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Published on: February 26, 2013
The Relationship Between Blood Parameters and Gastrointestinal Bleeding in Atrial Fibrillation Patients Receiving
Hayrullah Yurdakul1, Muhammet Cakas2, Seda Elcim Yildirim3
1Nizip City Hospital, 27300 Gaziantep, Turkey.
Insights
Systemic inflammatory markers predict gastrointestinal bleeding risk in atrial fibrillation (AF) patients on oral anticoagulants (OACs). These markers, especially in non-vitamin K antagonist oral anticoagulant (NOAC) users, can improve risk stratification and personalize OAC therapy.
Area of Science:
- Cardiology
- Internal Medicine
- Emergency Medicine
Background:
- Atrial fibrillation (AF) necessitates oral anticoagulant (OAC) therapy to prevent stroke but increases gastrointestinal (GI) bleeding risk.
- Accurate risk stratification for GI bleeding in AF patients on OACs is crucial, particularly in the emergency department (ED).
- Existing risk scores may not fully capture bleeding risk in patients receiving warfarin or non-vitamin K antagonist oral anticoagulants (NOACs).
Purpose of the Study:
- To evaluate systemic inflammatory markers as predictors of GI bleeding in AF patients treated with OACs.
- To compare the predictive value of inflammatory indices between NOAC and warfarin users.
- To explore the utility of inflammatory markers in refining GI bleeding risk stratification for personalized anticoagulation strategies.
Main Methods:
- Retrospective cohort study of 155 AF patients in an ED setting (2019-2023).
- Patients divided into GI bleeding (case) and no GI bleeding (control) groups.
- Analysis included demographics, comorbidities, CHA2DS2-VASc, HAS-BLED scores, and inflammatory indices (uric acid/albumin ratio, NLR, PLR, SII).
Main Results:
- In NOAC users, higher uric acid/albumin ratio, NLR, PLR, and SII were significantly associated with GI bleeding (p < 0.05).
- In warfarin users, only the uric acid/albumin ratio was significantly elevated in the bleeding group (p < 0.001).
- HAS-BLED scores were higher in bleeding groups; specific factors like hypolipidemia predicted bleeding in NOAC users, while hypoalbuminemia predicted bleeding in warfarin users.
Conclusions:
- Systemic inflammatory indices, particularly in NOAC users, show promise for stratifying GI bleeding risk in AF patients.
- These biomarkers may enhance personalized anticoagulation strategies, potentially reducing morbidity and mortality.
- Further integration of inflammatory markers into clinical practice is warranted for improved patient management.
Abstract:
Background/Objectives: Atrial fibrillation (AF) is a prevalent cardiac arrhythmia associated with significant morbidity, including stroke, heart failure, and increased mortality, necessitating oral anticoagulant (OAC) therapy to reduce thromboembolic risk. However, OACs, including warfarin and non-vitamin K antagonist oral anticoagulants (NOACs), increase the risk of gastrointestinal (GI) bleeding, a serious complication requiring precise risk stratification in the emergency department (ED). Methods: This retrospective cohort study was conducted in the Emergency Department of Balikesir University Hospital in Turkey between 2019 and 2023 and evaluates systemic inflammatory markers as predictors of GI bleeding in AF patients receiving OACs. A total of 155 patients were divided into case (GI bleeding) and control (no GI bleeding) groups, comparing demographics, comorbidities, CHA2DS2-VASc and HAS-BLED scores, and inflammatory indices (uric acid/albumin ratio, neutrophil-to-lymphocyte ratio [NLR], platelet-to-lymphocyte ratio [PLR], systemic immune inflammation index [SII]). Results: For patients receiving NOACs, the case group exhibited significantly higher uric acid/albumin ratio, NLR, PLR, and SII (p < 0.05). For patients receiving warfarin, only the uric acid/albumin ratio was significantly elevated (p < 0.001). Hypolipidemia and elevated uric acid were associated with bleeding risk in patients receiving NOACs, while hypoalbuminemia and elevated urea predicted bleeding in patients receiving warfarin. HAS-BLED scores were significantly higher in bleeding groups, unlike CHA2DS2-VASc scores. Conclusions: These findings suggest that inflammatory indices, particularly in patients taking NOACs, are associated with GI bleeding risk stratification. Integrating these biomarkers into clinical practice could optimize personalized anticoagulation strategies, reducing morbidity and mortality in AF patients.
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