Arpino Paul A, Demirjian Zareh, Van Cott Elizabeth M
Department of Pharmacy, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts 02114, USA.
Pharmacotherapy. 2005 Feb;25(2):157-64. doi: 10.1592/phco.25.2.157.56950.
To determine the clinical utility of the chromogenic factor X level for conversion from argatroban to warfarin in hospitalized patients.
Prospective observational study.
Sixty-two hospitalized patients with indications for anticoagulation in whom the chromogenic factor X assay was used for conversion from argatroban to warfarin.
University-affiliated hospital.
From December 2003-May 2004, data for all patients in whom the chromogenic factor X assay was used for conversion from argatroban to warfarin were screened for inclusion. When the chromogenic factor X level was satisfactory, the clinician discontinued the argatroban and a confirmatory international normalized ratio (INR) was obtained.
To determine the ability of the chromogenic factor X level to predict the INR free of argatroban influence, we calculated the sensitivity and specificity by using a cutoff chromogenic factor X level of 45% or less, or greater than 45%, which corresponded to an INR of 2 or greater, or less than 2, respectively. We constructed a receiver operating characteristic curve to illustrate various cutoff levels of chromogenic factor X. Of 146 patients screened, 62 had data that met criteria for analysis. An average of 6 +/- 3 doses of warfarin were administered before the confirmatory coagulation studies were obtained. The average time from the chromogenic factor X measurement to obtainment of confirmatory coagulation studies was 9 +/- 4 hours. Use of a chromogenic factor X level of 45% or less to predict an INR of 2 or greater absent of argatroban influence had a sensitivity of 93%, a specificity of 78%, and an accuracy of 89%. The area under the receiver operating characteristic curve was 0.91 (95% confidence interval 0.81-0.99, p<0.0001).
The chromogenic factor X level is an accurate alternative when converting hospitalized patients from argatroban to warfarin. A chromogenic factor X level of 45% or less is a reliable predictor that the INR will be therapeutic when argatroban therapy is discontinued.
确定发色底物法检测的X因子水平在住院患者从阿加曲班转换为华法林治疗中的临床应用价值。
前瞻性观察性研究。
62例有抗凝指征的住院患者,采用发色底物法检测X因子水平以指导从阿加曲班转换为华法林治疗。
大学附属医院。
2003年12月至2004年5月,筛选所有采用发色底物法检测X因子水平以指导从阿加曲班转换为华法林治疗的患者的数据。当发色底物法检测的X因子水平达标时,临床医生停用阿加曲班,并检测国际标准化比值(INR)以进行确认。
为确定发色底物法检测的X因子水平预测不受阿加曲班影响的INR的能力,我们计算了以发色底物法检测的X因子水平≤45%或>45%为界值时的敏感度和特异度,其分别对应INR≥2或<2。我们绘制了受试者工作特征曲线以展示发色底物法检测的X因子的不同界值水平。在筛选的146例患者中,62例患者的数据符合分析标准。在获得确认性凝血检查结果前,平均给予6±3剂华法林。从检测发色底物法检测的X因子水平到获得确认性凝血检查结果的平均时间为9±4小时。采用发色底物法检测的X因子水平≤45%来预测不受阿加曲班影响的INR≥2时,敏感度为93%,特异度为78%,准确度为89%。受试者工作特征曲线下面积为0.91(95%可信区间0.81-0.99,p<0.0001)。
在住院患者从阿加曲班转换为华法林治疗时,发色底物法检测的X因子水平是一种准确的替代指标。发色底物法检测的X因子水平≤45%是停用阿加曲班治疗后INR将达到治疗水平的可靠预测指标。