Abstract

BackgroundNigeria has one of the highest child mortality rates in the world, with an estimated 750,000 deaths annually among children under age five. The majority of these deaths are due to pneumonia, malaria, or diarrhea. Many parents do not seek sick-child care from trained, biomedical providers, contributing to this high rate of mortality.MethodsThis qualitative study explores factors enabling or preventing parents from seeking care for sick under-five children in Nigeria’s Kogi and Ebonyi states, including gender-related roles and social norms. Interviews were conducted with parents of sick under-five children and service providers, and focus group discussions were held with community leaders to assess how care-seeking behavior was influenced by four modes from the Colvin et al. conceptual framework for household decision-making and pathways to care. These include (1) caregivers’ recognition and response to illness, (2) seeking advice and negotiating access within the family, (3) making use of community-based treatment options, and (4) accessing biomedical services.ResultsParents were found to have a general understanding of illness symptoms but did not always attribute illness to biomedical causes. Intra-household decision-making processes were shaped by gender dynamics between men and women, and were found to have great effects on decisions to seek care. Use of traditional medicine and self-treatment were found to be common first steps in treatment before turning to the biomedical care system. Once the decision to seek biomedical care was taken, the route of seeking care varied between seeking care at chemists and then continuing to health facilities or starting with a health facility and then accessing prescriptions from a chemist.ConclusionWe conclude that care-seeking decisions do not follow a linear process; that intra-household decision-making processes particularly among parents should not be underestimated in addressing sick-child care seeking; and that, given the role of mothers as primary caregivers, their knowledge in illness recognition and agency in care-seeking decision-making, and seeking biomedical care, is deserving of future study.

Highlights

  • Nigeria has one of the highest child mortality rates in the world, with an estimated 750,000 deaths annually among children under age five

  • We interviewed a total of 12 mothers; 12 fathers; three primary health center in-charges and three Patent and Proprietary Medicine Vendors (PPMV); and held two focus group discussions with eight to ten community leaders in each Local government authority (LGA)

  • We present findings based on the four modes identified in the Colvin et al framework that influence care-seeking behavior in response to child diarrhea, pneumonia, and malaria

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Summary

Introduction

Nigeria has one of the highest child mortality rates in the world, with an estimated 750,000 deaths annually among children under age five. The majority of these deaths are due to pneumonia, malaria, or diarrhea. Malaria and diarrhea are the leading causes of death in the post-natal period representing more than two-thirds of all post-natal child deaths [3, 4] These illnesses contribute to high levels of child morbidity, with an estimate of over eight million episodes of clinical pneumonia occurring annually in Nigeria [5]. According to the 2016–17 Nigeria Multiple Indicator Cluster Survey, less than a third of children whose mother reported symptoms of pneumonia, fever, or diarrhea in the 2 weeks prior to the survey received care from a biomedical provider, such as a nurse at the primary health center [6]

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