Livshits Z, Sampson B A, Howland M A, Hoffman R S, Nelson L S
Division of Emergency Medicine, Department of Medicine, New York Presbyterian Weill Cornell Medical Center , New York, NY , USA.
Clin Toxicol (Phila). 2015 Feb;53(2):113-8. doi: 10.3109/15563650.2014.992528. Epub 2014 Dec 30.
The extent of non-absorbed drug burden in the GI tract following overdose is unknown. Patients who present with clinical signs of toxicity may not undergo decontamination due to assumption that the drug has already been completely absorbed and because of limited scientific evidence of benefit for routine GI decontamination in poisoned patients.
The goal of this study was to assess whether people who die of an oral overdose have unabsorbed drug present in the GI tract. The secondary goal was to analyze pharmacologic characteristics of retained drugs when present.
Retrospective review of autopsy reports from 2008 to 2010, whose cause of death was determined as "intoxication" or "overdose, was performed at the Office of Chief Medical Examiner of the City of New York (OCME NYC)." Decedents of all ages were identified via electronic OCME database. Inclusion criteria were as follows: 1) cause of death "intoxication" or "overdose" noted by forensic autopsy, 2) ingestion of a solid drug formulation.
92 out of 1038 autopsies (9%) that met inclusion criteria had documentation of retained pill fragments, granules, paste, sludge, slurry, or whole pills in the GI tract. The most common drugs found were opioids and anticholinergics. Ninety-eight percent (98%) of the retained drugs were either modified-release preparations or drugs known to slow GI transit. Most decedents were dead on arrival; there were twelve in-hospital deaths and eleven patients died in the Emergency Department. Bupropion and venlafaxine were responsible for four deaths in those who received medical care. One person died in the ICU following bupropion ingestion.
Overdose of an oral drug that either has modified-release properties or slows GI tract motility may result in substantial unabsorbed drug burden remaining in the GI tract.
过量用药后胃肠道中未吸收药物的负担程度尚不清楚。出现中毒临床症状的患者可能未进行去污处理,原因是认为药物已完全吸收,且中毒患者常规胃肠道去污处理益处的科学证据有限。
本研究的目的是评估死于口服过量用药的人胃肠道中是否存在未吸收药物。次要目的是分析留存药物存在时的药理学特征。
对纽约市首席法医办公室(OCME NYC)2008年至2010年死因确定为“中毒”或“过量用药”的尸检报告进行回顾性研究。通过OCME电子数据库识别所有年龄段的死者。纳入标准如下:1)法医尸检记录的死因是“中毒”或“过量用药”,2)摄入固体药物制剂。
在符合纳入标准的1038例尸检中,有92例(9%)记录了胃肠道中留存有药丸碎片、颗粒、糊剂、淤渣、浆液或完整药丸。发现的最常见药物是阿片类药物和抗胆碱能药物。留存药物的98%是缓释制剂或已知会减缓胃肠道转运的药物。大多数死者到达时已死亡;有12例住院死亡,11例患者在急诊科死亡。安非他酮和文拉法辛导致接受治疗的患者中有4例死亡。1例患者在摄入安非他酮后在重症监护病房死亡。
口服具有缓释特性或减缓胃肠道蠕动的药物过量可能导致大量未吸收药物残留于胃肠道中。