Editorials

Palliative care in people with chronic obstructive pulmonary disease

BMJ 2011; 342 doi: https://doi.org/10.1136/bmj.d106 (Published 24 January 2011) Cite this as: BMJ 2011;342:d106
  1. Andrew Thorns, consultant in palliative medicine,
  2. Declan Cawley, research fellow in palliative medicine
  1. 1Pilgrims Hospices, East Kent NHS University Hospitals Foundation Trust, University of Kent, Canterbury CT9 4AD, UK
  1. andrew_thorns{at}pilgrimshospice.org

Passive acceptance of the illness has implications for end of life care and delivery of services

The fact that chronic obstructive pulmonary disease (COPD) is a terminal illness comes as no surprise to clinicians on acute medical wards, especially as the winter takes hold. Why then are patients surprised when end of life issues are raised or referrals made to hospice services? In the linked study (doi:10.1136/bmj.d142), Pinnock and colleagues postulate that patients passively accept their lot and see the increasing disability as part of normal ageing.1 The researchers found that, unlike patients with other diseases (such as cancer and heart failure)—who can tell the story of how the illness occurred, events that have unfolded, and their current disease status2—patients with COPD seem to lack this narrative story. The realisation of illness, or “biographical disruption” to their life, is not a conscious thought for these patients. There is no clear point of diagnosis, especially one with a poor prognosis.

Dennis Hallinan/Alamy

This lack of biographical disruption stops patients …

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