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Kane RL, Guise JM, Hartman K, et al. Presentation of Future Research Needs [Internet]. Rockville (MD): Agency for Healthcare Research and Quality (US); 2012 Apr. (Methods Future Research Needs Reports, No. 9.)

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Presentation of Future Research Needs [Internet].

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Table 3Excerpt from “Future Research Needs for Angiotensin-Converting Enzyme Inhibitors (ACEIs), Angiotensin II Receptor Antagonists (ARBs), or Direct Renin Inhibitors (DRI) for Treating Hypertension”

Research areaRCT?Meta-analysis or individual patient data analysis across RCTs?Meta-analysis of observational studies?New observational study?Analysis of existing data?Model?
What is the comparative effectiveness of these medications on cardiovascular and cerebrovascular events measured over several years?Maybe: Large number of studies recently completed or ongoing in patients with other comorbidities may make new RCTs unnecessaryMaybe: If recent data is not included in original CER or if it is methodologically valid to combine studies of medication impact across different conditions (such as hypertension, ischemic heart disease, chronic kidney disease)Maybe: If sufficient number of studies available; adjustment for confounding could be an issueMaybe: Most direct way to address long-term outcomes; however, resource requirements for longer-term studies are potential limitationsYes: Most efficient method for evaluating long-term outcomes given the large number of existing studies; appropriate coding for covariates an issueMaybe: Potential role for helping determine clinically important differences
What is the impact of comorbidities (such as ischemic heart disease, CHF, diabetes, peripheral arterial disease, chronic kidney disease) on ACEI/ARB/DRI effectiveness or harms in patients with hypertension?Maybe: May be feasible for common comorbidities; existing or ongoing studies might be sufficient for someYes: If individual patient data or separate subgroup data not reported in current trials could be obtained and pooled for analysis; would require cooperation from the multiple sponsors of RCTs in this areaYes: If individual patient data or separate subgroup data not reported in current trials could be obtained and pooled for analysis; would require cooperation from the multiple sponsors; if available, could address less common comorbidities, long-term safety/effectivenessMaybe: Most direct way to address less common comorbidities; allows for adjustment for confounding; sample size and resources needed for longer follow-up are potential limitationsYes: Most efficient method for evaluating less common comorbidities over longer time frames; appropriate coding of covariates a potential limitationNo: Except for potential role in defining clinically or economically meaningful differences

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