Sickle cell disease in Nigerian children: A cross-sectional study on parental awareness and home management of pain

Submitted: 11 January 2021
Accepted: 26 March 2021
Published: 14 April 2021
Abstract Views: 2348
PDF: 310
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Pain, being the clinical trademark of Sickle Cell Disease (SCD), impacts negatively on clinical outcome in children. However, little is known regarding parental home pain management in children with SCD. We aimed to determine the parental awareness, use and perceived efficacy of pain relief techniques for children with SCD. This is a cross-sectional study involving 80 parents of children with SCD seen at General Hospital, Bwari, North-Central Nigeria. An interview-based, structured questionnaire was used to obtain information on socio-demographic characteristics, clinical history, parental awareness, use and perceived effectiveness of pain relief techniques. Data analysis was with SPSS version 20. Seventy-six (95.0%) respondents were aware of available pain relief technique(s) in SCD. Fifty-four (67.5%) respondents used pain relief techniques, 33 (61.1%) of whom used multiple pain relief techniques. The most commonly used drugs and Complementary and Alternative Medicine (CAM) were nonsteroidal anti-inflammatory drugs (47.0%) and massage (36.0%) respectively. Thirty-three (61.1%) respondents perceived their selected techniques as effective. A higher proportion (27.3%) of the children with multiple hospitalizations used multiple pain relief techniques when compared with 4.8% who used drugs alone (p=0.038). However, there was no significant difference based on age, gender, maternal education, genotype, age at diagnosis, pain episodes, regularity of routine drugs and packed cell volume of the children and pain relief techniques used (p>0.05). This study found high parental awareness and utilization of home pain relief techniques for children with SCD. The use of multiple pain relief techniques was influenced by multiple hospitalizations of the children.

