A cautionary tale of pediatric paracetamol poisoning in a low-resource setting in Kenya: a case report and review of the literature

Paracetamol has a wide safety margin at therapeutic doses but overdose may cause life-threatening hepatotoxicity particularly in children. We report a case of a 3-year-old African female who presented to Malindi Sub County Hospital (MSCH) with severe dehydration, pneumonia, and convulsions. A detailed clinical history from her grandmother and medication reconciliation at the hospital revealed that she had inadvertently received a 5000 mg supratherapeutic dose of paracetamol over 48 h. Liver function tests (LFTs) showed marked amino transferases (peak ALT: 1566.2 IU/L, AST: 302.3 IU/L), rising gamma-glutamyl transferase (GGT) and hypoalbuminemia. Clinical coagulopathy was suspected based on blood oozing at the cannula site and epistaxis triggered by nasogastric tube insertion. Given the resource-limited nature of MSCH, measurements on serum paracetamol, international normalized ratio (INR), and prothrombin time (PT) were not done prompting empirical administration of fresh frozen plasma (FFP). N-acetylcysteine (NAC) was initiated more than 84 h after paracetamol exposure due to regional stockouts and barriers in procurement. Despite this delay, patient liver enzymes improved rapidly (ALT: 431.1 IU/L, AST: 105.6 IU/L) and she regained consciousness several hours post-NAC administration. This case report highlights how system failures in a resource-limited setting may compromise the management of paracetamol poisoning. This case highlights how system failures such as medication errors, misdiagnosis, poor caregiver education, and limited antidote access in resource-limited healthcare settings may result in sub-optimal care in pediatric paracetamol poisoning. Proper history taking, patient examination, and medication reconciliation are key in managing suspected paracetamol poisoning. Fortunately, even the late administration of N-acetylcysteine (> 24 h) abrogates severe hepatotoxicity in children with paracetamol poisoning. The close monitoring of liver function and clinical status is essential in managing pediatric paracetamol poisoning.

Authors

Institutions

Publication Details

Journal
Discover Toxicology
Published
2026-03-02
DOI
https://doi.org/10.1007/s44339-026-00047-z
Primary Topic
Drug-Induced Hepatotoxicity and Protection
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A cautionary tale of pediatric paracetamol poisoning in a low-resource setting in Kenya: a case report and review of the literature

Aisha A Mongi, Mitchel Okumu, David Mang’ong’o, Salma Naji et al.
Discover Toxicology
Drug-Induced Hepatotoxicity and Protection
article

A cautionary tale of pediatric paracetamol poisoning in a low-resource setting in Kenya: a case report and review of the literature

Aisha A Mongi, Mitchel Okumu, David Mang’ong’o, Salma Naji, Yusuf Rasheed
article en

Abstract

Paracetamol has a wide safety margin at therapeutic doses but overdose may cause life-threatening hepatotoxicity particularly in children. We report a case of a 3-year-old African female who presented to Malindi Sub County Hospital (MSCH) with severe dehydration, pneumonia, and convulsions. A detailed clinical history from her grandmother and medication reconciliation at the hospital revealed that she had inadvertently received a 5000 mg supratherapeutic dose of paracetamol over 48 h. Liver function tests (LFTs) showed marked amino transferases (peak ALT: 1566.2 IU/L, AST: 302.3 IU/L), rising gamma-glutamyl transferase (GGT) and hypoalbuminemia. Clinical coagulopathy was suspected based on blood oozing at the cannula site and epistaxis triggered by nasogastric tube insertion. Given the resource-limited nature of MSCH, measurements on serum paracetamol, international normalized ratio (INR), and prothrombin time (PT) were not done prompting empirical administration of fresh frozen plasma (FFP). N-acetylcysteine (NAC) was initiated more than 84 h after paracetamol exposure due to regional stockouts and barriers in procurement. Despite this delay, patient liver enzymes improved rapidly (ALT: 431.1 IU/L, AST: 105.6 IU/L) and she regained consciousness several hours post-NAC administration. This case report highlights how system failures in a resource-limited setting may compromise the management of paracetamol poisoning. This case highlights how system failures such as medication errors, misdiagnosis, poor caregiver education, and limited antidote access in resource-limited healthcare settings may result in sub-optimal care in pediatric paracetamol poisoning. Proper history taking, patient examination, and medication reconciliation are key in managing suspected paracetamol poisoning. Fortunately, even the late administration of N-acetylcysteine (> 24 h) abrogates severe hepatotoxicity in children with paracetamol poisoning. The close monitoring of liver function and clinical status is essential in managing pediatric paracetamol poisoning.

Discover ToxicologyVol. 3(1)
Maseno University (KE), University of the Free State (ZA), Pwani University (KE), Jaramogi Oginga Odinga University of Science and Technology (KE), Mariakani Cottage Hospital (KE), Moving the GoalPosts (KE)
No poverty
Openalex Percentile: Top 35%
Drug-Induced Hepatotoxicity and Protection
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.