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Basic Concepts of Pathophysiology
Study Questions
Introduction
Explanation
Choice A reason: This is a correct definition of pathophysiology and does not indicate a need for further teaching.
Choice B reason: This is a correct definition of pathophysiology nursing and does not indicate a need for further teaching.
Choice C reason: This is a correct description of what pathophysiology nursing involves and does not indicate a need for further teaching.
Choice D reason: This is an incorrect statement that contradicts the text and indicates a need for further teaching.
Explanation
Choice A reason: This is a correct answer because family history of diabetes is a genetic risk factor that can increase the likelihood of inheriting defects in insulin production or action.
Choice B reason: This is a correct answer because obesity is a modifiable risk factor that can cause insulin resistance, a condition in which cells do not respond properly to insulin and glucose accumulates in the blood.
Choice C reason: This is an incorrect answer because smoking is not a risk factor for developing diabetes mellitus, although it can worsen its complications such as cardiovascular disease and kidney disease.
Choice D reason: This is an incorrect answer because hypertension is not a risk factor for developing diabetes mellitus, although it can be associated with it and increase the risk of cardiovascular complications.
Choice E reason: This is a correct answer because physical inactivity is a modifiable risk factor that can reduce insulin sensitivity and glucose utilization by muscles, leading to hyperglycemia.
Explanation
Choice A reason: This is a correct answer because it accurately describes the pathogenesis of asthma and its triggers. Asthma is caused by an overreaction of the immune system to certain triggers, such as allergens, infections, or irritants, that leads to inflammation, bronchoconstriction, mucus production, and coughing.
Choice B reason: This is an incorrect answer because it confuses asthma with another condition called pulmonary hypertension, which is characterized by high blood pressure in the lungs and reduced oxygen supply.
Choice C reason: This is an incorrect answer because it confuses asthma with another condition called pulmonary edema, which is characterized by fluid accumulation in the lungs and impaired gas exchange.
Choice D reason: This is an incorrect answer because it confuses asthma with another condition called cystic fibrosis, which is a genetic disorder that affects the mucus glands and causes thick and sticky mucus in the lungs and other organs.
Explanation
Choice A reason: This is an incorrect answer because feeling tired and weak are common symptoms of pneumonia, but not indicative of a complication.
Choice B reason: This is an incorrect answer because coughing up yellow-green sputum with some blood is a common sign of pneumonia, but not indicative of a complication.
Choice C reason: This is an incorrect answer because having chest pain that worsens with deep breathing is a common sign of pleurisy (inflammation of the lining of the lungs), which is often associated with pneumonia, but not indicative of a complication.
Choice D reason: This is a correct answer because having trouble breathing and cyanosis are signs of hypoxemia, which is a possible complication of pneumonia that can lead to respiratory failure and death.
Explanation
Choice A reason: This is a correct answer because obtaining a blood culture from the client before administering the antibiotic can help identify the causative microorganism and its sensitivity to different antibiotics, which can guide the selection of the most appropriate antibiotic therapy.
Choice B reason: This is an incorrect answer because checking the client's vital signs and oxygen saturation is an ongoing intervention that should be performed throughout the course of treatment, but not necessarily before administering the antibiotic.
Choice C reason: This is an incorrect answer because assessing the client's level of consciousness and orientation is an ongoing intervention that should be performed throughout the course of treatment, but not necessarily before administering the antibiotic.
Choice D reason: This is an incorrect answer because flushing the client's intravenous line with normal saline is an intervention that should be performed after administering the antibiotic, not before, to ensure that no residual antibiotic remains in the line.
Inflammation and Healing
Explanation
Choice A reason: Frostbite is caused by exposure to extreme cold, which is a physical factor that can damage the cells. Physical injury can result in cell membrane damage, cytoplasmic swelling, organelle dysfunction, or DNA breakage.
Choice B reason: Chemical injury is caused by exposure to toxic substances, poisons, or pollutants that can damage the cells. Chemical injury can result in cell membrane damage, cytoplasmic swelling, organelle dysfunction, or DNA breakage.
Choice C reason: Biological injury is caused by infection by microorganisms, such as bacteria, viruses, fungi, or parasites that can damage the cells. Biological injury can result in inflammation, immune response, or tissue damage.
Choice D reason: Genetic injury is caused by mutations or alterations in the DNA that can damage the cells. Genetic injury can result in abnormal protein synthesis, impaired cell function, or inherited diseases.
Explanation
Choice A reason: Bilirubin is a yellow pigment that is produced from the breakdown of hemoglobin in red blood cells. It is normally excreted by the liver into bile and then eliminated by the intestines. However, when there is an obstruction of bile flow in the liver due to cirrhosis, bilirubin accumulates in the blood and tissues, causing jaundice.
Choice B reason: Lipofuscin is a brown pigment that is derived from the oxidation of lipids and proteins in the cells. It is also known as "wear and tear" pigment because it accumulates with aging and reflects the cumulative damage to the cells.
Choice C reason: Steatosis is a condition where fat accumulates in the cytoplasm of hepatocytes (liver cells). It can be caused by various factors, such as alcohol abuse, obesity, diabetes, or malnutrition.
Choice D reason: Phenylketonuria is a genetic disorder where phenylalanine, an amino acid, cannot be converted into tyrosine, another amino acid, due to a deficiency of an enzyme called phenylalanine hydroxylase. This leads to a buildup of phenylalanine and its metabolites in the blood and tissues, causing brain damage and mental retardation.
Explanation
Choice A reason: "An unregulated and passive process of cell death that causes inflammation and tissue damage." This is a description of necrosis, not apoptosis. Necrosis is an abnormal and harmful process that occurs when the cells are exposed to severe or persistent stressors that overwhelm their adaptive capacity. It involves the loss of cell membrane integrity, the release of cellular contents into the extracellular space, and the initiation of an inflammatory response that can damage the surrounding tissues.
Choice B reason: Apoptosis is also known as programmed cell death or cell suicide. It is a normal and beneficial process that maintains the balance between cell proliferation and cell death. It involves a series of biochemical events that lead to the activation of enzymes called caspases, which degrade the cell's DNA, proteins, and organelles. The cell then shrinks and forms membrane-bound fragments called apoptotic bodies, which are phagocytosed by macrophages or neighboring cells without causing inflammation or tissue damage.
Choice C reason: "A reversible process of cell injury that occurs when the stressor is mild or removed." This is a description of reversible cell injury, not apoptosis. Reversible cell injury is a process that occurs when the cells are exposed to mild or transient stressors that do not exceed their adaptive capacity. It involves changes in cell metabolism, function, and structure that can be restored if the stressor is removed or the cells are able to adapt.
Choice D reason: "An irreversible process of cell injury that occurs when the stressor is severe or persistent." This is a description of irreversible cell injury, not apoptosis. Irreversible cell injury is a process that occurs when the cells are exposed to severe or persistent stressors that exceed their adaptive capacity. It involves changes in cell metabolism, function, and structure that cannot be restored and lead to cell death by necrosis or apoptosis.
Explanation
Choice A reason: Phenylketonuria (PKU) is a genetic disorder where phenylalanine, an amino acid, cannot be converted into tyrosine, another amino acid, due to a deficiency of an enzyme called phenylalanine hydroxylase. This leads to a buildup of phenylalanine and its metabolites in the blood and tissues, causing brain damage and mental retardation.
Choice B reason: Tyrosine is another amino acid that is normally produced from phenylalanine by the enzyme phenylalanine hydroxylase. However, in PKU, this enzyme is deficient, so tyrosine levels are low in the blood and tissues.
Choice C reason: Glucose is a simple sugar that is the main source of energy for the cells. It is not directly related to PKU, although some people with PKU may have low blood glucose levels due to dietary restrictions.
Choice D reason: Glycogen is a complex carbohydrate that is stored in the liver and muscles as a reserve source of energy. It is not directly related to PKU, although some people with PKU may have glycogen storage disease, which is a separate genetic disorder where glycogen cannot be broken down into glucose due to a deficiency of an enzyme called glucose-6-phosphatase.
Immunity and Hypersensitivity
Explanation
Choice A reason: Type II hypersensitivity is caused by the binding of IgG or IgM antibodies to antigens on the surface of target cells. This leads to complement activation, opsonization, phagocytosis, or antibody-dependent cellular cytotoxicity (ADCC) of the target cells. It is seen in conditions such as hemolytic anemia, transfusion reactions, or Graves' disease.
Choice B reason: Type III hypersensitivity is caused by the deposition of immune complexes in the tissues and blood vessels. This leads to complement activation, inflammation, and tissue damage. It is seen in conditions such as systemic lupus erythematosus (SLE), rheumatoid arthritis, or serum sickness.
Choice C reason: Type IV hypersensitivity is caused by the activation of cytotoxic T cells or helper T cells that release cytokines and recruit macrophages and other inflammatory cells. This leads to delayed and cell-mediated reactions, such as contact dermatitis, tuberculin reaction, or graft rejection.
Explanation
Choice A reason: Type I hypersensitivity is not involved in tuberculin skin test, as it does not involve IgE antibodies or mast cells.
Choice B reason: Type II hypersensitivity is not involved in tuberculin skin test, as it does not involve IgG or IgM antibodies or target cells.
Choice C reason: Type III hypersensitivity is not involved in tuberculin skin test, as it does not involve immune complexes or complement activation.
Choice D reason: Type IV hypersensitivity is involved in tuberculin skin test, as it involves the activation of helper T cells that recognize the mycobacterial antigens injected into the skin and release cytokines that recruit macrophages and other inflammatory cells. This leads to a delayed and indurated reaction at the site of injection.
Choice E reason: Type V hypersensitivity is also involved in tuberculin skin test, as it involves the activation of cytotoxic T cells that recognize the mycobacterial antigens presented by MHC class I molecules on infected cells and destroy them by releasing perforin and granzymes. This leads to a cell-mediated reaction at the site of infection.
Explanation
Choice B reason: An anaphylactic transfusion reaction is a type of transfusion reaction that occurs when the recipient has IgE antibodies against plasma proteins in the donor blood and causes a systemic allergic response. It manifests as urticaria, pruritus, bronchospasm, laryngeal edema, hypotension, or shock.
Choice C reason: A febrile nonhemolytic transfusion reaction is a type of transfusion reaction that occurs when the recipient has antibodies against leukocytes or platelets in the donor blood and causes a mild inflammatory response. It manifests as fever, chills, headache, or malaise.
Choice D reason: A transfusion-related acute lung injury is a type of transfusion reaction that occurs when the donor has antibodies against leukocytes in the recipient blood and causes pulmonary edema and respiratory distress. It manifests as dyspnea, hypoxia, hypotension, or fever.
Explanation
Choice B reason: A type II hypersensitivity reaction is not involved in bee sting allergy, as it does not involve IgG or IgM antibodies or target cells.
Choice C reason: A type III hypersensitivity reaction is not involved in bee sting allergy, as it does not involve immune complexes or complement activation.
Choice D reason: A type IV hypersensitivity reaction is not involved in bee sting allergy, as it does not involve cytotoxic T cells or helper T cells.
Explanation
Choice B reason: SLE is not an immunodeficiency disease, as it does not cause a reduced number or function of immune cells. Immunodeficiency diseases are characterized by increased susceptibility to infections and malignancies due to impaired immune response.
Choice C reason: SLE is not an infectious disease, as it is not caused by bacteria or viruses that invade the body. Infectious diseases are characterized by fever, malaise, lymphadenopathy, and organ-specific symptoms due to microbial invasion and replication.
Choice D reason: SLE is not a neoplastic disease, as it does not cause an abnormal growth and proliferation of immune cells. Neoplastic diseases are characterized by masses or tumors that result from uncontrolled cell division and differentiation.
Infection and Sepsis
Explanation
Choice C reason: Community-acquired infection is an infection that is acquired outside of a health care setting, such as a UTI caused by E. coli. E. coli is a common cause of UTI and is usually found in the intestinal tract or fecal matter.
Choice A reason: Nosocomial infection is an infection that is acquired in a health care setting, such as a surgical site infection or a catheter-associated bloodstream infection. Nosocomial infections are often caused by multidrug-resistant organisms, such as methicillin-resistant Staphylococcus aureus (MRSA) or vancomycin-resistant Enterococcus (VRE).
Choice B reason: Opportunistic infection is an infection that occurs in immunocompromised individuals, such as those with HIV/AIDS, cancer, or organ transplantation. Opportunistic infections are caused by microorganisms that are normally harmless or part of the normal flora, but become pathogenic when the host's defenses are weakened. Some examples of opportunistic infections are Pneumocystis jirovecii pneumonia, Candida albicans thrush, or cytomegalovirus retinitis.
Choice D reason: Latent infection is an infection that remains dormant or inactive in the host for a period of time, but can reactivate and cause disease when the host's immunity declines. Some examples of latent infections are herpes simplex virus, varicella-zoster virus, or Mycobacterium tuberculosis.
