Management of patients on Direct Oral Anti Coagulants (DOACs) and Antiplatelet Drugs presenting for EMERGENCY NOF fracture surgery

Key Points

  • The DOACs are oral anticoagulants that are an alternative to vitamin K antagonists (warfarin) and heparins. They include dabigatran (a direct thrombin inhibitor), rivaroxaban, edoxaban and apixaban (direct Xa inhibitors). The DOACs do not affect the results of coagulation tests (PT, INR, APTT, anti-Xa) in a predictable or linear fashion, unlike warfarin.
  • It is more important to focus on the time of the last dose of DOAC than on the laboratory results, as the clotting times do not correlate with bleeding risk, but normal clotting times are more reassuring than those that remain prolonged, particularly if there is uncertainty about the time of the last dose.
Version:2.0
Date Issued:03/04/2025
Review Date:01/04/2028
Key words:Fracture NOF DOAC, antiplatelet drugs

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Abbreviations

AAGBIAnaesthetists of Great Britain and Ireland
anti-XaLow-molecular-weight heparin
CrClcreatinine clearance
DOACsDirect Oral Anti Coagulants
ESAEuropean Society of Anaesthesiologist
LMWHLow Molecular Weight Heparin
INRInternational Normalized Ratio
TTthrombin time

Summary

The DOACs are oral anticoagulants that are an alternative to vitamin K antagonists (warfarin) and heparins. They include dabigatran (a direct thrombin inhibitor), rivaroxaban, edoxaban and apixaban (direct Xa inhibitors). The DOACs do not affect the results of coagulation tests (PT, INR, APTT, anti-Xa) in a predictable or linear fashion, unlike warfarin.

Standard coagulation assays will not predict the degree of anticoagulation in a given patient but abnormalities of APTT (dabigatran) and PT (rivaroxaban, edoxaban and apixaban) indicate possible ongoing presence of the anticoagulant and hence increased bleeding risk.

It is more important to focus on the time of the last dose of DOAC than on the laboratory results, as the clotting times do not correlate with bleeding risk, but normal clotting times are more reassuring than those that remain prolonged, particularly if there is uncertainty about the time of the last dose.

Good communication between the geriatric, orthopaedic, anaesthetic and eventually haematology teams is vital to coordinate optimal time of surgical intervention. It’s important to balance the benefit of early surgery (reduction of complications like delirium, pain,

pressure ulcers, reduction of the length of stay, targeting of the BPT criteria of surgery within 36 hours) and safety issues mainly related to safe spinal anaesthesia and surgery.

Recent literature and the AAGBI Proximal Neck of Femur Guidelines emphasise the need to consider the very small but serious risk of Vertebral Canal haematoma against the common and proven risks of delaying surgery beyond 36 hours.

Ideally the emergency surgery should be started at least 1-2 elimination half-lives after the last dose of anticoagulant if possible. The European Society of Anaesthesiologist (ESA) recommends that 2 elimination half- lives need to elapse between administration of the last dose of the drug and the performance of the neuraxial block. The estimated half- life varies according to the creatinine clearance (CrCl).

   
Drug   
   
Creatinine
   
Clearance   
   
Time from
   
dose to
   
insertion /
   
removal of
   
regional   
   
Time from
   
insertion   or
   
removal of   regional
   
to next   dose   
   
Administration   of
   
drug while   spinal
   
or epidural
   
catheter in   place   
   
Rivaroxaban   
   
CrCl > 30 ml/min   
   
24 hours   
   
6 hours
   
24 hours   if traumatic puncture   
   
Not recommended   
   
CrCl < 30   ml/min   
   
48 hours   
   
Dabigatran
   
CONSIDER   REVERSAL
   
WITH   PRAXBIND   
   
CrCl > 50 ml/min:   
   
48 hours   
   
6 hours   
   
Not recommended   
   
CrCl < 50   ml/min   
   
72 hours   
   
Apixaban   
   
CrCl > 30 ml/min   
   
24 hours   
   
6 hours   
   
Not recommended   
   
CrCl < 30   ml/min   
   
48 hours   
   
Edoxaban   
   
CrCl > 30 ml/min   
   
24 hours   
   
6 hours   
   
Not recommended   
   
CrCl < 30   ml/min   
   
48 hours   

Incorporating these time intervals, a pragmatic guideline approach, based on creatinine clearance, would be:

APIXABAN, RIVAROXABAN & EDOXABAN

DABIGATRAN

  • Stop agent

  • Confirm with patient time of last dose

List for theatre 24 hours after last dose ingested * with spinal anaesthesia if creatinine clearance equal or > 30 ml/min

  • Stop agent

  • Confirm with patient time of last dose

  • List for next afternoon theatre trauma slot

  • At 8am on day of surgery, send blood for “thrombin time” TT

If CrCl less than 30 ml/min, delay surgery to 48 hours OR discuss with Haematology on call.

Creatinine clearance = 1.23 x (140-age) x weight (x 0.85 if female) ÷ serum creatinine

(Age in years; weight in kg; creatinine in µmol/l)

TT normal -> proceed with surgery

TT abnormal -> discuss with haematologist for the use of Praxbind *

*Dabigatran:

Consider use of Praxbind, a specific antidote to dabigatran available in blood bank, active in 30 min/1 hour. This will neutralise the anticoagulant effect of dabigatran after approximately 1 hour when it is safe to proceed. Needs discussion between a senior member of orthopaedic or geriatric team (registrar, associate specialist, consultant) with on call haematologist consultant for authorisation.

