In line with the ESC mission, newly presented content is made available to all for a limited time (4 months for ESC Congress, 3 months for other events). ESC Professional Members, Association Members (Ivory & above) benefit from year-round access to all the resources from their respective Association, and to all content from previous years. Fellows of the ESC (FESC), and Professionals in training or under 40 years old, who subscribed to a Young Combined Membership package benefit from access to all ESC 365 content from all events, all editions, all year long. Find out more about ESC Memberships here.
Optimising heart failure treatment following cardiac resynchronisation therapy
Authors : A Jorsal (Aarhus,DK), K Pryds (Aarhus,DK), J Mcmurray (Glasgow,GB), H Wiggers (Aarhus,DK), A Sommer (Aarhus,DK), JC Nielsen (Aarhus,DK), RR Nielsen (Aarhus,DK)
A Jorsal1
,
K Pryds1
,
J Mcmurray2
,
H Wiggers1
,
A Sommer1
,
JC Nielsen1
,
RR Nielsen1
,
1Aarhus University Hospital, Department of Cardiology - Aarhus - Denmark
,
2University of Glasgow, Institute of Cardiovascular & Medical Sciences, University of Glasgow - Glasgow - United Kingdom of Great Britain & Northern Ireland
,
Topic(s): Chronic Heart Failure: Pharmacotherapy
BACKGROUND: Device therapy in addition to medical treatment improves prognosis in a subset of patients with heart failure and reduced ejection fraction. However, some patients remain symptomatic or their heart failure even progresses despite cardiac resynchronization therapy (CRT). The aim of the study was to evaluate the proportion of patients who could benefit from optimization of medical therapy by using sacubitril/valsartan, ivabradine or both following CRT implantation.
METHODS: Post-hoc analysis of a single-center, double blind, controlled trial, in which, patients scheduled for CRT were randomized to empiric (n=93) or imaging-guided left ventricular lead placement (n=89). All patients underwent clinical evaluation and blood sampling at baseline and 6 months following CRT implantation. The proportion of patients meeting the indication for sacubitril/valsartan (irrespective of angiotensin-converting enzyme inhibitor or angiotensin 2 receptor blocker dosage) and/or ivabradine in current guidelines was evaluated at baseline and after 6 months.
RESULTS: Of 182 patients with an indication for CRT, 146 (80%) also had an indication for optimization of medical therapy at baseline by adding sacubitril/valsartan, ivabradine or both. Of the 179 survivors at 6 months, 136 (76%) were still symptomatic after device implantation; of these, 51 (38%) patients had an indication for optimization of medical therapy: sacubitril/valsartanin 37 (27%), ivabradine in 7 (5%), and both drugs in 7 (5%) patients. Seven (18%) patients without indication at baseline developed an indication for medical optimization 6 months after CRT implantation.
CONCLUSION: In the present study, 38%of those who remained symptomatic 6 months after CRT implantation were eligible for optimization of medical therapy with sacubitril/valsartan, ivabradine or both. Patients with CRT may benefit from systematic follow-up including evaluation of medical treatment.