Literature DB >> 23332038

Safety of midazolam for sedation of HIV-positive patients undergoing colonoscopy.

E S Backman1, V A Triant, J M Ehrenfeld, Z Lu, P Arpino, E Losina, R T Gandhi.   

Abstract

OBJECTIVES: Because of concerns regarding interactions between midazolam and antiretroviral therapy (ART), alternative sedatives are sometimes used during procedural sedation. Our objective was to compare outcomes in patients on ART who received intravenous (iv) midazolam vs. iv diazepam, a second-line agent, during colonoscopy.
METHODS: We conducted a retrospective analysis of adult HIV-positive patients who underwent colonoscopy over a 3.5-year period. Primary outcomes were sedation duration, nadir systolic blood pressure (SBP), nadir oxygen saturation, abnormal cardiac rhythm, and change in level of consciousness using a standardized scale. We calculated rates of adverse events according to benzodiazepine use and identified risk factors for complications using univariate and multivariate analyses.
RESULTS: We identified 136 patients for this analysis: 70 received midazolam-based sedation and 66 received a diazepam-based regimen. There were no significant differences between the two groups with respect to sedation duration (mean 48.0 vs. 45.7 minutes for the midazolam and diazepam groups, respectively; P = 0.68), nadir SBP (mean 97.0 vs. 101.6 mmHg; P = 0.06), nadir oxygen saturation (mean 94.6 vs. 94.8%; P = 0.72) or rate of abnormal cardiac rhythm (11.4 vs. 19.7%; P = 0.18). More patients in the midazolam group experienced a depressed level of consciousness (91% vs. 74% in the diazepam group; P = 0.0075), but no patient required reversal of sedation or became unresponsive.
CONCLUSIONS: We did not find evidence that patients who received midazolam for procedural sedation had clinical outcomes statistically different from those who received diazepam. These findings should be confirmed in prospective studies or in a randomized controlled trial.
© 2013 British HIV Association.

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Year:  2013        PMID: 23332038      PMCID: PMC4120820          DOI: 10.1111/hiv.12014

Source DB:  PubMed          Journal:  HIV Med        ISSN: 1464-2662            Impact factor:   3.180


  26 in total

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Authors:  S P Nordt; R F Clark
Journal:  J Emerg Med       Date:  1997 May-Jun       Impact factor: 1.484

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Authors:  J Ahonen; K T Olkkola; P J Neuvonen
Journal:  Eur J Clin Pharmacol       Date:  1997       Impact factor: 2.953

3.  Saquinavir interaction with midazolam: pharmacokinetic considerations when prescribing protease inhibitors for patients with HIV disease.

Authors:  C Merry; F Mulcahy; M Barry; S Gibbons; D Back
Journal:  AIDS       Date:  1997-02       Impact factor: 4.177

4.  The effects of the systemic antimycotics, itraconazole and fluconazole, on the pharmacokinetics and pharmacodynamics of intravenous and oral midazolam.

Authors:  K T Olkkola; J Ahonen; P J Neuvonen
Journal:  Anesth Analg       Date:  1996-03       Impact factor: 5.108

5.  Effect of saquinavir on the pharmacokinetics and pharmacodynamics of oral and intravenous midazolam.

Authors:  V J Palkama; J Ahonen; P J Neuvonen; K T Olkkola
Journal:  Clin Pharmacol Ther       Date:  1999-07       Impact factor: 6.875

6.  A comparison of midazolam and diazepam for conscious sedation during colonoscopy in a prospective double-blind study.

Authors:  S F Zakko; H A Seifert; J B Gross
Journal:  Gastrointest Endosc       Date:  1999-06       Impact factor: 9.427

7.  Sedative drug requirements during flexible bronchoscopy.

Authors:  Prashant N Chhajed; Julia Wallner; Daiana Stolz; Florent Baty; Werner Strobel; Martin H Brutsche; Michael Tamm
Journal:  Respiration       Date:  2005 Nov-Dec       Impact factor: 3.580

8.  Ritonavir's role in reducing fentanyl clearance and prolonging its half-life.

Authors:  K T Olkkola; V J Palkama; P J Neuvonen
Journal:  Anesthesiology       Date:  1999-09       Impact factor: 7.892

9.  Midazolam should be avoided in patients receiving the systemic antimycotics ketoconazole or itraconazole.

Authors:  K T Olkkola; J T Backman; P J Neuvonen
Journal:  Clin Pharmacol Ther       Date:  1994-05       Impact factor: 6.875

10.  Diazepam metabolism by human liver microsomes is mediated by both S-mephenytoin hydroxylase and CYP3A isoforms.

Authors:  T Andersson; J O Miners; M E Veronese; D J Birkett
Journal:  Br J Clin Pharmacol       Date:  1994-08       Impact factor: 4.335

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