Effects of a perindopril-based blood pressure-lowering regimen on the risk of recurrent stroke according to stroke subtype and medical history - The PROGRESS trial

被引:184
作者
Chapman, N
Huxley, R
Anderson, C
Bousser, MG
Chalmers, J
Colman, S
Davis, S
Donnan, G
MacMahon, S
Neal, B
Warlow, C
Woodward, M
机构
[1] Univ Sydney, Inst Int Hlth, Progress Collaborat Grp, Sydney, NSW 2042, Australia
[2] St Marys Hosp, London, England
[3] Univ Auckland, Clin Trials Res Unit, Auckland 1, New Zealand
[4] Hop Lariboisiere, F-75475 Paris, France
[5] Univ Melbourne, Royal Melbourne Hosp, Melbourne, Vic 3050, Australia
[6] Natl Stroke Res Inst, Melbourne, Vic, Australia
[7] Western Gen Hosp, Dept Neurol, Edinburgh, Midlothian, Scotland
关键词
angiotensin converting enzyme inhibitors; blood pressure; intracerebral hemorrhage; randomized controlled trials; stroke; ischemic;
D O I
10.1161/01.STR.0000106480.76217.6F
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose - The Perindopril Protection Against Recurrent Stroke Study ( PROGRESS) showed that blood pressure lowering reduced stroke risk in patients with a history of cerebrovascular events. Here, we report the consistency of treatment effects across different stroke subtypes and among major clinical subgroups. Methods - PROGRESS was a randomized, double-blind trial among 6105 people with a prior history of cerebrovascular events. Participants were assigned to active treatment (perindopril for all participants and indapamide for those with neither an indication for nor a contraindication to a diuretic) or matching placebo(s). Results - During a mean of 3.9 years of follow-up, active treatment reduced the absolute rates of ischemic stroke from 10% to 8% ( relative risk reduction [RRR], 24%; 95% confidence interval [CI], 10 to 35) and the absolute rates of intracerebral hemorrhage from 2% to 1% (RRR, 50%; 95% CI, 26 to 67). The relative risk of any stroke during follow-up was reduced by 26% ( 95% CI, 12 to 38) among patients whose baseline cerebrovascular event was an ischemic stroke and by 49% ( 95% CI, 18 to 68) among those whose baseline event was an intracerebral hemorrhage. There was no evidence that treatment effects were modified by other drug therapies ( antiplatelet or other antihypertensive agents), residual neurological signs, atrial fibrillation, or the time since the last cerebrovascular event. Conclusions - Beneficial effects of a perindopril-based treatment regimen were observed for all stroke types and all major clinical subgroups studied. These data suggest that effective blood pressure - lowering therapy should be routinely considered for all patients with a history of cerebrovascular events.
引用
收藏
页码:116 / 121
页数:6
相关论文
共 18 条
[1]   CLASSIFICATION OF SUBTYPE OF ACUTE ISCHEMIC STROKE - DEFINITIONS FOR USE IN A MULTICENTER CLINICAL-TRIAL [J].
ADAMS, HP ;
BENDIXEN, BH ;
KAPPELLE, LJ ;
BILLER, J ;
LOVE, BB ;
GORDON, DL ;
MARSH, EE ;
KASE, CS ;
WOLF, PA ;
BABIKIAN, VL ;
LICATAGEHR, EE ;
ALLEN, N ;
BRASS, LM ;
FAYAD, PB ;
PAVALKIS, FJ ;
WEINBERGER, JM ;
TUHRIM, S ;
RUDOLPH, SH ;
HOROWITZ, DR ;
BITTON, A ;
MOHR, JP ;
SACCO, RL ;
CLAVIJO, M ;
ROSENBAUM, DM ;
SPARR, SA ;
KATZ, P ;
KLONOWSKI, E ;
CULEBRAS, A ;
CAREY, G ;
MARTIR, NI ;
FICARRA, C ;
HOGAN, EL ;
CARTER, T ;
GURECKI, P ;
MUNTZ, BK ;
RAMIREZLASSEPAS, M ;
TULLOCH, JW ;
QUINONES, MR ;
MENDEZ, M ;
ZHANG, SM ;
ALA, T ;
JOHNSTON, KC ;
ANDERSON, DC ;
TARREL, RM ;
NANCE, MA ;
BUDLIE, SR ;
DIERICH, M ;
HELGASON, CM ;
HIER, DB ;
SHAPIRO, RA .
STROKE, 1993, 24 (01) :35-41
[2]  
[Anonymous], 1989, Stroke, V20, P1407
[3]  
[Anonymous], 2000, Lancet, V355, P253, DOI DOI 10.1016/S0140-6736(99)12323-7
[4]   EPIDEMIOLOGY OF STROKE [J].
BONITA, R .
LANCET, 1992, 339 (8789) :342-344
[5]  
Chalmers J, 1996, J HYPERTENS, V14, pS41
[6]   BLOOD-PRESSURE, ANTIHYPERTENSIVE DRUG-TREATMENT AND THE RISKS OF STROKE AND OF CORONARY HEART-DISEASE [J].
COLLINS, R ;
MACMAHON, S .
BRITISH MEDICAL BULLETIN, 1994, 50 (02) :272-298
[7]  
CRUICKSHANK JM, 1987, LANCET, V1, P581
[8]   Treatment and secondary prevention of stroke: evidence, costs, and effects on individuals and populations [J].
Hankey, GJ ;
Warlow, CI .
LANCET, 1999, 354 (9188) :1457-1463
[9]   Long-term risk of first recurrent stroke in the Perth Community Stroke Study [J].
Hankey, GJ ;
Jamrozik, K ;
Broadhurst, RJ ;
Forbes, S ;
Burvill, PW ;
Anderson, CS ;
Stewart-Wynne, EG .
STROKE, 1998, 29 (12) :2491-2500
[10]   THE J-CURVE PHENOMENON IN STROKE RECURRENCE [J].
IRIE, K ;
YAMAGUCHI, T ;
MINEMATSU, K ;
OMAE, T .
STROKE, 1993, 24 (12) :1844-1849