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. 2022 Jan 18;34(2):322-325.
doi: 10.1093/icvts/ivab251.

Anticoagulation in syncardia total artificial heart recipients: anti-factor Xa or activated partial thromboplastin time?

Affiliations

Anticoagulation in syncardia total artificial heart recipients: anti-factor Xa or activated partial thromboplastin time?

María Monteagudo-Vela et al. Interact Cardiovasc Thorac Surg. .

Abstract

Although the activated partial thromboplastin time (aPTT) has historically been the method of choice for anticoagulation monitoring in patients undergoing mechanical circulatory support with intravenous unfractionated heparin, it is being progressively superseded by the anti-factor Xa (anti-Xa) method. A retrospective single-arm, single-centre analysis of 20 patients who underwent total artificial heart implantation entailed simultaneous determinations of aPTT and anti-Xa. Agreement between these parameters was assessed using the Bland-Altman method. Despite a positive correlation between aPTT and anti-Xa, normal target ranges were poorly aligned: from 5th to 30th postoperative day, for anti-Xa values of 0.2 and 0.4 U/ml corresponding aPTT values were 52.1 and 65.2 s, 7.9 and 14.8 lower than predicted values, respectively. This was not associated with thromboembolic sequalae. It was not possible to demonstrate a significant relationship between the predictor variables (postoperative day; white blood cell count; C-reactive protein concentration; alanine transaminase and alkaline phosphatase level; bilirubin; haemoglobin; albumin and total protein concentration) and the agreement between aPTT and anti-Xa levels. In summary, when anti-Xa levels were used to guide anticoagulation therapy, corresponding aPTT levels were low with respect to target range. Methodology applied in this study is generalizable to other forms of mechanical circulatory support.

Keywords: Anti-FXa assay; Anticoagulation protocol; Total artificial heart; aPTT.

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Figures

Figure 1:
Figure 1:
(A) Scatter plot of aPTT against anti-FXa (aggregate data from postoperative days 5–30, inclusive) with target ranges illustrated with dashed lines and linear regression in red. (B) Scatter plot of aPTT against anti-FXa (aggregate data from postoperative day 31 until termination of heparin therapy) with target ranges illustrated with dashed lines and linear regression in red. (C) Bland–Altman plot of the agreement term Δ (transformed aPTT − transformed anti-Xa) versus mean of transformed values for the early study period (postoperative days 5–30). Red dashed lines indicate 95% confidence limits. Anti-Xa: anti-factor Xa; aPTT, activated partial thromboplastin time.

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