Psychosocial impact of lymphedema: A systematic review of literature from 2004 to 2011

Mei R. Fu, Sheila H. Ridner, Sophia H. Hu, Bob R. Stewart, Janice N. Cormier, Jane M. Armer

研究成果: 雜誌貢獻文章

119 引文 (Scopus)

摘要

Objective This systematic review aimed to evaluate the level of evidence of contemporary peer-reviewed literature published from 2004 to 2011 on the psychosocial impact of lymphedema. Methods Eleven electronic databases were searched and 1311 articles retrieved; 23 met inclusion criteria. Twelve articles utilized qualitative methodology and 11 used quantitative methodology. An established quality assessment tool was used to assess the quality of the included studies. Results The overall quality of the 23 included studies was adequate. A critical limitation of current literature is the lack of conceptual or operational definitions for the concept of psychosocial impact. Quantitative studies showed statistically significant poorer social well-being in persons with lymphedema, including perceptions related to body image, appearance, sexuality, and social barriers. No statistically significant differences were found between persons with and without lymphedema in the domains of emotional well-being (happy or sad) and psychological distress (depression and anxiety). All 12 of the qualitative studies consistently described negative psychological impact (negative self-identity, emotional disturbance, and psychological distress) and negative social impact (marginalization, financial burden, perceived diminished sexuality, social isolation, perceived social abandonment, public insensitivity, and non-supportive work environment). Factors associated with psychosocial impact were also identified. Conclusions Lymphedema has a negative psychosocial impact on affected individuals. The current review sheds light on the conceptualization and operationalization of the definitions of psychosocial impact with respect to lymphedema. Development of a lymphedema-specific instrument is needed to better characterize the impact of lymphedema and to examine the factors contributing to these outcomes in cancer and non-cancer-related populations.

原文英語
頁(從 - 到)1466-1484
頁數19
期刊Psycho-Oncology
22
發行號7
DOIs
出版狀態已發佈 - 七月 2013
對外發佈Yes

指紋

Lymphedema
Sexuality
Psychology
Social Marginalization
Social Isolation
Affective Symptoms
Body Image
Social Change
Anxiety
Databases
Depression
Population
Neoplasms

ASJC Scopus subject areas

  • Oncology
  • Psychiatry and Mental health
  • Experimental and Cognitive Psychology

引用此文

Fu, M. R., Ridner, S. H., Hu, S. H., Stewart, B. R., Cormier, J. N., & Armer, J. M. (2013). Psychosocial impact of lymphedema: A systematic review of literature from 2004 to 2011. Psycho-Oncology, 22(7), 1466-1484. https://doi.org/10.1002/pon.3201

Psychosocial impact of lymphedema : A systematic review of literature from 2004 to 2011. / Fu, Mei R.; Ridner, Sheila H.; Hu, Sophia H.; Stewart, Bob R.; Cormier, Janice N.; Armer, Jane M.

於: Psycho-Oncology, 卷 22, 編號 7, 07.2013, p. 1466-1484.

研究成果: 雜誌貢獻文章

Fu, MR, Ridner, SH, Hu, SH, Stewart, BR, Cormier, JN & Armer, JM 2013, 'Psychosocial impact of lymphedema: A systematic review of literature from 2004 to 2011', Psycho-Oncology, 卷 22, 編號 7, 頁 1466-1484. https://doi.org/10.1002/pon.3201
Fu MR, Ridner SH, Hu SH, Stewart BR, Cormier JN, Armer JM. Psychosocial impact of lymphedema: A systematic review of literature from 2004 to 2011. Psycho-Oncology. 2013 7月;22(7):1466-1484. https://doi.org/10.1002/pon.3201
Fu, Mei R. ; Ridner, Sheila H. ; Hu, Sophia H. ; Stewart, Bob R. ; Cormier, Janice N. ; Armer, Jane M. / Psychosocial impact of lymphedema : A systematic review of literature from 2004 to 2011. 於: Psycho-Oncology. 2013 ; 卷 22, 編號 7. 頁 1466-1484.
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abstract = "Objective This systematic review aimed to evaluate the level of evidence of contemporary peer-reviewed literature published from 2004 to 2011 on the psychosocial impact of lymphedema. Methods Eleven electronic databases were searched and 1311 articles retrieved; 23 met inclusion criteria. Twelve articles utilized qualitative methodology and 11 used quantitative methodology. An established quality assessment tool was used to assess the quality of the included studies. Results The overall quality of the 23 included studies was adequate. A critical limitation of current literature is the lack of conceptual or operational definitions for the concept of psychosocial impact. Quantitative studies showed statistically significant poorer social well-being in persons with lymphedema, including perceptions related to body image, appearance, sexuality, and social barriers. No statistically significant differences were found between persons with and without lymphedema in the domains of emotional well-being (happy or sad) and psychological distress (depression and anxiety). All 12 of the qualitative studies consistently described negative psychological impact (negative self-identity, emotional disturbance, and psychological distress) and negative social impact (marginalization, financial burden, perceived diminished sexuality, social isolation, perceived social abandonment, public insensitivity, and non-supportive work environment). Factors associated with psychosocial impact were also identified. Conclusions Lymphedema has a negative psychosocial impact on affected individuals. The current review sheds light on the conceptualization and operationalization of the definitions of psychosocial impact with respect to lymphedema. Development of a lymphedema-specific instrument is needed to better characterize the impact of lymphedema and to examine the factors contributing to these outcomes in cancer and non-cancer-related populations.",
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