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      Clinical effect of dexmedetomidine combined with sufentanil on postoperative analgesia for transthoracic device closure of ventricular septal defects in children with ultrafast track anesthesia

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          Abstract

          Background

          To observe the effect of combining dexmedetomidine with sufentanil on postoperative analgesia in children who underwent transthoracic device closure of ventricular septal defects (VSDs) with ultrafast track anesthesia.

          Methods

          This was a retrospective study. Eighty-seven children who underwent transthoracic device closure of VSDs were retrospectively analyzed. Patients were divided into three groups based on the different drugs used for postoperative patient-controlled analgesia.

          Results

          No statistically significant differences in hemodynamic parameters were noted among the three groups after surgery ( p > 0.05). The FLACC score in the SD2 group was significantly greater than those in the S groups and SD1 groups after surgery ( p < 0.001). The Ramsay score in the S group was significantly lower than that of the SD1 and SD2 groups at 6 h ( p < 0.001 and p = 0.003), 12 h ( p = 0.002 and p = 0.012), and 24 h ( p < 0.001 and p < 0.001) after surgery. The pressing frequency of the analgesic pump 48 h after the operation in the SD2 group was significantly greater than that in the other two groups ( p < 0.05). The incidences of respiratory depression, nausea, and vomiting in the S group were significantly greater than those in the SD1 and SD2 groups ( p < 0.05).

          Conclusion

          The combination of 0.04 μg/kg/h dexmedetomidine and 0.04 μg/kg/h sufentanil intravenous analgesia was more effective than the other two analgesic strategies in children who underwent transthoracic device closure of ventricular septal defects (VSDs) with ultrafast track anesthesia.

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          Most cited references22

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          Controlled Sedation with Alphaxalone-Alphadolone

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            Systematic review of the Face, Legs, Activity, Cry and Consolability scale for assessing pain in infants and children: is it reliable, valid, and feasible for use?

            The Face, Legs, Activity, Cry and Consolability (FLACC) scale is one of the most widely used behavioural observation pain scales. However, the psychometrics of the scale have not been adequately summarised and evaluated to provide clear recommendations regarding its use. The aim of this study was to rigorously evaluate the reliability, validity, feasibility, and utility of the scale for clinical and research purposes and provide recommendations regarding appropriate use of the scale. Databases searched were MEDLINE, CINAHL, Embase, PsycINFO (using the Ovid, PubMed, and Ebscohost platforms), The Cochrane Database of Systematic reviews and Cochrane Controlled Trials, and Google Scholar. Psychometric evaluation studies reporting feasibility, reliability, validity, or utility data for the FLACC scale applied to children (birth to 18 years) and randomised controlled trials (RCT) using the FLACC scale to measure a study outcome in infants and children. Data extraction included study design, population demographics, and psychometric data. Analysis involved in this study are quality assessment of the psychometric evaluation studies and the RCTs using the COSMIN checklist and the Jadad scale, respectively, and narrative synthesis of all results. Twenty-five psychometric evaluations studies and 52 RCTs were included. The study population, circumstances, and quality of the studies varied greatly. Sufficient data addressing postoperative pain assessment in infants and children exist. Some positive data support the psychometrics of the scale used to assess postoperative pain in children with cognitive impairment. Limited and conflicting data addressing procedural pain assessment exist. Content validity and scale feasibility have had limited psychometric evaluation. There are insufficient data to support the FLACC scale for use in all circumstances and populations to which is currently applied.
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              Efficacy and safety of sedation with dexmedetomidine in critical care patients: a meta-analysis of randomized controlled trials.

              Dexmedetomidine may help physicians target a low level of sedation. Unfortunately, the impact of dexmedetomidine on major endpoints remains unclear in intensive care unit (ICU).
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                Author and article information

                Contributors
                wangjing202011@163.com
                xiewenpeng2020@163.com
                leiyuqing2020@163.com
                wangzengchun2071@163.com
                caohua0791@163.com
                chenqiang2228@163.com
                Journal
                J Cardiothorac Surg
                J Cardiothorac Surg
                Journal of Cardiothoracic Surgery
                BioMed Central (London )
                1749-8090
                28 July 2021
                28 July 2021
                2021
                : 16
                : 206
                Affiliations
                [1 ]GRID grid.256112.3, ISNI 0000 0004 1797 9307, Department of Cardiac Surgery, Fujian Maternity and Child Health Hospital, , Affiliated Hospital of Fujian Medical University, ; Fuzhou, China
                [2 ]GRID grid.415626.2, ISNI 0000 0004 4903 1529, Fujian Branch of Shanghai Children’s Medical Center, ; Fuzhou, China
                [3 ]Fujian Children’s Hospital, Fuzhou, China
                [4 ]Fujian Key Laboratory of Women and Children’s Critical Diseases Research, Fujian Maternity and Child Health Hospital, Fuzhou, China
                Author information
                http://orcid.org/0000-0003-3768-9000
                Article
                1592
                10.1186/s13019-021-01592-x
                8318323
                34321062
                b83519ef-8363-4e01-a5d3-9ce84ec4a15d
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 24 May 2021
                : 21 July 2021
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2021

                Surgery
                dexmedetomidine,sufentanil,fast-track anesthesia,vsd
                Surgery
                dexmedetomidine, sufentanil, fast-track anesthesia, vsd

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