Skip to main content
Log in

Optimising Outcomes in Secondary Prevention of Coronary Heart Disease

Current Evidence and Future Prospects

  • Review Article
  • Interventions & Outcomes
  • Published:
Disease Management & Health Outcomes

Summary

Atherosclerosis is a diffuse disease of arteries. It cannot be definitively treated by procedures such as bypass surgery or angioplasty which correct only discrete anatomical lesions. The only definitive treatments for atherosclerosis are medical. In both men and women with coronary disease, treatment includes interventions such as smoking cessation, lipid management and blood pressure lowering, restriction of dietary calories, fat, and salt, increased physical activity, body weight reduction, β-adrenoceptor blocking drugs during the first 6 to 12 months or so after an infarct, and, in patients with congestive heart failure, the use of angiotensin-converting enzyme (ACE) inhibitors.

Specific guidelines describing the use of these interventions have recently been released by a consensus panel of the American Heart Association. These guidelines apply to both men and women with coronary disease, even though the preponderance of evidence on which they are based has been derived from intervention trials that included mostly men. The application of these guidelines cannot guarantee that coronary disease will not recur. It is unclear what, if any, additive effects they may have. Unlike anatomical interventions, however, they attack the underlying process of atherogenesis in whatever vascular bed it occurs. Failure to include these interventions in the care of patients with established coronary disease is a serious and potentially life-threatening omission.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Moro CJL, Lopez AD. Mortality by cause for eight regions of the world: Global Burden of Disease Study. Lancet 1997; 349: 1269–76

    Article  Google Scholar 

  2. Smith S, Blair S, Criqui MH, et al., for the Secondary Prevention Panel. Preventing heart attack deaths in patients with coronary disease. Circulation 1995; 92: 2–4

    Article  PubMed  Google Scholar 

  3. Palmer JR, Rosenberg L, Shapiro S. ‘Low yield’ cigarettes and the risk of nonfatal myocardial infarction in women. N Engl J Med 1989; 320: 1569–73

    Article  PubMed  CAS  Google Scholar 

  4. Rosenberg L, Palmer JR, Shapiro S. Decline in the risk of myocardial infarction among women who stop smoking. N Engl J Med 1990; 322: 213–7

    Article  PubMed  CAS  Google Scholar 

  5. Roberts WC. Atherosclerotic risk factors: are there ten or is there only one? Am J Cardiol 1989; 64: 552–4

    Article  PubMed  CAS  Google Scholar 

  6. Alexander RW. Theodore Cooper Memorial Lecture. Hypertension and the pathogenesis of atherosclerosis: oxidative stress and the mediation of arterial inflammatory responses: a new perspective. Hypertension 1995; 25: 155–61

    Article  PubMed  CAS  Google Scholar 

  7. Scandinavian Simvastatin Survival Study Group. Randomised trial of cholesterol lowering in 4444 patients with coronary heart disease: the Scandinavian Survival Study. Lancet 1994; 344: 1383–9

    Google Scholar 

  8. Shepherd J, Cobbe SM, Ford I, et al. Prevention of coronary heart disease with pravastatin in men with hypercholesterolemia: West of Scotland Coronary Prevention Study Group. N Engl J Med 1995; 333: 1301–7

    Article  PubMed  CAS  Google Scholar 

  9. Sacks FM, Pfeffer MA, Moye LA, et al., for the Cholesterol and Recurrent Events Trial Investigators. The effect of pravastatin on coronary events after myocardial infarction in patients with average cholesterol levels. N Engl J Med 1996; 335: 1001–9

    Article  PubMed  CAS  Google Scholar 

  10. The Post Coronary Artery Bypass Graft Trial Investigators. The effect of aggressive lowering of low-density lipoprotein cholesterol levels and low-dose anticoagulation on obstructive changes in saphenous-vein coronary-artery bypass grafts. N Engl JMed 1997; 336: 153–62

    Article  Google Scholar 

  11. Carlson LA, Rosenhamer G. Reduction of mortality in the Stockholm Ischaemic Heart Disease Secondary Prevention Study by combined treatment with Clofibrate and nicotinic acid. Acta Med Scand 1988; 223: 405–18

    Article  PubMed  CAS  Google Scholar 

  12. Research Committee of the Scottish Society of Physicians. Ischaemic heart disease: a secondary prevention trial using Clofibrate. BMJ 1971; 4: 775–84

    Article  Google Scholar 

  13. Group of Physicians of the Newcastle upon Tyne Region. Trial of Clofibrate in the treatment of ischaemic heart disease. BMJ 1971; 4: 767–75

    Article  Google Scholar 

  14. Brown BG, Zhao X-Q, Sacco DE, et al. Arteriographic view of treatment to achieve regression of coronary atherosclerosis and to prevent plaque disruption and clinical cardiovascular events. Br Heart J 1993; 69 Suppl. 1: S48–53

    Article  PubMed  CAS  Google Scholar 

  15. Pitt B, Mancini J, Ellis SG, et al., for the PLAC I Investigators. Pravastatin limitation of atherosclerosis in the coronary arteries (PLAC I) [abstract no. 739-2]. J Am Coll Cardiol 1994; 1A-484A: 131A

