Decreases in Rhinology Care Utilization by People with Cystic Fibrosis on Highly Effective Modulator Therapy

被引:2
作者
Han, Ethan J. [1 ]
Beswick, Daniel M. [1 ]
Eshaghian, Patricia H. [2 ]
Turner, Grant A. [2 ]
Lee, Jivianne T. [1 ]
Li, Douglas A. [3 ]
Wang, Marilene B. [1 ]
Taylor-Cousar, Jennifer L. [4 ,5 ]
Suh, Jeffrey D. [1 ]
机构
[1] Univ Calif Los Angeles, Dept Head & Neck Surg, 10833 Le Conte Ave,CHS 62-235, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Pulm Med, Los Angeles, CA USA
[3] Univ Calif Los Angeles, Dept Pediat Pulmonol, Los Angeles, CA USA
[4] Natl Jewish Hlth, Dept Med, Denver, CO USA
[5] Natl Jewish Hlth, Dept Pediat, Denver, CO USA
关键词
cystic fibrosis; miscellaneous; chronic rhinosinusitis; endoscopic sinus surgery; patient care; clinical rhinology; rhinology; otolaryngology;
D O I
10.1177/00034894231211626
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Background: Many people with cystic fibrosis (PwCF) have chronic rhinosinusitis (CRS). CRS requires additional management beyond that of pulmonary disease and leads to increased utilization of healthcare resources. Elexacaftor/tezacaftor/ivacaftor (ETI) is a highly effective modulator therapy that has been shown to improve CRS in PwCF. However, the impact of ETI on rhinologic healthcare utilization is understudied. Objective: To compare rates of rhinologic healthcare utilization and procedures among PwCF prior to and after initiating ETI therapy. Methods: A single-center, cohort study investigating adult PwCF was performed in January 2023. Demographics, clinical characteristics, and data related to CF treatment were retrospectively abstracted. Characteristics of the cohort were compared over 2 periods: the 12-months prior to ETI initiation and the 12-months after ETI initiation. Post-ETI data were linearly extrapolated if a subject had not yet completed the full 12months of ETI. Paired t-testing, Wilcoxon signed rank testing, and regression analysis were performed. Results: Of 126 PwCF, 98 (77.8%) were on ETI therapy and 35 (27.7%) were both on ETI and concurrently followed by the rhinology service (ETI-ENT). Rhinology clinic visits (P=.007) and frequency of obtaining nasal cultures (P=.046) decreased for the ETI-ENT cohort after initiating ETI treatment. There were no significant changes in the number of endoscopic sinus surgeries (P=.452) performed. Beyond ETI use, regression analysis did not identify any factors associated with changes in utilization. Conclusion: Aspects of rhinology healthcare utilization by PwCF decreased after initiation of ETI therapy. Additional studies are needed to determine rhinologic healthcare requirements for PwCF who remain on ETI for the long-term and to evaluate larger cohorts of PwCF on ETI.
引用
收藏
页码:340 / 344
页数:5
相关论文
共 50 条
  • [41] Changes in vitamins and trace elements after initiation of highly effective CFTR modulator therapy in children and adults with cystic fibrosis - a real-life insight
    Fabricius, Dorit
    Knieling, Tina
    Zurmuehl, Noelle
    Makedon, Leandra
    Freihorst, Joachim
    Schmidt, Hanna
    Bode, Sebastian
    [J]. MOLECULAR AND CELLULAR PEDIATRICS, 2024, 11 (01)
  • [42] Men's sexual and reproductive health in cystic fibrosis in the era of highly effective modulator therapies-A qualitative study
    Clarke, Alison R.
    Stransky, Olivia M.
    Bernard, Miriam
    Hughan, Kara S.
    Ladores, Sigrid
    Sawicki, Gregory S.
    Stalvey, Michael S.
    Kazmerski, Traci M.
    [J]. JOURNAL OF CYSTIC FIBROSIS, 2022, 21 (04) : 657 - 661
  • [43] Update on Clinical Outcomes of Highly Effective Modulator Therapy
    Gifford, Alex H.
    Taylor-Cousar, Jennifer L.
    Davies, Jane C.
    McNally, Paul
    [J]. CLINICS IN CHEST MEDICINE, 2022, 43 (04) : 677 - 695
  • [44] Entering the era of highly effective CFTR modulator therapy
    Zemanick, Edith T.
    Accurso, Frank J.
    [J]. LANCET, 2019, 394 (10212) : 1886 - 1888
  • [45] In vitro modulator responsiveness of 655 CFTR variants found in people with cystic fibrosis
    Bihler, Hermann
    Sivachenko, Andrey
    Millen, Linda
    Bhatt, Priyanka
    Patel, Amita Thakerar
    Chin, Justin
    Bailey, Violaine
    Musisi, Isaac
    LaPan, Andre
    Allaire, Normand E.
    Conte, Joshua
    Simon, Noah R.
    Magaret, Amalia S.
    Raraigh, Karen S.
    Cutting, Garry R.
    Skach, William R.
    Bridges, Robert J.
    Thomas, Philip J.
    Mense, Martin
    [J]. JOURNAL OF CYSTIC FIBROSIS, 2024, 23 (04) : 664 - 675
  • [46] CFTR modulator therapies-Effect on life expectancy in people with cystic fibrosis
    Balfour-Lynn, I. M.
    King, J. A.
    [J]. PAEDIATRIC RESPIRATORY REVIEWS, 2022, 42 : 3 - 8
  • [47] CFTR Modulator Therapy and Its Impact on Lung Transplantation in Cystic Fibrosis
    Benden, Christian
    Schwarz, Carsten
    [J]. PULMONARY THERAPY, 2021, 7 (02) : 377 - 393
  • [48] Changes in the Cystic Fibrosis Airway Microbiome in Response to CFTR Modulator Therapy
    Yi, Buqing
    Dalpke, Alexander H.
    Boutin, Sebastien
    [J]. FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2021, 11
  • [49] CFTR Modulator Therapy and Its Impact on Lung Transplantation in Cystic Fibrosis
    Christian Benden
    Carsten Schwarz
    [J]. Pulmonary Therapy, 2021, 7 : 377 - 393
  • [50] Diagnosis of cystic fibrosis in adulthood and eligibility for novel CFTR modulator therapy
    Farley, Hannah
    Poole, Sarah
    Chapman, Stephen
    Flight, William
    [J]. POSTGRADUATE MEDICAL JOURNAL, 2022, 98 (1159) : 341 - 345