The burden of nosocomial SARS-CoV-2 infection remains poorly defined. We report on the outcomes of 2508 adults with molecularly-confirmed SARS-CoV-2 admitted across 18 major hospitals, representing over 60% of those hospitalised across Wales between 1 March and 1 July 2020. Inpatient mortality for nosocomial infection ranged from 38% to 42%, consistently higher than participants with community-acquired infection (31%–35%) across a range of case definitions. Those with hospital-acquired infection were older and frailer than those infected within the community. Nosocomial diagnosis occurred a median of 30 days following admission (IQR 21–63), suggesting a window for prophylactic or postexposure interventions, alongside enhanced infection control measures.
- clinical epidemiology
- infection control
- viral infection
- respiratory Infection
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Little is known regarding the prevalence and outcomes of in-hospital transmission of SARS-CoV-2 among medical patients.1 The largest and only multicentre cohort study to date reported outcomes in 1564 patients admitted with confirmed SARS-CoV-2 infection across 11 hospitals.2 Mortality in the nosocomial group appeared comparable to those with likely community-acquired infection (27.0% and 27.2%, respectively).2 This study was conducted early in the pandemic course, meaning reliable estimates of the true impact of hospital-acquired COVID-19 infection remain hampered by a paucity of publicly available data at national and regional levels.3 Here, we update assessment of the relative burden of community-acquired and nosocomial-acquired SARS-CoV-2 infection, using anonymised patient-level and hospital-level data collected via the National Pathway for Managing COVID-19 Infections in Secondary Care in Wales initiative (www.covid-19hospitalguideline.wales.nhs.uk).
The methods and data sources relating to this work are described in detail elsewhere.4 Briefly, positive SARS-CoV-2 PCR results recorded between 1 March 2020 and 1 July 2020 in adults with a recorded hospital admission were identified for retrospective notes review. Local clinical teams across 18 centres (online supplemental file S1) performed data entry using a standardised online tool. Mandatory fields included dates of PCR sampling, admission and discharge, age, sex, comorbidity count and outcome (death or discharge). Supplementary fields included Welsh Index of Multiple of Deprivation (WIMD) and preadmission Clinical Frailty Scale (CFS).
The primary outcome was all-cause mortality, grouped by probable origin of SARS-CoV-2 infection based on (1) clinician-recorded source and (2) standardised case definitions (online supplemental file S2). Time-to-event analysis used time in hospital following a positive PCR test, to avoid introducing survivorship bias. All analyses were performed using R and GraphPad Prism.
We identified 6005 SARS-CoV-2-positive results with a location in hospital, taken between 1 March 2020 and 1 July 2020 inclusive, of which 4112 were individual cases. Clinical information was obtained from 2584/4112 individuals (63%). A total of 76 individuals were excluded due to missing core data fields or initial PCR sampling date exceeding admission period by 31 days (online supplemental file S3). This left 2508 case records, representing approximately 61% of the total adult population hospitalised with COVID-19 within Wales. Admission features are summarised in table 1. The cohort had a median age of 74 years (IQR 62.5–85.5), of whom 54.3% were men and 45.7% were women. Individuals from the most-deprived WIMD quartile were over-represented relative to those in the least deprived quartile (31.2% vs 18.7%, χ2 test: p<0.0001).
Clinician-defined admission source was available in 2354 cases (93.9%). Hospital-acquired COVID-19 was documented in 433 cases (17.3% of cohort, 37.8% mortality), comparable to mortality in cases presenting by ambulance (553/1359, 40.7%). Walk-in and GP referrals together accounted for 20.4% of the cohort and had the lowest inpatient mortality rate (17.1%–23.6%). The small number of patients admitted from care or nursing homes showed the highest inpatient mortality rate (23/50, 46.0%).
We next applied a standardised definition for nosocomial COVID-19, based on the interval between admission and diagnostic testing exceeding 14 days, identifying 411 cases (16.4% of cohort, consistent with previous reports).2 Community-acquired cases constituted the majority (n=1604, 64.0%), defined by PCR sampling preceding or within 5 days of admission.2 Monthly prevalence estimates are shown in online supplemental file S4. Overall, 39.2% of patients with nosocomial-infection died, compared with 31.7% with community-acquired infection. This proved consistent across the majority of admission sites (figure 1). Using a random effects model, we found that the relative risk of mortality in patients with nosocomial-acquired COVID-19, averaged across sites, was 1.24 times that of community-acquired infection (95% CI 1.06 to 1.42, p=0.0047; online supplemental file S5). The median time from diagnostic sampling to discharge in patients with nosocomial infection was 17 days (IQR 7–38), compared with 7 days (IQR 3–15) in community-acquired COVID-19 cases. Nosocomial-infection cases had an increased cumulative incidence of inpatient mortality, when accounting for the competing risk of discharge (figure 2). Half of those with a nosocomial diagnosis had been admitted for at least 30 days prior to testing (IQR 21–63), with 48 admitted for over 100 days. Mortality by age group appeared similar for both nosocomial and community COVID-19 cases, but with a greater proportion of elderly individuals within the nosocomial COVID-19 group (online supplemental file S6).
As 95% of individuals display symptoms between 2.5 and 11.5 days of exposure,5 the above definition presents a conservative estimate of the burden of nosocomial infection. We extended analysis by varying the diagnostic interval across this range, thereby encompassing wider case definitions in use by UK Public Health agencies. Inpatient mortality rates for nosocomial COVID-19 ranged from 37.8% to 42.3% and remained greater than that for community-acquired infection (31.4%–34.7%, online supplemental files S7 and S8). By contrast, varying the case definition resulted in significant changes in nosocomial caseload and deaths. Applying the Public Health England definition (diagnosis>7 days following admission) identified 7247 (28.9%) admissions and 300 deaths (41.4% mortality). This rose to 827 cases (33.0%) and 341 deaths (41.2% mortality), when a 5-day interval between PCR testing and admission was used.6
Finally, we investigated the vulnerability of individuals with nosocomial COVID-19. To minimise selection bias inherent with previous case definitions requiring a prolonged preinfection admission,2 we considered a diagnostic interval of 2 days postadmission, commonly used for hospital-acquired bacterial pneumonia.7 Here, nosocomial-acquired cases had a median CFS score of 5 (IQR 4–7), compared with 3 (IQR 2–6) in community-acquired cases (online supplemental file S9). Marked differences in multimorbidity were evident, with 35.0% of nosocomial cases having at least four comorbidities compared with 26.7% of community-acquired patients.
Our findings expose the hitherto underestimated vulnerability and impact of nosocomial infection with SARS-CoV-2. Many potential mechanisms may underlie these observations, including the advanced age and frailty of patients who remain admitted to the hospital during the pandemic.2 8 These both predispose to severe disease9 and implicate personal care requirement as a causal link to exposure.10
Study strengths include the high proportion of patients hospitalised with COVID-19 (over 60%) across Wales with available core data, comparing favourably to similar reports.2 9 We employed simple but robust statistical methodology, acknowledging the competing risks of discharge and death and multiple case definitions. This is relevant to interpretation of publicly reported figures. For instance, defining nosocomial cases based on the median 5-day incubation period5 identified 14.2% additional cases and 13.7% more deaths than a commonly used 7-day threshold. This suggests the burden of nosocomial COVID-19 may be significantly under-reported, which has major public health implications for infection control policy globally, particularly given the rapid spread of more infectious and severe SARS-CoV-2 variants.
Our study also has limitations, including its retrospective nature. Although sites retrieved notes at random, we cannot fully exclude risk of ascertainment bias. As the total number of patients at risk of infection was unknown, we cannot infer the risk of acquiring SARS-CoV-2 within the hospital. Similarly, we did not collect data on recent hospitalisations, and it is possible that nosocomial COVID-19 cases have been classified as community. We also recognise our findings represent crude inpatient mortality rate estimates, based on all-cause mortality. Future studies using national linked datasets including genomic analysis and estimating excess mortality are suggested.
In conclusion, we performed a national service evaluation to document the burden of nosocomial-SARS-CoV-2 infection during and following the first wave in Wales. We found many of those dying with probable hospital-acquired COVID-19 had been in the hospital for at least a month prior to exposure. We suggest this highlights an opportunity for pre-exposure and early postexposure prophylactic measures, including inpatient vaccination and clinical trial enrolment.11 12
This work was presented to the Welsh Technical Advisory Group and Directors of Nursing Group, contributing to a recommendation to ministers supporting vaccination of inpatients without a diagnosis of COVID-19 within priority groups and those being admitted for a planned procedure at increased risk.
Patient consent for publication
This work was conducted as service evaluation. A formal waiver for ethical approval was received from Approvals Officer Dr Beresford (Welsh REC2). Requirement for ethical approval for this service evaluation was formally waived.
This work uses data collected by the NHS and Public Health Wales as part of the routine care and support for patients admitted with COVID-19. We are extremely grateful to the front-line NHS junior doctors for their commitment to inputting data from across Wales. Anonymised data handling and storage was supported by The Institute of Clinical Science and Technology, and we thank Gareth Davies and Bea Addison from Institute of Clinical Science and Technology for database management and coordination of data collection, and Dr Tom J C Ward for statistical guidance and careful reading of the manuscript.
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Twitter @WCATImmunology, @irhumphreys
Contributors SB conceived the study and worked with RJ and CD to create the COVID-19 guideline and the database. CW provided data on behalf of Public Health Wales. MJP led the data analysis supported by DF and wrote the first draft supervised by SB, DF, SJ, and IH. CD leads the Institute for Clinical Science and Technology, which created the digital interventions. MJP, RJ, CD and SB have verified the underlying data and act as guarantors. All authors contributed scientific and clinical guidance regarding study design and data collection, and reviewed the final draft. The corresponding author attested that all listed authors met authorship criteria and that no others meeting the criteria had been omitted.
Funding The Welsh Government funds the Respiratory Health Implementation Group (RHIG) of which SB is the lead and RJ the programme manager. RHIG fund the Institute for Clinical Science and Technology (ICST) which created the digital interventions including the Welsh Hospital covid-19COVID-19 guideline and the on-line data collection tool. This work was partly funded by UKRI/NIHR through the UK Coronavirus Immunology Consortium (UK-CIC). MJP is supported by the Welsh Clinical Academic Training (WCAT) programme and a Career Development Award from the Association of Clinical Pathologists and is a participant in the NIH Graduate Partnership Programme. IH is a Wellcome Trust Senior Research Fellow in Basic Biomedical Sciences.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.
Press Release For further information and interview requests contact: Gerry Holt, Cardiff University: 029 2087 5596 or Holtg2@cardiff.ac.uk