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Gabapentin's safety and impact on benzodiazepine exposure post-superior cavopulmonary anastomosis
Joshua W Branstetter1, Hania Zaki1, Samuel Van Horn2
1Department of Pharmacy, Children's Healthcare of Atlanta, Atlanta, GA, USA.
Insights
Gabapentin did not reduce opioid use in infants after heart surgery, but it did modestly lower benzodiazepine exposure. The medication was found to be safe for these pediatric patients.
Area of Science:
- Pediatric Cardiac Surgery
- Anesthesiology
- Pharmacology
Background:
- Superior cavopulmonary anastomosis is a common procedure in pediatric cardiac patients requiring staged palliation.
- Effective pain management is critical postoperatively to prevent adverse outcomes like increased pulmonary vascular resistance.
Purpose of the Study:
- To evaluate the impact of gabapentin on opioid and benzodiazepine exposure in infants undergoing superior cavopulmonary anastomosis.
- To assess the safety and efficacy of gabapentin in this patient population.
Main Methods:
- Retrospective cohort study of 85 infants between January 2018 and December 2022.
- Compared opioid and benzodiazepine exposure in infants who received perioperative gabapentin versus those who did not.
- Primary endpoint: opioid exposure (morphine milligram equivalents/kg).
Main Results:
- Gabapentin group had a higher proportion of males (70% vs. 47%, p=0.03).
- No significant difference in opioid exposure between groups (p=0.93).
- Gabapentin group showed significantly lower benzodiazepine exposure on postoperative day 2 (p=0.031) and cumulatively (p=0.031).
Conclusions:
- Gabapentin did not significantly reduce opioid requirements in infants undergoing superior cavopulmonary anastomosis.
- Gabapentin use was associated with a modest reduction in benzodiazepine exposure.
- Gabapentin appears safe in this population, but further research on optimal dosing is warranted.
Introduction:
In paediatric cardiac patients requiring staged palliation, superior cavopulmonary anastomosis is common. Pain control is a crucial aspect of postoperative care as agitation, untreated pain, and hypoventilation can cause increased pulmonary vascular resistance reduction and pulmonary blood flow.
Methods:
This was a large volume single-centre, retrospective cohort study evaluating the impact of gabapentin on opioid and benzodiazepine exposure in infants undergoing superior cavopulmonary anastomosis between January 2018 and December 2022. The primary endpoint was opioid exposure in morphine milligram equivalents per kilogram in infants receiving gabapentin compared to no gabapentin.
Results:
The study analysed 85 infants, 40 of which received perioperative gabapentin. Other than there being more males in the gabapentin group (70% versus 47%; p = 0.03), there was no difference in baseline characteristics. Opioid use, measured in morphine milligram equivalents per kilogram, was similar in the no gabapentin group compared to the gabapentin group during the first 5 POD's (2.66 (interquartile range1.76, 3.30) versus 2.27 (interquartile range R 1.75, 3.40); p = 0.93. However, there was a lower benzodiazepine exposure, measured in midazolam equivalents per kilogram, in the gabapentin group both on POD 2 (0.05 (interquartile range 0.00, 0.11) versus 0 (interquartile range 0.00, 0.08); p = 0.031) and cumulative (0.15 (interquartile range 0.00, 0.35) versus 0.05 (interquartile range 0.00, 0.15); p = 0.031).
Conclusions:
Gabapentin did not significantly reduce opioid exposure; however, its use was associated with modest reduction in benzodiazepine exposure. There were no differences in adverse events. Our findings suggest gabapentin is safe in infants undergoing superior cavopulmonary anastomosis; however, additional studies should be conducted to evaluate optimal gabapentin dosing.
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