2018
DOI: 10.1590/0034-7167-2016-0409
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Quality of life in adults with sickle cell disease: an integrative review of the literature

Abstract: Selected studies have shown that patients with sickle cell disease have worse scores than the general population. These indicators should be instrumental to the nurse in the proposal of interventions and strategies of assistance and socio-educational, with a view to improving the quality of life of this clientele.

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Cited by 29 publications
(26 citation statements)
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“…The sociodemographic characteristics of the pre-final sample in this study on the PMQ were similar to those of other investigations of patients with sickle cell anemia, highlighting the prevalence of single women, low schooling levels, poor physical condition and associated diseases. This corroborates the studies of [29] and [30], revealing a significant effect on a number of phases of life [3, 31–33]. There were no significant differences in age and sex for PMQ scores, similarly to that observed by [19].…”
Section: Discussionsupporting
confidence: 92%
“…The sociodemographic characteristics of the pre-final sample in this study on the PMQ were similar to those of other investigations of patients with sickle cell anemia, highlighting the prevalence of single women, low schooling levels, poor physical condition and associated diseases. This corroborates the studies of [29] and [30], revealing a significant effect on a number of phases of life [3, 31–33]. There were no significant differences in age and sex for PMQ scores, similarly to that observed by [19].…”
Section: Discussionsupporting
confidence: 92%
“…This is consistent with previous studies in the United States, Brazil and other countries that have reported unemployment rates of 25-81% among SCD adults [22,23]. The frequent medical visits and hospitalizations, as well as pain episodes contribute to missing work days and potentially neurocognitive effects of SCD all likely to contribute to this finding [24]. Our study has limitations.…”
Section: Discussionsupporting
confidence: 91%
“…Sickle cell disease is characterized by chronic hemolysis, recurrent pain episodes (which are described as sickle cell-related pain crises or vaso-occlusive crises, multiorgan dysfunction, and premature death. If these crises can be minimized, the risk of death of SCD patients can be minimized as well (13,14). A bone marrow transplantation list has been declared by the Turkish Social Security Institution, who also define frequent painful crises as 3 or more painful attacks experienced a year, and rare painful crises as less than three painful attacks experienced a year (15).…”
Section: Discussionmentioning
confidence: 99%