Pharmacology 3 Flashcards

1
Q

What is the mechanism of action of hydrochlorothiazide?

A

Hydrochlorothiazide is a diuretic used primarily for hypertension that works by blocking the Na-Cl co-transporters in the distal convoluted tubules of the kidney, thereby decreasing Na+ and Cl- reabsorption.

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2
Q

A 23-year-old 76 kg male is about to undergo surgery for an inguinal hernia. Standard ASA monitors are placed and the patient is preoxygenated for 3 minutes prior to induction. He receives 200 mg of propofol mixed with 40 mg of lidocaine, 100 mcg of fentanyl, and 8 mg of vecuronium for induction. Which of the following is TRUE regarding pain on injection with propofol?

A

Mixing propofol with lidocaine has been shown to decrease the stability of the propofol emulsion and may cause pulmonary embolism. The FDA recommends against mixing propofol with any other therapeutic medications prior to administration. The most effective methods to reduce pain are propofol injections using an antecubital vein and a modified Bier block prior to injection.

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3
Q

Amiloride is MOST commonly associated with which of the following electrolyte imbalances?

A

Potassium-sparing diuretics can cause hyperkalemia by blocking potassium secretion in the distal collecting ducts. Thiazide diuretics can cause hypercalcemia due to their effects on the sodium-calcium exchanger in the distal convoluted tubule. Loop diuretics can cause hypokalemia and hyponatremia by affecting the TAL. Carbonic anhydrase inhibitors can cause metabolic acidosis, which may lead to hyperkalemia if untreated.

TrueLearn Insight : Acetazolamide is the treatment of choice for high-altitude/mountain sickness due to its ability to eliminate CSF alkalosis. A mnemonic for the potassium-sparing diuretics is: “The K+ STAys,” for Spironolactone, Triamterene, and Amiloride.

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4
Q

Which of the following is MOST suggestive of a diagnosis of sodium nitroprusside toxicity?

A

Sodium nitroprusside administration has the potential for causing toxicity due to the accumulation of its metabolic byproducts: cyanide and thiocyanate. Common presenting signs of cyanide toxicity include elevated PVO2, tachyphylaxis to SNP, metabolic acidosis, and flushing. Symptoms of thiocyanate toxicity include hypoxia, nausea, tinnitus, muscle spasm, disorientation, and psychosis.

TrueLearn Insight : Amyl nitrate works as an antidote for cyanide poisoning by converting Hb to MetHb which avidly binds cyanide, converting it to the nontoxic cyanomethemoglobin.

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5
Q

Which of the following opioid drugs is the MOST nonionized at physiologic pH?

A

A unique characteristic of alfentanil relative to other opioids is its significantly lower pKa resulting in a very high fraction of the drug existing in the nonionized form. Coupled with its moderate lipid solubility, this allows alfentanil to very rapidly cross the blood-brain barrier and have an ultra-short onset of action. The plasma-brain equilibration half-time of alfentanil is 0.9-1.1 minutes compared to 6.2 minutes for sufentanil, 4.7-6.4 minutes for fentanyl, and 139 minutes for morphine.

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6
Q

Which of the following is TRUE regarding the effects of diuretics on electrolytes?

A

: Diuretics result in the excretion of sodium from the body. Calcium is excreted by loop diuretics and reabsorbed by thiazide diuretics.

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7
Q

You have just extubated a patient where antagonism of the nondepolarizing muscle blockade with neostigmine occurred. You need to urgently reintubate the patient and succinylcholine 1 mg/kg is administered. Which of the following do you expect for the duration of action of succinylcholine?

A

Following neostigmine administration, a dose of succinylcholine will result in an increased duration of phase I blockade when compared to the duration of action of succinylcholine administered alone. Phase I augmentation lasts about 30 minutes on average.

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8
Q

Which of the following statements is the LEAST descriptive of zero order kinetics?

A

First order kinetics describes a situation where a constant proportion (percentage) of a medication is removed per unit time, whereas zero order kinetics describes a situation where a constant amount of medication is removed per unit time.
Liver blood flow dependent elimination is characteristic of first-order kinetics, not zero-order kinetics.
It is important to remember that drug metabolism via first or second order kinetics is not an inherent property of a medication, but rather a way to describe mathematically how these drugs behave in vivo.
TrueLearn Insight : Drugs that typically follow zero-order kinetics are THE PAW: theophylline, heparin, ethanol, phenytoin, aspirin, warfarin.

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9
Q

A 29-year-old, 62 kg female undergoes an open reduction and external fixation of a distal radius fracture after a snowboarding accident. She takes loratadine for seasonal allergies, fluoxetine for depression, and oral contraceptive pills. During the procedure, she receives 70 mg of rocuronium and is reversed with sugammadex. Which of the following is MOST likely to be a side effect of sugammadex?

