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The effect of dexmedetomidine on neuroprotection in pediatric cardiac surgery patients: study protocol for a prospective randomized controlled trial

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dc.contributor.authorSang-Hwan Ji-
dc.contributor.authorPyoyoon Kang-
dc.contributor.authorIn-Sun Song-
dc.contributor.authorYoung-Eun Jang-
dc.contributor.authorJi-Hyun Lee-
dc.contributor.authorJin-Tae Kim-
dc.contributor.authorHee-Soo Kim-
dc.contributor.authorEun-Hee Kim-
dc.date.accessioned2022-05-10T01:46:26Z-
dc.date.available2022-05-10T01:46:26Z-
dc.date.issued2022-04-08-
dc.identifier.citationTrials. 2022 Vol 23(1):271ko_KR
dc.identifier.issn1745-6215-
dc.identifier.urihttps://hdl.handle.net/10371/179644-
dc.description.abstractInfants undergoing cardiac surgery under cardiopulmonary bypass are vulnerable to postoperative neurodevelopmental delays. Dexmedetomidine has been shown to have protective effects on the heart, kidneys, and brain in animals and adults undergoing cardiac surgery with cardiopulmonary bypass. We hypothesized that dexmedetomidine would have a neuroprotective effect on infants undergoing cardiopulmonary bypass and planned a prospective randomized controlled trial with postoperative neurodevelopment measurements.
This is a single-center, prospective, double-blinded, randomized controlled trial with 1:1 allocation. A cohort of 160 infants undergoing cardiac surgery with cardiopulmonary bypass will be enrolled. After induction, dexmedetomidine will be infused with a loading dose of 1 μg/kg and a maintenance dose of 0.5 μg/kg/h or the same amount of normal saline will be administered. Upon initiation of cardiopulmonary bypass, an additional dose of dexmedetomidine (0.01 μg/cardiopulmonary priming volume) will be mixed with the cardiopulmonary bypass circuit. The primary outcome will be the proportion of infants who score lower than 85 in any of the cognitive, language, or motor Bayley scales of infant development-III tests 1 year after the surgery. Other feasible outcome measures will include differences in plasma glial fibrillary acidic protein, troponin I, interleukin-6, urinary neutrophil gelatinase-associated lipocalin, and perioperative major adverse events. The results of the Bayley scales of infant development-III test from the study group and the control group will be compared using a chi-squared test under intention-to-treat analysis. A generalized estimating equation will be used to analyze repeated measurements over time.
This study will enable us to assess whether the use of dexmedetomidine can alter the early neurodevelopmental outcome in infants undergoing cardiac surgery with cardiopulmonary bypass and also estimate effects of dexmedetomidine on other organs.
ko_KR
dc.description.sponsorshipThis research was supported by the Institutional Source (SNU 800-20200331) and the National Research Foundation of Korea funded by the Ministry of Science and ICT, the government of Korea (Grant No.: 2020R1F1A1049067).
Expenses for purchasing dexmedetomidine and other consumables, laboratory tests, and Bayley Scales of Infant Development were provided. The funder has no role in the study design; collection, management, analysis, and interpretation of data; writing of the report; and the decision to submit the report for publication and will have no authority over any of these activities.
ko_KR
dc.language.isoenko_KR
dc.publisherBMCko_KR
dc.subjectDexmedetomidine-
dc.subjectInfant, Congenital heart disease-
dc.subjectCardiopulmonary bypass-
dc.subjectNeuroprotection-
dc.subjectRandomized controlled trial-
dc.titleThe effect of dexmedetomidine on neuroprotection in pediatric cardiac surgery patients: study protocol for a prospective randomized controlled trialko_KR
dc.typeArticleko_KR
dc.identifier.doihttps://doi.org/10.1186/s13063-022-06217-9ko_KR
dc.citation.journaltitleTrialsko_KR
dc.language.rfc3066en-
dc.rights.holderThe Author(s)-
dc.date.updated2022-04-10T03:16:23Z-
dc.citation.startpage271ko_KR
dc.citation.volume23ko_KR
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