2021
DOI: 10.22541/au.161577357.74566701/v1
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Primary Thromboprophylaxis to Prevent Thrombotic Events in Pediatric Oncology Patients with a Malignant Mediastinal Mass.

Abstract: Children with malignant mediastinal masses have increased thrombotic events (TE). We examined primary thromboprophylaxis in reducing TE. Eligible subjects were started on enoxaparin thromboprophylaxis and compared to a cohort without. There were 15 TEs among 76 subjects for an incidence of 19.7%. Mediastinal compression directly led to TE, (M-TE) in 9.2% of subjects requiring 2-fold longer duration of therapeutic anticoagulation. Primary thromboprophylaxis revealed a trend towards reduction in M-TE although no… Show more

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Cited by 1 publication
(2 citation statements)
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“…This study evaluated risk factors related to VTE. Consistent with previous studies, univariant analysis found that patients with a family history of thrombosis, a T‐ALL phenotype, a mediastinal mass at diagnosis, in a high‐risk treatment group or, at least, having an inherited thrombophilia defect, had statistically significant risk factors for VTE 2,3,6,29,30 …”
Section: Discussionsupporting
confidence: 84%
See 1 more Smart Citation
“…This study evaluated risk factors related to VTE. Consistent with previous studies, univariant analysis found that patients with a family history of thrombosis, a T‐ALL phenotype, a mediastinal mass at diagnosis, in a high‐risk treatment group or, at least, having an inherited thrombophilia defect, had statistically significant risk factors for VTE 2,3,6,29,30 …”
Section: Discussionsupporting
confidence: 84%
“…Consistent with previous studies, univariant analysis found that patients with a family history of thrombosis, a T-ALL phenotype, a mediastinal mass at diagnosis, in a high-risk treatment group or, at least, having an inherited thrombophilia defect, had statistically significant risk factors for VTE. 2,3,6,29,30 When each thrombophilia defect was evaluated independently, this association was not found, but when patients with factor II (G20210A) or/and factor V Leiden (G1691A) mutations were evaluated together, a statistically relationship was found.…”
Section: Discussionmentioning
confidence: 99%