Intubation in the delivery room: experience with nasal midazolam.

BACKGROUND

Neonates are often intubated in the delivery room (DR) without anesthesia because vascular access is impossible.

AIMS

To assess neonatal comfort and adverse events after use of nasal midazolam (nMDZ) for intubation in the DR.

STUDY DESIGN

Prospective data collection over 6months on the intubation of neonates with respiratory distress requiring tracheal instillation of surfactant.

SUBJECTS

Twenty-seven neonates with median (Q25-75) gestational age and birthweight of, respectively, 29 (27-33)weeks and 1270 (817-1942)g received a 0.1mg/kg dose of nMDZ, and intubation was performed at the onset of tonus resolution or apnea.

OUTCOME MEASURES

Comfort was assessed with a scale of hetero-pain assessment and electrical skin conductance monitoring. Continuous pulse oximetry was recorded in the first postnatal hour, with oscillometric blood pressure measurement every 10min.

RESULTS

Seventy percent of the patients required a single dose, with intubation performed 4.8 (3-9)min after administration. Combined electro-clinical assessment found adequate comfort during the procedure in 68% of neonates. Mean blood pressure decreased from 39 (34-44)mmHg before to 31 (25-33)mmHg 1h following nMDZ (p=0.011).

CONCLUSION

nMDZ provided rapid and effective sedation to intubate neonates in the DR but potentially exposed them to hypotension, thus requiring close hemodynamic monitoring.