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首页> 外文期刊>Pediatric emergency care >Nitrous Oxide 70% for Procedural Analgosedation in a Pediatric Emergency Department-With or Without Intranasal Fentanyl?
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Nitrous Oxide 70% for Procedural Analgosedation in a Pediatric Emergency Department-With or Without Intranasal Fentanyl?

机译:氧化亚氧化物70%用于在儿科急诊部中的程序性分支 - 有或没有鼻内芬太尼?

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Objectives Nitrous oxide 70% (N(2)0 70%) is an excellent medication for procedural analgosedation in a pediatric emergency department. However, its analgesic efficacy remains uncertain for painful procedures; therefore, a combination with intranasal fentanyl (INF), an opioid, was suggested. This study aimed at observing and assessing the analgesic efficacy and rate of adverse events using N(2)0 70% with and without INF. Methods Children who received N(2)0 70% in a tertiary children's hospital emergency department from January 1, 2014 to June 30, 2015 were included in this observational study with prospective data collection. Physicians decided individually whether INF was administered. Medical staff documented the child's behavior during the procedure, adverse events, and satisfaction rate. Results A total of 442 children were included; 206 (46.6%) received INF. Group differences regarding patient behavior were not statistically significant; however, N(2)0 70% application time was longer in the INF group (P = .02). Nausea was the most frequent adverse event with 13.1% in the INF group versus 8.1% without INF. Inadequate procedural analgosedation was documented only in the INF group, affecting 1.8% of all patients (P = .002). In contrast, anxiety was exclusively observed in the group without INF, which was presumably misjudged pain (P = .03); the satisfaction rate in the INF group was 95.6% compared with 98.7% without INF. Conclusions Because of the study design and limitations, no conclusions about adding INF to N(2)0 70% can be made. Additional research is needed to investigate the effect of combining N(2)0 70% with INF.
机译:氧化亚氮物体70%(N(2)0 70%)是一种优异的急诊急诊部分类药物药物。然而,其镇痛的疗效仍然不确定痛苦的程序;因此,提出了与鼻内芬太尼(INF),阿片类药物的组合。该研究旨在观察和评估使用N(2)0 70%的镇痛效果和不良事件的速率,其中没有INF。方法在2014年1月1日至2015年6月30日,在2015年1月1日至6月30日的第三级儿童医院急诊部门收到N(2)070%的儿童被纳入了本发明的课程研究。医生是否在单独决定inf是否被施用。医务人员在程序,不良事件和满足率期间记录了孩子的行为。结果共有442名儿童; 206(46.6%)收到INF。关于患者行为的群体差异在统计上没有统计学意义;然而,N(2)0 70%的施用时间在INF组中更长(p = .02)。恶心是INF组中最常见的不良事件,13.1%,而没有锑。不充分的程序性安静,仅在INF组中记录,影响所有患者的1.8%(P = .002)。相比之下,在没有缺乏的小组中专门观察到焦虑,这可能是误判疼痛(p = .03); INF组的满意度为95.6%,而无少数人则为98.7%。结论由于研究设计和局限性,可以在添加INF到N(2)0 70%的结论。需要进行额外的研究来研究与INF组合N(2)0 70%的效果。

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