Related Experiment Video
Updated: Jun 18, 2026

An Intestine/Liver Microphysiological System for Drug Pharmacokinetic and Toxicological Assessment
Published on: December 3, 2020
Pathophysiological changes that affect drug disposition in protein-energy malnourished children
Kazeem A Oshikoya1, Idowu O Senbanjo
1Pharmacology Department, Lagos State University College of Medicine, PMB 21266, Ikeja, Lagos, Nigeria. med_modhospital@yahoo.com.
Insights
Protein-energy malnutrition (PEM) in children alters drug metabolism, potentially requiring dosage adjustments. Further research is needed to confirm clinical relevance and establish safe drug dosages for treating this condition.
Area of Science:
- Pediatrics
- Public Health
- Pharmacology
Background:
- Protein-energy malnutrition (PEM) is a significant global health issue, particularly impacting children in developing nations.
- PEM is associated with high rates of childhood morbidity and mortality.
- Infections frequently complicate PEM, necessitating multiple drug treatments.
Purpose of the Study:
- To review the pathophysiological changes in children with PEM.
- To discuss how these changes affect drug disposition and metabolism.
- To highlight the need for therapeutic drug monitoring in PEM.
Main Methods:
- Literature review focusing on PEM pathophysiology and drug pharmacology.
- Analysis of existing studies on drug metabolism in malnourished pediatric populations.
- Synthesis of information regarding drug disposition alterations.
Main Results:
- Children with PEM exhibit abnormal drug disposition.
- These abnormalities suggest potential need for drug dosage modification.
- Current evidence for clinical relevance of dosage modification remains inconclusive.
Conclusions:
- Altered drug disposition in PEM may necessitate dosage adjustments.
- Further studies are required to confirm clinical relevance and establish precise drug dosages for safety.
- Rational and safe treatment of PEM requires understanding drug pharmacology and patient pathophysiology.
Abstract:
Protein-energy malnutrition (PEM) is a major public health problem affecting a high proportion of infants and older children world-wide and accounts for a high childhood morbidity and mortality in the developing countries. The epidemiology of PEM has been extensively studied globally and management guidelines formulated by the World Health Organization (WHO). A wide spectrum of infections such as measles, malaria, acute respiratory tract infection, intestinal parasitosis, tuberculosis and HIV/AIDS may complicate PEM with two or more infections co-existing. Thus, numerous drugs may be required to treat the patients. In-spite of abundant literature on the epidemiology and management of PEM, focus on metabolism and therapeutic drug monitoring is lacking. A sound knowledge of pathophysiology of PEM and pharmacology of the drugs frequently used for their treatment is required for safe and rational treatment. In this review, we discuss the pathophysiological changes in children with PEM that may affect the disposition of drugs frequently used for their treatment. This review has established abnormal disposition of drugs in children with PEM that may require dosage modification. However, the relevance of these abnormalities to the clinical management of PEM remains inconclusive. At present, there are no good indications for drug dosage modification in PEM; but for drug safety purposes, further studies are required to accurately determine dosages of drugs frequently used for children with PEM.
Related Concept Videos
Pharmacokinetics in Pediatric Patients: Drug Distribution
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Factors Affecting Protein-Drug Binding: Patient-Related Factors
Age stands as a key determinant in protein-drug binding. Neonates, characterized by low albumin content, experience heightened concentrations of unbound drugs such as phenytoin and...
Pharmacokinetics in Obese Patients: Drug Absorption and Distribution
Pharmacokinetics in Pediatric Patients: Drug Excretion