Mats L Junek,Iva Okaj,Sagar Patel,Angela Hu,Matthew A Jessome,Deborah Koh,Seungwon Choi,Sukhreet Atwal,John Koussiouris,Johan Pushani,Colin Stark,Farid Foroutan,Stephanie Garner,Nader Khalidi
{"title":"Multivariable models to predict a diagnosis of Giant Cell Arteritis: systematic review and meta-analysis.","authors":"Mats L Junek,Iva Okaj,Sagar Patel,Angela Hu,Matthew A Jessome,Deborah Koh,Seungwon Choi,Sukhreet Atwal,John Koussiouris,Johan Pushani,Colin Stark,Farid Foroutan,Stephanie Garner,Nader Khalidi","doi":"10.3899/jrheum.2022-1204","DOIUrl":null,"url":null,"abstract":"OBJECTIVE\r\nMultiple models to predict a diagnosis of Giant cell arteritis (GCA) have been developed to assist clinicians. We conducted a systematic review and meta-analysis of model variables and model performance.\r\n\r\nMETHODS\r\nWe searched Pubmed, Embase, and the Cochrane Library from January 1990 to April 2024 for studies that used multivariable models to diagnose GCA. Study characteristics, patient characteristics, method of and criteria for diagnosis, and model details were extracted. Metaanalysis of individual signs and symptoms was performed using generic inverse variance. The Prediction model Risk of Bias Assessment tool was used to assess individual model risk of bias. Certainty of the effect estimate for each predictor was assessed using Grading of Recommendations, Assessment, Development and Evaluations framework.\r\n\r\nRESULTS\r\nWe screened 2 254 abstracts and included 44 studies. A total of 15 409 patients and 4 340 diagnoses of GCA were included. Predictors with high certainty of effect and large effect size included jaw claudication, C-reactive protein elevation above 24.5 mg/dL, platelets above 400x109/L, positive temporal artery ultrasound, and presence of synovitis (predictive of a non-GCA diagnosis). Other factors classically associated with GCA including vision loss, symptoms of polymyalgia rheumatica, and headache were found to be predictive with lower certainty of effect. Models included were predominantly found to be at high risk of bias.\r\n\r\nCONCLUSION\r\nPredictors of GCA were consistent across models, however, models were of poor methodologic quality. Future models to predict a diagnosis of GCA should be constructed with improved methodologic rigor.","PeriodicalId":501812,"journal":{"name":"The Journal of Rheumatology","volume":"26 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Rheumatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3899/jrheum.2022-1204","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
OBJECTIVE
Multiple models to predict a diagnosis of Giant cell arteritis (GCA) have been developed to assist clinicians. We conducted a systematic review and meta-analysis of model variables and model performance.
METHODS
We searched Pubmed, Embase, and the Cochrane Library from January 1990 to April 2024 for studies that used multivariable models to diagnose GCA. Study characteristics, patient characteristics, method of and criteria for diagnosis, and model details were extracted. Metaanalysis of individual signs and symptoms was performed using generic inverse variance. The Prediction model Risk of Bias Assessment tool was used to assess individual model risk of bias. Certainty of the effect estimate for each predictor was assessed using Grading of Recommendations, Assessment, Development and Evaluations framework.
RESULTS
We screened 2 254 abstracts and included 44 studies. A total of 15 409 patients and 4 340 diagnoses of GCA were included. Predictors with high certainty of effect and large effect size included jaw claudication, C-reactive protein elevation above 24.5 mg/dL, platelets above 400x109/L, positive temporal artery ultrasound, and presence of synovitis (predictive of a non-GCA diagnosis). Other factors classically associated with GCA including vision loss, symptoms of polymyalgia rheumatica, and headache were found to be predictive with lower certainty of effect. Models included were predominantly found to be at high risk of bias.
CONCLUSION
Predictors of GCA were consistent across models, however, models were of poor methodologic quality. Future models to predict a diagnosis of GCA should be constructed with improved methodologic rigor.