Search Results - "RIVARD, G"

Magnetic resonance imaging and joint outcomes in boys with severe hemophilia A treated with tailored primary prophylaxis in Canada by KRAFT, J., BLANCHETTE, V., BABYN, P., FELDMAN, B., CLOUTIER, S., ISRAELS, S., PAI, M., RIVARD, G.‐E., GOMER, S., McLIMONT, M., MOINEDDIN, R., DORIA, A. S.

“…Background/objectives: Tailored primary prophylaxis (TPP) is a reduced‐intensity treatment program for hemophiliacs with the goal of preventing arthropathy…”
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Chitosan–glycerol phosphate/blood implants elicit hyaline cartilage repair integrated with porous subchondral bone in microdrilled rabbit defects by Hoemann, C.D., Ph.D, Sun, J., M.D., M.Sc, McKee, M.D., Ph.D, Chevrier, A., Ph.D, Rossomacha, E., M.D., Ph.D, Rivard, G.-E., M.D, Hurtig, M., D.V.M, Buschmann, M.D., Ph.D

“…Summary Objective We have previously shown that microfractured ovine defects are repaired with more hyaline cartilage when the defect is treated with in situ…”
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A retrospective cohort study of cancer incidence among patients treated with radiosynoviorthesis by INFANTE-RIVARD, C., RIVARD, G.-E., DEROME, F., CUSSON, A., WINIKOFF, R., CHARTRAND, R., GUAY, J.-P.

“…Radiosynoviorthesis (RS) is an intra‐articular injection of a radioactive colloid for the treatment of synovitis administered most often to patients with…”
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Emergence of Fluoroquinolones as the Predominant Risk Factor for Clostridium difficile–Associated Diarrhea: A Cohort Study during an Epidemic in Quebec by Pépin, Jacques, Saheb, Nathalie, Coulombe, Marie-Andrée, Alary, Marie-Eve, Corriveau, Marie-Pier, Authier, Simon, Leblanc, Michel, Rivard, Geneviève, Bettez, Mathieu, Primeau, Valérie, Nguyen, Martin, Jacob, Claude-Émilie, Lanthier, Luc

“…Background. Since 2002, an epidemic of Clostridium difficile–associated-diarrhea (CDAD) associated with a high case-fatality rate has involved >30 hospitals in…”
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The GBA p.Trp378Gly mutation is a probable French‐Canadian founder mutation causing Gaucher disease and synucleinopathies by Ruskey, J.A., Zhou, S., Santiago, R., Franche, L.‐A., Alam, A., Roncière, L., Spiegelman, D., Fon, E.A., Trempe, J.‐F., Kalia, L.V., Postuma, R.B., Dupre, N., Rivard, G.‐E., Assouline, S., Amato, D., Gan‐Or, Z.

“…Biallelic GBA mutations cause Gaucher disease (GD), and heterozygous carriers are at risk for synucleinopathies. No founder GBA mutations in French‐Canadians…”
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A prospective surveillance study of inhibitor development in haemophilia A patients following a population switch to a third‐generation B‐domain‐deleted recombinant factor VIII by Dubé, E., Bonnefoy, A., Merlen, C., Castilloux, J.‐F., Cloutier, S., Demers, C., Sabapathy, C. A., St‐Louis, J., Vezina, C., Warner, M., Rivard, G.‐É.

“…Introduction Following a provincial tender, most subjects with haemophilia A in Quebec switched their treatment to a third‐generation recombinant…”
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Incidence of hypotension and acute hypotensive transfusion reactions following platelet concentrate transfusions by Du Pont-Thibodeau, G., Robitaille, N., Gauvin, F., Thibault, L., Rivard, G.-É., Lacroix, J., Tucci, M.

“…Background and objectives Platelet concentrates (PCs) are associated with transfusion reactions involving hypotension, particularly bradykinin‐mediated acute…”
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Consequences of intra-articular bleeding in haemophilia: science to clinical practice and beyond by FORSYTH, A. L., RIVARD, G.-É., VALENTINO, L. A., ZOURIKIAN, N., HOFFMAN, M., MONAHAN, P. E., VAN MEEGEREN, M. E. R., FORRIOL, F.

“…Blood in the joint causes a number of physiological and pathological events that eventually lead to haemophilic arthropathy. Animal models show that blood in…”
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Epidemiological and Clinical Features of Brucellosis in the Country of Georgia by Akhvlediani, Tamar, Bautista, Christian T, Garuchava, Natalia, Sanodze, Lia, Kokaia, Nora, Malania, Lile, Chitadze, Nazibrola, Sidamonidze, Ketevan, Rivard, Robert G, Hepburn, Matthew J, Nikolich, Mikeljon P, Imnadze, Paata, Trapaidze, Nino

“…Brucellosis is an endemic disease in the country of Georgia. According to the National Center for Disease Control and Public Health of Georgia (NCDC), the…”
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Standardization of thromboelastography: a report from the TEG-ROTEM working group by CHITLUR, M., SORENSEN, B., RIVARD, G. E., YOUNG, G., INGERSLEV, J., OTHMAN, M., NUGENT, D., KENET, G., ESCOBAR, M., LUSHER, J.

“…Laboratory evaluation of bleeding disorders has been performed with the standard clotting assays such as the PT and PTT for several decades. Our improved…”
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Recommendations for performing thromboelastography/thromboelastometry in hemophilia: communication from the SSC of the ISTH by Chitlur, M., Rivard, G. E., Lillicrap, D., Mann, K., Shima, M., Young, G.

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Solidification mechanisms of chitosan–glycerol phosphate/blood implant for articular cartilage repair by Marchand, C, Rivard, G.-E, Sun, J, Hoemann, C.D

“…Summary Objective Chitosan–glycerol phosphate (chitosan-GP) is a unique polymer solution that is mixed with whole blood and solidified over microfractured or…”
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International workshop on immune tolerance induction: consensus recommendations by DIMICHELE, D. M., HOOTS, W. K., PIPE, S. W., RIVARD, G. E., SANTAGOSTINO, E.

“…Although immune tolerance induction (ITI) has been used for 30 years to eliminate inhibitors and restore normal factor pharmacokinetics in patients with…”
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Mode of delivery in hemophilia: vaginal delivery and Cesarean section carry similar risks for intracranial hemorrhages and other major bleeds by Andersson, Nadine G, Chalmers, Elizabeth A, Kenet, Gili, Ljung, Rolf, Mäkipernaa, Anne, Chambost, Hervé

“…The optimal mode of delivery for a pregnant hemophilia carrier is still a matter of debate. The aim of the study was to determine the incidence of intracranial…”
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An 'ice age' concept? The use of ice in the treatment of acute haemarthrosis in haemophilia by Forsyth, A. L., Zourikian, N., Rivard, G.-E., Valentino, L. A.

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The mutational spectrum of type 1 von Willebrand disease: results from a Canadian cohort study by James, P. D., Notley, C., Hegadorn, C., Leggo, J., Tuttle, A., Tinlin, S., Brown, C., Andrews, C., Labelle, A., Chirinian, Y., O'Brien, L., Othman, M., Rivard, G., Rapson, D., Hough, C., Lillicrap, D.

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Vaccinations are not associated with inhibitor development in boys with severe haemophilia A by Platokouki, H., Fischer, K., Gouw, S. C., Rafowicz, A., Carcao, M., Kenet, G., Liesner, R., Kurnik, K., Rivard, G. E., van den Berg, H. M.

“…Background Inhibitor development in previously untreated patients (PUPs) with severe haemophilia A is a multifactorial event. It is unknown whether paediatric…”
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An MRI scale for assessment of haemophilic arthropathy from the International Prophylaxis Study Group by Lundin, B., Manco-Johnson, M. L., Ignas, D. M., Moineddin, R., Blanchette, V. S., Dunn, A. L., Gibikote, S. V., Keshava, S. N., Ljung, R., Manco-Johnson, M. J., Miller, S. F., Rivard, G. E., Doria, A. S.

“…Summary Evaluation of prophylactic treatment of haemophilia requires sensitive methods. To design and test a new magnetic resonance imaging (MRI) scale for…”
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Evaluation of the profile of thrombin generation during the process of whole blood clotting as assessed by thrombelastography by RIVARD, G. E., BRUMMEL‐ZIEDINS, K. E., MANN, K. G., FAN, L., HOFER, A., COHEN, E.

“…The objective of this study was to evaluate the possibility of linking the tracing of whole blood clotting in a thrombelastograph® (TEG®) hemostasis system…”
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Tailored prophylaxis in severe hemophilia A: interim results from the first 5 years of the Canadian Hemophilia Primary Prophylaxis Study by FELDMAN, B. M., PAI, M., RIVARD, G. E., ISRAELS, S., POON, M.‐C., DEMERS, C., ROBINSON, S., LUKE, K.‐H., WU, J. K. M., GILL, K., LILLICRAP, D., BABYN, P., MCLIMONT, M., BLANCHETTE, V. S.

“…Background: Prophylactic treatment for severe hemophilia A is likely to be more effective than treatment when bleeding occurs, however, prophylaxis is costly…”
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