Write MD Anaesthesiology exam notes on guidelines for central neuroaxial blockade in patient taking anticoagulant based on recent Asra guidelines
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| Parameter | Recommendation |
|---|---|
| Pre-block | Discontinue 5 days before; verify INR ≤ 1.4 (ASRA: normal INR) |
| Monitoring | Check INR on day 1–2 after initiation if catheter in situ |
| Catheter removal | INR < 1.5; assess neurological status |
| Restart | 6 hours after catheter removal |
| Catheter + warfarin | Warfarin contraindicated with indwelling neuraxial catheter |
| Parameter | Recommendation (Grade 1A) |
|---|---|
| Pre-block | Discontinue infusion 4–6 hours before; verify normal aPTT |
| Needle timing | No other coagulopathy present |
| Post-needle heparinization | Delay IV heparin 1 hour after needle placement |
| Catheter removal | 4–6 hours after last heparin dose; assess coagulation status |
| Restart heparin | 1 hour after catheter removal |
The introduction of LMWH in North America in 1993 triggered a marked rise in SEH cases, prompting current guidelines.
| Dose | Pre-block interval | Catheter removal |
|---|---|---|
| Prophylactic (e.g., enoxaparin 40 mg OD) | ≥ 12 hours before | ≥ 12 hours after last prophylactic dose |
| Therapeutic (e.g., enoxaparin 1 mg/kg BD) | ≥ 24 hours before | ≥ 12–24 hours after last therapeutic dose |
| Renal impairment (CrCl < 30 mL/min) | Double the interval (≥ 24 h prophylactic; ≥ 48 h therapeutic) |
| Dose | Pre-block interval |
|---|---|
| Standard (15–20 mg OD) | ≥ 72 hours (Grade 2C) |
| Low dose (10 mg OD, CrCl > 15) | ≥ 24 hours (30 h if CrCl 15–30 mL/min) |
| Dose | Pre-block interval |
|---|---|
| Standard (5 mg BD) | ≥ 72 hours |
| Low dose (2.5 mg BD) | ≥ 36 hours |
| Dose | Pre-block interval |
|---|---|
| Standard (60 mg OD) | ≥ 72 hours |
| No low-dose guideline currently available | — |
| CrCl (mL/min) | Pre-block interval |
|---|---|
| ≥ 80 | 72 hours (3 days) |
| 50–79 | 96 hours (4 days) |
| 30–49 | 120 hours (5 days) |
| < 30 | Avoid neuraxial block |
| Unknown | 120 hours (5 days) |
| Drug | Discontinue before CNB |
|---|---|
| Clopidogrel | 5–7 days |
| Prasugrel | 7–10 days |
| Ticlopidine | 10 days |
| Drug | Discontinue before CNB |
|---|---|
| Ticagrelor | 5–7 days |
| Cangrelor (IV) | 3 hours |
| Herb | Effect | Discontinue |
|---|---|---|
| Garlic | Inhibits platelet aggregation | 7 days |
| Ginkgo | Inhibits PAF | 36 hours |
| Ginseng | Multiple effects | 7 days |
| Drug Class | Drug | Stop before CNB | Restart after CNB |
|---|---|---|---|
| UFH (IV therapeutic) | Heparin | 4–6 h | 1 h post-needle; 1 h post-catheter removal |
| UFH (SC prophylactic BID) | Heparin 5000 U | No contraindication | Per VTE protocol |
| UFH (SC therapeutic) | Heparin >10,000 U/dose | 24 h | — |
| LMWH prophylactic | Enoxaparin 40 mg | 12 h | 12 h post-needle; 4 h post-catheter removal |
| LMWH therapeutic | Enoxaparin 1 mg/kg | 24 h | 24 h post-needle |
| Warfarin | Warfarin | 5 days; INR ≤ 1.4 | 6 h post-catheter removal |
| DOAC Factor Xa (standard) | Rivaroxaban, Apixaban, Edoxaban | 72 h | 6 h post-catheter removal |
| DOAC Factor Xa (low dose) | Rivaroxaban 10 mg, Apixaban 2.5 mg | 24–36 h | 6 h |
| DTI | Dabigatran | 72–120 h (renal-dependent) | 6 h |
| Fondaparinux | Arixtra | 36–42 h | 12 h |
| Clopidogrel | Plavix | 5–7 days | 24 h (no loading dose) |
| Prasugrel | Effient | 7–10 days | 24 h |
| Ticagrelor | Brilinta | 5–7 days | Immediately |
| Cangrelor | IV | 3 h | Immediately |
| GP IIb/IIIa | Eptifibatide/Tirofiban | 8 h | — |
| GP IIb/IIIa | Abciximab | 48 h | — |
| Fibrinolytics | tPA, SK | 10 days | — |
| Drug | Useful Test |
|---|---|
| Warfarin | PT / INR |
| UFH | aPTT (therapeutic); anti-Xa (monitoring) |
| LMWH | Anti-Xa (if monitoring needed; not routine for neuraxial) |
| Dabigatran | Thrombin Time (TT), Ecarin Clotting Time (ECT) |
| Rivaroxaban/Apixaban | Calibrated anti-Xa (rivaroxaban or apixaban calibrated); NOT PT or aPTT |
| DOACs (general) | Calibrated anti-Xa < 30 ng/mL or anti-Xa ≤ 0.1 IU/mL = acceptable |
| General coagulation screen | TEG/ROTEM (viscoelastic) — comprehensive |
Important: Uncalibrated or heparin-calibrated anti-Xa assays cannot predict DOAC drug levels accurately.