Gandhi Manish J, Narra Vamsidhar R, Brown Jeffrey J, Guo Amy, Grosu Daniel S, Parvin Curtis A, Scott Mitchell G
Department of Pathology and Immunology, Washington University School of Medicine, 660 S Euclid Ave., Box 8118, St. Louis, MO 63110, USA.
AJR Am J Roentgenol. 2008 Mar;190(3):W213-7. doi: 10.2214/AJR.07.2923.
Gadolinium is administered as a contrast agent in MRI procedures. Two gadolinium-based contrast agents, gadodiamide and gadoversetamide, interfere with colorimetric total serum calcium methods. The purpose of this prospective observational study was to examine the incidence of calcium interference after gadoversetamide procedures, associated clinical outcomes, and costs 20 months after implementation of quality assurance and physician education programs.
Records of patients who received gadoversetamide from June 24, 2006, to October 7, 2006, were reviewed to determine if a routine calcium test had been performed after the injection. Calcium values were repeated with an alternate method that is less susceptible to gadoversetamide interference. If the difference was > or = 2.0 mg/dL or if the initial test value was < or = 7.0 mg/dL, patient charts were reviewed for any related treatment. Costs associated with this algorithm were tracked.
The initial calcium test was performed after gadoversetamide in 766 of 3,439 instances. The alternate test was performed in 633 of 766. One hundred twenty-five of 633 (20%) showed a difference in calcium values that was > or = 0.7 mg/dL, with 16 showing differences of > or = 1.6 mg/dL. Chart review for 56 instances revealed that calcium supplements were administered in 22 of 56 around the time of gadoversetamide injection. However, none appeared to be related to the spurious hypocalcemia. The total additional cost (reagent and technologist) for following this algorithm for just over 3 months was $6,807.
Approximately 20% of patients receiving gadoversetamide exhibited spurious hypocalcemia. No patients were identified who received inappropriate calcium because of this interference. This may be attributable to the quality assurance and physician education programs.
钆作为磁共振成像(MRI)检查中的造影剂使用。两种基于钆的造影剂,钆双胺和钆塞酸二钠,会干扰比色法测定血清总钙的方法。这项前瞻性观察性研究的目的是在实施质量保证和医师教育计划20个月后,检查钆塞酸二钠检查后钙干扰的发生率、相关临床结果及成本。
回顾2006年6月24日至2006年10月7日期间接受钆塞酸二钠检查的患者记录,以确定注射后是否进行了常规钙检测。采用一种不易受钆塞酸二钠干扰的替代方法重复检测钙值。如果差值≥2.0mg/dL或初始检测值≤7.0mg/dL,则查看患者病历以了解任何相关治疗情况。跟踪与该算法相关的成本。
在3439例检查中,766例在钆塞酸二钠检查后进行了初始钙检测。766例中的633例进行了替代检测。633例中的125例(20%)显示钙值差异≥0.7mg/dL,其中16例差异≥1.6mg/dL。对56例病历的审查显示,56例中有22例在钆塞酸二钠注射前后补充了钙。然而,似乎没有一例与假性低钙血症有关。按照该算法进行略超过3个月的跟踪,额外的总成本(试剂和技术人员)为6807美元。
接受钆塞酸二钠检查的患者中约20%出现假性低钙血症。未发现因这种干扰而接受不适当补钙的患者。这可能归因于质量保证和医师教育计划。