Quality of life of lower limb amputees’ caregivers

Authors

  • Marcos Henrique Dall´Aglio Foss Fisioterapeuta, Departamento de Ciências Neurológicas da Faculdade de Medicina de Rio Preto – FAMERP, São José do Rio Preto-SP, Brasil
  • Marielza R Ismael Martins Terapeuta Ocupacional, Doutora, Departamento de Ciências Neurológicas da Faculdade de Medicina de Rio Preto – FAMERP, São José do Rio Preto-SP, Brasil.
  • Mariana I Dias Martins Acadêmica de Medicina da Universidade do Vale do Sapucaí - UNIVAS, Pouso Alegre-MG, Brasil
  • José Maria Pereira Godoy

DOI:

https://doi.org/10.34024/rnc.2009.v17.8597

Keywords:

Caregivers, Quality of Life, Amputation

Abstract

Introduction. The amputation of lower limbs is still one of the major public health problems in Brazil. The process of rehabilitation means that the dependence of these patients is increasing, requiring almost all of the caregivers. Objective. To evaluate the quality of life of family caregivers of patients with amputation. Method. It is a prospective study and random 87 Caregivers of lower limb amputees of vascular surgery at the clinic of an School Hospital. We used the Caregiver Burden Scale (CBE) to evaluate the quality of the caregiver burden and a semi-structured for characterization of the family caregiver and the patient. Results. The caregivers were, in their majority, women (83.3%), married (65.2%), with mean age of 40.5 years. As a spouse (54.6%) and mothers (32.1%) and were moderately burdened (CBE total =2.33). The variables general tension, isolation and emotional involvement were below the median in 41 caregivers (47.5%) and disappointment and environment in 39 patients (45%). General tension and isolation versus emotion and emotion versus environment showed association (p <0.05). Conclusion. This study provides subsidies will team showing that effective public policies are necessary, to provide a network of support services for improving the quality of life for all.>

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References

Gamba MA, Gotlieb SLD, Bergamaschi DP, Vianna LAC. Amputações de extremidades inferiores por diabetes mellitus: estudo caso-controle. Rev Saúde Pub 2004;38(3):399-404

Buzato MAS, Tribulatto EC, Costa SM, Zorn WGW. Amputados de membros inferiores: a condição dos pacientes dois anos depois. Med Circ 2001; 128(4):111-9.

Chamlian TR, Masiero D. Perfil epidemiológico dos pacientes amputados tratados no Centro de Reabilitaçäo Lar Escola Säo Francisco. Acta Fisatr 1998;5(1):38-42.

Zarit SH, Todd P, Zarit J. Subjective burden of husbands and Wives as caregivers: a longitudinal study. Gerontol 1986;2:260-6.

Fink SV. The Influence of family resources and family demands on the strains and well being of caregiving families. Nurs Res 1995;44(3):139-46.

Holmes D, Terese J, Holmes M, Bergman S, King Y, Bentur N. Informal vesus formal supports for impaired elderly people: determinants of choice on Israli Kibbutzin. Gerontol 1989;29:195-202.

Freitas MC, Santana ME. Implementaçäo da estratégia de ensino-aprendizagem à família de paciente crônico. Rev Bras Enferm 2002;55(2): 146-50.

Belasco AGS. Qualidade de vida dos cuidadores de pacientes com insuficiência renal crônica em hemodiálise (Tese). São Paulo: UNIFESP, 2002, 84 p.

Albuquerque SMLA. Qualidade de vida: diferentes concepções. In: Albuquerque SMLA. Qualidade de vida do idoso. São Paulo: Casa do Psicólogo, 2003, 53-64.

Amendola F. Qualidade de vida de cuidadores de familiares de pacientes com perdas funcionais e dependência atendidos pelo PSF(Dissertação). São Paulo: USP, 2007, 142p.

Medeiros MMC, Ferraz MB, Quaresma MR. The Caregiver Burden Scale: a Brazilian cultural adaptation and validation. Braz J Rheumatol 1998;38:193-9.

Watanabe HAW, Dernt AM. Cuidadores de idosos: uma experiência em UBS. Rev Mun Sau 2005;29(4):639-44.

Juarez G, Ferrell B, Uman G, Podnos Y, Wagman LD. Distress and quality of life concerns of family caregivers of patients undergoing palliative surgery. Cancer Nurs 2008;31(1):2-10.

Faro ACM. Cuidar do lesado medular em casa: a vivência singular do cuidado familiar (Dissertação). São Paulo: USP, 1999, 127p.

Bromberg MB. Assessing quality of life in ALS. J Clin Neuromuscul Dis 2007;9(2):318-25.

Sorrell JM. Caring for the caregivers.J Psychosoc Nurs Ment Health Serv 2007; 45(11):17-20.

Simonelli C, Tripodi F, Rossi R, Fabrizi A, Lembo D, Cosmi V, et al. The influence of caregiver burden on sexual intimacy and marital satisfaction in couples with an Alzheimer spouse. Int J Clin Pract 2007;62(1):47-52.

Duayer MF, Oliveira MAC. Cuidados domiciliarios no SUS: uma resposta as necessidades especiais de pessoas com perdas funcionais e dependência. Rev Saúde Deb 2003;12:23-8.

Published

2009-03-31

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Section

Artigos Originais

How to Cite

1.
Foss MHD, Martins MRI, Martins MID, Godoy JMP. Quality of life of lower limb amputees’ caregivers. Rev Neurocienc [Internet]. 2009 Mar. 31 [cited 2025 Dec. 13];17(1):8-13. Available from: https://periodicos.unifesp.br/index.php/neurociencias/article/view/8597