Background An understanding of differences in clinical phenotypes and outcomes COVID-19 compared with other respiratory viral infections is important to optimise the management of patients and plan healthcare. Herein we sought to investigate such differences in patients positive for SARS-CoV-2 compared with influenza, respiratory syncytial virus (RSV) and other respiratory viruses.
Methods We performed a retrospective cohort study of hospitalised adults and children (≤15 years) who tested positive for SARS-CoV-2, influenza virus A/B, RSV, rhinovirus, enterovirus, parainfluenza viruses, metapneumovirus, seasonal coronaviruses, adenovirus or bocavirus in a respiratory sample at admission between 2011 and 2020.
Results A total of 6321 adult (1721 SARS-CoV-2) and 6379 paediatric (101 SARS-CoV-2) healthcare episodes were included in the study. In adults, SARS-CoV-2 positivity was independently associated with younger age, male sex, overweight/obesity, diabetes and hypertension, tachypnoea as well as better haemodynamic measurements, white cell count, platelet count and creatinine values. Furthermore, SARS-CoV-2 was associated with higher 30-day mortality as compared with influenza (adjusted HR (aHR) 4.43, 95% CI 3.51 to 5.59), RSV (aHR 3.81, 95% CI 2.72 to 5.34) and other respiratory viruses (aHR 3.46, 95% CI 2.61 to 4.60), as well as higher 90-day mortality, ICU admission, ICU mortality and pulmonary embolism in adults. In children, patients with SARS-CoV-2 were older and had lower prevalence of chronic cardiac and respiratory diseases compared with other viruses.
Conclusions SARS-CoV-2 is associated with more severe outcomes compared with other respiratory viruses, and although associated with specific patient and clinical characteristics at admission, a substantial overlap precludes discrimination based on these characteristics.
- respiratory infection
- viral infection
Data availability statement
No data are available. Data from deidentified electronic health records are not freely available due to protection of the personal integrity of the participants.
This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
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What is the key question?
What are the differences in clinical phenotypes and outcomes in patients with SARS-CoV-2 as compared with influenza, respiratory syncytial virus (RSV) and other respiratory viruses such as seasonal coronaviruses, rhinovirus and metapneumovirus?
What is the bottom line?
Adult SARS-CoV-2 was associated with more severe outcomes compared with influenza, RSV and other respiratory viruses, and although associated with specific patient and clinical characteristics at admission, a substantial overlap precluded discrimination based on these characteristics.
Why read on?
To our knowledge, this is the first extensive comparison of baseline characteristics, clinical presentation and patient outcomes in SARS-CoV-2 as compared with influenza and several other respiratory viruses.
The clinical presentation of SARS-CoV-2 infected adults in hospitals includes fever, cough or dyspnoea, which are similar to those of other respiratory viruses.1–3 Common characteristics of hospitalised patients with COVID-19 are male sex, cardiovascular disease, diabetes, hypertension or obesity.4–6 A substantial portion of patients with COVID-19 require intensive care unit (ICU) admission and develop severe complications such as pulmonary embolism or acute kidney failure.4 5 7 8 There is some evidence for lower susceptibility to SARS-CoV-2 infection in children, as well as more favourable disease outcome.9–12 These observations are primarily based on case series and how these characteristics and outcomes compares in similar cohorts of patients infected with other respiratory infections is less well studied.
SARS-CoV-2 will likely remain endemic and cocirculate in the population together with influenza and other respiratory viruses.13 14 To better understand the pathogenesis of SARS-CoV-2 and to optimise patient management and plan healthcare, it is important to understand variations in clinical phenotypes and outcomes associated with different respiratory viruses. In this study, the aim was to investigate differences in baseline characteristics, clinical presentation and outcomes for adult and paediatric patients with SARS-CoV-2 compared with other respiratory viruses.
Patient population and study setting
We conducted a retrospective cohort study of hospitalised patients from October 2011 to September 2020 at Karolinska University Hospital, Stockholm, Sweden, an academic centre with 1100 beds divided between two sites and serving a population of 2.3 million inhabitants. Patients with the following PCR-confirmed infections from respiratory samples (nasopharyngeal, throat, sputum, tracheal or bronchoalveolar lavage samples) on admission were included: influenza A (H3N2 and H1N1), influenza B (FluB), adenovirus, bocavirus, seasonal coronaviruses species 229E, NL63, OC43 and HKU1, enterovirus, metapneumovirus, rhinovirus (RV), parainfluenza viruses type 1–4 (PIV), respiratory syncytial virus (RSV) and SARS-CoV-2 (see online supplemental eMethods 1 for additioal descriptions of PCR-methods). Samples collected within −24 hours to +48 hours from the hospital admission were included. Repeated positive tests within 90 days were excluded.
