Main Michael L, Ryan Amy C, Davis Teresa E, Albano Maureen P, Kusnetzky Lisa L, Hibberd Mark
Saint Luke's Mid America Heart Institute, Kansas City, Missouri, USA.
Am J Cardiol. 2008 Dec 15;102(12):1742-6. doi: 10.1016/j.amjcard.2008.08.019. Epub 2008 Oct 23.
We sought to define acute mortality in a large multicenter cohort of hospitalized patients undergoing clinically indicated echocardiography with and without use of an ultrasound contrast agent. Although the United States Food and Drug Administration recently relaxed the issued warnings for perflutren-containing ultrasound contrast agents on May 13, 2008, concerns still exist regarding the safety of these compounds, particularly in critically ill patients. A retrospective analysis was performed using the Premier Perspective Database. Patients undergoing echocardiography during hospitalization were separated into those performed without contrast enhancement and those performed with perflutren lipid microsphere (PLM) injectable suspension contrast agent (Definity, Lantheus Medical Imaging, North Billerica, Massachusetts). Vital status within 1 day of the echocardiogram was available for all patients using hospital billing data. Between January 1, 2002 and October 31, 2007, 4,300,966 patients underwent transthoracic echocardiography at rest during hospitalization (unenhanced studies n = 4,242,712 and contrast-enhanced studies n = 58,254). Multivariate logistic regression analysis was used to compare 24-hour mortality, controlling for case mix and clinical covariates; 1-day mortality rates were 1.08% (n = 45,789 deaths) for patients undergoing noncontrast studies and 1.06% (n = 616 deaths) for patients undergoing contrast-enhanced examinations (p = 0.613). Multivariate logistic regression analysis revealed that, in patients undergoing an echocardiogram, patients receiving PLM injectable suspension contrast agent were 24% less likely to die within 1-day than patients not receiving a contrast agent (adjusted odds ratio = 0.76, 95% confidence interval 0.70 to 0.82). In conclusion, acute crude mortality was not increased in patients receiving PLM injectable suspension contrast agent. Multivariate logistic regression analysis revealed that, compared with patients not receiving a contrast agent, administration of PLM injectable suspension contrast agent during echocardiography was associated with a 24% decreased risk of mortality.
我们试图在一个大型多中心队列中,确定接受临床指征超声心动图检查且使用或未使用超声造影剂的住院患者的急性死亡率。尽管美国食品药品监督管理局于2008年5月13日放宽了对含全氟丙烷超声造影剂发布的警告,但对于这些化合物的安全性仍存在担忧,尤其是在重症患者中。我们使用Premier Perspective数据库进行了一项回顾性分析。住院期间接受超声心动图检查的患者被分为未使用造影剂增强的患者和使用全氟丙烷脂质微球(PLM)注射用混悬液造影剂(Definity,Lantheus Medical Imaging,马萨诸塞州北比勒里卡)的患者。利用医院计费数据,可获取所有患者在超声心动图检查后1天内的生命状态。在2002年1月1日至2007年10月31日期间,4300966例患者在住院期间接受了静息状态下的经胸超声心动图检查(未增强检查n = 4242712例,增强检查n = 58254例)。采用多因素logistic回归分析比较24小时死亡率,并对病例组合和临床协变量进行控制;未使用造影剂检查的患者1天死亡率为1.08%(n = 45789例死亡),使用造影剂增强检查的患者为1.06%(n = 616例死亡)(p = 0.613)。多因素logistic回归分析显示,在接受超声心动图检查的患者中,接受PLM注射用混悬液造影剂的患者1天内死亡的可能性比未接受造影剂的患者低2-4%(校正比值比 = 0.76,95%置信区间0.70至0.82)。总之,接受PLM注射用混悬液造影剂的患者急性粗死亡率并未增加。多因素logistic回归分析显示,与未接受造影剂的患者相比,在超声心动图检查期间给予PLM注射用混悬液造影剂可使死亡风险降低24%。