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A Survey Among Gastroenterologists to Understand Management of Inflammatory Bowel Disorder (IBD) in India with Focus on Therapy with Biologicals (REASSURANCE Study)

Survey Questionnaire Form
Doctor's details
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Questionnaire

  1. With which of the following statements regarding inflammatory bowel disease (IBD) phenotype in India you agree the most? (Multiple options can be selected) *
  2. What is your clinical experience about prevalence of IBD in young patients? *
  3. According to you which statement is true for gender distribution for patients of IBD in your practice? (Multiple options can be selected) *
  4. Which of the following type of ulcerative colitis is predominantly seen in your practice? *
  5. Which part of gastrointestinal tract is commonly affected by CD in most of your patients? (Multiple options can be selected) *
  6. What is the commonly observed disease behaviour of IBD patients in your practice? (Multiple options can be selected) *
  7. Which statement/s about extraintestinal manifestations (EIM) of IBD is/are true in your practice? (Multiple options can be selected) *
  8. Which organ system is most commonly affected in EIM in IBD as per your clinical experience?*
  9. What is/are the preferred test/s in your practice to diagnose IBD? (Multiple options can be selected) *
  10. What is your opinion about colonoscopy and intestinal ultrasound (IUS) in the management of IBD? (Multiple options can be selected) *
  11. Despite advances in diagnostic procedures differentiating CD from intestinal TB and vice versa, diagnosis of CD remains a major issue *
  12. Which scale/scoring system do you use to assess the severity of ulcerative colitis? (Multiple options can be selected) *
  13. Which guidelines do you follow in your practice for the management of IBD? (Multiple options can be selected) *
  14. How many mild to moderately active IBD patients in your practice do not respond adequately to conventional therapy and corticosteroids? *
  15. When do you consider to escalate treatment from conventional therapy or corticosteroids to biologicals in the management of IBD? (Multiple options can be selected) *
  16. How many patients of IBD do you treat with biologics in a year? *
  17. When do you prescribe adalimumab in the management of moderately to severely active UC and CD? *
  18. According to you which are the below parameters favour adalimumab in the management of moderately to severely active UC and CD? (Multiple options can be selected) *
  19. What is the average duration of adalimumab therapy for the management of IBD in your practice? (Multiple options can be selected) *
  20. How long does it take to achieve clinical remission with adalimumab in moderately to severely active UC? *
  21. How long does it take to achieve clinical remission with adalimumab in moderately to severely active CD? *
  22. What percentage of moderately to severely active IBD patients do not adequately respond to adalimumab in your practice? *
  23. What are the causes of inadequate response to adalimumab in patients with IBD as per your experience? (Multiple options can be selected) *
  24. High concentration adalimumab i.e., 40 mg in 0.4 ml can improve patient compliance as compared to low concentration adalimumab i.e., 40 mg in 0.8 ml as there is less injection related pain due to less volume is injected with high concentration formulation *
  25. High concentration adalimumab has favourable safety profile (lower incidence of injection site reactions or other adverse effects) compared to low concentration adalimumab *
  26. What is your observation about the efficacy of high concentration adalimumab compared to low concentration adalimumab in the management of IBD? *
  27. What is your experience about the development of anti-drug antibodies (ADA) with adalimumab? *
  28. % of patients
  29. What is your experience about relapse rate with adalimumab therapy once clinical remission is achieved in the management of IBD? (Multiple options can be selected) *
  30. What is your approach when patient comes with relapse after discontinuation of adalimumab? (Multiple options can be selected) *
  31. What is your clinical experience with adalimumab and azathioprine combination therapy Vs infliximab and azathioprine combination therapy in the management of IBD? *
  32. What is your approach to prevent reactivation of pulmonary or extra pulmonary tuberculosis with TNF-α blockers? *
  33. Which tests do you use to screen latent tuberculosis infection before initiating treatment with TNF-α blockers? (Multiple options can be selected) *
  34. What approach do you follow to reduce the risk of bacterial, viral and fungal infections with adalimumab in the management of IBD? (Multiple options can be selected) *
  35. What do you do if infection develops during treatment with adalimumab? *
  36. What approach is followed to minimize/ avoid risk of malignancies during treatment with adalimumab? *
  37. Which of the following drug is preferred when cardiac ailment such as myocarditis or ischemic heart disease or pericarditis is present as extraintestinal manifestations in your patient with IBD? *
  38. How do you manage pulmonary diseases such as pneumonitis or interstitial lung disease as extraintestinal manifestations of IBD? *
  39. How do you manage cutaneous diseases such as pyoderma gangrenosum or erythema nodosum as extraintestinal manifestations of IBD? *
  40. How do you manage ocular diseases such as uveitis or scleritis or episcleritis as extraintestinal manifestations of IBD? *