Explanation
Choice A reason: Sepsis is a life-threatening condition that occurs when the body has a systemic inflammatory response to an infection, which can be bacterial, viral, fungal, or parasitic. The inflammatory response involves the activation of immune cells, cytokines, complement, coagulation, and fibrinolysis pathways that cause widespread vasodilation, increased vascular permeability, and microvascular thrombosis.
Choice B reason: Sepsis can cause organ dysfunction or failure due to impaired tissue perfusion and oxygen delivery. The vasodilation and increased vascular permeability cause hypotension and hypovolemia, which reduce the cardiac output and blood pressure. The microvascular thrombosis causes obstruction and ischemia of the capillaries, which impair the oxygen and nutrient exchange to the tissues. The tissue hypoxia causes anaerobic metabolism and lactic acidosis, which further worsen the organ function.
Choice C reason: Sepsis can be diagnosed by measuring the blood lactate level, which indicates the severity of tissue hypoxia. Lactate is a product of anaerobic metabolism that accumulates in the blood when the oxygen delivery to the tissues is insufficient. A normal blood lactate level is less than 2 mmol/L. A blood lactate level of 2 to 4 mmol/L indicates moderate tissue hypoxia and sepsis. A blood lactate level of more than 4 mmol/L indicates severe tissue hypoxia and septic shock.
Choice D reason: Sepsis cannot be prevented by taking antibiotics regularly and avoiding contact with sick people. Taking antibiotics regularly can increase the risk of antibiotic resistance and superinfection by killing the normal flora and allowing opportunistic pathogens to grow. Avoiding contact with sick people can reduce the exposure to infectious agents, but it cannot eliminate the risk of sepsis completely, as some infections can be asymptomatic or latent.
Choice E reason: Sepsis can be treated by administering fluids, vasopressors, oxygen, and antibiotics as soon as possible. Fluids are given to restore the intravascular volume and improve the tissue perfusion and oxygen delivery. Vasopressors are given to increase the blood pressure and maintain the vital organ function. Oxygen is given to correct the hypoxemia and reduce the tissue hypoxia. Antibiotics are given to eradicate the causative microorganism and control the infection.
Explanation
Choice D reason: The client has signs and symptoms of cardiac, renal, and neurologic dysfunction due to sepsis.
Choice A reason: Cardiac dysfunction is indicated by tachycardia and hypotension, which reflect the impaired cardiac output and blood pressure due to sepsis. The cardiac dysfunction can lead to cardiogenic shock, myocardial ischemia, or arrhythmias.
Choice B reason: Renal dysfunction is indicated by oliguria, which reflects the reduced renal perfusion and glomerular filtration rate due to sepsis. The renal dysfunction can lead to acute kidney injury, electrolyte imbalance, or metabolic acidosis.
Choice C reason: Neurologic dysfunction is indicated by altered mental status, which reflects the reduced cerebral perfusion and oxygenation due to sepsis. The neurologic dysfunction can lead to delirium, coma, seizures, or stroke.
Explanation
Choice C reason: Purulent exudate is a type of exudate that contains pus, which is composed of dead neutrophils, bacteria, and cellular debris. It has a creamy white or yellow, purulent, and sometimes bloody appearance and a foul odor. It is seen in wound infections caused by pyogenic bacteria, such as S. aureus.
Choice A reason: Serous exudate is a type of exudate that contains clear or yellowish fluid that accumulates in body cavities or on the surface of tissues. It has a watery and thin appearance and no odor. It is seen in conditions such as blisters or pericarditis.
Choice B reason: Sanguineous exudate is a type of exudate that contains blood or blood cells that leak from damaged blood vessels. It has a red or brown appearance and no odor. It is seen in conditions such as trauma, surgery, or malignancy.
Choice D reason: Fibrinous exudate is a type of exudate that contains fibrin, which is a protein that forms a meshwork of fibers that seal and stabilize the wound. It has a sticky and thick appearance and no odor. It is seen in conditions such as rheumatic fever or pleurisy.
A nurse is administering antibiotics to a client who has septic shock. The nurse understands that the goal of antibiotic therapy in septic shock is to achieve what outcome?
Explanation
Choice A reason: Eradicate the causative microorganism within 24 hours. The goal of antibiotic therapy in septic shock is to eradicate the causative microorganism as soon as possible, preferably within 24 hours of diagnosis or sooner if possible. This can reduce the bacterial load, control the infection, and prevent further complications.
Choice B reason: Reduce the inflammatory response within 48 hours is not the goal of antibiotic therapy in septic shock, as antibiotics do not directly affect the inflammatory response. Antibiotics can indirectly reduce the inflammatory response by eradicating the microorganism that triggers it, but this may take longer than 48 hours to achieve.
Choice C reason: Restore the tissue perfusion and oxygen delivery within 72 hours is not the goal of antibiotic therapy in septic shock, as antibiotics do not directly affect the tissue perfusion and oxygen delivery. Antibiotics can indirectly restore the tissue perfusion and oxygen delivery by eradicating the microorganism that causes vasodilation, hypotension, hypovolemia, and microvascular thrombosis, but this may take longer than 72 hours to achieve.
Choice D reason: Prevent the development of multiple organ dysfunction syndrome within 96 hours is not the goal of antibiotic therapy in septic shock, as antibiotics do not directly prevent the development of multiple organ dysfunction syndrome. Antibiotics can indirectly prevent the development of multiple organ dysfunction syndrome by eradicating the microorganism that causes tissue hypoxia, lactic acidosis, and organ failure, but this may take longer than 96 hours to achieve.
Neoplasia
A nurse is caring for a client who has a benign neoplasm of the thyroid gland. The nurse understands that this type of neoplasm has which of the following characteristics? (Select all that apply.)
Explanation
Choice A reason:
A benign neoplasm grows slowly and remains localized within its site of origin. It does not spread to other parts of the body or cause systemic effects.
Choice B reason:
A malignant neoplasm invades surrounding tissues and organs and destroys their normal function. It can also penetrate blood vessels or lymphatics and disseminate to distant sites, forming secondary tumors or metastases.
Choice C reason:
A benign neoplasm can differentiate into normal cells that resemble the tissue of origin. It has a well-defined shape and structure and retains some of its normal functions.
Choice D reason:
A malignant neoplasm can metastasize to distant sites via blood or lymph, creating new foci of tumor growth and increasing the complexity and severity of the disease.
Choice E reason:
A benign neoplasm can cause compression or obstruction of nearby structures, such as nerves, blood vessels, ducts, or organs. This can result in pain, ischemia, inflammation, or dysfunction of the affected structures.
A nurse is teaching a client who has colon cancer about the staging system used to assess the extent of the tumor. The nurse explains that the most commonly used staging system is based on what criteria? (Select all that apply.)
Explanation
Choice A reason:
The size and number of primary tumors are important criteria for staging cancer, as they indicate the local growth and expansion of the tumor within its site of origin. The larger and more numerous the tumors are, the higher the stage of cancer is.
Choice B reason:
The presence or absence of regional lymph node involvement is another important criterion for staging cancer, as it indicates the spread of the tumor to the nearby lymphatic system. The more lymph nodes are affected, the higher the stage of cancer is.
Choice C reason:
The presence or absence of distant metastases is the most important criterion for staging cancer, as it indicates the spread of the tumor to other parts of the body via blood or lymph. The presence of any distant metastasis usually indicates the highest stage of cancer.
Choice D reason:
The degree of cellular differentiation and resemblance to normal tissue is a criterion for grading cancer, not staging cancer. Grading cancer assesses the severity and aggressiveness of the tumor based on its histologic appearance and behavior.
Choice E reason:
The level of tumor markers in the blood or other body fluids is a criterion for monitoring cancer, not staging cancer. Tumor markers are substances produced by tumor cells or by the body in response to tumor cells that can be detected in laboratory tests. They can help diagnose, prognose, or evaluate the response to treatment of cancer.
A nurse is administering chemotherapy to a client who has breast cancer. The client asks the nurse how chemotherapy works to treat cancer. Which of the following statements should the nurse include in the response?
Explanation
Choice A reason:
Chemotherapy kills cancer cells by interfering with their DNA synthesis and replication. Chemotherapy drugs are cytotoxic agents that target rapidly dividing cells, such as cancer cells, and disrupt their cell cycle, DNA repair, or DNA replication mechanisms. This leads to cell death or apoptosis.
Choice B reason:
Radiation therapy kills cancer cells by exposing them to high-energy radiation that damages their DNA. Radiation therapy uses ionizing radiation, such as x-rays, gamma rays, or protons, that create free radicals that break DNA strands and cause mutations or chromosomal aberrations in cancer cells.
Choice C reason:
Immunotherapy kills cancer cells by stimulating the immune system to recognize and destroy them. Immunotherapy uses biological agents, such as monoclonal antibodies, cytokines, vaccines, or adoptive cell transfer, that enhance the immune response against cancer cells or overcome their immune evasion strategies.
Choice D reason:
Hormone therapy kills cancer cells by blocking their hormone receptors and preventing their growth. Hormone therapy uses drugs that either inhibit the production or action of hormones, such as estrogen or testosterone, that stimulate the growth of hormone-dependent cancers, such as breast or prostate cancer.
A nurse is caring for a client who has a malignant neoplasm of the lung. The nurse notes that the client has dyspnea, cough, hemoptysis, and weight loss. The nurse recognizes that these findings are indicative of what type of manifestations of cancer?
Explanation
Choice D reason:
Metastatic manifestations are signs and symptoms of cancer that result from the spread of the tumor to distant organs or tissues. Lung cancer can metastasize to various sites, such as the brain, bone, liver, or adrenal glands, and cause organ-specific manifestations, such as dyspnea, cough, hemoptysis, and weight loss.
Choice A reason:
Local manifestations are signs and symptoms of cancer that result from the growth and expansion of the tumor within its site of origin. Lung cancer can cause local manifestations, such as chest pain, pleural effusion, or atelectasis.
Choice B reason:
Systemic manifestations are signs and symptoms of cancer that result from the effects of the tumor or its treatment on the whole body. Lung cancer can cause systemic manifestations, such as anorexia, cachexia, fatigue, or fever.
Choice C reason:
Paraneoplastic manifestations are signs and symptoms of cancer that result from the production of hormones or other substances by the tumor cells that affect normal body functions. Lung cancer can cause paraneoplastic manifestations, such as hypercalcemia, syndrome of inappropriate antidiuretic hormone secretion (SIADH), or Cushing's syndrome.
A nurse is teaching a client who has a family history of colon cancer about the risk factors and prevention strategies for the disease. Which of the following statements should the nurse include in the teaching?
Explanation
Choice B reason:
Dietary factors are important risk factors for colon cancer, as they can affect the composition and metabolism of the intestinal flora and the production of carcinogens or protective substances in the colon. Red meat, processed meat, and high-fat foods can increase the risk of colon cancer by increasing the production of heterocyclic amines, nitrosamines, or bile acids that can damage the colonic mucosa and promote tumor growth.
Choice A reason:
"You should have a colonoscopy every 10 years starting at age 50 to screen for colon cancer." This statement is not correct for a client who has a family history of colon cancer, as they have a higher risk of developing the disease than the general population. They should have a colonoscopy every 5 years starting at age 40 or 10 years earlier than the age at which their relative was diagnosed with colon cancer.
Choice C reason:
"You should take aspirin daily to prevent inflammation and polyp formation in your colon." This statement is not correct for a client who has a family history of colon cancer, as they may have other medical conditions or contraindications that make aspirin use unsafe or inappropriate for them. Aspirin is a nonsteroidal anti-inflammatory drug (NSAID) that can reduce the risk of colon cancer by inhibiting cyclooxygenase-2 (COX-2) enzyme that stimulates inflammation and angiogenesis in the colon. However, aspirin can also cause side effects such as bleeding, ulcers, or allergic reactions in some clients.
Choice D reason:
"You should increase your intake of calcium and vitamin D to protect your colon from cancer." This statement is not correct for a client who has a family history of colon cancer, as there is insufficient evidence to support the role of calcium and vitamin D in preventing colon cancer. Calcium and vitamin D may have some protective effects on the colon by binding to bile acids or regulating cell proliferation and differentiation in the colonic mucosa. However, they may also have adverse effects on other organs or systems, such as increasing the risk of kidney stones or cardiovascular disease.
Genetic and Congenital Disorders
A nurse is caring for a client who has a family history of Huntington disease. The nurse understands that this condition is caused by what type of mutation in a single gene?
Explanation
Choice B reason Huntington disease is caused by a mutation in the HTT gene that encodes for the huntingtin protein. The mutation involves an expansion of the CAG trinucleotide repeat in the gene, which results in an abnormal protein with an elongated polyglutamine tract. This protein gains a new toxic function that interferes with the normal function of other proteins and causes neuronal degeneration in the brain.
Choice A reason:
Loss-of-function mutation is a type of mutation that reduces or eliminates the normal function of a gene or protein. This can result in diseases such as cystic fibrosis, phenylketonuria, or sickle cell anemia.
