PMID- 33426938 OWN - NLM STAT- MEDLINE DCOM- 20211224 LR - 20211224 IS - 1651-2006 (Electronic) IS - 1401-7431 (Linking) VI - 55 IP - 3 DP - 2021 Jun TI - Clinical outcome of cardiac resynchronization therapy in patients randomized to an active fixation bipolar left ventricular lead versus a passive quadripolar lead. PG - 153-159 LID - 10.1080/14017431.2020.1869299 [doi] AB - Objectives: To compare the clinical outcome of cardiac resynchronization therapy (CRT) in patients receiving a bipolar left ventricular (LV) lead with a side helix for active fixation to the outcome in patients receiving a quadripolar passive fixation LV lead.Design: Sixty-two patients (mean age 72 +/- 11 years) were blindly and randomly assigned to the active fixation bipolar lead group (n = 31) or to the quadripolar lead group (n= 31). The LV leads were targeted to the basal LV segment in a vein concordant to the LV segment with the latest mechanical contraction chosen on the basis of preoperative radial strain (RS) echocardiography.Results: At the 6-month follow-up (FU), the reduction in LV end-systolic volume and LV reverse remodelling responder rate, defined as LV end-systolic volume reduction >15%, was 77% in the active fixation group and 83% in the quadripolar group, which was not significantly different. At the 12-month FU, the LV ejection fraction (LVEF) did not differ between the groups. There were no significant differences between the two groups in changes in New York Heart Association (NYHA) functional class or Minnesota Living with Heart Failure Questionnaire score. The occurrence of phrenic nerve stimulation (PNS) was 19% in the active fixation group versus 10% in the quadripolar group (p=.30), and all cases were resolved by reprogramming the device. All patients were alive at the 12-month FU. There was no device infection.Conclusions: There were no significant differences between the active fixation group of patients and the quadripolar group of patients concerning improvement in echocardiographic parameters or clinical symptoms.ClinicalTrials.gov number, NCT04632472. FAU - Keilegavlen, Havard AU - Keilegavlen H AUID- ORCID: 0000-0002-8190-9835 AD - Department of Heart Disease, Haukeland University Hospital, Bergen, Norway. AD - Department of Clinical Science, University of Bergen, Bergen, Norway. FAU - Schuster, Peter AU - Schuster P AD - Department of Heart Disease, Haukeland University Hospital, Bergen, Norway. AD - Department of Clinical Science, University of Bergen, Bergen, Norway. FAU - Hovstad, Thomas AU - Hovstad T AD - Department of Heart Disease, Haukeland University Hospital, Bergen, Norway. FAU - Faerestrand, Svein AU - Faerestrand S AD - Department of Heart Disease, Haukeland University Hospital, Bergen, Norway. AD - Department of Clinical Science, University of Bergen, Bergen, Norway. LA - eng SI - ClinicalTrials.gov/NCT04632472 PT - Journal Article PT - Randomized Controlled Trial DEP - 20210110 PL - England TA - Scand Cardiovasc J JT - Scandinavian cardiovascular journal : SCJ JID - 9708377 SB - IM MH - Aged MH - Aged, 80 and over MH - *Cardiac Resynchronization Therapy/methods MH - Humans MH - Middle Aged MH - Treatment Outcome OTO - NOTNLM OT - Cardiac resynchronization therapy OT - active fixation OT - heart failure OT - lead dislodgement OT - left ventricular lead placement EDAT- 2021/01/12 06:00 MHDA- 2021/12/25 06:00 CRDT- 2021/01/11 08:40 PHST- 2021/01/12 06:00 [pubmed] PHST- 2021/12/25 06:00 [medline] PHST- 2021/01/11 08:40 [entrez] AID - 10.1080/14017431.2020.1869299 [doi] PST - ppublish SO - Scand Cardiovasc J. 2021 Jun;55(3):153-159. doi: 10.1080/14017431.2020.1869299. Epub 2021 Jan 10.