Social Involvement of Critical and Emergency Medicine, CTS-609 Research Group, Hospital de Poniente, Almeria, Spain.
Division of Medicine, Nordland Hospital, Bodø, Norway.
BMC Geriatr. 2018 Sep 21;18(1):223. doi: 10.1186/s12877-018-0911-3.
With an ageing population and widening indications for pacemakers implantation, the number of persons carrying an implant is steadily increasing. The routine follow-up is thus a heavy burden for the respective NHS as well as for the patients and their relatives. Most of them of the studies have been performed in densely populated areas and nearby to the hospital. It is thus unknown whether these results could be applied also in rural areas such as Northern Norway with a more scattered population. The aim of this study was to assess the effectiveness of tele-monitoring (TM) in patients with pacemakers regarding reliability, safety and health-related quality of life, compared to traditional follow-up in outpatient clinic in a setting where geographical effects could possible influence the results.
The NORDLAND study is a controlled, randomized, non-masked clinical trial in pacemaker patients, with data collection carried out during the pre-implant stage and after 6 months. Between August of 2014 and November of 2015, 50 patients were assigned to either a tele-monitoring group (n = 25) or a conventional hospital monitoring (HM) group (n = 25). The EuroQol-5D (EQ-5D) utilities and visual analogue scale (VAS) and the Minnesota Living with Heart Failure Questionnaire (MLHFQ) were used to measure Health-Related Quality of Life. Baseline characteristics and number of hospital visits were also analyzed.
The baseline characteristics of the two study groups were similar for EQ-5D utilities (TM:0.81; HM:0.76; p = 0.47), EQ-5D VAS (TM: 64.00; HM:64.88; p = 0.86) and the MLHFQ (TM:20.20; HM:28.96; p = 0.07). At the 6 month follow-up, there were no significant differences between the groups in EQ-5D utilities (TM: 0.81; HM: 0.76; p = 0.54) and EQ-5D VAS scores (TM: 72.71; HM: 59.79; p = 0.08). The MLHFQ score was improved in both groups (TM: -4.40; HM: -15.13; p < 0.001). The number of in-office visits was similar in both groups (TM: 1.24 vs HM: 1.12; P = 0.30).
The NORDLAND trial shows that HRQoL is improved after implant in both groups. Without significant differences with regards to effectiveness and safety. In addition, provides a scientifically rigorous method to the field of HRQoL evaluations in patients with pacemakers.
ClinicalTrials.gov NCT02237404 , September 11, 2014.
随着人口老龄化和起搏器植入适应证的扩大,携带起搏器的人数稳步增加。因此,常规随访对各自的国民保健服务(NHS)以及患者及其家属来说都是一个沉重的负担。大多数研究都是在人口密集地区和医院附近进行的。因此,尚不清楚这些结果是否也适用于挪威北部等人口分布更为分散的农村地区。本研究的目的是评估远程监测(TM)在起搏器患者中的有效性,比较传统门诊随访,评估其在可靠性、安全性和健康相关生活质量方面的差异,在这种情况下,地理因素可能会影响结果。
NORDLAND 研究是一项起搏器患者的对照、随机、非盲临床试验,数据收集在植入前阶段和 6 个月后进行。2014 年 8 月至 2015 年 11 月,50 名患者被分配到远程监测组(n=25)或传统医院监测组(HM)(n=25)。使用 EuroQol-5D(EQ-5D)效用和视觉模拟量表(VAS)以及明尼苏达州心力衰竭生活质量问卷(MLHFQ)来衡量健康相关生活质量。还分析了基线特征和就诊次数。
两组患者的基线特征在 EQ-5D 效用(TM:0.81;HM:0.76;p=0.47)、EQ-5D VAS(TM:64.00;HM:64.88;p=0.86)和 MLHFQ(TM:20.20;HM:28.96;p=0.07)方面相似。6 个月随访时,两组间 EQ-5D 效用(TM:0.81;HM:0.76;p=0.54)和 EQ-5D VAS 评分(TM:72.71;HM:59.79;p=0.08)无显著差异。两组 MLHFQ 评分均有所改善(TM:-4.40;HM:-15.13;p<0.001)。两组门诊就诊次数相似(TM:1.24 次 vs HM:1.12 次;P=0.30)。
NORDLAND 试验表明,两组患者植入后生活质量均得到改善。在有效性和安全性方面无显著差异。此外,为起搏器患者的生活质量评估领域提供了一种科学严谨的方法。
ClinicalTrials.gov NCT02237404,2014 年 9 月 11 日。