Choice C reason:
Haploinsufficiency mutation is a type of mutation that reduces the amount or activity of a gene or protein to less than 50% of the normal level. This can result in diseases such as Marfan syndrome, familial hypercholesterolemia, or Waardenburg syndrome.
Choice D reason:
Dominant negative mutation is a type of mutation that produces an abnormal protein that interferes with the normal protein and prevents it from functioning properly. This can result in diseases such as osteogenesis imperfecta, Ehlers-Danlos syndrome, or Holt-Oram syndrome.
A nurse is teaching a pregnant client who has been diagnosed with gestational diabetes mellitus (GDM). The nurse explains that GDM can increase the risk of congenital disorders in the fetus, such as:
Explanation
Choice D reason: GDM can increase the risk of congenital disorders in the fetus, such as neural tube defects, cardiac defects, and cleft lip and palate. GDM is a condition that occurs when the mother develops insulin resistance and hyperglycemia during pregnancy. This can affect the fetal development and cause various complications, such as macrosomia, hypoglycemia, polycythemia, or respiratory distress syndrome.
Choice A reason:
Neural tube defects are congenital disorders that occur when the neural tube fails to close properly during the first month of embryonic development. This can result in defects such as spina bifida, anencephaly, or encephalocele. GDM can increase the risk of neural tube defects by altering the maternal-fetal glucose metabolism and affecting the folate metabolism.
Choice B reason:
Cardiac defects are congenital disorders that occur when the heart or blood vessels fail to form or function properly during the fetal development. This can result in defects such as atrial septal defect, ventricular septal defect, patent ductus arteriosus, or tetralogy of Fallot. GDM can increase the risk of cardiac defects by causing fetal hyperinsulinemia and hypoxia, which can impair the cardiac morphogenesis and differentiation.
Choice C reason:
Cleft lip and palate are congenital disorders that occur when the upper lip or palate fail to fuse completely during the first trimester of fetal development. This can result in defects such as unilateral or bilateral cleft lip, cleft palate, or both. GDM can increase the risk of cleft lip and palate by affecting the maternal-fetal glucose metabolism and causing oxidative stress and inflammation in the developing tissues.
A nurse is assessing a newborn who has Down syndrome. The nurse observes that the newborn has slanted eyes, a flat nose bridge, a protruding tongue, and a single palmar crease. The nurse recognizes that these findings are indicative of what type of chromosomal disorder?
Explanation
Choice A reason "Trisomy 21." Down syndrome is a chromosomal disorder that occurs when there is an extra copy of chromosome 21 in the cells. This can result in physical and mental developmental delays and various health problems. The features that the nurse observed are typical of Down syndrome, such as slanted eyes, a flat nose bridge, a protruding tongue, and a single palmar crease.
Choice B reason:
"Monosomy X." Turner syndrome is a chromosomal disorder that occurs when there is a missing or partially missing X chromosome in females. This can result in short stature, infertility, heart defects, and other health problems. The features that the nurse observed are not typical of Turner syndrome, which may include a webbed neck, a low hairline, a broad chest, or swollen hands and feet.
Choice C reason:
"XXY." Klinefelter syndrome is a chromosomal disorder that occurs when there is an extra X chromosome in males. This can result in low testosterone levels, infertility, gynecomastia, and other health problems. The features that the nurse observed are not typical of Klinefelter syndrome, which may include tall stature, small testes, sparse body hair, or learning difficulties.
Choice D reason:
"Deletion of 5p." Cri du chat syndrome is a chromosomal disorder that occurs when there is a deletion of part of the short arm of chromosome 5. This can result in intellectual disability, microcephaly, facial abnormalities, and other health problems. The features that the nurse observed are not typical of Cri du chat syndrome, which may include a high-pitched cat-like cry, epicanthal folds, low-set ears, or a small jaw.
A nurse is caring for a client who has a congenital disorder caused by an environmental factor. The nurse understands that this type of congenital disorder is caused by what type of factor?
Explanation
Choice A reason:
Teratogenic factor. A teratogenic factor is an environmental factor that can cause congenital disorders by interfering with the normal development of the fetus during the prenatal period. Teratogenic factors can include drugs, chemicals, infections, radiation, or maternal conditions that can affect the fetal growth and differentiation. Some examples of teratogenic factors are alcohol, thalidomide, rubella, ionizing radiation, or diabetes mellitus.
Choice B reason:
Mutagenic factor is an environmental factor that can cause genetic disorders by inducing changes in the DNA sequence or structure of the cells. Mutagenic factors can include chemicals, radiation, or viruses that can damage the DNA and cause mutations or chromosomal aberrations. Some examples of mutagenic factors are benzene, ultraviolet light, or human papillomavirus.
Choice C reason:
Carcinogenic factor is an environmental factor that can cause cancer by promoting the abnormal and uncontrolled growth of cells. Carcinogenic factors can include chemicals, radiation, or viruses that can interact with the DNA and cause mutations or epigenetic alterations that affect the gene expression or function. Some examples of carcinogenic factors are tobacco smoke, asbestos, or hepatitis B virus.
Choice D reason:
Epigenetic factor is an environmental factor that can cause genetic or congenital disorders by modifying the gene expression or function without changing the DNA sequence or structure. Epigenetic factors can include chemicals, nutrients, hormones, or stress that can affect the DNA methylation, histone modification, or microRNA expression that regulate the gene activity or silencing. Some examples of epigenetic factors are folate, estrogen, or cortisol.
Fluid, Electrolyte, and Acid-Base Balance
A nurse is caring for a client who has fluid overload due to heart failure. Which of the following clinical manifestations should the nurse expect to find in the client?
Explanation
The correct answer is: c. Crackles in the lungs
Choice A: Dry mucous membranes
Reason: Dry mucous membranes are typically associated with dehydration, not fluid overload. In fluid overload, the body retains excess fluid, leading to symptoms such as edema and pulmonary congestion, rather than dryness of mucous membranes.
Choice B: Decreased urine output
Reason: Decreased urine output can occur in conditions like dehydration or renal failure. In fluid overload due to heart failure, the kidneys may initially try to excrete excess fluid, leading to increased urine output. However, as heart failure progresses, renal perfusion may decrease, potentially leading to reduced urine output. This is not a primary or consistent symptom of fluid overload.
Choice C: Crackles in the lungs
Reason: Crackles in the lungs are a hallmark sign of fluid overload, particularly in the context of heart failure. This occurs due to pulmonary edema, where excess fluid accumulates in the alveoli, causing the characteristic crackling sound during auscultation. This is a direct result of the heart’s inability to effectively pump blood, leading to fluid backing up into the lungs.
Choice D: Hypotension
Reason: Hypotension, or low blood pressure, is not typically associated with fluid overload. In fact, fluid overload can often lead to hypertension (high blood pressure) due to the increased volume of fluid in the circulatory system. Hypotension might occur in severe heart failure if the heart’s pumping ability is significantly compromised, but it is not a primary manifestation of fluid overload.
A nurse is reviewing the laboratory results of a client who has metabolic acidosis. Which of the following electrolyte imbalances should the nurse anticipate? (Select all that apply.)
Explanation
Choice A reason:
Hyperkalemia is a common electrolyte imbalance in metabolic acidosis. The excess hydrogen ions in the blood cause a shift of potassium from the intracellular to the extracellular space, resulting in increased serum potassium levels.
Choice B reason:
Hyponatremia is a possible electrolyte imbalance in metabolic acidosis. The excess hydrogen ions in the blood can cause a dilutional effect on sodium, resulting in decreased serum sodium levels.
Choice C reason:
Hypercalcemia is not an electrolyte imbalance in metabolic acidosis. In fact, metabolic acidosis can cause hypocalcemia due to increased binding of calcium to albumin and decreased ionized calcium levels.
Choice D reason:
Hypophosphatemia is not an electrolyte imbalance in metabolic acidosis. In fact, metabolic acidosis can cause hyperphosphatemia due to increased renal excretion of hydrogen ions and decreased renal excretion of phosphate.
Choice E reason:
Hypochloremia is a common electrolyte imbalance in metabolic acidosis. The excess hydrogen ions in the blood cause a loss of chloride from the kidneys, resulting in decreased serum chloride levels.
A nurse is teaching a client who has respiratory alkalosis about the causes and prevention of this condition. Which of the following statements by the client indicates an understanding of the teaching?
Explanation
Choice A reason:
Aspirin or other salicylates can cause metabolic acidosis, not respiratory alkalosis, by increasing the production of organic acids and interfering with bicarbonate reabsorption in the kidneys.
Choice B reason:
Breathing into a paper bag when feeling anxious can help prevent or treat respiratory alkalosis by increasing the carbon dioxide levels in the blood and lowering the pH. Anxiety can cause respiratory alkalosis by stimulating hyperventilation, which decreases the carbon dioxide levels in the blood and raises the pH.
Choice C reason:
Drinking more fluids to prevent dehydration can help prevent or treat metabolic alkalosis, not respiratory alkalosis, by increasing the renal excretion of bicarbonate and lowering the pH. Dehydration can cause metabolic alkalosis by decreasing the renal excretion of bicarbonate and raising the pH.
Choice D reason:
Monitoring blood sugar levels regularly can help prevent or treat diabetic ketoacidosis, which is a type of metabolic acidosis, not respiratory alkalosis, by increasing the production of ketone bodies and lowering the pH. Diabetic ketoacidosis can occur when there is insufficient insulin to metabolize glucose and the body resorts to fat breakdown for energy.
A nurse is assessing a client who has diabetic ketoacidosis (DKA) and notes that the client has Kussmaul respirations. Which of the following explanations should the nurse give to the client about this type of breathing pattern?
Explanation
Choice A reason:
Kussmaul respirations are not a compensatory mechanism to increase oxygen intake, but rather to decrease carbon dioxide levels in the blood. Oxygen intake is not affected by Kussmaul respirations, which are characterized by deep and rapid breaths.
Choice B reason:
Kussmaul respirations are not a sign of respiratory failure and impending coma, but rather a sign of metabolic acidosis and an attempt to correct it. Respiratory failure and coma can occur in DKA if the condition is not treated promptly and effectively, but they are not indicated by Kussmaul respirations alone.
Choice C reason:
Kussmaul respirations are not an attempt to lower blood pressure by exhaling more air, but rather an attempt to lower blood acidity by exhaling more carbon dioxide. Blood pressure is not affected by Kussmaul respirations, which are caused by increased acidity in the blood due to the accumulation of ketone bodies from fat breakdown.
Choice D reason:
Kussmaul respirations are a response to lower blood acidity by exhaling more carbon dioxide. Carbon dioxide is an acidic gas that can lower the pH of the blood when it accumulates. By exhaling more carbon dioxide, the body tries to raise the pH of the blood and compensate for the metabolic acidosis caused by DKA.
A nurse is planning care for a client who has hypocalcemia. Which of the following interventions should the nurse include in the plan?
Explanation
Choice A reason:
Administering calcium gluconate IV as prescribed is an intervention that the nurse should include in the plan for a client who has hypocalcemia. Calcium gluconate is a calcium supplement that can increase the serum calcium levels and treat hypocalcemia. It should be given slowly and carefully to avoid extravasation and tissue necrosis.
Choice B reason:
Monitoring for Chvostek's sign and Trousseau's sign is an intervention that the nurse should include in the plan for a client who has hypocalcemia. Chvostek's sign is a facial twitching that occurs when the facial nerve is tapped near the ear. Trousseau's sign is a carpal spasm that occurs when a blood pressure cuff is inflated above the systolic pressure for several minutes. Both signs indicate increased neuromuscular excitability due to low calcium levels.
Choice C reason:
Encouraging intake of foods high in calcium and vitamin D is an intervention that the nurse should include in the plan for a client who has hypocalcemia. Calcium and vitamin D are essential nutrients for bone health and calcium metabolism. Foods high in calcium include dairy products, green leafy vegetables, tofu, sardines, and fortified cereals. Foods high in vitamin D include fatty fish, egg yolks, cheese, and fortified milk.
Summary
Explanation
Choice A reason:
Increased white blood cell count is a finding that the nurse should expect to indicate inflammation and healing. White blood cells are the main components of the immune system that fight against infection and promote tissue repair. An elevated white blood cell count reflects an increased production and mobilization of these cells in response to inflammation and healing.
Choice B reason:
Decreased erythrocyte sedimentation rate is not a finding that the nurse should expect to indicate inflammation and healing. Erythrocyte sedimentation rate is a measure of how fast red blood cells settle at the bottom of a test tube. A high erythrocyte sedimentation rate indicates increased inflammation, as inflammatory proteins cause red blood cells to clump together and fall faster. A low erythrocyte sedimentation rate indicates decreased inflammation or normal conditions.
