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Optimizing Antithrombotic Therapy in Patients With Coexisting Cardiovascular and Gastrointestinal Disease Publisher



Talasaz AH1 ; Sadeghipour P5 ; Ortegapaz L6 ; Kakavand H5, 7 ; Aghakouchakzadeh M8 ; Beavers C9 ; Fanikos J10 ; Eikelboom JW11 ; Siegal DM12 ; Monreal M13 ; Jimenez D14 ; Vaduganathan M15 ; Castellucci LA16 ; Cuker A17 Show All Authors
Authors
  1. Talasaz AH1
  2. Sadeghipour P5
  3. Ortegapaz L6
  4. Kakavand H5, 7
  5. Aghakouchakzadeh M8
  6. Beavers C9
  7. Fanikos J10
  8. Eikelboom JW11
  9. Siegal DM12
  10. Monreal M13
  11. Jimenez D14
  12. Vaduganathan M15
  13. Castellucci LA16
  14. Cuker A17
  15. Barnes GD18
  16. Connors JM19
  17. Secemsky EA20, 21, 22
  18. Van Tassell BW4
  19. De Caterina R24, 25
  20. Kurlander JE26, 27, 28
  21. Aminian A29
  22. Piazza G15, 30
  23. Goldhaber SZ15, 30
  24. Moores L31
  25. Middeldorp S32
  26. Kirtane AJ33, 34
  27. Elkind MSV35, 36
  28. Angiolillo DJ6
  29. Konstantinides S37
  30. Lip GYH38, 39
  31. Stone GW40
  32. Cushman M41
  33. Krumholz HM42, 43, 44
  34. Mehran R40
  35. Bhatt DL40
  36. Bikdeli B15, 28, 42
Show Affiliations
Authors Affiliations
  1. 1. Arnold & amp
  2. 2. Marie Schwartz College of Pharmacy and Health Sciences, Department of Pharmacy Practice, Long Island University, New York, NY, United States
  3. 3. Division of Pharmacy, New York-Presbyterian/Columbia University Irvine Medical Center, New York, NY, United States
  4. 4. Department of Pharmacotherapy and Outcome Sciences, Virginia Commonwealth University, Richmond, VA, United States
  5. 5. Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran
  6. 6. Division of Cardiology, University of Florida College of Medicine, Jacksonville, FL, United States
  7. 7. Department of Clinical Pharmacy, School of Pharmacy, Iran University of Medical Sciences, Tehran, Iran
  8. 8. Tehran Heart Center, Tehran University of Medical Sciences, Tehran, Iran
  9. 9. University of Kentucky College of Pharmacy, Lexington, KY, United States
  10. 10. Department of Pharmacy, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, United States
  11. 11. Population Health Research Institute, Hamilton Health Sciences, McMaster University, Hamilton, ON, Canada
  12. 12. Division of Hematology, Department of Medicine, University of Ottawa, Ottawa, ON, Canada
  13. 13. Department of Internal Medicine, Hospital Universitari Germans Trials i Pujol, Universidad Catolica San Antonio de Murcia, Barcelona, Spain
  14. 14. Respiratory Department, Hospital Ramon y Cajal and Medicine Department, Universidad de Alcala (IRYCIS), Centro de Investigacion Biomedica en Red de Enfermedades Respiratorias, ISCIII, Madrid, Spain
  15. 15. Cardiovascular Medicine Division, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, United States
  16. 16. Department of Medicine, Ottawa Hospital Research Institute at the University of Ottawa, Ottawa, ON, Canada
  17. 17. Department of Medicine and Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States
  18. 18. Frankel Cardiovascular Center, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, United States
  19. 19. Hematology Division, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, United States
  20. 20. Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States
  21. 21. Smith Center for Outcomes Research in Cardiology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States
  22. 22. Penn Cardiovascular Outcomes, Quality, & amp
  23. 23. Evaluative Research Center, Cardiovascular Medicine Division, Department of Medicine, University of Pennsylvania, Philadelphia, PA, United States
  24. 24. Cardiology Division, Pisa University Hospital, Pisa, Italy
  25. 25. Fondazione Villa Serena per la Ricerca, Pescara, Citta Sant’Angelo, Italy
  26. 26. Department of Internal Medicine, University of Michigan, Ann Arbor, MI, United States
  27. 27. Institute for Healthcare Policy and Innovation, University of Michigan, Ann Arbor, MI, United States
  28. 28. VA Ann Arbor Center for Clinical Management Research, Ann Arbor, MI, United States
  29. 29. Bariatric and Metabolic Institute, Department of General Surgery, Cleveland Clinic, Cleveland, OH, United States
  30. 30. Thrombosis Research Group, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, United States
  31. 31. F. Edward Hebert School of Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD, United States
  32. 32. Department of Internal Medicine, Radboud Institute of Health Sciences (RIHS), Radboud University Medical Center, Nijmegen, Netherlands
  33. 33. Cardiovascular Research Foundation, New York, NY, United States
  34. 34. Division of Cardiology, New York-Presbyterian Hospital/Columbia University Irving Medical Center, New York, NY, United States
  35. 35. Department of Neurology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY, United States
  36. 36. Department of Epidemiology, Mailman School of Public Health, Columbia University, New York, NY, United States
  37. 37. Center for Thrombosis and Hemostasis, Johannes Gutenberg, University of Mainz, Mainz, Germany
  38. 38. Liverpool Centre for Cardiovascular Science at University of Liverpool, Liverpool John Moores University and Liverpool Heart and Chest Hospital, Liverpool, United Kingdom
  39. 39. Danish Center for Health Services Research, Department of Clinical Medicine, Aalborg University, Aalborg, Denmark
  40. 40. Mount Sinai Heart, Icahn School of Medicine at Mount Sinai, New York, NY, United States
  41. 41. University of Vermont Medical Center, Burlington, VT, United States
  42. 42. Yale New Haven Hospital/Yale Center for Outcomes Research and Evaluation, New Haven, CT, United States
  43. 43. Department of Health Policy and Management, Yale School of Public Health, New Haven, CT, United States
  44. 44. Section of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, United States

