Back to Search Start Over

Design of CTP-PRO study (impact of stress Cardiac computed Tomography myocardial Perfusion on downstream resources and PROgnosis in patients with suspected or known coronary artery disease: A multicenter international study)

Authors :
Pontone, G
De Cecco, C
Baggiano, A
Guaricci, A
Guglielmo, M
Leiner, T
Lima, J
Maurovich-Horvat, P
Muscogiuri, G
Nance, J
Schoepf, U
Pontone G.
De Cecco C.
Baggiano A.
Guaricci A. I.
Guglielmo M.
Leiner T.
Lima J.
Maurovich-Horvat P.
Muscogiuri G.
Nance J. W.
Schoepf U. J.
Pontone, G
De Cecco, C
Baggiano, A
Guaricci, A
Guglielmo, M
Leiner, T
Lima, J
Maurovich-Horvat, P
Muscogiuri, G
Nance, J
Schoepf, U
Pontone G.
De Cecco C.
Baggiano A.
Guaricci A. I.
Guglielmo M.
Leiner T.
Lima J.
Maurovich-Horvat P.
Muscogiuri G.
Nance J. W.
Schoepf U. J.
Publication Year :
2019

Abstract

Background: CT myocardial perfusion imaging (CTP) represents one of the newly developed CT-based techniques but its cost-effectiveness in the clinical pathway is undefined. The aim of the study is to evaluate the usefulness of combined evaluation of coronary anatomy and myocardial perfusion in intermediate to high-risk patients for suspected CAD or with known disease in terms of clinical decision-making, resource utilization and outcomes in a broad variety of geographic areas and patient subgroups. Methods: CTP-PRO study is a cooperative, international, multicentre, prospective, open-label, randomized controlled study evaluating the cost-effectiveness of a CCTA+CTP strategy (Group A) versus usual care (Group B) in intermediate-high risk patients with suspected or known CAD who undergo clinically indicated diagnostic evaluation. A total sample size of 2000 subjects will be enrolled and followed up for 24 months. The primary endpoint is the reclassification rate of CCTA in group A due to the addition of CTP. The secondary endpoint will be the comparison between groups in terms of non-invasive and invasive downstream testing, prevalence of obstructive CAD at ICA, revascularization, cumulative ED and overall cost during the follow-up at 1- and 2-years. The tertiary endpoint will be the comparison between each group in terms of MACE and cost-effectiveness at 1- and 2-years. Conclusions: The study will provide information to patients, health care providers and other stakeholders about which strategy could be more effective in the diagnosis of suspected CAD in intermediate to high-risk patients or in the symptomatic patients with known CAD and previous history of revascularization.

Details

Database :
OAIster
Notes :
STAMPA, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1320814206
Document Type :
Electronic Resource