Choice C reason:
Decreased C-reactive protein level is not a finding that the nurse should expect to indicate inflammation and healing. C-reactive protein is a protein produced by the liver that increases in response to inflammation or tissue damage. A high C-reactive protein level indicates increased inflammation, as C-reactive protein binds to damaged cells and activates the complement system, which enhances the inflammatory response. A low C-reactive protein level indicates decreased inflammation or normal conditions.
Choice D reason:
Increased albumin level is not a finding that the nurse should expect to indicate inflammation and healing. Albumin is a protein produced by the liver that maintains the osmotic pressure and fluid balance in the blood vessels. A low albumin level indicates malnutrition, liver disease, kidney disease, or chronic inflammation, as albumin is lost or consumed by these conditions. A high albumin level indicates dehydration, steroid use, or normal conditions.
Explanation
Choice A reason:
Administering epinephrine as prescribed is an intervention that the nurse should implement for a client who has anaphylactic shock due to a hypersensitivity reaction to a medication. Epinephrine is a medication that can reverse the effects of anaphylaxis by stimulating the sympathetic nervous system, which causes bronchodilation, vasoconstriction, increased cardiac output, and decreased release of inflammatory mediators.
Choice B reason:
Monitoring blood pressure and pulse oximetry is an intervention that the nurse should implement for a client who has anaphylactic shock due to a hypersensitivity reaction to a medication. Anaphylactic shock can cause hypotension and hypoxia due to vasodilation, increased capillary permeability, bronchoconstriction, and laryngeal edema. The nurse should monitor the client's vital signs and oxygen saturation regularly and report any changes or deterioration.
Choice C reason:
Administering antihistamines as prescribed is an intervention that the nurse should implement for a client who has anaphylactic shock due to a hypersensitivity reaction to a medication. Antihistamines are medications that can block the effects of histamine, which is one of the inflammatory mediators released during anaphylaxis. Antihistamines can help reduce itching, hives, flushing, and swelling.
Choice D reason:
Administering corticosteroids as prescribed is an intervention that the nurse should implement for a client who has anaphylactic shock due to a hypersensitivity reaction to a medication. Corticosteroids are medications that can suppress the immune system and reduce inflammation by inhibiting the synthesis of prostaglandins, leukotrienes, and cytokines, which are other inflammatory mediators released during anaphylaxis. Corticosteroids can help prevent or treat delayed or prolonged reactions.
Choice E reason:
Administering antibiotics as prescribed is not an intervention that the nurse should implement for a client who has anaphylactic shock due to a hypersensitivity reaction to a medication. Antibiotics are medications that can treat bacterial infections, but they have no effect on anaphylaxis, which is an immune-mediated reaction. In fact, some antibiotics can cause anaphylaxis in some clients who are allergic to them.
Explanation
Choice A reason:
Antibodies are proteins produced by B lymphocytes that can recognize and bind to specific antigens, such as viruses, and mark them for destruction by other immune cells or mechanisms. Antibodies are part of the adaptive immune system, which provides specific and long-lasting immunity against pathogens.
Choice B reason:
Natural killer cells are lymphocytes that can directly kill infected or abnormal cells by releasing cytotoxic substances that induce apoptosis. Natural killer cells are part of the innate immune system, which provides nonspecific and immediate immunity against pathogens, but they do not directly kill viruses, which are intracellular parasites.
Choice C reason:
Macrophages are phagocytes that can engulf and digest foreign particles, such as bacteria, fungi, or cellular debris. Macrophages are part of the innate immune system, which provides nonspecific and immediate immunity against pathogens, but they are not very effective against viruses, which are intracellular parasites.
Choice D reason:
Complement proteins are plasma proteins that can activate a cascade of reactions that enhance inflammation, opsonization, and lysis of pathogens. Complement proteins are part of the innate immune system, which provides nonspecific and immediate immunity against pathogens, but they do not activate viruses, which are inert particles outside of host cells.
Explanation
Choice A reason:
Genetic mutations are a factor that can contribute to neoplasia. Genetic mutations are changes in the DNA sequence of a cell that can affect its normal function and regulation. Some genetic mutations are inherited, while others are acquired due to environmental factors, such as radiation, chemicals, or smoking. Genetic mutations can cause oncogenes to be activated or tumor suppressor genes to be inactivated, which can result in uncontrolled cell proliferation and resistance to apoptosis.
Choice B reason:
Hormonal imbalances are a factor that can contribute to neoplasia. Hormonal imbalances are abnormal levels of hormones in the body that can affect the growth and differentiation of cells. Some hormones, such as estrogen and progesterone, can stimulate the growth of certain types of cells, such as breast and endometrial cells. Hormonal imbalances can increase the risk of developing hormone-dependent cancers, such as breast cancer or endometrial cancer.
Choice C reason:
Chronic inflammation is a factor that can contribute to neoplasia. Chronic inflammation is a prolonged and persistent inflammatory response that can damage normal tissues and cause tissue repair and regeneration. Chronic inflammation can increase the production of reactive oxygen species (ROS) and cytokines, which can induce DNA damage and genetic mutations. Chronic inflammation can also stimulate angiogenesis and invasion of inflammatory cells, which can promote tumor growth and metastasis.
Choice D reason:
Viral infections are a factor that can contribute to neoplasia. Viral infections are invasions of viruses into host cells that can cause disease or harm. Some viruses, such as human papillomavirus (HPV), hepatitis B virus (HBV), hepatitis C virus (HCV), Epstein-Barr virus (EBV), and human immunodeficiency virus (HIV), can cause neoplasia by integrating their DNA into the host cell's genome and altering its normal function and regulation. Viral infections can also impair the immune system's ability to recognize and eliminate abnormal cells.
Choice E reason:
Nutritional deficiencies are not a factor that can contribute to neoplasia. Nutritional deficiencies are inadequate intake or absorption of essential nutrients that can affect the health and function of various organs and systems. Nutritional deficiencies can increase the risk of developing infections or chronic diseases, but they do not directly cause neoplasia. However, some nutrients, such as antioxidants, vitamins, minerals, and fiber, may have protective effects against neoplasia by preventing oxidative stress, enhancing immune function, or modulating hormonal levels.
Further Questions on this Topic
A nurse is interpreting the results of a diagnostic test for a client who has tuberculosis, a chronic infectious disease caused by Mycobacterium tuberculosis that primarily affects the lungs. The test involves injecting a purified protein derivative (PPD) of the bacterium under the skin and measuring the induration (raised area) after 48 to 72 hours.
Which of the following results indicates a positive reaction for the client?
Explanation
Choice A reason:
This is an incorrect answer because an induration of 5 mm or more is considered a positive reaction only for certain high-risk groups, such as people who are HIV-positive, have recent contact with a person with active tuberculosis, or have chest radiograph findings consistent with prior tuberculosis.
Choice B reason:
This is a correct answer because an induration of 10 mm or more is considered a positive reaction for most people, including those who are recent immigrants from high-prevalence countries, injection drug users, residents or employees of high-risk settings, children younger than 4 years old, or people with certain medical conditions that increase the risk of tuberculosis.
Choice C reason:
This is an incorrect answer because an induration of 15 mm or more is considered a positive reaction only for people who have no known risk factors for tuberculosis.
Choice D reason:
This is an incorrect answer because an induration of 20 mm or more is not a criterion for a positive reaction, as it exceeds the maximum threshold for any group.
A nurse is caring for a client who has heart failure, a condition in which the heart cannot pump enough blood to meet the body's needs. The nurse observes that the client has crackles in the lungs, jugular vein distension, and peripheral edema.
Which of the following terms best describes these clinical manifestations?
Explanation
Choice A reason:
This is an incorrect answer because cardiogenic shock is a severe form of heart failure that occurs when the heart cannot pump enough blood to maintain adequate tissue perfusion and oxygenation, resulting in hypotension, tachycardia, oliguria, altered mental status, and cold and clammy skin.
Choice B reason:
This is an incorrect answer because pulmonary embolism is a condition in which a blood clot travels to the lungs and blocks one or more pulmonary arteries, causing sudden dyspnea, chest pain, hemoptysis, tachypnea, and hypoxia.
Choice C reason:
This is a correct answer because right-sided heart failure occurs when the right ventricle of the heart fails to pump blood effectively to the lungs, causing blood to back up in the systemic circulation and leading to fluid accumulation in the lungs, neck veins, and extremities.
Choice D reason:
This is an incorrect answer because left-sided heart failure occurs when the left ventricle of the heart fails to pump blood effectively to the body, causing blood to back up in the pulmonary circulation and leading to pulmonary congestion, dyspnea, orthopnea, coughing, and fatigue.
A nurse is administering an oral medication to a client who has peptic ulcer disease (PUD), a condition in which there are ulcers in the lining of the stomach or duodenum caused by excessive acid secretion or infection with Helicobacter pylori.
The medication belongs to a class of drugs called proton pump inhibitors (PPIs), which reduce acid production by blocking the enzyme that pumps hydrogen ions into the stomach.
Which of the following are expected outcomes of PPI therapy for PUD? (Select all that apply.)
Explanation
Choice A reason:
This is a correct answer because healing of ulcers is an expected outcome of PPI therapy for PUD, as it occurs when the acid-induced damage to the mucosa is repaired and the ulcer is closed.
Choice B reason:
This is a correct answer because relief of pain is an expected outcome of PPI therapy for PUD, as it occurs when the acid-induced irritation and inflammation of the mucosa and the nerve endings are reduced.
Choice C reason:
This is an incorrect answer because eradication of H. pylori is not an expected outcome of PPI therapy for PUD, as it requires a combination of antibiotics and bismuth compounds to kill the bacteria and prevent its recurrence.
Choice D reason:
This is a correct answer because prevention of bleeding is an expected outcome of PPI therapy for PUD, as it occurs when the acid-induced erosion and perforation of the mucosa and the blood vessels are prevented.
Choice E reason:
This is a correct answer because reduction of inflammation is an expected outcome of PPI therapy for PUD, as it occurs when the acid-induced activation of inflammatory mediators and immune cells are inhibited.
A nurse is caring for a client who has liver failure due to alcohol abuse. The nurse observes that the client has ascites, which is an accumulation of fluid in the abdominal cavity.
The nurse understands that this condition is caused by:
Explanation
Choice A reason:
Increased hydrostatic pressure in the portal vein is one factor that causes ascites. The portal vein carries blood from the digestive organs to the liver for processing. However, when the liver is damaged by alcohol abuse, it becomes scarred and fibrotic, creating resistance to blood flow. This results in increased pressure in the portal vein and its branches, which forces fluid out of the capillaries into the abdominal cavity.
Choice B reason:
Decreased oncotic pressure in the plasma is another factor that causes ascites. Oncotic pressure is the force exerted by proteins in the plasma that attracts fluid into the capillaries from the interstitial space. However, when the liver is damaged by alcohol abuse, it cannot produce enough proteins, such as albumin and globulin, which are essential for maintaining oncotic pressure. This results in decreased oncotic pressure in the plasma and increased fluid movement into the interstitial space and the abdominal cavity.
Choice C reason:
Increased aldosterone secretion by the adrenal glands is another factor that causes ascites. Aldosterone is a hormone that regulates the balance of sodium and water in the body. It acts on the kidneys to increase the reabsorption of sodium and water from the urine into the blood. However, when the liver is damaged by alcohol abuse, it cannot metabolize aldosterone properly, leading to its accumulation in the blood. This results in increased sodium and water retention in the body and increased fluid movement into the interstitial space and the abdominal cavity.
Choice D reason:
Ascites is caused by a combination of factors that affect the fluid balance in the abdominal cavity.
A nurse is teaching a client who has a family history of breast cancer about the risk factors and prevention strategies.
The nurse informs the client that one of the cellular adaptations that can increase the risk of breast cancer is:
Explanation
Choice A reason:
Atrophy is a decrease in cell size or number in response to adverse stimuli, such as disuse, ischemia, or malnutrition. It does not increase the risk of cancer, but it can impair the function of tissues and organs.
Choice B reason:
Hypertrophy is an increase in cell size in response to normal or abnormal stimuli, such as exercise, hormones, or hypertension. It does not increase the risk of cancer, but it can affect the function of tissues and organs.
Choice C reason:
Hyperplasia is an increase in cell number in response to normal or abnormal stimuli, such as hormones, inflammation, or wound healing. It does not increase the risk of cancer, but it can cause excessive growth of tissues and organs.
Choice D reason:
Dysplasia is an abnormal and potentially reversible change in cell size, shape, and organization in response to persistent stressors. It can be a precursor to cancer if it is not detected and treated early.
Explanation
Choice B reason:
Transparent film dressing is a type of dressing that consists of a thin sheet of polyurethane with an adhesive coating. It allows oxygen and moisture vapor to pass through but prevents bacteria and water from entering the wound. It is suitable for wounds with minimal drainage, such as superficial abrasions or donor sites.
Choice C reason:
Calcium alginate dressing is a type of dressing that consists of fibers derived from seaweed that form a gel-like substance when they come in contact with wound exudate. It absorbs large amounts of drainage and supports autolytic debridement of necrotic tissue. It is suitable for wounds with heavy drainage, such as pressure ulcers or venous ulcers.
