Venous thromboembolism in pediatric patients with acute lymphoblastic leukemia under chemotherapy treatment. Risk factors and usefulness of thromboprophylaxis. Results of LAL-SEHOP-PETHEMA-2013
Autor: | Anna Ruiz‐Llobet, Susanna Gassiot, Edurne Sarrate, Josune Zubicaray, José Luis Dapena, Susana Rives, Julián Sevilla, Ángela Menárguez López, Melissa Panesso Romero, Catalina Montoya, José Manuel Vagace, José Ramón Molina Hurtado, Marina García‐Morín, Miriam García Abós, María Carmen Mendoza Sánchez, Francisco Lendínez, Pilar Palomo Moraleda, María Tallón, Berta González, Emilia Urrutia, José Vicente Serna, Irene Peláez Pleguezuelos, Marta Martínez Merino, Eduardo Ramos Elbal, Elena Orellana, Helga Benítez Muñoz, Rubén Berrueco |
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Rok vydání: | 2022 |
Předmět: | |
Zdroj: | JOURNAL OF THROMBOSIS AND HAEMOSTASIS r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante instname r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu |
ISSN: | 1538-7836 1538-7933 |
Popis: | Introduction: Symptomatic venous thromboembolism (VTE) is diagnosed in 3%14% of patients during pediatric acute lymphoblastic leukemia (ALL) therapy. There are well-known risk factors, but the role of others as inherited thrombophilia is still controversial. Prophylaxis with low molecular weight heparin (LMWH) has been described, but its use is not globally accepted. Methods: A retrospective multicentric study in ALL patients 1-18 years old following SEHOP-PETHEMA-2013 treatment guideline was performed to evaluate VTE rate, anticoagulant treatment, outcome, risk factors, and safety and usefulness of LMWH administration as primary thromboprophylaxis in children with inherited thrombophilia. Results: A total of 652 patients were included in the study. VTE incidence was 8.7%. Most of the cases occurred during induction therapy associated with central venous catheter. Univariant analysis showed that family history of thrombosis, presence of mediastinal mass, high-risk treatment group, and inherited thrombophilia were statistically significant risk factors. LMWH administration seemed to decrease VTE rate in patients with inherited thrombophilia and those with T-cell ALL phenotype. Conclusion: Most of the VTE cases occurred in patients without inherited thrombophilia, but when it is present, the VTE risk is higher. LMWH administration was useful to decrease VTE in these patients. |
Databáze: | OpenAIRE |
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