Suppr超能文献

右美托咪定可为儿科核医学成像提供安全有效的镇静选择。

Dexmedetomidine offers an option for safe and effective sedation for nuclear medicine imaging in children.

机构信息

Department of Anesthesiology, Perioperative and Pain Medicine, Boston Children's Hospital, Harvard Medical School, 300 Longwood Ave, Boston, MA 02115, USA.

出版信息

Radiology. 2013 Jun;267(3):911-7. doi: 10.1148/radiol.13121232. Epub 2013 Feb 28.

Abstract

PURPOSE

To determine the safety, efficacy, and outcomes of bradycardia, hypotension, and hypertension with dexmedetomidine (DEX), a recently approved sedative used for procedural sedation that has not been described previously for pediatric nuclear medicine imaging.

MATERIALS AND METHODS

Between March 2005 and August 2011, 669 patients (mean age, 5.7 years ± 4.5 [standard deviation]; median age, 4.5 years; age range, 0.1-22.5 years) received DEX in this HIPAA-compliant study. Sedation was administered with DEX, an α-2 adrenergic agonist, as an intravenous bolus (2 μg per kilogram of body weight) over a 10-minute period; this was followed by continuous infusion at a rate of 1 μg/kg/h until imaging was complete. The bolus could be repeated up to two times, if needed, to achieve the targeted level of a Ramsay sedation score of 4. After institutional review board approval, collected quality assurance data were reviewed.

RESULTS

Adequate sedation was achieved within 8.6 minutes ± 4.6 (median, 8.0 minutes; range, 1.0-40.0 minutes) on average in studies that averaged 41.3 minutes ± 25.5 (median, 31.5 minutes; range, 9.0-183.0 minutes). Of 669 studies, 667 (99.7%) were completed successfully. Six children (0.9%) had brief periods of oxygen desaturation below 95%, none of which required airway intervention. Hypotension, hypertension, and bradycardia (all defined as deviations of more than 20% from age-adjusted awake norms), occurred in 58.7% (n = 393), 2.1% (n = 14), and 4.3% (n = 29) of patients, respectively. Both hypotension and bradycardia were related to age (P = .033 and P = .002, respectively); older children tended to experience more of these events. None of these fluctuations required pharmacologic therapy. Discharge criteria (modified Aldrete score ≥ 9) were met, on average, within 41.4 minutes ± 27.9 (median, 36.0 minutes; range, 1.0-220.0 minutes).

CONCLUSION

DEX offers advantages for pediatric sedation for nuclear medicine imaging. DEX produces a condition similar to natural sleep, with no detrimental effect on respiration. The hemodynamic variability anticipated with DEX did not require pharmacologic treatment, and the drug was well tolerated.

摘要

目的

确定右美托咪定(DEX)镇静在儿科核医学成像中的安全性、有效性和结果。DEX 是一种最近批准的镇静药物,用于程序镇静,之前尚未描述用于儿科核医学成像。

材料和方法

2005 年 3 月至 2011 年 8 月期间,669 例患者(平均年龄 5.7 岁±4.5[标准差];中位年龄 4.5 岁;年龄范围 0.1-22.5 岁)接受了 HIPAA 合规性研究中的 DEX。DEX 是一种 α-2 肾上腺素能激动剂,以静脉推注(2μg/kg)的方式给药,持续 10 分钟;然后以 1μg/kg/h 的速度持续输注,直到成像完成。如果需要,推注可以重复两次,以达到 Ramsay 镇静评分 4 的目标水平。在机构审查委员会批准后,对收集的质量保证数据进行了审查。

结果

在平均持续 41.3 分钟±25.5(中位,31.5 分钟;范围,9.0-183.0 分钟)的研究中,平均在 8.6 分钟±4.6(中位数,8.0 分钟;范围,1.0-40.0 分钟)内达到充分镇静。669 项研究中,667 项(99.7%)成功完成。6 名儿童(0.9%)出现短暂的氧饱和度低于 95%,均无需气道干预。低血压、高血压和心动过缓(均定义为与年龄调整后清醒正常值相比偏差超过 20%)分别发生在 58.7%(n=393)、2.1%(n=14)和 4.3%(n=29)的患者中。低血压和心动过缓均与年龄有关(P=0.033 和 P=0.002);年龄较大的儿童更易发生这些事件。这些波动均无需药物治疗。平均在 41.4 分钟±27.9(中位数,36.0 分钟;范围,1.0-220.0 分钟)达到出院标准(改良 Aldrete 评分≥9)。

结论

DEX 为儿科核医学成像镇静提供了优势。DEX 产生类似于自然睡眠的状态,对呼吸无不良影响。DEX 预期的血液动力学变化不需要药物治疗,且药物耐受性良好。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验