Table 4.
Assay | Recommendations | Advantages | Disadvantages |
---|---|---|---|
Anti-Factor Xa chromogenic assay | • This assay is recommended (over PT measurement) and should always be used if possible | • Specific and sensitive quantitative measure • Determines plasma levels after all approved therapeutic doses of rivaroxaban have been administered • Rivaroxaban calibrators and controls are commercially available |
• Requires rivaroxaban calibrators and controls • Assay is not available in many hospitals • Results need to be interpreted in relation to the timing of the tablet intake, in accordance with the pharmacokinetic profile |
Prothrombin time | • Measurement of PT with a reagent sensitive to rivaroxaban (such as Neoplastin Plus; Roche Diagnostics, Mannheim, Germany) may be used for qualitative assessment only (measured in seconds) | • Assay is widely available • Simple assay • Quick results |
• Gives a qualitative assessment expressed in seconds • Notable variations with different reagents • Conventional INR must not be used because INR does not correct for variations • The use of PT/INR or CoaguCheck tests (Roche Diagnostics, Mannheim, Germany) or PT with insensitive reagents (such as Innovin® [Siemens HealthCare Diagnostic Products GmBH, Marburg, Germany]) is not recommended |
Note: Data from references 2, 19, 49, and 55.
Abbreviations: INR, international normalized ratio; PT, prothrombin time.