Predictors of non-referral of patients with cystic fibrosis for lung transplant evaluation in the United States

J Cyst Fibros. 2016 Mar;15(2):196-203. doi: 10.1016/j.jcf.2015.11.005. Epub 2015 Dec 17.

Abstract

Background: Lung transplantation is an intervention that improves survival for adult patients with cystic fibrosis (CF). Some patients with CF are never referred for lung transplant evaluation despite meeting physiologic criteria for referral.

Methods: We performed a retrospective analysis of adult patients (≥18years of age) in the Cystic Fibrosis Foundation Patient Registry (CFFPR), eligible for their first evaluation for lung transplantation during the years 2001-2008 based on FEV1<30% predicted in two consecutive years.

Results: Within the CFFPR, 1240 patients met eligibility criteria. Eight hundred and nine (65.2%) were referred for lung transplant evaluation, and 431 (34.8%) were not referred. In a multivariable model, Medicaid insurance (OR 1.79, 95% CI 1.29-2.47), older age (per 5year increase; OR 1.25, 95% CI 1.13-1.39), lack of high school graduate education (OR 2.27, 95% CI 1.42-3.64), and Burkholderia cepacia complex sputum culture positivity (OR 2.48, 95% CI 1.50-4.12) were associated with non-referral, while number of pulmonary exacerbations (OR 0.93, 95% CI 0.87-0.99) and supplemental oxygen use (OR 0.59, 95% CI 0.43-0.81) were associated with increased referral.

Conclusions: Despite meeting lung function criteria for lung transplant evaluation, 35% of patients with CF had not yet been referred to a lung transplant center. Predictors of non-referral included markers of low socioeconomic status, older age and B. cepacia complex sputum culture. Further work is needed to understand the outcomes for non-referred patients in order to refine referral recommendations in this population.

Keywords: Cystic fibrosis; Lung transplantation; Referral.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Cystic Fibrosis / diagnosis
  • Cystic Fibrosis / physiopathology
  • Cystic Fibrosis / surgery*
  • Disease Progression
  • Female
  • Follow-Up Studies
  • Humans
  • Lung Transplantation*
  • Male
  • Patient Selection*
  • Referral and Consultation
  • Respiratory Function Tests
  • Retrospective Studies
  • Severity of Illness Index
  • Time Factors
  • United States