کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5974990 | 1576200 | 2013 | 6 صفحه PDF | دانلود رایگان |

ObjectiveIn the SAVE-trial we evaluated the safety, reliability and improvements of patient management using the BIOTRONIK Home Monitoring®-System (HM) in pacemaker (PM) and implanted cardioverter defibrillator (ICD) patients.Design115 PM (Module A) and 36 ICD-patients (Module B) were recruited 3 months after implantation.Patients65 patients in Module A were randomised to HM-OFF and had one scheduled outpatient clinic follow-up (FU) per year, whereas patients randomised to HM-ON were equipped with the mobile transmitter and discharged without any further scheduled in-office FU. In Module B 18 patients were randomised to HM-OFF and followed by standard outpatient clinic controls every 6 months; 18 patients were randomised to HM-ON receiving remote monitoring plus one outpatient clinic visit per year; unscheduled follow-ups were performed when necessary.ResultsThe average follow-up period was 17.1 ± 9.2 months in Module A and 26.3 ± 8.6 months in Module B. In both modules, the number of FUs per year was significantly reduced (Module A HM-ON 0.29 ± 0.6 FUs/year vs HM-OFF 0.53 ± 0.5 FUs/year; p < 0.001; Module B HM-ON 0.87 ± 0.25 vs HM-OFF 1.73 ± 0.53 FU/year, p < 0.001). Cost analysis was significantly lower in the HM-ON group compared to the HM-OFF group (18.0 ± 41.3 and 22.4 ± 26.9⬠respectively; p < 0.003). 93% of the unscheduled visits in Module B were clinically indicated, whereas 55% of the routine FUs were classified as clinically unnecessary.ConclusionRemote home monitoring of pacemaker and ICD devices was safe, reduced overall hospital visits, and detected events that mandated unscheduled visits.
Journal: International Journal of Cardiology - Volume 169, Issue 6, 30 November 2013, Pages 402-407