Literature DB >> 31862306

Prevalence of unmet palliative care needs in adults with cystic fibrosis.

Elizabeth T Trandel1, Joseph M Pilewski1, Elisabeth P Dellon2, Kwonho Jeong1, Jonathan G Yabes1, Laura T Moreines3, Robert M Arnold1, Zachariah P Hoydich1, Dio Kavalieratos4.   

Abstract

BACKGROUND: Physical and emotional burdens impair quality of life (QoL) in many adults with cystic fibrosis (CF). Palliative care (PC) improves QoL in other serious illnesses, yet the full array of palliative needs amenable to PC are unknown in CF.
METHODS: We surveyed 164 adults with CF using the Supportive Care Needs Survey 34 (SCNS-34) to assess unmet PC needs across five domains, the Edmonton Symptom Assessment System (ESAS) to assess symptom burden, and the Cystic Fibrosis Questionnaire-Revised (CFQ-R) to assess CF-specific QoL. We assessed associations between SCNS-34 domain scores and respondent characteristics, including symptom burden and FEV1.
RESULTS: Median age was 29 years; 56% of respondents were male. Median FEV1 was 57% predicted. 78% of respondents reported ≥1 unmet PC need; physical and daily living (72%) and psychological (66%) needs were most prevalent. Symptom burden was correlated with all SCNS-34 domains scores, and strongly correlated with the physical (r = 0.79) and psychological (r = 0.72) domain scores. FEV1 was moderately inversely correlated with the physical domain score (r = -0.41). Forty-four of the 45 inverse correlations between SCNS-34 domain scores and CFQ-R domain scores were significant. Patient-reported depressive and anxiety symptoms were significantly associated with higher scores in five and four SCNS-34 domains, respectively.
CONCLUSIONS: Adults with CF have substantial unmet PC needs. Patient-reported symptom burden is more strongly associated with reporting unmet PC needs than FEV1. Routine screening of unmet PC needs, using tools such as the SCNS-34, may enable CF care teams to optimize the provision of primary and specialist PC.
Copyright © 2019 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Needs assessment; Palliative care; Patient-reported outcomes; Quality of life

Mesh:

Year:  2019        PMID: 31862306      PMCID: PMC8662333          DOI: 10.1016/j.jcf.2019.11.010

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  27 in total

1.  Needs assessment of cancer survivors in Connecticut.

Authors:  M Tish Knobf; Leah M Ferrucci; Brenda Cartmel; Beth A Jones; Denise Stevens; Maureen Smith; Andrew Salner; Linda Mowad
Journal:  J Cancer Surviv       Date:  2011-10-09       Impact factor: 4.442

Review 2.  Association Between Palliative Care and Patient and Caregiver Outcomes: A Systematic Review and Meta-analysis.

Authors:  Dio Kavalieratos; Jennifer Corbelli; Di Zhang; J Nicholas Dionne-Odom; Natalie C Ernecoff; Janel Hanmer; Zachariah P Hoydich; Dara Z Ikejiani; Michele Klein-Fedyshin; Camilla Zimmermann; Sally C Morton; Robert M Arnold; Lucas Heller; Yael Schenker
Journal:  JAMA       Date:  2016-11-22       Impact factor: 56.272

3.  End of life care in CF: patients, families and staff experiences and unmet needs.

Authors:  Maxine Braithwaite; Jennifer Philip; Heidi Tranberg; Felicity Finlayson; Michelle Gold; Tom Kotsimbos; John Wilson
Journal:  J Cyst Fibros       Date:  2011-03-27       Impact factor: 5.482

4.  Addressing the burden of illness in adults with cystic fibrosis with screening and triage: An early intervention model of palliative care.

