Literature DB >> 15934559

Pain, coping, and disability in adolescents and young adults with cystic fibrosis: a Web-based study.

Patrick A Hubbard1, Marion E Broome, Lauren A Antia.   

Abstract

PURPOSE: The purpose of this study was to develop a web-based education program tailored to patients with cystic fibrosis (CF) who may be experiencing pain, and to investigate, via the website, the pain experiences of those patients by studying their pain reports, disability, and coping strategies.
METHOD: This study was a cross-sectional survey of CF patients. Recruitment efforts focused on informing patients of the website and research study. A sample of 18 participants was recruited. Three separate questionnaires were employed: a demographic questionnaire, the Pain Disability Index, and the Pain Response Inventory.
FINDINGS: Approximately half of the sample reported experiencing daily pain episodes lasting two hours or less. The average intensity of a pain episode was reported to be in the moderate range. Participants reported pain disability highest in areas of recreation, occupation, and social activities. The most commonly used coping strategies included active and accommodative coping techniques such as problem solving, acceptance, and self-encouragement.
CONCLUSION: Pain management is clearly a problem for some young adults with CF. This study provided information about the areas of disability caused by pain, as well as common coping strategies used by patients. The findings of this study provide direction for the future of pain management in CF patients.

Entities:  

Mesh:

Year:  2005        PMID: 15934559

Source DB:  PubMed          Journal:  Pediatr Nurs        ISSN: 0097-9805


  4 in total

Review 1.  Pain and its clinical associations in individuals with cystic fibrosis: A systematic review.

Authors:  Annemarie L Lee; Sarah Rawlings; Katharine A Bennett; David Armstrong
Journal:  Chron Respir Dis       Date:  2016-02-12       Impact factor: 2.444

2.  Family caregiver perspectives on symptoms and treatments for patients dying from complications of cystic fibrosis.

Authors:  Elisabeth P Dellon; Mitchell D Shores; Katherine I Nelson; Joanne Wolfe; Terry L Noah; Laura C Hanson
Journal:  J Pain Symptom Manage       Date:  2010-09-17       Impact factor: 3.612

3.  Telemedicine and Virtual Reality at Time of COVID-19 Pandemic: An Overview for Future Perspectives in Neurorehabilitation.

Authors:  Marta Matamala-Gomez; Sara Bottiroli; Olivia Realdon; Giuseppe Riva; Lucia Galvagni; Thomas Platz; Giorgio Sandrini; Roberto De Icco; Cristina Tassorelli
Journal:  Front Neurol       Date:  2021-03-25       Impact factor: 4.003

4.  A pilot Internet "value of health" panel: recruitment, participation and compliance.

Authors:  Ken Stein; Matthew Dyer; Tania Crabb; Ruairidh Milne; Alison Round; Julie Ratcliffe; John Brazier
Journal:  Health Qual Life Outcomes       Date:  2006-11-27       Impact factor: 3.186

  4 in total

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