Consider the use of tranexamic acid 1 gram, to be administered upon induction by anaesthetist.

Postoperative resumption of DOACs: restart pre-op dose

The DOACs need to be restarted postoperatively cautiously once haemostasis is secure; be aware that the onset of action is far quicker than for warfarin. LMWH prophylaxis post- operatively can be considered until full anticoagulation is surgically safe if there is significant delay in restarting DOAC.

DrugTime from insertion or removal of regional to next dose
Rivaroxaban

6 hours

24 hours if traumatic puncture

Dabigatran6 hours
Apixaban6 hours
Edoxaban6 hours

Antiplatelet medications

Any single antiplatelet medication (including aspirin, clopidogrel, ticagrelor, prasugrel) is not a contraindication to spinal anaesthesia for acute hip fracture surgery, if this is the best option for an individual patient. This should be discussed with the patient.

Whilst dual antiplatelet therapy (e.g., aspirin and clopidogrel) is not an absolute contraindication to central neuraxial block in the context of acute hip fracture surgery, there would need to be good reason not to proceed with a general anaesthetic on a risk/benefit basis.

All high-risk patients should be monitored for signs of vertebral canal haematoma in the postoperative period (back pain, numbness, motor weakness, bladder/bowel incontinence).

References

  1. Smith, F. and Telford, R. (2014) Novel anti-platelet agents and anticoagulants. Available at: https://resources.wfsahq.org/atotw/novel-anti-platelet-agents-and-anticoagulants-anaesthesia-tutorial-of-the-week-309/ (Accessed: 17 February 2025).

  2. Horlocker, T.T. (2011) 'Regional anaesthesia in the patient receiving antithrombotic and antiplatelet therapy', British Journal of Anaesthesia, 107(Suppl 1), pp. i96-i106. Available at: https://doi.org/10.1093/bja/aer381

  3. Kietaibl S, Ferrandis R, Godier A, et al. (2022) 'Regional anaesthesia in patients on antithrombotic drugs: Joint ESAIC/ESRA guidelines', European Journal of Anaestehsiology, 39(2), pp. 100-132. Available at: https://doi.org/10.1097/eja.0000000000001600

  4. Baron, T.H., Kamath, P.S. and McBane, R.D. (2013) 'Management of antithrombotic therapy in patients undergoing invasive procedures', New England Journal of Medicine, 368(22), pp. 2113-2224. Available at: https://doi.org/10.1056/nejmra1206531

  5. Mayor, A. and White, S.M. (2020) 'Direct oral anticoagulants and delays to hip fracture repair', Anaesthesia, 75(9), pp. 1139-1141. Available at: https://doi.org/10.1111/anae.15008

  6. Mayor, A. and White, S.M. (2020) 'Direct oral anticoagulants and delays to hip fracture repair', Anaesthesia, 75(9), pp. 1139-1141. Available at: https://doi.org/10.1111/anae.15008

  7. Griffiths, R. et al. (2020) 'Guideline for the management of hip fractures 2020: guideline by the Association of Anaesthetists', Anaesthesia, 76(2), pp. 225-237. Available at: https://doi.org/10.1111/anae.15291

  8. NHS Networks (2022) Hip Fracture Perioperative Network (HipPeN). Available at: https://web.archive.org/web/20221006162506/https://www.networks.nhs.uk/nhs-networks/hip-fracture-anaesthesia (Accessed: 17 February 2025).

  9. Fragility Fracture Network [FFN] (2025) Fragility Fracture Network. Available at: https://fragilityfracturenetwork.org/ (Accessed: 17 February 2025).

  10. National Falls and Fragility Fracture Audit Programme [FFFAP] (2025) National hip fracture database. Available at: https://www.nhfd.co.uk/ (Accessed: 17 February 2025).

  11. National Office of Clinical Audit [NOCA] (2024) Irish hip fracture database. Available at: https://www.noca.ie/audits/irish-hip-fracture-database/ (Accessed: 17 February 2025).

  12. NHS National Services Scotland (2024) The Scottish hip fracture audit. Available at: https://www.shfa.scot.nhs.uk/index.htm (Accessed: 17 February 2025).

Full version control record

Version:2.0
Guidelines Lead(s):Dr Mark Reaveley Anaesthetic Consultant FPH, Dr Peter Sadeghi Anaesthetic Consultant WPH, Dr Marissa Hagan Orthogeriatric Consultant WPH
Contributor(s):Mr Rakesh Kucheria, Orthopaedic Consultant WPH Dr Nicola Philpott, Haematology Consultant WPH
Lead Director / Chief of Service:Dr Subodh Tote, CoS Anaesthesia
Library check completed:17/02/2025
Ratified at:Anaesthesia Clinical Governance 22.1.2025
Date Issued:03/04/2025
Review Date:01/04/2028
Pharmaceutical dosing advice and formulary compliance checked by:Laura Johnson Lead Critical Care Pharmacist 17/02/2025
Key words:Fracture NOF, DOAC, antiplatelet drugs

Version Control Sheet

VersionDateGuideline Lead(s)StatusComment
1June 2021Anaesthetic ConsultantFinal
1.1September 2022Clinical Guidelines AdministratorInterimTransferred to new Clinical Guidelines Template
2.0April 2025Anaesthetic ConsultantFinalScheduled review

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