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Pediatric patient dosages diverge from adults due to disparities in body surface area, total body water, and extracellular fluid per kilogram of body weight. The dosing regimen considers the variations in pharmacokinetics and pharmacology across distinct age groups, encompassing preterm newborns, infants, young children, older children, and adolescents. Calculation of pediatric patient doses is predicated on determining body surface area, which exhibits a superior correlation with the child's...
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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...
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Primaquine overdose in a toddler.

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Accidental primaquine overdose in a child with undiagnosed glucose-6-phosphate dehydrogenase (G6PD) deficiency led to severe methemoglobinemia and hemolytic anemia. Treatment involved ascorbic acid and blood transfusion, highlighting the need for awareness in pediatric antimalarial toxicity.

Keywords:
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Area of Science:

  • Toxicology
  • Pediatrics
  • Pharmacology

Background:

  • Antimalarial drugs like primaquine can cause serious side effects, including methemoglobinemia and hemolytic anemia.
  • Glucose-6-phosphate dehydrogenase (G6PD) deficiency amplifies these risks, potentially leading to life-threatening conditions.
  • Methylene blue, a common treatment for methemoglobinemia, can exacerbate hemolysis in G6PD-deficient individuals.

Observation:

  • A toddler with undiagnosed G6PD deficiency experienced an accidental primaquine overdose.
  • The patient developed severe methemoglobinemia and hemolytic anemia within two days.
  • Initial treatment with methylene blue preceded the diagnosis of G6PD deficiency.

Findings:

  • The patient received subsequent treatment with ascorbic acid and a blood transfusion.
  • Clinical condition improved gradually, leading to successful discharge.
  • This case highlights a rare instance of mixed methemoglobinemia and hemolytic toxicity in a pediatric patient due to primaquine overdose and G6PD deficiency.

Implications:

  • Pediatric patients constitute the majority of primaquine overdose cases.
  • Accurate diagnosis and prompt management of antimalarial toxicity in children with G6PD deficiency are critical.
  • Clinicians must maintain a high index of suspicion for G6PD deficiency in pediatric patients presenting with symptoms of antimalarial toxicity.