It is not recommended to perform neuraxial anaesthesia in patients with moderate to severe renal impairment (creatinine clearance ≤ 50mls/min i.e. 0.8 mls/sec) on therapeutic doses of Enoxaparin
Therapeutic anticoagulation doses of Enoxaparin (1 mg/kg twice daily or 1.5 mg/kg once daily) do not provide a safe window of opportunity for neuraxial anaesthesia. In patients with normal-mildly reduced renal function (GFR > 50mls/min, or 0.8mls/sec) a minimum of 24 hours must elapse from the last therapeutic anticoagulation dose of Enoxaparin to the time of needle/catheter insertion for neuroaxial anaesthesia/analgesia
To reduce the potential risk of bleeding associated with the concurrent use of Enoxaparin and neuraxial anaesthesia/ analgesia, the pharmacokinetic profile of the drug should be considered. Placement and removal of the needle/ catheter is best performed when the anticoagulant effect of Enoxaparin is low.
In patients with normal to mildly reduced renal function (as judged by GFR > 50mls/min or 0.8mls/sec) receiving therapeutic anticoagulation doses of Enoxaparin 1 mg/kg twice daily or 1.5 mg/kg once daily) placement and removal of epidural &/or spinal needle or catheter requires a delay of 24 hours from the last dose of Enoxaparin.
The decision to re-introduce Enoxaparin post-operatively MUST be made at Consultant level.
However subsequent Enoxaparin dose should be given no sooner than 4 hours after spinal needle/ catheter removal or insertion #.
The patient's regular Enoxaparin dose may need to be delayed to ensure this.
If blood is present during needle/ catheter placement, the subsequent dose of Enoxaparin should be delayed for 24 hours after placement #.