SICKLE CELL ANEMIA PATIENTS AND MENTAL DISTRESS: AN INTEGRATIVE REVIEW
DOI:
https://doi.org/10.56238/arev7n12-232Keywords:
Sickle Cell Anemia, Mental Health, Psychological Distress, Chronic Pain, Multidisciplinary ApproachAbstract
Sickle cell anemia, a chronic genetic disease and the most severe form of sickle cell disease, presents frequent pain crises and a complicated clinical picture with high mortality rates that cause great mental suffering. Given this, the present study aimed to verify, analyze, and synthesize the evidence found in the scientific literature on mental suffering in patients with sickle cell anemia, identifying the main psychological symptoms involved with the pathology and its course. This is an integrative literature review, conducted in April 2025. It included original articles published in the last ten years, in Portuguese, English, and Spanish. The selection followed the PRISMA guidelines. Studies conducted in Nigeria, the United States, and Ghana were included. The study identified that people with sickle cell anemia constantly suffer from anxiety, feelings of helplessness about the future, episodes of depression, isolation, and other symptoms that affect their mental health. Chronic pain and frequent hospitalizations negatively impact patients' daily lives, affecting school performance, professional integration, and social relationships. The selected studies showed that psychological symptoms are directly associated with increased pain frequency and intensity, worsening quality of life, and risk of opioid misuse. The review points to the need for further studies in this area and greater multidisciplinary involvement in the care of this population.
Downloads
References
ADELEKE, O.T. Et al. Unveiling the psychosocial and academic implications of living with sickle cell disease among undergraduates in a private university in Nigeria. Frontiers in Public Health, [S.l.], v. 13, 2025. DOI: https://doi.org/10.3389/fpubh.2025.1531161. Acesso em: 04 abril. 2025.
ALMEIDA R.A, BERETTA A.L.R.Z. Sickle Cell Disease and laboratory approach: a brief literature review. Revista Brasileira de Analise Clinicas, DOI: http://dx.doi.org/10.21877/2448-3877.201700530. Acesso em: 04 abril. 2025.
ANIM, M.T.; OSAFO, J.; YIRDON, F. Prevalence of psychological symptoms among adults with sickle cell disease in Korle-Bu Teaching Hospital, Ghana. BMC Psychology, [S.l.], v. 4, n. 1, p. 1–7, 2016. DOI: https://doi.org/10.1186/s40359-016-0162-z. Acesso em: 04 abril. 2025.
ARAÚJO, C. M.; FERREIRA, B. E. S.; MEIRA, M. S. J. N.; MUCUTA, N. J.; ANDRADE, R. R. G.; OLIVEIRA, T. H. C.; GONÇALVES, G. K. Conhecimento e prática de enfermagem no atendimento à doença falciforme e hemoglobinopatias na atenção primária. Texto & Contexto Enfermagem, Florianópolis, v. 32, e20220276, 2023. DOI: https://doi.org/10.1590/1980-265X-TCE-2022-0276pt. Acesso em: 3 ago. 2025.
BALLAS, S. K.; GUPTA, K.; ADAMS-GRAVES, P. Sickle cell pain: a critical reappraisal. Blood, v. 120, n. 18, p. 3647-3656, 1 nov. 2012 DOI: http://dx.doi.org/10.1182/blood-2012-04-383430. Acesso em: 10 ago. 2025.
BARRETO, F. J. N.; CIPOLOTTI, R. Sintomas depressivos em crianças e adolescentes com anemia falciforme. Jornal brasileiro de psiquiatria. v. 60, n. 4, 2011. DOI: https://doi.org/10.1590/S0047-20852011000400008. Acesso em: 18 jul. 2025.
CAMARGO, L. C.; CAMARGO, N. C.; COSTA, L. H. A.; LUCENA, J. B.; SILVA, M. S.; SOUSA, R. B. N. S. Transtorno depressivo e doença falciforme: o estado da arte. Psicologia e Saúde em Debate, v. 10, n. 1, p. 174-190, 2024 DOI: https://doi.org/10.22289/2446-922X.V10N1A11. Acesso em: 20 ago. 2025.
COSTA, J.L. et al. Experiências e estratégias de pessoas com doença falciforme no Distrito Federal: a ruptura biográfica. Ciência & Saúde Coletiva, Rio de Janeiro, v. 29, n. 3, e11782023, 2024. DOI: https://doi.org/10.1590/1413-81232024293.11782023.
