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尿中人乳头瘤病毒检测用于宫颈人乳头瘤病毒存在情况的准确性:系统评价与荟萃分析

Accuracy of urinary human papillomavirus testing for presence of cervical HPV: systematic review and meta-analysis.

作者信息

Pathak Neha, Dodds Julie, Zamora Javier, Khan Khalid

机构信息

Women's Health Research Unit, Centre for Primary Care and Public Health, Blizard Institute, Barts and The London School of Medicine and dentistry, London E1 2AB, UK.

Women's Health Research Unit, Centre for Primary Care and Public Health, Blizard Institute, Barts and The London School of Medicine and dentistry, London E1 2AB, UK Clinical Biostatistics Unit, Hospital Ramon y Cajal (IRYCIS) and CIBER Epidemiologia y Salud Publica, Madrid, Spain

出版信息

BMJ. 2014 Sep 16;349:g5264. doi: 10.1136/bmj.g5264.

Abstract

OBJECTIVE

To determine the accuracy of testing for human papillomavirus (HPV) DNA in urine in detecting cervical HPV in sexually active women.

DESIGN

Systematic review and meta-analysis.

DATA SOURCES

Searches of electronic databases from inception until December 2013, checks of reference lists, manual searches of recent issues of relevant journals, and contact with experts.

ELIGIBILITY CRITERIA

Test accuracy studies in sexually active women that compared detection of urine HPV DNA with detection of cervical HPV DNA.

DATA EXTRACTION AND SYNTHESIS

Data relating to patient characteristics, study context, risk of bias, and test accuracy. 2 × 2 tables were constructed and synthesised by bivariate mixed effects meta-analysis.

RESULTS

16 articles reporting on 14 studies (1443 women) were eligible for meta-analysis. Most used commercial polymerase chain reaction methods on first void urine samples. Urine detection of any HPV had a pooled sensitivity of 87% (95% confidence interval 78% to 92%) and specificity of 94% (95% confidence interval 82% to 98%). Urine detection of high risk HPV had a pooled sensitivity of 77% (68% to 84%) and specificity of 88% (58% to 97%). Urine detection of HPV 16 and 18 had a pooled sensitivity of 73% (56% to 86%) and specificity of 98% (91% to 100%). Metaregression revealed an increase in sensitivity when urine samples were collected as first void compared with random or midstream (P=0.004).

LIMITATIONS

The major limitations of this review are the lack of a strictly uniform method for the detection of HPV in urine and the variation in accuracy between individual studies.

CONCLUSIONS

Testing urine for HPV seems to have good accuracy for the detection of cervical HPV, and testing first void urine samples is more accurate than random or midstream sampling. When cervical HPV detection is considered difficult in particular subgroups, urine testing should be regarded as an acceptable alternative.

摘要

目的

确定检测性活跃女性尿液中人乳头瘤病毒(HPV)DNA以检测宫颈HPV的准确性。

设计

系统评价和荟萃分析。

数据来源

检索自数据库建立至2013年12月的电子数据库、检查参考文献列表、手工检索相关期刊近期各期,并与专家联系。

纳入标准

性活跃女性中比较尿液HPV DNA检测与宫颈HPV DNA检测的检测准确性研究。

数据提取与合成

与患者特征、研究背景、偏倚风险和检测准确性相关的数据。构建2×2表格,并通过双变量混合效应荟萃分析进行合成。

结果

16篇报道14项研究(1443名女性)的文章符合荟萃分析的条件。大多数研究对首次晨尿样本采用商业聚合酶链反应方法。尿液中检测到任何HPV的合并敏感性为87%(95%置信区间78%至92%),特异性为94%(95%置信区间82%至98%)。尿液中检测到高危HPV的合并敏感性为77%(68%至84%),特异性为88%(58%至97%)。尿液中检测到HPV 16和18的合并敏感性为73%(56%至86%),特异性为98%(91%至100%)。元回归分析显示,与随机或中段尿相比,收集首次晨尿样本时敏感性增加(P=0.004)。

局限性

本综述的主要局限性在于缺乏严格统一的尿液HPV检测方法,且各研究之间准确性存在差异。

结论

检测尿液中的HPV对宫颈HPV检测似乎具有良好的准确性,且检测首次晨尿样本比随机或中段尿采样更准确。当在特定亚组中认为宫颈HPV检测困难时,尿液检测应被视为一种可接受的替代方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fd9/4793832/cbec7f381b61/patn020452.f1_default.jpg

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