Self-Reported Physical and Psychological Symptom Burden in Adults with Cystic Fibrosis
Author:
Publisher
Elsevier BV
Subject
Anesthesiology and Pain Medicine,Clinical Neurology,General Nursing
Reference22 articles.
1. Patient registry annual data report for 2004;Cystic Fibrosis Foundation,2005
2. Assessing the usefulness of outcomes measured in a cystic fibrosis treatment trial;Suri;Respir Med,2007
3. Linking clinical variables with health-related quality of life. A conceptual model of patient outcomes;Wilson;JAMA,1995
4. Defining a pulmonary exacerbation in cystic fibrosis;Rosenfeld;J Pediatr,2001
5. The psychosocial and psychiatric side of cystic fibrosis in adolescents and adults;Pfeffer;J Cyst Fibros,2003
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1. Validation of the Integrated Palliative Care Outcome Scale (IPOS) in adults with cystic fibrosis;Pediatric Pulmonology;2024-06-27
2. Scoring Abdominal Symptoms in People with Cystic Fibrosis;Journal of Clinical Medicine;2024-03-13
3. Symptoms and quality of life in adults with cystic fibrosis: A cross-sectional analysis of the InSPIRe:CF trial;Journal of Cystic Fibrosis;2024-03
4. Pulmonary Function and Quality of Life in Adults with Cystic Fibrosis;Lung;2023-11-16
5. Clinician perspectives on barriers and solutions to symptom management in cystic fibrosis;Journal of Cystic Fibrosis;2023-11
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