一氧化碳中毒成人入院时血清神经元特异性烯醇化酶与迟发性神经精神后遗症风险之间的关系:荟萃分析

0 MEDICINE, RESEARCH & EXPERIMENTAL
Yu Zhang, Nan Gao, Yingbo Wang, Wenxin Hu, Zhihao Wang, Li Pang
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引用次数: 0

摘要

延迟性神经精神后遗症(DNS)严重影响急性一氧化碳中毒(COP)患者的生活质量。本系统综述和荟萃分析旨在评估急性一氧化碳中毒成人入院时血清神经元特异性烯醇化酶(NSE)水平与DNS风险之间的关系。通过在PubMed、Embase、Web of Science、万方和中国国家知识基础设施数据库中检索,确定了相关的纵向随访观察性研究。考虑到潜在的异质性,采用随机效应模型对结果进行汇总。共分析了九项队列研究,包括 1501 名患者,其中 254 人(16.9%)在随访期间出现 DNS。汇总数据显示,早期血清 NSE 升高与随后发生 DNS 的较高风险有关(NSE 每增加 1 ng/mL 的几率比:1.10,95% 置信区间:1.06 至 1.15,P <0.001)。研究之间的中度异质性(I2 = 46%)完全归因于一项随访时间最长的研究(22.3 个月;排除该研究后,I2 = 0%)。根据国家、研究设计、样本量、年龄、性别、入院碳氧血红蛋白水平、DNS 发生率、随访时间和质量评分进行的亚组分析得出了一致的结果(亚组差异的 P 均大于 0.05)。总之,急性 COP 早期血清 NSE 水平高与随访期间发生 DNS 的风险增加有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association between serum neuron-specific enolase at admission and the risk of delayed neuropsychiatric sequelae in adults with carbon monoxide poisoning: A meta-analysis.

Delayed neuropsychiatric sequelae (DNS) significantly impact the quality of life in patients following acute carbon monoxide poisoning (COP). This systematic review and meta-analysis aimed to assess the relationship between serum neuron-specific enolase (NSE) levels at admission and the risk of DNS in adults after acute COP. Relevant observational studies with longitudinal follow-up were identified through searches in PubMed, Embase, Web of Science, Wanfang, and China National Knowledge Infrastructure databases. The random-effects model was used to aggregate results, accounting for potential heterogeneity. Nine cohort studies, including 1501 patients, were analyzed, with 254 (16.9%) developing DNS during follow-up. The pooled data indicated that elevated serum NSE in the early phase was linked to a higher risk of subsequent DNS (odds ratio per 1 ng/mL increase in NSE: 1.10, 95% confidence interval: 1.06 to 1.15, P < 0.001). Moderate heterogeneity (I2 = 46%) among the studies was entirely attributed to one study with the longest follow-up duration (22.3 months; I2 = 0% after excluding this study). Subgroup analyses based on country, study design, sample size, age, sex, admission carboxyhemoglobin levels, DNS incidence, follow-up duration, and quality score yielded consistent results (P for subgroup differences all > 0.05). In summary, high serum NSE levels in the early phase of acute COP are associated with an increased risk of developing DNS during follow-up.

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