Benzodiazepines and Development of Delirium in Critically Ill Children: Estimating the Causal Effect*

被引:4
作者
Mody, Kalgi [1 ]
Kaur, Savneet [2 ]
Mauer, Elizabeth A. [3 ]
Gerber, Linda M. [3 ]
Greenwald, Bruce M. [2 ]
Silver, Gabrielle [4 ]
Traube, Chani [2 ]
机构
[1] Mt Sinai Sch Med, Dept Pediat, New York, NY USA
[2] Weill Cornell Med Coll, Dept Pediat, New York, NY 10065 USA
[3] Weill Cornell Med Coll, Dept Healthcare Policy & Res, New York, NY USA
[4] Weill Cornell Med Coll, Dept Psychiat, New York, NY USA
基金
美国国家卫生研究院;
关键词
benzodiazepines; critical care; delirium; intensive care; pediatric; sedation; INTENSIVE-CARE-UNIT; MECHANICALLY VENTILATED PATIENTS; DECREASED DURATION; PEDIATRIC DELIRIUM; BRAIN-DYSFUNCTION; ABCDEF BUNDLE; SEDATION; ANALGESIA; DEXMEDETOMIDINE; EPIDEMIOLOGY;
D O I
10.1097/CCM.0000000000003194
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Objectives: Benzodiazepine use may be associated with delirium in critically ill children. However, benzodiazepines remain the first-line sedative choice in PICUs. Objectives were to determine the temporal relationship between administration of benzodiazepines and delirium development, control for time-varying covariates such as mechanical ventilation and opiates, and evaluate the association between dosage of benzodiazepines and subsequent delirium. Design: Retrospective observational study. Setting: Academic tertiary care PICU. Patients: All consecutive admissions from January 2015 to June 2015. Interventions: Retrospective assessment of benzodiazepine exposure in a population that had been prospectively screened for delirium. Measurements and Main Results: All subjects were prospectively screened for delirium throughout their stay, using the Cornell Assessment for Pediatric Delirium, with daily cognitive status assigned as follows: delirium, coma, or normal. Multivariable mixed effects modeling determined predictors of delirium overall, followed by subgroup analysis to assess effect of benzodiazepines on subsequent development of delirium. Marginal structural modeling was used to create a pseudorandomized sample and control for time-dependent variables, obtaining an unbiased estimate of the relationship between benzodiazepines and next day delirium. The cumulative daily dosage of benzodiazepines was calculated to test for a dose-response relationship. Benzodiazepines were strongly associated with transition from normal cognitive status to delirium, more than quadrupling delirium rates (odds ratio, 4.4; CI, 1.7-11.1; p < 0.002). Marginal structural modeling demonstrated odds ratio 3.3 (CI, 1.4-7.8), after controlling for time-dependent confounding of cognitive status, mechanical ventilation, and opiates. With every one log increase in benzodiazepine dosage administered, there was a 43% increase in risk for delirium development. Conclusions: Benzodiazepines are an independent and modifiable risk factor for development of delirium in critically ill children, even after carefully controlling for time-dependent covariates, with a dose-response effect. This temporal relationship suggests causality between benzodiazepine exposure and pediatric delirium and supports limiting the use of benzodiazepines in critically ill children.
引用
收藏
页码:1486 / 1491
页数:6
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