Literature DB >> 34030782

Idiopathic Thrombocytopenic Purpura and the Moderna Covid-19 Vaccine.

Jeffrey A Julian, Douglas R Mathern, Dinali Fernando1.   

Abstract

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Year:  2021        PMID: 34030782      PMCID: PMC7879100          DOI: 10.1016/j.annemergmed.2021.02.011

Source DB:  PubMed          Journal:  Ann Emerg Med        ISSN: 0196-0644            Impact factor:   5.721


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To the Editor: Recently, it was reported that a physician developed petechiae 3 days after receiving the Pfizer-BioNTech Covid-19 vaccine, was diagnosed with idiopathic thrombocytopenic purpura, and ultimately died of a cerebral hemorrhage. Here, we report a case of idiopathic thrombocytopenic purpura in a 72-year-old woman 1 day after receiving the first dose of the Moderna COVID-19 vaccine. The day after receiving her vaccination, the patient woke up with a rash, spontaneous oral bleeding, and headache. She denied any history of easy bruising or abnormal bleeding. Her medical history included gout, type 2 diabetes mellitus, and seasonal contact dermatitis. She denied any new medications or changes to her allopurinol and sitagliptin within the last 5 years. She denied any family history of autoimmune disorders. On examination, she had diffuse petechiae across her arms, legs, and abdomen and hemorrhagic bullae of the gingival mucosa. Laboratory tests were notable for an initial platelet count of 12,000/μL, decreasing to 1,000/μL within 12 hours of arrival. Other laboratory tests are as shown in Table 1 . Of note, normal prothrombin time, activated partial-thromboplastin time, d-dimer, and fibrinogen ruled out disseminated intravascular coagulation. Further, normal hemoglobin, haptoglobin, lactate dehydrogenase, and peripheral smear without schistocytes were inconsistent with hemolytic uremic syndrome or thrombotic thrombocytopenic purpura. Viral studies, including hepatitis A, B, and C, Epstein-Barr virus, HIV, cytomegalovirus, influenza A and B, and SARS-CoV-2, revealed no evidence of current or prior infection. Parvovirus IgG but not IgM antibodies were present, indicating prior resolved infection. Antinuclear antibody titers were undetectable, making rheumatic etiology less likely.
Table 1

Clinical laboratory results.

MeasureReference RangeHospital Day 1Hospital Day 3Hospital Day 5Hospital Day 8
Hemoglobin (g/dL)12.0–16.013.312.210.811.1
Hematocrit (%)37.0–47.041.236.333.934.5
Platelet count (per μL)150,000–400,00012,0009,00011,0001,000
White-cell count (per μL)4,800–10,8005,3205,3603,0203,300
Mean corpuscular volume (fL)80.0–99.092.690.592.692.5
Mean corpuscular hemoglobin (pg)27.0–31.029.930.429.529.8
Mean corpuscular hemoglobin concentration (g/dL)29.8–35.232.333.631.932.2
Red-cell distribution width (%)12.0–15.012.312.312.012.0
Differential count (per μL)
Neutrophils2,100–7,6003,5103,63016002,350
Lymphocytes1,000–4,9001,2601,160980580
Monocytes100–1,100410480350290
Eosinophils100–40011060∗5080
Basophils0–2002121
Sodium (mmol/L)136–145140141138137
Potassium (mmol/L)3.5–5.13.74.13.93.8
Chloride (mmol/L)98–108100104104101
Carbon dioxide (mmol/L)22–2926252828
Urea nitrogen (mg/dL)6.0–23.014192116
Creatinine (mg/dL)0.50–1.200.760.680.730.76
Glucose (mg/dL)74–110103105102112
Calcium (mg/dL)8.6–10.39.39.18.99
Total protein (g/dL)6.6–8.77.26.48.2
Albumin (g/dL)3.5–5.24.64.03.7
Aspartate aminotransferase (U/L)5–32211618
Alanine aminotransferase (U/L)0–33131012
Alkaline phosphatase (U/L)35–104988273
Total bilirubin (mg/dL)0.0–1.22.82.11.9
Direct bilirubin (mg/dL)0.0–0.30.40.30.3
Magnesium (mg/dL)1.6–2.62.12.12.1
Phosphorus (mg/dL)2.5–4.53.42.63.92.8
Prothrombin time (seconds)10.0–13.011.8
International normalized ratio1
Activated partial-thromboplastin time (seconds)25.1–36.531.7
Fibrinogen (mg/dL)200–393359
D-dimer (ng/mL DDU)0–243216
Iron (ng/μL)37–14545
Unsaturated iron-binding capacity (ng/μL)112.0–347.0275.5
Total iron-binding capacity (ng/μL)220–430320
Haptoglobin (mg/dL)34–200106
Central venous oxygen saturation (%)60.0–85.078.9
Ionized calcium (mmol/L)1.16–1.321.22
Lactic acid (mmol/L)0.6–1.41.5
Thyroid stimulating hormone (mlU/L)0.27–4.201.29
Vitamin B12 (pg/mL)211–946299
SARS-CoV-2 RNANANot detected
SARS-CoV-2 antibody index<0.990.08
Influenza A RNANANot detected
Influenza B RNANANot detected
Hepatitis A IgM antibodiesNANon-reactive
Hepatitis B surface antibodyNAReactive
Hepatitis B surface antigenNANon-reactive
Hepatitis B core IgM antibodyNANon-reactive
Hepatitis C RNANANot detected
HIV 1,2 antigen and antibody assayNANon-reactive
Cytomegalovirus PCRNANot detected
Epstein-Barr virus PCRNANot detected
Parvovirus B19 IgM antibodiesNANegative
Parvovirus B19 IgG antibodiesNAPositive
H. pylori stool antigenNANot detected
Antinuclear antibodyNANegative

NA, not applicable; PCR, polymerase chain reaction.

The value in this patient was below normal.

The value in this patient was above normal.

Clinical laboratory results. NA, not applicable; PCR, polymerase chain reaction. The value in this patient was below normal. The value in this patient was above normal. The patient received an initial 40-mg intravenous dose of dexamethasone and additional doses of 20 mg/day for 3 days thereafter. Intravenous immunoglobulin, aminocaproic acid, and rituximab were administered, and she received multiple platelet transfusions. However, her platelets continued to fluctuate between 1,000/μL and 40,000/μL. Non-contrast computed tomography of the head was without evidence of intracranial bleeding. Her course was complicated by multiple episodes of melena. Idiopathic thrombocytopenic purpura postvaccination has been reported in the measles, mumps, and rubella vaccine and has been associated with the use of attenuated vaccines and vaccine adjuvants, with one review identifying 45% of drug-induced idiopathic thrombocytopenic purpura occurring postvaccination. While hypersensitivity reactions are a known adverse event related to mRNA COVID-19 vaccines, this is, to our knowledge, the second known case of acute idiopathic thrombocytopenic purpura following administration.
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