Literature DB >> 11374521

Ways of coping with cystic fibrosis: implications for treatment adherence.

J Abbott1, M Dodd, L Gee, K Webb.   

Abstract

PURPOSE: How individuals cope with aspects of cystic fibrosis (CF) has the potential to influence their self management and the course of their disease. To evaluate how individuals cope with CF, a disease specific coping scale was developed and validated. A second objective of the work was to examine the relationship between coping styles and treatment adherence.
METHODS: The development of the coping scale constituted a longitudinal design. A cross-sectional questionnaire design was used to examine the coping-adherence relationship. The development and validation of the coping scale comprised three phases: (1) Initially, 60 patients were interviewed to identify CF concerns. From this information a list of 23 concerns were recorded; (2) Eighty-three patients were interviewed to identify CF coping responses. For each concern, they were asked what they did or thought to ease the worry. A list of 24 coping strategies were recorded that formed a comprehensive set of items as to how people with CF act, feel and think about aspects of their disease; and (3) Further development and testing of the questionnaire involved 174 patients completing the measure. Four distinct ways of coping with CF were identified by factor analysis. These were termed optimistic acceptance, hopefulness, distraction and avoidance. The cronbach alpha coefficients were 0.74 (optimistic acceptance), 0.69 (hopefulness). 0.71 (distraction) and 0.76 (avoidance). To evaluate the relationship between coping and treatment adherence 60 patients completed the CF Coping Questionnaire and the Manchester Adult Cystic Fibrosis Compliance Questionnaire.
RESULTS: Compared with patients who were non-adherent, those who were adherent scored higher on the optimistic acceptance scale (physiotherapy p < 0.05, enzymes p < 0.003, vitamins p < 0.05) and hopefulness scale (physiotherapy p < 0.002, enzymes p < 0.001). Those who were partially adherent reported using distraction as a way of coping to a greater extent than adherent or non-adherent patients (all p's < 0.05). Non-adherent patients used avoidance strategies to a greater extent than those who were adherent (physiotherapy p < 0.05, enzymes p < 0.04), although interestingly, adherence with exercise was associated with avoidant coping (p < 0.004).
CONCLUSIONS: The degree of adherence to treatments was influenced by a person's style of coping. The identification of effective coping strategies to aid both long-term psychological and clinical well-being should improve the management of non-adherence.

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Mesh:

Year:  2001        PMID: 11374521     DOI: 10.1080/09638280010004171

Source DB:  PubMed          Journal:  Disabil Rehabil        ISSN: 0963-8288            Impact factor:   3.033


  14 in total

Review 1.  Coping with cystic fibrosis.

Authors:  Janice Abbott
Journal:  J R Soc Med       Date:  2003       Impact factor: 5.344

2.  Adherence to treatment in adolescents.

Authors:  Danielle Taddeo; Maud Egedy; Jean-Yves Frappier
Journal:  Paediatr Child Health       Date:  2008-01       Impact factor: 2.253

3.  Associations between illness perceptions and health-related quality of life in adults with cystic fibrosis.

Authors:  Gregory S Sawicki; Deborah E Sellers; Walter M Robinson
Journal:  J Psychosom Res       Date:  2010-08-10       Impact factor: 3.006

4.  We can handle this: parents' use of religion in the first year following their child's diagnosis with cystic fibrosis.

Authors:  Daniel H Grossoehme; Judy Ragsdale; Jamie L Wooldridge; Sian Cotton; Michael Seid
Journal:  J Health Care Chaplain       Date:  2010

5.  We were chosen as a family: parents' evolving use of religion when their child has cystic fibrosis.

Authors:  Daniel H Grossoehme; Judith R Ragsdale; Amy Snow; Michael Seid
Journal:  J Relig Health       Date:  2012-12

6.  The impact of COVID-19 shielding on the wellbeing, mental health and treatment adherence of adults with cystic fibrosis.

Authors:  Kristina A Westcott; Frances Wilkins; Amelia Chancellor; Alan Anderson; Simon Doe; Carlos Echevarria; Stephen J Bourke
Journal:  Future Healthc J       Date:  2021-03

7.  Reciprocal Links Between Physical Health and Coping Among Adolescents With Cystic Fibrosis.

Authors:  Christina M D'Angelo; Sylvie Mrug; Daniel Grossoehme; Kevin Leon; Lacrecia Thomas; Bradley Troxler
Journal:  J Pediatr Psychol       Date:  2021-02-19

8.  Avoidance and inhibition do not predict nonrespondent bias among patients with inflammatory bowel disease.

Authors:  Rafael J A Cámara; Stefan Begré; Roland von Känel
Journal:  J Epidemiol       Date:  2010-11-13       Impact factor: 3.211

9.  Qualitative Assessment of the Symptoms and Impact of Pancreatic Exocrine Insufficiency (PEI) to Inform the Development of a Patient-Reported Outcome (PRO) Instrument.

Authors:  Colin D Johnson; Rob Arbuckle; Nicola Bonner; Gary Connett; Enrique Dominguez-Munoz; Philippe Levy; Doris Staab; Nicola Williamson; Markus M Lerch
Journal:  Patient       Date:  2017-10       Impact factor: 3.883

10.  Telemonitoring in Cystic Fibrosis: A 4-year Assessment and Simulation for the Next 6 Years.

Authors:  Irene Tagliente; Leopoldo Trieste; Terje Solvoll; Fabrizio Murgia; Sergio Bella
Journal:  Interact J Med Res       Date:  2016-05-03
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