Background: In Ireland physician transfer to utilisation of Low Molecular W
eight Heparin for Venous Thromboembolism has been slow, despite evidence of
efficacy and concern about the level of anticoagulation achieved with Unfr
actionated Heparin.
Objective: To examine the effectiveness of Unfractionated Heparin administr
ation in a teaching hospital in Ireland. Primary outcomes measured were tim
e to therapeutic APTT and length of hospital stay.
Methods: We identified 50 consecutive eligible patients treated with contin
uous intravenous unfractionated heparin for Venous Thromboembolism from the
period August 1994 to December 1996 at Beaumont Hospital, Dublin, Ireland.
Data analysed included length of hospital stay, costing data and anticoagu
lation parameters (time to therapeutic APTT, percentage of time within ther
apeutic range, number of diagnostic tests, heparin dosages).
Results: A significant number of patients (22%) never achieved therapeutic
APTT levels. Of those who did achieve therapeutic APTT levels at some time
during their therapy, therapeutic range APTT was maintained only 28% of the
time on heparin. 57% of the time results mere below therapeutic while 15%
of the time results were above therapeutic. Also 26% of the patients were d
ischarged with INR results outside the therapeutic range despite an average
length of stay of 13.3 days (over twice the ideal of 6 days). Ineffective
anticoagulation influenced hospital length of stay in 60% of cases in our e
valuation. Average cost of treatment with Unfractionated Heparin was pound
5897.86 versus the projected cost of Low Molecular Weight Heparin at pound
2562.78 for 6 days of in-patient therapy or pound 60.78 for outpatient ther
apy (excluding physician visit costs).
Conclusions: Unfractionated Heparin therapy as reviewed in our study is sub
-optimal with inadequate anti coagulation and prolonged hospitalisation. Lo
w Molecular Weight heparin, with comparable therapeutic effect documented e
lsewhere, overall may cost less.
Acknowledgement: Funding for this study was received from Leo Laboratories,
Ireland.