A medication diary-book for pediatric patients with acute lymphoblastic leukemia in Indonesia

Mei N Sitaresmi1, Saskia Mostert, Chad M Gundy

  • 1Department of Pediatrics, Dr Sardjito Hospital, Yogyakarta, Indonesia.

Insights

A medication diary improved event-free survival for children with acute lymphoblastic leukemia (ALL) in Indonesia, especially when mothers had higher education. This tool may enhance outcomes in resource-limited settings.

Area of Science:

  • Pediatric Oncology
  • Hematology
  • Public Health

Background:

  • Event-free survival (EFS) for pediatric acute lymphoblastic leukemia (ALL) in Yogyakarta, Indonesia was critically low at 20%.
  • Addressing low survival rates in childhood ALL is a significant challenge, particularly in resource-limited settings.

Purpose of the Study:

  • To evaluate the effectiveness of a medication diary-book intervention on the treatment outcomes of childhood ALL.
  • To assess the impact of the diary on event-free survival (EFS) in pediatric ALL patients.

Main Methods:

  • A randomized controlled trial involving 109 pediatric ALL patients in Yogyakarta, Indonesia.
  • Intervention group received a medication diary alongside standard care (parental education, donated chemotherapy); control group received standard care only.
  • Event-free survival (EFS) at 3 years was the primary outcome measure.

Main Results:

  • Pediatric ALL patients with highly educated mothers showed significantly improved 3-year EFS in the intervention group (62%) compared to the control group (29%, P=0.04).
  • No significant difference in 3-year EFS was observed between intervention (26%) and control (18%) groups for patients with less educated mothers (P=0.86).

Conclusions:

  • A medication diary-book intervention shows potential to improve survival for pediatric ALL patients in resource-limited settings.
  • The intervention's effectiveness appears particularly pronounced in children whose mothers have higher educational attainment.
Abstract

Related Concept Videos

Pharmacokinetics in Pediatric Patients: Drug Excretion01:26

Pharmacokinetics in Pediatric Patients: Drug Excretion

In pediatric medicine, understanding the renal function and drug elimination nuances is crucial for administering safe and effective treatments. Newborns, in particular, display markedly slower renal functions than adults, profoundly affecting how drugs are cleared from their bodies. This slower drug clearance requires clinicians to extend the dosing intervals for many medications to prevent drug accumulation and toxicity while ensuring therapeutic efficacy.One key area where these adjustments...
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 a challenge in...
Pharmacokinetics in Pediatric Patients: Drug Distribution01:17

Pharmacokinetics in Pediatric Patients: Drug Distribution

Drug distribution in the pediatric population exhibits unique challenges and considerations due to the physiological differences between children, particularly neonates and infants, and adults. A crucial aspect of pediatric pharmacology is understanding how these differences impact the pharmacokinetics of various drugs, necessitating age-specific dosing strategies to ensure efficacy and safety.Neonates and infants have a higher total body water content, ~75%–90% of their body weight, compared...