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Published on: July 29, 2014
Suspected opioid-induced hyperalgesia in an infant
1Department of Paediatric Anaesthesia and Pain Management, Royal Children's Hospital, Parkville, Victoria, Australia. benhallett@benhallett.com.au
Insights
Opioid-induced hyperalgesia (OIH) is a condition where pain worsens despite increased opioid use. This case study details the first reported instance of OIH in an infant, highlighting a critical challenge in pediatric pain management.
Area of Science:
- Pediatric Critical Care
- Pain Management
- Neonatology
Background:
- Opioid-induced hyperalgesia (OIH) is a known phenomenon that can diminish opioid analgesic efficacy.
- Gastroschisis is a congenital defect requiring extensive surgical management and often prolonged intensive care.
Observation:
- A neonate with gastroschisis developed escalating pain scores and signs of hyperalgesia and allodynia despite increasing opioid doses.
- The infant exhibited irritability, photophobia, and increased pain upon handling, unresponsive to further opioid escalation.
Findings:
- This case represents the first documented instance of opioid-induced hyperalgesia in an infant.
- Opioid de-escalation, rotation to hydromorphone, and the addition of ketamine led to a rapid reduction in pain scores and irritability.
- Successful weaning from opioid infusions and sedatives was achieved after managing OIH.
Implications:
- This report underscores the importance of recognizing OIH in infants, even in the context of complex surgical conditions.
- It suggests that opioid de-escalation and multimodal analgesia strategies, including non-opioid agents like ketamine, are crucial for managing OIH in neonates.
- Further research is warranted to understand the pathophysiology and optimal management of OIH in pediatric populations.
Abstract:
One explanation for diminished opioid analgesic efficacy is opioid-induced hyperalgesia (OIH). We report a case of OIH in an infant with gastroschisis, requiring multiple surgical interventions and prolonged sedation for ventilation. This is the first report of OIH in an infant. On day 41 of life after nine separate surgical interventions, the patient's pain scores increased and remained elevated, despite increasing opioid administration. The patient also developed hyperalgesia, allodynia, and photophobia and became extremely irritable upon handling. Other possible causes were excluded, including interruption to opioid delivery, sepsis, acid-base and electrolyte disturbance, and ongoing surgical pathology. An opioid rotation to hydromorphone was initiated and ketamine was commenced. Sedation for ventilation was achieved with dexmedetomidine and midazolam infusions. Over a period of 24 h after opioid de-escalation, pain scores reduced rapidly and the patient became significantly less irritable with handling. All infusions were gradually weaned and eventually ceased.
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