Literature DB >> 8128399

Treatment compliance in adults with cystic fibrosis.

J Abbott1, M Dodd, D Bilton, A K Webb.   

Abstract

BACKGROUND: The study comprised three interrelated aims: (1) to ascertain (a) patient compliance with physiotherapy, exercise, enzyme and vitamin regimens, (b) how compliance was perceived by patients, and (c) the reasons for poor compliance (2) to identify demographic and clinical variables associated with compliance; and (3) to determine how accurately patient compliance can be predicted by carers.
METHODS: Demographic and medical history data were obtained from medical records and a patient questionnaire. The data obtained included age, sex, employment status, inpatient or outpatient status, frequency of contact with the clinic, age at diagnosis, and the number of years practising physiotherapy. Measures of clinical status, including FEV1 and FVC percentage predicted, Shwachman score, and 24 hour sputum weight were recorded before completion of the questionnaire. The questionnaire, administered by a psychologist, assessed the reported degree of patient compliance, their perception of compliance, and their reasons for poor compliance.
RESULTS: Sixty patients participated in the study and 51/60 and 41/55 patients were considered compliant with enzyme and exercise therapies, respectively. Compliance was lower with physiotherapy (32/60) and vitamin treatment (21/45). Patients reporting immediate benefits following exercise and physiotherapy were more compliant than those reporting no improvement. The perception by patients that compliance was sufficient ("about right") was physiotherapy 67%, exercise 37%, enzymes 78%, and vitamins 9%. Compliance was not influenced by demographic details nor by severity of disease, although patients producing large amounts of sputum and receiving help with physiotherapy were more compliant with physiotherapy. The physiotherapist and physician judged correctly the degree of compliance with physiotherapy in 83% and 75% of cases, respectively, and with exercise in 68% and 67% of cases, respectively.
CONCLUSIONS: The reported degree of compliance and reasons for poor compliance were treatment specific. Demographic and disease severity variables were not associated with compliance. Those involved in the care of patients with cystic fibrosis were able to predict patient compliance.

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Year:  1994        PMID: 8128399      PMCID: PMC474321          DOI: 10.1136/thx.49.2.115

Source DB:  PubMed          Journal:  Thorax        ISSN: 0040-6376            Impact factor:   9.139


  8 in total

1.  The benefits of exercise combined with physiotherapy in the treatment of adults with cystic fibrosis.

Authors:  D Bilton; M E Dodd; J V Abbot; A K Webb
Journal:  Respir Med       Date:  1992-11       Impact factor: 3.415

2.  A comparative study of the psychosocial assets of adults with cystic fibrosis and their healthy peers.

Authors:  S L Shepherd; M F Hovell; I R Harwood; L E Granger; C R Hofstetter; C Molgaard; R M Kaplan
Journal:  Chest       Date:  1990-06       Impact factor: 9.410

3.  Profiles of non-compliance with antituberculous therapy.

Authors:  A G Wardman; A J Knox; M F Muers; R L Page
Journal:  Br J Dis Chest       Date:  1988-07

4.  Diagnosing potential noncompliance. Physicians' ability in a behavioral dimension of medical care.

Authors:  A I Mushlin; F A Appel
Journal:  Arch Intern Med       Date:  1977-03

5.  Psychosocial adaptation in older cystic fibrosis patients.

Authors:  G D Strauss; D K Wellisch
Journal:  J Chronic Dis       Date:  1981

6.  Idiopathic thrombocytopenic purpura in two children with Graves disease.

Authors:  C Chintu; P McClure
Journal:  Am J Dis Child       Date:  1975-01

7.  Medical compliance and coping with cystic fibrosis.

Authors:  D R Czajkowski; G P Koocher
Journal:  J Child Psychol Psychiatry       Date:  1987-03       Impact factor: 8.982

8.  Patient-reported compliance with cystic fibrosis therapy.

Authors:  M A Passero; B Remor; J Salomon
Journal:  Clin Pediatr (Phila)       Date:  1981-04       Impact factor: 1.168

  8 in total
  34 in total

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2.  Evidence for using nebulised antibiotics in cystic fibrosis.

Authors:  S P Conway
Journal:  Arch Dis Child       Date:  1999-04       Impact factor: 3.791

Review 3.  Understanding non-compliance with treatment in adults with cystic fibrosis.

Authors:  M E Dodd; A K Webb
Journal:  J R Soc Med       Date:  2000       Impact factor: 5.344

Review 4.  The role of vitamins in cystic fibrosis.

Authors:  S B Carr; J McBratney
Journal:  J R Soc Med       Date:  2000       Impact factor: 5.344

5.  Comparison of lung deposition of colomycin using the HaloLite and the Pari LC Plus nebulisers in patients with cystic fibrosis.

Authors:  N M Byrne; P M Keavey; J D Perry; F K Gould; D A Spencer
Journal:  Arch Dis Child       Date:  2003-08       Impact factor: 3.791

Review 6.  Coping with cystic fibrosis.

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

7.  Exercise and sport in cystic fibrosis: benefits and risks.

Authors:  A K Webb; M E Dodd
Journal:  Br J Sports Med       Date:  1999-04       Impact factor: 13.800

8.  Individualised unsupervised exercise training in adults with cystic fibrosis: a 1 year randomised controlled trial.

Authors:  A J Moorcroft; M E Dodd; J Morris; A K Webb
Journal:  Thorax       Date:  2004-12       Impact factor: 9.139

9.  Compliance with treatment in adult patients with cystic fibrosis.

Authors:  S P Conway; M N Pond; T Hamnett; A Watson
Journal:  Thorax       Date:  1996-01       Impact factor: 9.139

10.  Adherence and psychopathology in children and adolescents with cystic fibrosis.

Authors:  Tonya White; Judith Miller; Gail L Smith; William M McMahon
Journal:  Eur Child Adolesc Psychiatry       Date:  2008-09-20       Impact factor: 4.785

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