Point-of-care testing for emergency assessment of coagulation in patients treated with direct oral anticoagulants
© The Author(s). 2017
Received: 24 June 2016
Accepted: 27 January 2017
Published: 15 February 2017
Point-of-care testing (POCT) of coagulation has been proven to be of great value in accelerating emergency treatment. Specific POCT for direct oral anticoagulants (DOAC) is not available, but the effects of DOAC on established POCT have been described. We aimed to determine the diagnostic accuracy of Hemochron® Signature coagulation POCT to qualitatively rule out relevant concentrations of apixaban, rivaroxaban, and dabigatran in real-life patients.
We enrolled 68 patients receiving apixaban, rivaroxaban, or dabigatran and obtained blood samples at six pre-specified time points. Coagulation testing was performed using prothrombin time/international normalized ratio (PT/INR), activated partial thromboplastin time (aPTT), and activated clotting time (ACT+ and ACT-low range) POCT cards. For comparison, laboratory-based assays of diluted thrombin time (Hemoclot) and anti-Xa activity were conducted. DOAC concentrations were determined by liquid chromatography-tandem mass spectrometry.
Four hundred and three samples were collected. POCT results of PT/INR and ACT+ correlated with both rivaroxaban and dabigatran concentrations. Insufficient correlation was found for apixaban. Rivaroxaban concentrations at <30 and <100 ng/mL were detected with >95% specificity at PT/INR POCT ≤1.0 and ≤1.1 and ACT+ POCT ≤120 and ≤130 s. Dabigatran concentrations at <30 and <50 ng/mL were detected with >95% specificity at PT/INR POCT ≤1.1 and ≤1.2 and ACT+ POCT ≤100 s.
Hemochron® Signature POCT can be a fast and reliable alternative for guiding emergency treatment during rivaroxaban and dabigatran therapy. It allows the rapid identification of a relevant fraction of patients that can be treated immediately without the need to await the results of much slower laboratory-based coagulation tests.
Unique identifier, NCT02371070. Retrospectively registered on 18 February 2015.
KeywordsPoint-of-care testing POCT Direct oral anticoagulants DOAC Non-vitamin K antagonist oral anticoagulants NOAC Emergency surgery Anticoagulation reversal Thrombolysis Stroke
Direct oral anticoagulants (DOAC) are being increasingly prescribed. Consequentially, more DOAC-treated patients are admitted to emergency units across all clinical specialties. Importantly, emergency coagulation testing in DOAC-treated patients has not been solved, which complicates emergency treatment decisions such as emergency surgery, anticoagulation reversal, and thrombolysis in ischaemic stroke.
In patients receiving vitamin K antagonists (VKA), point-of-care testing (POCT) of coagulation has proven its great value in accelerating emergency treatment . Although DOAC-specific POCT is not currently available, results obtained by our group suggest that relevant plasma concentrations of rivaroxaban can be qualitatively ruled out with CoaguChek® (Roche, Basel, Switzerland), a prothrombin time/international normalized ratio (PT/INR) POCT designed for VKA monitoring . However, CoaguChek® lacked sensitivity to apixaban and dabigatran.
Hemochron® Signature (ITC, Edison, NJ, USA) is another coagulation POCT that uses a different PT/INR assay to CoaguChek® and has additional measuring capability for activated partial thromboplastin time (aPTT) and activated clotting time (ACT). Previous reports indicate that Hemochron® Signature is responsive to rivaroxaban and dabigatran [3–7]. However, these reports aimed at quantitative measurements rather than qualitatively ruling out low but relevant DOAC concentrations, and used either artificially DOAC-spiked plasma samples [3, 4] or they only comprised a few samples with low DOAC concentrations [5–7]. Furthermore, the utility of Hemochron® Signature to measure the effects of apixaban on coagulation effects has never been reported. Thus, the diagnostic value of Hemochron® Signature in guiding emergency treatment decisions in DOAC-treated patients has not been clarified.
Study aim and design
We aimed to determine the diagnostic accuracy of Hemochron® Signature to qualitatively rule out relevant concentrations of apixaban, rivaroxaban, and dabigatran in real-life patients.