Data source and definitions
Data were obtained from a database of electronic health records of all patients admitted between January 2010 and September 2020, including demographics, International Classification of Diseases (ICD)-10 codes, body mass index (BMI), laboratory findings, vital signs, microbiology, intensive care and mortality. The study period start time of October 2011 was chosen to ensure at least 1.5 years of data on previous comorbidities and other variables. Specific individual comorbidities as well as Charlson Comorbidity Index (CCI) and Elixhauser Comorbidity Index (ECI) scores were based on ICD-10 codes recorded from 5 years before and up until admission.15 BMI was based on the most updated height and weight available. For laboratory parameters and vital signs, the worst value −24 hours to +24 hours from admission was used. See online supplemental eMethods 1 for additional descriptions.
The primary outcome was 30-day mortality from hospital admission. Secondary outcomes were length of stay (LOS) at hospital, 90-day mortality, ICU admission (defined as units that provide inotropic and non-invasive or invasive respiratory treatment), LOS at ICU, mortality after ICU admission (calculated from ICU admission), acute kidney injury (AKI; based on the Kidney Disease: Improving Global Outcomes (KDIGO) criteria16 but without urine volume measurements), pulmonary embolism (based on ICD-10 discharge code), acute myocardial injury (AMI; cardiac troponin T>50 ng/mL) and hospital-onset bacteraemia (HOB; significant findings in blood cultures taken >48 hours after admission).17 See online supplemental eMethods 2 for detailed definitions. Patients were followed for 30 days for outcome measures, except for pulmonary embolism where patients were followed until discharge and 90-day mortality.
Children (≤15 years of age) and adults were analysed separately. Analyses were performed using 10 virus categories as well as four virus groups in adults—SARS-CoV-2, influenza, RSV and other viruses—to correspond to differential virus testing indications. Testing for other viruses is preferentially performed in patients with more severe disease, with immunosuppression and tested negative for other viruses. All analyses were restricted to patients positive for only one virus group, in order to distinguish clinical phenotypes and outcomes for each virus group. For rhinoviruses and enteroviruses, PCR cross-reactivity, preventing classification of 572 health care episodes (HCE) (82 adult and 490 paediatric) into virus-specific groups.18 These 572 HCEs were excluded from virus-specific analyses, but adults were included in the other viruses group.
Multiple imputation with predictive mean matching was used to account for missing values for BMI, laboratory parameters and vital signs (proportion missing values 5%–13%) with other baseline characteristics and outcomes used as predictors (detailed description in online supplemental file).
Comparisons between all 10 virus groups were performed using χ2 test for nominal and Kruskal-Wallis test for continuous variables. Sex- and age category adjusted logistic regression analyses were performed to compare baseline characteristics, laboratory parameters and vital signs in patients with SARS-CoV-2 compared with influenza, RSV and other respiratory viruses. To investigate overall differences in baseline characteristics and clinical presentation between SARS-CoV-2 and influenza, RSV and other respiratory viruses, three logistic regression models were used. Predictors in the first model were age category, sex and BMI category, the second also included specific comorbidities and the third included laboratory parameters and vital signs as well. Model performance was assessed using area under the receiver operating characteristics (AUROC).
Clinical outcomes were compared among different virus groups using regression analyses with adjustment for sex, age category, BMI category and individual comorbidities: Cox regression HRs for 30-day and 90-day mortality, ICU admission, AMI, AKI and HOB, logistic regression ORs for pulmonary embolism and negative binomial regression rate ratios for LOS. The proportional hazards assumption was checked by Schoenfeld residuals. Kaplan-Meier curves and standardised adjusted survival functions were calculated for 30-day and 90-day mortality.15 In order to address potential time-related drifts in clinical management as well as more extensive testing of SARS-CoV-2 as compared with other viruses, predefined sensitivity analyses were performed for the outcomes mortality and ICU admission: (1) restriction to years 2015–2020, (2) restriction to patients with admission temperature ≥38°C, or oxygen saturation <95%, or respiratory rate >20, (3) stratification according to calendar time of SARS-CoV-2 positivity (February–April 2020 vs May–September 2020) and (4) restriction to the index HCE for each patient.
Statistical analyses were performed in R V.4.0.3.
