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Prevention of Withdrawal in Pediatric Patients Receiving Long-term Dexmedetomidine Infusions
Insights
Adding clonidine during dexmedetomidine weaning did not reduce withdrawal symptoms like agitation or blood pressure changes. However, it did decrease abnormal heart rates, though clinical significance requires further study.
Area of Science:
- Pediatric Critical Care Medicine
- Pharmacology
- Clinical Therapeutics
Background:
- Prolonged dexmedetomidine infusions are used for sedation in pediatric intensive care units (PICUs).
- Dexmedetomidine withdrawal can manifest as hemodynamic instability and agitation.
- Clonidine is sometimes used as an adjunct to manage withdrawal symptoms.
Purpose of the Study:
- To investigate whether adding clonidine reduces the incidence of dexmedetomidine withdrawal in pediatric patients receiving prolonged infusions.
- To assess the impact of clonidine on specific withdrawal symptoms, including blood pressure changes, heart rate abnormalities, and agitation.
Main Methods:
- Retrospective observational cohort study in a single-center pediatric intensive care unit.
- Included children aged 1 month to 18 years receiving dexmedetomidine infusions for ≥5 days.
- Compared outcomes between patients who received clonidine and those who did not.
Main Results:
- No significant difference in blood pressure changes or documented agitation between groups.
- Patients not receiving clonidine had a higher, though not statistically significant, number of abnormal heart rate readings post-discontinuation.
- Clonidine addition did not impact the duration of dexmedetomidine weaning or PICU length of stay.
Conclusions:
- Clonidine addition during long-term dexmedetomidine weaning did not lower blood pressure or agitation.
- A decreased percentage of heart rates above the age-appropriate range was observed with clonidine, but clinical significance is uncertain.
- Clonidine did not reduce time to dexmedetomidine weaning or shorten PICU length of stay, warranting further investigation.
Objective:
Determine if the addition of clonidine was associated with a decreased incidence of dexmedetomidine withdrawal in patients who received prolonged dexmedetomidine infusions.
Methods:
This was a retrospective observational cohort study conducted at a single-center PICU in an academic children's hospital. Children 1 month to 18 years of age who received dexmedetomidine infusion for 5 days or longer were included in the study.
Results:
Fifty patients met the inclusion criteria with 15 patients who received clonidine and 35 who received a dexmedetomidine wean alone. Withdrawal criteria included blood pressure changes, heart rate changes, and documented agitation. Overall, there was no difference in change in blood pressure or documented agitation between groups. Patients who did not receive clonidine had a greater number of heart rate readings above normal for age following discontinuation of the infusion, yet this was not statistically significant. Potentially more importantly, the addition of clonidine did not impact the duration of dexmedetomidine wean or the PICU length of stay after dexmedetomidine discontinuation.
Conclusions:
The addition of clonidine while weaning a long-term dexmedetomidine infusion did not lead to lower blood pressures or agitation, but did lead to decreased percentage of heart rates above the age-appropriate range. The clinical significance of this is unknown, and further investigation is warranted. The addition of clonidine did not decrease time to weaning off dexmedetomidine or shorten PICU length of stay.
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