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An evaluation of dexmedetomidine in combination with midazolam in pediatric sedation: a systematic review and meta-analysis.
Nie, Juan; Li, Chenxi; Yang, Ge; Chang, Huihui; Ding, Guicong.
Afiliação
  • Nie J; Shenzhen Children's Hospital, Shenzhen, 518026, China.
  • Li C; Department of Pediatric Dentistry, Sichuan Hospital of Stomatology, Chengdu, 61000, China.
  • Yang G; Oncological Department of Oral and Maxillofacial Surgery, School of Stomatology, Stomatology Research Institute of Xinjiang Autonomous Region, The First Affiliated Hospital of Xinjiang Medical University, Xinjiang Medical University, Urumqi, 830054, People's Republic of China.
  • Chang H; Shenzhen Children's Hospital, Shenzhen, 518026, China.
  • Ding G; Shenzhen Children's Hospital, Shenzhen, 518026, China.
BMC Anesthesiol ; 24(1): 210, 2024 Jun 21.
Article em En | MEDLINE | ID: mdl-38907338
ABSTRACT

BACKGROUND:

Dexmedetomidine and midazolam are commonly used sedatives in children. We conducted a systematic review and meta-analysis to compare the safety and effectiveness of sedation provided by dexmedetomidine combined with midazolam versus other sedatives including chloral hydrate, midazolam and other sedatives in pediatric sedation.

METHODS:

The Embase, Web of Science, Cochrane Library, and PubMed databases, and Clinicaltrials.gov register of controlled trials were searched from inception to June 2022. All randomized controlled trials used dexmedetomidine-midazolam in pediatric sedation were enrolled. The articles search, data extraction, and quality assessment of included studies were performed independently by two researchers. The success rate of sedation was considered as the primary outcome. The secondary outcomes included onset time of sedation, recovery time of sedation and occurrence of adverse events.

RESULTS:

A total of 522 studies were screened and 6 RCTs were identified; 859 patients were analyzed. The administration of dexmedetomidine combined with midazolam was associated with a higher sedation success rate and a lower incidence of nausea and vomiting in computed tomography, magnetic resonance imaging, Auditory Brainstem Response test or fiberoptic bronchoscopy examinations than the other sedatives did (OR = 2.92; 95% CI 1.39-6.13, P = 0.005, I2 = 51%; OR = 0.23, 95% CI 0.07-0.68, P = 0.008, I2 = 0%, respectively). Two groups did not differ significantly in recovery time and the occurrence of adverse reactions (WMD = - 0.27, 95% CI - 0.93 to - 0.39, P = 0.42; OR 0.70; 95% CI 0.48-1.02, P = 0.06, I2 = 45%. respectively). However, the results of the subgroup analysis of ASA I-II children showed a quicker onset time in dexmedetomidine-midazolam group than the other sedatives (WMD=-3.08; 95% CI -4.66 to - 1.49, P = 0.0001, I2 = 30%).

CONCLUSIONS:

This meta-analysis showed that compared with the control group, dexmedetomidine combined with midazolam group provided higher sedation success rates and caused a lower incidence of nausea and vomiting in completing examinations, indicating a prospective outpatient clinical application for procedural sedation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Midazolam / Dexmedetomidina / Hipnóticos e Sedativos Limite: Child / Humans Idioma: En Revista: BMC Anesthesiol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Midazolam / Dexmedetomidina / Hipnóticos e Sedativos Limite: Child / Humans Idioma: En Revista: BMC Anesthesiol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China