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Impact of sickle cell disease on work activity
Rosana Paula Pires1, Mário Cézar Oliveira1, Lucio Borges Araújo2
1Agência Transfusional do Hospital de Clínicas, Universidade Federal de Uberlândia (UFU), Uberlândia, MG, Brazil.
Introduction:
Sickle cell disease is a group of conditions caused by anomalous hemoglobin that predisposes people to some clinical syndromes. Because of these recurrent syndromes, patients have difficulty finding and, often, keeping a job.
Objectives:
To evaluate the impact of sickle cell disease on the job situation of people with the condition.
Methods:
Thirty-two working-age people with sickle cell disease were recruited using the snowball sampling method and underwent semistructured interviews for demographic, socioeconomic, and clinical data collection.
Results:
Only 28.1% of the interviewees engaged in paid work, 46.9% had already worked but were not working at the time of the interview, and 25% had never worked. About 6% of participants lived in extreme poverty, and 28.4% lived on the poverty line. Monthly per capita income was less than one minimum salary in 56.2% of cases and less than 1.5 minimum salaries in 9.4%.
Conclusions:
Sickle cell disease has an important negative impact on employment situation, as about 70% of working-age people were inactive. This results in a high social cost represented by a very low monthly per capita income (≤ 1 minimum salary) in 93.7% of the participants.
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