Clinical Abacavir Hypersensitivity Reaction among Children in India

Jaya Chakravarty1, Saurabh Sharma2, Anuradha Johri2

  • 1Department of Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh, 221005, India. tapadar@gmail.com.

Insights

Abacavir hypersensitivity reactions (HSR) occurred in 7.9% of children. Overdiagnosis is common; treating concurrent illnesses before abacavir may reduce HSR incidence.

Area of Science:

  • Pediatric infectious diseases
  • Clinical pharmacology
  • Pharmacogenomics

Background:

  • Abacavir is a key component of first-line antiretroviral therapy recommended by the National AIDS Control Organization.
  • Abacavir hypersensitivity reaction (HSR) is a significant concern in patients receiving this medication.
  • Understanding the incidence and characteristics of HSR in pediatric populations is crucial for optimizing treatment.

Purpose of the Study:

  • To determine the incidence of clinically diagnosed abacavir hypersensitivity reaction (HSR) in children receiving abacavir-based therapy within a national program.
  • To investigate the association between HLA-B*5701 allele status and the occurrence of abacavir HSR in pediatric patients.
  • To identify clinical features differentiating HSR from other conditions in children.

Main Methods:

  • An observational study was conducted including all children initiated on abacavir.
  • Clinical diagnosis of abacavir HSR was made according to national guidelines.
  • HLA-B*5701 testing was performed on children diagnosed with clinical abacavir HSR.

Main Results:

  • Out of 101 children who started abacavir, 8 (7.9%) developed clinically diagnosed abacavir HSR.
  • Four of the 8 children with HSR had concomitant illnesses and were HLA-B*5701 negative.
  • Only 2 (25%) of the children with HSR carried the HLA-B*5701 allele. Fever and abdominal symptoms were more frequent in HLA-B*5701 positive cases.

Conclusions:

  • Clinically diagnosed abacavir HSR appears to be overdiagnosed in the pediatric population.
  • The presence of concomitant illness may complicate the clinical diagnosis of abacavir HSR.
  • Pre-treatment management of concurrent illnesses before initiating abacavir may help reduce the incidence of overdiagnosed HSR.

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