Table 2.
Section | Population | Intervention and Comparator | Outcomes | Available Methodology |
Patients receiving warfarin therapy | ||||
2.1 |
Patients receiving warfarin therapy who require an elective surgery or invasive procedure |
In patients who require warfarin interruption before surgery to attain normal or near-normal INR at surgery, stopping warfarin 5-6 d before surgery vs stopping warfarin < 5 d before surgery |
Hemostasis at time of surgery (INR) |
Observational studies |
2.2 |
In patients with warfarin interruption before surgery, resuming warfarin 12-24 h after surgery (evening of or next day) and when there is hemostasis vs resuming warfarin > 24 h from surgery |
Hemostasis at time of surgery |
Observational studies |
|
2.3 |
INR testing to monitor anticoagulant effect of warfarin before and after surgery vs no testing |
Hemostasis at time of surgery (aPTT, antifactor Xa) |
Observational studies |
|
2.4 |
Need for bridging anticoagulation during perioperative warfarin interruption |
Bridging anticoagulation with heparin/LMWH vs no bridging |
Stroke, other systemic embolism, major hemorrhage |
Observational studies |
Patients considered at high risk for perioperative thromboembolism | ||||
Patients considered at moderate risk for perioperative thromboembolism |
Bridging anticoagulation with heparin/LMWH vs no bridging |
Stroke, other systemic embolism, major hemorrhage |
Observational studies |
|
Patients considered at low risk for perioperative thromboembolism |
Bridging anticoagulation with heparin/LMWH vs no bridging |
Stroke, other systemic embolism, major hemorrhage |
Observational studies |
|
2.5 |
Patients having minor dental, skin, or eye procedures |
Continuing warfarin and coadministering an oral prohemostatic drug vs stopping warfarin 5-6 d before the procedure without administering a prohemostatic drug |
ATE or VTE, major hemorrhage |
RCTs, observational studies |
Patients receiving warfarin therapy and having a minor dental procedure | ||||
Patients receiving warfarin therapy and having a minor skin procedure |
Continuing warfarin around the time of the procedure vs stopping warfarin 5-6 d before the procedure |
ATE or VTE, major hemorrhage |
RCTs, observational studies |
|
Patients receiving warfarin therapy and having cataract procedure |
Continuing warfarin around the time of the procedure vs stopping warfarin 5-6 d before the procedure |
ATE or VTE, postoperative bleeding |
RCTs, observational studies |
|
Patients receiving antiplatelet therapy | ||||
3.4 |
Patients receiving antiplatelet therapy and having minor dental, skin, or eye procedure |
Continuing antiplatelet drugs around the time of the procedure vs stopping antiplatelet drugs 7-10 d before procedure |
Myocardial ischemia, postoperative bleeding |
Observational |
3.5 |
Patients receiving antiplatelet therapy and having elective noncardiac surgery |
Continuing antiplatelet drugs around the time of the procedure vs stopping antiplatelet drugs 7-10 d before noncardiac surgery |
Myocardial ischemia, postoperative bleeding |
RCTs, observational studies |
3.6 |
Patients receiving antiplatelet therapy and having elective CABG surgery |
Continue antiplatelet drugs around the time of surgery vs stopping antiplatelet drugs 7-10 d before CABG |
Myocardial ischemia, postoperative bleeding |
Observational studies |
3.7 |
Patients with a coronary stent receiving antiplatelet therapy and having elective surgery |
In patients with a bare-metal coronary stent who require surgery within 6 wk of stent placement or patients with a drug-eluting coronary stent who require surgery within 6 mo of stent placement, continuing antiplatelet drugs around the time surgery vs stopping antiplatelet drugs 7-10 d before surgery |
Myocardial ischemia, postoperative bleeding |
Observational studies |
Patients receiving heparin bridging anticoagulation | ||||
4.2 |
Patients who are receiving bridging anticoagulation with therapeutic-dose IV UFH |
Stopping UFH 4-6 h before surgery vs stopping UFH closer to surgery |
Postoperative bleeding |
Observational studies |
4.3 |
Patients who are receiving bridging anticoagulation with therapeutic-dose SC LMWH |
Administering the last preoperative dose of LMWH ~24 h before surgery vs administering the last preoperative dose of LMWH ~12 h before surgery |
Postoperative bleeding |
Observational studies |
4.4 | Patients who are receiving bridging anticoagulation with therapeutic-dose SC LMWH |
Resuming therapeutic-dose LMWH ≤ 24 h after surgery vs resuming LMWH > 24 h after surgery |
Postoperative bleeding |
Observational studies |
Having surgery associated with high bleeding risk | ||||
Having surgery associated with low to moderate bleeding risk | Resuming therapeutic-dose LMWH ≤ 24 h after surgery vs resuming LMWH > 24 h after surgery | Postoperative bleeding | Observational studies |
aPPT = activated partial thromboplastin time; ATE = aterial thromboembolism; CABG = coronary artery bypass graft; INR = international normalized ratio; LMWH = low-molecular-weight heparin; RCT = randomized controlled trial; SC = subcutaneous; UFH = unfractionated heparin.