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warfarin guidelines


Warfarin Guidelines CPG

Warfarin is the most commonly used oral anticoagulant of which there are two brands.

Brands are not interchangeable.




Availability of tablet strengths


The following table describes the availability of tablet strengths and their corresponding colour.

1mg
2mg
3mg
5mg
Coumadin
Light tan
Lavender
n/a
Green
Marevan
Brown
n/a
Blue
Pink

Guidelines


For acute thrombosis or thromboembolism, commence warfarin when the patient is receiving heparin. A minimum of 5 days of heparin should be given, even if the INR reaches the desired level beforehand.

Most patients require 3-5 days of warfarin before achieving a stable maintenance phase.


Target INR range for clinical indication (individual patients may vary)


Indication
Target
Target range
Venous thromboembolism
2.5
2.0-3.0
Prosthetic heart valves
3.0
2.5-3.5
Cardiomyopathy
2.5
2.0-3.0
Atrial fibrillation
2.0
1.5-2.5


Warfarin dosing


Warfarin is NOT evenly distributed within each tablet. Doses should be given in whole tablet sizes. Many patients will require alternate day doses or dose reduction.

If the woman has previously been taking warfarin and is recommencing warfarin after surgery, begin warfarin therapy at the usual dose.


Loading dose: day 1
For adult patients commencing warfarin begin with a loading dose of 5 -10mg. The lower dose should be used if there is poor oral intake, liver impairment concurrent antimicrobial therapy or age>60.

Loading dose: days 2-4
Subsequent loading doses are based on individual INR response.

The dose reductions in the table below are critical to avoid 'over-shooting' the target range.


INR
Warfarin adjustment
1.1-1.3
Repeat initial loading dose
1.4-1.9
50% of initial loading dose
2.0-3.0
50% of initial loading dose
3.1-3.5
25% of initial loading dose
>3.5
Hold until INR <3.5 then restart at 50% less than previous dose.

If the INR is not >1.5 on Day 4, the patient should be reassessed and the dose increased gradually until the INR is in the desired range.

If the patient is receiving other medicines (e.g. antibiotics) the loading dose may need to be adjusted accordingly. Check with Pharmacy or Haematology.


Patient/consumer education


Thorough patient education is the key to successful management of patients on oral anticoagulants.

Factors affecting the INR include:
  • other medicine use
  • Vitamin K content of diet
  • alcohol
  • many naturopathic or dietary supplements
  • herbal medicines.

Women taking warfarin may notice that their periods are slightly heavier.

Women should be advised of the importance of effective contraception if there are taking warfarin.

Avoid aspirin or other NSAIDS unless specifically prescribed by the woman’s physician.



Outpatient follow-up


Heparin can be ceased when the INR is therapeutic for two consecutive days.

Monitor INR within three days of discharge - refer patient to their GP or local pathology provider.

The duration of therapy is dependent upon the indication for anticoagulation.


ALWAYS CHECK THE INR within 5 days:
  • of a dose change
  • if a concurrent illness develops e.g. diarrhoea or vomiting
  • if a new medicine is prescribed

Warfarin interactions


It must be assumed that all medications will influence the individual's response to warfarin. The INR may increase or decrease, depending on the medicine.

Pregnancy


Warfarin embryopathy occurs in approximately 5% of fetuses exposed to warfarin between 6-13 weeks gestation. Warfarin embryopathy is variable in severity and ranges from mild nasal flattening to severe mid face flattening with shortened limbs (dwarfism). Exposure in the second or third trimester carries an additional 5% risk of fetal intracerebral haemorrhage.

All women of reproductive age should be informed of the teratogenic effects of warfarin and advised to seek urgent medical attention if pregnancy occurs.

Women who conceive on warfarin and who wish to continue the pregnancy should be given vitamin K 10mg orally to reverse the warfarin effect and commenced immediately on therapeutic LMWH at a weight adjusted twice daily dose. Each case should be discussed with the woman’s physician, haematologist or cardiologist before the warfarin is ceased.

Perioperative anticoagulation


Warfarin may not need to be stopped for minor procedures such as D&C or Mirena insertion. Check with the consultant gynaecologist.

Women undergoing more major surgery may require bridging anticoagulation.

Advice regarding the need for bridging anticoagulation should be obtained from the treating haematologist or cardiologist. If the warfarin is managed by a pathology provider or general practitioner, refer the patient to the Women’s haematology outpatients.

Adverse events


One of the major adverse events associated with warfarin is bleeding. If a patient on warfarin suffers significant bleeding, withhold any further doses, and seek urgent Haematology consult.

Urgent surgery


If a woman taking warfarin requires urgent surgery, obtain urgent Haematology consult.

Further information can be obtained by referring to the following journal article:
  • Baker RI, Coughlin PB, Gallus AS, Harper PL, Salem HH, Wood EM, The Warfarin Reversal Consensus Group. Warfarin reversal: consensus guidelines, on behalf of the Australasian Society of Thrombosis and Haemostasis. Medical Journal of Australia; MJA 181:9, 1 November 2004. http://www.mja.com.au/public/issues/181_09_011104/bak10441_fm.pdf.

References


Refer to: References: Anticoagulants.




Revised and updated: 14 May 2009



Royal Women's Hospital Clinical Practice Guidelines (CPGs) are intended to provide guidance to health care professionals, based on a thorough evaluation of research evidence, on the practical assessment and management of specific clinical issues or situations. The guidelines allow some flexibility on the part of the health care professional based on the needs of the specific patient for whom they are caring.

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