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首页> 外文期刊>Investigative radiology >A Structured Survey on Adverse Events Occurring Within 24 Hours After Intravenous Exposure to Gadodiamide or Gadoterate Meglumine A Controlled Prospective Comparison Study
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A Structured Survey on Adverse Events Occurring Within 24 Hours After Intravenous Exposure to Gadodiamide or Gadoterate Meglumine A Controlled Prospective Comparison Study

机译:在静脉内暴露于钆胺或再现Meglumine后24小时内发生的不良事件的结构化调查或受控前瞻性比较研究

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Objective This study compares the incidence of new-onset symptoms within 24 hours after enhanced magnetic resonance imaging (eMRI) with intravenous administration of gadodiamide or gadoterate meglumine compared with a control group undergoing unenhanced MRI (uMRI). Materials and Methods A prospective cohort study (n = 1088 patients) was designed to assess the incidence of symptoms within 24 hours after administration of gadodiamide or gadoterate meglumine. The participants underwent a structured questionnaire by phone call before and 24 hours after the MRI scan to check for symptoms that were not present before the scan. The questionnaire included a list of active questions aimed to test the prevalence of symptoms that have been proposed in the debated definition of gadolinium deposition disease (GDD) and that we recorded in this study as GDD-like. In particular, the following symptoms and signs were tested: central torso pain, arm or leg pain, bone pain, headache, skin redness (any site of the body), fatigue, and mental confusion. Fisher exact test was used to test differences between groups with significance threshold set at P < 0.05. Results Within the 24 hours after the MRI scan, 8.3% of patients reported at least one new-onset symptom in the uMRI group versus 17.4% in the gadodiamide eMRI versus 17.8% in the gadoterate meglumine eMRI group. The difference between the eMRI and the uMRI group was statistically significant (P < 0.001 for gadodiamide and P < 0.001 for gadoterate meglumine). There was not a different incidence of symptoms between the gadodiamide and the gadoterate meglumine eMRI groups. For gadodiamide, fatigue (P < 0.05) and dizziness (P < 0.05) were symptoms significantly more frequent than uMRI group; for gadoterate meglumine, fatigue (P < 0.01), mental confusion (P < 0.01), and diarrhea (P < 0.01) were significantly more frequent than uMRI group. Conclusions We found that the onset of new symptoms within 24 hours after exposure to gadolinium-based contrast agent was more frequent than after uMRI. Among GDD-like symptoms, fatigue and mental confusion were the most frequent symptoms reported after eMRI. The other GDD-like symptoms were not overreported after eMRI versus uMRI. Thus, these results are questioning the term GDD.
机译:目的本研究比较了在静脉施用的磁共振成像(EMRI)后24小时内对新发病症状的发病率与静脉施用的Gadodiamide或GadoTate Meglumine相比,与未加薪MRI(UMRI)进行比较。材料和方法预期队列研究(N = 1088名患者)旨在评估施用青霉菌或再生Meglumine后24小时内的症状发生率。参与者在MRI扫描之前和24小时之前通过电话拨打了一个结构化问卷,以检查扫描前未存在的症状。调查问卷包括一个积极问题的清单,旨在测试争论沉积疾病(GDD)的讨论定义中提出的症状的患病率,并且我们在本研究中记录为GDD样。特别是,测试了以下症状和迹象:中央躯干疼痛,臂或腿部疼痛,骨痛,头痛,皮肤发红(任何部位的身体),疲劳和心理混乱。 Fisher精确测试用于在P <0.05处设定具有意义阈值的组之间的差异。结果在MRI扫描后24小时内,8.3%的患者报告了UMRI群中的至少一个新发病症状,在Gadoderate Meglumine EMRI集团中的17.8%。 EMRI和UMRI组之间的​​差异是统计学上显着的(Gadodiamide的P <0.001,对于再生Meglumine的P <0.001)。 Gadodiamide和GadoTate Meglumine EMRI组之间没有不同的症状发生率。对于青霉素,疲劳(P <0.05)和头晕(P <0.05)症状明显多于Umri组;对于生长的Meglumine,疲劳(P <0.01),心理混乱(P <0.01)和腹泻(P <0.01)比UMRI组显着更频繁。结论我们发现在暴露于基于钆的造影剂后24小时内发生新症状的发生比在Umri之后更频繁。在类似GDD的症状中,疲劳和心理混乱是EMRI后最常见的症状。在EMRI与Umri,其他类似GDD样症状不会被过度报告。因此,这些结果正在质疑GDD术语。

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