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儿科心脏导管插入术中的造影剂给药:剂量与不良事件

Contrast administration in pediatric cardiac catheterization: dose and adverse events.

作者信息

Senthilnathan Selvi, Gauvreau Kimberlee, Marshall Audrey C, Lock James E, Bergersen Lisa

机构信息

Department of Pediatrics, Children's Hospital at Dartmouth, Lebanon, New Hampshire, USA.

出版信息

Catheter Cardiovasc Interv. 2009 May 1;73(6):814-20. doi: 10.1002/ccd.21902.

Abstract

BACKGROUND

In pediatrics, contrast-related AE such as allergic reactions, seizures, and nephropathy have been reported to occur after cardiac catheterization, but their incidence remains unknown.

OBJECTIVE

We sought to report adverse event (AE) rates attributed to contrast administration in a pediatric cardiac catheterization lab and identify characteristics related to higher doses.

METHODS

A single institution prospective cardiac catheterization AE database identified AE in children <18 years old exposed to contrast. All AE were reviewed and classified by relationship to contrast. Medical records for the 50 cases who received highest contrast doses were retrospectively reviewed for AE. Patient and procedural characteristics were compared in the top quartile of contrast dose versus remaining cases.

RESULTS

Over 3 years, 2,321 consecutive cases required median 3.9 cm(3)/kg [IQR: 2.0, 6.0] of contrast. Patients receiving high dose contrast (top quartile) were more likely to be <1 year (51% vs. 24%), weigh <10 kg (66% vs. 29%), have complex 2 ventricle disease (56% vs. 35%), be in a high procedure type risk group (57% vs. 26%), and undergo procedures >2 h (67% vs. 28%), all P < 0.001. Only 2 of 2,321 cases (0.09%, 95% CI 0.01-0.31%) had AE possibly related to contrast. These events were an acute neurological change and transient nephropathy. In 50 cases receiving the most contrast, no AE were attributed to contrast.

CONCLUSION

A large volume pediatric cardiac catheterization lab administered >or= 6 cm(3)/kg of contrast in a quarter of cases; however, AE related to contrast exposure were exceedingly rare.

摘要

背景

在儿科学领域,据报道心脏导管插入术后会发生与造影剂相关的不良事件,如过敏反应、癫痫发作和肾病,但其发生率仍不清楚。

目的

我们试图报告儿科心脏导管插入实验室中因使用造影剂导致的不良事件(AE)发生率,并确定与高剂量相关的特征。

方法

一个单一机构的前瞻性心脏导管插入术不良事件数据库确定了18岁以下接受造影剂的儿童中的不良事件。所有不良事件均根据与造影剂的关系进行审查和分类。对接受最高造影剂剂量的50例患者的病历进行回顾性不良事件审查。比较造影剂剂量最高四分位数组与其余病例的患者和手术特征。

结果

在3年多的时间里,连续2321例病例使用造影剂的中位数为3.9 cm³/kg[四分位间距:2.0,6.0]。接受高剂量造影剂(最高四分位数)的患者更可能年龄小于1岁(51%对24%)体重小于10 kg(66%对29%)、患有复杂的双心室疾病(56%对35%)、属于高手术类型风险组(57%对26%)以及接受超过2小时的手术(67%对28%),所有P<0.001。在2321例病例中,只有两例(0.09%,95%CI 0.01-0.31%)出现了可能与造影剂相关的不良事件。这些事件为急性神经功能改变和短暂性肾病。在接受造影剂最多的50例病例中,没有不良事件归因于造影剂。

结论

一个大型儿科心脏导管插入实验室在四分之一的病例中使用了≥6 cm³/kg的造影剂;然而,与造影剂暴露相关的不良事件极为罕见。

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