Acesso em: 3 ago. 2025.
ESSIEN, E.A. et al. Psychosocial challenges of persons with sickle cell anemia: A narrative review. Medicine. 2023. DOI: https://doi.org/10.1097/MD.0000000000036147. Acesso em: 15 ago. 2025.
HARRIS, et al. Examining Mental Health, Education, Employment, and Pain in Sickle Cell Disease. Jama NetWork, v. 6, n. 5, May, p. e2314070, 2023. DOI: http://dx.doi.org/10.1001/jamanetworkopen.2023.14070. Acesso em: 04 abril. 2025.
JONASSAINT, C.R. et al. Mental health, pain and likelihood of opioid misuse among adults with sickle cell disease. Br J Haematol, v. 204, p. 1029-1038, 2024. DOI: https://doi.org/10.1111/bjh.19243. Acesso em: 18 ago. 2025.
LOPES, W. S. L.; MOREIRA, M. C. N.; GOMES, R. A experiência de adoecimento falciforme pelas lentes qualitativas. Ciência & Saúde Coletiva, Rio de Janeiro, v. 28, n. 9, p. 2489-2500, 2023. DOI: https://doi.org/10.1590/1413-81232023289.03812023. Acesso em: 3 ago. 2025.
MARQUES, L. N.; SOUZA, A. C. A.; PEREIRA, A. R. O viver com a doença falciforme: percepção de adolescentes. Revista de Terapia Ocupacional da Universidade de São Paulo, São Paulo, v. 26, n. 1, p. 109-117, jan./abr. 2015. DOI: https://doi.org/10.11606/issn.2238-6149.v26i1p109-117. Acesso em: 04 abril. 2025.
MASTANDREA, E. B.; LUCCHESI, F.; KITAYAMA, M. M. G.; FIGUEIREDO, M. S.; CITERO, V. A. The relationship between genotype, psychiatric symptoms and quality of life in adult patients with sickle cell disease in São Paulo, Brazil: a cross-sectional study. São Paulo Medical Journal, São Paulo, v. 133, n. 5, p. 421-427, 2015. DOI: https://doi.org/10.1590/1516-3180.2015.00171105. Acesso em: 3 ago. 2025.
MENDES, K. D. S.; SILVEIRA, R. C. C. P.; GALVÃO, C. M. Revisão integrativa: método de pesquisa para a incorporação de evidências na saúde e na enfermagem. Texto & Contexto Enfermagem, Florianópolis, v. 17, n. 4, p. 758–764, 2008. DOI: https://doi.org/10.1590/S0104-07072008000400018. Acesso em: 20 jul. 2025.
NAGEL, R. L. et al. Hematologically and genetically distinct forms of sickle cell anemia in Africa. The New England Journal of Medicine, v. 312, p. 880-884, 1985. DOI: https://doi.org/10.1056/NEJM198504043121403. Acesso em: 04 abril. 2025.
PELLEGRINO, B. C. P.; GALHARDI, M. P. W.; OLIVEIRA, E. H. B. M.; JÚNIOR, A. C. P. F.; CURCINO, D. R.; SOARES, T. M.; XAVIER, V. M. A.; RODRIGUES, R.; CAMPOS, F. L.; NAKAMURA, G. Y.; FARIAS, S. B.; ALVES, S. M. A. Doença falciforme e saúde pública: desafio para a assistência multiprofissional. Caderno Pedagógico, v. 22, n. 9, e18675, 2025. DOI: https://doi.org/10.54033/cadpedv22n9-451. Acesso em: 20 jul. 2025.
RAMSAY, Z. et al. Sickle Cell Disease and Pain: Is it all Vaso-occlusive Crises? Clinic Journal Pain, v. 37, n.8, p.583-590, 2021. DOI: http://dx.doi.org/10.1097/AJP.0000000000000949. Acesso em: 3 ago. 2025.
SEAKINS, M.; GIBBS, W. N.; MILNER, P. F.; BERTLES, J. F. Concentração de Hb-S em eritrócitos: um fator importante na baixa afinidade do sangue pelo oxigênio na anemia falciforme. The Journal of Clinical Investigation v. 52, p. 422-432, 1973. DOI: https://doi.org/10.1172/JCI107199. Acesso em: 3 ago. 2025.