Uptake and Use of Biologic Therapies in Paediatric Immune-Mediated Inflammatory Diseases: An Australian

Jun Ni Ho1, Jodie Hillen1,2, Natasha Nassar3,4,5

  • 1Quality Use of Medicines and Pharmacy Research Centre, College of Health, Adelaide University, Adelaide, Australia.

Insights

Biologic medicine use in Australian children with immune-mediated inflammatory diseases (IMIDs) significantly increased from 2014 to 2020. Many children required extended treatment, with nearly one in five receiving multiple biologic medications.

Area of Science:

  • Paediatric Rheumatology
  • Immunology
  • Pharmacovigilance

Background:

  • Immune-mediated inflammatory diseases (IMIDs) impact children, necessitating effective treatments.
  • Biologic medicines offer targeted therapies for IMIDs, but their real-world use in paediatrics requires characterization.

Purpose of the Study:

  • To quantify the real-world utilization of biologic medicines in Australian paediatric patients diagnosed with IMIDs.
  • To describe the demographic characteristics and treatment patterns of children initiating biologic therapy for IMIDs.

Main Methods:

  • Analysis of Australian dispensing claims data for patients under 18 years from 2013 to 2020.
  • Calculation of incidence and prevalence rates of biologic use, patient demographics, and the number of unique biologic medicines dispensed per child.

Main Results:

  • Biologic medicine incidence and prevalence in children with IMIDs substantially increased between 2014 and 2020.
  • Infliximab, adalimumab, and etanercept were the most commonly dispensed biologics, accounting for 80% of treatments.
  • Children initiated on biologics were typically 14 years old, with inflammatory bowel diseases and inflammatory arthropathies being the primary indications; 18% received multiple unique biologic agents.

Conclusions:

  • Paediatric patients with IMIDs often require prolonged biologic therapy, with a significant proportion receiving multiple agents over time.
  • The findings highlight the need for ongoing post-market surveillance to monitor the safety and effectiveness of biologic treatments in children.
Abstract

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