Authors:  Lara Dhingra; Patricia Walker; Maria Berdella; Amy Plachta; Jack Chen; Ashley Fresenius; Julie Balzano; Malcolm Barrett; Marilyn Bookbinder; Kenya Wilder; Myra Glajchen; Elinor Langfelder-Schwind; Russell K Portenoy
Journal:  J Cyst Fibros       Date:  2019-08-27       Impact factor: 5.482

5.  End-of-life practice patterns at U.S. adult cystic fibrosis care centers: A national retrospective chart review.

Authors:  Elaine Chen; Karen Homa; Jessica Goggin; Kathryn A Sabadosa; Sarah Hempstead; Bruce C Marshall; Albert Faro; Elisabeth P Dellon
Journal:  J Cyst Fibros       Date:  2017-09-13       Impact factor: 5.482

6.  The Edmonton Symptom Assessment System (ESAS): a simple method for the assessment of palliative care patients.

Authors:  E Bruera; N Kuehn; M J Miller; P Selmser; K Macmillan
Journal:  J Palliat Care       Date:  1991       Impact factor: 2.250

7.  Supportive care needs in patients with cardiovascular disorders.

Authors:  Sebastian Kohlmann; Mara S Kilbert; Kristin Ziegler; Karl-Heinz Schulz
Journal:  Patient Educ Couns       Date:  2013-02-04

8.  A service evaluation of an integrated model of palliative care of cystic fibrosis.

Authors:  Stephen J Bourke; Zoe Booth; Simon Doe; Alan Anderson; Sarah Rice; Alistair Gascoigne; Rachel Quibell
Journal:  Palliat Med       Date:  2016-01-26       Impact factor: 4.762

9.  Brief assessment of adult cancer patients' perceived needs: development and validation of the 34-item Supportive Care Needs Survey (SCNS-SF34).

Authors:  Allison Boyes; Afaf Girgis; Christophe Lecathelinais
Journal:  J Eval Clin Pract       Date:  2009-06-10       Impact factor: 2.431

10.  International Committee on Mental Health in Cystic Fibrosis: Cystic Fibrosis Foundation and European Cystic Fibrosis Society consensus statements for screening and treating depression and anxiety.

Authors:  Alexandra L Quittner; Janice Abbott; Anna M Georgiopoulos; Lutz Goldbeck; Beth Smith; Sarah E Hempstead; Bruce Marshall; Kathryn A Sabadosa; Stuart Elborn
Journal:  Thorax       Date:  2015-10-09       Impact factor: 9.139

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  6 in total

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

Authors:  Melissa Basile; Lincy Jojan; Mara R Hobler; Elisabeth P Dellon; Anna M Georgiopoulos; Jessica L Goggin; Elaine Chen; Christopher H Goss; Sarah E Hempstead; Albert Faro; Dio Kavalieratos
Journal:  J Palliat Med       Date:  2021-04-20       Impact factor: 2.947

Review 2.  The role of palliative care in lung transplantation.

Authors:  Eric Nolley; Matt Morrell
Journal:  J Thorac Dis       Date:  2021-11       Impact factor: 3.005

3.  A Systematic Review of the Development and Implementation of Needs-Based Palliative Care Tools in Heart Failure and Chronic Respiratory Disease.

Authors:  Amy Waller; Breanne Hobden; Kristy Fakes; Katherine Clark
Journal:  Front Cardiovasc Med       Date:  2022-04-13

4.  Integrating specialist palliative care to improve care and reduce suffering: cystic fibrosis (InSPIRe:CF) - study protocol for a multicentre randomised clinical trial.

Authors:  Jane Lowers; Elisabeth P Dellon; Anne Stephenson; Robert Arnold; Andrew Althouse; Kwonho Jeong; Ethan Dubin; Jesse Soodalter; Cade Hovater; Marie Bakitas; Jessica Goggin; William Hunt; Sigrid Ladores; Kimberly Curseen; Gretchen Winter; George Solomon; Jonathan Ailon; Douglas Conrad; Dio Kavalieratos
Journal:  BMJ Open Respir Res       Date:  2022-09

Review 5.  Pulmonary Complications in Cystic Fibrosis: Past, Present, and Future: Adult Cystic Fibrosis Series.

Authors:  Christina M Mingora; Patrick A Flume
Journal:  Chest       Date:  2021-06-17       Impact factor: 10.262

6.  Models of Palliative Care Delivery for Individuals with Cystic Fibrosis: Cystic Fibrosis Foundation Evidence-Informed Consensus Guidelines.

Authors:  Dio Kavalieratos; Anna M Georgiopoulos; Lara Dhingra; Melissa J Basile; Elliot Rabinowitz; Sarah E Hempstead; Albert Faro; Elisabeth P Dellon
Journal:  J Palliat Med       Date:  2020-09-16       Impact factor: 2.947

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