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Review
. 2013 Feb;13(1):63-70.
doi: 10.7861/clinmedicine.13-1-63.

Pharmacological treatment of chronic stable angina pectoris

Affiliations
Review

Pharmacological treatment of chronic stable angina pectoris

Jason M Tarkin et al. Clin Med (Lond). 2013 Feb.

Abstract

Chronic stable angina is the most common manifestation of ischaemic heart disease in the developed world and is associated with impaired quality of life and increased mortality. The pathogenesis of stable angina is complex and often, albeit not always, involves flow-limiting epicardial coronary artery stenoses (atheromatous plaques) that reduce the ability of the coronary circulation to deliver appropriate blood supply to the myocardium. The coronary microcirculation can also play an important role. An imbalance between myocardial oxygen supply and metabolic oxygen demand causes the symptoms of angina pectoris and represents a major therapeutic target. Rational treatment requires a multi-faceted approach combining lifestyle changes, aggressive management of modifiable coronary artery disease risk factors, pharmacological therapy and myocardial revascularisation when appropriate. Despite modern therapies, many patients continue to suffer from angina. Several new anti-anginal drugs have been introduced that might allow more effective symptom control. These novel agents have specific mechanisms of action and fewer side effects compared to conventional drugs. The combined use of traditional and novel treatments is likely to increase the proportion of patients who are managed successfully with medical therapy alone. This article briefly reviews recent advances in the pharmacological management of chronic stable angina pectoris, highlighting how an understanding of the prevailing pathogenic mechanisms in the individual patient can aid appropriate selection of therapeutic strategies and improve clinical outcome.

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Figures

Fig 1.
Fig 1.
Proposed practical algorithm for pharmacological treatment of chronic stable angina based on NICE guidance. BB = beta-blocker; CCB = calcium channel blocker; DM = diabetes mellitus; GTN = glyceryltrinitrate; HF = heart failure; MI = myocardial infarction. *added cardio-protective properties; †improves HbA1c in DM; ‡prognostic benefit in HF.

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References

    1. Silverman ME. William Heberden and some account of a disorder of the breast. Clin Cardiol. 1987;10:211–3. doi: 10.1002/clc.4960100314. - DOI - PubMed
    1. Kaski JC. Arrebola-Moreno A. Dungu J. Treatment strategies for chronic stable angina. Expert Opin Pharmacother. 2011;12:2833–44. doi: 10.1517/14656566.2011.634799. - DOI - PubMed
    1. Lloyd-Jones DM. Hong Y. Labarthe D. Mozaffarian D, et al. on behalf of the American Heart Association Strategic Planning Task Force and Statistics Committee. Defining and setting national goals for cardiovascular health promotion and disease reduction. The American Heart Association's strategic impact goal through 2020 and beyond. Circulation. 2010;121:586–613. doi: 10.1161/CIRCULATIONAHA.109.192703. - DOI - PubMed
    1. National Institute for Health and Clinical Excellence. Clinical guideline CG126. London: NICE; 2011. Management of stable angina. http://guidance.nice.org.uk/CG126 [Accessed 3 January 2013]. - PubMed
    1. Fox K. Garcia MA. Ardissino D, et al. Guidelines on the management of stable angina pectoris: executive summary: the task force on the management of stable angina pectoris of the European Society of Cardiology. Eur Heart J. 2006;27:1341–81. doi: 10.1093/eurheartj/ehl001. - DOI - PubMed

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