When to start cholesterol-lowering therapy in patients with coronary heart disease. A statement for healthcare professionals from the American Heart Association Task Force on Risk Reduction

作者: Scott M. Grundy , Gary J. Balady , Michael H. Criqui , Gerald Fletcher , Philip Greenland

DOI: 10.1161/01.CIR.95.6.1683

关键词: MedicineFramingham Risk ScorePravastatinRisk factorCoronary atherosclerosisAnginaMyocardial infarctionCardiologyInternal medicineNational Cholesterol Education ProgramCoronary arteries

摘要: Strong evidence denotes benefit from reducing serum cholesterol levels in patients with established coronary heart disease (CHD).1 Treatment to decrease recurrent events and reduce total mortality can be called secondary prevention. Support for aggressive cholesterol-lowering therapy as a component of prevention comes meta-analysis earlier trials2 recent large clinical trials.3 4 5 Among the latter, Scandinavian Simvastatin Survival Study (4S),3 which hypercholesterolemic CHD received simvastatin therapy, documented 34% reduction major events, 42% mortality, 30% mortality. Investigators Cholesterol Recurrent Events (CARE) study5 likewise observed significant benefits when pravastatin was given average levels. Several other trials6 7 8 angiographic end points were used show that retards progression atherosclerosis; acute thrombolic arteries also noted. The summed results these different categories trials justify management most CHD. The National Education Program (NCEP)1 calls intensive any form atherosclerotic disease, specifically, myocardial infarction or angina pectoris, artery angioplasty, peripheral arterial abdominal aortic aneurysm, symptomatic carotid history bypass graft. These carry fivefold sevenfold elevated risk developing new thus need reduction. Despite proven CHD, many patients—up two thirds—receive no lower LDL (National Heart, Lung, Blood Institute; unpublished data; 1995). are being deprived valuable treatment will likelihood their having thrombotic …

参考文章(18)
Joel M. Gore, Robert J. Goldberg, Alan S. Matsumoto, William P. Castelli, Patricia M. McNamara, James E. Dalen, Validity of serum total cholesterol level obtained within 24 hours of acute myocardial infarction American Journal of Cardiology. ,vol. 54, pp. 722- 725 ,(1984) , 10.1016/S0002-9149(84)80197-6
D. Yeshurun, A.M. Gotto, Drug treatment of hyperlipidemia The American Journal of Medicine. ,vol. 60, pp. 379- 396 ,(1976) , 10.1016/0002-9343(76)90755-5
T Pearson, E Rapaport, M Criqui, C Furberg, V Fuster, L Hiratzka, W Little, I Ockene, G Williams, Optimal risk factor management in the patient after coronary revascularization. A statement for healthcare professionals from an American Heart Association Writing Group. Circulation. ,vol. 90, pp. 3125- 3133 ,(1994) , 10.1161/01.CIR.90.6.3125
Yaakov Henkin, Albert Oberman, Robert A. Kreisberg, Principles and Management of Lipid Disorders: A Primary Care Approach ,(1992)
Arlene W. Caggiula, Cholesterol-Lowering Intervention Program Archives of Internal Medicine. ,vol. 156, pp. 1205- 1213 ,(1996) , 10.1001/ARCHINTE.1996.00440100103012
G. B. John Mancini, Robert P. Byington, J. Wouter Jukema, Jukka T. Salonen, Bertram Pitt, Albert V. Bruschke, Helena Hoen, Curt D. Furberg, Reduction in cardiovascular events during pravastatin therapy. Pooled analysis of clinical events of the Pravastatin Atherosclerosis Intervention Program Circulation. ,vol. 92, pp. 2419- 2425 ,(1995) , 10.1161/01.CIR.92.9.2419
J. Tuomilehto, G. Vidgren, L. Toivanen, E. Tuomilehto-Wolf, K. Kohtamaki, J. Stengård, P. Zimmet, I.R. Mackay, Mj Rowley, P. Koskela, Antibodies to glutamic acid decarboxylase as predictors of insulin-dependent diabetes mellitus before clinical onset of disease. The Lancet. ,vol. 343, pp. 1383- 1385 ,(1994) , 10.1016/S0140-6736(94)92521-6