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AIDS Care
Psychological and Socio-medical Aspects of AIDS/HIV
Volume 17, 2005 - Issue 6
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Original Articles

Coping strategies of HIV patients with peripheral neuropathy

Germaine A. Griswold Weill Medical College of Cornell University, New YorkCorrespondence[email protected]
,
Susan Evans Weill Medical College of Cornell University, New York
,
Lisa Spielman Weill Medical College of Cornell University, New York
&
Baruch Fishman Weill Medical College of Cornell University, New York
Pages 711-720 | Published online: 20 Aug 2006

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Read on this site (5)

Cory Toth, Shauna Brady & Melinda Hatfield. (2014) The importance of catastrophizing for successful pharmacological treatment of peripheral neuropathic pain. Journal of Pain Research 7, pages 327-338.
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Marinda Kotzé, Maretha Visser, Jennifer Makin, Kathy Sikkema & Brian Forsyth. (2013) The coping strategies used over a two-year period by HIV-positive women who had been diagnosed during pregnancy. AIDS Care 25:6, pages 695-701.
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BrendanP. Lucey, DavidB. Clifford, Jason Creighton, RobertR. Edwards, JustinC. McArthur & Jennifer Haythornthwaite. (2011) Relationship of depression and catastrophizing to pain, disability, and medication adherence in patients with HIV-associated sensory neuropathy. AIDS Care 23:8, pages 921-928.
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C Narasimooloo, SS Naidoo & BM Gaede. (2011) Adequacy of pain management in HIV-positive patients. South African Family Practice 53:1, pages 71-76.
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P. K. Nicholas, J. K. Kemppainen, G. E. Canaval, I. B. Corless, E. F. Sefcik, K. M. Nokes, C. A. Bain, K. M. Kirksey, L. Sanzero Eller, P. J. Dole, M. J. Hamilton, C. L. Coleman, W. L. Holzemer, N. R. Reynolds, C. J. Portillo, E. H. Bunch, D. J. Wantland, J. Voss, R. Phillips, Y.-F. Tsai, M. Rivero Mendez, T. G. Lindgren, S. M. Davis & D. M. Gallagher. (2007) Symptom management and self-care for peripheral neuropathy in HIV/AIDS. AIDS Care 19:2, pages 179-189.
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Articles from other publishers (16)

Tony V Pham, James Doorley, Martha Kenney, Jin Hui Joo, Amanda J Shallcross, Michael Kincade, Jonathan Jackson & Ana-Maria Vranceanu. (2023) Addressing chronic pain disparities between Black and White people: a narrative review of socio-ecological determinants. Pain Management 13:8, pages 473-496.
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Peter Puplampu, Vincent Ganu, Ernest Kenu, William Kudzi, Patrick Adjei, Leticia Grize & Michael Käser. (2019) Peripheral neuropathy in patients with human immunodeficiency viral infection at a tertiary hospital in Ghana. Journal of NeuroVirology 25:4, pages 464-474.
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Michael A. Owens, Romy Parker, Rachael L. Rainey, Cesar E. Gonzalez, Dyan M. White, Anooshah E. Ata, Jennifer I. Okunbor, Sonya L. Heath, Jessica S. Merlin & Burel R. Goodin. (2018) Enhanced facilitation and diminished inhibition characterizes the pronociceptive endogenous pain modulatory balance of persons living with HIV and chronic pain. Journal of NeuroVirology 25:1, pages 57-71.
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Whitney Scott, Chinar Arkuter, Kitty Kioskli, Harriet Kemp, Lance M. McCracken, Andrew S.C. Rice & Amanda C. de C. Williams. (2018) Psychosocial factors associated with persistent pain in people with HIV: a systematic review with meta-analysis. Pain 159:12, pages 2461-2476.
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Marcin Rzeszutek. (2017) Health-related quality of life and coping strategies among people living with HIV: the moderating role of gender. Archives of Women's Mental Health 21:3, pages 247-257.
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Romy Parker, Jennifer Jelsma & Dan J Stein. (2017) Pain in amaXhosa women living with HIV/AIDS: a cross-sectional study of ambulant outpatients. BMC Women's Health 17:1.
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Marcin Rzeszutek, Ewa Gruszczyńska & Ewa Firląg-Burkacka. (2017) Coping profiles and subjective well-being among people living with HIV: less intensive coping corresponds with better well-being. Quality of Life Research 26:10, pages 2805-2814.
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Mélanie Racine, Dwight E. Moulin, Warren R. Nielson, Patricia K. Morley-Forster, Mary Lynch, Alexander J. Clark, Larry Stitt, Allan Gordon, Howard Nathan, Catherine Smyth, Mark A. Ware & Mark P. Jensen. (2016) The reciprocal associations between catastrophizing and pain outcomes in patients being treated for neuropathic pain: a cross-lagged panel analysis study. Pain 157:9, pages 1946-1953.
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Montserrat Durán, Manuel García-Fernández, Juan Carlos Fernández & Beatriz Sanjurjo. (2016) Afrontamiento, estrés parental y calidad de vida de los cuidadores principales de personas TEA || Coping, parental stress and quality of life of primary caregivers of people with ASD. Revista de Estudios e Investigación en Psicología y Educación 3:1, pages 60-68.
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Gwenyth R. WallenKimberly R. MiddletonNancy AmesAlyssa T. BrooksDaniel Handel. (2014) Randomized Trial of Hypnosis as a Pain and Symptom Management Strategy in Adults with Sickle Cell Disease. Integrative Medicine Insights 9, pages IMI.S18355.
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Marinda Kotzé, Maretha Visser, Jenny Makin, Kathleen Sikkema & Brian Forsyth. (2012) Psychosocial Variables Associated with Coping of HIV-Positive Women Diagnosed During Pregnancy. AIDS and Behavior 17:2, pages 498-507.
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Abby L. Braden, James C. Overholser & Eden Silverman. (2011) Depression and Reasons for Living among Aids Patients: Protecting Quality of Life When the End is in Sight. The International Journal of Psychiatry in Medicine 41:2, pages 173-185.
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Karen O. Anderson, Carmen R. Green & Richard Payne. (2009) Racial and Ethnic Disparities in Pain: Causes and Consequences of Unequal Care. The Journal of Pain 10:12, pages 1187-1204.
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Lisa C. Campbell, Norah Andrews, Cindy Scipio, Brian Flores, Miriam H. Feliu & Francis J. Keefe. (2009) Pain Coping in Latino Populations. The Journal of Pain 10:10, pages 1012-1019.
Crossref
Inger Utne, Christine Miaskowski, Kristin Bjordal, Bruce A. Cooper, Berit T. Valeberg & Tone Rustøen. (2009) Confirmatory Factor Analysis of the Coping Strategies Questionnaire-Revised in Samples of Oncology Outpatients and Inpatients With Pain. The Clinical Journal of Pain 25:5, pages 391-400.
Crossref
Salimah H. Meghani & Arlene D. Houldin. (2007) The Meanings of and Attitudes About Cancer Pain Among African Americans. Oncology Nursing Forum 34:6, pages 1179-1186.
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