    Google Scholar 

  16. Crouse JR III, Byington RP, Bond MG, et al. Pravastatin, lipids, and atherosclerosis in the carotid arteries (PLAC-II). Am J Cardiol 1995; 75: 455–9

    Article  PubMed  Google Scholar 

  17. Waters D, Higginson L, Gladstone P, et al., and the CCAIT Study Group. Effects of monotherapy with an HMG-CoA reductase inhibitor on the progression of coronary atherosclerosis as assessed by serial quantitative arteriography: the Canadian Coronary Atherosclerosis Intervention Trial. Circulation 1994; 89: 959–68

    Article  PubMed  CAS  Google Scholar 

  18. MAAS Investigators. Effect of simvastatin on coronary atheroma: the Multicentre Anti-Atheroma Study (MAAS). Lancet 1994; 344: 633–8

    Article  Google Scholar 

  19. Jukema JW, Bruschke AVG, van Boven AJ, et al., on behalf of the REGRESS Study Group. Effects of lipid lowering by pravastatin on progression and regression of coronary artery disease in symptomatic men with normal to moderately elevated serum cholesterol levels: the Regression Growth Evaluation Statin Study (REGRESS). Circulation 1995; 91: 2528–40

    Article  PubMed  CAS  Google Scholar 

  20. Furberg CD, Adams Jr HP, Applegate WB, et al., for the Asymptomatic Carotid Artery Progression Study (ACAPS) Research Group. Effect of lovastatin on early carotid atherosclerosis and cardiovascular events. Circulation 1994; 90: 1679–87

    Article  PubMed  CAS  Google Scholar 

  21. Blankenhorn DH, Azen SP, Kramsch DM, et al., and the MARS Research Group. Coronary angiographic changes with lovastatin therapy: the Monitored Atherosclerosis Regression Study (MARS). Ann Intern Med 1993; 119: 969–76

    PubMed  CAS  Google Scholar 

  22. Kane JP, Malloy MJ, Ports TA, et al. Regression of coronary atherosclerosis during treatment of familial hypercholesterolemia with combined drug regimens. JAMA 1990; 264: 3007–12

    Article  PubMed  CAS  Google Scholar 

  23. Waters D, Higginson L, Gladstone P, et al. Effects of cholesterol lowering on the progression of coronary atherosclerosis in women: a Canadian Coronary Atherosclerosis Intervention Trail (CCAIT) substudy. Circulation 1995; 92: 2404–10

    Article  PubMed  CAS  Google Scholar 

  24. Buchwald H, Vargo RL, Matts JP, et al. Effect of partial ileal bypass surgery on mortality and morbidity from coronary heart disease in patients with hypercholesterolemia. N Engl J Med 1990; 323: 946–55

    Article  PubMed  CAS  Google Scholar 

  25. Ericsson CG, Hamsten A, Nilsson J, et al. Angiographie assessment of effects of bezafibrate on progression of coronary artery disease in young male postinfarction patients. Lancet 1996; 347: 849–53

    Article  PubMed  CAS  Google Scholar 

  26. Nawrocki JW, Weiss SR, Davidson MH, et al. Reduction of LDL cholesterol by 25% to 60% in patients with primary hypercholesterolemia by atorvastatin, a new HMG-CoA reductase inhibitor. Arterioscler Thromb Vase Biol 1995; 15: 678–82

    Article  CAS  Google Scholar 

  27. Rimm EB, Klatsky A, Grobbee D, et al. Review of moderate alcohol consumption and reduced risk of coronary heart disease: is the effect due to beer, wine, or spirits? BMJ 1996; 312: 731–6

    Article  PubMed  CAS  Google Scholar 

  28. Antiplatelets Trialists’ Collaboration. Collaborative overview of randomised trials of antiplatelet therapy: I. Prevention of death, myocardial infarction, and stroke by prolonged anti-platelet therapy in various categories of patients. BMJ 1994; 308: 81–106

    Article  Google Scholar 

  29. Pfeffer MA, Braunwald E, Moye LA, et al., on behalf of the SAVE Investigators. Effect of Captopril on mortality and morbidity in patients with left ventricular dysfunction after myocardial infarction: results of the survival and ventricular enlargement trial. N Engl J Med 1992; 327: 669–77

    Article  PubMed  CAS  Google Scholar 

  30. Yusuf A, Pepine CJ, Garces C, et al. Effect of enalapril on myocardial infarction and unstable angina in patients with low ejection fractions. Lancet 1992; 340: 1173–8

    Article  PubMed  CAS  Google Scholar 

  31. Yusuf S, Peto R, Lewis J, et al. Beta blockade during and after myocardial infarction: an overview of randomized trials. Prog Cardiovasc Dis 1985; 27; 5: 335–71

    Article  Google Scholar 

  32. Henderson BE, Pagnini-Hill A, Ross RK. Decreased mortality in users of estrogen replacement therapy. Arch Intern Med 1991; 151: 75–8

