Society GuidelinesCanadian Cardiovascular Society Guidelines for the Diagnosis and Management of Stable Ischemic Heart Disease
Section snippets
Establishing Diagnosis and Prognosis
In patients with symptoms suggestive of SIHD, the probability of having obstructive coronary artery disease (CAD) is primarily obtained using a thorough history. Classically, angina is described as a dull retrosternal discomfort/ache/heaviness that might or might not radiate to the jaw, neck, shoulders or arms, is provoked by exertion or emotional stress, and is relieved within 5 minutes of rest or nitroglycerine use.2 However, nonclassical symptoms are common, particularly among diabetic
Initiation of Medical Treatment in Patients With Established CAD
Therapy for SIHD involves a combination of approaches to improve quality of life by minimizing or abolishing symptoms, and to improve prognosis by preventing myocardial infarction (MI) and premature death. Medical management can be implemented more expeditiously in most settings than can the steps required in anticipation of possible revascularization. However, expeditious revascularization therapy might be considered in parallel based on prognostic features of the diagnostic tests as discussed
Consideration of Revascularization Therapy
Revascularization therapy is also indicated to improve symptoms or quality of life and/or to reduce the risk of MI and premature death. There is no controversy regarding the need to explore revascularization in SIHD patients with inadequate symptom relief, suboptimal quality of life, or emergence of acute chest pain syndromes while using medical therapy. However, because of the success of available medical therapy, and new forms of medical and revascularization therapies, categorical statements
Provision of Appropriate Clinical Follow-up
The most appropriate clinical follow-up in patients with SIHD is difficult to clearly define because of the paucity of robust research. However, there is a need for regular communication between primary care practitioners and specialists expert in the provision of chronic disease care for such patients.3 Follow-up visits should include a focused history, physical examination, and clinically appropriate laboratory testing, with an emphasis on ensuring optimal risk factor control. The history
Summary
SIHD is common, requires expeditious diagnosis, implementation of medical therapies, correction of CV risk factors, timely consideration of revascularization options, and appropriate follow-up. This Canadian perspective provides a practical approach applicable in most practice settings for optimization of longevity and quality of life, with ample regard for rational resource utilization.
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The disclosure information of the authors and reviewers is available from the CCS on their guidelines library at www.ccs.ca.
This statement was developed following a thorough consideration of medical literature and the best available evidence and clinical experience. It represents the consensus of a Canadian panel comprised of multidisciplinary experts on this topic with a mandate to formulate disease-specific recommendations. These recommendations are aimed to provide a reasonable and practical approach to care for specialists and allied health professionals obliged with the duty of bestowing optimal care to patients and families, and can be subject to change as scientific knowledge and technology advance and as practice patterns evolve. The statement is not intended to be a substitute for physicians using their individual judgment in managing clinical care in consultation with the patient, with appropriate regard to all the individual circumstances of the patient, diagnostic and treatment options available and available resources. Adherence to these recommendations will not necessarily produce successful outcomes in every case.