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Citations

WHO Regional Office for Africa. Sickle-cell disease: a strategy for the WHO African region: report of the regional director (AFR/RC60/68). Geneva, Switzerland: World Health Organization; 2010.
Wastnedge E, Waters D, Patel S, et al. The global burden of sickle cell disease in children under five years of age: a systematic review and meta-analysis. J Glob Health 2018;8:021103. DOI: https://doi.org/10.7189/jogh.08.021103
Federal Ministry of Health. National guideline for the control and management of sickle cell disease. Nigeria: FMOH 2014; pp. 1-61.
Piel FB, Patil AP, Howes RE, et al. Global epidemiology of sickle haemoglobin in neonates : a contemporary geostatistical model-based map and population estimates. Lancet 2013;381:142–51. DOI: https://doi.org/10.1016/S0140-6736(12)61229-X
Piel FB, Hay SI, Gupta S, et al. Global burden of sickle cell anaemia in children under five, 2010-2050: modelling based on demographics, excess mortality, and interventions. PLoS Med 2013;10:e1001484. DOI: https://doi.org/10.1371/journal.pmed.1001484
Inusa BP, Daniel Y, Lawson JO, et al. Sickle cell disease screening in northern Nigeria: the co-existence of Β- Thalassemia inheritance. Pediatr Therapeut 2015;5:262-5. DOI: https://doi.org/10.4172/2161-0665.1000262
Nwogoh B, Adewoyin A, Iheanacho O, et al. Prevalence of haemoglobin variants in Benin City, Nigeria. Ann Biomed Sci 2012;11:60–4.
Diwe K, Iwu AC, Uwakwe K, et al. Prevalence and patterns of sickle cell disease among children attending tertiary and non-tertiary health care institutions in a South Eastern State, Nigeria: A 10 year survey. J Res Med Dent Sci 2017;4:183–9. DOI: https://doi.org/10.5455/jrmds.2016432
Adewoyin AS. Management of sickle cell disease: a review for physician education in Nigeria (Sub-Saharan Africa). Anemia 2015;2015:7914981. DOI: https://doi.org/10.1155/2015/791498
Williams H, Tanabe P. Sickle Cell Disease: A review of non-pharmacological approaches for pain. HHS Public Access 2017;51:163–77.
Al-Jafar H, Al-Feeli A, Alozairi A. Non-Conventional pain management for sickle cell disease. Ann Hematol Oncol 2017;4:1161. DOI: https://doi.org/10.26420/annhematoloncol.2017.1161
WHO. WHO guidelines on the pharmacological treatment of persisting pain in children with medical illnesses. 2012. Accessed: Mar 2019. Available from: https://www.ncbi.nlm.nih.gov/books/NBK138354/
Mulumba LL, Wilson L. Sickle cell disease among children in Africa: An integrative literature review and global recommendations. Int J Africa Nurs Sci 2015;3:56–64. DOI: https://doi.org/10.1016/j.ijans.2015.08.002
Nwogoh B, Ofovwe CE, Omoti CE. Health-related quality of life in sickle cell disease subjects in Benin City, Nigeria. Afr J Med Health Sci 2016;15:80-85. DOI: https://doi.org/10.4103/2384-5589.197965
Federal Ministry of Health. Guidelines for the management of pain in Nigeria. Nigeria: FMOH 2018; pp. 1–92.
National Heart Lung, and Blood Institute. Evidence-based management of sickle cell disease. Expert panel report, 2014. Accessed: Apr 2019. Available from: http://www.nhlbi.nih.gov/sites/www.nhlbi.nih.gov/files/sickle-cell-disease-report.pdf
Oshikoya KA, Edun B, Oreagba IA. Acute pain management in children with sickle cell anaemia during emergency admission to a teaching hospital in Lagos, Nigeria. S Afr J Child Health 2015;9:119–23. DOI: https://doi.org/10.7196/SAJCH.2015.v9i4.968
Po C, Colombatti R, Cingliano A, et al. The management of sickle cell pain in the emergency department: a priority for health systems. Clin J Pain 2013;29:60–3. DOI: https://doi.org/10.1097/AJP.0b013e318245764b
National Bureau of Statistics. Annual abstract of statistics, 2016. Accessed: Mar 2019. Available from: https://www.nigerianstat.gov.ng/pdfuploads/ANNUAL ABSTRACT STATISTICS VOLUME-1.pdf
Olusanya O, Okpere E, Ezimokhai M. The importance of social class in voluntary fertility control in a developing country. West Afr J Med 1985;4:205–11.
Naing L, Winn T, Rusli BN. Practical issues in calculating the sample size for prevalence studies. Arch Orofac Sci 2006;1:9–14.
Hughes E, Jacobs B, Berman BN. In: Tierney L, SJ M, Papadakis M, editors. Complementary and alternative medicine in current medical diagnosis and treatment. McGraw-Hill: 2005; pp. 1696-1719.
Sibinga EMS, Shindell DL, Casella JF, et al. Pediatric patients with sickle cell disease: Use of complementary and alternative therapies. J Altern Complement. Med 2006;12:291–8.
Yoon SL, Black S. Comprehensive, integrative management of pain for patients. J Altern Complement Med 2006;12:995–1001. DOI: https://doi.org/10.1089/acm.2006.12.995
Busari AA, Mufutau MA. High prevalence of complementary and alternative medicine use among patients with sickle cell disease in a tertiary hospital in Lagos, South West, Nigeria. BMC Complement Altern Med 2017;17:299-306. DOI: https://doi.org/10.1186/s12906-017-1812-2
Majumdar S, Thompson W, Ahmad N, et al. The use and effectiveness of complementary and alternative medicine for pain in sickle cell anemia. Complement Ther Clin Pract 2013;19:184–7. DOI: https://doi.org/10.1016/j.ctcp.2013.05.003
Thompson WE, Eriator I. Pain control in sickle cell disease patients: Use of complementary and alternative medicine. Pain Med 2014;15:241–6. DOI: https://doi.org/10.1111/pme.12292
Smith K, Reinman L, Schatz J, Roberts CW. Parent perspectives on pain management in preschool-age children with sickle cell disease. J Pediatr Oncol Nurs 2018;35:16-24. DOI: https://doi.org/10.1177/1043454217735829
Oshikoya KA, Senbanjo IO, Njokanma OF, et al. Use of complementary and alternative medicines for children with chronic health conditions in Lagos, Nigeria. BMC Complement Altern Med 2008;8:66-73. DOI: https://doi.org/10.1186/1472-6882-8-66
Ahmadi M, Ilkhani M, Beiranvand S, et al. Massage for pain management in patients with sickle cell disease: a review study. J Chronic Dis Care 2018; 7:e62315. DOI: https://doi.org/10.5812/jjcdc.62315

How to Cite

Afolabi, O. F., & Esomonu, S. N. (2021). Sickle cell disease in Nigerian children: A cross-sectional study on parental awareness and home management of pain. Annals of Clinical and Biomedical Research, 2(1). https://doi.org/10.4081/acbr.2021.131