试点以黑人患者为重点的高血压团队远程医疗护理。

IF 1.6 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Srista Manandhar, Sunit Chhetri, Danielle Sutton, Animita C Saha, Suneet Kaur, Josh Brown, Jeff Williamson, Kathryn E Callahan, Justin B Moore, Yhenneko J Taylor, Hayden B Bosworth, Yashashwi Pokharel
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引用次数: 0

摘要

背景:在美国,与白人患者相比,目前远程医疗项目在黑人患者中管理高血压的效果较差。对自我照顾技能的支持不足和未解决的社会需求可能解释了这些差异。我们评估了一个基于团队的远程医疗项目的可行性,该项目使用家庭血压监测(HBPM)指导药物治疗,并支持患者的自我保健技能和社会需求。方法:我们在北卡罗来纳州的两个安全网诊所进行了一项单臂试点研究,招募了20名高血压未控制的成年人,他们采用稳定的降压方案,使用智能手机,英语熟练。我们排除了有妨碍家庭血压监测、复杂慢性疾病或近期急性健康事件的个体。为期12周的干预包括每日HBPM, HBPM指导的药物治疗,由训练有素的护士提供的基于电话的自我管理支持,以及社区卫生工作者和社会工作者的社会支持。我们评估了招募、保留和完成干预组件的可行性,预先指定≥70%的预期HBPM(7次/周/患者)和≥80%的自我管理呼叫/患者(临床1 8次,临床2 12次)。结果:135例患者中,28.9% (n = 39)符合条件。我们招募了20例患者(17例黑人患者,9例女性),其中18例(90%)完成了研究。患者平均每周测量血压9.4次(SD 8.6)(预期的134.3%),完成预期呼叫的78.3%。我们为11名患者提供了19次社会支持,包括卫生保健员的家访支持,主要是食物和药物。在支持住房等其他社会需求方面存在挑战。平均(SD)为1.1(0.8)个药物激活/患者(剂量或药物变化),HBPM/远程监护应用使用的小技术问题8个,均得到及时解决。结论:基于团队的高血压远程医疗干预在招募、保留和HBPM方面具有可行性,在社会支持方面具有部分可行性,在自我管理支持方面具有基本可行性。社区知情的方法可以进一步改善项目的实施。试验注册:ClinicalTrials.gov, NCT05424744, 2022年6月9日注册,https://clinicaltrails.gov/study/NCT05424744。试验资助:维克森林大学医学院心血管医学系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Piloting a team-based telemedicine care for hypertension focused on Black patients.

Piloting a team-based telemedicine care for hypertension focused on Black patients.

Piloting a team-based telemedicine care for hypertension focused on Black patients.

Piloting a team-based telemedicine care for hypertension focused on Black patients.

Background: Current telemedicine programs to manage hypertension are less effective in Black compared with White patients in the US. Insufficient support for self-care skills and unaddressed social needs may explain the differences. We evaluated feasibility of a team-based telemedicine program using home blood pressure (BP) monitoring (HBPM) guided pharmacotherapy and supporting patients' self-care skills and social needs.

Methods: We conducted a single-arm pilot study in two safety-net clinics in North Carolina, enrolling 20 adults with uncontrolled hypertension on stable antihypertensive regimen with smartphone access, and English proficiency. We excluded individuals with conditions impairing home BP monitoring, complex chronic illnesses, or recent acute health events. The 12-week intervention included daily HBPM, HBPM-guided pharmacotherapy, telephone-based self-management support by trained nurses, and social support from community health workers (CHW) and social workers. We evaluated feasibility for recruitment and retention and completion of intervention components, pre-specified as ≥ 70% of expected HBPM (7 times/week/patient) and ≥ 80% self-management calls/patient (8 in clinic 1 and 12 in clinic 2).

Results: Among 135 patients approached, 28.9% (n = 39) were eligible. We enrolled 20 patients (17 Black patients, 9 women) and 18 (90%) completed the study. Patients measured their BP an average of 9.4 (SD 8.6) times/week (134.3% of expected) and completed 78.3% of expected calls. We provided social support to 11 patients 19 times including support at home visits by CHWs, mostly for food and medications. There were challenges in supporting other social needs like housing. There was mean (SD) of 1.1 (0.8) medication activation/patient (dose or medication changes), and 8 minor technical issues about HBPM/telemonitoring application use, which were promptly resolved.

Conclusion: Our team-based telemedicine hypertension intervention shows feasibility for recruitment, retention, and HBPM, partial feasibility for social support, and almost met feasibility for self-management support. Community informed approaches can further improve program implementation.

Trial registration: ClinicalTrials.gov, NCT05424744, Registered 9 June 2022, https://clinicaltrails.gov/study/NCT05424744 .

Trial funding: Department of Cardiovascular Medicine, Wake Forest University School of Medicine.

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来源期刊
Pilot and Feasibility Studies
Pilot and Feasibility Studies Medicine-Medicine (miscellaneous)
CiteScore
2.70
自引率
5.90%
发文量
241
审稿时长
9 weeks
期刊介绍: Pilot and Feasibility Studies encompasses all aspects of the design, conduct and reporting of pilot and feasibility studies in biomedicine. The journal publishes research articles that are intended to directly influence future clinical trials or large scale observational studies, as well as protocols, commentaries and methodology articles. The journal also ensures that the results of all well-conducted, peer-reviewed, pilot and feasibility studies are published, regardless of outcome or significance of findings. Pilot and feasibility studies are increasingly conducted prior to a full randomized controlled trial. However, these studies often lack clear objectives, many remain unpublished, and there is confusion over the meanings of the words “pilot” and “feasibility”. Pilot and Feasibility Studies provides a forum for discussion around this key aspect of the scientific process, and seeks to ensure that these studies are published, so as to complete the publication thread for clinical research.
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