Source: Nature Reviews Cardiology Published:2024


Abstract

Balancing the safety and efficacy of antithrombotic agents in patients with gastrointestinal disorders is challenging because of the potential for interference with the absorption of antithrombotic drugs and for an increased risk of bleeding. In this Review, we address considerations for enteral antithrombotic therapy in patients with cardiovascular disease and gastrointestinal comorbidities. For those with gastrointestinal bleeding (GIB), we summarize a general scheme for risk stratification and clinical evidence on risk reduction approaches, such as limiting the use of concomitant medications that increase the risk of GIB and the potential utility of gastrointestinal protection strategies (such as proton pump inhibitors or histamine type 2 receptor antagonists). Furthermore, we summarize the best available evidence and potential gaps in our knowledge on tailoring antithrombotic therapy in patients with active or recent GIB and in those at high risk of GIB but without active or recent GIB. Finally, we review the recommendations provided by major medical societies, highlighting the crucial role of teamwork and multidisciplinary discussions to customize the antithrombotic regimen in patients with coexisting cardiovascular and gastrointestinal diseases. © Springer Nature Limited 2024.; Balancing the safety and efficacy of antithrombotic therapy in patients with gastrointestinal disorders is challenging because of the potential for interference with the absorption of antithrombotic drugs or for an increased risk of bleeding. Various clinical states, including malabsorption syndromes, bariatric surgery, short-bowel syndrome or enteral tube feeding, can influence the absorption and bioavailability of oral antithrombotic agents. Bleeding events are an essential prognosticator in patients with cardiovascular diseases — at times as important as thrombotic events — and using antithrombotic agents in patients at high risk of gastrointestinal bleeding (GIB) is very challenging. Most of the existing models to predict the risk of bleeding in patients with coronary artery disease do not estimate the risk of GIB specifically. Identifying patients at high risk of GIB, modifying the bleeding risk by using gastroprotective agents, and determining the appropriate antithrombotic therapy regimen have crucial roles in preventing GIB. After an episode of acute GIB, determining the duration of antithrombotic therapy interruption and the regimen for re-initiation requires consideration of the balance between the bleeding severity and the risk of thrombotic events. © Springer Nature Limited 2024..