Related Experiment Videos
The Pharmaceutical Benefits Scheme and implications for paediatric prescribing
Yashwant Sinha1, Jo-Anne E Brien, Jonathan C Craig
1Centre for Kidney Research, The Children's Hospital at Westmead, NSW, Australia. yashwans@chw.edu.au
Insights
Access to new medicines for children in Australia is limited as most applications target adult conditions. Pharmaceutical Benefits Scheme (PBS) processes help improve children's access by removing age restrictions.
Area of Science:
- Health Services Research
- Paediatric Pharmacology
- Health Policy
Background:
- The Pharmaceutical Benefits Advisory Committee (PBAC) influences medicine access in Australia.
- Understanding PBAC decisions' impact on paediatric medicine access is crucial.
Purpose of the Study:
- To evaluate the Pharmaceutical Benefits Advisory Committee (PBAC) decisions' impact on children's access to medicines listed on the Pharmaceutical Benefits Scheme (PBS).
Main Methods:
- Analysis of PBAC public summary documents (July 2005-November 2006).
- Comparison with Therapeutic Goods Administration (TGA) recommendations for paediatric use.
- Assessment of medicine cost, therapeutic class, and concordance between TGA and PBS information.
Main Results:
- Only 7% of 102 submissions were for new paediatric indications.
- 60% of submissions lacked age specification, targeting adult conditions.
- Listings specifically including children were more likely to be recommended.
- Fair concordance (kappa 0.21) between TGA and PBS information on age, with 46% of recommendations being age-unrestricted versus adult-only TGA information.
Conclusions:
- Children's access to new subsidised medicines in Australia lags behind adults.
- PBAC processes can enhance paediatric access by avoiding age restrictions on PBS listings.
Aims:
To evaluate the impact of the Pharmaceutical Benefits Advisory Committee (PBAC) decisions on access to medicines listed on the Pharmaceutical Benefits Scheme (PBS) for children.
Methods:
We analysed all public summary documents from PBAC meetings from July 2005 to November 2006 and compared these with the Therapeutic Goods Administration (TGA) recommendations for children for the same medicine. Main outcome measures stratified by age, the total number of medicines for specific indications (accepted and rejected) by therapeutic class; estimated cost to the PBS per annum for each medicine recommended for listing; comparison of TGA-approved product information and PBS listing for recommended medicines.
Results:
Of the 102 medicines for specific indications considered by the PBAC, 7% (7/102) of submissions were for new paediatric indications. Most submissions (60%, 61/102) did not specify age for the PBS recommendation and were for conditions which only affect adults. Listings which specifically included children were more likely to have a positive PBAC recommendation. Of the six recommended medicines for children, four were estimated to cost between $10-30 million per year. There was fair concordance between PBS- and TGA-approved product information for age (kappa 0.21) but in 46%, PBAC recommendations were for age-unrestricted listing compared with adults-only use in the TGA-approved product information.
Conclusion:
Access to new subsidised medicines for children in Australia lags behind adults because most applications to the PBAC for new medicines are for conditions which only affect adults. PBS processes facilitate access for children to new medicines by avoiding age restrictions.
Related Concept Videos
Pharmacokinetics in Pediatric Patients: Overview and Drug Absorption
Pharmacokinetics in Pediatric Patients: Drug Distribution
Pharmacokinetics in Pediatric Patients: Drug Excretion
Pharmacokinetics in Pediatric Patients: Drug Metabolism
Drug Dosing: Infants and Children
Pharmaceutical Poisoning: Potential Scenarios