Prognostic Value of Ambulatory Blood-Pressure Recordings in Patients with Treated Hypertension
Denis L. Clement, M.D., Ph.D., Marc L. De Buyzere, B.Sc., Dirk A. De Bacquer, Ph.D., Peter W. de Leeuw, M.D., Ph.D., Daniel A. Duprez, M.D., Ph.D., Robert H. Fagard, M.D., Ph.D., Peter J. Gheeraert, M.D., Luc H. Missault, M.D., Jacob J. Braun, M.D., Roland O. Six, M.D., Patricia Van Der Niepen, M.D., Eoin O'Brien, M.D., Ph.D., for the Office versus Ambulatory Pressure Study Investigators
Background It is uncertain whether ambulatory blood-pressuremeasurements recorded for 24 hours in patients with treatedhypertension predict cardiovascular events independently ofblood-pressure measurements obtained in the physician's officeand other cardiovascular risk factors.
Methods We assessed the association between base-line ambulatoryblood pressures in treated patients and subsequent cardiovascularevents among 1963 patients with a median follow-up of 5 years(range, 1 to 66 months).
Results We documented new cardiovascular events in 157 patients.In a Cox proportional-hazards model with adjustment for age,sex, smoking status, presence or absence of diabetes mellitus,serum cholesterol concentration, body-mass index, use or nonuseof lipid-lowering drugs, and presence or absence of a historyof cardiovascular events, as well as blood pressure measuredat the physician's office, higher mean values for 24-hour ambulatorysystolic and diastolic blood pressure were independent riskfactors for new cardiovascular events. The adjusted relativerisk of cardiovascular events associated with a 1-SD incrementin blood pressure was 1.34 (95 percent confidence interval,1.11 to 1.62) for 24-hour ambulatory systolic blood pressure,1.30 (95 percent confidence interval, 1.08 to 1.58) for ambulatorysystolic blood pressure during the daytime, and 1.27 (95 percentconfidence interval, 1.07 to 1.57) for ambulatory systolic bloodpressure during the nighttime. For ambulatory diastolic bloodpressure, the corresponding relative risks of cardiovascularevents associated with a 1-SD increment were 1.21 (95 percentconfidence interval, 1.01 to 1.46), 1.24 (95 percent confidenceinterval, 1.03 to 1.49), and 1.18 (95 percent confidence interval,0.98 to 1.40).
From the Departments of Cardiovascular Diseases (D.L.C., M.L.D.B., D.A.D., P.J.G.) and Public Health (D.A.D.B.), Ghent University, Ghent, Belgium; the Department of Medicine, University Hospital Maastricht, Maastricht, the Netherlands (P.W.L.); the Cardiovascular Division, University of Minnesota, Minneapolis (D.A.D.); the Hypertension and Cardiovascular Rehabilitation Unit, University of Leuven, Leuven, Belgium (R.H.F.); the Department of Cardiology, Algemeen Ziekenhuis St. Jan, Bruges, Belgium (L.H.M.); the Department of Internal Medicine, Vlietland Hospital, Schiedam, the Netherlands (J.J.B.); the Department of Internal Medicine and Hypertension, Vrije Universiteit Brussel, Brussels, Belgium (R.O.S., P.V.D.N.); and the Blood Pressure Unit and Arterial Disease, Assessment, Prevention, and Treatment Centre, Beaumont Hospital, Dublin, Ireland (E.O.).
Address reprint requests to Dr. Clement at the Department of Cardiology and Angiology, University Hospital, De Pintelaan 185, B-9000 Ghent, Belgium, or at denis.clement{at}skynet.be.
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