QUALITY-OF-LIFE OF 125 ADULTS SURVIVING 6-18 YEARS AFTER BONE-MARROW TRANSPLANTATION

Citation
Ne. Bush et al., QUALITY-OF-LIFE OF 125 ADULTS SURVIVING 6-18 YEARS AFTER BONE-MARROW TRANSPLANTATION, Social science & medicine, 40(4), 1995, pp. 479-490
Citations number
57
Categorie Soggetti
Social Sciences, Biomedical","Public, Environmental & Occupation Heath
Journal title
ISSN journal
02779536
Volume
40
Issue
4
Year of publication
1995
Pages
479 - 490
Database
ISI
SICI code
0277-9536(1995)40:4<479:QO1AS6>2.0.ZU;2-3
Abstract
Background: Recent studies examining the medical and psychosocial sequ elae of bone marrow transplantation have reported most survivors do re latively well while a smaller group continues to experience less than optimal quality of life (QOL). Many of these studies are limited by sm all sample sizes, limited scope, and focus on a narrow (1-4 year) wind ow of survival. Methods: The descriptive survey examined the QOL, late medical complications, psychological distress, demands of long-term r ecovery, and health perceptions of 125 adults surviving 6-18 (mean 10) years after marrow transplantation. Seven wide-ranging tests covering 271 items were completed on average in 90 min. Two tests were develop ed by the authors specifically for assessing QOL in this population. R esults: 74% of long-term survivors of bone marrow transplantation repo rted their current QOL was the same or better than before transplantat ion, 80% rated their current health status and QOL as good to excellen t, and 88% said the benefits of transplantation outweighted the side e ffects. Ten years or more post-transplantation, long-term survivors co ntinued to experience a moderate incidence of lingering complications and demands, including emotional and sexual dysfunction, fatigue, eye problems, sleep disturbance, general pain and cognitive dysfunction. H owever, the severity or degree of distress attributed to those complic ations was, for most survivors, consistently low. Nearly all were back to work or school. Only 5% rated both their QOL and health status as poor. Long-term survivors demonstrated good mood and low psychological distress compared to cancer and population norms, and had the same pe rceptions as the general population of their current health and expect ation of future health. Demands attributed to long-term survival appea red to impose little hardship. The most frequently cited demand of rec overy was the perceived lack of social support as time went on. Conclu sions: Almost all long-term survivors were leading full and meaningful lives. Persistent complications were, on the whole, dismissed as rela tively trivial and the overwhelming majority viewed themselves as cure d and well.