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降钙素原与因感染导致的婴儿猝死有关。

Procalcitonin is associated with sudden unexpected death in infancy due to infection.

机构信息

Pediatric Emergency Department, Children's Hospital, University Hospital of Nancy, Vandoeuvre-Les-Nancy, France.

Inserm, Clinical Investigation Centre 1413, University Hospital of Nantes, Nantes, France.

出版信息

Eur J Pediatr. 2023 Sep;182(9):3929-3937. doi: 10.1007/s00431-023-05064-3. Epub 2023 Jun 23.

Abstract

Infection is an important cause of death during infancy worldwide and is a frequent etiology of sudden unexpected death in infancy (SUDI). Procalcitonin (PCT) is a useful marker to diagnose infection in patients, and several studies report the stability of PCT after death. The added value of a biological marker, such as the PCT level in the blood, remains controversial in investigating SUDI. The aim of this study was to determine if PCT can help clinicians determine whether infection caused SUDI. We conducted a retrospective, multicenter study with the French SUDI registry (Observatoire National des Morts Inattendues du Nourrisson; OMIN). We collected data from this registry on children who died between May 2015 and June 2021. The levels of PCT in the blood of 540 SUDI patients were measured. We compared PCT and other biological tests performed in terms of infection status, autopsy results, and cause of death using clinical and biological data compiled by pediatricians at the SUDI referral center. PCT levels were significantly higher in the children who died from infection than in those who did not (0.12 µg/L vs. 0.08 µg/L, p < 0.001). A PCT blood level exceeding 0.2 µg/L was more frequently observed when infection was present than in the absence of infection (44.3% vs. 15.4%, p < 0.001). The same data were obtained with a 0.5 µg/L cut-off (36.1% with infection vs. 9.2% without, p < 0.001).  Conclusions: PCT is a sensitive biomarker for detecting infections postmortem; thus, additional samples may be necessary during autopsy. What is known: • PCT is a stable marker postmortem and increases earlier than CRP, i.e., 2-4 h after the beginning of an infection vs. 6 h. • PCT can be measured up to 140 h after death. What is new: • PCT is a sensitive marker for detecting infection in SUDI patients postmortem. • This test can reveal an infection from non-standardized samples obtained during autopsy if such an infection was not determined before death.

摘要

感染是全球婴儿死亡的重要原因,也是婴儿猝死综合征 (SUDI) 的常见病因。降钙素原 (PCT) 是一种用于诊断患者感染的有用标志物,多项研究报告了死亡后 PCT 的稳定性。在调查 SUDI 时,生物标志物(例如血液中的 PCT 水平)的附加值仍然存在争议。本研究旨在确定 PCT 是否可以帮助临床医生确定感染是否导致 SUDI。我们进行了一项回顾性、多中心研究,使用法国 SUDI 登记处(国家婴儿意外死亡观察站;OMIN)。我们从该登记处收集了 2015 年 5 月至 2021 年 6 月期间死亡的儿童的数据。测量了 540 名 SUDI 患者的血液 PCT 水平。我们比较了 PCT 和其他生物测试在感染状态、尸检结果和死因方面的差异,使用儿科医生在 SUDI 转诊中心收集的临床和生物数据进行比较。死于感染的儿童的 PCT 水平明显高于未死于感染的儿童(0.12µg/L 比 0.08µg/L,p<0.001)。当存在感染时,血液 PCT 水平超过 0.2µg/L 的情况比不存在感染时更为常见(44.3%比 15.4%,p<0.001)。当使用 0.5µg/L 截止值时,也获得了相同的数据(感染时为 36.1%,无感染时为 9.2%,p<0.001)。结论:PCT 是一种检测死后感染的敏感生物标志物;因此,尸检时可能需要额外的样本。已知:• PCT 是一种稳定的死后标志物,并且比 CRP 更早增加,即在感染开始后 2-4 小时增加,而 CRP 则在 6 小时后增加。• 可以在死后 140 小时内测量 PCT。新发现:• PCT 是一种检测 SUDI 患者死后感染的敏感标志物。• 如果在死亡前未确定感染,则可以通过尸检时获得的非标准化样本检测到感染。

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