Occurrence of cholelithiasis in patients with sickle cell anemia: an integrative literature review

Authors

DOI:

https://doi.org/10.33448/rsd-v11i3.26868

Keywords:

Sickle cell anemia; Cholelithiasis

Abstract

Due to premature destruction of sickled erythrocytes, individuals with sickle cell anemia (SCA) are more likely to form gallstones through the accumulation of indirect bilirubin resulting from this hemolysis. Some risk factors, when present, may be associated with an increased prevalence and number of complications in the condition. In this sense, it is essential to recognize these relationships described, so that it is possible to avoid as much as possible the occurrence of cholelithiasis in SCA patients and to promote a better quality of life for them. Thus, the objective was to evaluate the risk factors and prevalence of cholelithiasis in SCA. This is an integrative literature review that searched for articles on the PubMed platform, using the descriptors "Sickle Cell Anemia" AND "Cholelithiasis" AND "Prevalence", in the time frame from 2010 to 2020. Of the 28 articles found, 16 were excluded by avoidance of the topic or impossibility of access to the full text. From the 12 selected articles, 2 thematic axes were identified: I) Risk factors for the development of cholelithiasis in SCA and II) Prevalence of cholelithiasis in SCA. relevance of risk factors and prevalence of cholelithiasis in SCA, it is essential to carry out prophylactic measures through an early diagnosis together with adequate guidance to the patient, in addition to further studies that enrich the knowledge already acquired on the subject in question.

References

Alhawsawi, Z. M., Alshenqeti, A. M., Alqarafi, A. M., Alhussayen, L. K., & Turkistani, W. A. (2019). Cholelithiasis in patients with paediatric sickle cell anaemia in a Saudi hospital. Journal of Taibah University Medical Sciences, 14(2), 187.

Alkindi, S. Y., Pathare, A., Al Zadjali, S., Panjwani, V., Wasim, F., Khan, H. & Alkindi, S. (2015). Serum total bilirubin, not cholelithiasis, is influenced by UGT1A1 polymorphism, alpha thalassemia and βs haplotype: first report on comparison between Arab-Indian and African βs genes. Mediterranean Journal of Hematology and Infectious Diseases, 7(1).

Al Talhi, Y., Shirah, B. H., Altowairqi, M., & Yousef, Y. (2017). Laparoscopic cholecystectomy for cholelithiasis in children with sickle cell disease. Clinical Journal of Gastroenterology, 10(4), 320-326.

Attalla, B. A. I., Karrar, Z. A., Ibnouf, G., Mohamed, A. O., Abdelwahab, O., Nasir, E. M., & Seed, M. A. (2013). Outcome of cholelithiasis in Sudanese children with Sickle Cell Anaemia (SCA) after 13 years follow-up. African Health Sciences, 13(1), 154-159.

Cawich, S. O., Arthurs, M., Murphy, T., Bonadie, K. O., Roberts, H. A., & Naraynsingh, V. (2015). Complications of ERCP for choledocholithiasis in a sickle cell cohort. Tropical Doctor, 45(1), 15-20.

Ercole, F. F., Melo, L. S., & Alcoforado, C. L. G. C. (2014). Revisão integrativa versus revisão sistemática. Revista Mineira de Enfermagem, 18 (1), 09-12.

Froed, A., Crespo, A., Quirino, B., Silva, C., de Matos, F., Belém, F., Ribeiro, L., & Santos, R. (2012). Colelitíase em paciente com doença falciforme. Revista Médica de Minas Gerais, 3.

Gumiero, A. P. S., Brandão, M. Â. B., Pinto, E. A. L. C., & Anjos, A. C. D. (2007). Colelitíase no paciente pediátrico portador de doença falciforme. Revista Paulista de Pediatria, 25(4), 377–381.

Hamad, Z., Aljedai, A., Halwani, R., & AlSultan, A. (2013). UGT1A1 promoter polymorphism associated with serum bilirubin level in saudi patients with sickle cell disease. Annals of Saudi Medicine, 33(4), 372-376.

