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Impact of antithrombotic therapy resumption in patients with gastrointestinal bleeding: a multicenter retrospective
1Department of Gastroenterology, Xuanwu Hospital Capital Medical University, Changchun Street 45#, 100053 Beijing, China.
Insights
Antithrombotic therapy for gastrointestinal bleeding reduces 28-day mortality but significantly increases rebleeding risk. Early resumption of these therapies may also elevate mortality risk.
Area of Science:
- Gastroenterology
- Clinical Medicine
- Pharmacology
Background:
- Gastrointestinal bleeding (GIB) is a serious condition with high mortality.
- Increased use of antithrombotic agents (antiplatelets, anticoagulants) correlates with rising GIB incidence.
Purpose of the Study:
- To investigate the impact of antithrombotic therapy on 28-day mortality and rebleeding in GIB patients.
- To compare risks associated with different antithrombotic agents and timing of resumption.
Main Methods:
- Retrospective cohort study utilizing data from three independent databases (2008-2022).
- Propensity score matching and inverse probability of treatment weighting (IPTW) to control for confounding factors.
- Weighted logistic regression to analyze outcomes across antiplatelet, anticoagulant, and combination therapy subgroups.
Main Results:
- Antithrombotic therapy was associated with a significantly lower 28-day mortality (8.2% vs 12.5%).
- However, antithrombotic therapy significantly increased rebleeding rates (19.9% vs 10.5%) and risk (OR=2.118).
- Anticoagulants or combination therapy showed the highest rebleeding risk; early resumption (within 3 days) increased mortality risk.
Conclusions:
- Antithrombotic therapy presents a trade-off: reduced mortality but increased rebleeding risk in GIB.
- Specific agents (anticoagulants, combination therapy) and early resumption timing require careful consideration due to elevated risks.
Background:
Gastrointestinal bleeding (GIB) is a critical clinical emergency associated with high morbidity and mortality. The widespread use of antithrombotic agents, including antiplatelet and anticoagulant medications, has increased the incidence of GIB.
Objectives:
Our study aims to address this gap by evaluating the impact of antithrombotic therapy on both 28-day mortality and rebleeding risk.
Design:
Retrospective cohort study using propensity score-based methods to address confounding.
Methods:
Data were extracted from three independent databases (MIMIC-IV, NWICU, and Xuanwu Hospital) spanning 2008-2022. inverse probability of treatment weighting (IPTW) was applied to balance baseline characteristics. Weighted logistic regression models assessed outcomes across antiplatelet, anticoagulant, and combination therapy subgroups.
Results:
After inverse probability of treatment weighting (IPTW) adjustment, the antithrombotic group maintained a significantly elevated rebleeding rate (19.9% vs 10.5%, p < 0.001) and an increased risk of rebleeding (odds ratio (OR) = 2.118, 95% confidence interval (CI): 1.577-2.845, p < 0.001). Conversely, the 28-day mortality was significantly lower in the antithrombotic group postadjustment (8.2% vs 12.5%, p = 0.022; OR = 0.621, 95% CI: 0.412-0.935, p = 0.023). Notably, early resumption of antithrombotic therapy (within 3 days) significantly increased the risk of mortality.
Conclusion:
Our study suggests that while antithrombotic therapy reduces 28-day mortality, it significantly increases rebleeding risk. Notably, the use of anticoagulants or combination therapy is linked to the highest rebleeding risk, compared to antiplatelets. Additionally, resuming antithrombotic therapy too early (i.e., within 3 days) may further elevate the risk of mortality.
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