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Inverse association with COVID-19 vaccination status of the incidence of pneumonia after SARS-CoV-2 infection: A nationwide retrospective cohort study

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dc.contributor.author최준용-
dc.date.accessioned2024-12-06T03:05:47Z-
dc.date.available2024-12-06T03:05:47Z-
dc.date.issued2024-04-
dc.identifier.issn1876-0341-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/200985-
dc.description.abstractBackground: Although one of the characteristics of COVID-19 is accompanied by acute pneumonia immediately after infection, large-scale cohort studies focused on this issue are lacking. In addition, there is interest in how COVID-19 vaccinations reduce the incidence of acute pneumonia for people infected with different strains of SARS-CoV-2. Thus, we assess the short-term incidence of pneumonia after COVID-19 with the vaccination and SARS-CoV-2 variants. Methods: As data for 2136,751 COVID-19 patients between January 01, 2020 and February 28, 2022 was collected, they were observed for one month from the day of infection. Patients in retrospective cohort study were classified according to doses of the received vaccine and the epidemic phase when SARS-CoV-2 variants prevailed. Multivariable logistic regression analysis calculated adjusted odds ratios (aOR) and 95% confidence intervals (CIs) for the pneumonia risk. Results: In B.1.1.7-B.1.351, B.1.617.2, and B.1.617.2 variants, the aORs (95% CIs; p-value) for incidence of pneumonia were 0.93 (0.89–0.98; <0.001), 0.74 (0.70–0.78; <0.001), and 0.04 (0.038–0.043; <0.001), respectively, compared to the original strain. More than 80% of patients have received the second and more doses of the vaccine (average age=44.67 years). The aORs (95% CIs; p-value) for pneumonia were 0.61 (0.58–0.64; <0.001), 0.39 (0.38–0.40; <0.001), and 0.18 (0.166–0.184; <0.001) in patients who received the first (N = 68,216), second (N = 898,838), and ≥ third doses (N = 836,173), respectively, compared to unvaccinated patients. According to the received vaccine (second dose of mRNA or viral vector), those who received BNT162b2 and mRNA-1273 (N = 787,980) had lower risk of pneumonia, compared to that in those who received h ChAdOx1 nCov-19 and AD26. COV2-S (N = 89,024). Conclusions: Our findings suggest that the second and ≥ third doses (61% and 82% of risk aversion effect increased, respectively) of the COVID-19 vaccine can prevent the COVID-19-related pneumonia, regardless of the variants.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherElsevier-
dc.relation.isPartOfJOURNAL OF INFECTION AND PUBLIC HEALTH-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAdult-
dc.subject.MESHBNT162 Vaccine-
dc.subject.MESHCOVID-19 Vaccines-
dc.subject.MESHCOVID-19* / epidemiology-
dc.subject.MESHCOVID-19* / prevention & control-
dc.subject.MESHChAdOx1 nCoV-19-
dc.subject.MESHHumans-
dc.subject.MESHIncidence-
dc.subject.MESHPneumonia* / epidemiology-
dc.subject.MESHPneumonia* / prevention & control-
dc.subject.MESHRetrospective Studies-
dc.subject.MESHSARS-CoV-2-
dc.subject.MESHVaccination-
dc.titleInverse association with COVID-19 vaccination status of the incidence of pneumonia after SARS-CoV-2 infection: A nationwide retrospective cohort study-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorJihun Song-
dc.contributor.googleauthorSeogsong Jeong-
dc.contributor.googleauthorSeulggie Choi-
dc.contributor.googleauthorYun Hwan Oh-
dc.contributor.googleauthorSun Jae Park-
dc.contributor.googleauthorJoo Young Chang-
dc.contributor.googleauthorYoosun Cho-
dc.contributor.googleauthorKyeonghyang Byeon-
dc.contributor.googleauthorJun Yong Choi-
dc.contributor.googleauthorSeju Lee-
dc.contributor.googleauthorJaehun Jung-
dc.contributor.googleauthorSang Min Park-
dc.identifier.doi10.1016/j.jiph.2024.02.005-
dc.contributor.localIdA04191-
dc.relation.journalcodeJ04249-
dc.identifier.eissn1876-035X-
dc.identifier.pmid38430718-
dc.subject.keywordCOVID-19 vaccine-
dc.subject.keywordPneumonia-
dc.subject.keywordSARS-CoV-2 infection-
dc.subject.keywordSARS-CoV-2 variants-
dc.contributor.alternativeNameChoi, Jun Yong-
dc.contributor.affiliatedAuthor최준용-
dc.citation.volume17-
dc.citation.number4-
dc.citation.startPage650-
dc.citation.endPage656-
dc.identifier.bibliographicCitationJOURNAL OF INFECTION AND PUBLIC HEALTH, Vol.17(4) : 650-656, 2024-04-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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