A

The two most important adverse effects of sugammadex include anaphylaxis/hypersensitivity reactions and potentially severe bradycardia. Other important adverse effects include, but are not limited to arrhythmias, tachycardia, hypotension, prolongation of PT/INR and aPTT, and increased risk of unintentional pregnancy due to inactivation of hormonal contraceptives.

TrueLearn Insight : Sugammadex has no affinity for succinylcholine or benzylisoquinolinium neuromuscular blocking drugs (e.g. cisatracurium) and will not reverse their effects.

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10
Q

A patient undergoing laparoscopic appendectomy has received rocuronium for muscle relaxation at intubation. What is the mechanism of action for this medication?

A

All non-depolarizing neuromuscular blockers act as competitive antagonists at the postsynaptic nicotinic acetylcholine receptor.

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11
Q

Which of the following hemodynamic effects is MOST LIKELY to be seen immediately following 0.5 g/kg administration of mannitol given intravenously over twenty minutes?

A

After administration of mannitol, an increase in plasma volume will occur which will result in an increase in blood pressure and cardiac output. This may lead to an increase in pulmonary capillary wedge pressure, especially in patients with heart failure.

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12
Q

Which of the following is the FIRST expected sign or symptom of central nervous system toxicity from intravenous lidocaine administration?

A

Lidocaine toxicity is dependent on dose and site of injection. The most common cause is dosing error. The maximum dose (commonly cited) of lidocaine with and without epinephrine is 7 mg/kg and 5mg/kg, respectively. Central nervous system toxicity is first noted by circumoral and tongue numbness. Areas of regional anesthesia from highest to lowest vascularity include: intravenous > tracheal > intercostal > caudal/paracervical > epidural > brachial plexus > sciatic/femoral > spinal > subcutaneous.

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13
Q

Which of the following describes the mechanism by which the duration of action of rocuronium is prolonged when desflurane is used?

A

Volatile anesthetics potentiate neuromuscular blockade by DECREASING sensitivity of the postjunctional membrane to depolarization and INCREASING skeletal muscle blood flow which both augment neuromuscular blockade. In addition, potentiation of neuromuscular blockade occurs by depression of upper motor neurons.

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14
Q

Which of the following statements regarding milrinone is TRUE?

A

Milrinone is a second generation phosphodiesterase III (PDE III) inhibitor. Both PDE I and PDE II hydrolyze all cyclic nucleotides, but PDE III acts on cAMP specifically. Milrinone is excreted via the kidneys in its unconjugated form and therefore dosage should be adjusted in the setting of renal failure. Milrinone is unique in its ability to increase cardiac index without increasing myocardial oxygen demand. It also improves myocardial relaxation (lusitropy) and augments coronary circulation.
Milrinone increases cardiac index while reducing systemic and pulmonary vascular resistance.

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15
Q

A 68-year-old male is undergoing a hemicolectomy for colon cancer. He is maintained on 1% isoflurane and fentanyl boluses. Rocuronium is used for paralysis and is titrated to a single twitch on the peripheral nerve stimulator. Intraoperatively the surgeon complains of inadequate paralysis and requests further relaxation. Assessment of which of the following muscles is the MOST representative of abdominal muscle paralysis?

A

After laryngeal muscles and diaphragm, the corrugator supercilii (eyebrow movement) is the most resistant to neuromuscular blockade and most closely resembles the abdominal and laryngeal muscles. The adductor pollicis is more sensitive to neuromuscular blockade and is the best choice to monitor for extubating conditions. The flexor hallucis (big toe flexion) and orbicularis oculi (eyelid movement) correlate more closely with the adductor pollicis.

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16
Q

Which of the following immunosuppressants is MOST likely to prolong nondepolarizing neuromuscular blockade?

A

Cyclosporine is an immunosuppressant drug that can prolong the action of NDNBDs. In addition, it has potentially neurotoxic effects, including generalized seizures, and is nephrotoxic.

17
Q

Which of the following statements about buprenorphine is CORRECT?

A

Buprenorphine is a partial μ-agonist and κ-antagonist with 25-40 times the potency of morphine. There are ceiling effects, particularly for respiratory depression, at high doses. Cessation of buprenorphine is typically associated with only mild withdrawal symptoms.

18
Q

A 23-year-old male is undergoing general anesthesia for an inguinal hernia. Shortly following induction, the patient becomes hypotensive with increased peak airway pressures. Which of the following is MOST commonly associated with perioperative anaphylaxis?

A

Neuromuscular blocking drugs are the most common agents associated with perioperative anaphylaxis. Epinephrine is the drug of choice for anaphylaxis as is supports hemodynamics, promotes bronchodilation, and stabilizes mast cells. Serum mast cell tryptase levels can aid in diagnosis.

TrueLearn Insight : Allergy to neuromuscular blockers is more common in women than men, which is believed to be due to cross-reactive tertiary or quaternary ammonium groups found in both neuromuscular blockers and a variety of topical cosmetics and personal products, as well as certain over-the-counter cough remedies.

