02808nas a2200277   4500000000100000008004100001100001400042700001500056700001200071700001400083700001400097700001200111700001500123700001200138700001300150700001400163700001500177700001400192700001300206700001900219245012000238250001500358490003200373520207400405020005102479       2015                            d1 aHawley C.1 aPilmore H.1 aGarg A.1 aPascoe E.1 aIerino F.1 aKrum H.1 aRoberts M.1 aCass A.1 aBadve S.1 aScaria A.1 aVergara L.1 aTonkin A.1 aIsbel N.1 aPerkovic Vlado00aThe beta-Blocker to Lower Cardiovascular Dialysis Events (BLOCADE) Feasibility Study: A Randomized Controlled Trial  a2016/01/010 vpii: S0272-6386(15)01394-3.3 a<p>
BACKGROUND: beta-Blocking agents reduce cardiovascular mortality in patients with heart disease, but their potential benefit in dialysis patients is unclear. We aimed to determine the feasibility of a randomized controlled trial (RCT). STUDY DESIGN: Pilot RCT. SETTING &amp; PARTICIPANTS: Patients who received dialysis for 3 or more months and were 50 years or older (or &gt;/=18 years with diabetes or cardiovascular disease) were recruited from 11 sites in Australia and New Zealand. We aimed to recruit 150 participants. INTERVENTION: After a 6-week run-in with the beta-blocker carvedilol, we randomly assigned participants to treatment with carvedilol or placebo for 12 months. OUTCOMES &amp; MEASUREMENTS: The prespecified primary outcome was the proportion of participants who tolerated carvedilol, 6.25mg, twice daily during the run-in period. After randomization, we report participant withdrawal and the incidence of intradialytic hypotension (IDH). RESULTS: Of 1,443 patients screened, 354 were eligible, 91 consented, and 72 entered the run-in stage. 49 of 72 run-in participants (68%; 95% CI, 57%-79%) achieved the primary outcome. 5 of the 23 withdrawals from run-in were attributable to bradycardia or hypotension. After randomization, 10 of 26 allocated to carvedilol and 4 of 23 allocated to placebo withdrew. 4 participants randomly assigned to carvedilol withdrew because of bradycardia or hypotension. Overall, there were 4 IDH events per 100 hemodialysis sessions; in participants allocated to carvedilol versus placebo, respectively, there were 7 versus 2 IDH events per 100 hemodialysis sessions (P=0.1) in the 2 weeks immediately following a dose increase and 4 versus 3 IDH events per 100 hemodialysis sessions after no dose increase (P=0.7). LIMITATIONS: Unable to recruit planned sample size. CONCLUSIONS: Recruiting patients receiving dialysis to an RCT of beta-blocker versus placebo will prove challenging. Possible solutions include international collaboration and exploring novel trial designs such as a registry-based RCT.
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  a1523-6838 (Electronic)<br/>0272-6386 (Linking)