Literature DB >> 33664607

Determinants of Care-Seeking Practices for Children with Sickle Cell Disease in Ekiti, Southwest Nigeria.

Oladele Simeon Olatunya1,2, Adefunke Olarinre Babatola1,2, Adewuyi Temidayo Adeniyi1,2, Olubunmi Adeola Lawal3, Alaba Olanrewaju Daramola4, Tosin Anthony Agbesanwa5, Temitope Olumuyiwa Ojo6, Paul Oladapo Ajayi7, Adeleke Ajayi Ibijola8, Akinwumi Kolawole Komolafe2, Adekunle Adekile9.   

Abstract

BACKGROUND: Due to the chronic nature of sickle cell disease (SCD), affected individuals may seek help from diverse places thus raising the need to understand their health-seeking behavior (HSB) in order to design an appropriate management policy for them. AIM: The aim of this study was to evaluate the HSB among pediatric SCD patients relative to their non-SCD counterparts attending a tertiary facility in Southwest Nigeria and identified predictors of poor HSB among SCD patients.
METHODS: A total of 110 children with SCD were recruited and studied for their HSPs which were compared with 110 non-SCD patients with other chronic medical conditions. Questionnaires were used to obtain self-reported information on participants' socio-demographic data and HSB. Logistic regression was used to determine the predictors of poor HSB among the SCD cohort.
RESULTS: More SCD patients received treatments at private hospitals, patent medicine stores and faith-based centers compared to their non-SCD counterparts (p=0.0052; 0.006; and 0.007), respectively. No difference was observed in the patronage of traditional care centres 10 (9.1%) vs 6 (5.5%). More SCD patients 61 (55.5%) vs 35 (31.8%) exhibited poor HSB (p=0.0004). SCD patients who were not enrolled on health insurance scheme were 18 times more likely to have poor HSB (OR=18.38, 95% CI (4.41-76.57), p value= <0.0001) while absence of VOC within the preceding year reduces the risk of poor HSB by 91.5% (OR=0.085, 95% CI (0.028-0.258), p value= <0.0001).
CONCLUSION: SCD patients in the study locality had poor HSB. This raises the need for their education on proper HSB. More enrollment into health insurance scheme and the prevention of VOC will lessen the burden of poor HSB. The high patronage of non-hospital care facilities in this study raises the need for stakeholders to monitor activities and train the operators at these informal care centres.
© 2021 Olatunya et al.

Entities:  

Keywords:  Nigeria; health-seeking behavior; non-orthodox care; sickle cell disease

Year:  2021        PMID: 33664607      PMCID: PMC7921626          DOI: 10.2147/JBM.S294952

Source DB:  PubMed          Journal:  J Blood Med        ISSN: 1179-2736


  36 in total

Review 1.  Health seeking behaviour and health service utilization in Pakistan: challenging the policy makers.

Authors:  Babar T Shaikh; Juanita Hatcher
Journal:  J Public Health (Oxf)       Date:  2004-12-08       Impact factor: 2.341

2.  Current sickle cell disease management practices in Nigeria.

Authors:  N Galadanci; B J Wudil; T M Balogun; G O Ogunrinde; A Akinsulie; F Hasan-Hanga; A S Mohammed; M O Kehinde; J A Olaniyi; I N Diaku-Akinwumi; B J Brown; S Adeleke; O E Nnodu; I Emodi; S Ahmed; A O Osegbue; N Akinola; H I O Opara; S A Adegoke; J Aneke; A D Adekile
Journal:  Int Health       Date:  2013-10-10       Impact factor: 2.473

3.  Scarification in sub-Saharan Africa: social skin, remedy and medical import.

Authors:  Roland Garve; Miriam Garve; Jens C Türp; Julius N Fobil; Christian G Meyer
Journal:  Trop Med Int Health       Date:  2017-05-09       Impact factor: 2.622

Review 4.  Insight into the complex pathophysiology of sickle cell anaemia and possible treatment.

Authors:  Andrea Piccin; Ciaran Murphy; Elva Eakins; Maria Beatrice Rondinelli; Massimo Daves; Cinzia Vecchiato; Dominik Wolf; Corrina Mc Mahon; Owen P Smith
Journal:  Eur J Haematol       Date:  2019-02-21       Impact factor: 2.997

5.  Complementary and alternative medicines use in children with epilepsy in Ibadan, Nigeria.

Authors:  I A Lagunju
Journal:  Afr J Med Med Sci       Date:  2013-03

6.  Understanding health seeking behavior.

Authors:  Simmi Oberoi; Neha Chaudhary; Siriesha Patnaik; Amarjit Singh
Journal:  J Family Med Prim Care       Date:  2016 Apr-Jun

7.  Haptoglobin Gene Polymorphism in Patients with Sickle Cell Anemia: Findings from a Nigerian Cohort Study.

Authors:  Oladele Simeon Olatunya; Dulcineia Martins Albuquerque; Magnun Nueldo Nunes Santos; Tolorunju Segun Kayode; Adekunle Adekile; Fernando Ferreira Costa
Journal:  Appl Clin Genet       Date:  2020-05-08

8.  Global epidemiology of sickle haemoglobin in neonates: a contemporary geostatistical model-based map and population estimates.

Authors:  Frédéric B Piel; Anand P Patil; Rosalind E Howes; Oscar A Nyangiri; Peter W Gething; Mewahyu Dewi; William H Temperley; Thomas N Williams; David J Weatherall; Simon I Hay
Journal:  Lancet       Date:  2012-10-25       Impact factor: 79.321

9.  Seeking care for epilepsy and its impacts on households in a rural district in southern Malawi.

Authors:  Alister Munthali; Stine H Braathen; Lisbet Grut; Yusman Kamaleri; Benedicte Ingstad
Journal:  Afr J Disabil       Date:  2013-09-30

10.  Perceptions and Practice of Early Diagnosis of Sickle Cell Disease by Parents and Physicians in a Southwestern State of Nigeria.

Authors:  Oladele Simeon Olatunya; Adefunke Olarinre Babatola; Ezra Olatunde Ogundare; Babatunde Ajayi Olofinbiyi; Olubunmi Adeola Lawal; Jacob Olumuyiwa Awoleke; Olusola Peter Aduloju; Alaba Olanrewaju Daramola; Eyitayo Ebenezer Emmanuel; Oyebanji Anthony Olajuyin; Akinwumi Kolawole Komolafe; Abiola Olukayode Olaleye
Journal:  ScientificWorldJournal       Date:  2020-05-31
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