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COVID-19 Vaccine-Associated Pneumonitis in the Republic of Korea: A Nationwide Multicenter Survey

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dc.contributor.authorYoo, H-
dc.contributor.authorKim, SY-
dc.contributor.authorPark, MS-
dc.contributor.authorJeong, SH-
dc.contributor.authorPark, SW-
dc.contributor.authorLee, HL-
dc.contributor.authorLee, HK-
dc.contributor.authorYang, SH-
dc.contributor.authorJegal, Y-
dc.contributor.authorYoo, JW-
dc.contributor.authorLee, J-
dc.contributor.authorKang, HK-
dc.contributor.authorChoi, SM-
dc.contributor.authorPark, J-
dc.contributor.authorKim, YW-
dc.contributor.authorSong, JW-
dc.contributor.authorPark, JH-
dc.contributor.authorChoi, WI-
dc.contributor.authorChoi, HS-
dc.contributor.authorPark, C-
dc.contributor.authorPark, JW-
dc.contributor.authorChung, MP-
dc.date.accessioned2023-05-04T06:41:39Z-
dc.date.available2023-05-04T06:41:39Z-
dc.date.issued2023-
dc.identifier.issn1011-8934-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/25289-
dc.description.abstractBACKGROUND: Recent reports have suggested that pneumonitis is a rare complication following vaccination against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). However, its clinical features and outcomes are not well known. The aim of this study was to identify the clinical characteristics and outcomes of patients with vaccine-associated pneumonitis following vaccination against SARS-CoV-2. METHODS: In this nationwide multicenter survey study, questionnaires were distributed to pulmonary physicians in referral hospitals. They were asked to report cases of development or exacerbation of interstitial lung disease (ILD) associated with the coronavirus disease 2019 vaccine. Vaccine-associated pneumonitis was defined as new pulmonary infiltrates documented on chest computed tomography within 4 weeks of vaccination and exclusion of other possible etiologies. RESULTS: From the survey, 49 cases of vaccine-associated pneumonitis were identified between February 27 and October 30, 2021. After multidisciplinary discussion, 46 cases were analyzed. The median age was 66 years and 28 (61%) were male. The median interval between vaccination and respiratory symptoms was 5 days. There were 20 (43%), 17 (37%), and nine (19%) patients with newly identified pneumonitis, exacerbation of pre-diagnosed ILD, and undetermined pre-existing ILD, respectively. The administered vaccines were BNT162b2 and ChAdOx1 nCov-19/AZD1222 each in 21 patients followed by mRNA-1273 in three, and Ad26.COV2.S in one patient. Except for five patients with mild disease, 41 (89%) patients were treated with corticosteroid. Significant improvement was observed in 26 (57%) patients including four patients who did not receive treatment. However, ILD aggravated in 9 (20%) patients despite treatment. Mortality was observed in eight (17%) patients. CONCLUSION: These results suggest pneumonitis as a potentially significant safety concern for vaccines against SARS-CoV-2. Clinical awareness and patient education are necessary for early recognition and prompt management. Additional research is warranted to identify the epidemiology and characterize the pathophysiology of vaccine-associated pneumonitis.-
dc.language.isoen-
dc.subject.MESHAd26COVS1-
dc.subject.MESHAged-
dc.subject.MESHBNT162 Vaccine-
dc.subject.MESHChAdOx1 nCoV-19-
dc.subject.MESHCOVID-19-
dc.subject.MESHCOVID-19 Vaccines-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHPneumonia-
dc.subject.MESHRepublic of Korea-
dc.subject.MESHSARS-CoV-2-
dc.subject.MESHVaccination-
dc.titleCOVID-19 Vaccine-Associated Pneumonitis in the Republic of Korea: A Nationwide Multicenter Survey-
dc.typeArticle-
dc.identifier.pmid37038643-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086377-
dc.subject.keywordCOVID-19-
dc.subject.keywordInterstitial Lung Disease-
dc.subject.keywordPneumonitis-
dc.subject.keywordSARS-CoV-2-
dc.subject.keywordVaccine-
dc.contributor.affiliatedAuthorPark, JH-
dc.type.localJournal Papers-
dc.identifier.doi10.3346/jkms.2023.38.e106-
dc.citation.titleJournal of Korean medical science-
dc.citation.volume38-
dc.citation.number14-
dc.citation.date2023-
dc.citation.startPagee106-
dc.citation.endPagee106-
dc.identifier.bibliographicCitationJournal of Korean medical science, 38(14). : e106-e106, 2023-
dc.identifier.eissn1598-6357-
dc.relation.journalidJ010118934-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Pulmonary & Critical Care Medicine
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