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.
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

CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
StumbleUpon
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