共 32 条
Long-Term Follow-Up of Health-Related Quality of Life and Short-Term Intervention with CFTR Modulator Therapy in Adults with Cystic Fibrosis: Evaluation of Changes over Several Years with or without 33 Weeks of CFTR Modulator Therapy
被引:5
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Blosch, Christopher
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Univ Duisburg Essen, Childrens Hosp, Cyst Fibrosis Ctr, Pediat Pulmonol & Sleep Med, D-45147 Essen, Germany Univ Duisburg Essen, Childrens Hosp, Cyst Fibrosis Ctr, Pediat Pulmonol & Sleep Med, D-45147 Essen, Germany

Dillenhoefer, Stefanie
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Ruhr Univ Bochum, Univ Childrens Hosp, Dept Pediat Pulmonol, D-44801 Bochum, Germany Univ Duisburg Essen, Childrens Hosp, Cyst Fibrosis Ctr, Pediat Pulmonol & Sleep Med, D-45147 Essen, Germany

Olivier, Margarete
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Univ Duisburg Essen, Childrens Hosp, Cyst Fibrosis Ctr, Pediat Pulmonol & Sleep Med, D-45147 Essen, Germany Univ Duisburg Essen, Childrens Hosp, Cyst Fibrosis Ctr, Pediat Pulmonol & Sleep Med, D-45147 Essen, Germany

Brinkmann, Folke
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Ruhr Univ Bochum, Univ Childrens Hosp, Dept Pediat Pulmonol, D-44801 Bochum, Germany Univ Duisburg Essen, Childrens Hosp, Cyst Fibrosis Ctr, Pediat Pulmonol & Sleep Med, D-45147 Essen, Germany

Koerner-Rettberg, Cordula
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Marienhospital Wesel, Childrens Hosp, D-46483 Wesel, Germany Univ Duisburg Essen, Childrens Hosp, Cyst Fibrosis Ctr, Pediat Pulmonol & Sleep Med, D-45147 Essen, Germany

Sutharsan, Sivagurunathan
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Univ Duisburg Essen, Univ Hosp Essen Ruhrlandklin, Adult Cyst Fibrosis Ctr, Dept Pulm Med, D-45239 Essen, Germany Univ Duisburg Essen, Childrens Hosp, Cyst Fibrosis Ctr, Pediat Pulmonol & Sleep Med, D-45147 Essen, Germany

Mellies, Uwe
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Univ Duisburg Essen, Childrens Hosp, Cyst Fibrosis Ctr, Pediat Pulmonol & Sleep Med, D-45147 Essen, Germany Univ Duisburg Essen, Childrens Hosp, Cyst Fibrosis Ctr, Pediat Pulmonol & Sleep Med, D-45147 Essen, Germany

Taube, Christian
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Univ Duisburg Essen, Univ Hosp Essen Ruhrlandklin, Adult Cyst Fibrosis Ctr, Dept Pulm Med, D-45239 Essen, Germany Univ Duisburg Essen, Childrens Hosp, Cyst Fibrosis Ctr, Pediat Pulmonol & Sleep Med, D-45147 Essen, Germany

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[1] Univ Duisburg Essen, Childrens Hosp, Cyst Fibrosis Ctr, Pediat Pulmonol & Sleep Med, D-45147 Essen, Germany
[2] Christian Albrechts Univ Kiel, Inst Human Nutr & Food Sci, D-24118 Kiel, Germany
[3] Univ Duisburg Essen, Univ Hosp Essen Ruhrlandklin, Adult Cyst Fibrosis Ctr, Dept Pulm Med, D-45239 Essen, Germany
[4] Ruhr Univ Bochum, Univ Childrens Hosp, Dept Pediat Pulmonol, D-44801 Bochum, Germany
[5] Marienhospital Wesel, Childrens Hosp, D-46483 Wesel, Germany
来源:
关键词:
cystic fibrosis;
adults;
health-related quality of life;
Elexacaftor/Tezacaftor/Ivacaftor;
longitudinal changes;
PEOPLE;
QUESTIONNAIRE;
IVACAFTOR;
D O I:
10.3390/healthcare11212873
中图分类号:
R19 [保健组织与事业(卫生事业管理)];
学科分类号:
摘要:
Background: Longitudinal data on changes in health-related quality of life (HRQoL) in adult people with cystic fibrosis (pwCF) and the longitudinal effects of Elexacaftor/Tezacaftor/Ivacaftor therapy (ETI) on HRQoL or HRQoL domains are currently scarce. This study aimed to investigate the effects of ETI on HRQoL and compare them with those of pwCF who did not receive highly effective CFTR modulators over a longer period. Methods: Baseline assessment and follow-up data for 5.6 years in pwCF with (n = 21) and 6.5 years in pwCF without (n = 6) ETI (>= 18 years) were evaluated. The assessment of HRQoL and clinical parameters was identical at both time points. HRQoL was assessed using the CFQ-R, and clinical outcomes included BMI, ppFEV1, and FEV1 z-score. Results: ETI was found to improve all HRQoL domains at more than four points over time, and their increases were significant except for vitality, digestion, treatment burden, and social functioning (p < 0.05). Without ETI, psychosocial domains remained almost constant, whereas most physical domains decreased over time. Conclusions: The results of the present study show that ETI therapy has a positive effect on HRQoL and clinical outcomes over time but not in pwCF without ETI treatment. Furthermore, our results suggest that disease progression over time affects the physical domains of HRQoL more than the psychosocial domains. Due to the small sample size and the heterogeneity of the study population (CFTR mutation genotype), the results should be interpreted with some caution.
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机构:
Johns Hopkins Univ, Eudowood Div Pediat Resp Sci, Sch Med, Baltimore, MD 21224 USA Johns Hopkins Univ, Eudowood Div Pediat Resp Sci, Sch Med, Baltimore, MD 21224 USA
[10]
Longitudinal Trends in Health-Related Quality of Life in Adults With Cystic Fibrosis
[J].
Dill, Edward J.
;
Dawson, Ree
;
Sellers, Deborah E.
;
Robinson, Walter M.
;
Sawicki, Gregory S.
.
CHEST,
2013, 144 (03)
:981-989

Dill, Edward J.
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Univ Colorado Anschutz Med Campus, Colorado Sch Publ Hlth, Ctr Amer Indian, Aurora, CO USA
Univ Colorado Anschutz Med Campus, Colorado Sch Publ Hlth, Ctr Alaska Native Hlth, Aurora, CO USA Univ Colorado Anschutz Med Campus, Colorado Sch Publ Hlth, Ctr Amer Indian, Aurora, CO USA

Dawson, Ree
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Frontier Sci & Technol Res Fdn Inc, Boston, MA USA Univ Colorado Anschutz Med Campus, Colorado Sch Publ Hlth, Ctr Amer Indian, Aurora, CO USA

Sellers, Deborah E.
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机构:
Educ Dev Ctr Inc, Ctr Appl Eth, Newton, MA USA Univ Colorado Anschutz Med Campus, Colorado Sch Publ Hlth, Ctr Amer Indian, Aurora, CO USA

Robinson, Walter M.
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Educ Dev Ctr Inc, Ctr Appl Eth, Newton, MA USA Univ Colorado Anschutz Med Campus, Colorado Sch Publ Hlth, Ctr Amer Indian, Aurora, CO USA

Sawicki, Gregory S.
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h-index: 0
机构:
Harvard Univ, Childrens Hosp, Sch Med, Div Resp Dis, Boston, MA 02115 USA Univ Colorado Anschutz Med Campus, Colorado Sch Publ Hlth, Ctr Amer Indian, Aurora, CO USA