Key result
The ClotChip dielectric microsensor accurately detected DOAC anticoagulant effects, with AUCs of 0.83 for rivaroxaban, 0.82 for apixaban, and 1.0 for dabigatran (all p<0.01).
Why the study?
Due to variability among routine coagulation tests, there is an unmet need for a rapid assay to assess the anticoagulant effect of DOACs in acute settings.
Does the ClotChip dielectric microsensor accurately detect DOAC anticoagulant effects in whole blood samples from patients?
Observational (n=154)
No
Does the ClotChip dielectric microsensor accurately detect DOAC anticoagulant effects in whole blood samples from patients?
Effect estimate: AUC 0.83 (95% CI 0.75-0.91)
p-value: p=<0.01
The ClotChip dielectric microsensor provides a rapid, sensitive point-of-care method to detect the anticoagulant effects of DOACs using a small whole blood sample.
May support point-of-care DOAC monitoring; hypothesis-generating pending prospective outcome validation.
Background There are acute settings where assessing the anticoagulant effect of direct oral anticoagulants (DOACs) can be useful. Due to variability among routine coagulation tests, there is an unmet need for an assay that detects DOAC effects within minutes in the laboratory or at the point of care. Methods We developed a novel dielectric microsensor, termed ClotChip, and previously showed that the time to reach peak permittivity (T peak) is a sensitive parameter of coagulation function. We conducted a prospective, single-center, pilot study to determine its clinical utility at detecting DOAC anticoagulant effects in whole blood. Results We accrued 154 individuals: 50 healthy volunteers, 49 rivaroxaban patients, 47 apixaban, and 8 dabigatran patients. Blood samples underwent ClotChip measurements and plasma coagulation tests. Control mean T peak was 428 seconds (95% confidence interval [CI]: 401–455 seconds). For rivaroxaban, mean T peak was 592 seconds (95% CI: 550–634 seconds). A receiver operating characteristic curve showed that the area under the curve (AUC) predicting rivaroxaban using T peak was 0.83 (95% CI: 0.75–0.91, p < 0.01). For apixaban, mean T peak was 594 seconds (95% CI: 548–639 seconds); AUC was 0.82 (95% CI: 0.73–0.91, p < 0.01). For dabigatran, mean T peak was 894 seconds (95% CI: 701–1,086 seconds); AUC was 1 (p < 0.01). Specificity for all DOACs was 88%; sensitivity ranged from 72 to 100%. Conclusion This diagnostic study using samples from “real-world” DOAC patients supports that ClotChip exhibits high sensitivity at detecting DOAC anticoagulant effects in a disposable portable platform, using a miniscule amount of whole blood (<10 µL).
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Maji et al. (2020) conducted an observational in DOAC therapy (n=154). ClotChip dielectric microsensor vs. Healthy volunteers was evaluated on Predicting rivaroxaban use using T peak (AUC 0.83, 95% CI 0.75-0.91, p=<0.01). The ClotChip dielectric microsensor accurately detected DOAC anticoagulant effects, with AUCs of 0.83 for rivaroxaban, 0.82 for apixaban, and 1.0 for dabigatran (all p<0.01).
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