In Touch newsletter: Summer 2016

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INTOUCH SUMMER 2016

Dr. Katerina Pavenski and Lesley Asiedu, a TTP patient, discuss platelet levels and treatment in the Medical Daycare Unit. (Photo by Katie Cooper, Medical Media Centre)

New ‘virtual’ clinic for rare blood disease a hybrid of patient care and research By Elizabeth Kosturik

A new “virtual” clinic at St. Michael’s combines treatment and research for patients with thrombotic thrombocytopenic purpura, or TTP, an extremely rare blood disorder. TTP is an acute disease that causes blood clots in the small blood vessels of the brain, heart and kidneys, which can cause permanent organ damage. TTP patients have low platelet counts and little or no ADAMTS13, a protein that prevents abnormal clotting. The most effective treatment is plasmapheresis, Printed on 100 per cent recycled paper

a procedure that removes a patient’s “bad” plasma and replaces it with healthy plasma. Once a patient is in remission, his or her platelet levels must be checked regularly to monitor for possible relapse. Coordinating follow-up appointments with different physicians, including hematologists and nephrologists, as well as plasmapheresis nurses, can be tricky. In the new clinic, a patient’s visit is tracked with a special code while he or she attends different appointments. He or she is able to keep in touch with the medial team through phone, email

or drop-in. The medical team can collect statistics and implement research and quality improvement initiatives. “It’s extremely important to monitor patients so we can quickly treat them if they relapse,” said Dr. Katerina Pavenski, the head of the Transfusion Medicine division and medical director of the

TTP affects three per one million people. If it goes untreated, TTP can kill 80 per cent of patients within two days. Continued on page 2 SUMMER 2016 | IN TOUCH | 1


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In Touch newsletter: Summer 2016 by St. Michael's Hospital - Issuu