Unbound MEDLINE

Health-related quality of life of patients receiving low-toxicity immunosuppressive regimens: a substudy of the Symphony study. Transplantation [Transplantation] Journal article

 
TitleHealth-related quality of life of patients receiving low-toxicity immunosuppressive regimens: a substudy of the Symphony study.
Author(s)Oppenheimer F, Rebollo P, Grinyo JM, Ortega F, Sanchez-Plumed J, Gonzalez-Molina M, Hernandez D, Anaya F, Ekberg H 
InstitutionRenal Transplant Unit, Hospital Clínico, Barcelona, Spain.
SourceTransplantation 2009 Apr 27; 87(8):1210-3.
MeSHAdrenal Cortex Hormones
Adult
Antibodies, Monoclonal
Creatinine
Cyclosporine
Dose-Response Relationship, Drug
Female
Follow-Up Studies
Health Status
Health Surveys
Humans
Immunoglobulin G
Immunosuppressive Agents
Kidney Transplantation
Male
Middle Aged
Mycophenolic Acid
Quality of Life
Time Factors
AbstractOBJECTIVE: To evaluate health-related quality of life (HRQoL) in patients with different low-toxicity regimens posttransplantation.
METHODS: One hundred fifty-six patients were randomized to standard-dose cyclosporine A (CsA), mycophenolate mofetil, and corticosteroids or daclizumab induction, mycophenolate mofetil, and corticosteroids with a low dose of CsA, tacrolimus (Low-Tac), or sirolimus. SF-36 Health survey was completed at baseline, 3, 6, and 12 months.
RESULTS: There were no differences between groups in SF-36 at baseline or at month 12. Low-Tac showed higher scores at month 3 than standard-dose CsA and low dose of CsA. Patients with serum creatinine less than or equal to 1.5 mg/mL had better HRQoL at 6 and 12 months. Proportion of these patients was higher in Low-Tac at 6 months. Physical component summary of Patients increased during follow-up, but mental component summary did not. Patients with acute rejection showed lower mental component summary at 6 months.
CONCLUSIONS: No HRQoL differences were identified among groups, but the low-dose Tac group showed the fastest improvement.
Languageeng
Pub Type(s)Journal Article
Multicenter Study
Research Support, Non-U.S. Gov't
PubMed ID19384168
  
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