scholarly journals Discrimination capability of pretest probability of stable coronary artery disease: a systematic review and meta-analysis suggesting how to improve validation procedures

BMJ Open ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. e047677
Author(s):  
Pierpaolo Mincarone ◽  
Antonella Bodini ◽  
Maria Rosaria Tumolo ◽  
Federico Vozzi ◽  
Silvia Rocchiccioli ◽  
...  

ObjectiveExternally validated pretest probability models for risk stratification of subjects with chest pain and suspected stable coronary artery disease (CAD), determined through invasive coronary angiography or coronary CT angiography, are analysed to characterise the best validation procedures in terms of discriminatory ability, predictive variables and method completeness.DesignSystematic review and meta-analysis.Data sourcesGlobal Health (Ovid), Healthstar (Ovid) and MEDLINE (Ovid) searched on 22 April 2020.Eligibility criteriaWe included studies validating pretest models for the first-line assessment of patients with chest pain and suspected stable CAD. Reasons for exclusion: acute coronary syndrome, unstable chest pain, a history of myocardial infarction or previous revascularisation; models referring to diagnostic procedures different from the usual practices of the first-line assessment; univariable models; lack of quantitative discrimination capability.MethodsEligibility screening and review were performed independently by all the authors. Disagreements were resolved by consensus among all the authors. The quality assessment of studies conforms to the Quality Assessment of Diagnostic Accuracy Studies (QUADAS-2). A random effects meta-analysis of area under the receiver operating characteristic curve (AUC) values for each validated model was performed.Results27 studies were included for a total of 15 models. Besides age, sex and symptom typicality, other risk factors are smoking, hypertension, diabetes mellitus and dyslipidaemia. Only one model considers genetic profile. AUC values range from 0.51 to 0.81. Significant heterogeneity (p<0.003) was found in all but two cases (p>0.12). Values of I2 >90% for most analyses and not significant meta-regression results undermined relevant interpretations. A detailed discussion of individual results was then carried out.ConclusionsWe recommend a clearer statement of endpoints, their consistent measurement both in the derivation and validation phases, more comprehensive validation analyses and the enhancement of threshold validations to assess the effects of pretest models on clinical management.PROSPERO registration numberCRD42019139388.

2013 ◽  
Vol 169 (4) ◽  
pp. 262-270 ◽  
Author(s):  
Gianluigi Savarese ◽  
Giuseppe Rosano ◽  
Carmen D'Amore ◽  
Francesca Musella ◽  
Giuseppe Luca Della Ratta ◽  
...  

2020 ◽  
Author(s):  
Pierpaolo Mincarone ◽  
Antonella Bodini ◽  
Maria Rosaria Tumolo ◽  
Federico Vozzi ◽  
Silvia Rocchiccioli ◽  
...  

ABSTRACTAn overuse of invasive and non-invasive anatomical testing for the diagnosis of coronary artery disease (CAD) affects patients’ and healthcare professionals’ safety, and the sustainability of Healthcare Systems. Pre-test probability (PTP) models can be routinely used as gatekeeper for initial patient management. Although with different positions, international organizations clearly underline the need for more information on the various risk factors acting as modifier of the PTP.This systematic review addresses validation of PTP models adopting variables available at the first-line assessment of a suspected stable CAD. A comprehensive search has been done in MEDLINE®, HealthSTAR, and Global Health databases.Nearly all the models considered in the 27 analysed papers include age, sex, and chest pain symptoms. Other common risk factors are smoking, hypertension, diabetes mellitus and dyslipidaemia. Only one model considers genetic profile. Reported AUCs range from 0.51 to 0.81. Relevant heterogeneity sources have been highlighted, such as the sample size, the presence of a PTP cut-off and the adoption of different definitions of CAD which can prevent comparisons of results. Very few papers address a complete validation, making then impossible to understand the reasons why the model does not show a good discrimination capability on a different data set.We consequently recommend a more clear statement of endpoints, their consistent measurement both in the derivation and validation phases, more comprehensive validation analyses and the enhancement of threshold validations of PTP to assess the effects of PTP on clinical management.


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