The study was a single-centre, prospective observational trial with blinded end-point assessment. The Clinical Trial Registration Information unique identifier is NCT02371070.
Setting and eligibility criteria
The study was conducted at the Department of Neurology & Stroke and the Department of Cardiology and Cardiovascular Medicine of Tübingen University Hospital, Tübingen, Germany, a tertiary care facility. Patients receiving first doses of apixaban, rivaroxaban, or dabigatran were enrolled. Exclusion criteria were known coagulopathy, abnormal coagulation at baseline (PT >13 s/Quick <70%/INR >1.2 or aPTT >37 s), intake of VKA or DOAC within 14 days, low-molecular-weight heparins within 24 h or unfractionated heparin within 12 h prior to DOAC intake. Use of antiplatelet agents was permitted.
Predominantly low dabigatran concentrations in these samples required inclusion of additional samples from patients on maintenance therapy with dabigatran. The same exclusion criteria as above applied, except that abnormal coagulation at baseline (due to dabigatran intake) was allowed.
Six blood samples were collected from each subject via an indwelling venous catheter or venipuncture: before DOAC intake, 30 min and 1, 2, and 8 h after intake, and at trough (12 h for apixaban and dabigatran, 24 h for rivaroxaban).
POCT and laboratory-based coagulation testing
Bedside POCT of PT/INR, aPTT and ACT was conducted from whole blood. ACT was measured using ACT plus (ACT+) and ACT-low range (ACT-LR) test cards that contain different reagents and cover different measurement ranges. Further samples were collected in 3.2% sodium-citrate tubes (Sarstedt, Nümbrecht, Germany), and instantly centrifuged to acquire plasma. Laboratory-based anti-Xa activity was measured using Chromogenix COAMATIC Heparin Test on an ACL TOP 700 (Instrumentation Laboratory, Kirchheim, Germany). TECHNOVIEW calibrators (Technoclone, Vienna, Austria) were used to determine apixaban and rivaroxaban concentrations with limits of quantification of 10 and 18 ng/mL. Remaining plasma aliquots were stored at –80 °C until testing of diluted thrombin time (dTT; Hemoclot assay, Hyphen BioMed, Neuville-sur-Oise, France). As the gold standard, DOAC concentrations were determined by ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS) . All coagulation testing was performed according to manufacturers’ instructions by thoroughly trained investigators and technicians.
All laboratory-based tests, including UPLC-MS, were conducted and interpreted by technicians blinded to POCT results.
Definition of relevant DOAC concentrations
For test performance analyses, results of samples (all baseline samples, all samples per DOAC) were pooled in order to obtain a clinically relevant concentration spectrum. SPSS v23 (IBM, Armonk, NY, USA) was used for statistics. Confidence intervals for proportions, i.e. diagnostic sensitivity and specificity, were calculated according to the efficient-score method using the free online VassarStats Clinical Calculator 1 . Pearson’s correlation coefficient was used to estimate the strength of correlations between coagulation assays and DOAC concentrations. Correlation strength was graded as proposed by Evans: <0.20 very weak, 0.20–0.39 weak, 0.40–0.59 moderate, 0.60–0.79 strong, and >0.80 very strong . Fisher’s exact test was calculated to determine differences in the proportions of baseline POCT results between the study groups and to examine the association between coagulation test results and DOAC concentrations dichotomized to concentrations below and above the chosen safe-for-treatment thresholds (Table 1). Diagnostic accuracy of coagulation tests at different cut-off points was expressed in terms of sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and likelihood ratio. Sensitivity was defined as the percentage of samples with DOAC concentrations below the chosen safe-for-treatment threshold that were correctly identified as eligible for treatment. Correspondingly, specificity was defined as the percentage of samples with DOAC concentrations above the corresponding threshold that were correctly identified as not eligible. Specificity >95% was defined as sufficient for clinical application. PPV was defined as the percentage of samples with DOAC concentrations below the chosen safe-for-treatment threshold of all samples identified as eligible for treatment. NPV was defined as the percentage of samples with DOAC concentrations above the chosen safe-for-treatment threshold of all samples identified as not eligible for treatment. All DOAC concentrations are reported as median and interquartile range (IQR). Sensitivity and specificity are given with two-sided 95% confidence intervals.
