Literature DB >> 2746688

Use of naloxone in septic shock.

J Canady, W Williams, I Thompson, G S Vincent, E Hoover.   

Abstract

Experimental and clinical evidence show that endogenous opiates (endorphins) contribute to the pathophysiology of circulatory shock. The authors evaluated the effectiveness and safety of continuous infusion of naloxone in five septic patients with prolonged hypotension unresponsive to volume replacement and dopamine infusion. Naloxone (2 mg bolus) was intravenously administered and continued at 0.25 mg/hr for 24 to 48 hours. All five patients had significant increase in mean arterial pressure of between 20 and 30 mmHg (P less than 0.0012). Cardiac index, systemic vascular resistance, and pulmonary arterial pressure were not significantly altered; however, there was a significant difference in pulmonary capillary wedge pressure (P less than 0.034) and urinary output (P less than 0.0273). Subjects did not experience side effects with naloxone. We conclude that continuous infusion of naloxone can reverse endorphin-mediated hypotension in septic shock patients.

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Year:  1989        PMID: 2746688      PMCID: PMC2625808     

Source DB:  PubMed          Journal:  J Natl Med Assoc        ISSN: 0027-9684            Impact factor:   1.798


  44 in total

1.  Hemodynamic effects of dopamine in critically ill septic patients.

Authors:  R F Wilson; W J Sibbald; J L Jaanimagi
Journal:  J Surg Res       Date:  1976-03       Impact factor: 2.192

2.  Effects of dobutamine on left ventricular performance, coronary dynamics, and distribution of cardiac output in conscious dogs.

Authors:  S F Vatner; R J McRitchie; E Braunwald
Journal:  J Clin Invest       Date:  1974-05       Impact factor: 14.808

Review 3.  Cardiogenic shock: a review.

Authors:  M G Perlroth; D C Harrison
Journal:  Clin Pharmacol Ther       Date:  1969 Jul-Aug       Impact factor: 6.875

4.  Dopamine-induced alterations in coronary hemodynamics in dogs.

Authors:  H L Brooks; P D Stein; J L Matson; J W Hyland
Journal:  Circ Res       Date:  1969-05       Impact factor: 17.367

5.  Acidosis lowers in-vivo potency of narcotics and narcotic antagonists and can even abolish narcotic antagonist activity.

Authors:  J J Kaufman
Journal:  Lancet       Date:  1982-03-06       Impact factor: 79.321

6.  Response to naloxone in septic shock.

Authors:  W R Swinburn; P Phelan
Journal:  Lancet       Date:  1982-01-16       Impact factor: 79.321

7.  Reduced ambient temperature blocks the ability of naloxone to prevent endotoxin-induced hypotension.

Authors:  H F Janssen; J L Pugh; L O Lutherer
Journal:  Adv Shock Res       Date:  1982

8.  Reversal of hypotension by continuous naloxone infusion in a ventilator-dependent patient.

Authors:  T L Higgins; E D Sivak; D M O'Neil; J W Graves; D G Foutch
Journal:  Ann Intern Med       Date:  1983-01       Impact factor: 25.391

9.  beta-Endorphin and adrenocorticotropin are selected concomitantly by the pituitary gland.

Authors:  R Guillemin; T Vargo; J Rossier; S Minick; N Ling; C Rivier; W Vale; F Bloom
Journal:  Science       Date:  1977-09-30       Impact factor: 47.728

10.  Naloxone treatment of endotoxin shock: stereospecificity of physiologic and pharmacologic effects in the rat.

Authors:  A I Faden; J W Holaday
Journal:  J Pharmacol Exp Ther       Date:  1980-03       Impact factor: 4.030

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  1 in total

Review 1.  Naloxone for shock.

Authors:  B Boeuf; V Poirier; F Gauvin; A M Guerguerian; C Roy; C A Farrell; J Lacroix
Journal:  Cochrane Database Syst Rev       Date:  2003
  1 in total

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