This protocol is intended to standardize the anticoagulation management for critically-ill
patients with COVID19 pneumonia requiring admission to intensive care unit.
Indications:
Adult patients admitted to Intensive Care Unit with COVID19 Pneumonia OR as per your local guidance for high risk patients.
Contraindication:
Patients with active bleeding.
Platelets less than 50,000 per microliter.
Fibrinogen level less than 1.5 gram per liter.
Protocol
LOW-RISK GROUP: D-Dimer less than 1.2 mg/L
If CrCl ≥ 30 ml/min
Enoxaparin 40 mg subcutaneous once daily for patients with weight < 90 kg.
Enoxaparin 60 mg subcutaneous once daily for patients with weight ≥ 90 kg.
If CrCl < 30 ml/min
Dalteparin 5,000 units subcutaneous once daily for patients with weight < 90 kg.
Dalteparin 7,500 units subcutaneous once daily for patients with weight ≥ 90 kg.
For patients on Renal Replacement Therapy (RRT),
Unfractionated Heparin 5000 units subcutaneous every 12 hours.
INTERMEDIATE-RISK GROUP: D-Dimer ≥ 1.2 mg/L and P/F ratio < 200
If CrCl ≥ 30 ml/min
Enoxaparin 40 mg subcutaneous every 12 hours for patients with weight < 90 kg.
Enoxaparin 60 mg subcutaneous every 12 hours for patients with weight ≥ 90 kg.
If CrCl < 30 ml/min,
Dalteparin 7,500 units subcutaneous once daily for patients with weight < 90 kg.
Dalteparin 10,000 units subcutaneous once daily for patients with weight ≥ 90 kg.
For patients on Renal Replacement Therapy,
Unfractionated Heparin 5000 units subcutaneous every 8 hours.
HIGH-RISK GROUP: D-Dimer ≥ 1.2 mg/L, P/F ratio < 100, acutely worsening oxygenation or increasing dead space or rapid increase in D-Dimer ( ≥ 5 folds in 48 hours).
If CrCl ≥ 30 ml/min,
Administer Enoxaparin 1 mg/kg subcutaneous every 12 hours.
If CrCl < 30 ml/min,
Administer Dalteparin 100 units/kg subcutaneous every 12 hours.
For patients on Renal Replacement Therapy,
Administer Unfractionated Heparin intravenous infusion at 18 units/kg/hour targeting aPTT as per protocol.
MONITORING PATIENTS RECEIVING ANTICOAGULATION
For low-risk patients:
Receiving LMWH (Enoxaparin or Dalteparin), target Anti-Factor Xa level of 0.2-0.4 units/ml. Blood sample to be collected for analysis 4 hours after the 3rd dose.
For intermediate-risk patients
Receiving LMWH (Enoxaparin or Dalteparin), target Anti-Factor Xa level of 0.4-0.6 units/ml. Blood sample to be collected for analysis 4 hours after the 3rd dose.
For high-risk patients
Rreceiving LMWH (Enoxaparin or Dalteparin), target Anti- Factor Xa level of 0.6-1.0 units/ml. Blood sample to be collected for analysis 4 hours after the 3rd dose.
For all patients assess bleeding risk daily (platelet count < 50,000 per microliter, fibrinogen level < 1.5 gm/L).
Algorithm
References
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