A randomized trial comparing two different approaches of pacemaker selection

Europace. 2007 Dec;9(12):1185-90. doi: 10.1093/europace/eum231. Epub 2007 Oct 19.

Abstract

Aims: DDD-pacemakers are favoured in patients with sick-sinus-syndrome or AV-block. However, AAI-pacemakers for sick-sinus-syndrome or VDD-pacemakers for AV-block may provide similar benefit with lower costs. The aim is to show that a tailored approach (TA) with arrhythmia-specific pacemaker selection was equal to a standard approach (SA) regarding quality of life (QoL) at lower costs.

Methods and results: The study was prospective and randomized with QoL as primary endpoint. Secondary endpoints were a combined endpoint of all-cause mortality, worsening heart failure or angina, atrial fibrillation (AF), stroke, these endpoints individually and costs. Of 198 patients (age 77 +/- 10 years, 43% female, ejection fraction 54 +/- 12%, follow-up 38 +/- 15 months), 94 were randomized to SA and 104 to TA. Thirty-two patients (34%) died in the SA group vs. 25 (24%) in the TA (P= ns). QoL showed no differences in all dimensions. The combined secondary endpoint was reached more frequently with SA (51%) compared to TA (37%, P = 0.045). There was no difference regarding all single secondary endpoints. Hardware costs were reduced by 15% (P < 0.0001).

Conclusion: In long-term follow-up, a TA is equal to SA regarding the primary endpoint QoL and secondary endpoints as AF and mortality. Depending on the healthcare system, it may significantly reduce costs.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Aged, 80 and over
  • Atrial Fibrillation / etiology
  • Atrioventricular Block / therapy*
  • Endpoint Determination
  • Female
  • Health Care Costs
  • Humans
  • Male
  • Pacemaker, Artificial* / economics
  • Prospective Studies
  • Quality of Life
  • Risk Factors
  • Sick Sinus Syndrome / therapy*
  • Treatment Outcome