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Management of cancer‐associated thrombosis with thrombocytopenia: Impact of the ISTH guidance statement

BACKGROUND: Optimal management of cancer‐associated thrombosis (CAT) in patients with thrombocytopenia remains difficult given competing risks of recurrent thrombosis and increased bleeding. We determine the impact of the ISTH Scientific and Standardization Committee (SCC) guidance on CAT management...

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Autores principales: Held, Nicole, Jung, Benjamin, Baumann Kreuziger, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133434/
https://www.ncbi.nlm.nih.gov/pubmed/35664532
http://dx.doi.org/10.1002/rth2.12726
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author Held, Nicole
Jung, Benjamin
Baumann Kreuziger, Lisa
author_facet Held, Nicole
Jung, Benjamin
Baumann Kreuziger, Lisa
author_sort Held, Nicole
collection PubMed
description BACKGROUND: Optimal management of cancer‐associated thrombosis (CAT) in patients with thrombocytopenia remains difficult given competing risks of recurrent thrombosis and increased bleeding. We determine the impact of the ISTH Scientific and Standardization Committee (SCC) guidance on CAT management and thrombocytopenia on platelet transfusion, bleeding, and recurrent thrombosis. METHODS: A retrospective review was performed of patients with CAT and thrombocytopenia who required anticoagulation for VTE for 11 months before and after implementation of the ISTH SCC guidance. Medical records were reviewed to identify the type of VTE event, number of platelet transfusions, incidence of bleeding, and VTE recurrence within pre‐ and postintervention time periods. RESULTS: A total of 41 and 80 cases were included in the preintervention and postintervention periods, respectively. The preintervention group showed a trend toward less acute VTE events (39% vs 55%; P = .05). The postintervention period had an increased per‐patient platelet transfusion (median, 2.5 vs 4; P = .05). Nonmajor bleeding was increased in the postintervention group (2% vs 16%; P = 0.03) and included all six (8%) major hemorrhages (P = .09). There was numerically less recurrent thrombosis in the postintervention group (20% vs 8%; P = .07), which was not significantly different when accounting for acuity of VTE. Management adherence was strong, at 91%, in the postintervention group. CONCLUSION: The ISTH guidance on management of cancer‐associated thrombosis in patients with thrombocytopenia was successfully implemented in an academic medical center. There was no significant difference in bleeding or recurrent thrombosis outcomes after adjusting for acuity of VTE.
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spelling pubmed-91334342022-06-04 Management of cancer‐associated thrombosis with thrombocytopenia: Impact of the ISTH guidance statement Held, Nicole Jung, Benjamin Baumann Kreuziger, Lisa Res Pract Thromb Haemost Original Articles BACKGROUND: Optimal management of cancer‐associated thrombosis (CAT) in patients with thrombocytopenia remains difficult given competing risks of recurrent thrombosis and increased bleeding. We determine the impact of the ISTH Scientific and Standardization Committee (SCC) guidance on CAT management and thrombocytopenia on platelet transfusion, bleeding, and recurrent thrombosis. METHODS: A retrospective review was performed of patients with CAT and thrombocytopenia who required anticoagulation for VTE for 11 months before and after implementation of the ISTH SCC guidance. Medical records were reviewed to identify the type of VTE event, number of platelet transfusions, incidence of bleeding, and VTE recurrence within pre‐ and postintervention time periods. RESULTS: A total of 41 and 80 cases were included in the preintervention and postintervention periods, respectively. The preintervention group showed a trend toward less acute VTE events (39% vs 55%; P = .05). The postintervention period had an increased per‐patient platelet transfusion (median, 2.5 vs 4; P = .05). Nonmajor bleeding was increased in the postintervention group (2% vs 16%; P = 0.03) and included all six (8%) major hemorrhages (P = .09). There was numerically less recurrent thrombosis in the postintervention group (20% vs 8%; P = .07), which was not significantly different when accounting for acuity of VTE. Management adherence was strong, at 91%, in the postintervention group. CONCLUSION: The ISTH guidance on management of cancer‐associated thrombosis in patients with thrombocytopenia was successfully implemented in an academic medical center. There was no significant difference in bleeding or recurrent thrombosis outcomes after adjusting for acuity of VTE. John Wiley and Sons Inc. 2022-05-25 /pmc/articles/PMC9133434/ /pubmed/35664532 http://dx.doi.org/10.1002/rth2.12726 Text en © 2022 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosisand Haemostasis (ISTH). https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Held, Nicole
Jung, Benjamin
Baumann Kreuziger, Lisa
Management of cancer‐associated thrombosis with thrombocytopenia: Impact of the ISTH guidance statement
title Management of cancer‐associated thrombosis with thrombocytopenia: Impact of the ISTH guidance statement
title_full Management of cancer‐associated thrombosis with thrombocytopenia: Impact of the ISTH guidance statement
title_fullStr Management of cancer‐associated thrombosis with thrombocytopenia: Impact of the ISTH guidance statement
title_full_unstemmed Management of cancer‐associated thrombosis with thrombocytopenia: Impact of the ISTH guidance statement
title_short Management of cancer‐associated thrombosis with thrombocytopenia: Impact of the ISTH guidance statement
title_sort management of cancer‐associated thrombosis with thrombocytopenia: impact of the isth guidance statement
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9133434/
https://www.ncbi.nlm.nih.gov/pubmed/35664532
http://dx.doi.org/10.1002/rth2.12726
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