Dispelling the myth: the use of renin-angiotensin blockade in atheromatous renovascular disease

被引:71
作者
Chrysochou, Constantina [1 ]
Foley, Robert N. [2 ]
Young, James F. [1 ]
Khavandi, Kaivan [1 ]
Cheung, Ching M. [1 ]
Kalra, Philip A. [1 ]
机构
[1] Univ Manchester, Renal Dept, Salford Royal Hosp, Manchester Acad Hlth Sci Ctr, Salford, Lancs, England
[2] Univ Minnesota Twin Cities, Sch Med, Chron Dis Res Grp, Minneapolis, MN USA
关键词
angiotensin-converting enzyme inhibitors; angiotensin receptor blockers; atheromatous renovascular disease; cardiovascular events; dialysis; CONVERTING-ENZYME-INHIBITORS; RENAL-ARTERY-STENOSIS; ANTI HYPERTENSIVE DRUGS; CHRONIC KIDNEY-DISEASE; HEART-FAILURE; CARDIOVASCULAR EVENTS; RISK-FACTORS; DOUBLE-BLIND; INSUFFICIENCY; MANAGEMENT;
D O I
10.1093/ndt/gfr496
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background. Many physicians retain reservations regarding the routine prescription of renin-angiotensin blockade (RAB) in patients with atheromatous renovascular disease (ARVD). Conversely, these patients are in most need of the cardio-and renal protection offered by RAB. This reservation is mostly because of fear of precipitating acute renal deterioration. We aimed to study whether RAB can be used safely in ARVD patients and whether it altered their outcome. Methods. Prospective observational study of all ARVD patients presenting to our tertiary referral centre from 1999-2009. Data capture included usage and tolerability of RAB, and correlation with endpoints of cardiovascular events, dialysis or death. Results. Six hundred and twenty-one subjects were available for analysis. Mean age (SD) of the cohort was 71.3 (8.8) years, median (interquartile range) follow-up 3.1 (2.1, 4.8), range 0.2-10.61 years. Seventy-four patients had an intolerance to RAB at study entry. When utilized prospectively, RAB was tolerated in 357 of 378 patients (92%), and this was even seen in 54/69 (78.3%) patients with bilateral >60% renal artery stenosis (RAS) or occlusion. Patients (4/21) who were intolerant of RAB during follow-up (and 12 retrospectively intolerant), underwent renal revascularization which facilitated safe use of these medications post-procedure. On multivariate time-adjusted analysis, patients receiving RAB were significantly less likely to die (P = 0.02). Conclusion. RAB is well tolerated even in patients with bilateral severe RAS and reduced mortality in a large group of ARVD patients. We recommend all ARVD patients be considered for RAB therapy unless an absolute contraindication exists. Intolerance of these agents due to renal dysfunction should be considered an emerging indication for renal revascularization to facilitate their re-introduction.
引用
收藏
页码:1403 / 1409
页数:7
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