Assessing Practices,Beliefs,and Attitudes about Palliative Care among People with Cystic Fibrosis,Their Caregivers,and Clinicians: Results of a Content Analysis

Abstract

Background:

Individuals with cystic fibrosis (CF) experience symptoms affecting quality of life and may benefit from palliative care (PC).

Objectives:

To present results of content analysis from open-ended survey questions assessing knowledge and experiences with PC among CF stakeholders.

Design, Setting, Subjects:

Online surveys were sent to CF stakeholders through CF-specific listservs predominantly in the United States.

Measurements:

Responses to five open-ended questions about CF PC—delivery, health care provider training, and lung transplant—underwent content analysis. Responses were coded using NVivo12 Software™.

Results:

Forty-eight CF adults, 59 caregivers, and 229 providers responded to the open-ended survey questions. Analysis showed 5 primary categories related to CF PC: (1) stakeholder perceptions of PC for CF, (2) delivering PC to people with CF, (3) conversations about PC for CF, (4) perceptions that PC services are underutilized for people with CF, and (5) beliefs that PC services are critical for people with CF considering or pursuing lung transplant. Analysis showed variation among and within groups in defining PC for CF, when, and how to deliver it. Many respondents felt PC was underutilized in CF. Most saw PC as particularly important when considering lung transplant, managing anxiety around transplant, and for goals of care discussions. Some believed PC and lung transplant were mutually exclusive.

Conclusion:

Respondents felt PC is underutilized for CF, and that people with CF may miss out on the benefits of PC. Among stakeholders, respondents felt people with CF would benefit from access to primary and secondary PC services.