19
Q

Which of the following would result in the biggest decrease in minimum alveolar concentration (MAC) in a 35-year-old adult patient who is undergoing anesthesia for a laparoscopic appendectomy with a volatile anesthetic?

A

Intravenous opioids result in a decreased minimum alveolar concentration (MAC). The synthetic opioids cause a higher reduction in MAC compared to morphine. Gabapentin has not been shown to alter MAC values.

20
Q

In an anuric patient, which of the following treatments would BEST eliminate potassium from the body?

A

The mainstays of treatment for hyperkalemia include calcium chloride to stabilize the myocardium, insulin +/- dextrose to temporarily shift potassium intracellularly, and elimination of potassium via diuresis (usually loop diuretics such as furosemide), gastrointestinal loss (via the potassium binders patiromer or sodium zirconium cyclosilicate), or removal via hemodialysis. Intravenous insulin is the most rapid way to lower serum potassium, but this must be followed up by a method of eliminating the potassium, such as with furosemide, as the effects of insulin are only temporary.

21
Q

A previously healthy 7-year-old on postoperative day one from an open small bowel resection complains of pain and nausea. Which of the following options is MOST likely to control pain and decrease adverse events?

A

Intravenous patient controlled analgesia is an excellent form of pain management when a patient is unable to tolerate oral medications. It usually results in a more continuous plasma concentration of medication and also helps the patient became more able to be in control of their pain. Basal rates for intravenous PCAs are not advisable because they are associated with an increased risk of respiratory depression, especially in a patient who is opioid naïve

22
Q

Which of the following BEST approximates the time until the maximum plasma fentanyl concentration is reached following placement of a transdermal fentanyl patch?

A

The median time to peak plasma fentanyl concentration is approximately 30 hours following placement of a transdermal fentanyl patch. Onset is approximately 6-8 hours after placement.

23
Q

Which of the following BEST describes the amnestic effects of midazolam?

A

Midazolam causes anterograde but not retrograde amnesia, even at large doses. Typical anxiolysis doses (e.g. 2mg IV in an adult) do not guarantee amnesia.

24
Q

A 75-year-old patient with coronary artery disease presents in septic shock. Fluids are given and norepinephrine is started, which is rapidly titrated up to control hypotension. Which of the following is NOT a potential mechanism for the development of myocardial ischemia in this patient?

A

The deleterious side effects of vasopressors may result in significant morbidity and possibly mortality in certain patient populations. In patients with preexisting cardiac dysfunction, medication induced tachycardia may result in increased myocardial oxygen demand. If supply is not increased, myocardial ischemia and then infarction can result.

25
Q

he mechanism of the action of which of the following medications LEAST resembles that of glucagon?

A

Glucagon activates adenylyl cyclase to increase cyclic AMP levels. Glucagon increases cardiac index, mean arterial pressure, and ventricular contractility.
least similar to phenylephrine

26
Q

A patient has been receiving enoxaparin for a history of deep vein thrombosis. Which of the following would be the most appropriate test to assess the effectiveness of this anti-coagulation therapy?

A

LMWH exerts its anticoagulation effect by inactivation of factor Xa. Although laboratory monitoring in non-pregnant patients is not necessary, the anti-Xa assay is the best test to document the adequacy of anticoagulation with LMWH.

27
Q

Which of the following is an accurate description regarding the mechanism of action for angiotensin converting enzyme inhibitors?

A

The antihypertensive effects of ACE inhibitors are the result of decreasing the action of aldosterone within the renin-angiotensin-aldosterone system and increasing bradykinin’s vasodilatory and kidney natriuretic effects.

TrueLearn Insight : ACE inhibitors can cause a decrease in glomerular filtration in the setting of hypoperfusion because of a decrease in efferent arteriolar resistance.

28
Q

Which of the following intravenous medications reduces minimum alveolar concentration the MOST?

A

The opioids, particularly fentanyl type, have significant MAC reducing properties at analgesic doses. Midazolam and dexmedetomidine can reduce MAC. Gabapentin does not affect MAC. Magnesium and ephedrine increase MAC requirements.

29
Q

A 37-year-old woman presents for repair of a fractured radius. She reports several allergies, including amoxicillin. Upon further discussion, she states she had a fever and sore throat as a child, received the antibiotic, and then developed a rash without any other symptoms. Which of the following antibiotics would be MOST appropriate for this patient’s surgical procedure today?

A

Patients with a history of a delayed reaction to penicillin can be given cephalosporins. In a patient reporting an immediate penicillin reaction with concerning features including flushing, hives, pruritis, angioedema, urticaria, bronchospasm, or hypotension, an alternate drug should be chosen.

30
Q

During induction, the patient complains of pain at the site of intravenous administration. Which of the following medications is MOST likely the cause of this pain?

A

Pain on injection is common with some medications commonly used in anesthesia, with the most common being propofol, etomidate, methohexital, diazepam, and rocuronium. Methods to minimize the pain include injecting into a larger or central vein and the administration of lidocaine and/or opioids before the injection of the medication causing the pain on injection