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Mary S. Hinds

Researcher at University of Washington

Publications -  5
Citations -  1797

Mary S. Hinds is an academic researcher from University of Washington. The author has contributed to research in topics: Hepatic veno-occlusive disease & Transplantation. The author has an hindex of 5, co-authored 5 publications receiving 1722 citations.

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Veno-occlusive Disease of the Liver and Multiorgan Failure after Bone Marrow Transplantation: A Cohort Study of 355 Patients

TL;DR: The clinical impression is that the current incidence of VOD at the institution is much higher than the 21% rate reported 9 years ago and that more patients have severe liver disease, which may explain the apparent increased incidence and severity of this complication.
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Etiology and outcome of diarrhea after marrow transplantation: a prospective study.

TL;DR: Most cases of diarrhea after marrow transplant are not caused by infection, and clinical signs and symptoms of infection and GVHD were similar, and no clear etiology could be found for self-limited diarrhea.
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Venoocclusive disease of the liver: development of a model for predicting fatal outcome after marrow transplantation.

TL;DR: The course of VOD after cytoreductive therapy can be predicted by knowing the serum bilirubin and weight gained within 1 to 2 weeks of transplantation, and probability estimates derived from patient data are highly specific and moderately sensitive.
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Recombinant Human Tissue Plasminogen Activator for the Treatment of Established Severe Venocclusive Disease of the Liver After Bone Marrow Transplantation

TL;DR: It is concluded that recombinant human tPA can be administered to patients with severe VOD at the dosage described and five patients responded to therapy with prompt reduction in total serum bilirubin within 96 hours of starting tPA.
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A phase I/II study of prostaglandin E1 for the prevention of hepatic venocclusive disease after bone marrow transplantation

TL;DR: It is concluded that P GE1 causes significant toxicity in patients undergoing marrow transplantation and the ability of PGE1 to prevent severe VOD in patients at high risk remains unproven.