Register for email alerts and news feeds:
This journal | BMJ Group
rss
Thorax 1995;50:794-796; doi:10.1136/thx.50.7.794
Copyright © 1995 BMJ Publishing Group Ltd & British Thoracic Society.

Different perceptions of disease severity and self care between patients with cystic fibrosis, their close companions, and physician.

J Abbott, M Dodd, A K Webb

Bradbury Adult Cystic Fibrosis Unit, Wythenshawe Hospital, Manchester, UK.

BACKGROUND--An investigation was carried out to determine whether patients with cystic fibrosis, their close companions, and physician perceived the severity of the disease and the level of patient self care similarly. METHODS--Sixty adults with cystic fibrosis (16-44 years), their close companion, and physician independently completed scales measuring their perceptions of disease severity and patient self care on three occasions over a two year period. Percentage predicted forced expiratory volume in one second (FEV1) and forced vital capacity (FVC), Shwachman score, and weight for height were recorded following each assessment. RESULTS--Patients and close companions considered the disease to be less severe than their physician. Fifty patients (83%) rated their health as "above/well above average", and 49 (82%) close companions rated the patient's health in the same way, but only 21 (35%) patients were considered by their physician to have mild disease. Differences also emerged in the estimation of patient self care; 48 close companions (80%) rated patients as "very good" or "excellent" in their self care, compared with 26 (44%) of the patients themselves. Only nine patients (15%) were considered to achieve this level of self care by their physician. Over the two year period the physician's ratings of severity increased in accordance with the decline in lung function. Patients' perceptions remained unchanged. CONCLUSIONS--From the physician's view-point, patients and close companions underestimate the severity of cystic fibrosis and overestimate patient self care. Patients' perceptions remain constant over time even when their health is clinically deteriorating.


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

This article has been cited by other articles:

  • Connelly, M., Wagner, J. L., Brown, R. T., Rittle, C., Cloues, B., Taylor, L. C. (2005). Informant Discrepancy in Perceptions of Sickle Cell Disease Severity. J Pediatr Psychol 30: 443-448 [Abstract] [Full Text]  
  • Kettler, L J, Sawyer, S M, Winefield, H R, Greville, H W (2002). Determinants of adherence in adults with cystic fibrosis. Thorax 57: 459-464 [Abstract] [Full Text]  
  • Powers, P. M., Gerstle, R., Lapey, A. (2001). Adolescents With Cystic Fibrosis: Family Reports of Adolescent Health-Related Quality of Life and Forced Expiratory Volume in One Second. Pediatrics 107: 70e-70 [Abstract] [Full Text]  

This Article

Services
Citing Articles
Google Scholar
PubMed
Bookmark with

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.

Chest Medicine Jobs

Chest Medicine Jobs