2014
DOI: 10.1016/j.jacc.2014.01.087
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Worsening Renal Function and Outcome in Heart Failure Patients With Preserved Ejection Fraction and the Impact of Angiotensin Receptor Blocker Treatment

Abstract: The incidence of WRF in HFpEF was similar to that previously reported in HFrEF but more frequent with irbesartan than with placebo. WRF after initiation of irbesartan treatment in HFpEF was associated with excess risk, in contrast to WRF occurring with RAAS blockade in HFrEF.

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Cited by 70 publications
(73 citation statements)
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“…For example, a recent study showed that WRF induced by initiating renin-angiotensin-aldosterone system inhibitors was associated with a poor prognosis in those with HFpEF, not with HFrEF. 27 In another study, although WRF was established as a predictor of poor prognosis in patients, the association was less evident in patients with HFpEF. 1 The diversity in the causes of WRF and the pathology of heart failure may explain these findings.…”
Section: Discussionmentioning
confidence: 96%
“…For example, a recent study showed that WRF induced by initiating renin-angiotensin-aldosterone system inhibitors was associated with a poor prognosis in those with HFpEF, not with HFrEF. 27 In another study, although WRF was established as a predictor of poor prognosis in patients, the association was less evident in patients with HFpEF. 1 The diversity in the causes of WRF and the pathology of heart failure may explain these findings.…”
Section: Discussionmentioning
confidence: 96%
“…Whereas WRF was an independent risk factor for all analyzed outcomes, the effect size was larger in HFpEF; particularly for in‐hospital outcomes, effect size was 3‐fold larger in HFpEF. No current studies have compared the effect size of WRF in HF subtypes, whereas a previous study showed that WRF was a predictor of adverse events in HFpEF …”
Section: Discussionmentioning
confidence: 98%
“…If the decrease in GFR itself is the cause for the inferior outcomes, then in HFpEF where RAAS antagonism has no benefit, we would expect the risk of death associated with WRF to be identical in the placebo and RAAS antagonist groups. 21 To the contrary, the risk of death associated with RAAS antagonist-induced WRF was 53% greater than WRF in the placebo group. Notably, WRF in the placebo group was not actually significantly associated with worse outcomes (p=0.21).…”
mentioning
confidence: 94%