Why the study?
Does the addition of losartan to atenolol reduce the early left ventricular hypertrophic response in end-stage kidney disease patients undergoing arteriovenous fistula creation?
RCT (n=26)
Double-blind
1:1
No
Does the addition of losartan to atenolol reduce the early left ventricular hypertrophic response in end-stage kidney disease patients undergoing arteriovenous fistula creation?
Answers are grounded in this paper and cite their sources.
Losartan addition to atenolol does not mitigate early post-AVF LV mass increase in ESKD; leaves open optimal RAAS inhibition strategies.
BACKGROUND: Haemodialysis results in a left ventricular hypertrophic response. It is unclear whether tight blood pressure control or particular medications might attenuate this response. We sought to determine, in a pre-dialysis cohort on atenolol, whether Losartan might attenuate left ventricular hypertrophy post arteriovenous fistula creation in end stage kidney disease. MATERIALS AND METHODS: Placebo controlled double blind randomisation of 26 patients to fixed dose atenolol plus fixed dose losartan or placebo occurred 1 day prior to fistula creation. Pre-randomisation echocardiography was repeated at 1 week and 1-month. Measurement was undertaken of blood pressure, heart rate, brain natriuretic peptide, serum creatinine and estimated glomerular filtration rate. The primary pre-specified endpoint was the change in left ventricular mass at 1 month. Non-parametric statistical comparison was performed within and between groups. RESULTS: There was no difference in left ventricular mass between our groups 1-month post fistula creation. In the entire cohort, change in left ventricular mass was driven by changes in blood pressure and volume loading. Blood pressure changes correlated with left ventricular mass changes seen shortly post arteriovenous fistula creation, suggesting blood pressure control during this time period may be an important part of the management of end stage kidney disease. CONCLUSIONS: We did not see an advantage with the use of losartan with respect to diminution of the LVM response. However, our demonstrated change in LVM was relatively small compared to previous literature and suggests a possible role for beta blockade as a neurohormonal modulator around the time of arteriovenous fistula creation. TRIAL REGISTRATION: Clinical trials.gov (NCT00602004).
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Zentner et al. (2012) conducted an RCT in End stage kidney disease undergoing arteriovenous fistula creation (n=26). Losartan vs. Placebo was evaluated on Change in left ventricular mass at 1 month (p=ns).
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