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Sources of variation in assessing male and female responses to pain

Identifieur interne : 003481 ( Istex/Corpus ); précédent : 003480; suivant : 003482

Sources of variation in assessing male and female responses to pain

Auteurs : Stuart W. G. Derbyshire

Source :

RBID : ISTEX:6AD0950527B4903619CAA4323B68E7B45CC88AE4

English descriptors

Abstract

Abstract: The question of differential pain response between men and women has recently received much attention. In general, women present with pain and ill-health problems at least twice as often as do men and are therefore greater users of the health care system. One common explanation of this disproportionate use is that women respond to stimuli as painful at a lower intensity than do men. Thus, in the same situation, more women are liable to present with pain and illness than are men. Such a suggestion, however, is at odds with the highly variable psychological responses to painful stimuli in both men and women and returns to an essentially Cartesian understanding of pain which draws on the largely discredited ‘direct transmission model’. It is suggested here that differential ill-health and pain response between the sexes can be understood through an extension of the biopsychosocial model of pain and ill-health which is used to describe three types of clinical pain disorder: post extraction pain, rheumatoid arthritis and atypical facial pain. The differential experiences of men and women give women both greater opportunity and reason to be ill by altering the factors influencing the biopsychosocial model of pain.

Url:
DOI: 10.1016/S0732-118X(97)00009-3

Links to Exploration step

ISTEX:6AD0950527B4903619CAA4323B68E7B45CC88AE4

Le document en format XML

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<p>Abstract: The question of differential pain response between men and women has recently received much attention. In general, women present with pain and ill-health problems at least twice as often as do men and are therefore greater users of the health care system. One common explanation of this disproportionate use is that women respond to stimuli as painful at a lower intensity than do men. Thus, in the same situation, more women are liable to present with pain and illness than are men. Such a suggestion, however, is at odds with the highly variable psychological responses to painful stimuli in both men and women and returns to an essentially Cartesian understanding of pain which draws on the largely discredited ‘direct transmission model’. It is suggested here that differential ill-health and pain response between the sexes can be understood through an extension of the biopsychosocial model of pain and ill-health which is used to describe three types of clinical pain disorder: post extraction pain, rheumatoid arthritis and atypical facial pain. The differential experiences of men and women give women both greater opportunity and reason to be ill by altering the factors influencing the biopsychosocial model of pain.</p>
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<ce:given-name>Stuart W.G.</ce:given-name>
<ce:surname>Derbyshire</ce:surname>
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<ce:textfn>University of Pittsburgh Medical Centre, PET Facility, B-938 PUH, 200 Lothrop Street, Pittsburgh, PA 15213, U.S.A.</ce:textfn>
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<ce:simple-para>The question of differential pain response between men and women has recently received much attention. In general, women present with pain and ill-health problems at least twice as often as do men and are therefore greater users of the health care system. One common explanation of this disproportionate use is that women respond to stimuli as painful at a lower intensity than do men. Thus, in the same situation, more women are liable to present with pain and illness than are men. Such a suggestion, however, is at odds with the highly variable psychological responses to painful stimuli in both men and women and returns to an essentially Cartesian understanding of pain which draws on the largely discredited ‘direct transmission model’. It is suggested here that differential ill-health and pain response between the sexes can be understood through an extension of the biopsychosocial model of pain and ill-health which is used to describe three types of clinical pain disorder: post extraction pain, rheumatoid arthritis and atypical facial pain. The differential experiences of men and women give women both greater opportunity and reason to be ill by altering the factors influencing the biopsychosocial model of pain.</ce:simple-para>
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<ce:text>gender</ce:text>
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<ce:text>somatic response</ce:text>
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<ce:text>chronic pain</ce:text>
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<abstract lang="en">Abstract: The question of differential pain response between men and women has recently received much attention. In general, women present with pain and ill-health problems at least twice as often as do men and are therefore greater users of the health care system. One common explanation of this disproportionate use is that women respond to stimuli as painful at a lower intensity than do men. Thus, in the same situation, more women are liable to present with pain and illness than are men. Such a suggestion, however, is at odds with the highly variable psychological responses to painful stimuli in both men and women and returns to an essentially Cartesian understanding of pain which draws on the largely discredited ‘direct transmission model’. It is suggested here that differential ill-health and pain response between the sexes can be understood through an extension of the biopsychosocial model of pain and ill-health which is used to describe three types of clinical pain disorder: post extraction pain, rheumatoid arthritis and atypical facial pain. The differential experiences of men and women give women both greater opportunity and reason to be ill by altering the factors influencing the biopsychosocial model of pain.</abstract>
<subject lang="en">
<genre>Keywords</genre>
<topic>gender</topic>
<topic>somatic response</topic>
<topic>chronic pain</topic>
<topic>health</topic>
</subject>
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<title>New Ideas in Psychology</title>
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<publisher>ELSEVIER</publisher>
<dateIssued encoding="w3cdtf">199704</dateIssued>
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<identifier type="ISSN">0732-118X</identifier>
<identifier type="PII">S0732-118X(00)X0070-0</identifier>
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<date>199704</date>
<detail type="volume">
<number>15</number>
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<start>1</start>
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<start>83</start>
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<identifier type="DOI">10.1016/S0732-118X(97)00009-3</identifier>
<identifier type="PII">S0732-118X(97)00009-3</identifier>
<identifier type="ArticleID">97000093</identifier>
<accessCondition type="use and reproduction" contentType="copyright">©1997 Elsevier Science Ltd.</accessCondition>
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