A provider has ordered oral voriconazole [Vfend] which is an azole medication for a patient who has a systemic fungal infection. The nurse obtains a medication history and learns that the patient takes anticoagulant medication Warfarin. The nurse will contact the provider to discuss which possibility?

Choice A reason:
Fatty acids are essential components of many lipids, but they are not the primary building blocks of bile salts. Bile salts are synthesized from cholesterol. Fatty acids mainly function as energy storage molecules and are involved in forming complex lipids, like triglycerides and phospholipids. They don't participate directly in the production of bile salts, which are crucial for digesting and absorbing dietary fats.

Choice B reason:
Testosterone is a steroid hormone that plays a vital role in male reproductive tissues and secondary sexual characteristics. It is not involved in the synthesis of bile salts. Bile salts are derived from cholesterol, not hormones. Testosterone’s primary function is related to endocrine activities rather than hepatic functions like bile salt synthesis.

Choice C reason:
Cholesterol is the correct answer. Bile salts are synthesized from cholesterol in the liver. This process involves the conversion of cholesterol into bile acids, which are then conjugated with amino acids to form bile salts. These bile salts are critical for the digestion and absorption of fats in the small intestine. The liver’s conversion of cholesterol to bile salts helps in maintaining cholesterol homeostasis in the body.

Choice D reason:
Lecithin is a type of phospholipid that plays a significant role in cell membrane structure and function. While it is an important component of bile, it is not the substance from which bile salts are synthesized. Lecithin helps in the emulsification of fats in the digestive process but is not a precursor to bile salts. The synthesis of bile salts specifically involves cholesterol.

Choice A reason:
Morphine is not most effective when given orally due to the high first-pass effect. The first-pass effect refers to the metabolism of a drug in the liver immediately after it enters the bloodstream from the gastrointestinal tract, significantly reducing the amount of active drug that reaches systemic circulation. Therefore, oral administration of morphine is not the most effective route because much of it is metabolized before it can exert its effect.

Choice B reason:
Morphine will be more effective when given via a non-enteral route such as intravenous (IV) or subcutaneous (SQ) because these routes bypass the liver, thereby avoiding the first-pass metabolism. This allows a higher concentration of the active drug to reach the systemic circulation, providing a more potent and effective pain relief.

Choice C reason:
Oral and IV administration of morphine do not have the same effect due to the first-pass metabolism. When morphine is administered orally, a significant amount is metabolized by the liver before it reaches the systemic circulation, whereas IV administration delivers the drug directly into the bloodstream, bypassing the liver and allowing a higher active concentration.

Choice D reason:
Morphine is not primarily excreted by the lungs; it is mainly metabolized by the liver and excreted by the kidneys. This statement does not accurately demonstrate an understanding of the first-pass effect or the pharmacokinetics of morphine.