当前位置: X-MOL 学术BMJ › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Prediction models for diagnosis and prognosis of covid-19 infection: systematic review and critical appraisal.
The BMJ ( IF 105.7 ) Pub Date : 2020-04-07 , DOI: 10.1136/bmj.m1328
Laure Wynants 1, 2 , Ben Van Calster 2, 3 , Gary S Collins 4, 5 , Richard D Riley 6 , Georg Heinze 7 , Ewoud Schuit 8, 9 , Marc M J Bonten 8, 10 , Darren L Dahly 11, 12 , Johanna A A Damen 8, 9 , Thomas P A Debray 8, 9 , Valentijn M T de Jong 8, 9 , Maarten De Vos 2, 13 , Paul Dhiman 4, 5 , Maria C Haller 7, 14 , Michael O Harhay 15, 16 , Liesbet Henckaerts 17, 18 , Pauline Heus 8, 9 , Michael Kammer 7, 19 , Nina Kreuzberger 20 , Anna Lohmann 21 , Kim Luijken 21 , Jie Ma 5 , Glen P Martin 22 , David J McLernon 23 , Constanza L Andaur Navarro 8, 9 , Johannes B Reitsma 8, 9 , Jamie C Sergeant 24, 25 , Chunhu Shi 26 , Nicole Skoetz 19 , Luc J M Smits 1 , Kym I E Snell 6 , Matthew Sperrin 27 , René Spijker 8, 9, 28 , Ewout W Steyerberg 3 , Toshihiko Takada 8 , Ioanna Tzoulaki 29, 30 , Sander M J van Kuijk 31 , Bas van Bussel 1, 32 , Iwan C C van der Horst 32 , Florien S van Royen 8 , Jan Y Verbakel 33, 34 , Christine Wallisch 7, 35, 36 , Jack Wilkinson 22 , Robert Wolff 37 , Lotty Hooft 8, 9 , Karel G M Moons 8, 9 , Maarten van Smeden 8
Affiliation  

OBJECTIVE To review and critically appraise published and preprint reports of prediction models for diagnosing coronavirus disease 2019 (covid-19) in patients with suspected infection, for prognosis of patients with covid-19, and for detecting people in the general population at risk of being admitted to hospital for covid-19 pneumonia. DESIGN Rapid systematic review and critical appraisal. DATA SOURCES PubMed and Embase through Ovid, Arxiv, medRxiv, and bioRxiv up to 24 March 2020. STUDY SELECTION Studies that developed or validated a multivariable covid-19 related prediction model. DATA EXTRACTION At least two authors independently extracted data using the CHARMS (critical appraisal and data extraction for systematic reviews of prediction modelling studies) checklist; risk of bias was assessed using PROBAST (prediction model risk of bias assessment tool). RESULTS 2696 titles were screened, and 27 studies describing 31 prediction models were included. Three models were identified for predicting hospital admission from pneumonia and other events (as proxy outcomes for covid-19 pneumonia) in the general population; 18 diagnostic models for detecting covid-19 infection (13 were machine learning based on computed tomography scans); and 10 prognostic models for predicting mortality risk, progression to severe disease, or length of hospital stay. Only one study used patient data from outside of China. The most reported predictors of presence of covid-19 in patients with suspected disease included age, body temperature, and signs and symptoms. The most reported predictors of severe prognosis in patients with covid-19 included age, sex, features derived from computed tomography scans, C reactive protein, lactic dehydrogenase, and lymphocyte count. C index estimates ranged from 0.73 to 0.81 in prediction models for the general population (reported for all three models), from 0.81 to more than 0.99 in diagnostic models (reported for 13 of the 18 models), and from 0.85 to 0.98 in prognostic models (reported for six of the 10 models). All studies were rated at high risk of bias, mostly because of non-representative selection of control patients, exclusion of patients who had not experienced the event of interest by the end of the study, and high risk of model overfitting. Reporting quality varied substantially between studies. Most reports did not include a description of the study population or intended use of the models, and calibration of predictions was rarely assessed. CONCLUSION Prediction models for covid-19 are quickly entering the academic literature to support medical decision making at a time when they are urgently needed. This review indicates that proposed models are poorly reported, at high risk of bias, and their reported performance is probably optimistic. Immediate sharing of well documented individual participant data from covid-19 studies is needed for collaborative efforts to develop more rigorous prediction models and validate existing ones. The predictors identified in included studies could be considered as candidate predictors for new models. Methodological guidance should be followed because unreliable predictions could cause more harm than benefit in guiding clinical decisions. Finally, studies should adhere to the TRIPOD (transparent reporting of a multivariable prediction model for individual prognosis or diagnosis) reporting guideline. SYSTEMATIC REVIEW REGISTRATION Protocol https://osf.io/ehc47/, registration https://osf.io/wy245.
更新日期:2020-04-08
down
wechat
bug