Choice D reason:
Hydrogel dressing is a type of dressing that consists of water or glycerin-based gel that provides moisture to dry wounds and supports autolytic debridement of necrotic tissue. It is suitable for wounds with minimal to moderate drainage, such as partial-thickness burns or radiation injuries.
Explanation
Choice A reason:
Vascular stage is the stage of inflammation that involves the changes in blood flow and vascular permeability at the site of injury or infection. It manifests as redness and warmth due to vasodilation and increased blood flow, and swelling due to fluid leakage from the vessels into the interstitial space.
Choice B reason:
Cellular stage is the stage of inflammation that involves the migration of white blood cells from the vessels into the tissues to eliminate the causative agent and remove the damaged tissue. It manifests as pain due to the release of chemical mediators that stimulate nerve endings, and purulent drainage due to the accumulation of dead cells and microorganisms.
Choice D reason:
Resolution stage is the stage of inflammation that involves the restoration of normal tissue structure and function after the elimination of the causative agent and the removal of the damaged tissue. It manifests as decreased redness, warmth, swelling, pain, and drainage due to the cessation of inflammatory response.
Explanation
Choice A reason:
Applying a moist dressing to the wound provides a moist environment for wound healing and protects the wound from contamination and trauma. Moisture prevents dehydration and necrosis of the wound bed and promotes cell migration and growth.
Choice B reason:
Assessing the wound for signs of infection is important to detect and treat any infection that may impair wound healing or cause systemic complications. Signs of infection include increased redness, warmth, swelling, pain, drainage, odor, fever, or leukocytosis.
Choice C reason:
Debriding necrotic tissue from the wound is essential to remove any dead or devitalized tissue that may interfere with wound healing or serve as a source of infection. Debridement can be done by surgical, mechanical, enzymatic, or autolytic methods.
Choice D reason:
Elevating the affected leg above the heart level reduces edema and improves blood circulation to the wound. Edema can impair wound healing by causing tissue hypoxia, increasing bacterial growth, and delaying granulation tissue formation.
Choice E reason:
Massaging the wound edges gently is not recommended for chronic wounds, as it may cause trauma or bleeding to the wound bed or delay epithelialization. Massaging may be beneficial for preventing hypertrophic scars or contractures in healed wounds.
Explanation
Choice A reason:
B cells are not involved in contact dermatitis, as they do not produce antibodies or form immune complexes.
Choice B reason:
T cells are the type of cells that mediate contact dermatitis, which is a type of type IV hypersensitivity. T cells recognize the poison ivy antigens that bind to the skin proteins and release cytokines that recruit macrophages and other inflammatory cells. This leads to a delayed and localized reaction that manifests as erythema, edema, vesicles, and pruritus.
Choice C reason:
T cells are not the same as B cells, as they have different receptors and functions in the immune system.
Choice D reason:
Mast cells are not involved in contact dermatitis, as they do not express IgE antibodies or release histamine.
Explanation
Choice A reason:
Type I hypersensitivity is not involved in Graves' disease, as it does not involve IgE antibodies or mast cells.
Choice B reason:
Type II hypersensitivity is involved in Graves' disease, as it involves IgG antibodies that bind to the thyroid-stimulating hormone (TSH) receptors on the thyroid gland and stimulate the production of thyroid hormones. This leads to hyperthyroidism and manifestations such as goiter, exophthalmos, tachycardia, weight loss, or tremors.
Choice C reason:
Type III hypersensitivity is not involved in Graves' disease, as it does not involve immune complexes or complement activation.
Choice D reason:
Type IV hypersensitivity is not involved in Graves' disease, as it does not involve cytotoxic T cells or helper T cells.
Choice E reason:
Type V hypersensitivity is also involved in Graves' disease, as it involves the stimulation of target cells by antibodies that act as agonists for cell surface receptors. This leads to an increased function of the target organ or tissue.
Explanation
Choice A reason:
Gram-positive cocci are bacteria that have a spherical shape and stain purple with Gram stain due to their thick peptidoglycan cell wall. Streptococcus pyogenes is an example of gram-positive cocci that can cause infections such as pharyngitis, impetigo, cellulitis, necrotizing fasciitis, or rheumatic fever.
Choice B reason:
Gram-negative cocci are bacteria that have a spherical shape and stain pink with Gram stain due to their thin peptidoglycan cell wall and outer membrane. Neisseria gonorrhoeae and Neisseria meningitidis are examples of gram-negative cocci that can cause infections such as gonorrhea, meningitis, or septicemia.
Choice C reason:
Gram-positive bacilli are bacteria that have a rod-shaped shape and stain purple with Gram stain due to their thick peptidoglycan cell wall. Bacillus anthracis and Clostridium botulinum are examples of gram-positive bacilli that can cause infections such as anthrax, botulism, or tetanus.
Choice D reason:
Gram-negative bacilli are bacteria that have a rod-shaped shape and stain pink with Gram stain due to their thin peptidoglycan cell wall and outer membrane. Escherichia coli and Pseudomonas aeruginosa are examples of gram-negative bacilli that can cause infections such as urinary tract infection, wound infection, or sepsis.
Explanation
Choice A reason:
Bacteria are microorganisms that have a cell wall composed of peptidoglycan and a cell membrane composed of phospholipids. They can be classified by their shape (cocci or bacilli), their Gram stain (positive or negative), or their oxygen requirement (aerobic or anaerobic).
Choice B reason:
Viruses are microorganisms that have a nucleic acid core (DNA or RNA) surrounded by a protein coat (capsid) and sometimes an envelope derived from the host cell membrane. They can only replicate inside living cells and cause various diseases such as influenza, herpes, hepatitis, or AIDS.
Choice C reason:
Fungi are microorganisms that have a cell wall composed of chitin and a cell membrane composed of ergosterol. They can exist as yeasts or molds depending on the environmental conditions. Candida albicans is an example of fungi that can cause infections such as thrush, vaginitis, or systemic candidiasis.
Choice D reason:
Parasites are microorganisms that live on or in another organism (host) and derive nutrients from it. They can be classified by their size (protozoa or helminths) or their mode of transmission (vector-borne or direct contact). They can cause infections such as malaria, giardiasis, or schistosomiasis.
Explanation
Choice D reason:
Malignant neoplasia of bone marrow cells. Leukemia is a type of cancer that originates from the abnormal and uncontrolled growth of hematopoietic stem cells or progenitor cells in the bone marrow. These cells can proliferate and differentiate into various types of blood cells, such as lymphocytes, granulocytes, monocytes, or erythrocytes. Leukemia can be classified by the type of cell involved (myeloid or lymphoid) and the rate of progression (acute or chronic).
Choice A reason:
Benign neoplasia of blood cells is not a correct term for leukemia, as leukemia is a malignant condition that can invade and destroy normal blood cells and tissues. Benign neoplasia of blood cells is a rare condition that involves the overproduction of normal blood cells, such as polycythemia vera or essential thrombocythemia.
Choice B reason:
Malignant neoplasia of blood cells is not a correct term for leukemia, as leukemia does not originate from blood cells, but from bone marrow cells. Malignant neoplasia of blood cells is a term that can be used for lymphoma, which is a type of cancer that originates from lymphocytes in the lymphatic system.
Choice C reason:
Benign neoplasia of bone marrow cells is not a correct term for leukemia, as leukemia is a malignant condition that can spread to other organs or systems. Benign neoplasia of bone marrow cells is a term that can be used for myelodysplastic syndrome, which is a condition that involves the abnormal development and maturation of bone marrow cells.
Explanation
Choice A reason:
Decreased hematocrit is an indicator of improvement for a client who has hypovolemia and is receiving IV fluid therapy. Hematocrit is the percentage of red blood cells in the blood. Hypovolemia causes hemoconcentration, which increases the hematocrit level. IV fluid therapy restores the blood volume and dilutes the red blood cells, which decreases the hematocrit level.
Choice B reason:
Increased urine specific gravity is not an indicator of improvement for a client who has hypovolemia and is receiving IV fluid therapy. Urine specific gravity is a measure of the concentration of solutes in the urine. Hypovolemia causes dehydration, which increases the urine specific gravity. IV fluid therapy rehydrates the body and lowers the urine specific gravity.
Choice C reason:
Decreased central venous pressure is not an indicator of improvement for a client who has hypovolemia and is receiving IV fluid therapy. Central venous pressure is a measure of the pressure in the right atrium and vena cava. Hypovolemia causes decreased preload, which lowers the central venous pressure. IV fluid therapy increases preload and raises the central venous pressure.
Choice D reason:
Increased blood urea nitrogen is not an indicator of improvement for a client who has hypovolemia and is receiving IV fluid therapy. Blood urea nitrogen is a measure of the amount of urea in the blood. Urea is a waste product of protein metabolism that is excreted by the kidneys. Hypovolemia causes decreased renal perfusion, which increases the blood urea nitrogen level. IV fluid therapy improves renal perfusion and lowers the blood urea nitrogen level.
A nurse is caring for a client who has metabolic alkalosis due to prolonged vomiting. Which of the following interventions should the nurse implement? (Select all that apply.)
Explanation
Choice A reason:
Administering antiemetics as prescribed is an intervention that the nurse should implement for a client who has metabolic alkalosis due to prolonged vomiting. Antiemetics are medications that can prevent or treat nausea and vomiting, which are the main causes of metabolic alkalosis in this case. By stopping vomiting, antiemetics can help prevent further loss of gastric acid and bicarbonate retention, which can correct metabolic alkalosis.
Choice B reason:
Monitoring serum potassium levels is an intervention that the nurse should implement for a client who has metabolic alkalosis due to prolonged vomiting. Metabolic alkalosis can cause hypokalemia due to increased renal excretion of potassium and intracellular shift of potassium in exchange for hydrogen ions. Hypokalemia can worsen metabolic alkalosis by impairing renal acid excretion and increasing bicarbonate reabsorption. The nurse should monitor serum potassium levels regularly and report any abnormalities or signs of hypokalemia, such as muscle weakness, cramps, arrhythmias, or ECG changes.
Choice C reason:
Administering sodium bicarbonate IV as prescribed is not an intervention that the nurse should implement for a client who has metabolic alkalosis due to prolonged vomiting. Sodium bicarbonate is an alkalinizing agent that can increase serum bicarbonate levels and pH, which can worsen metabolic alkalosis. Sodium bicarbonate IV should be avoided or used with caution in clients who have metabolic alkalosis, unless they have severe acid-base imbalance or coexisting metabolic acidosis.
Choice D reason:
Encouraging intake of acidic foods and beverages is not an intervention that the nurse should implement for a client who has metabolic alkalosis due to prolonged vomiting. Acidic foods and beverages can lower the pH of the stomach, but they have little effect on the pH of the blood or urine, which are regulated by other mechanisms such as buffers, lungs, and kidneys. Acidic foods and beverages can also irritate the gastric mucosa and trigger more vomiting, which can aggravate metabolic alkalosis.
Choice E reason:
Providing supplemental oxygen as needed is an intervention that the nurse should implement for a client who has metabolic alkalosis due to prolonged vomiting. Metabolic alkalosis can cause respiratory compensation by decreasing the respiratory rate and depth, which can lead to hypoxemia and hypercapnia. Supplemental oxygen can help maintain adequate oxygenation and prevent tissue hypoxia and organ damage. The nurse should monitor the client's oxygen saturation and arterial blood gas levels and adjust the oxygen therapy accordingly.
A nurse is caring for a client who has hypernatremia. Which of the following actions should the nurse take? (Select all that apply.)
Explanation
Choice A reason:
Restricting fluid intake is not an action that the nurse should take for a client who has hypernatremia. Fluid restriction can worsen hypernatremia by increasing the concentration of sodium in the blood. Fluid intake should be increased or replaced with isotonic or hypotonic fluids to dilute sodium and correct hypernatremia.
Choice B reason:
Monitoring neurological status is an action that the nurse should take for a client who has hypernatremia. Hypernatremia can cause neurological symptoms such as confusion, agitation, seizures, coma, and death due to cellular dehydration and brain shrinkage. The nurse should assess the client's level of consciousness, orientation, memory, behavior, and reflexes regularly and report any changes or deterioration.
Choice C reason:
Administering hypotonic IV fluids is an action that the nurse should take for a client who has hypernatremia. Hypotonic fluids have a lower concentration of solutes than normal body fluids and can help lower serum sodium levels by moving water into the cells from the blood vessels. The nurse should administer hypotonic fluids slowly and carefully to avoid fluid overload or cerebral edema.
Choice D reason:
Encouraging foods high in sodium is not an action that the nurse should take for a client who has hypernat
A nurse is assessing a client who has septic shock. The nurse notes that the client has a blood pressure of 80/50 mmHg, a heart rate of 120 beats per minute, a respiratory rate of 28 breaths per minute, and a temperature of 39°C.
