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Comparison between patients included in randomized controlled trials of ischemic heart disease and real-world data. A nationwide study - 30/10/18

Doi : 10.1016/j.ahj.2018.05.018 
Peter Nørkjær Laursen, MD a, , Lene Holmvang, DMSc a, Jacob Lønborg, DMSc a, Lars Køber, DMSc a, Dan E. Høfsten, PhD a, Steffen Helqvist, DMSc a, Peter Clemmensen, DMSc g, h, i, Henning Kelbæk, DMSc f, Erik Jørgensen, DMSc a, Jens Flensted Lassen, DMSc a, Frants Pedersen, PhD a, Thomas Høi-Hansen, DMSc d, Christian Juhl Therkelsen, PhD b, Hans-Henrik Tilsted, DMSc c, Lisette Okkels Jensen, DMSc e, Lars Nepper-Christensen, MD a, Golnaz Sadjadieh, MD a, Thomas Engstrøm, DMSc a, j
a Department of Cardiology, The Heart Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark 
b Department of Cardiology, Aarhus University Hospital, Skejby, Aarhus, Denmark 
c Department of Cardiology, Aalborg University Hospital, Aalborg, Denmark 
d Department of Cardiology, Herlev-Gentofte Hospital, Copenhagen, Denmark 
e Department of Cardiology, Odense University Hospital, Odense, Denmark 
f Department of Cardiology, Zealand University Hospital, Roskilde, Denmark 
g Department of General and Interventional Cardiology, University Heart Center, Hamburg, Germany 
h Department of Medicine, Division of Cardiology, Nykoebing F Hospital, Nykøbing Falster, Denmark 
i University of Southern Denmark, Odense, Denmark 
j University of Lund, Lund, Sweden 

Reprint requests: Peter Nørkjær Laursen, MD, The Heart Centre, Department of Cardiology, Copenhagen University Hospital, Rigshospitalet, Blegdamsvej 9, 2100 Copenhagen.Department of CardiologyCopenhagen University Hospital, RigshospitaletBlegdamsvej 9Copenhagen2100

Abstract

Background

The objective was to compare patients with ischemic heart disease (IHD) undergoing percutaneous coronary intervention (PCI) who were included in randomized controlled trials (RCTs) (trial participants) with patients who were not included (nonparticipants) on a trial-by-trial basis and according to indication for PCI.

Methods

In this cohort study, we compared patients with IHD who were randomized in RCTs in relation to undergoing PCI in Denmark between 2011 and 2015 were considered as RCT-participants in this study. The RCT-participants were compared with contemporary nonparticipants with IHD undergoing PCI in the same period, and they were identified using unselected national registry data. The primary end point was all-cause mortality.

Results

A total of 10,317 (30%) patients were included in 10 relevant RCTs (trial participants), and a total of 23,644 (70%) contemporary patients did not participate (nonparticipants). In all the included RCTs, nonparticipants had higher hazard ratios for mortality compared to trial participants (P < .001). Among all patients treated with PCI, the pooled estimates showed a significantly higher mortality rate for nonparticipants compared to trial participants (hazard ratio: 2.03, 95% CI: 1.88-2.19) (P < .001). When patients were stratified according to indication for PCI, the pooled estimates showed a significantly lower mortality rate for trial participants compared to nonparticipants in all strata (P for all < .001).

Conclusions

Trial participants in recently performed RCTs including patients undergoing PCI were not representative of the general population of patients with IHD treated with PCI according to clinical characteristics and mortality. The difference in mortality was found irrespective of the indication for PCI. Thus, results from RCTs including patients undergoing PCI should be extrapolated with caution to the general patient population.

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 Declarations of interest: none.


© 2018  Publié par Elsevier Masson SAS.
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Vol 204

P. 128-138 - octobre 2018 Retour au numéro
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