Figure 1.
Residual DOAC levels according to preprocedural DOAC-interruption interval in hours. Patients undergoing low- and high-bleeding-risk procedures had their DOAC stopped 1 and 2 days prior to the procedure, respectively. Patients undergoing low-bleeding-risk procedures are indicated in black, whereas patients undergoing high-bleeding-risk procedures are indicated in blue. (A) The median preoperative-interruption intervals for low- and high-bleeding-risk procedures for apixaban were 39.4 hours (IQR, 37.5, 41.5) and 63.8 hours (IQR, 61.0, 67.0), respectively. (B) The median preoperative-interruption intervals for dabigatran for low- and high-bleeding-risk procedures were 40.5 (IQR, 38.4, 44.7) and 63.8 (IQR, 61.7, 74.3), respectively. (C) The median preoperative-interruption intervals for rivaroxaban for low- and high-bleeding-risk procedures were 48.0 (IQR, 40.8, 51.0) and 72.0 (IQR, 66.1, 75.0), respectively.

Residual DOAC levels according to preprocedural DOAC-interruption interval in hours. Patients undergoing low- and high-bleeding-risk procedures had their DOAC stopped 1 and 2 days prior to the procedure, respectively. Patients undergoing low-bleeding-risk procedures are indicated in black, whereas patients undergoing high-bleeding-risk procedures are indicated in blue. (A) The median preoperative-interruption intervals for low- and high-bleeding-risk procedures for apixaban were 39.4 hours (IQR, 37.5, 41.5) and 63.8 hours (IQR, 61.0, 67.0), respectively. (B) The median preoperative-interruption intervals for dabigatran for low- and high-bleeding-risk procedures were 40.5 (IQR, 38.4, 44.7) and 63.8 (IQR, 61.7, 74.3), respectively. (C) The median preoperative-interruption intervals for rivaroxaban for low- and high-bleeding-risk procedures were 48.0 (IQR, 40.8, 51.0) and 72.0 (IQR, 66.1, 75.0), respectively.

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