The nurse calculates that the client has a Sequential Organ Failure Assessment (SOFA) score of what value?
Explanation
The SOFA score is a tool that assesses the degree of organ dysfunction or failure in septic shock. It is based on six parameters: blood pressure, Glasgow coma scale, PaO2/FiO2 ratio, platelet count, bilirubin level, and creatinine level. Each parameter is assigned a score from 0 to 4 based on the severity of the abnormality. The total SOFA score ranges from 0 to 24, with higher scores indicating worse organ dysfunction or failure.
The client's blood pressure of 80/50 mmHg corresponds to a SOFA score of 1, as it indicates hypotension.
The client's Glasgow coma scale is not given, so it is assumed to be normal (15), which corresponds to a SOFA score of 0.
The client's PaO2/FiO2 ratio is not given, so it is assumed to be normal (>400), which corresponds to a SOFA score of 0.
The client's platelet count is not given, so it is assumed to be normal (>150 x 10^9/L), which corresponds to a SOFA score of 0.
The client's bilirubin level is not given, so it is assumed to be normal (<20 micromol/L), which corresponds to a SOFA score of 0.
The client's creatinine level is not given, so it is assumed to be normal (<110 micromol/L), which corresponds to a SOFA score of 0.
The total SOFA score is the sum of the scores for each parameter: 1 + 0 + 0 + 0 + 0 + 0 = 1. Therefore, the client has a SOFA score of 1.
A nurse is caring for a client who has rheumatoid arthritis (RA). The nurse understands that this condition is caused by what type of hypersensitivity?
Explanation
Choice A reason:
Type I hypersensitivity is not involved in RA, as it does not involve IgE antibodies or mast cells.
Choice B reason:
Type II hypersensitivity is not involved in RA, as it does not involve IgG or IgM antibodies or target cells.2
Choice C reason:
RA is caused by type III hypersensitivity, which involves the formation and deposition of immune complexes in the synovial membranes of the joints. This triggers complement activation, inflammation, and tissue damage.
Choice D reason:
Type IV hypersensitivity is not involved in RA, as it does not involve cytotoxic T cells or helper T cells.
Exams on Basic Concepts of Pathophysiology
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Objectives
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Define and explain the terms related to pathophysiology, such as etiology, pathogenesis, clinical manifestations, diagnosis, prognosis, and treatment.
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Describe the cellular adaptations, injuries, and death that occur in response to stressors and their implications for health and disease.
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Explain the process of inflammation and healing, including the types, stages, mediators, and outcomes of inflammation, and the factors that affect wound healing.
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Understand the basic concepts of immunity and hypersensitivity, including the components, functions, and disorders of the immune system, and the types, mechanisms, and manifestations of hypersensitivity reactions.
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Identify the causes, transmission, prevention, and control of infection and sepsis, including the types, characteristics, and virulence factors of microorganisms, systemic inflammatory response syndrome (SIRS), and septic shock.
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Define neoplasia and describe the characteristics, classification, diagnosis, staging, grading, treatment, and complications of benign and malignant tumors.
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Recognize the genetic and congenital disorders that affect human health and development, including the types, patterns, mechanisms, and testing of genetic diseases, and the types, causes, diagnosis, and treatment of congenital anomalies.
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Analyze the fluid, electrolyte, and acid-base balance in the body, including the regulation, distribution, composition, and disorders of body fluids; the sources, functions, regulation, imbalances, and replacement of electrolytes; and the sources, regulation, imbalances, assessment, and correction of acid-base status.
Introduction
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Pathophysiology is the study of how normal physiological processes are altered by disease or injury.
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It involves understanding the causes (etiology), mechanisms (pathogenesis), signs and symptoms (clinical manifestations), diagnostic tests (diagnosis), outcomes (prognosis), and interventions (treatment) of various health conditions.
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Pathophysiology is an essential component of nursing education and practice because it provides the scientific basis for assessing, diagnosing, planning, implementing, and evaluating nursing care for individuals or groups with health problems.
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Pathophysiology nursing is a branch of nursing that applies the knowledge of pathophysiology, the study of the underlying changes in body physiology that result from disease or injury, to the assessment, diagnosis, and management of patients with various health problems12.
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Pathophysiology nursing requires an understanding of the normal structure and function of the human body, as well as the mechanisms of disease development, progression, and resolution12.
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Pathophysiology nursing also involves the recognition of risk factors, precipitating factors, etiology, signs, symptoms, and complications of different diseases and disorders, as well as their impact on the patient’s physical, psychological, and social well-being12.
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Pathophysiology nursing uses various tools and methods to collect and analyze data, such as history taking, physical examination, laboratory tests, diagnostic imaging, and monitoring devices12.
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Pathophysiology nursing employs evidence-based practice and clinical reasoning to formulate nursing diagnoses, plan and implement appropriate interventions, and evaluate outcomes12.
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Pathophysiology nursing collaborates with other health care professionals and disciplines to provide holistic and patient-centered care12.
Inflammation and Healing
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Inflammation is the body’s protective response to injury or infection. It involves the activation of vascular, cellular, and chemical mediators that aim to eliminate the causative agent, limit the tissue damage, and initiate the healing process.
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Inflammation can be acute or chronic, depending on the duration and nature of the stimulus. Some examples of inflammation are:
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Acute inflammation: a rapid and short-lived response to a mild or transient injury or infection. It is characterized by the cardinal signs of inflammation: redness (rubor), heat (calor), swelling (tumor), pain (dolor), and loss of function (functio laesa). It involves three main stages: vascular changes, cellular changes, and chemical changes.
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Vascular changes: include vasodilation (increased blood flow) and increased vascular permeability (leakage of fluid and proteins) that result in local hyperemia (increased blood volume) and edema (accumulation of fluid).
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Cellular changes: include the migration of white blood cells (WBCs) from the blood vessels to the site of injury or infection through a process called chemotaxis. The main WBCs involved in acute inflammation are neutrophils, which phagocytose (ingest) and destroy the causative agent and release enzymes that digest the necrotic tissue.
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Chemical changes: include the release of various inflammatory mediators that amplify and regulate the inflammatory response. The main mediators involved in acute inflammation are histamine, serotonin, prostaglandins, leukotrienes, cytokines, complement, and clotting factors.
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Chronic inflammation: a prolonged and persistent response to a severe or recurrent injury or infection. It is characterized by the presence of lymphocytes, macrophages, plasma cells, fibroblasts, and granulomas (nodules of chronic inflammatory cells). It involves four main features: tissue destruction, fibrosis (scar formation), angiogenesis (new blood vessel formation), and impaired healing.
The outcome of healing depends on several factors, such as the type, extent, and location of tissue injury; the presence of infection or foreign bodies; the nutritional and immunological status of the individual; and the quality and timing of medical intervention. Some possible outcomes are:
Resolution: is the complete restoration of normal tissue structure and function after an injury that involves minimal tissue damage and no complications. For example: healing of a superficial cut or a mild sunburn.
Primary intention: is the healing of a clean surgical incision or a small wound that involves minimal tissue loss and no complications. It is characterized by a thin scar that is barely visible. For example: healing of an appendectomy or a sutured laceration.
Secondary intention: is the healing of a large wound that involves significant tissue loss or complications, such as infection, necrosis, or foreign bodies. It is characterized by a wide scar that may impair function or appearance. For example: healing of a pressure ulcer or a burn wound.
Tertiary intention: is the delayed closure of a wound that was initially left open to allow for drainage, debridement, or infection control. It is characterized by a deep scar that may require grafting or reconstruction. For example: healing of an abdominal wound after peritonitis or a gunshot wound.
Inflammation: is the same as described above, but in the context of repair, it also prepares the wound for healing by removing debris, bacteria, and necrotic tissue.
Proliferation: is the phase of repair that involves the formation of granulation tissue, which is a highly vascularized and cellular tissue that fills the wound defect. It also involves the re-epithelialization of the wound surface by the migration and proliferation of epithelial cells from the wound edges or hair follicles.
Remodeling: is the phase of repair that involves the maturation and reorganization of collagen fibers and other extracellular matrix components to form a scar that strengthens the wound. It also involves the contraction of the wound by the action of myofibroblasts, which are specialized fibroblasts that have contractile properties.
The process of repair involves four main phases: hemostasis, inflammation, proliferation, and remodeling.
Hemostasis: is the cessation of bleeding from injured blood vessels. It involves the formation of a platelett plug and a fibrin clot that seal the wound and prevent further blood loss.
Healing is the process of restoring the normal structure and function of injured or infected tissues. It involves two main mechanisms: regeneration and repair. Regeneration is the replacement of damaged cells with identical cells that restore the original tissue structure and function. Repair is the replacement of damaged cells with connective tissue that forms a scar that restores some but not all tissue structure and function. Some examples of healing are:
Regeneration: occurs in tissues that have a high capacity for cell division, such as epithelial tissues, bone marrow, liver, and lymphoid organs. It depends on the presence of stem cells that can differentiate into various cell types.
Repair: occurs in tissues that have a low capacity for cell division, such as cardiac muscle, skeletal muscle, nervous tissue, and cartilage. It depends on the presence of fibroblasts that synthesize collagen and other extracellular matrix components.
Immunity and Hypersensitivity
Immunity is the ability of the body to recognize and defend itself against foreign substances or organisms that may cause disease or harm. It involves two main types: innate immunity and adaptive immunity. Innate immunity is the first line of defense that provides immediate and nonspecific protection against any potential invader. Adaptive immunity is the second line of defense that provides delayed and specific protection against a particular invader. Some examples of immunity are:
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Innate immunity: consists of physical barriers (skin, mucous membranes), mechanical barriers (cilia, coughing, sneezing), chemical barriers (acid, enzymes, lysozyme), cellular barriers (natural killer cells, phagocytes), and inflammatory barriers (complement, cytokines, acute phase proteins). It does not require prior exposure to an antigen (a foreign substance that elicits an immune response) and does not generate immunological memory (a long-lasting response to a specific antigen).
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Adaptive immunity: consists of humoral immunity (mediated by antibodies produced by B lymphocytes) and cell-mediated immunity (mediated by T lymphocytes). It requires prior exposure to an antigen and generates immunological memory. It can be further classified into active immunity (acquired by natural infection or vaccination) or passive immunity (acquired by maternal transfer or immunoglobulin injection).
Hypersensitivity is an exaggerated or inappropriate immune response to an antigen that results in tissue damage or disease. It involves four main types: type I, type II, type III, and type IV. Some examples of hypersensitivity are:
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Type I hypersensitivity: also known as immediate hypersensitivity or allergic reaction. It is mediated by IgE antibodies that bind to mast cells and basophils and trigger the release of histamine and other mediators that cause vasodilation, increased vascular permeability, smooth muscle contraction, mucus secretion, and itching. It occurs within minutes after exposure to an antigen and can range from mild (urticaria, rhinitis, conjunctivitis) to severe (anaphylaxis).
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Type II hypersensitivity: also known as antibody-mediated hypersensitivity or cytotoxic reaction. It is mediated by IgG or IgM antibodies that bind to antigens on the surface of target cells and activate complement or phagocytes that destroy the target cells. It occurs within hours to days after exposure to an antigen and can affect various tissues and organs (hemolytic anemia, transfusion reaction, autoimmune hemolytic anemia, autoimmune hemolytic anemia, Graves’ disease, myasthenia gravis, Goodpasture syndrome).
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Type III hypersensitivity: also known as immune complex-mediated hypersensitivity or serum sickness. It is mediated by IgG or IgM antibodies that form antigen-antibody complexes that deposit in various tissues and activate complement or phagocytes that cause inflammation and tissue damage. It occurs within hours to days after exposure to an antigen and can affect various tissues and organs (glomerulonephritis, rheumatoid arthritis, systemic lupus erythematosus, Arthus reaction).
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Type IV hypersensitivity: also known as cell-mediated hypersensitivity or delayed-type hypersensitivity. It is mediated by T lymphocytes that recognize antigens on the surface of target cells and secrete cytokines or cytotoxic molecules that cause inflammation and tissue damage. It occurs within days to weeks after exposure to an antigen and can affect various tissues and organs (contact dermatitis, tuberculin reaction, graft rejection, type 1 diabetes mellitus, multiple sclerosis).
Infection and Sepsis
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Infection is the invasion and multiplication of microorganisms in the body that cause disease or harm.
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It involves three main components: the host, the pathogen, and the environment.
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The host is the individual who is infected by the pathogen.
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The pathogen is the microorganism that causes the infection.
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The environment is the external or internal factor that facilitates or hinders the infection. Some examples of infection are:
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Host factors: include innate and adaptive immunity, normal flora (beneficial microorganisms that colonize certain body sites), and the risk factors (conditions or behaviors that increase the susceptibility or severity of infection). For example: immunodeficiency, diabetes mellitus, antibiotic use, surgery, catheterization, sexual activity, etc.
