使用 TECCU 对活动性炎症性肠病进行远程监控并不比标准护理差:GETECCU多中心随机对照试验的短期结果。

IF 5.8 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Journal of Medical Internet Research Pub Date : 2024-11-18 DOI:10.2196/60966
Mariam Aguas, Javier Del Hoyo, Raquel Vicente, Manuel Barreiro-de Acosta, Luigi Melcarne, Alejandro Hernandez-Camba, Lucía Madero, María Teresa Arroyo, Beatriz Sicilia, María Chaparro, María Dolores Martin-Arranz, Ramón Pajares, Francisco Mesonero, Miriam Mañosa, Pilar Martinez, Silvia Chacón, Joan Tosca, Sandra Marín, Luciano Sanroman, Marta Calvo, David Monfort, Empar Saiz, Yamile Zabana, Ivan Guerra, Pilar Varela, Virginia Baydal, Raquel Faubel, Pilar Corsino, Sol Porto-Silva, Eduard Brunet, Melodi González, Ana Gutiérrez, Pilar Nos
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The study included adult patients with IBD who were starting immunosuppressive or biological therapy. Participants were randomized into 2 groups: the telemonitoring group (G_TECCU) and the standard care group (G_Control). The follow-up schedule for the telemonitoring group (G_TECCU) was based on contacts via the TECCU app, while the control group (G_Control) adhered to standard clinical practice, which included in-person visits and telephone calls. In both groups, treatment adjustments were made based on the progression of disease activity and medication adherence, assessed using specific indices and biological markers at each check-up. The primary outcome was the duration of remission after 12 weeks, while secondary outcomes included quality of life, medication adherence, adverse events, and patient satisfaction.</p><p><strong>Results: </strong>Of the 169 patients enrolled, 158 were randomized and 150 were analyzed per protocol: telemonitoring (n=71) and control (n=79). 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引用次数: 0

摘要

背景:在炎症性肠病(IBD)的治疗中,远程监测并不总是优于标准治疗,但如果远程治疗更有效,非劣效性可能是可以接受的结果:目的:比较活动性 IBD 患者通过标准疗法或 TECCU 应用程序(克罗恩病和溃疡性结肠炎远程监控)控制病情的缓解时间和生活质量:西班牙 24 家医院对开始接受免疫抑制剂或生物疗法的成年 IBD 患者进行了一项双臂、随机、多中心试验,该试验采用非劣效性设计。患者被随机分为远程监控组(G_TECCU)或标准护理组(G_Control)。在 G_TECCU 组中,随访计划基于通过 TECCU 应用程序进行的远程监测联系,而在 G_Control 组中,随访计划则与临床实践相同,基于亲自访问和电话联系。两组患者的治疗均根据疾病活动性和用药依从性的变化进行调整,每次检查都会通过特定指数和生物标记物对疾病活动性和用药依从性进行测量。12周后的缓解时间为主要结果,生活质量、用药依从性、不良反应和患者满意度为次要结果:在入组的 169 名患者中,158 人被随机分配,150 人按方案进行了分析:远程监控(71 人);对照组(79 人)。12周后,远程监测的临床缓解时间(4.20 ±3.73 周)不低于对照组(4.32 ±3.28 周),两组间的平均差异为-0.12周(95% CI -1.25-,1.01 ),非劣效性 p=0.017)。G_TECCU的CRP值平均降低-15.40毫克/升(SD=90.15,P=0.195),G_control的CRP值平均降低-13.16毫克/升(SD=54.61,P=0.053),两组间无显著差异(P=0.726)。同样,G_TECCU 的 FC 水平平均提高了 832.3 毫克/升(SD=1825.0,P=.003),G_对照组提高了 1073.5 毫克/升(SD=3105.7,P=.03),但差异不显著(P=.965)。两组患者的生活质量均有所改善,G_TECCU 组的 IBDQ-9 评分平均上升了 13.44 分(SD=19.1;PC 结论:在实现和维持短期缓解方面,对活动性 IBD 患者进行远程监测并不比标准治疗差。如果改善的健康结果和成本在长期得到证实,TECCU 可能是一种替代性随访工具:该试验已在ClinicalTrials.gov网站注册,标识符为NCT06031038;https://classic.clinicaltrials.gov/ct2/show/NCT06031038.International 注册报告:RR2-10.2196/resprot.9639.
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Telemonitoring of Active Inflammatory Bowel Disease Using the App TECCU: Short-Term Results of a Multicenter Trial of GETECCU.