    Article  PubMed  CAS  Google Scholar 

  33. Falkeborn M, Persson I, Adami H-O. The risk of acute myocardial infarction after oestrogen and oestrogen-progestogen replacement. Br J Obstet Gynaecol 1992; 99: 821–8

    Article  PubMed  CAS  Google Scholar 

  34. Psaty BM, Heckbert SR, Atkins D, et al. The risk of myocardial infarction associated with the combination use of estrogens and progestins in postmenopausal women. Arch Intern Med 1994; 154: 1333–9

    Article  PubMed  CAS  Google Scholar 

  35. Grodstein F, Stampfer JJ, Manson JE, et al. Postmenopausal estrogen and progestin use and the risk of cardiovascular disease. N Engl J Med 1996; 335: 453–61

    Article  PubMed  CAS  Google Scholar 

  36. Grodstein F, Stampfer MJ, Colditz GA, et al. Postmenopausal hormone therapy and mortality. N Engl J Med 1997; 336: 1769–75

    Article  PubMed  CAS  Google Scholar 

  37. LaRosa JC. Estrogen: risk versus benefit for the prevention of coronary artery disease: review in depth. Coronary Artery Dis 1993; 4: 588–94

    Article  CAS  Google Scholar 

  38. Writing Group for the PEPI Trial. Effects of estrogen or estrogen/progestin regimens on heart’ disease risk factors in postmenopausal women: the Postmenopausal Estrogen/Progestin Interventions (PEPI) Trial. JAMA 1995; 273: 199–208

    Article  Google Scholar 

  39. Kim CJ, Min YK, Ryu WS, et al. Effect of hormone replacement therapy on lipoprotein (a) and lipid levels in postmenopausal women: influence of various progestogens and duration of therapy. Arch Intern Med 1996; 156: 1693–700

    Article  PubMed  CAS  Google Scholar 

  40. Adams MR, Clarkson TB, Loritnik DR, et al. Contraceptive steroids and coronary artery atherosclerosis in cynomolgus macaques. Fertil Steril 1987; 47: 1010–8

    PubMed  CAS  Google Scholar 

  41. Gaziano JM, Manson JE, Ridker PM, et al. Beta carotene therapy for chronic stable angina. Circulation 1991; 82 Suppl. 111: 201

    Google Scholar 

  42. Hennekens CH, Buring JE, Manson JE, et al. Lack of effect of long-term supplementation with beta carotene on the incidence of malignant neoplasms and cardiovascular disease. N Engl J Med 1996; 334: 1145–9

    Article  PubMed  CAS  Google Scholar 

  43. Gaziano JM, Manson JE, Branch LG, et al. Dietary beta carotene and decreased cardiovascular mortality in an elderly cohort [abstract]. J Am Coll Cardiol 1992; 19 Suppl A: 377A

    Google Scholar 

  44. Omenn GS, Goodman GE, Thornquist MD, et al. Effects of a combination of beta-carotene and vitamin A on lung cancer and cardiovascular disease. N Engl J Med 1996; 334: 1150–5

    Article  PubMed  CAS  Google Scholar 

  45. The Alpha-Tocopherol, Beta Carotene Cancer Prevention Study Group. The effect of vitamin E and beta carotene on the incidence of lung cancer and other cancers in male smokers. N Engl J Med 1994; 330: 1029–35

    Article  Google Scholar 

  46. Hebert PR, Gaziano JM, Chanks H. Cholesterol lowering with statin drugs, risk of stroke, and total mortality. An overview of randomised trials. JAMA 1997; 278: 313–21

    Article  PubMed  CAS  Google Scholar 

  47. Hebert PR, Moser M, Mayer J, et al. Recent evidence on drug therapy of mild to moderate hypertension and decreased risk of cardiovascular heart disease. Arch Intern Med 1993; 153: 578–81

    Article  PubMed  CAS  Google Scholar 

  48. SHEP Cooperative Research Group. Prevention of stroke by antihypertensive drug treatment in older persons with isolated systolic hypertension: final results of the Systolic Hypertension in the Elderly Program (SHEP). JAMA 1991; 265: 3255–64

    Article  Google Scholar 

  49. Ruderman NB, Schneider SH. Diabetes, exercise, and atherosclerosis. Diabetes Care 1992; 15: 1787–93

    Article  PubMed  CAS  Google Scholar 

  50. Pyorala K, Pedersen TR, Kjekshus J, et al., for the Scandinavian Simvastatin Survival Study (4S) Group. Cholesterol lowering with simvastatin improves prognosis of diabetic patients with coronary artery disease: a sub-group analysis of the Scandinavian Simvastatin Survival Study (4S). Diabetes Care 1997; 20: 614–20

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

LaRosa, J.C. Optimising Outcomes in Secondary Prevention of Coronary Heart Disease. Dis-Manage-Health-Outcomes 2, 281–290 (1997). https://doi.org/10.2165/00115677-199702060-00003

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.2165/00115677-199702060-00003

Keywords

Navigation