Medicines
- Ketamine: increase cardiac work, O2 use, secretions, BP. No respiratory
depression. Hallucinations
- Methoxyflurane has renal toxicity
- Halothane is hepatotoxic
- Succinylcholine is the only depolarizing agent used; generalized
contractions; hyperkalemia in burn patients; fast on/fast off; risk
aspiration, glaucoma
- Clindamycin prolongs neuromuscular blockade
- Demerol should be avoided in patients on MAOI's
- Octreotide: long acting somatostatin analog
- Reglan = metoclopromaide: DA blocker, increase LES tone, increase gastric
motility
- Omeprazole: mech is blocking H pump (ATPase); associated with
enterochromaffin hyperplasia in rats. No evidence for carcinogenesis in humans
- Digoxin: glycosides, inhibits Na-K ATPase to increase Ca in heart. Slows
AV conduction. Inotrope, but does not increase O2 consumption. Associated with
ischemic gut, decreases splanchnic flow. Avoid hypokalemia
- Amrinone: phosphodiesterase inhibitor; inotrope, increase cardiac output,
decrease SVR
- Metyrapone and Aminoglutethimide: 'medical adrenalectomy'
- Leuprolide: 'medical orchiectomy'
- Vasopressin: reduces splanchnic flow, portal flow ~40%. Useful in GI
bleeds, give with beta-blocker to avoid angina
- Sodium Nitroprusside relaxes arteries and veins; has cyanide toxicity
- Nitroglycerin primarily relaxes veins
- Aspirin irreversibly binds cyclooxygenase, effective for life of platelet
(~7 days)
- Indomethacin blocks PG production, used to close PDA (effective in 70%).
Decrease renal blood flow
- Misoprostil replaces PGE2 (cytoprotective) for pt on nsaids, to reduce PUD
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