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Rivaroxaban – Evaluating NoVel and Effective AnticoaguLant Action (REVEAL Survey)

Survey Questionnaire Form
Doctor's details
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Questionnaire

  1. In recent years, have you observed an increase in the number of patients suffering from thromboembolic disorders? *
  2. If you agree with the increased incidence of thromboembolic events in recent years, which may be the factors leading to this observed rise? (Can select multiple answers)
  3. In your daily practice, how frequently do you prescribe an Anticoagulant? *
  4. While prescribing an Anticoagulant in your practice, what is your primary desired objective? *
  5. Do you find any gender preferences in these conditions (male: female) *
  6. Which is the most frequent age group of your patients to receive an Anticoagulant? *
  7. According to you, while selecting an Anticoagulant, which of the following parameters are important? (Can select multiple answers) *
  8. Which class of Anticoagulants do you prefer and prescribe the most in your patients? (Can select multiple answers) *
  9. Have you been prescribing the newer anticoagulants – Non vitamin K antagonist oral anticoagulants (NOACs*)? *
  10. If you regularly prescribe the NOACs, which ones are preferred by you? (Can select multiple answers)
  11. What is the one key feature of NOACs due to which you prefer to prescribe these in your patients? Please specify in brief *
  12. In the treatment and management of post-operative thromboprophylaxis, prevention of stroke in patients with non-valvular atrial fibrillation, which of the DOACs* you prefer to prescribe in your patients? *
  13. How has been your clinical experience while prescribing Rivaroxaban in your patients? Please specify in brief *
  14. Can you enlist the most important and essential treatment benefits while using Rivaroxaban? (Can select multiple answers) *
  15. In your experience, does Rivaroxaban show better/equal anticoagulant efficacy as compared to Apixaban? *
  16. Recently, rivaroxaban has also been approved for secondary prevention after acute coronary syndrome (ACS) or peripheral arterial disease (PAD) as an add-on to clopidogrel and aspirin therapy after stabilization with initial management. Do you think the vascular protection benefit is clinically advantageous for patients with ACS and PAD? *
  17. At therapeutic concentrations of rivaroxaban (173–274 μg L−1), INR* rarely exceeds 1.5 and may even be in the reference range (≤1.2). Do you consider this as an important parameter influencing the bleeding risk in patients on Rivaroxaban? *
  18. Rivaroxaban is excreted via kidneys to a large extent. When do you recommend dosage modification? *
  19. Have you observed an increased risk of spinal/epidural hematoma during anesthesia in a patient on Rivaroxaban? *
  20. How frequently do you observe side effects in your patients on Rivaroxaban? Please specify in brief *
  21. Which are the most reported side effects of Rivaroxaban? (Can select multiple answers) *
  22. Do you agree that routine coagulation testing is not necessary for Rivaroxaban? *
  23. If you recommend routine coagulation testing in your patients, please specify which category of patients do you prescribe the testing in.
  24. When do you advise the patient to take Rivaroxaban? *
  25. In your clinical practice, which is the most prescribed/effective dose for Rivaroxaban for management and treatment of DVT*/PE*? *
  26. After the procedure, Rivaroxaban therapy is restarted at the same dose, following adequate hemostasis. Do you agree? *
  27. Post a procedure, what is you preferred method/dose to re-initiate Rivaroxaban? Please specify in brief *
  28. It is seen that premature discontinuation of Rivaroxaban increases the risk of thrombotic events. Do you agree with this statement? *
  29. The increased risk of thrombotic events post premature discontinuation of Rivaroxaban is evident in which type of patients? Please specify in brief *
  30. In a case where there is no evident risk of bleeding in a patient, do you prescribe Rivaroxaban in comparison to Apixaban? *
  31. It has been clinically seen that a lower dose of Rivaroxaban (2.5 mg twice per day) in combination with dual antiplatelet therapy significantly improves ischemic outcome in ACS*, including rates of stent thrombosis. This is unlike apixaban and dabigatran which resulted in unfavorable efficacy and safety profiles. In your patients with ACS*, do you prescribe Rivaroxaban for improved outcomes for this clinical benefit? *
  32. Do you think it is safe to prescribe Rivaroxaban in patients with hepatic impairment? Please give your opinion *
  33. Do you think Obesity as a parameter influences the anticoagulant action of Rivaroxaban? *
  34. Do you practice estimating the CHADS2* grading score in your patients to evaluate the risk of stroke secondary to atrial fibrillation? *
  35. Do you feel that the CHADS2* grading score is useful in estimating the risk? Please give your opinion. Also specify if you use any other score/ tool. *
  36. In your clinical practice, have you observed any detrimental effect on the platelet count of a patient receiving Rivaroxaban? *
  37. Rivaroxaban shows a 21% relative risk reduction in stroke and systemic embolism as compared to Warfarin. Please specify if you have observed this in your clinical practice *
  38. In which type of patients, do you prefer prescribing Rivaroxaban instead of Warfarin? (Can select multiple answers) *
  39. In the Rocket AF trial, Rivaroxaban showed significantly lower incidence of major bleeding and intracerebral bleeding, especially in elderly patients with diabetes as compared to Warfarin. Do you prefer prescribing Rivaroxaban in such patients and why? *
  40. How do you perceive cardiovascular safety of Rivaroxaban in comparison to other Novel anticoagulants? Please give your opinion *
  41. DOAC use in MHV*s has been halted due to the failure of both dabigatran and apixaban in two major clinical trials. However, Rivaroxaban has shown encouraging clinical outcomes in patients with mechanical prosthetic heart valves. Do you advise the use of Rivaroxaban in these patients? *
  42. In patients with renal impairment (Crcl*>30 mL/minute), which would be your preferred drug – Rivaroxaban or Dabigatran or Apixaban? *
  43. Which would be important parameters of preference while prescribing Rivaroxaban over Dabigatran for stroke prevention in NVAF*? (Can select multiple answers) *
  44. Similar efficacy in stroke prevention in AF*

  45. Rivaroxaban is one and the only anticoagulant indicated to reduce the risk of heart attack, stroke, or cardiovascular death in patients with CAD and PAD. Please specify your clinical experience *
  46. Do you advise Rivaroxaban in patients with CAD and PAD as an add-on for improved outcomes. *
  47. In your opinion, which of the following outcomes project Rivaroxaban as an influential add-on in patients with CAD? (Can select multiple answers) *
  48. COMPASS study has shown that the reduction in CVE* was evident without increasing the risk of fatal and intracranial bleeding when Rivaroxaban was added to Aspirin. *
  49. Do you predict this as an important factor to address the residual risk and prevent the CVEs*? Please specify in brief

  50. In patients with PAD*, Rivaroxaban has shown significant reduction in the risk of major cardiovascular events and acute limb ischemia along with aspirin. *
  51. Have you observed this in your practice? Please specify in brief

  52. Do you prefer Rivaroxaban in PAD* patients *
  53. What would be the major influential outcomes enhanced by addition of Rivaroxaban to aspirin in PAD* patients? (Can select multiple answers) *
  54. Rivaroxaban necessitates no bridge with Heparin or LMWH* for DVT* and PE* treatment indications. Do you consider this as an advantageous parameter in the VTE* management? *
  55. Please specify the reasons

  56. Most of the clinical studies conducted for Rivaroxaban involve high risk patients. Do you consider this as an important feature to simulate real world clinical experience Rivaroxaban? *
  57. What key points should be highlighted in the promotion of RIVAFLO for managing thromboembolism, CAD* and PAD*? (Subjective question) *