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巨细胞动脉炎:常见治疗方法的检测准确性、益处及危害的系统评价与荟萃分析

Giant Cell Arteritis: A Systematic Review and Meta-Analysis of Test Accuracy and Benefits and Harms of Common Treatments.

作者信息

Dua Anisha B, Husainat Nedaa M, Kalot Mohamad A, Byram Kevin, Springer Jason M, James Karen E, Chang Lin Yih, Turgunbaev Marat, Villa-Forte Alexandra, Abril Andy, Langford Carol, Maz Mehrdad, Chung Sharon A, Mustafa Reem A

机构信息

Northwestern University Feinberg School of Medicine, Chicago, Illinois.

St. Mary's Hospital, St. Louis, Missouri.

出版信息

ACR Open Rheumatol. 2021 Jul;3(7):429-441. doi: 10.1002/acr2.11226. Epub 2021 Apr 2.

DOI:10.1002/acr2.11226
PMID:33811481
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8280815/
Abstract

This systematic review compares treatment options for patients with giant cell arteritis (GCA) and evaluates the test accuracy of studies used in diagnosing and monitoring GCA. These studies were used to inform evidence-based recommendations for the American College of Rheumatology (ACR)/Vasculitis Foundation (VF) vasculitis management guidelines. A systematic review and search of articles in English in Ovid Medline, PubMed, Embase, and the Cochrane Library was conducted. Articles were screened for suitability, and studies presenting the highest level of evidence were given preference. Three hundred ninety-nine full-text articles addressing GCA questions were reviewed to inform 27 Population, Intervention, Comparison, and Outcome questions. No benefit was found with intravenous glucocorticoids (GCs) compared with high-dose oral GCs in patients with cranial ischemic symptoms (27.4% vs 12.3%; odds ratio [OR] 2.39 [95% confidence interval (CI) 0.75-7.62], [very low certainty of evidence]). Weekly tocilizumab with a 26-week GC taper was superior to a 52-week GC taper in patients achieving remission (risk ratio 4.00 [95% CI 1.97-8.12], [low certainty of evidence]). Non-GC immunosuppressive therapies with GCs compared with GCs alone showed no statistically significant in relapse at 1 year (OR 0.87 [95% CI 0.73-1.04], [moderate certainty of evidence]) or serious adverse events (OR 0.81 [95% CI 0.54-1.20]; [moderate certainty of evidence]). Temporal artery biopsy has a sensitivity of 61% (95% CI 38%-79%) and a specificity of 98% (95% CI 95%-99%) in patients with a clinical diagnosis of suspected GCA. This comprehensive systematic review synthesizes and evaluates the benefits and harms of different treatment options and the accuracy of commonly used tests for the diagnosis and monitoring of GCA.

摘要

本系统评价比较了巨细胞动脉炎(GCA)患者的治疗方案,并评估了用于诊断和监测GCA的研究的检测准确性。这些研究用于为美国风湿病学会(ACR)/血管炎基金会(VF)血管炎管理指南提供循证建议。对Ovid Medline、PubMed、Embase和Cochrane图书馆中收录的英文文章进行了系统评价和检索。对文章进行适用性筛选,优先选择证据水平最高的研究。对399篇涉及GCA问题的全文文章进行了综述,以回答27个关于人群、干预措施、对照和结局的问题。在有颅缺血症状的患者中,与大剂量口服糖皮质激素(GCs)相比,静脉注射GCs未显示出益处(27.4%对12.3%;优势比[OR]2.39[95%置信区间(CI)0.75 - 7.62],[证据确定性极低])。在实现缓解的患者中,每周使用托珠单抗并进行26周GC减量优于进行52周GC减量(风险比4.00[95%CI 1.97 - 8.12],[证据确定性低])。与单独使用GCs相比,联合使用非GC免疫抑制疗法与GCs在1年复发率(OR 0.87[95%CI 0.73 - 1.04],[证据确定性中等])或严重不良事件方面(OR 0.81[95%CI 0.54 - 1.20];[证据确定性中等])无统计学显著差异。对于临床诊断为疑似GCA的患者,颞动脉活检的敏感性为61%(95%CI 38% - 79%),特异性为98%(95%CI 95% - 99%)。这项全面的系统评价综合并评估了不同治疗方案的益处和危害,以及用于诊断和监测GCA的常用检测方法的准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7696/8280815/776de307a44f/ACR2-3-429-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7696/8280815/e0b0a31cb299/ACR2-3-429-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7696/8280815/a765acc22989/ACR2-3-429-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7696/8280815/9e90caf93d94/ACR2-3-429-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7696/8280815/c0eed7339b3e/ACR2-3-429-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7696/8280815/4e38b0cb57b5/ACR2-3-429-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7696/8280815/776de307a44f/ACR2-3-429-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7696/8280815/e0b0a31cb299/ACR2-3-429-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7696/8280815/a765acc22989/ACR2-3-429-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7696/8280815/9e90caf93d94/ACR2-3-429-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7696/8280815/c0eed7339b3e/ACR2-3-429-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7696/8280815/4e38b0cb57b5/ACR2-3-429-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7696/8280815/776de307a44f/ACR2-3-429-g003.jpg

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