Article Text

Download PDFPDF
Tezacaftor-ivacaftor use in routine care of adults with cystic fibrosis: a medicine use evaluation
  1. Iona Paterson1,
  2. Chris Johnson2,
  3. Gordon MacGregor3
  1. 1Pharmacy, Queen Elizabeth University Hospital Campus, Glasgow, UK
  2. 2Pharmacy Services, NHS Greater Glasgow and Clyde Primary Care Division, Glasgow, Glasgow, UK
  3. 3Department of Respiratory Medicine, Queen Elizabeth University Hospital Campus, Glasgow, Glasgow, UK
  1. Correspondence to Iona Paterson, Pharmacy, Queen Elizabeth University Hospital Campus, Glasgow G51 4TF, UK; iona.paterson{at}ggc.scot.nhs.uk

Abstract

Objectives Cystic fibrosis is a devastating life-limiting genetic condition characterised by a progressive decline in lung function, respiratory infections and premature death. Tezacaftor-ivacaftor is a combined cystic fibrosis transmembrane conductance regulator (CFTR) modulator that targets the underlying cause of the disease. This study aimed to assess the impact of tezacaftor-ivacaftor use in routine clinical practice for adults with cystic fibrosis.

Methods A retrospective observational longitudinal cohort study design was applied to examine the clinical effect of tezacaftor-ivacaftor in routine practice in the West of Scotland Adult Cystic Fibrosis Unit. Adults receiving tezacaftor-ivacaftor for at least 4 weeks were included in this medicine use evaluation.

A standardised data form was used to collect patient-level data: demographics, genotype, complications of cystic fibrosis, medicine access process. Fifty-two weeks pre and post tezacaftor-ivacaftor initiation data: lung function, body mass index (BMI), days spent in hospital, days receiving antibiotic treatment for respiratory exacerbations. Anonymised data were collated and analysed using SPSS V.26.

Results Of 121 potential patients, 45 received treatment with tezacaftor-ivacaftor; median age 30 years (range 17–64) at initiation, 56% were male, 76% were deemed to be homozygote and 41 patients continued treatment for at least 52 weeks. There was no significant change in % predicted FEV1; median difference 0 (IQR −3 to 6). There was a significant improvement in BMI, mean 0.6 kg/m2 (95% CI 0.2 to 1.0), as well as a median 4 (IQR −17 to 0) day reduction in days in hospital and 21 (IQR −42 to 0) day reduction in days receiving antibiotics.

Conclusions The use of tezacaftor-ivacaftor in routine practice for people with cystic fibrosis was associated with improvements in weight, as well as reducing the number of days people needed to spend in hospital and receive antibiotics.

  • clinical medicine
  • evidence-based medicine
  • pharmacy service
  • hospital
  • pulmonary medicine
  • drug monitoring

Data availability statement

Data are available on reasonable request. Individual participant data that underlie the results reported in this article, after deidentification, will be made available, beginning 3 months and ending 5 years after article publication. Data will be shared with researchers providing a methodologically sound proposal in order to achieve the aims in the approved proposal. Proposals should be directed to iona.paterson@ggc.scot.nhs.uk.

Statistics from Altmetric.com

Data availability statement

Data are available on reasonable request. Individual participant data that underlie the results reported in this article, after deidentification, will be made available, beginning 3 months and ending 5 years after article publication. Data will be shared with researchers providing a methodologically sound proposal in order to achieve the aims in the approved proposal. Proposals should be directed to iona.paterson@ggc.scot.nhs.uk.

View Full Text

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.