Highlights
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We identified, that of our adult patients, only 45% were primary COVID-19 cases.
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Patients with primary COVID-19 and incidental COVID-19 are different patient populations.
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The total number of COVID-19 hospitalizations should be interpreted with caution.
ABSTRACT
Objectives
SARS-CoV-2 Omicron variants BA.1 and BA.2 seem to show reduced clinical severity compared with earlier variants. Therefore, we aimed to assess and classify the cause of hospitalization for patients with COVID-19 identified with these Omicron variants in our hospital.
Methods
A retrospective analysis was performed on all patients identified with the SARS-CoV-2 Omicron variant between December 23, 2021, and February 27, 2022. Patients with a positive SARS-CoV-2 polymerase chain reaction (PCR) upon clinical admission or during clinical admission were classified into four categories: (1) primary COVID-19, (2) admission-contributing COVID-19, (3) incidental COVID-19, and (4) undetermined COVID-19.
Results
We classified 172 COVID-19 Omicron patient admissions, including 151 adult and 21 pediatric patients. Of the adult patients, 45% were primary COVID-19 cases, 21% were admission-contributing, 31% were incidental, and 3% were undetermined. Of the pediatric patients, 19% were primary COVID-19 cases, 29% were admission-contributing, 38% were incidental, and 14% were undetermined.
Conclusion
In the evolving landscape of COVID-19, the number of hospitalized patients with COVID-19 should be interpreted with caution. The different patient categories should be considered in public health policy decision-making and when informing the general public.
Introduction
Monitoring national hospitalization rates for COVID-19 has been essential throughout the pandemic to guide public health decision-making and to evaluate vaccine efficacy. However, with the rapid worldwide spread of the SARS-CoV-2 Omicron variant of concern (associated with a decreased severity) and increasing immunity against SARS-CoV-2, interpreting the true impact of these hospitalization rates has been complicated (
Viana et al., 2022- Viana R
- Moyo S
- Amoako DG
- Tegally H
- Scheepers C
- Althaus CL
- et al.
Rapid epidemic expansion of the SARS-CoV-2 Omicron variant in southern Africa.
;
).
Due to the high SARS-CoV-2 incidence in the population with this variant, not all hospitalized SARS-CoV-2–positive patients were hospitalized solely because of COVID-19. We aimed to assess and classify the cause of hospitalization for patients with COVID-19 identified with the Omicron variant within our hospital to provide more insight into its burden on hospitalizations.
Methods
This study was performed at the Erasmus MC University Medical Center in Rotterdam, The Netherlands (Erasmus MC), a large tertiary care hospital with 1125 beds, including 121 intensive care unit (ICU) beds. The majority of our adult clinic consists of single-occupancy rooms with private bathrooms, whereas our pediatric clinic mainly consists of multiple-occupancy rooms with shared bathrooms. A retrospective analysis was performed on all patients identified with the SARS-CoV-2 Omicron variant between December 23, 2021, and February 27, 2022. During this period, the SARS-CoV-2 testing strategy of the hospital was symptom-based with a low threshold and included a wide range of symptoms and clinical signs. Only for select patient groups, a PCR was performed regardless of symptoms. These groups were (1) patients who were admitted to a multiple-occupancy room in the adult oncology ward and pediatric ICU, (2) patients who had to undergo upper respiratory tract or major surgery, or (3) patients who had been in unprotected close contact with a proven COVID-19 case (usually a family member). Isolation measures were the same for all SARS-CoV-2 positive patients.
SARS-CoV-2 infection was identified by real-time transcription–mediated amplification with the Aptima® SARS-CoV-2 assay using the Panther system (Hologic, Marlborough, USA), or by the Xpert® Xpress SARS-CoV-2 assay on a GeneXpert® system (Cepheid®, Sunnyvale, USA). SARS-CoV-2 positive samples were further characterized by variant-specific PCR using VirSNiP (TIBmolbiol, Berlin, Germany) assays targeting S371-S373 and K417 as a proxy for the Omicron variant. While detection of K417N was considered indicative for the Omicron variant, S371L-S373P was considered indicative for BA.1 and S371F-S373P for BA.2.
SARS-CoV-2 Omicron variant positive patients at admission were divided into the following categories: (1) patients hospitalized >24 hours within 7 days of first positive SARS-CoV-2 PCR, (2) patients hospitalized <24 hours within 7 days of first positive SARS-CoV-2 PCR, and (3) patients with visits only to the Erasmus MC outpatient clinic within 7 days of first positive SARS-CoV-2 PCR. Data were collected from electronic health records (EHRs).
The main cause of hospitalization during the full length of stay of patients with a positive SARS-CoV-2 PCR upon or during clinical admission was classified. Classifications were defined by modified definitions developed by the National Intensive Care Evaluation Foundation (
Table 1) (
). Classifications were performed by two epidemiologists through the evaluation of the patient's history in the EHR.
