Nursing care in pain management in children with sickle cell anemia: na integrative review
DOI:
https://doi.org/10.33448/rsd-v9i5.3353Keywords:
Nursing; Handling; Pain; Child; Anemia; Sickle Cell.Abstract
Objective: to analyze the nursing care strategies employed in pain management in children with sickle cell anemia. Method: integrative literature review on the topic in the virtual databases Scielo, Lilacs, PubMed, MEDLINE and BDENF in the months of January and February. Results: 17 articles were selected and two analytical categories were identified: knowledge of professionals and education of children and family members about the pathological process of pain and pharmacological and non-pharmacological treatment for pain management. Conclusions: as strategies for coping with pain in children, there is adequate pharmacological and non-pharmacological treatment, in addition to nursing knowledge that prevents complications, as well as the education of children and family members about the disease, which favors improvement and adaptation to symptoms.
References
Brasil. (2015). Doença falciforme: diretrizes básicas da linha de cuidado. Ministério da Saúde. Departamento de Atenção Especializada e Temática. Secretaria de Atenção à Saúde. Brasília (DF).
Carvalho, E.M.M.S., Santos, F.H.E.S. & Anjos, C.D. (2015). Doença falciforme nas pesquisas em enfermagem: uma revisão integrativa. Rev. baiana enferm. 29(1):86-93
Campelo, L.M.N., Oliveira, N.F., Magalhães, J.M., Julião, A.M.S., Amorim, F.C.M. & Coelho, M.C.V.S. (2018). The pain of children with sickle cell disease: the nursing approach. Rev. bras. enferm. 71(Suppl 3):1381-7.
Sousa EQ, Sales AA, Santos CVS, Andrade SM, Neto MPL & Oliveira EH. (2020). Use of hydroxyurea in sickle cell anemia: a literature review. Research, Society and Development. 9(2):e102922058.
Soares, A.B., Gobbi, D.R., Silva, G.D., Siqueira, I.C.G.L. & Cruz, M.P. (2012). A assistência de enfermagem em crianças e adolescentes portadores de anemia falciforme. Rev. recien. 2(5):5-10.
Miranda, F.P. & Brito, M.B. (2016). Assistência multidisciplinar ao paciente com anemia falciforme na internação de crises álgicas: uma revisão integrativa. Rev. enfer. contemp. 5(1):143-150.
Brasil. (2016). Internações, valor total segundo região/ Unidade da federação. (2016). Tratamento de anemias aplásticas e outras anemias no período de Jan. 2016. Ministério da Saúde. Tecnologia de Informação a Serviço do SUS (DATASUS). Brasília (DF).
Tanabe, P., Dias, N. & Gorman, L. (2013). Care of children with sickle cell disease in the emergency department: parent and provider perspectives inform quality improvement efforts. J. pediatr. oncol. nurs. 30(4):205–217.
Brigida, E.C.S.S., Andrade, G.C.F & Araújo, R.B.S. (2018). Humanization of nursing in the neonatal intensive theapy unit (NICU) Journal of specialist. 2(2):2-12.
Ercpe, F.F., Melo, L.S. & Alcoforado, C.L.G.C. (2014). Integrative review versus systematic review. REME rev. min. enferm. 18(1): 09-11.
Botelho, L.L.R., Cunha, C.C.A. & Macedo M. (2011). O método da revisão integrativa nos estudos organizacionais. Gestão e sociedade. 5(11):121-36.
Campelo, L.M.N., Oliveira, N.F., Magalhães, J.M., Julião, A.M.S., Amorim, F.C.M. & Coelho, M.C.V.S. (2018). The pain of children with sickle cell disease: the nursing approach. Rev. bras. enferm. 71(suppl 3):1463-9.
Jacob, E., Duran, J., Stinson, J., Lewis, M.A. & Zeltzer, L. (2013). Remote monitoring of pain and symptoms using wireless technology in children and adolescents with sickle cell disease. J Am Assoc Nurse Pract. 25(1):42-54.
Souza, A.A.M., Ribeiro, C.A. & Borba, R.I.H. (2011). Ter anemia falciforme: nota prévia sobre seu significado para a criança expresso através da brincadeira. Rev. gaúch. enferm. 32(1):194-6.
Jayaram, A., Nagel, R.W. & Jasty, R. (2010). Impact of clinical pathway on quality of care in sickle cell patients. J. pediatr. hematol. oncol. 32(7):537-9.
Bernier, K.M., Strobel, M. & Lucas, R. (2018). Assessing the effect of an educational intervention on nurses' and patient care assistants' comprehension and documentation of functional ability in pediatric patients with sickle cell disease. J. pediatr. nurs. 13. pii:S0882-5963(17)30623-1.
Kato-Lin, Y.C., Krishnamurti, L., Padman, R. & Seltman, H.J. (2014). Does e-pain plan improve management of sickle cell disease associated vaso-occlusive pain crisis? a mixed methods evaluation. Int. j. med. inf. 83(11):814-24.
Silva, D.G. & Marques, I.R. (2007). Nursing interventions for patients with sickle cell during pain crisis. Rev bras. enferm. 60(3):327-30.
Turaç, A. & Rumeli Atici, Ş. (2016). Evaluation of the effectiveness of patient-controlled analgesia in children with sickle cell anemia from the perspective of healthcare professionals and parents. Agri. 28(3):150-154.
Rees, A.L. (2016). Hydroxyurea in pediatric patients with sickle cell disease: what nurses need to know. J pediatr. oncol. nurs. 33(5):339-44.
Graves, J.K. & Jacob, E. (2014). Pain, coping, and sleep in children and adolescents with sickle cell disease. J. child. adolesc. psychiatr. nurs. 27(3):109-20.
Pack-Mabien, U. & Haynes, J.J. (2009). A primary care provider's guide to preventive and acute care management of adults and children with sickle cell disease. J. Am. Acad. Nurse Pract. 21(5):250-7.
Carvalho, E.M.M.S., Santo, F.H.E., Izidoro, C., Santos, M.L.S.C. & Santos, R.B. (2016). Nursing care to people suffering with sickle cell disease in emergency unit. Ciênc. cuid. saúde. 15(2):328-335.
Tavares, N.B.F., Nascimento, N.M.A., Neto, R.T.L., Junior, J.C. & Christofolini. (2017). Self-care practice in people with sickle cell anemia. Rev. bras. promoç. saúde. 30(4):1-7.
Carvalho, E.M.M.S., Santo, F.H.E. & Anjos, C. (2015). Sickle cell research in nursing: an integrative review. Rev. baiana enferm 29(1):86-93.
Jacob, E., Childress, C. & Nathanson, J.D. (2016). Barriers to care and quality of primary care services in children with sickle cell disease. J. adv. nurs. 72(6):1417-29.
Lakkakula, B.V.K.S., Sahoo, R., Verma, H. & Lakkakula, S. (2018). Pain management issues as part of the comprehensive care of patients with sickle cell disease. Pain manag. nurs. 19(6):558-572.
Jacob, E., Miaskowski, C., Savedra, M., Beyer, J.E., Treadwell, M. & Styles, L. (2006). Changes in sleep, food intake, and activity levels during acute painful episodes in children with sickle cell disease. J. pediatr. nurs. 21(1):23-34.
Filho, N.A. & Rouquayrol, M.Z. (2006). Introdução à Epidemiologia (4th ed.). Rio de Janeiro (RJ): Guanabara Koogan.
Orem, D.E. (2001). Nursing: concepts of pratice (6th ed.). St Louis: Mosby.
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