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Article: Serial intervals and case isolation delays for Coronavirus Disease 2019: a systematic review and meta-analysis

TitleSerial intervals and case isolation delays for Coronavirus Disease 2019: a systematic review and meta-analysis
Authors
KeywordsCOVID-19
Isolation delays
Regression analysis
Serial intervals
Systematic review and meta-analysis
Issue Date2021
PublisherOxford University Press, published in association with Clinical Infectious Diseases. The Journal's web site is located at http://www.oxfordjournals.org/our_journals/cid/
Citation
Clinical Infectious Diseases, 2021, Feb., 74 n. 4, p. 685-694 How to Cite?
AbstractBackground: Estimates of the serial interval distribution contribute to our understanding of the transmission dynamics of coronavirus disease 2019 (COVID-19). Here, we aimed to summarize the existing evidence on serial interval distributions and delays in case isolation for COVID-19. Methods: We conducted a systematic review of the published literature and preprints in PubMed on 2 epidemiological parameters, namely, serial intervals and delay intervals relating to isolation of cases for COVID-19 from 1 January 2020 to 22 October 2020 following predefined eligibility criteria. We assessed the variation in these parameter estimates using correlation and regression analysis. Results: Of 103 unique studies on serial intervals of COVID-19, 56 were included, providing 129 estimates. Of 451 unique studies on isolation delays, 18 were included, providing 74 estimates. Serial interval estimates from 56 included studies varied from 1.0 to 9.9 days, while case isolation delays from 18 included studies varied from 1.0 to 12.5 days, which were associated with spatial, methodological, and temporal factors. In mainland China, the pooled mean serial interval was 6.2 days (range, 5.1-7.8) before the epidemic peak and reduced to 4.9 days (range, 1.9-6.5) after the epidemic peak. Similarly, the pooled mean isolation delay related intervals were 6.0 days (range, 2.9-12.5) and 2.4 days (range, 2.0-2.7) before and after the epidemic peak, respectively. There was a positive association between serial interval and case isolation delay. Conclusions: Temporal factors, such as different control measures and case isolation in particular, led to shorter serial interval estimates over time. Correcting transmissibility estimates for these time-varying distributions could aid mitigation efforts.
Persistent Identifierhttp://hdl.handle.net/10722/300208
ISSN
2023 Impact Factor: 8.2
2023 SCImago Journal Rankings: 3.308
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorAli, ST-
dc.contributor.authorYeung, A-
dc.contributor.authorShan, S-
dc.contributor.authorWang, L-
dc.contributor.authorGao, H-
dc.contributor.authorDu, Z-
dc.contributor.authorXu, X-
dc.contributor.authorWu, P-
dc.contributor.authorLau, EHY-
dc.contributor.authorCowling, BJ-
dc.date.accessioned2021-06-04T08:39:40Z-
dc.date.available2021-06-04T08:39:40Z-
dc.date.issued2021-
dc.identifier.citationClinical Infectious Diseases, 2021, Feb., 74 n. 4, p. 685-694-
dc.identifier.issn1058-4838-
dc.identifier.urihttp://hdl.handle.net/10722/300208-
dc.description.abstractBackground: Estimates of the serial interval distribution contribute to our understanding of the transmission dynamics of coronavirus disease 2019 (COVID-19). Here, we aimed to summarize the existing evidence on serial interval distributions and delays in case isolation for COVID-19. Methods: We conducted a systematic review of the published literature and preprints in PubMed on 2 epidemiological parameters, namely, serial intervals and delay intervals relating to isolation of cases for COVID-19 from 1 January 2020 to 22 October 2020 following predefined eligibility criteria. We assessed the variation in these parameter estimates using correlation and regression analysis. Results: Of 103 unique studies on serial intervals of COVID-19, 56 were included, providing 129 estimates. Of 451 unique studies on isolation delays, 18 were included, providing 74 estimates. Serial interval estimates from 56 included studies varied from 1.0 to 9.9 days, while case isolation delays from 18 included studies varied from 1.0 to 12.5 days, which were associated with spatial, methodological, and temporal factors. In mainland China, the pooled mean serial interval was 6.2 days (range, 5.1-7.8) before the epidemic peak and reduced to 4.9 days (range, 1.9-6.5) after the epidemic peak. Similarly, the pooled mean isolation delay related intervals were 6.0 days (range, 2.9-12.5) and 2.4 days (range, 2.0-2.7) before and after the epidemic peak, respectively. There was a positive association between serial interval and case isolation delay. Conclusions: Temporal factors, such as different control measures and case isolation in particular, led to shorter serial interval estimates over time. Correcting transmissibility estimates for these time-varying distributions could aid mitigation efforts.-
dc.languageeng-
dc.publisherOxford University Press, published in association with Clinical Infectious Diseases. The Journal's web site is located at http://www.oxfordjournals.org/our_journals/cid/-
dc.relation.ispartofClinical Infectious Diseases-
dc.rightsThis is a pre-copyedited, author-produced version of an article accepted for publication in [insert journal title] following peer review. The version of record [insert complete citation information here] is available online at: xxxxxxx [insert URL and DOI of the article on the OUP website].-
dc.subjectCOVID-19-
dc.subjectIsolation delays-
dc.subjectRegression analysis-
dc.subjectSerial intervals-
dc.subjectSystematic review and meta-analysis-
dc.titleSerial intervals and case isolation delays for Coronavirus Disease 2019: a systematic review and meta-analysis-
dc.typeArticle-
dc.identifier.emailAli, ST: alist15@hku.hk-
dc.identifier.emailYeung, A: amy99@HKUCC-COM.hku.hk-
dc.identifier.emailShan, S: swshan@hku.hk-
dc.identifier.emailDu, Z: zwdu@hku.hk-
dc.identifier.emailWu, P: pengwu@hku.hk-
dc.identifier.emailLau, EHY: ehylau@hku.hk-
dc.identifier.emailCowling, BJ: bcowling@hku.hk-
dc.identifier.authorityAli, ST=rp02673-
dc.identifier.authorityDu, Z=rp02777-
dc.identifier.authorityWu, P=rp02025-
dc.identifier.authorityLau, EHY=rp01349-
dc.identifier.authorityCowling, BJ=rp01326-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1093/cid/ciab491-
dc.identifier.pmid34037748-
dc.identifier.pmcidPMC8241473-
dc.identifier.hkuros322668-
dc.identifier.volumeciab491-
dc.identifier.issue4-
dc.identifier.spage685-
dc.identifier.epage694-
dc.identifier.isiWOS:000755840800001-
dc.publisher.placeUnited States-

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