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Review of Pharmacology - 9E (2015)

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Anaesthesia<br />

• The patient underwent rapid sequence intubation (RSI). A depolarizing neuromuscular blocking drug is commonly<br />

administered for RSI, because onset <strong>of</strong> action is generally more rapid (within 60 seconds) than for most available nondepolarizing<br />

blockers.<br />

• The patient still exhibits residual muscle paralysis even after neostigmine, an anti-cholinesterase. The persistence <strong>of</strong><br />

paralysis indicates that Drug A is a depolarizing blocker. Anticholinesterases do not reverse the action <strong>of</strong> depolarizing<br />

and may, in fact, enhance them.<br />

The only depolarizing blocker listed among the options is succinylcholine. In patients with atypical pseudocholinesterase,<br />

SCh may produce prolonged paralysis and apnea.<br />

71. Ans. (d) Suxamethonium (Ref: Katzung 11/e p454)<br />

Suxamethonium is the other name <strong>of</strong> succinylcholine. It is the shortest acting muscle relaxant due to metabolism by pseudocholinesterase<br />

72. Ans. (a) Atracurium (Ref: KDT 6/e p345)<br />

73. Ans. (d) Quinidine (Ref: Clinical Anesthesiology by Murray and Morgan/189;KDT 6/e p346)<br />

Non-depolarizing blockade is potentiated by<br />

Hypothermia<br />

Hypokalemia<br />

Hypermagnesemia<br />

Aminoglycosides, Tetracyclines, Polymyxin B<br />

Trimethaphan<br />

MgSO 4<br />

Ketamine<br />

74. Ans. (a) Chloramphenicol (Ref: KDT 6/e p346)<br />

Drugs causing curare like effect are:<br />

• Aminoglycosides<br />

• Polypeptide antibiotics:<br />

––<br />

Polymyxin B<br />

––<br />

Bacitracin<br />

––<br />

Colistin<br />

––<br />

Tyrothricin<br />

• Tetracycline<br />

• Clindamycin, lincomycin<br />

Respiratory acidosis<br />

Hypocalcemia<br />

Neonatal period<br />

Quinine, Lignocaine, CCBs, Procainamide<br />

Dantrolene<br />

Local Anaesthetics<br />

General Anaesthesia <strong>Pharmacology</strong><br />

75. Ans. (b) Vecuronium (Ref: KDT 5/e p345)<br />

It does not cause ganglion blockade or histamine release and is having good cardiovascular stability.<br />

76. Ans. (b) Depolarising muscle relaxant (Ref: KDT 6/e p339 )<br />

77. Ans. (a) Centrally acting muscle relaxant (Ref: Katzung 11/e p463)<br />

78. Ans. (d) All <strong>of</strong> the above (Ref: Katzung 11/e p457)<br />

79. Ans. (c) Succinylcholine (Ref: KDT 6/e p343)<br />

80. Ans. (c) Pancuronium (Ref: KDT 6/e p343)<br />

81. Ans. (d) Amitryptiline (Ref: Katzung 11/e p462-464)<br />

82. Ans. (a) Atracurium (Ref: KDT 6/e p345)<br />

83. Ans. (b) Mivacurium (Ref: KDT 6/e p339)<br />

84. Ans. (c) Progression to dual blockade (Ref: Katzung 11/e p457)<br />

85. Ans. (d) All <strong>of</strong> the above (Ref: KDT 6/e p348)<br />

86. Ans. (c) Ketamine (Ref: Goodman and Gilman 12/e p538-539)<br />

Ketamine increases all pressures (blood pressure, intracranial tension, intraocular pressure) in the body. It is therefore<br />

intravenous anaesthetic <strong>of</strong> choice for shock (increases blood pressure).<br />

431<br />

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