HealthDay News — The transition to use of buprenorphine products with unit-dose packaging (UDP) starting in 2010 correlated with a reduction in unintentional pediatric exposures to buprenorphine-naloxone, according to a study published online May 3 in Pediatrics.

George Sam Wang, MD, from the University of Colorado Anschutz Medical Campus in Aurora, and colleagues conducted an observational surveillance study using the Researched Abuse, Diversion, and Addiction-Related Surveillance System Poison Center Program. Cases of unintentional ingestions involving children aged younger than 6 years and buprenorphine-naloxone products were identified during three periods: pre-UDP (first quarter 2008 through fourth quarter 2010), transition to UDP (first quarter 2011 through fourth quarter 2012), and post-UDP (first quarter 2013 through fourth quarter 2016).

A total of 6,217 exposures to combination products were identified. The researchers found that there were 20.57 pediatric unintentional exposures per 100,000 prescriptions dispensed in the pre-UDP period. In the transition to UDP period and post-UDP period, there were 8.77 and 4.36 pediatric unintentional exposures, respectively, per 100,000 prescriptions dispensed. From the pre-UDP period, this represented a 78.8% relative decrease.

“The shift from non-UDP to UDP in over 80% of buprenorphine-naloxone products was associated with a significant decrease in unintentional pediatric exposures reported to poison centers,” the authors write. “Packaging controls should be a mainstay in the approach to the prevention of unintentional buprenorphine pediatric exposures as well as exposures to other prescription opioids.”

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The study was funded by Indivior.

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