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First results from major European patient survey show devastating impact of living with breakthrough cancer pain
Date:9/11/2009

Lisbon, Portugal 11 September, 2009 The first results of the first European survey of cancer patients experience of breakthrough pain were presented today at the 6th congress of the European Federation of Chapters of the International Association for the Study of Pain (EFIC).

Previous surveys have looked at the overall management of pain in cancer patients but this is the first international study to look in detail at Breakthrough Cancer Pain (BTCP) from a patient perspective. These results for the first 200 patients from the UK, Sweden and Denmark offer valuable insight into cancer patients experiences with breakthrough pain management and the impact of the condition on their daily lives.

  • The median number of BTCP episodes per patient per day was 3
  • Each episode had a median duration of 60 minutes
  • 96% of the pain episodes were described as moderate to severe
  • For 90% of patients their BTCP interfered with their daily living including their ability to sleep, walk and get on with other people

The study documents that breakthrough pain has a significant impact on cancer patients daily lives, explained Dr. Andrew Davies, Department of Palliative Medicine, Royal Marsden Hospital, UK and the principal investigator of this survey. Breakthrough pain is very different to background pain. Background pain is a continuous, chronic pain requiring around-the-clock medication. Breakthrough pain is a fast onset, short duration, intense pain that breaks through the chronic pain even when this is being controlled with medication. It is incapacitating and very distressing to the patient.

For this kind of pain episode the ideal treatment would be fast acting with a short duration of action to most closely match the nature of BTCP episodes. Moreover, it must be easy to use to improve patient compliance. However, the results of the survey show that:

  • At least 95% of patients were using orally administered dr
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Contact: Mette Thorn Srensen
mts@cohnwolfe.dk
454-138-4300
Cohn & Wolfe, Copenhagen
Source:Eurekalert

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