首页> 外文期刊>Acta Radiologica >Safety and patient comfort with iodixanol: a postmarketing surveillance study in 9515 patients undergoing diagnostic CT examinations.
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Safety and patient comfort with iodixanol: a postmarketing surveillance study in 9515 patients undergoing diagnostic CT examinations.

机译:碘克沙醇的安全性和患者舒适度:一项针对9515例接受CT诊断检查的患者的上市后监测研究。

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BACKGROUND: Iodinated radiographic contrast media are considered safe diagnostic drugs with a low incidence of adverse drug reactions. PURPOSE: To determine prospectively the incidence and nature of immediate and delayed adverse drug reactions occurring after administration of iodixanol for contrast-enhanced computed tomography (CT) in routine practice in nonselected patients, and to assess patient comfort (pain and sensations of heat or coldness). MATERIAL AND METHODS: Patient characteristics (including demographics, risk factors, indication for CT, and status of the vein used to administer iodixanol) and aspects of iodixanol administration (including dose and volume) were documented on a standardized case report form. Patients were asked to report immediate (during the visit) or delayed (occurring up to 7 days after administration of iodixanol) adverse reactions; those deemed related or possibly related to iodixanol were documented on a standardized adverse drug reaction form. Discomfort was rated by patients on a scale of 0-10 for pain, heat, and coldness; individual scores were combined into a composite score (0-30). RESULTS: Evaluable documentation was provided for 9515 patients in 77 centers across Germany. Adverse drug reactions were reported in 70 patients (0.74%), including hypersensitivity reactions in 55 patients. Thirty patients experienced immediate reactions and 40 experienced delayed reactions. Serious adverse drug reactions were evident in five patients (0.05%). Patients with allergic diathesis appeared to be at increased risk of immediate and delayed adverse drug reactions. Discomfort was generally mild, with 72% of patients reporting a composite score of 0-3. CONCLUSION: In the outpatient setting, where it is often difficult to properly assess patients for specific risk factors, it was reassuring that iodixanol demonstrated an excellent safety profile in over 9500 patients undergoing diagnostic CT examinations. There were no unexpected serious adverse drug reactions, and patient discomfort during administration was mild or absent in most patients.
机译:背景:碘化射线造影剂被认为是安全的诊断药物,药物不良反应的发生率低。目的:前瞻性确定在非选定患者的常规实践中使用碘克沙醇作对比增强计算机断层扫描(CT)后立即和延迟发生的药物不良反应的发生率和性质,并评估患者的舒适度(疼痛或热感或冷感) )。材料和方法:在标准病例报告表中记录了患者特征(包括人口统计学,危险因素,CT指征以及用于碘克沙醇的静脉状况)和碘克沙醇使用的各个方面(包括剂量和体积)。要求患者报告立即(就诊期间)或延迟(发生在碘克沙醇给药后最多7天)的不良反应。那些被认为与碘克沙醇有关或可能与碘克沙醇有关的物质均记录在标准化的药物不良反应表中。患者对疼痛,热和冷的不适等级为0-10。将单个分数合并为综合分数(0-30)。结果:在德国的77个中心为9515名患者提供了可评估的文档。据报告有70例患者发生药物不良反应(0.74%),其中55例患者出现超敏反应。 30名患者立即反应,40例延迟反应。 5名患者(0.05%)出现严重的药物不良反应。具有过敏素质的患者似乎有立即和延迟药物不良反应的风险增加。不适感一般较轻,有72%的患者综合评分为0-3。结论:在门诊环境中,通常很难正确评估患者的特定危险因素,因此可以放心,碘克沙醇在接受诊断性CT检查的9500多例患者中显示出优异的安全性。没有意外的严重药物不良反应,大多数患者在服药期间患者的不适轻微或没有。

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