We enrolled 60 patients (n = 20 per DOAC) receiving first doses of DOAC and eight patients on dabigatran maintenance therapy between February 2014 and November 2015. Patient characteristics and baseline laboratory values are provided as part of Additional file 1: Tables S1 and S2).
Samples and DOAC concentrations
Of 408 planned samples, 403 were collected (apixaban n = 117, rivaroxaban n = 118, dabigatran n = 168). Five samples could not be analysed due to POCT malfunction.
DOAC were not detected by UPLC-MS in any baseline sample acquired before first DOAC intake (n = 60). Samples collected after DOAC intake contained a median concentration of 57.2 ng/mL apixaban (IQR 35.3–101.2, n = 97), 99.3 ng/mL rivaroxaban (IQR 25.7–184.3, n = 98), and 29.0 ng/mL dabigatran (IQR 10.7–72.3, n = 148). Median trough dabigatran concentrations were significantly lower after the first dose than during maintenance therapy (16.3 versus 81.8 ng/mL, p < 0.001).
Correlation between POCT results and DOAC concentrations
Due to insufficient correlation strength for apixaban, we limited all further analyses to rivaroxaban and dabigatran. To maximize clinical applicability, we focused on the two test cards that provided strong correlation to both rivaroxaban and dabigatran, i.e. PT/INR and ACT+.
Diagnostic accuracy of POCT
Diagnostic accuracy of Hemochron® Signature POCT for rivaroxaban
Coagulation test result
POCT PT ≤1.0
POCT PT ≤1.1
POCT ACT+ ≤120 s
POCT ACT+ ≤130 s
Diagnostic accuracy of Hemochron® Signature POCT for dabigatran
Coagulation test result
POCT PT ≤1.1
POCT PT ≤1.2
POCT ACT+ ≤100 s
POCT ACT+ ≤100 s
Rivaroxaban concentrations at <30 and <100 ng/mL were detected with >95% specificity at PT/INR POCT ≤1.0 and ≤1.1 and ACT+ POCT ≤120 and ≤130 s. Dabigatran concentrations at <30 and <50 ng/mL were detected with >95% specificity at PT/INR POCT ≤1.1 and ≤1.2 and ACT+ POCT ≤100 s (for both thresholds). Likelihood ratio (LR) was highest for rivaroxaban and ACT+ POCT (<30 ng/mL, LR 15.7; <100 ng/mL, LR 16.2), and dabigatran and PT POCT (<30 ng/mL, LR 34.6; <50 ng/mL, LR 33.5).
Performance of laboratory-based DOAC-specific coagulation assays
The calibrated anti-Xa assay (Chromogenix COAMATIC Heparin Test) showed the highest correlation to rivaroxaban levels of all evaluated coagulation tests (r = 0.94, p < 0.001). Test results predicted rivaroxaban concentrations <30 and <100 ng/mL with a respective specificity of 99% and 92%, and a sensitivity of 98% and 97%.
Correlation between dTT (Hemoclot) and dabigatran concentrations was also very strong (r = 0.86, p < 0.001). Test results predicted dabigatran concentrations <30 and <50 ng/mL with a respective specificity of 95% and 84%, and a sensitivity of 77% and 82%.
Results of Hemochron® Signature coagulation POCT correlate with rivaroxaban and dabigatran, but not with apixaban concentrations. PT/INR and ACT+ test cards are of particular interest, as they are influenced by both rivaroxaban and dabigatran. POCT-specific cut-offs can be used to exclude relevant rivaroxaban and dabigatran concentrations (Table 1) at the bedside with high specificity.
Data on what constitutes a relevant DOAC concentration, i.e. a concentration that leads to clinically significant coagulation impairment, are scarce. Current guidelines are predominantly time-based. Urgent surgical procedures may be performed at trough [9, 17], i.e. 12 or 24 h after last intake of apixaban/dabigatran [18, 19] or rivaroxaban , respectively. Thrombolysis for ischaemic stroke can be performed >48 h after the last intake of any DOAC . However, significant DOAC concentrations have been observed in patients even beyond 48 h after the last intake . Hence, the usefulness of time-based guidelines is limited. Furthermore, obtaining information on last DOAC intake might be impossible in patients with stroke and aphasia or dementia.
