2015
DOI: 10.4172/2329-8790.1000185
|View full text |Cite
|
Sign up to set email alerts
|

Risk of Thromboembolism in Patients with Immune Thrombocytopenia

Abstract: Immune thrombocytopenia (ITP) comprises a heterogeneous group of disorders characterized by autoimmunemediated platelet destruction and impairment of platelet production. Thromboembolic events have been reported in up to 8% of patients with ITP, suggesting that thromboembolism requires special precaution in this patient group. Thromboembolism can be caused by a disease (i.e. pro-thrombotic disease state) after the introduction of ITP therapies such as corticosteroids, splenectomy, and thrombopoietin receptor a… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0
1

Year Published

2020
2020
2021
2021

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(2 citation statements)
references
References 98 publications
(129 reference statements)
0
1
0
1
Order By: Relevance
“…Treatment should always be personalised to the individual to minimise bleeding and risk of thromboembolism. 17 For the treatment of thrombosis in patients with ITP (with no bleeding, petechiae, hematomas or stable hb (WHO grade 0-II), anticoagulation should be started at standard doses with a platelet count of ≥50 10⁹/L/ or at half-standard doses with a platelet count of <50 000/μL and increased to full doses if platelet counts rise to ≥50 000/μL. 18 There have been multiple reports in the literature highlighting the thrombotic manifestations of COVID-19, including venous thromboembolic disease and arterial thrombosis.…”
Section: Discussionmentioning
confidence: 99%
“…Treatment should always be personalised to the individual to minimise bleeding and risk of thromboembolism. 17 For the treatment of thrombosis in patients with ITP (with no bleeding, petechiae, hematomas or stable hb (WHO grade 0-II), anticoagulation should be started at standard doses with a platelet count of ≥50 10⁹/L/ or at half-standard doses with a platelet count of <50 000/μL and increased to full doses if platelet counts rise to ≥50 000/μL. 18 There have been multiple reports in the literature highlighting the thrombotic manifestations of COVID-19, including venous thromboembolic disease and arterial thrombosis.…”
Section: Discussionmentioning
confidence: 99%
“…Развитие тромботических процессов у больных ПИТ стало предметом специальных исследований и породило концепцию «тромбоцитопенической тромбофилии», озвученной в специальной статье под названием: «Является ли иммунная тромбоцитопения (ИТП) тромбофилией?» [3]. По данным метаанализа нескольких исследований, у больных ПИТ выявлен высокий риск артериальных и венозных тромбозов по сравнению с показателями в популяции [4][5][6][7][8][9].…”
unclassified