Literature DB >> 21056811

Dexmedetomidine and ketamine for sedation during spinal anesthesia in children.

Janette D McVey1, Joseph D Tobias.   

Abstract

STUDY
OBJECTIVE: To evaluate the combination of dexmedetomidine and ketamine for sedation during lumbar puncture and sedation for spinal anesthesia in children.
DESIGN: Retrospective analysis of quality assurance data sheets and anesthetic records.
SETTING: Developing countries with the humanitarian group, Kids First. PATIENTS: 12 infants and children, ranging in age from two to 9 years.
INTERVENTIONS: A bolus dose of ketamine (two mg/kg) and dexmedetomidine (one μg/kg) was given over three minutes followed by a continuous infusion of dexmedetomidine (two μg/kg/hr for the first 30 min, followed by one μg/kg/hr for the duration of the case). Supplemental analgesia/sedation was provided by ketamine (0.5 mg/kg) as needed. MEASUREMENTS: The need for supplemental ketamine, the ability to complete the procedure, and heart rate (HR), blood pressure, end-tidal carbon dioxide (ETCO(2)), and oxygen saturation values were recorded. MAIN
RESULTS: Effective sedation for lumbar puncture and performance of spinal anesthesia were achieved in all patients. One patient required a supplemental dose of ketamine (0.5 mg/kg). Following the bolus dose of ketamine and dexmedetomidine, HR increased by 11 ± 4 bpm. The greatest HR increase was 20 bpm. No patient had a HR increase ≥ 20% from baseline. The HR decrease was ≤ 30 bpm in 10 of the 12 patients, and the greatest HR decrease was 58 bpm. Systolic blood pressure (SBP) increased from baseline by 10 ± 3 mmHg after administration of the bolus dose of ketamine and dexmedetomidine. During the subsequent dexmedetomidine infusion, SBP decreased by 11 ± 9 mmHg. No patient's respiratory rate decreased to less than 10 breaths/min or increased above 24 breaths/min during the procedural sedation. The highest ETCO(2) was 45 ± 2 mmHg (P < 0.0001). Oxygen saturation remained ≥ 95% during the procedure in all patients.
CONCLUSION: A combination of ketamine and dexmedetomidine provides effective sedation during spinal anesthesia in infants and children, with limited effects on cardiovascular and ventilatory function.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 21056811     DOI: 10.1016/j.jclinane.2010.03.002

Source DB:  PubMed          Journal:  J Clin Anesth        ISSN: 0952-8180            Impact factor:   9.452


  9 in total

Review 1.  Intranasal Dexmedetomidine for Procedural Sedation in Children, a Suitable Alternative to Chloral Hydrate.

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2.  Dexmedetomidine-ketamine sedation during bone marrow aspirate and biopsy in a patient with duchenne muscular dystrophy.

Authors:  Andrew Rozmiarek; Marco Corridore; Joseph D Tobias
Journal:  Saudi J Anaesth       Date:  2011-04

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4.  Dexmedetomidine premedication in relevance to ketamine anesthesia: A prospective study.

Authors:  Kumkum Gupta; Amit Gupta; Prashant K Gupta; Bhawna Rastogi; Salony Agarwal; Mahima Lakhanpal
Journal:  Anesth Essays Res       Date:  2011 Jan-Jun

5.  Dexmedetomidine and fentanyl combination for procedural sedation in a case of Duchenne muscular dystrophy.

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6.  Safety and efficacy of ketamine-dexmedetomidine versus ketamine-propofol combinations for sedation in patients after coronary artery bypass graft surgery.

Authors:  Mona Mohamed Mogahd; Mohammed Shafik Mahran; Ghada Foad Elbaradi
Journal:  Ann Card Anaesth       Date:  2017 Apr-Jun

7.  Addition of dexmedetomidine, tramadol and neostigmine to lidocaine 1.5% increasing the duration of postoperative analgesia in the lower abdominal pain surgery among children: A double-blinded randomized clinical study.

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8.  Intranasal dexmedetomidine and intravenous ketamine for procedural sedation in a child with alpha-mannosidosis: a magic bullet?

Authors:  Matteo Trevisan; Sara Romano; Egidio Barbi; Irene Bruno; Flora Maria Murru; Giorgio Cozzi
Journal:  Ital J Pediatr       Date:  2019-09-03       Impact factor: 2.638

9.  Procedural sedation for a child with a mediastinal mass and superior vena caval syndrome.

Authors:  Aparna Williams; Georgene Singh; Sajan Philip George
Journal:  J Anaesthesiol Clin Pharmacol       Date:  2015 Jul-Sep
  9 in total

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