Joly, P., Renoux, C., Lacan, P., Bertrand, Y., Cannas, G., Garnier, N., Cuzzubbo, D., Kebaili, K., Renard, C., Gauthier, A., Pialoux, V., Martin, C., Romana, M., & Connes, P. (2017). UGT 1A1 (TA) n genotype is not the major risk factor of cholelithiasis in sickle cell disease children. European Journal of Hematology, 98(3), 296-301.

McCarville, M. B., Rogers, Z. R., Sarnaik, S., Scott, P., Aygun, B., Hilliard, L., Lee, M. T., Kalinyak, k., Owen, W., Garro, J., Schultz, W., Yovetch, N., Ware, R. E., & SWiTCH Investigators. (2012). Effects of chronic transfusions on abdominal sonographic abnormalities in children with sickle cell anemia. The Journal of Pediatrics, 160(2), 281-285.

Oguntoye, O. O., Ndububa, D. A., Yusuf, M., Bolarinwa, R. A., & Ayoola, O. O. (2017). Hepatobiliary ultrasonographic abnormalities in adult patients with sickle cell anaemia in steady state in Ile-Ife, Nigeria. Polish Journal of Radiology, 82, 1.

Santos, C. M. D. C., Pimenta, C. A. D. M., & Nobre, M. R. C. (2007). A estratégia PICO para a construção da pergunta de pesquisa e busca de evidências. Revista Latino-Americana de Enfermagem, 15, 508-511.

Sarat, C. N. F., Ferraz, M. B., Ferreira, M. A., Corrêa, R. A. C., Souza, A. S. D., Cardoso, A. I. D. Q., & Ivo, M. L. (2019). Prevalência da doença falciforme em adultos com diagnóstico tardio. Acta Paulista de Enfermagem, 32, 202-209.

Seixas, M. O., Rocha, L. C., Carvalho, M. B., Menezes, J. F., Lyra, I. M., Nascimento, V. M., Couto. R. D., Atta, A. M., Reis, M. G., & Goncalves, M. S. (2010). Levels of high-density lipoprotein cholesterol (HDL-C) among children with steady-state sickle cell disease. Lipids in Health and Disease, 9(1), 1-9.

Silva, I. V., Reis, A. F., Palaré, M. J., Ferrão, A., Rodrigues, T., & Morais, A. (2015). Sickle cell disease in children: chronic complications and search of predictive factors for adverse outcomes. European Journal of Haematology, 94(2), 157-161.

Souza, M. T. D., Silva, M. D. D., & Carvalho, R. D. (2010). Revisão integrativa: o que é e como fazer. Einstein, 8, 102-106.

Sousa, L. M. M., Marques-Vieira, C. M. A., Severino, S. S. P., & Antunes, A. V. (2017). A metodologia de revisão integrativa da literatura em enfermagem. Revista Investigação em Enfermagem, 17.

Van Tuijn, C. F., Schimmel, M., van Beers, E. J., Nur, E., & Biemond, B. J. (2017). Prospective evaluation of chronic organ damage in adult sickle cell patients: A seven‐year follow‐up study. American Journal of hematology, 92(10), E584-E590.

Sundd, P., Gladwin, M. T., Novelli, E. M. (2018). Pathophysiology of Sickle Cell Disease. Annual Review of Pathology: Mechanisms of Disease, 14, 263-292.

Published

08/03/2022

How to Cite

NASCIMENTO, B. M. R. do .; ROCHA, M. F. de A. .; UCHÔA, S. M. .; MONTENEGRO, I. O. .; BARBOSA, N. M. .; OLIVEIRA, K. A. de; BEZERRA, R. E. de A. .; MENDES, A. L. de A. C. .; NORÕES, M. E. de A. T. .; LUCENA, A. B. de . Occurrence of cholelithiasis in patients with sickle cell anemia: an integrative literature review. Research, Society and Development, [S. l.], v. 11, n. 3, p. e58911326868, 2022. DOI: 10.33448/rsd-v11i3.26868. Disponível em: https://www.rsdjournal.org/index.php/rsd/article/view/26868. Acesso em: 25 apr. 2024.

Issue

Section

Review Article