Your browser doesn't support javascript.
loading
Severe, Refractory Immune Thrombocytopenia Occurring After SARS-CoV-2 Vaccine.
Helms, Jackie M; Ansteatt, Kristin T; Roberts, Jonathan C; Kamatam, Sravani; Foong, Kap Sum; Labayog, Jo-Mel S; Tarantino, Michael D.
Afiliación
  • Helms JM; The Bleeding and Clotting Disorders Institute, Peoria, IL, USA.
  • Ansteatt KT; The Bleeding and Clotting Disorders Institute, Peoria, IL, USA.
  • Roberts JC; The Bleeding and Clotting Disorders Institute, Peoria, IL, USA.
  • Kamatam S; Department of Medicine, University of Illinois College of Medicine-Peoria, Peoria, IL, USA.
  • Foong KS; Department of Medicine, Saint Francis Medical Center, Peoria, IL, USA.
  • Labayog JS; Department of Medicine, University of Illinois College of Medicine-Peoria, Peoria, IL, USA.
  • Tarantino MD; Department of Medicine, Saint Francis Medical Center, Peoria, IL, USA.
J Blood Med ; 12: 221-224, 2021.
Article en En | MEDLINE | ID: mdl-33854395
ABSTRACT
The rollout of the SARS-CoV-2 vaccine is underway, and millions have already been vaccinated. At least 25 reports of "immune thrombocytopenia" (ITP) or "thrombocytopenia" following the Moderna or Pfizer vaccine have been added to the Vaccine Adverse Event Reporting System (VAERS) in the US. ITP is a rare but known complication of several vaccinations. SARS-CoV-2 vaccine is new, with a novel mechanism of action, and understanding the epidemiology, clinical manifestations, treatment success and natural history of post-vaccination thrombocytopenia is evolving. We report a 74-year-old man who developed refractory thrombocytopenia within one day of receiving the Moderna SARS-CoV-2 vaccine. Several hours after vaccination, he developed significant epistaxis and cutaneous purpura. Severe thrombocytopenia was documented the following day, and he developed extremity weakness and encephalopathy with facial muscle weakness. Over a 14-day period, thrombocytopenia was treated first with high dose dexamethasone, intravenous immunoglobulin, platelet transfusions, rituximab, plasma exchange (for presumed acute inflammatory demyelinating polyneuropathy (AIDP)), and four daily doses of the thrombopoietin receptor agonist (TPO-RA) eltrombopag (Promacta™), without a platelet response. Three days later, he received the TPO-RA romiplostim (Nplate™). Five days later, his platelet count began to rise and by post-vaccination day 25, his platelet count was in the normal range. Thrombocytopenia was refractory to frontline and second-line treatment. The eventual rise in his platelet count suggests that one or both TPO-RAs may have impacted platelet recovery. Possibly, but less likely given the temporality, the drug-induced thrombocytopenia was subsiding. The aggressive use of immunosuppressive treatment may jeopardize the intended purpose of the SARS-CoV-2 vaccine, and earlier use of non-immunosuppressive second-line treatment for vaccine-related severe thrombocytopenia, such as with TPO-RAs, should be considered. While it is imperative to continue the global vaccination program, vigilance to the occurrence of post-vaccination severe thrombocytopenia is warranted.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Blood Med Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Blood Med Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos