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Evaluation of an Enteral Clonidine Taper following Prolonged Dexmedetomidine Exposure in Critically Ill Children
Mara F Crabtree1, Cheryl L Sargel1, Colleen P Cloyd1
1Department of Pharmacy, Nationwide Children's Hospital, Columbus, Ohio, United States.
Insights
Enteral clonidine effectively prevents and manages dexmedetomidine withdrawal symptoms in critically ill children. This transition strategy showed a low rate of taper modification, indicating its efficacy in pediatric intensive care settings.
Area of Science:
- Pediatric Critical Care Medicine
- Pharmacology
- Sedation Management
Background:
- Dexmedetomidine is commonly used for sedation in critically ill children.
- Withdrawal symptoms can occur after discontinuing continuous dexmedetomidine infusions.
- Alternative strategies for managing dexmedetomidine withdrawal are needed.
Purpose of the Study:
- To evaluate the effectiveness of enteral clonidine as a transition strategy.
- To assess the prevention and management of dexmedetomidine withdrawal symptoms.
- To identify risk factors for withdrawal in pediatric patients.
Main Methods:
- Retrospective, single-center study of pediatric intensive care unit patients.
- Inclusion criteria: ≤ 18 years, ≥ 24 hours of dexmedetomidine infusion, enteral clonidine initiated within 72 hours of discontinuation.
- Assessment of withdrawal symptoms including hypertension, tachycardia, and agitation.
Main Results:
- 105 patients received enteral clonidine; only 12.4% required taper modification for withdrawal.
- Higher cumulative dexmedetomidine dose and duration were associated with increased need for taper modification.
- Enteral clonidine was effective in preventing or managing withdrawal symptoms in most patients.
Conclusions:
- Enteral clonidine is an effective strategy for preventing and managing dexmedetomidine withdrawal in critically ill children.
- Identifying high-risk patients based on dexmedetomidine exposure may optimize intervention.
- This transition approach can reduce the incidence and severity of withdrawal symptoms.
Abstract:
The aim of the current study is to evaluate the use of an enteral clonidine transition for the prevention or management of dexmedetomidine withdrawal symptoms in critically ill children not exposed to other continuous infusion sedative agents. A retrospective, single-center study was conducted in patients ≤ 18 years of age admitted to the pediatric intensive care unit who received a continuous infusion of dexmedetomidine for ≥ 24 hours and who were prescribed enteral clonidine within 72 hours of dexmedetomidine discontinuation. Predefined withdrawal terminology was established to assess for hypertension, tachycardia, agitation, tremors, and decreased sleep. A total of 105 patients were included and received enteral clonidine for prevention or management of dexmedetomidine withdrawal symptoms, with 13 patients (12.4%) requiring a taper modification to manage withdrawal symptoms. The median duration of dexmedetomidine infusion was 120.5 hours (95.5, 143.5) and median peak infusion rate was 1 µg/kg/h (1, 1.2). A higher cumulative dexmedetomidine dose of 119.2 µg/kg (96.6, 154.9) and duration of 142.9 hours (122.6, 158.3) were noted in patients who required a taper modification. Risk factors for dexmedetomidine withdrawal such as dexmedetomidine duration and cumulative dose may help predict patients at the highest risk of withdrawal that would benefit from an enteral clonidine taper to prevent dexmedetomidine withdrawal symptoms. An enteral clonidine taper can be effective in the prevention and management of dexmedetomidine withdrawal symptoms.
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