Table 2.

Association of IVCF usage and brain metastases with 30-day mortality in patients diagnosed with melanoma, kidney, breast, or lung cancers and a VTE by the presence or absence of active bleeding

Variable HR (95% CI)
Active bleeding (no interaction between IVCF and brain metastasis)  
Brain metastases  
Yes 1.27 (0.98-1.65) 
No Reference 
IVCF  
Yes 0.53 (0.42-0.68) 
No Reference 
No active bleeding (interaction between IVCF & brain metastasis)  
Brain metastases  
IVCF  
Yes 0.72 (0.60-0.85) 
No Reference 
No brain metastases  
IVCF  
Yes 0.91 (0.80-1.05) 
No Reference 
Variable HR (95% CI)
Active bleeding (no interaction between IVCF and brain metastasis)  
Brain metastases  
Yes 1.27 (0.98-1.65) 
No Reference 
IVCF  
Yes 0.53 (0.42-0.68) 
No Reference 
No active bleeding (interaction between IVCF & brain metastasis)  
Brain metastases  
IVCF  
Yes 0.72 (0.60-0.85) 
No Reference 
No brain metastases  
IVCF  
Yes 0.91 (0.80-1.05) 
No Reference 

Inverse propensity-weighted Cox proportional hazard regression models were used. IVCF was included as time-dependent covariate. All models were also adjusted for age, year, and location of VTE; prior history of VTE; sex; race/ethnicity; health insurance; neighborhood socioeconomic status; cancer site; stage at diagnosis; comorbidities; and each contraindication for anticoagulation (in the active bleeding model, aortic dissection and brain, orthopedic, and spine surgeries were consolidated into 1 variable).

There was an interaction between IVCF and active bleeding (P = .0006) warranting stratified models.

Active bleeding: there was no interaction between IVCF and brain metastases (P = .7046).

No active bleeding: there was an interaction between IVCF and brain metastases (P = .0318).

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