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. 2012 Feb;141(2 Suppl):e326S–e350S. doi: 10.1378/chest.11-2298

Table 2.

—[Section 1.2] Structured Clinical Questions

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.