Specific concentration thresholds that increase bleeding risk can currently only be estimated based on retrospective analyses , pharmacodynamic considerations , and expert opinions [12, 14]. For surgical procedures, concentrations of rivaroxaban <30 ng/mL , and dabigatran <30 , <48 , and <50 ng/mL  have been proposed as safe. For apixaban, such concentration thresholds are currently unknown . For acute ischaemic stroke, DOAC concentrations that may permit thrombolysis have been suggested by an expert group (see Table 1) . It should be noted that these latter concentrations represent an expert opinion rather than quantitatively determined values.
Coagulation testing for rivaroxaban and dabigatran
Quantification of DOAC concentrations using DOAC-specific assays is the recommended clinical standard for coagulation testing during DOAC treatment, i.e. anti-Xa activity for rivaroxaban and dTT or ecarin-based assays for dabigatran [17, 23]. Our study confirms that these assays provide high diagnostic accuracy for all tested DOAC. However, we found that Hemoclot had limited specificity and sensitivity for dabigatran concentrations <50 ng/mL, a threshold considered safe for surgery [11, 12] and thrombolysis . At such low dabigatran concentrations, the reduced accuracy of Hemoclot has also been reported by others .
In many institutions, availability of DOAC-specific coagulation assays is limited . For this reason, several authors have argued that unspecific global coagulation assays might suffice to rule out relevant DOAC concentrations [14, 26, 27].
Prompt availability and instantaneous results makes coagulation POCT an attractive option in emergency situations. We have previously shown that relevant concentrations of rivaroxaban can be qualitatively ruled out with CoaguChek®, a POCT designed for VKA monitoring . The results of our current trial suggest Hemochron® Signature as a more versatile alternative: while CoaguChek® was only responsive to rivaroxaban, results of Hemochron® Signature PT/INR and ACT+ test cards were altered by both rivaroxaban and dabigatran.
Interestingly, the two factor Xa inhibitors, rivaroxaban and apixaban, differed in their effects on Hemochron® Signature POCT results. While POCT results at different apixaban concentrations were almost randomly distributed (Fig. 1), a strong correlation was found for rivaroxaban. Similar findings have been previously reported by our group and others for POCT and laboratory-based assays [2, 28]. To our knowledge, no convincing explanation for this difference has yet been provided.
Irregularities of Hemochron® Signature POCT results in the presence of dabigatran were noted early . Recently, three trials evaluated this POCT (or the equivalent GEM® PCL Plus) for coagulation monitoring in patients treated with rivaroxaban , dabigatran , or both . These studies reported that, in the case of low DOAC concentrations, coagulation test results frequently fell into a “normal range” previously established in untreated volunteers and concluded that the device cannot sufficiently distinguish between patients at trough concentrations and untreated patients [5–7]. We contest the usefulness of a “normal range” found in untreated volunteers for the monitoring of DOAC. In agreement with the previous reports, we observed that the alterations in coagulation results in the presence of DOAC often did not exceed values found in untreated patients. Nevertheless, our analyses show that POCT results below DOAC-specific cut-offs are highly predictive when used to qualitatively rule out relevant concentrations of rivaroxaban and dabigatran.
Translation into the real world
Although both rivaroxaban and dabigatran can be detected with PT/INR or ACT+ POCT, our likelihood ratio calculations support the use of ACT+ test cards for rivaroxaban and PT/INR test cards for dabigatran.
Importantly, since there is no single POCT cut-off value that can safely rule out all DOAC, knowledge of the patient’s medication history is necessary. Furthermore, the blood concentration of all DOAC increase rapidly after intake. Therefore, coagulation results obtained within the first 4 h after intake are not reliable.
