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4CPS-136 Dexmedetomidine treatment for the sedation of preterm neonates
  1. R Escrig-Fernández1,
  2. AA Garcia Robles2,
  3. O Ballesta-López3,
  4. MJ Company-Albir3,
  5. A Gimeno-Navarro1,
  6. JL Poveda-Andrés3,
  7. I Izquierdo-Macián1
  1. 1Hospital Universitario Y Politécnico La Fe, Neonatology, Valencia, Spain
  2. 2Hospital Universitario Y Politécnico La Fe, Neonatology/Pharmacy, Valencia, Spain
  3. 3Hospital Universitario Y Politécnico La Fe, Pharmacy, Valencia, Spain


Background and importance The control of pain and sedation is a challenge in the neonatal intensive care unit (NICU). Traditionally, opioids and benzodiazepines have been the most commonly used, but they have side effects. Dexmedetomidine, an alpha adrenergic agonist with a sedative and analgesic effect, could be an alternative in neonates (off-label use) because it offers advantages such as the absence of gastrointestinal effects and depression of the respiratory centre. Its pharmacokinetic profile appears to be different in neonates compared with older children and adults, exhibiting a longer half-life and a larger AUC, indicating that lower doses may be required.

Aim and objectives To analyse the effectiveness and safety of dexmedetomidine in neonates.

Material and methods A retrospective observational study was conducted in neonates admitted to a level III NICU and treated with dexmedetomidine perfusion over ≥ 24 hours between July 2017 and September 2018.

Results Thirty-one patients were analysed, 35% female. Median gestational age was 25 weeks (IQR 25–27), 74% were <32 weeks. The initial dose was 0.3 mg/kg/hour (IQR 0.2–0.4) and the maximum dose was 0.8 mg/kg/hour (IQR 0.7–1). The initial loading bolus dose was administered to four patients and two of them presented bradycardia that required atropine treatment. Treatment duration was 178 hours (IQR 96–255), 11 patients were extubated during the infusion and no reintubation was needed in the following 72 hours. Comparisons between heart rate (HR), systolic blood pressure (SBP) and diastolic blood pressure (DBP) before and after starting dexmedetomidine are shown in table 1. The most used concomitant sedoanalgesic medication was fentanyl (29 patients, 93.5%). Fentanyl dose was reduced in the first 24 hours from the start of dexmedetomidine treatment in 16 patients (55%).

Abstract 4CPS-136 Table 1

Conclusion and relevance Dexmedetomidine is an innovative option to manage sedation. Our experience showed that its administration as a perfusion was safe (reduction in HR and DBP were statistically significant but without clinical impact). However, cautious is needed with bolus administration. Also, extubation was possible during its administration without impact on respiratory activity level. It had better sedoanalgesic effects with the possibility of lowering the dose of concomitant drugs.

References and/or acknowledgements None.

No conflict of interest.

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