Table 1

Study design, participants and inclusion criteria for patients with non-LBBB QRS morphology who did or did not receive CRT

StudyDesignDateCountrySample sizeAgeSexParticipant inclusion criteria
MADIT-CRT5 15 20Randomised controlled trialDecember 2004 to September 201388 centres in USA, Canada and Europe1820 total:
1281 LBBB, 536 non-LBBB, 3 unknown
Total mean 64 years; non-LBBB mean 64 yearsTotal 75% male; non-LBBB 90% maleAge >21 years with ischaemic (NYHA I–II) or non-ischaemic (NYHA II) cardiomyopathy, sinus rhythm, QRS≥130 msec and LVEF ≤30%
CARE-HF1 18Randomised controlled trialJanuary 2001 to March 200382 European centres775 total:
730 LBBB,
45 non-LBBB
Total mean 67 yearsTotal 73% maleAge ≥18 years with NHYA III–IV, LVEF ≤35%, height-adjusted LVEDD ≥30 mm, QRS≥120 msec and sinus rhythm (additional dyssynchrony criteria required for QRS 120–149 msec)
COMPANION2Randomised controlled trialJanuary 2000 to November 2002128 US centres1520 total:
1075 LBBB,
444 non-LBBB.
Total mean 67 yearsTotal 67% maleNHYA class III–IV ischaemic or non-ischaemic cardiomyopathy, sinus rhythm, QRS ≥120 msec, LVEF ≤35% and HF hospitalisation within preceding 12 months
RAFT4 12Randomised controlled trialJanuary 2003 to February 200934 centres in Canada, Europe, Turkey and AustraliaTotal 1798: 1295 LBBB,
503 non-LBBB
Total mean 66 yearsTotal 83% maleNYHA II–III ischaemic or non-ischaemic cardiomyopathy, LVEF ≤30%, QRS duration ≥120 msec (or paced QRS ≥200 msec)
REVERSE6 14Randomised controlled trialSeptember 2004 to September 200673 centres in USA, Canada and EuropeTotal 610:
369 LBBB,
238 non-LBBB, 3 unknown
Total 63 years; non-LBBB 63 yearsTotal 79%. Non-LBBB 88% maleNHYA I–II, sinus rhythm, QRS ≥120 msec, LVEF ≤40%, LVEDD ≥55 mm
  • 6MWT, 6-min walk test; CRT, cardiac resynchronisation therapy; HF, heart failure; LBBB, left bundle branch block; LVEDD, left ventricular end-diastolic dimension; NYHA, New York Heart Association.