BMJ 1998;316:130-132 (10 January)

Clinical review

ABC of palliative care: Communication with patients, families, and other professionals

Ann Faulkner 

There is increasing awareness of the need for effective communication in health care, particularly with people who face a frightening diagnosis and an uncertain future for themselves or someone close to them.


Communication problems when dealing with incurable and life threatening disease

  • Breaking bad news

  • Denial

  • Collusion

  • Difficult questions

  • Emotional reactions

Recent research suggests that most patients wish to know their diagnosis and the progress of treatment and disease. This may conflict with health professionals' need to protect their patients and retain an optimistic message even when the outlook is very poor.


Effective communication depends not only on the professionals but also on patients and carers. Language may be ambivalent, leading to genuine misunderstandings, and the needs of patients and carers do not always match. This may lead to health professionals feeling as though they are "pig in the middle" as they try to meet the needs of their patient and those of relatives.


Available Only
in the Full Text
Recommended manner of breaking bad . . . [Full text of this article]

Denial

Dealing with collusion

Difficult questions

Dealing with difficult questions

Major emotional reactions

Costs to professionals of dealing with dying patients and their families

Further reading


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 StumbleUpon StumbleUpon   Add to Technorati Technorati    What's this?

Relevant Articles

Exploring preferences for place of death with terminally ill patients: qualitative study of experiences of general practitioners and community nurses in England
Daniel Munday, Mila Petrova, and Jeremy Dale
BMJ 2009 339: b2391. [Abstract] [Full Text] [PDF]

What oncologists tell patients about survival benefits of palliative chemotherapy and implications for informed consent: qualitative study
Suzanne Audrey, Julian Abel, Jane M Blazeby, Stephen Falk, and Rona Campbell
BMJ 2008 337: a752. [Abstract] [Full Text] [PDF]

This article has been cited by other articles:

  • Braithwaite, M., Philip, J., Finlayson, F., Tranberg, H., Gold, M., Kotsimbos, T., Wilson, J. (2009). Adverse events arising from a palliative care survey. Palliat Med 23: 665-669 [Abstract]  
  • Thistlethwaite, J. (2009). Breaking bad news--skills and evidence. InnovAiT 2: 605-612 [Abstract] [Full text]  
  • Munday, D., Petrova, M., Dale, J. (2009). Exploring preferences for place of death with terminally ill patients: qualitative study of experiences of general practitioners and community nurses in England. BMJ 339: b2391-b2391 [Abstract] [Full text]  
  • Audrey, S., Abel, J., Blazeby, J. M, Falk, S., Campbell, R. (2008). What oncologists tell patients about survival benefits of palliative chemotherapy and implications for informed consent: qualitative study. BMJ 337: a752-a752 [Abstract] [Full text]  
  • Weaver, N., Murtagh, M., Thomson, R. (2006). How do newly diagnosed hypertensives understand 'risk'? Narratives used in coping with risk. Fam Pract 23: 637-643 [Abstract] [Full text]  
  • Arnold, S. J., Koczwara, B. (2006). Breaking Bad News: Learning Through Experience. JCO 24: 5098-5100 [Full text]  
  • Gore, J M, Brophy, C J, Greenstone, M A (2000). How well do we care for patients with end stage chronic obstructive pulmonary disease (COPD)? A comparison of palliative care and quality of life in COPD and lung cancer. Thorax 55: 1000-1006 [Abstract] [Full text]  
  • Enck, R. E. (1999). Anger at the end. AM J HOSP PALLIAT CARE 16: 692-693  



Access jobs at BMJ Careers
Whats new online at Student 

BMJ