Abstract
Sodium nitroprusside (SNP) entered into clinical practice in 1955 and gained popularity as a vasodilator for hypertensive emergencies because of its rapid onset of action and short duration, which allowed for bedside titration to the desired effect [1]. The introduction of a freeze-dried preparation in 1974 was followed by an additional increase in popularity, and it continued to gain favor for producing controlled hypotension during anesthesia and afterload reduction during low cardiac output states. Availability of alternative agents has more recently limited use of SNP for hypertensive emergencies. However, novel applications, such as for the treatment of schizophrenia, are under investigation [2].
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References
Page IH, Corcoran AC, Dustan HP, et al. Cardiovascular actions of sodium nitroprusside in animals and hypertensive patients. Circulation. 1955;11:188–98.
Hallak JE, Maia de Oliveira JP, Abrao J, et al. Rapid improvement of acute schizophrenia symptoms after intravenous sodium nitroprusside: a randomized, double blind, placebo controlled trial. JAMA Psychiatry. 2013;70:668–76.
Curry SC, Arnold-Capell P. Nitroprusside, nitroglycerin, and angiotensin-converting enzyme inhibitors. Crit Care Clin. 1991;7:555–81.
Kreye VAW, Reske SN. Possible site of the in vivo disposition of sodium nitroprusside in the rat. Arch Pharmacol. 1982;32:260–5.
Schulz V. Clinical pharmacokinetics of nitroprusside, cyanide, thiosulphate and thiocyanate. Clin Pharmacokinet. 1984;9:239–51.
Rodkey FL, Collison HA. Determination of cyanide and nitroprusside in blood and plasma. Clin Chem. 1977;23:1969–75.
Schulz V, Bonn R, Kindler J. Kinetics of elimination of thiocyanate in seven healthy subjects and in eight subjects with renal failure. Klin Wochenschr. 1979;57:243–7.
Ivankovich AD, Braverman B, Stephens TS, et al. Sodium thiosulfate disposition in humans: relation to sodium nitroprusside toxicity. Anesthesiology. 1983;58:11–7.
Rutkowski JV, Roebuck BD, Smith RP. Liver damage does not increase the sensitivity of mice to cyanide given acutely. Toxicology. 1986;38:305–14.
Jack RD. Toxicity of sodium nitroprusside (letter). Br J Anaesth. 1974;46:952.
MacRae WR, Owen M. Severe metabolic acidosis following hypotension induced with sodium nitroprusside. Br J Anaesth. 1974;46:795–7.
Mellino M, Phillips DF. Severe lactic acidosis in a case of nitroprusside resistance. Cleve Clin Q. 1980;47:119–22.
Humphrey SH, Nash DA. Lactic acidosis complicating sodium nitroprusside therapy. Ann Intern Med. 1978;88:58–9.
Aitken D, West D, Smith F, et al. Cyanide toxicity following nitroprusside-induced hypotension. Can Anaesth Soc J. 1977;24:651–60.
Vesey CJ, Cole PV, Simpson PJ. Cyanide and thiocyanate concentrations following sodium nitroprusside infusion in man. Br J Anaesth. 1976;48:651–60.
Vesey CJ, Cole PV. Blood cyanide and thiocyanate concentrations produced by long-term therapy with sodium nitroprusside. Br J Anaesth. 1985;57:148–55.
Vesey CJ, Wilson J. Red cell cyanide. J Pharm Pharmacol. 1978;30:20–6.
Patel CB, Laboy V, Venus B, et al. Use of sodium nitroprusside in post-coronary bypass surgery: a plea for conservatism. Chest. 1986;89:663–7.
Cole PV, Vesey CJ. Sodium thiosulphate decreases blood cyanide concentration following sodium nitroprusside (letter). Br J Anaesth. 1988;60:745.
Schulz V, Gross R, Pasch T, et al. Cyanide toxicity of sodium nitroprusside in therapeutic use with and without sodium thiosulphate. Klin Wochenschr. 1982;60:1393–400.
Pahl MV, Vaziri ND. In-vivo and in-vitro hemodialysis studies of thiocyanate. J Toxicol Clin Toxicol. 1982;19:965–74.
Elberg AJ, Gorman HM, Baker R, et al. Prolonged nitroprusside and intermittent hemodialysis as therapy for intractable hypertension. Am J Dis Child. 1978;132:988–9.
Rigg D, McDonogh A. Use of sodium nitroprusside for deliberate hypotension during pregnancy. Br J Anaesth. 1981;53:985–7.
Donchin Y, Amirav G, Sahar A, et al. Sodium nitroprusside for aneurysm surgery in pregnancy. Br J Anaesth. 1978;50:849–51.
Stempel JE, O’Grady JP, Morton MJ, et al. Use of sodium nitroprusside in complications of gestational hypertension. Obstet Gynecol. 1982;60:533–8.
Ellis SC, Wheeler AS, James III FM, et al. Fetal and maternal effects of sodium nitroprusside used to counteract hypertension in gravid ewes. Am J Obstet Gynecol. 1982;143:766–70.
Curry SC, Carlton MW, Raschke RA. Prevention of fetal and maternal cyanide toxicity from nitroprusside with coinfusion of sodium thiosulfate in gravid ewes. Anesth Analg. 1997;84:1121–6.
Naulty J, Cefalo RC, Lewis PE. Fetal toxicity of nitroprusside in the pregnant ewe. Am J Obstet Gynecol. 1981;139:708–11.
Graeme KA, Curry SC, Bikin DS, et al. The lack of transplacental movement of the cyanide antidote thiosulfate in gravid ewes. Anesth Analg. 1999;89:1448–52.
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Grading System for Levels of Evidence Supporting Recommendations in Critical Care Toxicology, 2nd Edition
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I
Evidence obtained from at least one properly randomized controlled trial.
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II-1
Evidence obtained from well-designed controlled trials without randomization.
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II-2
Evidence obtained from well-designed cohort or case–control analytic studies, preferably from more than one center or research group.
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II-3
Evidence obtained from multiple time series with or without the intervention. Dramatic results in uncontrolled experiments (such as the results of the introduction of penicillin treatment in the 1940s) could also be regarded as this type of evidence.
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III
Opinions of respected authorities, based on clinical experience, descriptive studies and case reports, or reports of expert committees.
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Curry, S.C., Spyres, M.B. (2017). Sodium Nitroprusside. In: Brent, J., et al. Critical Care Toxicology. Springer, Cham. https://doi.org/10.1007/978-3-319-17900-1_10
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DOI: https://doi.org/10.1007/978-3-319-17900-1_10
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