1 / 19

FOLLOW UP IN THALASSEMIA CLINIC

FOLLOW UP IN THALASSEMIA CLINIC. Presented by: Dr. Afsana Jahan (PGT) Dr. Aditi Baruah (MD); Dr. P. Bishwanath (MD) Department of Paediatrics Assam Medical College & Hospital, Dibrugarh. Introduction.

joie
Télécharger la présentation

FOLLOW UP IN THALASSEMIA CLINIC

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. FOLLOW UP IN THALASSEMIA CLINIC Presented by: Dr. Afsana Jahan(PGT) Dr. Aditi Baruah (MD); Dr. P. Bishwanath (MD) Department of Paediatrics Assam Medical College & Hospital, Dibrugarh

  2. Introduction • Thalassemia is the commonest chronic haematological disease needing repeated blood transfusion. • North-East specially Assam is a reservoir of abnormal haemoglobins & also thalassemia because of ethnic diversity of the inhabitants. • Present thalassemia clinic was established in April’2005, AMCH, Dibrugarh where regular follow-up of thalassemia pateints are done.

  3. Aim of the Study To study the follow-up cases of haemo-globinopathy with special reference to thalassemia in thalassemia clinic

  4. Materials & Methods • Place of Study : Thalassemia clinic, AMCH • Period of Study : May’2005 to Oct’2007 • Study universe : 50 diagnosed and registered cases of Haemoglobinopathy • Selection criteria : Cases of Haemoglobinopathy diagnosed by HPLC.

  5. Age & Sex distribution at registration

  6. Distribution of haemoglobinopathies

  7. Caste & Community distribution

  8. Showing status of spleen

  9. Photograph showing facial features and heptosplenomegaly

  10. Complications of Haemoglobinopathy

  11. PHOTOGRAPH SHOWING BONY CHANGES IN SKULL X-RAY

  12. Effect of chelation on Serum Ferritin

  13. Effect of use of filter on transfusion reaction

  14. Parental HPLC study

  15. Chromatogram

  16. Problems in Thalassemia clinic • Family study and convincing parents and relatives for necessity of the test. • Irregular follow-up visits. • Irregular blood transfusion • Lack of voluntary blood donation. • Cost of filters and chelation therapy limits their use. • Cost of different laboratory tests.

  17. Need of the HOUR! • Public awareness. • Education of health professional. • Antenatal diagnosis. • Emphasis on conventional treatment in particular chelation in view of its high efficacy. • Cure of the disease with increasing possibility of bone marrow transplantation and gene therapy. • Concrete support for achieving high standard for management of thalassemia in this part of Country.

  18. Conclusion Thalassemia clinic is playing an important role in making thalassemia a preventable, manageable and curable disease in prospect of high incidence in this region.

  19. THANK YOU & wish you all a very HAPPY NEW YEAR

More Related