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BMJ 2004;329:1404 (11 December), doi:10.1136/bmj.329.7479.1404
EDITORLike Wennberg and Zimmermann, I am troubled by the interpretation of the results of PROGRESS published in the original Lancet article and reiterated by others; by the amalgamation of the perindopril and perindopril-indapamide arms under the rubric "perindopril based therapy"; and by the chief conclusions about such treatment attributed by the trialists.1 2
Interestingly, this has affected my own work. A neurologist referee of a recent article on secondary stroke prevention I published with Kapral in the Canadian Journal of Neurological Sciences strongly criticised our paper for simply noting the difference in efficacy between the two active treatment arms of PROGRESS3; this anonymous reviewer adamantly stated that the trial was not sufficiently powered to show a distinction. Perhaps the best way to look at PROGRESS is that it is really two parallel but different randomised trials with the same control group. Therefore, combining these two very different treatment arms for analysis may be an oversimplification.
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One pill or two? Credit: BSIP/HUBERT/SPL
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Moreover, the article by Wennberg and Zimmermann does not at all distract from implementation of the trial results, as argued by the PROGRESS trialists. With combination treatment with angiotensin converting enzyme inhibitors and diuretics we get the best of both worlds, and a combination indapamide-perindopril regimen exists and is manufactured by Servier. I also find it interesting that a higher dose of perindopril monotherapy (8 mg) did not prevent stroke in the recent massive EUROPA study, despite a reduction of 5/3 mm Hg in blood pressure.4
Daniel G Hackam, research fellow
Institute for Clinical Evaluative Sciences, Division of Clinical Pharmacology, Sunnybrook and Women's College Health Sciences Centre, University of Toronto, Canada M4N 3M5 danhackam{at}cogeco.ca