Clinico-biochemical profile of sick children with severe acute malnutrition

Dhilip Kumar1, Sunil Kumar Rao2, Tej Bali Singh3

  • 1Resident Pediatrics, IMS, BHU, Uttar Pradesh, India.

Insights

Edematous malnutrition, a severe form of acute malnutrition, is common in young children and associated with higher risks of death and medical complications. This study details the clinical and biochemical profiles of these children.

Area of Science:

  • Pediatrics
  • Nutritional Science
  • Clinical Medicine

Background:

  • Severe acute malnutrition (SAM) presents with edematous and marasmic phenotypes.
  • Kwashiorkor is the most severe form of edematous malnutrition.
  • Understanding the clinico-biochemical profile of SAM is crucial for effective management.

Purpose of the Study:

  • To describe the clinico-biochemical profile of sick children diagnosed with severe acute malnutrition.
  • To compare the characteristics of edematous versus non-edematous malnutrition in children.

Main Methods:

  • A descriptive, cross-sectional study involving 122 children aged 6-60 months meeting WHO criteria for SAM.
  • Data collected included demographics, anthropometry, clinical history, and physical examination.
  • Biochemical investigations included blood gas analysis, serum electrolytes, calcium, albumin, and blood sugar.

Main Results:

  • 65% of children had edematous malnutrition, predominantly in younger children (25.7 vs. 34.5 months).
  • Edematous malnutrition was linked to higher rates of pneumonia, gastroenteritis, hyponatremia, metabolic acidosis, and hypocalcemia.
  • Children with edematous malnutrition faced a 1.3-1.4 times higher risk of death or leaving against medical advice.

Conclusions:

  • Edematous malnutrition is prevalent in children aged 1-3 years.
  • Clinical and biochemical abnormalities are frequent comorbidities in edematous malnutrition.
  • Prompt recognition and management of edematous malnutrition are vital to reduce mortality.
Abstract

Related Concept Videos

Overview of Protein Metabolism01:21

Overview of Protein Metabolism

Proteins are broken down into amino acids during digestion. Unlike fats and carbohydrates, which are stored for later use, proteins are not. Instead, amino acids are either used to produce ATP through oxidation or contribute to the creation of new proteins for the growth and repair of the body. Any surplus amino acids from the diet are converted into glucose or triglycerides rather than excreted.
Amino acids play various roles in the body once they are absorbed into cells. They are restructured...
3.2K
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption01:23

Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption

Understanding the physiological differences in the pediatric population is crucial for effective pharmacotherapy. Neonates, infants, and children exhibit significant variations in gastric pH, gastric emptying time, intestinal transit time, and biliary function. These variations profoundly affect oral drug absorption, necessitating a nuanced approach to pediatric dosing.Neonates present with a unique physiological profile, having a gastric pH greater than 4 and faster and more irregular gastric...
147
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
111
Inborn Errors of Metabolism01:20

Inborn Errors of Metabolism

Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
614