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4470 Appropriateness of Thrombophilia Testing in Tertiary Care Centers in Edmonton

Health Services and Outcomes Research – Non-Malignant Conditions
Program: Oral and Poster Abstracts
Session: 901. Health Services and Outcomes Research – Non-Malignant Conditions: Poster III
Monday, December 7, 2015, 6:00 PM-8:00 PM
Hall A, Level 2 (Orange County Convention Center)

Alabdurubalnabi Zainab, MBBS1,2*, Salma Shivji, MD3* and Cynthia Wu, MD4

1University of Alberta Hospital, Edmonton, AB, Canada
2University of British Columbia, Vancouver, BC, Canada
3University of Alberta, Edmonton, AB, Canada
4Department of Medicine, University of Alberta, Edmonton, AB, Canada

INTRODUCTION

Thrombophilia is associated with an increased risk of venous thromboembolism (VTE). Despite this link, determining the presence or absence of such conditions has no role in VTE management including determining the choice or duration of anticoagulant therapy. Testing can be potentially harmful when results are misinterpreted or impact patient anxiety and insurance eligibility.

METHODS

We performed a retrospective chart review of adult patients presenting to the emergency department (ED) or were admitted to the University of Alberta Hospital (UAH), Royal Alexandra Hospital (RAH) and Grey Nuns Hospital (GNH) and underwent any number of thrombophilia tests (including factor V Leiden [FVL], prothrombin gene mutation [PT20210], protein C [PC], protein S [PS], antithrombin [AT] and antiphospholipid antibody testing). To assess for appropriateness of testing, categories of data were collected including presence of other strong risk factors obviating the need to look for other causes, indicators for higher yield (age of patient, presence of family history of VTE, idiopathic nature of VTE), presence of factors that confound testing (such as therapeutic anticoagulation) and relevant follow up (appropriate repeat testing when necessary). We also collected basic patient demographics, VTE details and ordering physician/service details to evaluate under what circumstances testing may be ordered more frequently.

RESULTS

134 charts of patients tested for thrombophilia were reviewed between 2007-2013 at UAH and RAH Hospitals. A total of 965 thrombophilia tests were done (see analysis table). 13.4% of the testing was ordered by hematologists, 23.1% by neurologists, 52.2% by other internists. Overall, all patients had tests performed inappropriately, lacked appropriate follow up or had uninterpretable results and none had documented counseling prior to thrombophilia testing.

CONCLUSIONS

Thrombophilia testing is frequently ordered inappropriately and not adequately followed up. Strategies to educate physicians on indications and limitations of testing are warranted.  These strategies can help decrease over/under/misinterpretation of thrombophilia testing as well as result in significant savings to the health care system if testing can be reduced.

Demographics

Sample Size

Males

Females

Total

74 (55.22%)

60 (44.78%)

134 (100%)

Age at time of testing (Yrs)

Range

19-88

Average

48.7

Patients’ Test Results

Test

Times Performed

Abnormal Results

APCR

134 (100%)

32 (23.8%)

FVL genetic test

58 (43%)

21 (39%)

PT20210

105 (77%)

4 (3.8%)

Protein C

100 (74.1%)

8 (8%)

Protein S

99 (73.3%)

16 (16.2%)

AT levels

99 (73.3%)

19 (19.2%)

Anticardiolipin Ab

117 (86.7%)

4 (3.4%)

Lupus Anticoagulant

109 (81.3%)

10 (10.2%)

Provoking Factors

Patients with One or More Provoking Factors

Major

10

7.4%

Moderate

74

56%

Minor

29

21.8%

No Provoking Factors

49

36.8%

Family History of VTE

12

8.9%

Protein C and Protein S Testing

Done During Acute VTE

64

64%

Patient was on Warfarin

25

25%

Number of Abnormal Test Results

24

16%

Number of Repeated Abnormal Tests

0

0%

AT Testing

Total Tests Performed

99

73.3%

Done During Acute VTE

62

63%

Patient was on Therap. Heparin or LMWH

62

62.6%

Number of Abnormal Test Results

19

19.2%

Abnormal Tests Repeated?

7

37%

Repeat Tests Showing Normal Results

3

57%

APA Testing

Tests were Repeated After 12 Weeks for Confirmation

11%

Disclosures: Wu: Leo Pharma: Consultancy , Honoraria , Membership on an entity’s Board of Directors or advisory committees ; Pfizer: Consultancy , Honoraria , Membership on an entity’s Board of Directors or advisory committees .

*signifies non-member of ASH