Washington State University, Global Health Programs (Kenya Office), Nairobi, Kenya.
College of Health Sciences, University of Nairobi, Nairobi, Kenya.
Clin Infect Dis. 2021 Dec 15;73(Suppl_5):S360-S367. doi: 10.1093/cid/ciab810.
We used postmortem minimally invasive tissue sampling (MITS) to assess the effect of time since death on molecular detection of pathogens among respiratory illness-associated deaths.
Samples were collected from 20 deceased children (aged 1-59 months) hospitalized with respiratory illness from May 2018 through February 2019. Serial lung and/or liver and blood samples were collected using MITS starting soon after death and every 6 hours thereafter for up to 72 hours. Bodies were stored in the mortuary refrigerator for the duration of the study. All specimens were analyzed using customized multipathogen TaqMan® array cards (TACs).
We identified a median of 3 pathogens in each child's lung tissue (range, 1-8; n = 20), 3 pathogens in each child's liver tissue (range, 1-4; n = 5), and 2 pathogens in each child's blood specimen (range, 0-4; n = 5). Pathogens were not consistently detected across all collection time points; there was no association between postmortem interval and the number of pathogens detected (P = .43) and no change in TAC cycle threshold value over time for pathogens detected in lung tissue. Human ribonucleoprotein values indicated that specimens collected were suitable for testing throughout the study period.
Results suggest that lung, liver, and blood specimens can be collected using MITS procedures up to 4 days after death in adequately preserved bodies. However, inconsistent pathogen detection in samples needs careful consideration before drawing definitive conclusions on the etiologic causes of death.
我们使用死后微创组织取样(MITS)来评估死后时间对与呼吸道疾病相关死亡的病原体分子检测的影响。
从 2018 年 5 月至 2019 年 2 月期间因呼吸道疾病住院的 20 名已故儿童(年龄 1-59 个月)中采集样本。使用 MITS 尽快在死后并随后每 6 小时收集一次连续的肺和/或肝和血样,最多持续 72 小时。在研究期间,尸体被储存在太平间冰箱中。所有标本均使用定制的多病原体 TaqMan®阵列卡(TAC)进行分析。
我们在每个儿童的肺组织中鉴定出中位数为 3 种病原体(范围为 1-8;n=20),在每个儿童的肝组织中鉴定出中位数为 3 种病原体(范围为 1-4;n=5),在每个儿童的血液标本中鉴定出中位数为 2 种病原体(范围为 0-4;n=5)。病原体未在所有采集时间点上均被检测到;死后间隔与检测到的病原体数量之间无关联(P=0.43),并且在肺组织中检测到的病原体的 TAC 循环阈值值在整个研究期间没有随时间变化。人类核糖核蛋白值表明,在整个研究期间,收集的标本均适合进行测试。
结果表明,在适当保存的尸体中,MITS 程序最多可在死亡后 4 天内采集肺、肝和血样。然而,样本中病原体的不一致检测需要在得出关于死亡病因的明确结论之前进行仔细考虑。