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Preliminary consultation on preferred product characteristics of benzathine penicillin G for secondary prophylaxis of rheumatic fever

  • Rosemary Wyber*
  • , Ben J. Boyd
  • , Samantha Colquhoun
  • , Bart J. Currie
  • , Mark Engel
  • , Joseph Kado
  • , Ganesan Karthikeyan
  • , Mark Sullivan
  • , Anita Saxena
  • , Meru Sheel
  • , Andrew Steer
  • , Joseph Mucumbitsi
  • , Liesl Zühlke
  • , Jonathan Carapetis
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

32 Citations (Scopus)

Abstract

Rheumatic fever is caused by an abnormal immune reaction to group A streptococcal infection. Secondary prophylaxis with antibiotics is recommended for people after their initial episode of rheumatic fever to prevent recurrent group A streptococcal infections, recurrences of rheumatic fever and progression to rheumatic heart disease. This secondary prophylaxis must be maintained for at least a decade after the last episode of rheumatic fever. Benzathine penicillin G is the first line antibiotic for secondary prophylaxis, delivered intramuscularly every 2 to 4 weeks. However, adherence to recommended secondary prophylaxis regimens is a global challenge. This paper outlines a consultation with global experts in rheumatic heart disease on the characteristics of benzathine penicillin G formulations which could be changed to improve adherence with secondary prophylaxis. Characteristics included dose interval, pain, administration mechanism, cold chain independence and cost. A sample target product profile for reformulated benzathine penicillin G is presented.

Original languageEnglish
Pages (from-to)572-578
Number of pages7
JournalDrug Delivery and Translational Research
Volume6
Issue number5
DOIs
Publication statusPublished - 1 Oct 2016
Externally publishedYes

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