Table 1Classifications for primary, admission-contributing, and incidental COVID-19.
Results
A total of 333 adult patients were identified with the Omicron variant, of which 287 patients were identified with BA.1 (86.1%), 28 patients with BA.2 (8.4%), and 18 patients with either BA.1 or BA.2 (5.4%). Of patients with BA.1 , 39.4% had a clinical admission of >24 hours, 9.8% had a clinical admission of <24 hours, and 50.9% had an outpatient visit only. For adult patients with BA.2, 50% were clinically admitted to the hospital and 50% had an outpatient visit. Ninety-six pediatric patients were identified with the Omicron variant. BA.1 was identified in 57 children (82.6%), BA.2 in 16 children (15.9%), and one child was identified with either BA.1 or BA.2 (1.4%). Of children identified with BA.1, 26.3% were clinically admitted >24 hours, whereas 1.8% had a clinical admission of <24 hours, and 71.9% had an outpatient visit only. For children with BA.2, 36.4% had a clinical admission of >24 hours and 63.6% only had an outpatient visit.
One hundred seventy-two patients were hospitalized for >24 hours and were identified with the Omicron variant of SARS-CoV-2 at admission or during admission (
Table 2). Patients were classified (
Table 1) and characterized (
Table 2).
Table 2Characteristics of included hospitalized adults and pediatric patients with COVID-19 for each classification.
Clas, classification; ICU, intensive care unit; NA, not available; PCR, polymerase chain reaction; pos, positive.
Discussion
We identified that only 45% of our hospitalized adult patients with either BA.1 or BA.2, and 19% of pediatric patients, were primary COVID-19 cases. Patients with primary COVID-19 were significantly more often solid organ transplant recipients and showed significantly less BA.1 than patients with incidental COVID-19. They also seemed older and seemed to have a higher 28-day in-hospital mortality rate than patients with incidental COVID-19. They had, however, higher COVID-19 vaccination rates compared with patients with incidental COVID-19 (
Sun et al., 2022- Sun J
- Zheng Q
- Madhira V
- Olex AL
- Anzalone AJ
- Vinson A
- et al.
Association between immune dysfunction and COVID-19 breakthrough infection after SARS-CoV-2 vaccination in the US.
).
Initial studies on patients with the Omicron variant mainly assessed the clinical severity of hospitalized patients with COVID-19. However, these studies did not differentiate between primary and incidental COVID-19, thereby providing a general conclusion for all patients, while inherent differences are to be expected (
Maslo et al., 2022- Maslo C
- Friedland R
- Toubkin M
- Laubscher A
- Akaloo T
- Kama B.
Characteristics and outcomes of hospitalized patients in South Africa during the COVID-19 omicron wave compared with previous waves.
;
Wolter et al., 2022- Wolter N
- Jassat W
- Walaza S
- Welch R
- Moultrie H
- Groome M
- et al.
Early assessment of the clinical severity of the SARS-CoV-2 omicron variant in South Africa: a data linkage study.
). We suggest including our classification system when assessing the clinical severity of SARS-CoV-2 variants.
Although both primary and incidental COVID-19 hospitalizations have implications for workload and isolation capacity, patients with incidental COVID-19 generally interfere less with routine care. Our study population mainly consisted of patients with COVID-19 identified through our symptom-based testing strategy. Therefore, the number of patients with incidental COVID-19 may have been underestimated because asymptomatic COVID-19 cases may have gone unnoticed. Counting patients with incidental COVID-19 as primary COVID-19 admissions gives a skewed image of hospital workload and the COVID-19 burden. One should be careful to base health care and public health decisions solely on the total number of hospitalized COVID-19 patients. We recommend policy makers to consider the different groups of hospitalized COVID-19 patients in their decision-making.
Declaration of Competing Interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Conflict of interest
The authors declare no conflict of interest relevant to this article.
Funding source
This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.
Ethical approval statement
This study was approved by the medical ethical research committee of Erasmus MC (MEC-2021-0845-A-0002) and was not subject to the Medical Research Involving Human Subjects Act.
Acknowledgments
None.
Authors’ contributions
AV, CH, JR, RM, EN, LT, RP, AR, and JS conceptualized the study. AV and CH collected and analyzed the data. AV, CH, JR, RM, EN, LT, RP, AR, and JS interpreted the data. AV and CH drafted the work. All authors read, reviewed, and approved the final manuscript, and all authors have read and agreed to the published version of the manuscript.
References
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Article info
Publication history
Published online: July 12, 2022
Accepted:
July 8,
2022
Received in revised form:
July 7,
2022
Received:
May 20,
2022
Copyright
© 2022 The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases.