Q&A with Peter Higgins: Why Dialogue about Nutrition is Key for IBD Patients
December 12th 2015Peter Higgins, MD, PhD, University of Michigan Health System, talked about how patients these days are often answering their own nutritional questions on the "Wild Wild West" of the Internet, so it's up to the experts to provide thorough answers to assuage their concerns.
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Q&A with Peter Higgins: How to Implement a Nutrition Program for IBD Patients
December 12th 2015At the 2015 Advances in Inflammatory Bowel Diseases (AIBD) meeting in Orlando, Florida, Peter Higgins, MD, PhD, the University of Michigan Health System shared his insight about the importance and value of careful nutritional guidance for IBD patients.
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Q&A with Eva Szigethy: Prevent & Treat Opioid Dependence in Pediatric IBD Patients
December 11th 2015Eva Szigethy, MD, PhD, University of Pittsburgh discussed at the 2015 Advances in Inflammatory Bowel Diseases (AIBD) how to continue the conversation and implement methods to treat the burgeoning concern of opioid dependence among pediatric IBD patients.
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Q&A with Russell Cohen: Healthcare Economics and Its Impact on IBD
December 10th 2015Russell Cohen, MD, director of the Inflammatory Bowel Diseases Center at The University of Chicago Medicine continued to discuss the relevance of healthcare economics specific to IBD at the 2015 Advances in Inflammatory Bowel Diseases.
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Q&A with Russell Cohen: Does the Westernization of Countries Lead to Westernized Diseases?
December 10th 2015Russell Cohen, MD, director of the Inflammatory Bowel Diseases Center at The University of Chicago Medicine, discussed the progress made not only in the clinical care of IBD, but also in the basic science group and translational core at the 2015 Advances in Inflammatory Bowel Diseases meeting in Orlando, FL.
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Q&A with Barbara Cappelli: HLA- Sibling Transplants Works in Sickle Cell Disease
December 8th 2015Barbara Cappelli, MD, Eurocord International Registry, Paris, France, shared an overview from her team's study that found further evidence that for patients with severe sickle cell disease who have an HLA-identical sibling available as a donor, HSCT can be safe and effective.
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Q&A with Christine Cserti-Gazdewich: The Progression in Blood Storage Duration
December 6th 2015At the 57th American Society of Hematology Annual Meeting, Christine Cserti-Gazdewich, BSc, MD, Blood Transfusion Laboratory, Toronto General Hospital discussed the progress made in blood unit storage.
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Q&A with Christine Cserti-Gazdewich: Blood Storage Duration, How Long Is Too Long?
December 6th 2015Christine Cserti-Gazdewich, BSc, MD, Blood Transfusion Laboratory, Toronto General Hospital, and colleagues wanted to address the burgeoning concern that the longer blood units are stored, the likelier it may be to introduce harm or simply not work as well.
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Q&A with Seth Karol, MD: Treating Pediatric Osteonecrosis
December 5th 2015Seth Karol, MD, St. Jude's Children's Research Center and his team focused their research on the 10-20 age group, the "sweet spot" where the bones are still finishing up development and thus going to be susceptible to therapy.
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Q&A with Seth Karol, MD: Risk Factors for Bone Toxicity for Patients with ALL
December 5th 2015Seth Karol, MD, St. Jude's Children's Research Center discussed several ways in which he and his colleagues intensified therapy over the years and referred to a key toxicity that had emerged from the two drugs they used.
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Epoetin Alfa Biosimilar Is Effective in Treating Patients with CIA and Lymphoma or Myeloma
December 4th 2015Researchers assessed the effect of epoetin alfa biosimilar both with and without iron supplementation on CIA in patients undergoing treatment for oncologic and hematologic malignancies.
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Equations with Both Serum Cystatin C and Creatinine Inaccurately Estimate Glomerular Filtration Rate
December 3rd 2015Sickle cell disease, as debilitating as it is, is associated with the progressive complication of renal damage – beginning with hyerfiltration in childhood to glomerular filtration rate (GFR) decline and chronic renal failure in approximately 12 % of HbSS sickle cell adults.
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How to Manage Anticoagulation in Patients with Bleeding Disorders
December 2nd 2015Patients suffering from the most common hereditary bleeding disorder von Willebrand disease (VWD) also undergoing surgical procedures are recommended specific treatment methods to manage perioperative anticoagulation.
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