Use of aPTT and PT in the Raschke Heparin Protocol
The Raschke protocol uses aPTT exclusively for monitoring unfractionated heparin (UFH) therapy, targeting an aPTT of 1.5-2 times control (typically 46-70 seconds), while PT/INR is not used for heparin monitoring and should only be checked when transitioning to warfarin therapy. 1, 2
aPTT Monitoring in the Raschke Protocol
The Raschke protocol is a weight-based heparin dosing nomogram that relies entirely on aPTT for dose adjustments:
- Initial dosing: 80 units/kg IV bolus, followed by 18 units/kg/hour continuous infusion 1
- Target aPTT range: 46-70 seconds (corresponding to anti-Xa activity of 0.3-0.7 units/mL) 1
- Monitoring frequency:
Dose Adjustment Algorithm Based on aPTT
The protocol provides specific dose adjustments based on aPTT results 1:
- aPTT <35 seconds: Give 80 units/kg bolus, increase infusion by 4 units/kg/hour
- aPTT 35-45 seconds: Give 40 units/kg bolus, increase infusion by 2 units/kg/hour
- aPTT 46-70 seconds (therapeutic): No change
- aPTT 71-90 seconds: Decrease infusion by 2 units/kg/hour
- aPTT >90 seconds: Hold infusion for 1 hour, then decrease by 3 units/kg/hour
PT/INR Has No Role in Heparin Monitoring
PT should not be used to monitor heparin therapy. The evidence is clear on this separation:
- Heparin prolongs PT minimally and unpredictably 2, 3
- PT is insensitive to therapeutic heparin levels 3
- Within therapeutic aPTT ranges, PT changes are not statistically significant 3
When PT Becomes Relevant
PT/INR only becomes important during warfarin bridging when transitioning from heparin to oral anticoagulation 4, 2:
- Wait at least 5 hours after last IV heparin dose before drawing PT for warfarin monitoring 2
- Wait 24 hours after last subcutaneous heparin dose 2
- This prevents heparin interference with obtaining a valid PT/INR for warfarin dose adjustment
Critical Pitfalls to Avoid
Do not use PT to guide heparin dosing - this is a common error that can lead to inadequate anticoagulation. The Raschke protocol achieved therapeutic aPTT in 91% of low-bleeding-risk patients using aPTT-guided dosing alone 5.
Local aPTT calibration is essential - the therapeutic range of 46-70 seconds must be validated at your institution to correspond to anti-Xa levels of 0.3-0.7 units/mL 1, 6. Different aPTT reagents have varying sensitivities to heparin 7, 6.
Consider anti-Xa monitoring in heparin resistance - if patients require >35,000 units/day to achieve therapeutic aPTT, switch to anti-Xa level monitoring (target 0.35-0.7 units/mL) 1.
Additional Monitoring Beyond aPTT
While aPTT drives dosing decisions, comprehensive monitoring includes 2:
- Platelet counts (periodically throughout therapy to detect HIT)
- Hematocrit
- Occult blood in stool
- These parameters assess safety but do not guide dose adjustments