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

被引:0
作者
Albon, Dana [1 ]
Ong, Thida [2 ]
Horton, Bethany [3 ]
Brighton, David [3 ]
Shen, Shiyi [3 ]
List, Rhonda [1 ]
Antos, Nicholas [4 ]
Asfour, Fadi [5 ]
Balasa, Ella [6 ]
Beachler, Danielle [7 ]
Daines, Cori [8 ]
Froh, Deborah [9 ]
Kier, Catherine [10 ]
Nasr, Samya [11 ]
Sathe, Meghana [12 ]
Sawicki, Gregory [13 ]
Schechter, Michael [14 ]
Solomon, George [15 ]
Powers, Michael [16 ]
机构
[1] Univ Virginia, Dept Internal Med, Div Pulm & Crit Care, Charlottesville, VA 22904 USA
[2] Univ Washington, Seattle Childrens Hosp, Sch Med, Pulm & Sleep Med,Pediat, Seattle, WA USA
[3] Univ Virginia, Dept Publ Hlth Sci, Charlottesville, VA USA
[4] Med Coll Wisconsin, Dept Pediat, Milwaukee, WI USA
[5] Univ Utah, Dept Pediat, Salt Lake City, UT USA
[6] Virginia Commonwealth Univ, Pulm & Crit Care, Richmond, VA USA
[7] Dell Childrens Med Ctr Cent Texas, Dept Pediat, Austin, TX USA
[8] Univ Arizona, Med Ctr, Pediat, Univ Campus, Tucson, AZ USA
[9] Univ Virginia, Dept Pediat, Charlottesville, VA USA
[10] SUNY Stony Brook, Dept Pediat, Stony Brook, NY USA
[11] Univ Michigan Hlth Syst, Dept Pediat, Ann Arbor, MI USA
[12] UT Southwestern Med Ctr, Div Pediat Gastroenterol & Nutr, Dallas, TX USA
[13] Childrens Hosp Boston, Div Resp Dis, Boston, MA USA
[14] Virginia Commonwealth Univ, Dept Pediat, Richmond, VA USA
[15] Univ Alabama Birmingham, Gregory Fleming James Cyst Fibrosis Res Ctr, Dept Med, Birmingham, AL USA
[16] Oregon Hlth & Sci Univ, Dept Pediat, Portland, OR USA
关键词
cystic fibrosis; cystic fibrosis learning network; innovation laboratory; quality improvement; telehealth;
D O I
10.1002/ppul.71102
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BackgroundCystic 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.MethodsAll 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.ResultsIn 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.ConclusionIntegrating 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.
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页数:12
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[31]   Long-Term Safety and Efficacy of Elexacaftor/Tezacaftor/Ivacaftor in Children Aged ≥6 Years with Cystic Fibrosis and at Least One F508del Allele A Phase 3, Open-Label Clinical Trial [J].
Wainwright, Claire ;
McColley, Susanna A. ;
McNally, Paul ;
Powers, Michael ;
Ratjen, Felix ;
Rayment, Jonathan H. ;
Retsch-Bogart, George ;
Roesch, Erica ;
Ahluwalia, Neil ;
Chin, Anna ;
Chu, Chenghao ;
Lu, Mengdi ;
Menon, Prema ;
Waltz, David ;
Weinstock, Tanya ;
Zelazoski, Laura ;
Davies, Jane C. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2023, 208 (01) :68-78
[32]   A Phase 3 Open-Label Study of Elexacaftor/Tezacaftor/lvacaftor in Children 6 through 11 Years of Age with Cystic Fibrosis and at Least One F508del Allele [J].
Zemanick, Edith T. ;
Taylor-Cousar, Jennifer L. ;
Davies, Jane ;
Gibson, Ronald L. ;
Mall, Marcus A. ;
McKone, Edward F. ;
McNally, Paul ;
Ramsey, Bonnie W. ;
Rayment, Jonathan H. ;
Rowe, Steven M. ;
Tullis, Elizabeth ;
Ahluwalia, Neil ;
Chu, Chenghao ;
Ho, Thang ;
Moskowitz, Samuel M. ;
Noel, Sabrina ;
Tian, Simon ;
Waltz, David ;
Weinstock, Tanya G. ;
Xuan, Fengjuan ;
Wainwright, Claire E. ;
McColley, Susanna A. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2021, 203 (12) :1522-1532