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Short-term effects of Lumacaftor/Ivacaftor (Orkambi™) on exertional symptoms, exercise performance, and ventilatory responses in adults with cystic fibrosis.
Quon, Bradley S; Ramsook, Andrew H; Dhillon, Satvir S; Mitchell, Reid A; Boyle, Kyle G; Wilcox, Pearce G; Guenette, Jordan A.
Affiliation
  • Quon BS; Clinician-Scientist, UBC Centre for Heart Lung Innovation, Providence Health Care Research Institute, University of British Columbia, St. Paul's Hospital, #166 - 1081 Burrard Street, Vancouver, BC, V6Z 1Y6, Canada. bradley.quon@hli.ubc.ca.
  • Ramsook AH; Division of Respiratory Medicine, Department of Medicine, University of British Columbia, Vancouver, BC, Canada. bradley.quon@hli.ubc.ca.
  • Dhillon SS; Clinician-Scientist, UBC Centre for Heart Lung Innovation, Providence Health Care Research Institute, University of British Columbia, St. Paul's Hospital, #166 - 1081 Burrard Street, Vancouver, BC, V6Z 1Y6, Canada.
  • Mitchell RA; Department of Physical Therapy, University of British Columbia, Vancouver, BC, Canada.
  • Boyle KG; Clinician-Scientist, UBC Centre for Heart Lung Innovation, Providence Health Care Research Institute, University of British Columbia, St. Paul's Hospital, #166 - 1081 Burrard Street, Vancouver, BC, V6Z 1Y6, Canada.
  • Wilcox PG; Clinician-Scientist, UBC Centre for Heart Lung Innovation, Providence Health Care Research Institute, University of British Columbia, St. Paul's Hospital, #166 - 1081 Burrard Street, Vancouver, BC, V6Z 1Y6, Canada.
  • Guenette JA; Department of Physical Therapy, University of British Columbia, Vancouver, BC, Canada.
Respir Res ; 21(1): 135, 2020 Jun 01.
Article in En | MEDLINE | ID: mdl-32487229
RATIONALE: Lumacaftor/ivacaftor (LUM/IVA) modestly improves lung function following 1 month of treatment but it is unknown if this translates into improvements in exercise endurance and exertional symptoms. METHODS: Adult CF participants completed a symptom-limited constant load cycling test with simultaneous assessments of dyspnea and leg discomfort ratings pre- and 1 month post-initiation of LUM/IVA. RESULTS: Endurance time, exertional dyspnea and leg discomfort ratings at submaximal exercise did not change significantly. There was a significant inverse correlation between changes in leg discomfort and endurance time (r = - 0.88; p = 0.009) following 1-month of LUM/IVA. CONCLUSIONS: Overall, 1-month of LUM/IVA did not increase endurance time or modify exertional dyspnea or leg discomfort ratings. However, individuals who experienced a reduction in leg discomfort following LUM/IVA had an improvement in endurance time. Future studies with a larger sample size are needed to verify these findings and to assess the long-term effects of LUM/IVA on exercise outcomes. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT02821130. Registered July 1, 2016.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Forced Expiratory Volume / Quinolones / Pulmonary Ventilation / Cystic Fibrosis / Benzodioxoles / Exercise Test / Physical Exertion / Aminophenols / Aminopyridines Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Respir Res Year: 2020 Document type: Article Affiliation country: Canada Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Forced Expiratory Volume / Quinolones / Pulmonary Ventilation / Cystic Fibrosis / Benzodioxoles / Exercise Test / Physical Exertion / Aminophenols / Aminopyridines Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Respir Res Year: 2020 Document type: Article Affiliation country: Canada Country of publication: United kingdom