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红细胞分布宽度(RDW)作为急性阑尾炎诊断的无创生物标志物的效用:对5222例病例的系统评价和荟萃分析

Utility of Red Cell Distribution Width (RDW) as a Noninvasive Biomarker for the Diagnosis of Acute Appendicitis: A Systematic Review and Meta-Analysis of 5222 Cases.

作者信息

Anand Sachit, Krishnan Nellai, Jukić Miro, Križanac Zvonimir, Llorente Muñoz Carlos Martin, Pogorelić Zenon

机构信息

Department of Pediatric Surgery, All India Institute of Medical Sciences, New Delhi 110029, India.

Department of Pediatric Surgery, University Hospital of Split, 21000 Split, Croatia.

出版信息

Diagnostics (Basel). 2022 Apr 17;12(4):1011. doi: 10.3390/diagnostics12041011.

Abstract

Background: Despite great advances in medicine, numerous available laboratory markers, and radiological imaging, the diagnosis of acute appendicitis (AA) in some cases still remains controversial and challenging for clinicians. Because of that, clinicians are still looking for an ideal marker that would be specific to AA. The red blood cell distribution width (RDW) has been recently investigated in several studies as a potential biomarker for AA. The aim of this systematic review and meta-analysis was to systematically summarize and compare all relevant data on RDW as a diagnostic biomarker for AA. Methods: This systematic review and meta-analysis were performed as per the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Scientific databases (PubMed, Scopus, Web of Science, and Excerpta Medica database—EMBASE) were systematically searched for relevant comparative studies by two independent researches using keywords ((red cell distribution width) OR rdw) AND (appendicitis). An independent assessment of the methodological quality was performed by two authors using the Downs and Black scale. RevMan 5.4 software was used to perform the meta-analysis. Results: Fifteen studies were included in the final meta-analysis; the majority of the studies was retrospective. Nine studies compared the RDW values between AA and non-AA; four studies compared the same between AA and healthy controls, while two studies compared the RDW values among all three groups. The estimated heterogeneity among the studies for all outcome was statistically significant (I2 = 92−99%, p < 0.00001). The pooling the data demonstrated no statistically significant difference in the RDW values (weighted mean difference (WMD) = 0.03, 95% CI = (−0.46, 0.52), p = 0.91) between AA and healthy controls as well as between AA and non-AA cases (WMD = 0.23, 95%CI = (−0.19, 0.65), p = 0.28). A separate subanalysis was performed to evaluate the utility of this biomarker for the pediatric age group. Pooling the data demonstrated no significant difference among the AA and non-AA groups in terms of the RDW values (WMD = 0.99, 95% CI = (−0.35, 2.33), p = 0.15). Conclusion: The RDW value difference demonstrated no statistically significant difference in AA versus healthy individuals and AA versus non-AA individuals. At the moment, there is no evidence of RDW utility in diagnostic testing of AA. Further research with prospective, multicenter studies and studies targeting special patient groups with a large sample size are needed in this field.

摘要

背景

尽管医学取得了巨大进步,有众多可用的实验室指标和放射影像学检查,但在某些情况下,急性阑尾炎(AA)的诊断对临床医生而言仍存在争议且具有挑战性。正因如此,临床医生仍在寻找一种针对AA的理想指标。红细胞分布宽度(RDW)最近在多项研究中被作为AA的潜在生物标志物进行了调查。本系统评价和荟萃分析的目的是系统地总结和比较关于RDW作为AA诊断生物标志物的所有相关数据。

方法

本系统评价和荟萃分析按照系统评价和荟萃分析的首选报告项目(PRISMA)指南进行。由两名独立研究人员使用关键词((红细胞分布宽度)或RDW)和(阑尾炎)在科学数据库(PubMed、Scopus、科学网和医学文摘数据库——EMBASE)中系统检索相关的比较研究。由两名作者使用唐斯和布莱克量表对方法学质量进行独立评估。使用RevMan 5.4软件进行荟萃分析。

结果

最终的荟萃分析纳入了15项研究;大多数研究为回顾性研究。9项研究比较了AA组和非AA组之间的RDW值;4项研究比较了AA组和健康对照组之间的RDW值,而2项研究比较了所有三组之间的RDW值。所有结局研究之间的估计异质性具有统计学意义(I² = 92−99%,p < 0.00001)。汇总数据显示,AA组与健康对照组之间以及AA组与非AA组病例之间的RDW值无统计学显著差异(加权平均差(WMD)= 0.03,95%置信区间 =(−0.46,0.52),p = 0.91)。进行了一项单独的亚组分析以评估该生物标志物在儿童年龄组中的效用。汇总数据显示,AA组和非AA组之间的RDW值无显著差异(WMD = 0.99,95%置信区间 =(−0.35,2.33),p = 0.15)。

结论

RDW值差异在AA与健康个体以及AA与非AA个体之间无统计学显著差异。目前,没有证据表明RDW在AA诊断检测中有用。该领域需要进行进一步的前瞻性、多中心研究以及针对特殊患者群体的大样本量研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1765/9032964/eab9f87d1872/diagnostics-12-01011-g001.jpg

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