TY - JOUR
T1 - A practical guide to the management of immune thrombocytopenia co-existing with acute coronary syndrome
AU - Rahhal, Alaa
AU - Provan, Drew
AU - Ghanima, Waleed
AU - González-López, Tomás José
AU - Shunnar, Khaled
AU - Najim, Mostafa
AU - Ahmed, Ashraf Omer
AU - Rozi, Waail
AU - Arabi, Abdulrahman
AU - Yassin, Mohamed
N1 - Publisher Copyright:
Copyright © 2024 Rahhal, Provan, Ghanima, González-López, Shunnar, Najim, Ahmed, Rozi, Arabi and Yassin.
PY - 2024
Y1 - 2024
N2 - Introduction: Immune thrombocytopenia (ITP) management with co-existing acute coronary syndrome (ACS) remains challenging as it requires a clinically relevant balance between the risk and outcomes of thrombosis and the risk of bleeding. However, the literature evaluating the treatment approaches in this high-risk population is scarce. Methods and Results: In this review, we aimed to summarize the available literature on the safety of ITP first- and second-line therapies to provide a practical guide on the management of ITP co-existing with ACS. We recommend holding antithrombotic therapy, including antiplatelet agents and anticoagulation, in severe thrombocytopenia with a platelet count < 30 × 109/L and using a single antiplatelet agent when the platelet count falls between 30 and 50 × 109/L. We provide a stepwise approach according to platelet count and response to initial therapy, starting with corticosteroids, with or without intravenous immunoglobulin (IVIG) with a dose limit of 35 g, followed by thrombopoietin receptor agonists (TPO-RAs) to a target platelet count of 200 × 109/L and then rituximab. Conclusion: Our review may serve as a practical guide for clinicians in the management of ITP co-existing with ACS.
AB - Introduction: Immune thrombocytopenia (ITP) management with co-existing acute coronary syndrome (ACS) remains challenging as it requires a clinically relevant balance between the risk and outcomes of thrombosis and the risk of bleeding. However, the literature evaluating the treatment approaches in this high-risk population is scarce. Methods and Results: In this review, we aimed to summarize the available literature on the safety of ITP first- and second-line therapies to provide a practical guide on the management of ITP co-existing with ACS. We recommend holding antithrombotic therapy, including antiplatelet agents and anticoagulation, in severe thrombocytopenia with a platelet count < 30 × 109/L and using a single antiplatelet agent when the platelet count falls between 30 and 50 × 109/L. We provide a stepwise approach according to platelet count and response to initial therapy, starting with corticosteroids, with or without intravenous immunoglobulin (IVIG) with a dose limit of 35 g, followed by thrombopoietin receptor agonists (TPO-RAs) to a target platelet count of 200 × 109/L and then rituximab. Conclusion: Our review may serve as a practical guide for clinicians in the management of ITP co-existing with ACS.
UR - https://www.scopus.com/pages/publications/85191234139
UR - https://www.scopus.com/inward/citedby.url?scp=85191234139&partnerID=8YFLogxK
U2 - 10.3389/fmed.2024.1348941
DO - 10.3389/fmed.2024.1348941
M3 - Review article
C2 - 38665297
AN - SCOPUS:85191234139
SN - 2296-858X
VL - 11
JO - Frontiers in Medicine
JF - Frontiers in Medicine
M1 - 1348941
ER -