Hunt Christopher H, Hartman Robert P, Hesley Gina K
Department of Radiology, Mayo Clinic, Rochester, MN 55905, USA.
AJR Am J Roentgenol. 2009 Oct;193(4):1124-7. doi: 10.2214/AJR.09.2520.
The purpose of this study was to determine the frequency and characteristics of adverse effects of low-osmolar iodinated and gadolinium contrast agents in a single-center experience with a large number of cases.
A retrospective review of all intravascular doses of low-osmolar iodinated and gadolinium contrast materials administered from 2002 through 2006 was conducted. Adverse effects were identified through the use of radiologist and nurse event recording. Adverse effects were examined for type and severity of reaction, treatment required, and outcome.
A total of 456,930 contrast doses (298,491 low-osmolar iodinated, 158,439 gadolinium) were administered over the study period. A total of 522 cases of adverse effects (0.11% of total) were identified (458 low-osmolar iodinated, 64 gadolinium). The most common adverse effects were hives (274, 52.5%) and nausea (92, 17.6%). Of all adverse effects, 79 of low-osmolar iodinated and 15 of gadolinium contrast material necessitated treatment. Most treatments were performed in the radiology department alone. Only 16 cases of adverse effects necessitated transfer for further observation or treatment. Epinephrine was used to manage an adverse effect in nine instances. Thirty-two of the adverse effects of low-osmolar iodinated contrast material (6.9%) occurred in patients with a history of allergy who received premedication. Only two of these premedication reactions necessitated transfer to the emergency department. The one death in the study period occurred after administration of low-osmolar iodinated contrast material. The patient had no symptoms during the contrast administration or imaging but died suddenly within 30 minutes of receiving the dose.
Both iodinated and gadolinium contrast agents are associated with a very low rate of adverse effects. Most adverse effects are mild and can be managed in the radiology department. Transfer for additional treatment or observation is rarely needed.
本研究的目的是在单中心大量病例经验中确定低渗碘化造影剂和钆造影剂不良反应的频率及特征。
对2002年至2006年期间血管内注射的所有低渗碘化造影剂和钆造影剂剂量进行回顾性研究。通过放射科医生和护士的事件记录来识别不良反应。检查不良反应的反应类型、严重程度、所需治疗及结果。
在研究期间共注射了456,930剂造影剂(298,491剂低渗碘化造影剂,158,439剂钆造影剂)。共识别出522例不良反应(占总数的0.11%)(458例低渗碘化造影剂相关,64例钆造影剂相关)。最常见的不良反应是荨麻疹(274例,52.5%)和恶心(92例,17.6%)。在所有不良反应中,79例低渗碘化造影剂和15例钆造影剂需要治疗。大多数治疗仅在放射科进行。仅16例不良反应需要转院进行进一步观察或治疗。肾上腺素用于处理9例不良反应。低渗碘化造影剂的32例不良反应(6.9%)发生在有过敏史且接受了预处理的患者中。这些预处理反应中仅2例需要转至急诊科。研究期间有1例死亡发生在注射低渗碘化造影剂后。患者在注射造影剂或成像过程中无任何症状,但在接受剂量后30分钟内突然死亡。
碘化造影剂和钆造影剂的不良反应发生率均非常低。大多数不良反应较轻,可在放射科处理。很少需要转院进行额外治疗或观察。