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Original articles |
1 Erasmus MC - Sophia, Netherlands
2 Isala Clinics, Netherlands
3 Erasmus MC, Netherlands
* To whom correspondence should be addressed. E-mail: j.illsley{at}erasmusmc.nl.
Accepted 27 July 2005
| Abstract |
|---|
Objective:To study the effects of continuous morphine infusion on arterial blood pressure in ventilated neonates.
Design:Blinded randomised placebo-controlled trial.
Setting:Level III Neonatal Intensive Care Unit in two centres.
Patients:144 ventilated neonates (Inclusion criteria: postnatal age < 3 days, ventilation < 8 hours, indwelling arterial line. Exclusion criteria: severe asphyxia, severe IVH, major congenital anomalies, neuromuscular blockers).
Intervention:Arterial blood pressure was measured before the start and during the first 48 hours of masked medication infusion (morphine/placebo; 100 µg/kg + 10 µg/kg/h).
Outcome measures:arterial blood pressure and blood pressure variability.
Results:There were no significant differences in overall MAP (mean arterial blood pressures) between the morphine group (median 36 mmHg; IQR 6) and the placebo group (median 38 mmHg; IQR 6)(p=0.11). Although significantly more morphine treated patients (70%) showed hypotension compared to the placebo group (47%) (p=0.004), the use of volume expanders and vasopressor drugs was not significantly different (morphine group: 44 %; placebo group: 48 %; p=0.87) indicating the limited clinical significance of this side effect. Blood pressure variability was not influenced by routine morphine analgesia (p=0.81) and additional morphine (p=0.80). Patients with and without intraventricular haemorrhage showed no differences in blood pressures (Mann Whitney U-tests:1953; p=0.14) and incidence of hypotension (÷2 test: 1.16; df: 1; p=0.28).
Conclusions:Overall arterial blood pressures, use of inotropic therapy and blood pressure variability were not influenced by morphine infusion. Therefore, the clinical impact of hypotension as a side effect of low dose morphine treatment in neonates is negligible.
Keywords: randomised controlled trial, opioids, hypotension, blood pressure variability
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