Strengths and limitations
Our study adds considerable insight to previous reports. We are the first to evaluate the diagnostic accuracy of Hemochron® Signature to qualitatively rule out relevant DOAC concentrations of apixaban, rivaroxaban, and dabigatran. To the best of our knowledge, apixaban has never been tested with this device before. In a departure from previous studies, we aimed at establishing DOAC-specific cut-offs to provide clinicians with a practical tool for decision making during emergency treatment. All samples were acquired from real-life patients, avoiding the use of spiked plasma. Primarily collecting samples during treatment initiation rather than a steady state provided a high number of samples containing very low DOAC concentrations. Compared to previous studies [5–7], this allowed superior assessment of how such low concentrations influence coagulation assays. Due to low dabigatran concentrations in samples collected during treatment initiation, we decided to include samples from eight patients on maintenance therapy. Although this adds heterogeneity to our patient population, we did not find differences in correlation to POCT results between the two groups. Six sequential samples were acquired from each patient. Hence, a bias due to repeated measurements in individual patients cannot be excluded but this approach allowed us to cover a wide spectrum of DOAC concentrations. Due to the use of venous blood in this study, our results cannot be extended to test results obtained from capillary samples. However, as venous access is routinely obtained in all emergency patients we do not expect this to limit the clinical applicability of our results.
What constitutes a clinically relevant DOAC concentration is a matter for debate, and the concentration thresholds investigated in our study, albeit based on current literature, have not been confirmed by prospective clinical trials. Furthermore, generalizability of our results is limited by the single-centre nature of our trial. For these reasons, validation of our data is warranted, ideally including clinical outcome-oriented end-points.
Our results suggest that Hemochron® Signature POCT in combination with PT/INR or ACT+ test cards can be used to qualitatively rule out relevant concentrations of rivaroxaban and dabigatran, but not of apixaban.
Thus, Hemochron® Signature POCT can be a fast and reliable alternative for guiding emergency treatment during rivaroxaban and dabigatran therapy. It allows the rapid identification of a relevant fraction of patients that can be treated immediately without the need to await the results of much slower laboratory-based coagulation tests. The high clinical relevance of this question warrants a large-scale trial to investigate the clinical safety of this approach.
Activated clotting time
Activated clotting time plus
Activated clotting time-low range
Activated partial thromboplastin time
Direct oral anticoagulants
Diluted thrombin time
Negative predictive value
Positive predictive value
Prothrombin time/international normalized ratio
Ultra-performance liquid chromatography-tandem mass spectrometry
Vitamin K antagonists
We thank Louise Härtig for language revision of the manuscript. We acknowledge support from Deutsche Forschungsgemeinschaft and the Open Access Publishing Fund of the University of Tübingen.
No financial support. One Hemochron® Signature Elite device was allocated by Keller Medical GmbH (Bad Soden/Taunus, Germany) for research purposes. The company had no influence whatsoever on patient enrolment, acquisition of data, interpretation of data, or drafting the manuscript.
Availability of data and materials
The datasets supporting the conclusions of this article are included within the article and its additional file.
ME and SP designed the study, participated in enrolment and data acquisition, and headed preparation of the manuscript. CS and FH enrolled patients and performed POCT at the bedside. IB, AP, and JK conducted all laboratory-based coagulation tests and UPLC-MS. GB assisted with statistical data analyses. CSZ, UZ, and FH helped with patient recruitment and supervised the preparation of the manuscript. All authors have reviewed and approved the final version of the manuscript.
SP received speaker’s honoraria and consulting honoraria from Bayer, Boehringer-Ingelheim, Bristol-Myers Squibb/Pfizer, and Daiichi Sankyo, and reimbursement for congress traveling and accommodation from Bayer and Boehringer-Ingelheim. ME and FH received reimbursement for congress traveling and accommodation from Bayer. IB received speaker’s honoraria and reimbursement for congress traveling from Bristol-Myers Squibb and CSL Behring. UZ received research support from Bristol-Myers Squibb/Pfizer and speaker’s honoraria and reimbursement for congress traveling and accommodation from Biogen Idec and Medtronic. The remaining authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
Institutional Review Board approval was obtained from the ethics committee of Tübingen University Hospital (protocol no. 259/2013BO1; additional patients receiving dabigatran were enrolled using protocol no. 270/2015B01). The study was performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments. Written informed consent was obtained from all patients prior to enrolment.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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