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Review Article

The experience of amputation and prosthesis use for adults: a metasynthesis

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Pages 1133-1142 | Received 25 May 2012, Accepted 20 Aug 2012, Published online: 04 Oct 2012
 

Abstract

Purpose: To identify and synthesize qualitative literature on the experience of amputation and prosthesis use for adults, and to make recommendations based on these findings for rehabilitation services. Methods: A systematic search of three databases for qualitative research exploring the experience of amputation and prosthesis use for adults was undertaken. Included papers were evaluated using the Critical Appraisal Skills Programme (CASP) quality guidelines. Data were extracted and themes synthesized in accordance with accepted procedures for qualitative metasyntheses. Results: From the 15 papers (13 studies) included in there view, five concepts were identified: (i) Becoming an amputee and facing prosthesis use; (ii) Adjustment to and coping with amputation and prosthesis use; (iii) The role of valued relationships in recovery; (iv) Amputation and prosthesis use in social interaction; and (v) Prosthetically enabled identities. Conclusions: The findings provide a base from which to make suggestions regarding the provision of health rehabilitation services for this population. It is recommended that such services make greater use of psychological interventions and education, include patients’ social support networks, use psychotherapy to support and develop positive coping strategies, and facilitate peer support from those who have already made positive adjustments to amputation and prosthesis use.

Implications for Rehabilitation

  • Amputation of a limb and subsequent prosthesis use present major physical, psychological and social challenges.

  • Qualitative research on these topics is important in informing the design, organisation and delivery of health rehabilitation services which meet the needs of this population.

  • The findings of this systematic review indicate that rehabilitation for this group make greater use of psychological interventions and education, involve patients’ social support networks, use psychotherapy to support positive coping strategies, and provide peer support from patients who have already made positive adjustments.

Declaration of Interest: The authors report no conflicts of interest.

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