Background: Telemonitoring for inflammatory bowel disease (IBD) has not consistently demonstrated superiority over standard care; however, noninferiority may be an acceptable outcome if remote care proves to be more efficient.

Objective: This study aims to compare the remission time and quality of life of patients with active IBD managed through standard care versus the TECCU (Telemonitoring of Crohn Disease and Ulcerative Colitis) app.

Methods: A 2-arm, randomized, multicenter trial with a noninferiority design was conducted across 24 hospitals in Spain. The study included adult patients with IBD who were starting immunosuppressive or biological therapy. Participants were randomized into 2 groups: the telemonitoring group (G_TECCU) and the standard care group (G_Control). The follow-up schedule for the telemonitoring group (G_TECCU) was based on contacts via the TECCU app, while the control group (G_Control) adhered to standard clinical practice, which included in-person visits and telephone calls. In both groups, treatment adjustments were made based on the progression of disease activity and medication adherence, assessed using specific indices and biological markers at each check-up. The primary outcome was the duration of remission after 12 weeks, while secondary outcomes included quality of life, medication adherence, adverse events, and patient satisfaction.

Results: Of the 169 patients enrolled, 158 were randomized and 150 were analyzed per protocol: telemonitoring (n=71) and control (n=79). After 12 weeks, the time in clinical remission was not inferior in the telemonitoring group (mean 4.20, SD 3.73 weeks) compared with the control group (mean 4.32, SD 3.28 weeks), with a mean difference between arms of -0.12 weeks (95% CI -1.25 to 1.01; noninferiority P=.02). The mean reduction in C-reactive protein values was -15.40 mg/L (SD 90.15 mg/L; P=.19) in the G_TECCU group and -13.16 mg/L (SD 54.61 mg/L; P=.05) in the G_Control group, with no significant differences between the 2 arms (P=.73). Similarly, the mean improvement in fecal calprotectin levels was 832.3 mg/L (SD 1825.0 mg/L; P=.003) in the G_TECCU group and 1073.5 mg/L (SD 3105.7 mg/L; P=.03) in the G_Control group; however, the differences were not statistically significant (P=.96). Quality of life improved in both groups, with a mean increase in the 9-item Inflammatory Bowel Disease Questionnaire score of 13.44 points (SD 19.1 points; P<.001) in the G_TECCU group and 18.23 points (SD 22.9 points; P=.001) in the G_Control group. Additionally, the proportion of patients who adhered to their medication significantly increased from 35% (25/71) to 68% (48/71) in the G_TECCU group (P=.001) and from 46% (36/79) to 73% (58/79) in the G_Control group (P=.001). The satisfaction rate remained stable at around 90%, although noninferiority was not demonstrated for the secondary outcomes.

Conclusions: Telemonitoring patients with active IBD is not inferior to standard care for achieving and maintaining short-term remission. The TECCU app may serve as a viable alternative follow-up tool, pending confirmation of improved health outcomes and cost-effectiveness over the long-term.

Trial registration: ClinicalTrials.gov NCT06031038; https://clinicaltrials.gov/ct2/show/NCT06031038.

International registered report identifier (irrid): RR2-10.2196/resprot.9639.

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来源期刊
CiteScore
14.40
自引率
5.40%
发文量
654
审稿时长
1 months
期刊介绍: The Journal of Medical Internet Research (JMIR) is a highly respected publication in the field of health informatics and health services. With a founding date in 1999, JMIR has been a pioneer in the field for over two decades. As a leader in the industry, the journal focuses on digital health, data science, health informatics, and emerging technologies for health, medicine, and biomedical research. It is recognized as a top publication in these disciplines, ranking in the first quartile (Q1) by Impact Factor. Notably, JMIR holds the prestigious position of being ranked #1 on Google Scholar within the "Medical Informatics" discipline.
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