2004
DOI: 10.7326/0003-4819-141-2-200407200-00016
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Is Improved Survival a Class Effect of Angiotensin-Converting Enzyme Inhibitors?

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Cited by 12 publications
(11 citation statements)
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“…Patients who were prescribed antihypertensives other than ACEIs ( n = 420 074) were excluded because the focus of this analysis was CA ACEIs and non‐CA ACEIs (see Appendix Table 1 for list of ACEI classification). Non‐CA ACEI users were selected as the comparison group in this analysis because the CA properties of certain ACEIs have not been promoted and are not readily apparent to clinicians and many clinicians consider ACEIs to be an undifferentiated class of drug . Consequently, clinicians are unlikely to select an ACEI on the basis of its pharmacodynamic properties or the cognitive characteristics of the patient, which reduces the likelihood of selection bias or confounding by indication.…”
Section: Methodsmentioning
confidence: 99%
“…Patients who were prescribed antihypertensives other than ACEIs ( n = 420 074) were excluded because the focus of this analysis was CA ACEIs and non‐CA ACEIs (see Appendix Table 1 for list of ACEI classification). Non‐CA ACEI users were selected as the comparison group in this analysis because the CA properties of certain ACEIs have not been promoted and are not readily apparent to clinicians and many clinicians consider ACEIs to be an undifferentiated class of drug . Consequently, clinicians are unlikely to select an ACEI on the basis of its pharmacodynamic properties or the cognitive characteristics of the patient, which reduces the likelihood of selection bias or confounding by indication.…”
Section: Methodsmentioning
confidence: 99%
“…The most robust CHF evidence lies with Ramipril/ Enalapril (ACE-I) and Candersartan/Valsartan (ARB). If the playing field was level the benefits are likely a "class effect" with minor variations [49][50][51]. Difference in glucose metabolism and IR favor ARB [26,49].…”
Section: Beta Blockersmentioning
confidence: 99%
“…The extrapolation of the benefit of these drugs to their pharmacological families or other drugs or doses in the prevention of vascular disease recurrences following TIA or stroke, would be inappropriate [37, 107, 108]. …”
Section: Therapeutic Objectives Following Stroke: Analysis Of Currentmentioning
confidence: 99%