Safety of midazolam for sedation of HIV-positive patients undergoing colonoscopy.
Safety of midazolam for sedation of HIV-positive patients undergoing colonoscopy.
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DOI:
10.1111/hiv.12014
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发表时间:
2013-07
期刊:
影响因子:
3
通讯作者:
Gandhi RT
中科院分区:
文献类型:
--
作者:
Backman ES;Triant VA;Ehrenfeld JM;Lu Z;Arpino P;Losina E;Gandhi RT
Concerns regarding possible interactions between midazolam and antiretroviral medicines have caused clinicians to use second-line sedatives, such as diazepam, instead. We demonstrated that patients who received midazolam during colonoscopy had similar clinical outcomes as those who received diazepam. 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 versus IV diazepam, a second-line agent, during colonoscopy. We conducted a retrospective analysis of adult HIV-infected patients who underwent colonoscopy over a 3.5-year period. Primary outcomes were sedation duration, nadir systolic blood pressure, 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. 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 (48 versus 45.7 minutes, P = 0.68), nadir systolic blood pressure (97 versus 101.6 mmHg, P = 0.06), nadir oxygen saturation (94.6 versus 94.8%, P = 0.72), or rate of abnormal cardiac rhythm (11.4 versus 19.7%, P = 0.18). More patients in the midazolam group experienced a depressed level of consciousness (91 versus 74%, P = 0.0075), but no patient required reversal of sedation or became unresponsive. Although IV midazolam interacts with ART, we did not find evidence that patients who received this agent 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.
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DOI:
10.1016/j.atc.2004.06.001
发表时间:
2004-09-01
期刊:
Anesthesiology clinics of North America
影响因子:
--
作者:
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通讯作者:
Hughes, Samuel C
影响因子:
7.7
作者:
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通讯作者:
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作者:
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通讯作者:
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影响因子:
4.1
作者:
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通讯作者:
Davey, R
影响因子:
4.1
作者:
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通讯作者:
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