Linked Life Data

8707686

Source:http://linkedlifedata.com/resource/pubmed/id/8707686

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1996-9-12
pubmed:abstractText
Women who have used the New Zealand health services for chronic pelvic pain have reported problems with diagnosis, communication with the doctor, lack of information, and inappropriate treatment. Six focus groups were conducted in which women talked about their experiences of using the health services for chronic pelvic pain. A discourse analysis of this material provided a conceptual basis for understanding the key dimensions structuring women's experience. Themes of particular concern were that (a) doctors negated the woman's own experience of the pain and its meaning to her and this negation affected her ability to take responsibility for her condition; (b) the medical "extraction" of symptoms through technology overshadows the woman's discursive interpretation of, and voicing of, her symptoms; and (c) the concept of "pelvic pain without organic pathology" implies an absence that becomes filled with the specter of neurosis or psychological problems.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
N
pubmed:status
MEDLINE
pubmed:issn
0739-9332
pubmed:author
pubmed:issnType
Print
pubmed:volume
16
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
509-19
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed:articleTitle
Problems women patients experience in the medical encounter for chronic pelvic pain: a New Zealand study.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't