Pain management experiences in adults living with HIV/AIDS

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dc.contributor.advisor Carter , Patricia A .
dc.contributor.committeeMember Acton , Gayle
dc.contributor.committeeMember Fredholm , Leigh
dc.contributor.committeeMember Garcia , Alexandra
dc.contributor.committeeMember Volker , Deborah
dc.creator Mikan , Sabrina Quintanilla
dc.date.accessioned 2011 -10 -31T21 :29 :04Z
dc.date.available 2011 -10 -31T21 :29 :04Z
dc.date.created 2011 -08
dc.date.issued 2011 -10 -31
dc.date.submitted August 2011
dc.identifier.uri http : / /hdl .handle .net /2152 /ETD -UT -2011 -08 -3864
dc.description.abstract Even though pain is common and often chronic in people living with HIV /AIDS (PLWHA ) , the management of pain is complicated and frequently woefully inadequate . Many factors influence the way PLWHA experience and communicate their pain . These factors can be categorized as both physiological and emotional . PLWHA often resort to self -care activities to control their pain because of the pervasive lack of adequate pain management by health care providers . The purposes of this study were to increase understanding of the pain management experiences in people living with HIV /AIDS (PLWHA ) who report chronic pain and to elucidate the factors that influence this experience . Recruitment was conducted at 3 locations in Central Texas , USA ; serving over 3 ,000 clients /year . A cross -sectional descriptive design and open -ended questions were used to explore PLWHA experiences in reporting chronic pain needs for at least 3 months and to describe pain management choices (self -care and /or seeking care activities ) and communication with health care providers . Variables of interest were assessed with paper -pencil surveys (HIV -Self Efficacy Questionnaire , Coping Inventory for Pain in Persons Living with HIV /AIDS and Pain Self -Efficacy Questionnaire ) and open -ended questions . Interviews ranged from 7 -35 minutes each . One hundred PLWHA participated in the study , 53 % African -American , 21 % Hispanic and 25 % Caucasian . They were primarily male (66 % ) , 34 % female , reported a mean age of 48 years and a mean of 13 years living with HIV . 83 % of the participants rated their pain as consistently moderate to high levels ; 82 % rated they are likely to “tolerate the pain .” A majority of the participants (63 % ) reported they exercise or walk as a way of self -managing their pain . There was a significant association between use of pain management choices (self -care and /or seeking care activities ) and confidence in performing life activities (r= 0 .344 , p <0 .05 ) . These findings indicate a need for health care providers to move beyond quantitative measures for this complex problem . Clinicians can use this information to understand the coping strategies used by PLWHA to manage pain . Future implications will be to develop appropriate pain management approaches (behavioral and pharmacological ) for health care providers to improve control of chronic pain in PLWHA . Longitudinal studies are needed to explore the causative relationships between pain management choices (self -care and /or seeking care activities ) and functional outcomes in PLWHA .
dc.format.mimetype application /pdf
dc.language.iso eng
dc.subject HIV /AIDS
dc.subject Pain management
dc.subject Coping
dc.subject Self -efficacy
dc.title Pain management experiences in adults living with HIV /AIDS
dc.description.department Nursing
dc.type.genre thesis *
dc.type.material text *
thesis.degree.name Doctor of Philosophy
thesis.degree.level Doctoral
thesis.degree.discipline Nursing
thesis.degree.grantor University of Texas at Austin
thesis.degree.department Nursing
dc.date.updated 2011 -10 -31T21 :29 :18Z
dc.identifier.slug 2152 /ETD -UT -2011 -08 -3864

Citation

Pain management experiences in adults living with HIV/AIDS. Doctoral dissertation, University of Texas at Austin. Available electronically from http : / /hdl .handle .net /2152 /ETD -UT -2011 -08 -3864 .

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