Identification of newborns affected by both opioids and gabapentin during pregnancy could with more appropriate care for newborns experiencing withdrawal symptoms.

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Gabapentin is an FDA-approved medication for nerve pain, epilepsy and in combination with medication-assisted treatment for opioid use disorder, but its misuse has been documented. Because maternal self-reporting can underestimate prenatal exposure to substances, Marshall researchers examined the impact of universal, post-delivery maternal toxicology screening including gabapentin.
"Our study found an increase in identification of co-exposure, which led to more timely treatment and likely shorter hospital stays for those newborns experiencing withdrawal," said Sean Loudin, M.D., lead author and associate professor of pediatrics at the Marshall University Joan C. Edwards School of Medicine, a board-certified neonatologist with Marshall Health and medical director of the Neonatal Therapeutic Unit at Cabell Huntington Hospital and Lily’s Place.
Before universal screening, newborns with co-exposure began treatment around day 20, on average. After universal screening began, newborns with co-exposure began treatment around day 14 of life, on average. Likewise, before universal screening, newborns with co-exposure had an average hospital stay of 58 days. After universal screening began, newborns with co-exposure had an average hospital stay of 48 days.
"While the charge for laboratory testing did increase slightly with the additional testing, the potential cost savings by reducing the average length of stay in a medical facility was much greater," Loudin said.
Amy Saunders, managing director of the Marshall University Center of Excellence for Recovery, said the research was an excellent example of interdisciplinary work at an academic medical center.
Source-Eurekalert
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