Mode
Text Size
Log in / Sign up

Thromboembolic events cost 2.5-fold more per event than bleeding after high-risk endoscopyHigh Risk Endoscopy Procedures Linked to Bleeding in Patients

AI-generated summary of the cited source, checked by automated accuracy review. How we work

Key Takeaway
Note that thromboembolic events after high-risk endoscopy are associated with 2.5-fold higher costs than bleeding.

This retrospective cohort study analyzed 2,486 unique patients (1,933 with linked cost data) on DOAC or warfarin therapy who underwent high-risk endoscopy. The study assessed peri-procedural adverse events and associated healthcare costs over a 90-day follow-up period.

Bleeding rates were reported at 18.0% at 7 days and 22.9% at 90 days. Stroke or TIA rates were lower, recorded at 0.5% at 7 days and 1.7% at 90 days. Adjusted costs for bleeding were $3,157 (cost ratio 1.33; 95% CI 1.18-1.50; p<0.001). In contrast, adjusted costs for stroke/TIA were $5,798 (cost ratio 1.56; 95% CI 1.11-2.20; p=0.011). Patients experiencing both bleeding and stroke/TIA had the highest mean cost of $23,716.

The study is limited by its retrospective design and the use of claims data, which may not capture all clinical nuances. While it highlights a significant cost disparity where thromboembolic events cost 2.5-fold more than bleeding, it does not provide randomized evidence on optimal DOAC resumption timing.

How this fits prior evidence

How this fits prior evidence: This study addresses a gap in the economic impact of peri-procedural complications for patients with atrial fibrillation. While previous coverage established that early DOAC initiation is safe regardless of infarct volume and that shortened dual antithrombotic therapy reduces bleeding risk, this data adds specific cost dimensions to these risks. It quantifies the higher healthcare costs associated with thromboembolic events compared to bleeding events following high-risk endoscopy.

This observational study looked at over 2,400 adults with atrial fibrillation who were taking blood thinners like warfarin or direct oral anticoagulants. The researchers tracked these patients after they underwent a high-risk endoscopy procedure to see how often they experienced bleeding or stroke.

The results showed that about 18% of patients experienced bleeding within seven days of the procedure, and this number rose to nearly 23% by ninety days. While the rate of stroke or TIA was lower, at around 0.5% to 1.7%, these events were associated with much higher healthcare costs. Patients who experienced both a bleed and a stroke faced the highest average costs.

Because this was an observational study using insurance claims data, the evidence is not definitive. It shows a link between certain procedures and complications but does not provide specific instructions on when to start or stop medications. Patients should talk to their doctors about managing these risks during medical procedures.

What this means for you:
Patients with atrial fibrillation may face bleeding risks after high-risk endoscopy, which can impact healthcare costs.

Common questions

What are the risks of endoscopy if I have atrial fibrillation?

Patients with atrial fibrillation undergoing high-risk endoscopy showed a 18.0% bleeding rate at 7 days and a 22.9% bleeding rate at 90 days. While stroke or TIA rates were lower, at 0.5% and 1.7% respectively, these events are linked to higher healthcare costs.

How much does a stroke cost compared to bleeding after a procedure?

The study found that thromboembolic events like stroke or TIA cost the healthcare system 2.5 times more per event than bleeding. Patients who experienced both bleeding and a stroke faced the highest average costs of $23,716.

Is this study enough to change how doctors treat patients?

No, because this was an observational study using claims data, the evidence is not definitive. It identifies a need for more research on the best timing for restarting medications after procedures like endoscopy.

Study Details

Study typeRct
Sample sizen = 2,486
EvidenceLevel 2
PublishedAug 2026
View Original Abstract ↓
ABSTRACT Background and study aims: Patients on direct oral anticoagulants (DOACs) undergoing high-risk endoscopy face competing risks of bleeding and thromboembolism during peri-procedural anticoagulant interruption. We quantified peri-procedural adverse event (AE) rates and incremental healthcare costs. Patients and methods: Retrospective cohort study using the TriNetX Linked Claims database (2015-2025), a US-wide multi-payer claims network. Adults on DOAC or warfarin therapy who underwent high-risk endoscopy were included (N=2,486 unique patients; N=1,933 with linked cost data). Peri-procedural bleeding and thromboembolic events were identified using principal-diagnosis codes in acute care encounters (emergency department or inpatient) within 90 days of the index procedure. Unadjusted and multivariable-adjusted incremental 90-day costs were compared between patients with and without each AE type using generalized linear models. Results: Among 2,486 anticoagulated patients (median age 65; 61.5% male; 81% with atrial fibrillation), bleeding occurred in 18.0% at 7 days and 22.9% at 90 days. Stroke/TIA occurred in 0.5% at 7 days and 1.7% at 90 days. Each thromboembolic event cost approximately 2.5 times more than each bleeding event. Stroke/TIA added $8,874 unadjusted (p<0.001) and $5,798 adjusted (cost ratio 1.56; 95% CI 1.11-2.20; p=0.011); bleeding added $3,471 unadjusted and $3,157 adjusted (cost ratio 1.33; 95% CI 1.18-1.50; p<0.001). Patients experiencing both bleeding and subsequent stroke/TIA had the highest costs (mean $23,716). Conclusions: Peri-procedural thromboembolic events cost the healthcare system 2.5-fold more per event than bleeding, underscoring the clinical and economic importance of periprocedural DOAC management and motivating randomized evidence on optimal DOAC resumption timing strategies.
Free Newsletter

Clinical research that matters. Delivered to your inbox.

Join thousands of clinicians and researchers. No spam, unsubscribe anytime.