Clinical Audit of Low Dose Prophylaxis Programme for Nigerian Children with Haemophilia

T U Nwagha1, H C Okoye1, C E Udo2

  • 1Department of Haematology and Immunology, College of Medicine, University of Nigeria, Ituku Ozalla Campus, Enugu, Nigeria.

Insights

Low dose prophylaxis significantly reduced joint bleeds and improved joint function in Nigerian children with haemophilia. This treatment enhances quality of life, despite limited access in developing countries.

Area of Science:

  • Pediatrics
  • Hematology
  • Public Health

Background:

  • Low-dose prophylaxis is a proven treatment for haemophilia.
  • Access to prophylaxis is limited for children in developing nations, including Nigeria.

Purpose of the Study:

  • To audit the effectiveness of low-dose prophylaxis in Nigerian children with haemophilia.
  • To assess improvements in joint bleeding, function, and quality of life.

Main Methods:

  • A multicentre clinical audit involving five Nigerian haemophilia treatment centers.
  • Eighteen children with haemophilia were enrolled in a low-dose prophylaxis program.
  • Data collected on joint bleeds, joint function, and quality of life over a median of 7 months.

Main Results:

  • A 74% overall reduction in joint bleeds was observed (162 to 42).
  • Joint function improved in 94.1% of affected joints.
  • School attendance, sports participation, and daily activities showed moderate to significant improvements.

Conclusions:

  • Low-dose prophylaxis is beneficial for reducing joint bleeds in Nigerian children with haemophilia.
  • The treatment improves joint function and overall quality of life.
  • This highlights the importance of expanding access to such protocols in resource-limited settings.
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...
8
Drug Dosing: Infants and Children01:29

Drug Dosing: Infants and Children

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...
19
Pharmacovigilance01:19

Pharmacovigilance

Post-marketing surveillance is a critical component of pharmaceutical regulation, often uncovering unanticipated adverse drug reactions (ADRs) once a drug is widely used over an extended period.
This process, termed pharmacovigilance, aims to detect, evaluate, and minimize harmful effects related to medication use. The data collection for pharmacovigilance depends on spontaneous reporting systems, where healthcare professionals or patients voluntarily report suspected ADRs.
In some cases, there...
1.0K