Your browser doesn't support javascript.
loading
COVID-19-induced immune thrombocytopenia management approach: A case report and literature review.
Alahwal, Hatem Mahmoud; Alsharif, Mansour Hani; Alsharif, Mada Hani; Almohammadi, Abdullah Talal; Al-Marzouki, Adel Fahad; Barefah, Ahmed Saleh; Bahashwan, Salem Mohammad; Radhwi, Osman Omer; Damanhouri, Ghazi Abdullah.
Afiliação
  • Alahwal HM; Hematology Department, Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia.
  • Alsharif MH; Hematology Research Unit, King Fahd Medical Research Center King Abdulaziz University Jeddah Saudi Arabia.
  • Alsharif MH; Internal Medicine Department, Al-Thagher General Hospital Jeddah Saudi Arabia.
  • Almohammadi AT; Department of Preventive Medicine - Directorate of Health Affairs Jeddah Saudi Arabia.
  • Al-Marzouki AF; Hematology Department, Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia.
  • Barefah AS; Hematology Research Unit, King Fahd Medical Research Center King Abdulaziz University Jeddah Saudi Arabia.
  • Bahashwan SM; Hematology Department, Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia.
  • Radhwi OO; Hematology Research Unit, King Fahd Medical Research Center King Abdulaziz University Jeddah Saudi Arabia.
  • Damanhouri GA; Hematology Department, Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia.
Clin Case Rep ; 12(6): e9070, 2024 Jun.
Article em En | MEDLINE | ID: mdl-38883219
ABSTRACT
Key Clinical Message Vincristine therapy can be effective in refractory Immune thrombocytopenia (ITP) following COVID-19 vaccination. Our case report highlights the need for further research to establish standard management guidelines for COVID-19-vaccine-associated ITP. Abstract Adult immune thrombocytopenia (ITP) can occur as a rare complication following several viral infections or a rare adverse event or complication of vaccination. In this paper, we report a case of a 39-year-old male patient with severe refractory ITP that began 4-weeks after receiving his third (booster) dose of the COVID-19 vaccine (BNT162b2, Pfizer-BioNTech). He was given oral dexamethasone 40 mg daily for 4 days followed by prednisone at 1 mg/kg (85 mg daily) for 10 days. In the following weeks, we attempted several other lines of therapy to treat his ITP, including anti-RhD immunoglobulin, which, unfortunately, caused moderate hemolysis requiring packed red blood cell transfusion, intravenous immunoglobulin (given at a subtherapeutic dose of 0.4 g/kg for only 1 day since it was not available), rituximab, and eltrombopag. The patient, unfortunately, showed no response to any of these treatments. This was an indicator to initiate salvage therapy with vincristine 2 mg weekly for 3 weeks. The patient's platelet count started to increase remarkably during the third week of vincristine and normalized after 4 weeks. We review the findings, clinical characteristics, and management approaches that were reported in the literature regarding COVID-19-vaccine-induced ITP. More in-depth research is needed to delineate standard guidelines for the management of such cases. This report underscores the importance of resorting to vincristine and eltrombopag as great options for severe and refractory ITP related to the COVID-19 vaccine.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Clin Case Rep Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Clin Case Rep Ano de publicação: 2024 Tipo de documento: Article