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Estimation of the serial interval and proportion of pre-symptomatic transmission events of COVID- 19 in Ireland using contact tracing data.
McAloon, Conor G; Wall, Patrick; Griffin, John; Casey, Miriam; Barber, Ann; Codd, Mary; Gormley, Eamonn; Butler, Francis; McV Messam, Locksley L; Walsh, Cathal; Teljeur, Conor; Smyth, Breda; Nolan, Philip; Green, Martin J; O'Grady, Luke; Culhane, Kieran; Buckley, Claire; Carroll, Ciara; Doyle, Sarah; Martin, Jennifer; More, Simon J.
  • McAloon CG; School of Veterinary Medicine, University College Dublin, Belfield, Dublin 4, Ireland. conor.mcaloon@ucd.ie.
  • Wall P; School of Public Health, Physiotherapy and Sports Science, University College Dublin, Belfield, Dublin 4, Ireland.
  • Griffin J; Centre for Veterinary Epidemiology and Risk Analysis, School of Veterinary Medicine, University College Dublin, Belfield, Dublin, Ireland.
  • Casey M; Centre for Veterinary Epidemiology and Risk Analysis, School of Veterinary Medicine, University College Dublin, Belfield, Dublin, Ireland.
  • Barber A; Centre for Veterinary Epidemiology and Risk Analysis, School of Veterinary Medicine, University College Dublin, Belfield, Dublin, Ireland.
  • Codd M; School of Public Health, Physiotherapy and Sports Science, University College Dublin, Belfield, Dublin 4, Ireland.
  • Gormley E; School of Veterinary Medicine, University College Dublin, Belfield, Dublin 4, Ireland.
  • Butler F; School of Biosystems and Food Engineering, University College Dublin, Belfield, Dublin 4, Ireland.
  • McV Messam LL; School of Veterinary Medicine, University College Dublin, Belfield, Dublin 4, Ireland.
  • Walsh C; Department of Mathematics and Statistics, University of Limerick, Limerick, Ireland.
  • Teljeur C; Health Information and Quality Authority, George's Court, Dublin 7, Ireland.
  • Smyth B; Department of Public Health, Health Service Executive West, Galway, Ireland.
  • Nolan P; National University of Ireland Maynooth, Kildare, Ireland.
  • Green MJ; School of Veterinary Medicine and Science, University of Nottingham, Nottingham, UK.
  • O'Grady L; School of Veterinary Medicine, University College Dublin, Belfield, Dublin 4, Ireland.
  • Culhane K; School of Veterinary Medicine and Science, University of Nottingham, Nottingham, UK.
  • Buckley C; Central Statistics Office, Ardee Road, Rathmines, Dublin, Ireland.
  • Carroll C; COVID-19 Contact Management Programme, Health Service Executive, Dublin, Ireland.
  • Doyle S; School of Public Health, University College Cork, Cork, Ireland.
  • Martin J; COVID-19 Contact Management Programme, Health Service Executive, Dublin, Ireland.
  • More SJ; COVID-19 Contact Management Programme, Health Service Executive, Dublin, Ireland.
BMC Public Health ; 21(1): 805, 2021 04 27.
Article in English | MEDLINE | ID: covidwho-1204065
ABSTRACT

BACKGROUND:

The serial interval is the period of time between the onset of symptoms in an infector and an infectee and is an important parameter which can impact on the estimation of the reproduction number. Whilst several parameters influencing infection transmission are expected to be consistent across populations, the serial interval can vary across and within populations over time. Therefore, local estimates are preferable for use in epidemiological models developed at a regional level. We used data collected as part of the national contact tracing process in Ireland to estimate the serial interval of SARS-CoV-2 infection in the Irish population, and to estimate the proportion of transmission events that occurred prior to the onset of symptoms.

RESULTS:

After data cleaning, the final dataset consisted of 471 infected close contacts from 471 primary cases. The median serial interval was 4 days, mean serial interval was 4.0 (95% confidence intervals 3.7, 4.3) days, whilst the 25th and 75th percentiles were 2 and 6 days respectively. We found that intervals were lower when the primary or secondary case were in the older age cohort (greater than 64 years). Simulating from an incubation period distribution from international literature, we estimated that 67% of transmission events had greater than 50% probability of occurring prior to the onset of symptoms in the infector.

CONCLUSIONS:

Whilst our analysis was based on a large sample size, data were collected for the primary purpose of interrupting transmission chains. Similar to other studies estimating the serial interval, our analysis is restricted to transmission pairs where the infector is known with some degree of certainty. Such pairs may represent more intense contacts with infected individuals than might occur in the overall population. It is therefore possible that our analysis is biased towards shorter serial intervals than the overall population.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Contact Tracing / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Limits: Aged / Humans Country/Region as subject: Europa Language: English Journal: BMC Public Health Journal subject: Public Health Year: 2021 Document Type: Article Affiliation country: S12889-021-10868-9

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Contact Tracing / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Limits: Aged / Humans Country/Region as subject: Europa Language: English Journal: BMC Public Health Journal subject: Public Health Year: 2021 Document Type: Article Affiliation country: S12889-021-10868-9