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Pathogen factors: include the type, characteristics, and virulence factors of the microorganism that determine its ability to cause infection. For example bacteria, viruses, fungi, parasites, prions; gram-positive or gram-negative, aerobic or anaerobic, encapsulated or non-encapsulated, motile or non-motile; toxins, enzymes, adhesins, invasins, etc.
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Environment factors: include the source, mode, and route of transmission of the microorganism that determine how it reaches and infects the host. For example: endogenous (from the host’s own flora) or exogenous (from another person, animal, object, or environment); contact (direct or indirect), droplet, airborne, vector-borne (by insects or animals), vehicle-borne (by food, water, blood, etc.); skin, mucous membranes, respiratory tract, gastrointestinal tract, genitourinary tract, etc.
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Sepsis is a life-threatening condition that occurs when a systemic inflammatory response syndrome (SIRS) is triggered by an infection.
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SIRS is a generalized inflammatory response that involves two or more of the following criteria: fever (>38°C) or hypothermia (<36°C), tachycardia (>90 beats per minute), tachypnea (>20 breaths per minute), leukocytosis (>12 x 10^9/L) or leukopenia (<4 x 10^9/L).
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Sepsis is diagnosed when SIRS is associated with a confirmed or suspected infection. Some examples of sepsis are:
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Sepsis: a systemic inflammatory response to infection that may cause organ dysfunction or failure. It is characterized by signs and symptoms such as fever, chills, rigors, malaise, nausea, vomiting, diarrhea, confusion, altered mental status, hypotension, oliguria, dyspnea, hypoxemia, etc.
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Severe sepsis: sepsis with evidence of organ dysfunction or hypoperfusion. It is characterized by signs and symptoms such as lactic acidosis, coagulopathy, thrombocytopenia, acute kidney injury, acute liver injury, acute lung injury, acute cardiac injury, etc.
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Septic shock: sepsis with persistent hypotension despite adequate fluid resuscitation. It is characterized by signs and symptoms such as refractory hypotension, tissue hypoxia, multiple organ failure, coma, death.
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The pathophysiology of sepsis involves a complex interaction of inflammatory mediators (cytokines, complement, coagulation factors), immune cells (neutrophils, monocytes, macrophages), endothelial cells (lining of blood vessels), and organ systems (cardiovascular, respiratory, renal, hepatic, neurologic). The main mechanisms involved are:
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Vasodilation: caused by nitric oxide and other mediators that relax the smooth muscle of blood vessels and reduce vascular resistance. This leads to hypotension and decreased tissue perfusion.
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Increased vascular permeability: caused by histamine and other mediators that increase the gaps between endothelial cells and allow fluid and proteins to leak out of blood vessels. This leads to edema and hypovolemia.
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Microvascular thrombosis: is caused by tissue factors and other mediators that activate the coagulation cascade and form clots in small blood vessels. This leads to ischemia and organ damage.
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Impaired fibrinolysis: caused by plasminogen activator inhibitor-1 (PAI-1) and other mediators that inhibit the breakdown of clots by plasmin. This leads to persistent thrombosis and organ damage.
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Apoptosis: caused by caspases and other mediators that induce programmed cell death in various tissues and organs. This leads to cell loss and organ dysfunction.
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The treatment of sepsis involves early recognition and diagnosis; source control (removal or drainage of infected site); antimicrobial therapy (broad-spectrum antibiotics); fluid resuscitation (isotonic crystalloids); vasopressors (norepinephrine, dopamine, etc.); corticosteroids (hydrocortisone); and supportive care (oxygen, mechanical ventilation, renal replacement therapy, etc.).
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The prognosis of sepsis depends on several factors, such as the type and severity of infection, the presence and extent of organ dysfunction, the age and comorbidities of the patient, and the quality and timing of medical intervention. The mortality rate of sepsis ranges from 10% to 50%, depending on the criteria used to define it.
Neoplasia
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Neoplasia is the abnormal and uncontrolled growth of cells that form a mass or tumor. It can be benign or malignant, depending on the characteristics and behavior of the tumor cells. Some examples of neoplasia are:
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Benign neoplasia: a non-cancerous tumor that grows slowly, does not invade surrounding tissues, and does not metastasize (spread) to distant sites. It is usually encapsulated (surrounded by a fibrous capsule) and well-differentiated (resembles the normal tissue of origin). It is named according to the tissue of origin and the suffix -oma. For example: adenoma (glandular tissue), lipoma (fat tissue), leiomyoma (smooth muscle tissue), etc.
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Malignant neoplasia: a cancerous tumor that grows rapidly, invades surrounding tissues, and metastasizes to distant sites. It is usually non-encapsulated and poorly differentiated (does not resemble the normal tissue of origin). It is named according to the tissue of origin and the suffix -carcinoma (epithelial tissue) or -sarcoma (connective tissue). For example: adenocarcinoma (glandular epithelium), squamous cell carcinoma (squamous epithelium), osteosarcoma (bone tissue), etc.
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The pathophysiology of neoplasia involves a multistep process of genetic and epigenetic alterations that result in the transformation of normal cells into tumor cells. The main mechanisms involved are:
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Initiation: the exposure of normal cells to a carcinogen (a substance or agent that causes cancer) that induces DNA damage or mutation. For example: tobacco smoke, ultraviolet radiation, asbestos, etc.
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Promotion: the stimulation of initiated cells by a promoter (a substance or agent that enhances cell proliferation) that induces clonal expansion or growth. For example: hormones, inflammation, chronic irritation, etc.
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Progression: the acquisition of additional mutations or alterations by tumor cells that confer them with malignant characteristics, such as increased growth rate, invasiveness, angiogenesis (new blood vessel formation), immuno-evasion (escape from immune surveillance), and metastasis.
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The diagnosis of neoplasia involves various methods, such as physical examination, imaging studies (x-ray, ultrasound, computed tomography, magnetic resonance imaging, etc.), laboratory tests (blood tests, tumor markers, etc.), biopsy (removal and examination of a tissue sample), cytology (examination of cells from body fluids or secretions), and histopathology (examination of tissue sections under a microscope).
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The staging and grading of neoplasia involve the assessment of the extent and severity of the tumor. The main systems used are:
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Staging: based on the TNM system that evaluates the size and spread of the primary tumor (T), the involvement of regional lymph nodes (N), and the presence or absence of distant metastases (M). For example: T1N0M0 indicates a small tumor with no lymph node involvement and no metastases; T4N3M1 indicates a large tumor with extensive lymph node involvement and metastases.
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Grading: based on the degree of differentiation and anaplasia (loss of normal cell features) of the tumor cells. For example: G1 indicates well-differentiated tumor cells that resemble normal cells; G4 indicates poorly differentiated tumor cells that do not resemble normal cells.
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The treatment of neoplasia involves various modalities, such as surgery, radiation therapy, chemotherapy, immunotherapy, hormone therapy, targeted therapy, and palliative care.
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The choice and combination of modalities depend on several factors, such as the type, stage, grade, location, and molecular profile of the tumor; the age, health status, and preferences of the patient; and the availability and effectiveness of medical resources.
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The prognosis of neoplasia depends on several factors, such as the type, stage, grade, location, and molecular profile of the tumor; the response to treatment; and the occurrence of complications or recurrence.
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The survival rate of neoplasia varies widely depending on these factors. For example: breast cancer has a 5-year survival rate of about 90% if detected early and treated appropriately; pancreatic cancer has a 5-year survival rate of about 10% regardless of detection and treatment.
Genetic and Congenital Disorders
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Genetic disorders are diseases or conditions that are caused by abnormalities in the genes or chromosomes. They can be inherited from one or both parents or acquired during development or life.
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They can affect any aspect of human health and development. Some examples of genetic disorders are:
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Chromosomal disorders: caused by changes in the number or structure of chromosomes. For example: Down syndrome (trisomy 21), Turner syndrome (monosomy X), Klinefelter syndrome (XXY), Cri du chat syndrome (deletion of 5p), etc.
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Single-gene disorders: caused by mutations in a single gene. They can be classified into autosomal dominant, autosomal recessive, or X-linked depending on the mode of inheritance. For example: Huntington disease (autosomal dominant), cystic fibrosis (autosomal recessive), hemophilia (X-linked), etc.
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Multifactorial disorders: caused by the interaction of multiple genes and environmental factors. For example: diabetes mellitus, hypertension, coronary artery disease, etc.
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Mitochondrial disorders: caused by mutations in the mitochondrial DNA or genes that affect mitochondrial function. For example: Leber hereditary optic neuropathy, mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS), etc.
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The pathophysiology of genetic disorders involves the disruption of normal gene expression or function that results in abnormal protein synthesis or metabolism. The main mechanisms involved are:
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Loss-of-function mutations: reduce or eliminate the function of a gene product. For example: cystic fibrosis is caused by a mutation in the CFTR gene that encodes a chloride channel that regulates fluid and electrolyte balance in various tissues. The mutation impairs the function of the channel and causes thick and sticky mucus to accumulate in the lungs, pancreas, and other organs.
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Gain-of-function mutations: increase or alter the function of a gene product. For example: Huntington disease is caused by a mutation in the HTT gene that encodes a protein called huntingtin that is involved in nerve cell function. The mutation expands a repeated sequence of three nucleotides (CAG) in the gene and causes the protein to become toxic and aggregate in the brain cells.
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Haploinsufficiency: occur when one copy of a gene is mutated or deleted and the remaining copy is not enough to maintain normal function. For example: Cri du chat syndrome is caused by a deletion of part of chromosome 5 that includes several genes. The deletion reduces the dosage of these genes and causes various developmental abnormalities, such as microcephaly, intellectual disability, and a distinctive cry.
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Dominant negative mutations: occur when a mutated gene product interferes with the function of the normal gene product. For example: Marfan syndrome is caused by a mutation in the FBN1 gene that encodes a protein called fibrillin-1 that is involved in connective tissue structure and elasticity. The mutation produces an abnormal fibrillin-1 that disrupts the formation of normal fibrillin-1 fibers and causes various skeletal, cardiovascular, and ocular defects.
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The diagnosis of genetic disorders involves various methods, such as family history, physical examination, laboratory tests (blood tests, biochemical tests, etc.), cytogenetic tests (karyotype, fluorescence in situ hybridization, etc.), molecular tests (polymerase chain reaction, molecular tests (polymerase chain reaction, DNA sequencing, microarray, etc.), and prenatal tests (amniocentesis, chorionic villus sampling, etc.). The genetic counseling of genetic disorders involves the provision of information, education, and support to individuals or families who are affected by or at risk of a genetic disorder. It aims to help them understand the nature, inheritance, diagnosis, treatment, and prevention of the disorder; to assess their risk and options; and to cope with the psychological and social implications of the disorder.
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Congenital disorders are diseases or conditions that are present at birth or develop during the prenatal period. They can be caused by genetic or environmental factors or a combination of both. They can affect any aspect of human health and development. Some examples of congenital disorders are:
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Genetic congenital disorders: caused by inherited or acquired genetic abnormalities that affect the development of the embryo or fetus. For example: Down syndrome, Turner syndrome, Klinefelter syndrome, cystic fibrosis, hemophilia, etc.
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Environmental congenital disorders: caused by exposure to teratogens (substances or agents that cause birth defects) during the critical period of embryonic or fetal development. For example: fetal alcohol syndrome (alcohol), thalidomide syndrome (thalidomide), congenital rubella syndrome (rubella virus), etc.
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Multifactorial congenital disorders: caused by the interaction of genetic and environmental factors that affect the development of the embryo or fetus. For example: cleft lip and palate, spina bifida, congenital heart defects, etc.
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The pathophysiology of congenital disorders involves the disruption of normal embryonic or fetal development that results in structural or functional abnormalities. The main mechanisms involved are:
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Malformation: a defect in the formation of an organ or a part of an organ. For example: anencephaly (absence of brain), holoprosencephaly (incomplete separation of brain hemispheres), ectopia cordis (displacement of heart outside the chest), etc.
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Deformation: a distortion of an organ or a part of an organ by mechanical forces. For example: clubfoot (abnormal bending of foot), torticollis (abnormal twisting of neck), plagiocephaly (asymmetrical flattening of skull), etc.
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Disruption: a destruction of an organ or a part of an organ by a vascular accident or an external agent. For example: amniotic band syndrome (entrapment of limbs by fibrous bands), gastroschisis (rupture of abdominal wall), hydrops fetalis (accumulation of fluid in fetal tissues), etc.
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Dysplasia: a disorder in the differentiation or maturation of cells or tissues. For example: achondroplasia (defective growth of cartilage), osteogenesis imperfecta (defective synthesis of collagen), ectodermal dysplasia (defective development of ectodermal structures), etc.
