Tolerability of COVID-19 Infection and Messenger RNA Vaccination Among Patients With a History of Kawasaki Disease.
2019-nCoV Vaccine mRNA-1273
Adolescent
BNT162 Vaccine
COVID-19
/ complications
COVID-19 Vaccines
/ adverse effects
Child
Cough
/ etiology
Fatigue
/ etiology
Humans
Male
Mucocutaneous Lymph Node Syndrome
RNA, Messenger
SARS-CoV-2
Systemic Inflammatory Response Syndrome
Vaccination
/ adverse effects
Vaccines, Inactivated
/ adverse effects
Vaccines, Synthetic
Viral Vaccines
/ adverse effects
mRNA Vaccines
Journal
JAMA network open
ISSN: 2574-3805
Titre abrégé: JAMA Netw Open
Pays: United States
ID NLM: 101729235
Informations de publication
Date de publication:
01 08 2022
01 08 2022
Historique:
entrez:
12
8
2022
pubmed:
13
8
2022
medline:
17
8
2022
Statut:
epublish
Résumé
Kawasaki disease (KD) symptoms significantly overlap with multisystem inflammatory syndrome in children due to COVID-19. Patients with KD may be at risk for adverse outcomes from exposure to SARS-CoV-2 infection or vaccination. To describe the outcomes of patients with KD to SARS-CoV-2 infection or vaccination. This case series evaluated 2 cohorts using an existing KD database and reviewed individual electronic medical records for the period spanning January 1, 2020, through January 31, 2022, via electronic medical records that include Washington state immunization records. Vaccine cohort inclusion criteria consisted of being 21 years or younger at immunization and receiving 1 or more BNT162b2 (Pfizer-BioNTech) or messenger RNA (mRNA)-1273 (Moderna) vaccine doses. The COVID-19 cohort included patients 21 years or younger with positive polymerase chain reaction or nuclear capsid IgG findings for SARS-CoV-2. Participants included 826 patients from a preexisting KD database. One hundred fifty-three patients received at least 1 BNT162b2 or mRNA-1273 vaccine dose and were included in the mRNA vaccine cohort. Thirty-seven patients had positive test results for SARS-CoV-2 and were included in the COVID-19 cohort. SARS-CoV-2 vaccination and/or infection. Adverse events after mRNA vaccination and/or COVID-19, including clinician visits, emergency department encounters, or hospitalizations. Among the 153 patients included in the mRNA vaccination cohort (mean [SD] age, 13.0 [4.3] years; 94 male [61.4%]), the BNT162b2 vaccine was provided for 143 (93.5%), and the remaining 10 (6.5%) received mRNA-1273 or a combination of both. Among patients in the vaccine cohort, 129 (84.3%) were fully vaccinated or received a third-dose booster. No clinically severe adverse events occurred, and there were no reports of vaccine-related hospitalizations or outpatient visits. The COVID-19 cohort included 37 patients (mean [SD] age, 11.0 [5.5] years; 22 male [59.5%]). No patients required hospitalization due to COVID-19. The most common symptoms included low-grade fever, fatigue, cough, and myalgia with resolution within a few days. Two patients, aged 9 and 19 years, had extended cough and fatigue for 3 to 4 weeks. One patient developed COVID-19 within 6 weeks of receiving intravenous immunoglobulin for KD. These findings suggest that the mRNA vaccines may be safe and COVID-19 may not be severe for patients with a history of KD.
Identifiants
pubmed: 35960521
pii: 2795162
doi: 10.1001/jamanetworkopen.2022.26236
pmc: PMC9375169
mid: NIHMS1830296
doi:
Substances chimiques
COVID-19 Vaccines
0
RNA, Messenger
0
Vaccines, Inactivated
0
Vaccines, Synthetic
0
Viral Vaccines
0
mRNA Vaccines
0
2019-nCoV Vaccine mRNA-1273
EPK39PL4R4
BNT162 Vaccine
N38TVC63NU
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
e2226236Subventions
Organisme : NHLBI NIH HHS
ID : R01 HL146130
Pays : United States
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