Skip to main navigation Skip to search Skip to main content

Power of their stories: faces of kernicterus – experience and perception of caregivers and their children in Northern Nigeria

  • Z. L. Farouk
  • , T. M. Slusher
  • , A. Ali
  • , I. Abdulkadir
  • , U. M. Diala
  • , K. M. Satrom
  • , L. Hassan
  • , F. L. Abdullahi
  • , K. Gurama
  • , Y. N. Jibril
  • , S. Shehu
  • , P. U. Kanhu
  • , B. O. Toma
  • , N. H. Usman
  • , L. Remme
  • , F. Bode-Thomas
  • , S. Oguche
  • , W. N. Ogala
  • , V. K. Bhutani

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Our qualitative study was conducted to explore real-life experiences and challenges of caregivers and individuals with kernicterus spectrum disorder (KSD) in Northern Nigeria, where it remains a significant cause of neurological impairment. The lived experiences of affected individuals and their caregivers are largely undocumented. These stories of caregivers living with children with KSD and survivors with KSD highlight challenges and obstacles they face beyond bilirubin levels and quantitative measures. Methods: We conducted focus group discussions (FGDs; n=7), caregivers (n=54 or 6–8 per FGD) and case studies (n=4 individuals with KSD). Data were analysed using thematic analysis at three teaching hospitals in Northern Nigeria, all members of the Stop Kernicterus and Infection in Northern Nigeria+ collaborative. Caregivers with a child who had acute bilirubin encephalopathy and now has KSD and those living with KSD were interviewed. Results: Key features identified among caregivers were remarkably limited awareness of neonatal jaundice (NNJ) and its consequences, as well as reliance on traditional remedies, resulting in delays accessing care and pervasive stigma. Caregivers reported significant physical, long-term emotional and financial burdens, while individuals with KSD faced real-life challenges with mobility, communication and social inclusion. Despite these obstacles, participants demonstrated incredible resilience and inspiring aspirations. Conclusions: Our study highlights the lives and stories of caregivers and individuals affected by KSD and the urgent need for public health interventions that could prevent KSD through timely access to screening, diagnosis and treatment of NNJ. For those individuals who do progress to KSD, we need not only improved care and support for caregivers but also to value their stories, insisting they not be victimised but given every opportunity to achieve their dreams and full potential.

Original languageEnglish (US)
Article numbere004535
JournalBMJ Paediatrics Open
Volume10
Issue number1
DOIs
StatePublished - 2026

Bibliographical note

Publisher Copyright:
© Author(s) (or their employer(s)) 2026. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ Group. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: https://creativecommons.org/licenses/by-nc/4.0/.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 10 - Reduced Inequalities
    SDG 10 Reduced Inequalities

Keywords

  • Child Health
  • Jaundice
  • Low and Middle Income Countries
  • Neonatology
  • Qualitative research

PubMed: MeSH publication types

  • Journal Article

Fingerprint

Dive into the research topics of 'Power of their stories: faces of kernicterus – experience and perception of caregivers and their children in Northern Nigeria'. Together they form a unique fingerprint.

Cite this