Pedersen Susanne S, Skovbakke Søren J, Wiil Uffe K, Schmidt Thomas, dePont Christensen Rene, Brandt Carl J, Sørensen Jan, Vinther Michael, Larroudé Charlotte E, Melchior Thomas M, Riahi Sam, Smolderen Kim G E, Spertus John A, Johansen Jens B, Nielsen Jens C
Department of Psychology, University of Southern Denmark, Campusvej 55, DK-5230, Odense M, Denmark.
Department of Cardiology, Odense University Hospital, Odense, Denmark.
BMC Cardiovasc Disord. 2018 Jul 3;18(1):136. doi: 10.1186/s12872-018-0872-7.
In Denmark and other countries, there has been a shift in the management of patients with an implantable cardioverter defibrillator (ICD) with remote device monitoring largely replacing in-hospital visits. Less patient-nurse and patient-physician interaction may lead to gaps in patients' quality of care and impede patients' adaptation to living successfully with the ICD. A comprehensive eHealth intervention that include goal-setting, monitoring of symptoms of depression, anxiety, and quality of life, psychological treatment, information provision, supportive tools, online dialogues with nursing staff and access to an online community network, may help fill these gaps and be particularly beneficial to patients who suffer from anxiety and depression. This study will evaluate the effectiveness of the ACQUIRE-ICD care innovation, a comprehensive and interactive eHealth intervention, on patient-reported and clinical outcomes.
The ACQUIRE-ICD study is a multicenter, prospective, two-arm, unblinded randomised controlled superiority trial that will enroll 478 patients implanted with a first-time ICD or ICD with cardiac synchronisation therapy (CRT-D) from the six implanting centers in Denmark. The trial will evaluate the clinical effectiveness and cost-effectiveness of the ACQUIRE-ICD care innovation, as add-on to usual care compared with usual care alone. The primary endpoint, device acceptance, assessed with the Florida Patient Acceptance Survey, is evaluated at 12 months' post implant. Secondary endpoints, evaluated at 12 and 24 months' post implant, include patient-reported outcomes, return to work, time to first ICD therapy and first hospitalisation, mortality and cost-effectiveness.
The effectiveness of a comprehensive and interactive eHealth intervention that relies on patient-centred and personalised tools offered via a web-based platform targeted to patients with an ICD has not been assessed so far. The ACQUIRE-ICD care innovation promotes and facilitates that patients become active participants in the management of their disease, and as such addresses the need for a more patient-centered disease-management approach. If the care innovation proves to be beneficial to patients, it may not only increase patient empowerment and quality of life but also free up time for clinicians to care for more patients.
The trial has been registered on https://clinicaltrials.gov/ct2/show/NCT02976961 on November 30, 2016 with registration number [ NCT02976961 ].
在丹麦和其他国家,植入式心脏复律除颤器(ICD)患者的管理方式已发生转变,远程设备监测在很大程度上取代了住院就诊。患者与护士以及患者与医生之间的互动减少,可能导致患者护理质量出现差距,并阻碍患者成功适应佩戴ICD的生活。一项全面的电子健康干预措施,包括目标设定、抑郁、焦虑症状及生活质量监测、心理治疗、信息提供、支持工具、与护理人员的在线对话以及接入在线社区网络,可能有助于填补这些差距,对患有焦虑和抑郁的患者尤其有益。本研究将评估ACQUIRE-ICD护理创新(一种全面且交互式的电子健康干预措施)对患者报告结局和临床结局的有效性。
ACQUIRE-ICD研究是一项多中心、前瞻性、双臂、非盲随机对照优势试验,将从丹麦的六个植入中心招募478例首次植入ICD或植入心脏同步治疗除颤器(CRT-D)的患者。该试验将评估ACQUIRE-ICD护理创新作为常规护理补充与单纯常规护理相比的临床有效性和成本效益。主要终点为设备接受度,采用佛罗里达患者接受度调查进行评估,在植入后12个月时进行。次要终点在植入后12个月和24个月时进行评估,包括患者报告的结局、重返工作岗位情况、首次ICD治疗时间和首次住院时间、死亡率以及成本效益。
迄今为止,尚未评估一种依赖通过针对ICD患者的基于网络平台提供的以患者为中心且个性化工具的全面且交互式电子健康干预措施的有效性。ACQUIRE-ICD护理创新促进并推动患者成为其疾病管理的积极参与者,从而满足了对更以患者为中心的疾病管理方法的需求。如果该护理创新被证明对患者有益,它不仅可能增强患者的自主权和生活质量,还可能为临床医生腾出时间来照顾更多患者。
该试验于2016年11月30日在https://clinicaltrials.gov/ct2/show/NCT02976961上注册,注册号为[NCT02976961]。