1 | Impact of comorbidities (such as hypertension, CHF with or without preserved LV function, diabetes, peripheral arterial disease, chronic kidney disease, prior coronary revascularization; single-vs. multi-vessel coronary artery disease) on ACEI/ARB effectiveness or harms in patients with stable IHD |
2 | The impact of ACEI/ARB in patients with stable IHD on progression of renal insufficiency or development of dialysis dependence |
2 | The impact of ACEI/ARB in patients with stable IHD on utilization and cost of therapy |
3 | Impact of demographic differences (such as age, race, sex) on ACEI/ARB effectiveness or harms in patients with stable IHD |
3 | Impact of concurrent medications (such as antiplatelet agents, lipid-lowering medications, other antihypertensives) on ACEI/ARB effectiveness or harms in patients with stable IHD |
3 | The benefit of ACEIs/ARBs relative to alternative medication classes (calcium channel blocker, diuretic, or beta-blocker) with respect to their effectiveness or harms in patients with stable IHD |
3 | Strategies to enhance greater evidence-based use of ACEIs/ARBs |
3 | The impact of ACEI/ARB in patients with stable IHD on cardiovascular outcomes (such as cardiovascular death, nonfatal MI, CVA, hospitalization for CHF, and surrogates such as blood pressure control, measures of atherosclerosis, etc.) |
3 | The impact of ACEI/ARB in patients with stable IHD on incidence of new diagnoses (such as diabetes, atrial fibrillation, CHF with or without preserved LV function) |
4 | Impact of genetic differences (such as ACE or angiotensin II receptor gene polymorphisms) on ACEI/ARB effectiveness or harms in patients with stable IHD |
4 | The impact of ACEI/ARB adherence (including differential adherence within and between medication classes) on their effectiveness or harms in patients with stable IHD |
4 | The impact of ACEI/ARB in patients with stable IHD on patient quality of life |
5 | Impact of the dose response (impact of medication dose or dosing interval) of ACEIs and ARBs on their effectiveness or harms in patients with stable IHD |
5 | Impact of class effect (impact of differences between specific agents within each class) of ACEIs and ARBs on their effectiveness or harms in patients with stable IHD |
5 | The impact of ACEI/ARB in patients with stable IHD on development of nonangioedema adverse effects (such as hypotensive symptoms, cough, syncope, diarrhea, renal insufficiency, hyperkalemia) |
6 | The impact of ACEI/ARB in patients with stable IHD on development of angioedema |