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美国 2007-2011 年终端住院期间儿童接触阿片类药物和镇静药物情况。

Pediatric exposure to opioid and sedation medications during terminal hospitalizations in the United States, 2007-2011.

机构信息

Kentucky Children's Hospital, Lexington, KY.

The Children's Hospital of Philadelphia, Philadelphia, PA.

出版信息

J Pediatr. 2015 Mar;166(3):587-93.e1. doi: 10.1016/j.jpeds.2014.10.017. Epub 2014 Nov 21.

DOI:10.1016/j.jpeds.2014.10.017
PMID:25454928
Abstract

OBJECTIVE

To describe the use of opioids and sedatives to pediatric patients dying in the hospital in the 2 weeks preceding death.

STUDY DESIGN

We conducted a retrospective study on opioid and sedation medication exposure among children who die in hospitals in the US by using large administrative data sources. We described patterns of exposure to these medications for deceased inpatients (<21 years of age) between 2007 and 2011 (n = 37,459) and factors associated with the exposure. Multivariable logistic regression models were used to estimate the ORs.

RESULTS

Overall, 74% patients were exposed to opioids or sedatives in the 14 days before death. Among patients with 6 or more hospital days before death, the daily exposure rate ranged from 73% (the sixth day before death) to 89% (the day of death). The most commonly used medications were fentanyl (52%), midazolam (44%), and morphine (40%). Older age (ORs 1.6-3.7), black race (ORs 0.8), longer hospital stay (ORs 6.6-9.3), receiving medical interventions (including mechanical ventilation, surgery, and stay in the intensive care unit, ORs 1.7-2.6), having comorbidities (ORs 1.7-2.4), and being hospitalized in children's hospitals (ORs 4.0-4.5) were associated with exposure of opioid and sedation medication on adjusted analysis.

CONCLUSION

Although most pediatric patients terminally hospitalized are exposed to opioid and sedation medication, some patients do not receive such medications before death. Given that patient and hospital characteristics were associated with opioid/sedative exposure, these findings suggest areas of potential quality improvement and further research.

摘要

目的

描述在死亡前两周内,医院中死亡的儿科患者使用阿片类药物和镇静剂的情况。

研究设计

我们使用大型行政数据源,对美国医院死亡儿童的阿片类药物和镇静剂药物暴露情况进行回顾性研究。我们描述了 2007 年至 2011 年(n=37459)期间,<21 岁住院死亡患者暴露于这些药物的模式,并探讨了与暴露相关的因素。多变量逻辑回归模型用于估计比值比(ORs)。

结果

总体而言,74%的患者在死亡前 14 天内暴露于阿片类药物或镇静剂。在死亡前有 6 天或以上住院时间的患者中,每日暴露率从第六天(死亡前一天)的 73%到死亡当天(死亡前一天)的 89%不等。最常用的药物是芬太尼(52%)、咪达唑仑(44%)和吗啡(40%)。年龄较大(ORs 1.6-3.7)、黑人种族(ORs 0.8)、住院时间较长(ORs 6.6-9.3)、接受医疗干预(包括机械通气、手术和重症监护病房入住,ORs 1.7-2.6)、合并症(ORs 1.7-2.4)和在儿童医院住院(ORs 4.0-4.5)与阿片类药物和镇静剂药物暴露相关。

结论

尽管大多数终末期住院的儿科患者都接受了阿片类药物和镇静剂治疗,但有些患者在死亡前并未接受此类药物治疗。鉴于患者和医院特征与阿片类药物/镇静剂暴露相关,这些发现提示存在潜在的质量改进和进一步研究的领域。

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