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The diagnosis of congenital disorders involves various methods, such as physical examination, imaging studies (ultrasound, computed tomography, magnetic resonance imaging, etc.), laboratory tests (blood tests, biochemical tests, etc.), cytogenetic tests (karyotype, fluorescence in situ hybridization, etc.), molecular tests (polymerase chain reaction, DNA sequencing, microarray, etc.), and prenatal tests (amniocentesis, chorionic villus sampling, etc.). The treatment and prevention of congenital disorders depend on several factors, such as the type, cause, severity, and prognosis of the disorder; the availability and effectiveness of medical resources; and the ethical and legal issues involved. Some possible interventions are:
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Treatment: aimed at correcting or improving the structural or functional abnormalities caused by the disorder. It may involve surgery, medication, therapy, or supportive care. For example: surgery for cleft lip and palate, medication for phenylketonuria, therapy for cerebral palsy, or supportive care for trisomy 18.
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Prevention: aimed at reducing or eliminating the risk factors that cause or contribute to the disorder. It may involve genetic screening, genetic counseling, prenatal diagnosis, prenatal treatment, or termination of pregnancy. For example: genetic screening for cystic fibrosis, genetic counseling for Down syndrome, prenatal diagnosis for spina bifida, prenatal treatment for congenital adrenal hyperplasia, or termination of pregnancy for anencephaly.
Fluid, Electrolyte, and Acid-Base Balance
Fluid, electrolyte, and acid-base balance are the processes that maintain the optimal composition and distribution of body fluids in relation to water, solutes, and hydrogen ions. They are essential for maintaining homeostasis and normal physiological functions. They involve various organs and systems, such as the kidneys, lungs, heart, blood vessels, hormones, and buffers. Some examples of fluid, electrolyte, and acid-base balance are:
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Fluid balance: the regulation of the intake and output of water and the maintenance of the osmolality (concentration) and volume of body fluids. It involves two main compartments: intracellular fluid (ICF) and extracellular fluid (ECF). ICF is the fluid within the cells that accounts for about 40% of body weight. ECF is the fluid outside the cells that accounts for about 20% of body weight. ECF can be further divided into interstitial fluid (fluid between the cells), plasma (fluid in the blood vessels), and transcellular fluid (fluid in specialized cavities, such as cerebrospinal fluid, synovial fluid, etc.).
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Electrolyte balance: the regulation of the intake and output of solutes and the maintenance of the concentration and charge of electrolytes in body fluids. Electrolytes are substances that dissociate into ions (charged particles) in solution and conduct electricity. They include cations (positively charged ions) and anions (negatively charged ions). The main electrolytes in body fluids are sodium (Na+), potassium (K+), calcium (Ca2+), magnesium (Mg2+), chloride (Cl-), bicarbonate (HCO3-), phosphate (PO4 3-), and sulfate (SO4 2-).
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Acid-base balance: the regulation of the production and elimination of hydrogen ions (H+) and the maintenance of the pH (a measure of acidity or alkalinity) of body fluids. pH is determined by the ratio of bicarbonate to carbonic acid in body fluids. Bicarbonate is a base that accepts H+ and carbonic acid is an acid that releases H+. The normal pH range of body fluids is 7.35 to 7.45. A pH below 7.35 is called acidosis and a pH above 7.45 is called alkalosis.
The pathophysiology of fluid, electrolyte, and acid-base imbalance involves the disruption of normal regulatory mechanisms that result in abnormal changes in the composition or distribution of body fluids. The main mechanisms involved are:
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Fluid imbalance: caused by changes in water intake or output that affect the osmolality or volume of body fluids. For example: dehydration (water deficit), overhydration (water excess), hypovolemia (volume deficit), hypervolemia (volume excess), etc.
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Electrolyte imbalance: caused by changes in electrolyte intake or output that affect the concentration or charge of electrolytes in body fluids. For example: hyponatremia (low sodium), hypernatremia (high sodium), hypokalemia (low potassium), hyperkalemia (high potassium), hypocalcemia (low calcium), hypercalcemia (high calcium), etc.
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Acid-base imbalance: caused by changes in acid or base production or elimination that affect the pH of body fluids. For example: metabolic acidosis (low bicarbonate), metabolic alkalosis (high bicarbonate), respiratory acidosis (high carbonic acid), respiratory alkalosis (low carbonic acid), etc.
The diagnosis of fluid, electrolyte, and acid-base imbalance involves various methods, such as physical examination, vital signs, laboratory tests (blood tests, urine tests, etc.), and clinical manifestations. The treatment and prevention of fluid, electrolyte, and acid-base imbalance depend on several factors, such as the type, cause, severity, and complications of the imbalance; the age, health status, and preferences of the patient; and the availability and effectiveness of medical resources. Some possible interventions are:
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Treatment: aimed at correcting or improving the abnormal changes in the composition or distribution of body fluids. It may involve fluid therapy (administration of fluids by oral, intravenous, or other routes to restore or maintain fluid balance), electrolyte therapy (administration of electrolytes by oral, intravenous, or other routes to restore or maintain electrolyte balance), acid-base therapy (administration of acids, bases, or buffers by oral, intravenous, or other routes to restore or maintain acid-base balance), or pharmacological therapy (administration of drugs that affect fluid, electrolyte, or acid-base balance, such as diuretics, antidiuretics, antacids, etc.).
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Prevention: aimed at reducing or eliminating the risk factors that cause or contribute to the imbalance. It may involve lifestyle modifications (diet, exercise, hydration, etc.), disease management (control of diabetes mellitus, hypertension, etc.), infection control (prevention and treatment of infections), or environmental control (avoidance of exposure to heat, cold, altitude, etc.).
Conclusion
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Pathophysiology is the study of how normal physiological processes are altered by disease or injury.
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Pathophysiology involves understanding the causes, mechanisms, signs and symptoms, diagnostic tests, outcomes, and interventions of various health conditions.
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Pathophysiology is an essential component of nursing education and practice because it provides the scientific basis for assessing, diagnosing, planning, implementing, and evaluating nursing care for individuals or groups with health problems.
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The main topics covered in this module are:
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Cellular adaptation, injury, and death: the changes in cell size, number, shape, or function in response to stressors and their implications for health and disease.
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Cells can adapt to changes in their environment by altering their size (atrophy or hypertrophy), number (hyperplasia or hypoplasia), shape (metaplasia), or function (dysplasia).
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Cells can also be injured by various physical, chemical, biological, or genetic factors that disrupt their structure or function.
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Cell death is the ultimate outcome of irreversible cell injury. There are two main types of cell death: necrosis and apoptosis.
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Inflammation and healing: the process of tissue response to injury or infection and the restoration of normal structure and function.
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Inflammation is the body’s protective response to injury or infection. It involves the activation of vascular, cellular, and chemical mediators that aim to eliminate the causative agent, limit tissue damage, and initiate the healing process. Inflammation can be acute or chronic.
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Healing is the process of restoring the normal structure and function of injured or infected tissues. It involves two main mechanisms: regeneration and repair. Regeneration is the replacement of damaged cells with identical cells that restore the original tissue structure and function. Repair is the replacement of damaged cells with connective tissue that forms a scar that restores some but not all tissue structure and function. The process of repair involves four main phases: hemostasis, inflammation, proliferation, and remodeling. The outcome of healing depends on several factors, such as the type, extent, and location of tissue injury; the presence of infection or foreign bodies; the nutritional and immunological status of the individual; and the quality and timing of medical intervention.
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Immunity and hypersensitivity: the ability of the body to recognize and defend itself against foreign substances or organisms and the exaggerated or inappropriate immune response that results in tissue damage or disease.
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Immunity involves two main types: innate immunity and adaptive immunity. Innate immunity is the first line of defense that provides immediate and nonspecific protection against any potential invader. Adaptive immunity is the second line of defense that provides delayed and specific protection against a particular invader. It requires prior exposure to an antigen and generates immunological memory.
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Hypersensitivity involves four main types: type I, type II, type III, and type IV. Type I hypersensitivity is also known as immediate hypersensitivity or allergic reaction. Type II hypersensitivity is also known as antibody-mediated hypersensitivity or cytotoxic reaction. Type III hypersensitivity is also known as immune complex-mediated hypersensitivity or serum sickness. Type IV hypersensitivity is also known as cell-mediated hypersensitivity or delayed-type hypersensitivity.
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Infection and sepsis: the invasion and multiplication of microorganisms in the body that cause disease or harm and the life-threatening condition that occurs when a systemic inflammatory response syndrome (SIRS) is triggered by an infection.
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Infection involves three main components: the host, the pathogen, and the environment. The host is the individual who is infected by the pathogen. The pathogen is the microorganism that causes the infection. The environment is the external or internal factor that facilitates or hinders the infection.
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Sepsis is a life-threatening condition that occurs when an infection triggers a systemic inflammatory response syndrome (SIRS). SIRS is a generalized inflammatory response that involves two or more of the following criteria: fever (>38°C) or hypothermia (<36°C), tachycardia (>90 beats per minute), tachypnea (>20 breaths per minute), leukocytosis (>12 x 10^9/L) or leukopenia (<4 x 10^9/L). Sepsis is diagnosed when SIRS is associated with a confirmed or suspected infection. Sepsis can progress to severe sepsis (sepsis with evidence of organ dysfunction or hypoperfusion) or septic shock (sepsis with persistent hypotension despite adequate fluid resuscitation).
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Neoplasia: the abnormal and uncontrolled growth of cells that form a mass or tumor that can be benign or malignant.
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Benign neoplasia is a non-cancerous tumor that grows slowly, does not invade surrounding tissues, and does not metastasize (spread) to distant sites. It is usually encapsulated and well-differentiated. It is named according to the tissue of origin and the suffix -oma.
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Malignant neoplasia is a cancerous tumor that grows rapidly, invades surrounding tissues, and metastasizes to distant sites. It is usually non-encapsulated and poorly differentiated. It is named according to the tissue of origin and the suffix -carcinoma (epithelial tissue) or -sarcoma (connective tissue).
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The pathophysiology of neoplasia involves a multistep process of genetic and epigenetic alterations that result in the transformation of normal cells into tumor cells. The main mechanisms involved are initiation, promotion, and progression.
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Genetic and congenital disorders: the diseases or conditions that are caused by abnormalities in the genes or chromosomes or by exposure to teratogens during the prenatal period.
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Genetic disorders are caused by inherited or acquired genetic abnormalities that affect the function of genes or chromosomes. They can be classified into chromosomal disorders, single-gene disorders, multifactorial disorders, and mitochondrial disorders.
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Congenital disorders are caused by exposure to teratogens during the critical period of embryonic or fetal development. They can be classified into genetic congenital disorders, environmental congenital disorders, and multifactorial congenital disorders.
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The pathophysiology of genetic and congenital disorders involves the disruption of normal gene expression or function or normal embryonic or fetal development that results in structural or functional abnormalities. The main mechanisms involved are malformation, deformation, disruption, and dysplasia.
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Fluid, electrolyte, and acid-base balance: the processes that maintain the optimal composition and distribution of body fluids in relation to water, solutes, and hydrogen ions.
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Fluid balance involves two main compartments: intracellular fluid (ICF) and extracellular fluid (ECF). Fluid balance is regulated by the intake and output of water and the osmolality and volume of body fluids.
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Electrolyte balance involves various electrolytes that dissociate into ions in solution and conduct electricity. Electrolyte balance is regulated by the intake and output of solutes and the concentration and charge of electrolytes in body fluids.
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Acid-base balance involves the production and elimination of hydrogen ions (H+) and the pH of body fluids. Acid-base balance is regulated by the ratio of bicarbonate to carbonic acid in body fluids.
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The pathophysiology of fluid, electrolyte, and acid-base imbalance involves the disruption of normal regulatory mechanisms that result in abnormal changes in the composition or distribution of body fluids. The main mechanisms involved are fluid imbalance, electrolyte imbalance, and acid-base imbalance.
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Summary
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Pathophysiology is the study of how normal physiological processes are altered by disease or injury.
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Pathophysiology involves understanding the causes, mechanisms, signs and symptoms, diagnostic tests, outcomes, and interventions of various health conditions.
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Pathophysiology is an essential component of nursing education and practice because it provides the scientific basis for assessing, diagnosing, planning, implementing, and evaluating nursing care for individuals or groups with health problems.
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The main topics covered in this module are:
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Cellular adaptation, injury, and death: the changes in cell size, number, shape, or function in response to stressors and their implications for health and disease.
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Inflammation and healing: the process of tissue response to injury or infection and the restoration of normal structure and function.
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Immunity and hypersensitivity: the ability of the body to recognize and defend itself against foreign substances or organisms and the exaggerated or inappropriate immune response that results in tissue damage or disease.
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Infection and sepsis: the invasion and multiplication of microorganisms in the body that cause disease or harm and the life-threatening condition that occurs when a systemic inflammatory response syndrome is triggered by an infection.
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Neoplasia: the abnormal and uncontrolled growth of cells that form a mass or tumor that can be benign or malignant.
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Genetic and congenital disorders: the diseases or conditions that are caused by abnormalities in the genes or chromosomes or by exposure to teratogens during the prenatal period.
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Fluid, electrolyte, and acid-base balance: the processes that maintain the optimal composition and distribution of body fluids in relation to water, solutes, and hydrogen ions.
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