Abstract 4359

Introduction:

Venous Thromboembolism (VTE) remains the number one preventable cause of hospital acquired morbidity and mortality (1). To mitigate this, guidelines are published for the prevention of VTE (2). Currently, the rate of adherence to guidelines is between 16 and 60% (3). Studies show even short periods of immobilization can increase risk for VTE (4), thus we postulated that delays in prophylaxis may correlate with more VTEs.

Methods:

Between January 2009 and December 2011, hospital acquired VTEs were identified at a 600 bed teaching hospital. Control cases were selected from consecutive admissions in February 2011 to match the VTE cases by risk category, age and gender. Patients younger than 18 years, or initiated on therapeutic anticoagulation were excluded.VTE was confirmed by imaging, and timing was recorded from time of presentation to time of administration. Prophylaxis appropriateness was determined according to published guidelines (2).

Categorical variables were compared using Chi-squared test for independence. Normally distributed continuous variables were compared using 2 tailed T-test.

Results:

179 cases of hospital acquired VTE were found between 2009 and 2011. 9 cases were excluded due to age or therapeutic anticoagulation. 170 control cases were matched by risk category, age and gender. The patient characteristics are summarized in Table 1. Appropriate prophylaxis rate was lower in the VTE group.(p< 0.0001)(55% vs 80%) There was a higher rate in VTE risk assessment in the VTE group (p=0.021) (90% vs 82%). There was no significant difference (p=0.67) in the timing of initial prophylaxis. (33.4hrs vs 34.8hrs)

Table 1.

Patient Characteristics

VTE Cases (n=170)Control cases (n=170)p-value
Male 66 69 0.64 
Female 104 101  
Age (median) 71.5 68 0.89 
VTE Risk Category   0.80 
    Medical Admission, moderate VTE risk 56 63  
    General Surgery 29 28  
    Neurosurgery/Spinal Cord Injury 17 20  
    Elective Spinal Surgery 10  
    Orthopedic Surgery 19 19  
    Thoracic Surgery 10  
    Contraindication to chemical prophylaxis 24 20  
    Low VTE risk  
Appropriate prophylaxis given   <0.0001 
    Yes 93 (55%) 136 (80%)  
    No 58 (34%) 12 (7%)  
Ordered, not documented 19 (11%) 22 (13%)  
VTE Risk Assessed   0.021 
    Yes 153 (90%) 139 (82%)  
    No 15 (9%) 28 (16%)  
    No opportunity 2 (1%) 4 (2%)  
Initial prophylaxis time (hrs) 33.4 34.8 0.67 
VTE Cases (n=170)Control cases (n=170)p-value
Male 66 69 0.64 
Female 104 101  
Age (median) 71.5 68 0.89 
VTE Risk Category   0.80 
    Medical Admission, moderate VTE risk 56 63  
    General Surgery 29 28  
    Neurosurgery/Spinal Cord Injury 17 20  
    Elective Spinal Surgery 10  
    Orthopedic Surgery 19 19  
    Thoracic Surgery 10  
    Contraindication to chemical prophylaxis 24 20  
    Low VTE risk  
Appropriate prophylaxis given   <0.0001 
    Yes 93 (55%) 136 (80%)  
    No 58 (34%) 12 (7%)  
Ordered, not documented 19 (11%) 22 (13%)  
VTE Risk Assessed   0.021 
    Yes 153 (90%) 139 (82%)  
    No 15 (9%) 28 (16%)  
    No opportunity 2 (1%) 4 (2%)  
Initial prophylaxis time (hrs) 33.4 34.8 0.67 

Prophylaxis choices are summarized in Table 2. The rate of sequential compression devices (SCDs) ordered but undocumented is high in both groups. In many cases, it was the sole prophylaxis ordered, and would have been sufficient (11% VTE, 12% control). Documented contraindications to chemical prophylaxis are shown in table 3. Notably, several cases were listed as “high bleeding risk” but had no identifiable risk. Also among the cases listing thrombocytopenia, only one had less than 50k platelets.

Table 2.

Prophylaxis choice

VTE CasesControl Cases
Fondaparinux 2.5mg 
Undocumented fondaparinux 
Enoxaparin 40mg or 30mg 34 48 
Heparin 5000U TID or BID 28 45 
Documented SCDs 42 29 
Undocumented SCDs 30 23 
ASA 325mg BID 
None 29 14 
VTE CasesControl Cases
Fondaparinux 2.5mg 
Undocumented fondaparinux 
Enoxaparin 40mg or 30mg 34 48 
Heparin 5000U TID or BID 28 45 
Documented SCDs 42 29 
Undocumented SCDs 30 23 
ASA 325mg BID 
None 29 14 
Table 3.

Contraindications to chemical prophylaxis

VTE CasesControl Cases
Active Bleeding 22 10 
Bleeding risk 18 
Impeding procedure 10 
Thrombocytopenia 
Low risk assessment 
Anemia 
Same day discharge 
Patient Refusal 
Heparin antibody testing 
None documented 32 38 
VTE CasesControl Cases
Active Bleeding 22 10 
Bleeding risk 18 
Impeding procedure 10 
Thrombocytopenia 
Low risk assessment 
Anemia 
Same day discharge 
Patient Refusal 
Heparin antibody testing 
None documented 32 38 
Conclusion:

Between 2009 to 2011, 170 evaluable cases of VTE were compared against matched controls. There was no difference in the time to prophylaxis in both groups; however the 34 hour delay shows a need for improvement. The statistically lower adherence rate to guidelines in the VTE group is in keeping with other published series (3). This is made more poignant by the higher risk assessment rate in the VTE group, which should increase adherence rates. The low documentation rate of SCDs in both groups stresses the need for standardized documentation. Adherence rates would be higher since SCDs would be sufficient in many cases. Incorrect risk assessment, especially with regard to bleeding risk and thrombocytopenia highlight the need for improved understanding of true chemical prophylaxis contraindications. This study demonstrates the importance of continued adherence to prophylaxis throughout hospitalization.

Disclosures:

No relevant conflicts of interest to declare.

(1)
(2)
(3)
(4)

Author notes

*

Asterisk with author names denotes non-ASH members.

Sign in via your Institution