External applicability of the ISCHEMIA trial: an analysis of a prospective, nationwide registry of patients with stable coronary artery disease

被引:26
作者
De Luca, Leonardo [1 ]
Uguccioni, Massimo [1 ]
Meessen, Jennifer [2 ]
Temporelli, Pier Luigi [3 ]
Tomai, Fabrizio [4 ]
De Rosa, Francesco Mario [5 ]
Passamonti, Enrico [6 ]
Formigli, Dario [7 ]
Riccio, Carmine [8 ]
Gabrielli, Domenico [9 ]
Colivicchi, Furio [10 ]
Gulizia, Michele Massimo [11 ]
Perna, Gian Piero [12 ]
机构
[1] AO San Camillo Forlanini, Dept Cardiosci, Rome, Italy
[2] Ist Ric Farmacol Mario Negri IRCCS, Dept Cardiovasc Med, Milan, Italy
[3] IRCCS, Div Cardiol, Ist Clin Sci Maugeri, Novara, Italy
[4] European Hosp, Aurelia Hosp, Div Cardiol, Rome, Italy
[5] PO Annunziata, Div Cardiol, Cosenza, Italy
[6] Ist Osped, Div Cardiol, Cremona, Italy
[7] AOG Rummo, Div Cardiol, Benevento, Italy
[8] Azienda Osped St Anna & San Sebastian, Div Cardiol, Caserta, Italy
[9] A Murri Hosp, Div Cardiol, Fermo, Italy
[10] S Filippo Neri Hosp, Div Cardiol, Rome, Italy
[11] Garibaldi Nesima Hosp, Div Cardiol, Catania, Italy
[12] Azienda Osped Univ Osped Riuniti, Div Cardiol, Ancona, Italy
关键词
clinical research; quality of life; stable angina; CARDIOLOGISTS; MANAGEMENT;
D O I
10.4244/EIJ-D-20-00610
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: We sought to assess the proportion of patients eligible for the ISCHEMIA trial and to compare the characteristics and outcomes of these patients with those without ISCHEMIA inclusion or with ISCHEMIA exclusion criteria in a contemporary, nationwide cohort of patients with stable coronary artery disease (CAD). Methods and results: Among the 5,070 consecutive patients enrolled in the START registry, 4,295 (84.7%) did not fulfil the inclusion criteria (ISCHEMIA-Not Included or ISCHEMIA-Unclassifiable), 582 (11.5%) had exclusion criteria (ISCHEMIA-Excluded), and the remaining 193 (3.8%) were classified as ISCHEMIA-Like. At one year, the incidence of the primary outcome, a composite of death from cardiovascular (CV) causes, myocardial infarction (MI), or hospitalisation for unstable angina and heart failure, was 0.5% in the ISCHEMIA-Like versus 3.3% in other patients (p=0.03). The composite secondary outcome of CV mortality and MI occurred in 0.5% of the ISCHEMIA-Like patients and in 1.4% of the remaining patients (p=0.1). Conclusions: In a contemporary real-world cohort of stable CAD patients, only 4% resulted in being eligible for the ISCHEMIA trial. These patients presented an extremely low annual risk of adverse events, especially when compared with other groups of stable CAD patients.
引用
收藏
页码:E966 / +
页数:15
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