Johnson H D, Morgan M S, Koenig G R, Utley J R, Leyland S A, Whittle T B, Conn J M
Spartanburg Regional Medical Center, SC, USA.
J Extra Corpor Technol. 1997 Jun;29(2):83-7.
The Hemochron Rx/Dx uses an ACT and a heparin response tube to calculate the heparin dose to identify heparin sensitive/resistant patients. We evaluated the Rx/Dx system in 37 patients to determine if the ACT after the predicted heparin loading dose was adequate to initiate CPB. The mean heparin dose calculated by the Rx/Dx was 31,700 IU +/- 8,700 IU (370 IU/kg) with a mean post ACT of 463 +/- 124 sec. Our standard heparin dose (400 IU/kg) would have given an additional 2,800 IU over the Rx/Dx. Four patients (6.5%) were predicted to be heparin sensitive and all four achieved an ACT over 450 sec. Twenty-one patients (56.8%) were predicted to be resistant and yet failed to raise the ACT over 450 sec in 17 (81.0%). Twelve patients (32.4%) were predicted to have a normal heparin response, and four (33.3%) did not achieve an ACT over 450 sec. In all, 21 patients (56.8%) did not achieve an ACT greater than 450 sec. Each institution should evaluate their heparin loading dose and the resultant ACT. In this study, we found the number of times the Rx/Dx system did not raise the ACT over 450 sec too great to justify the additional expense.
Hemochron Rx/Dx系统使用活化凝血时间(ACT)和肝素反应管来计算肝素剂量,以识别对肝素敏感/抵抗的患者。我们对37例患者的Rx/Dx系统进行了评估,以确定在预测的肝素负荷剂量后ACT是否足以启动体外循环(CPB)。Rx/Dx计算出的平均肝素剂量为31,700国际单位±8,700国际单位(370国际单位/千克),ACT后的平均值为463±124秒。我们的标准肝素剂量(400国际单位/千克)比Rx/Dx计算出的剂量多2,800国际单位。预测有4例患者(6.5%)对肝素敏感,这4例患者的ACT均超过450秒。预测有21例患者(56.8%)对肝素抵抗,但其中17例(81.0%)未能使ACT升高至450秒以上。预测有12例患者(32.4%)肝素反应正常,但其中4例(33.3%)未能使ACT超过450秒。总共有21例患者(56.8%)的ACT未超过450秒。每个机构都应评估其肝素负荷剂量以及由此产生的ACT。在本研究中,我们发现Rx/Dx系统未能使ACT升高至450秒以上的次数过多,以至于额外费用不合理。