Cystic Fibrosis Learning Network Telehealth Innovation Lab During the COVID-19 Pandemic: Impact on Access to Care, Outcomes, and a New CF Care Model.

IF 2.7 3区 医学 Q1 PEDIATRICS
Dana Albon, Thida Ong, Bethany Horton, David Brighton, Shiyi Shen, Rhonda List, Nicholas Antos, Fadi Asfour, Ella Balasa, Danielle Beachler, Cori Daines, Deborah Froh, Catherine Kier, Samya Nasr, Meghana Sathe, Gregory Sawicki, Michael Schechter, George Solomon, Michael Powers
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Abstract

Background: Cystic fibrosis (CF) is a chronic genetic disorder requiring regimented visits for maintenance of care. The COVID-19 pandemic accelerated the accessibility of telehealth (TH) and forced a trial of incorporating remote care into routine CF care. The CF Learning Network (CFLN) organized for data sharing into a telehealth innovation lab (TH-iLab) to improve access to the interdisciplinary care team and co-produced shared agenda-setting.

Methods: All persons with CF (PwCF) with a CF diagnosis in the CF Foundation Registry (CFFPR) from 1/2020-12/2021 were included and categorized into CFLN TH-iLab, CFLN TH-iLab non-participants, and non-CFLN programs.

Hypothesis: standardized TH implementation in the CFLN TH-iLab is associated with increased access to the CF care model and results in similar lung function and nutrition health outcomes.

Results: In 2020 and 2021, the average number of TH visits per person per year and the percentage of PwCF with one or more TH visits per year were higher in the CFLN TH-iLab than in the other groups. Lung function was highest in PwCF, followed by a program that was part of the CFLN TH-iLab in 2020 and 2021. Anthropometric measurements, spirometry, and attainment of microbiology cultures were similar among all three groups. Access to interdisciplinary care was highest in the CFLN non-TH-iLab group.

Conclusion: Integrating TH into CF care in the CFLN TH-iLab provided access to care during the COVID-19 pandemic without compromising clinical outcomes. Further research on optimizing the telehealth experience for PwCF can help better understand TH's long-term impact on CF care.

COVID-19大流行期间囊性纤维化学习网络远程医疗创新实验室:对获得护理、结果和新的CF护理模式的影响。
背景:囊性纤维化(CF)是一种慢性遗传性疾病,需要定期就诊以维持护理。2019冠状病毒病大流行加速了远程医疗的可及性,并迫使将远程医疗纳入常规CF治疗的试验。CF学习网络(CFLN)组织将数据共享到远程保健创新实验室(TH-iLab),以改善与跨学科护理团队的联系,并共同制定共享议程。方法:纳入2020年1月至2021年12月在CF基金会注册表(cfffpr)中诊断为CF的所有CF (PwCF)患者,并将其分为CFLN TH-iLab、CFLN TH-iLab非参与者和非CFLN项目。假设:CFLN TH- ilab的标准化TH实施与CF护理模型的可及性增加相关,并导致相似的肺功能和营养健康结果。结果:2020年和2021年,CFLN TH- ilab组每年人均TH就诊次数和每年一次或多次TH就诊的PwCF百分比均高于其他组。PwCF患者的肺功能最高,其次是2020年和2021年CFLN TH-iLab的一个项目。三组的人体测量、肺活量测定和微生物培养结果相似。在CFLN非th - ilab组中,获得跨学科护理的机会最高。结论:在CFLN TH- ilab中,将TH纳入CF治疗提供了COVID-19大流行期间获得治疗的机会,而不会影响临床结果。进一步研究优化PwCF的远程医疗体验有助于更好地了解TH对CF护理的长期影响。
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来源期刊
Pediatric Pulmonology
Pediatric Pulmonology 医学-呼吸系统
CiteScore
6.00
自引率
12.90%
发文量
468
审稿时长
3-8 weeks
期刊介绍: Pediatric Pulmonology (PPUL) is the foremost global journal studying the respiratory system in disease and in health as it develops from intrauterine life though adolescence to adulthood. Combining explicit and informative analysis of clinical as well as basic scientific research, PPUL provides a look at the many facets of respiratory system disorders in infants and children, ranging from pathological anatomy, developmental issues, and pathophysiology to infectious disease, asthma, cystic fibrosis, and airborne toxins. Focused attention is given to the reporting of diagnostic and therapeutic methods for neonates, preschool children, and adolescents, the enduring effects of childhood respiratory diseases, and newly described infectious diseases. PPUL concentrates on subject matters of crucial interest to specialists preparing for the Pediatric Subspecialty Examinations in the United States and other countries. With its attentive coverage and extensive clinical data, this journal is a principle source for pediatricians in practice and in training and a must have for all pediatric pulmonologists.
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