| Literature DB >> 29551585 |
Angela Ju1, Mark Unruh2, Sara Davison3, Juan Dapueto4, Mary Amanda Dew5, Richard Fluck6, Michael Germain7, Sarbjit V Jassal8, Gregorio Obrador9, Donal O'Donoghue10, Michelle A Josephson11, Jonathan C Craig12, Andrea Viecelli13, Emma O'Lone12, Camilla S Hanson12, Braden Manns14, Benedicte Sautenet15, Martin Howell12, Bharathi Reddy16, Caroline Wilkie17, Claudia Rutherford18, Allison Tong12.
Abstract
Fatigue is one of the most highly prioritized outcomes for patients and clinicians, but remains infrequently and inconsistently reported across trials in hemodialysis. We convened an international Standardized Outcomes in Nephrology-Hemodialysis (SONG-HD) consensus workshop with stakeholders to discuss the development and implementation of a core outcome measure for fatigue. 15 patients/caregivers and 42 health professionals (clinicians, researchers, policy makers, and industry representatives) from 9 countries participated in breakout discussions. Transcripts were analyzed thematically. 4 themes for a core outcome measure emerged. Drawing attention to a distinct and all-encompassing symptom was explicitly recognizing fatigue as a multifaceted symptom unique to hemodialysis. Emphasizing the pervasive impact of fatigue on life participation justified the focus on how fatigue severely impaired the patient's ability to do usual activities. Ensuring relevance and accuracy in measuring fatigue would facilitate shared decision making about treatment. Minimizing burden of administration meant avoiding the cognitive burden, additional time, and resources required to use the measure. A core outcome measure that is simple, is short, and includes a focus on the severity of the impact of fatigue on life participation may facilitate consistent and meaningful measurement of fatigue in all trials to inform decision making and care of patients receiving hemodialysis.Entities:
Keywords: Clinical trials; consensus; core outcome; dialysis symptoms; end-stage renal disease (ESRD); fatigue; hemodialysis; kidney disease; life participation; nephrology research; outcome; outcome measure; patient-centered research; patient-reported outcome (PRO); quality of life; tiredness
Mesh:
Year: 2018 PMID: 29551585 DOI: 10.1053/j.ajkd.2017.12.018
Source DB: PubMed Journal: Am J Kidney Dis ISSN: 0272-6386 Impact factor: 8.860