Bhaskar Bhardwaj1, John A Spertus2, Kevin F Kennedy3, W Schuyler Jones4, David Safley3, Thomas T Tsai5, Herbert D Aronow6, Amit N Vora4, Yashashwi Pokharel2, Arun Kumar7, Robert R Attaran8, Dmitriy N Feldman9, Ehrin Armstrong10, Anand Prasad11, Bruce Gray12, Adam C Salisbury13. 1. Division of Cardiovascular Diseases, University of Missouri, Columbia, Missouri; Department of Internal Medicine, University of Missouri-Kansas City, Kansas City, Missouri. 2. Department of Internal Medicine, University of Missouri-Kansas City, Kansas City, Missouri; Division of Cardiovascular Medicine, Saint Luke's Mid-America Heart Institute, Kansas City, Missouri. 3. Division of Cardiovascular Medicine, Saint Luke's Mid-America Heart Institute, Kansas City, Missouri. 4. Division of Cardiology, Duke University Health System, Duke Heart Center, Durham, North Carolina. 5. Division of Cardiovascular Medicine, University of Colorado and Institute for Health Research, Kaiser Permanente, Denver, Colorado. 6. Division of Cardiovascular Medicine, Warren Alpert Medical School of Brown University and Lifespan Cardiovascular Institute, Providence, Rhode Island. 7. Division of Cardiovascular Diseases, University of Missouri, Columbia, Missouri. 8. Department of Cardiovascular Medicine, Yale University School of Medicine, New Haven, Connecticut. 9. Division of Cardiology, Weill Cornell Medical College, New York, New York. 10. Division of Cardiovascular Medicine, University of Colorado, Denver, Colorado and Denver Veterans Affairs Medical Center, Denver, Colorado. 11. Division of Cardiology, Department of Medicine, UT Health San Antonio, San Antonio, Texas. 12. Department of Surgery at Greenville Health System, Greenville, South Carolina. 13. Department of Internal Medicine, University of Missouri-Kansas City, Kansas City, Missouri; Division of Cardiovascular Medicine, Saint Luke's Mid-America Heart Institute, Kansas City, Missouri. Electronic address: asalisbury@saint-lukes.org.
Abstract
OBJECTIVES: This study sought to assess periprocedural bleeding complications in lower-extremity peripheral vascular interventions (PVIs). BACKGROUND: Few studies have examined the incidence, predictors, or outcomes of periprocedural bleeding after lower-extremity PVI. METHODS: The study examined patients undergoing PVI at 76 hospitals in the National Cardiovascular Data Registry PVI registry from 2014 to 2016. Post-PVI major bleeding was defined as any overt bleeding with a hemoglobin (Hb) drop of ≥3 g/dl, any Hb decline of ≥4 g/dl, or blood transfusion in patients with pre-procedure Hb >8 g/dl within 72 h of their procedure. Hierarchical multivariable logistic regression was used to identify factors independently associated with post-PVI bleeding. The study also examined adjusted in-hospital mortality among patients with or without major bleeding complications. RESULTS: Among 18,289 PVI procedures, major bleeding occurred in 744 (4.10%). Patient characteristics independently associated with bleeding included age, female sex, heart failure, pre-procedural hemoglobin <12 g/dl, nonelective PVI, and critical limb ischemia on presentation. Procedural characteristics associated with bleeding included nonfemoral vascular access, use of thrombolytic therapy, PVI of the aortoiliac segment, and multilesion interventions, whereas use of closure devices was associated with less bleeding. All-cause in-hospital mortality was higher in patients who experienced bleeding than in those who did not (6.60% vs. 0.30%; p < 0.001; adjusted hazard ratio: 10.9; 95% confidence interval: 6.9 to 17.0). CONCLUSIONS: Major bleeding occurred in 4.10% of lower-extremity PVI procedures and was associated with several patient and procedural characteristics, as well as in-hospital mortality. These insights can be incorporated into strategies to reduce periprocedural bleeding after PVI.
OBJECTIVES: This study sought to assess periprocedural bleeding complications in lower-extremity peripheral vascular interventions (PVIs). BACKGROUND: Few studies have examined the incidence, predictors, or outcomes of periprocedural bleeding after lower-extremity PVI. METHODS: The study examined patients undergoing PVI at 76 hospitals in the National Cardiovascular Data Registry PVI registry from 2014 to 2016. Post-PVI major bleeding was defined as any overt bleeding with a hemoglobin (Hb) drop of ≥3 g/dl, any Hb decline of ≥4 g/dl, or blood transfusion in patients with pre-procedure Hb >8 g/dl within 72 h of their procedure. Hierarchical multivariable logistic regression was used to identify factors independently associated with post-PVI bleeding. The study also examined adjusted in-hospital mortality among patients with or without major bleeding complications. RESULTS: Among 18,289 PVI procedures, major bleeding occurred in 744 (4.10%). Patient characteristics independently associated with bleeding included age, female sex, heart failure, pre-procedural hemoglobin <12 g/dl, nonelective PVI, and critical limb ischemia on presentation. Procedural characteristics associated with bleeding included nonfemoral vascular access, use of thrombolytic therapy, PVI of the aortoiliac segment, and multilesion interventions, whereas use of closure devices was associated with less bleeding. All-cause in-hospital mortality was higher in patients who experienced bleeding than in those who did not (6.60% vs. 0.30%; p < 0.001; adjusted hazard ratio: 10.9; 95% confidence interval: 6.9 to 17.0). CONCLUSIONS: Major bleeding occurred in 4.10% of lower-extremity PVI procedures and was associated with several patient and procedural characteristics, as well as in-hospital mortality. These insights can be incorporated into strategies to reduce periprocedural bleeding after PVI.
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