In total, 782 345 inpatient admissions in 412 115 patients were registered between October 2011 and September 2020, of which 6700 adult and 8477 paediatric episodes tested positive for a respiratory virus at admission (figure 1). There were 661 episodes with repeated positive tests within 90 days. In the analysis, 12 700 episodes with one respiratory virus detected were included, 6321 adults (1721 SARS-CoV-2, 2468 influenza, 624 RSV and 1508 other viruses) and 6379 children (101 SARS-CoV-2, 871 influenza, 2425 RSV and 2982 other viruses).
Patient characteristics and clinical presentation of SARS-CoV-2 compared with other respiratory viruses among adults
Adult patients with SARS-CoV-2 were younger and more often male (median age 58 years (IQR 42–71), 59% male) compared with influenza (median age 68 years (IQR 51–79), 48% male), RSV (median age 71 years (IQR 60–81), 44% male) and other viruses (median age 61 years (IQR 40–72), 56% male) (p<0.001) (table 1 and online supplemental eTable 4). After adjustment for sex and age, SARS-CoV-2 admission was associated with overweight and obesity, as well as lower CCI and ECI compared with influenza, RSV and other viruses (table 1). The only comorbidities that were over-represented among patients with SARS-CoV-2 compared with influenza, RSV or other viruses were diabetes and hypertension.
Patients with SARS-CoV-2 more often presented with normal white cell count (WCC), platelet count and creatinine values (table 1, online supplemental eTable 5 and eFigure 2). In sex-adjusted and age-adjusted analyses, SARS-CoV-2 was associated with tachypnoea and less often hypotension or tachycardia, compared with all other virus groups, and less often fever (temperature >38°C) compared with influenza (online supplemental eTable 6 and eFigure 3). The prediction model that included age, sex, BMI, comorbidity, laboratory parameters and vital signs performed better compared with the simpler models, mean AUROC 0.74 for SARS-CoV-2 versus influenza, 0.83 for SARS-CoV-2 versus RSV and 0.82 for SARS-CoV-2 versus other viruses (online supplemental eFigure 4 and eTable 7).
Paediatric SARS-CoV-2 in relation to other respiratory viruses
Children with SARS-CoV-2 were older, while the sex distribution was similar compared with other respiratory viruses: SARS-CoV-2 median age 7 years (IQR 1–12), 55% male; influenza median age 2 years (IQR 0–5), 56% male; RSV median age 0 years (IQR 0–1), 56% male; and RV median age 1 year (IQR 0–3), 58% male (p<0.001 and 0.80) (table 2). The proportion of patients with at least one comorbidity differed between the viruses, being 20% (20/101) in SARS-CoV-2, 23% (198/871) in influenza and 16% (396/2425) in RSV, while it was higher (28%–43%) for the other viruses (p<0.001). Immunosuppression was the most prevalent comorbidity among patients with SARS-CoV-2 (10/101, 10%). Chronic respiratory disease, congenital malformations and chromosomal abnormalities were more prevalent in all nine other virus groups compared with SARS-CoV-2 (p<0.001). In the SARS-CoV-2 paediatric cohort, 41% presented with a temperature >38°C and 24% with increased respiratory rate or desaturation, which was lower than in all other virus groups (online supplemental eFigure 3). In children with SARS-CoV-2, the median LOS was 3 days (IQR 1–8), the 30-day and 90-day mortality were both 1% (1/101), 4% (4/101) were admitted to ICU and acute kidney injury based on modified KDIGO stage 1 criteria was detected in 8% (8/101).
Clinical outcomes in SARS-CoV-2 compared with other respiratory viruses among adults
The LOS in patients with SARS-CoV-2 was longer (6 days (IQR 3–11)) compared with influenza (4 days (IQR 2–7)), RSV (5 days (IQR 3–9)) and other viruses (4 days (IQR 2–8)). The 30-day mortality was 13% among patients with SARS-CoV-2 as compared with 5% for influenza, 7% for RSV and 5% for the other virus group (table 3 and figure 2). The adjusted 30-day mortality HR (aHR) for SARS-CoV-2 was 4.43 (95% CI 3.51 to 5.59), 3.81 (95% CI 2.72 to 5.34) and 3.46 (95% CI 2.61 to 4.60) compared with influenza, RSV and other viruses, respectively. This resulted in the following standardised 30-day survival probabilities: SARS-CoV-2 0.83 (95% CI 0.79 to 0.87), influenza 0.96 (95% CI 0.95 to 0.97), RSV 0.95 (95% CI 0.94 to 0.97) and other viruses 0.96 (95% CI 0.95 to 0.97) (figure 2). The SARS-CoV-2 30-day mortality was 16% (154/981) from February to April 2020 and 8% (62/740) from May to September 2020. For patients with SARS-CoV-2 admitted from May to September 2020, the 30-day mortality aHR compared with influenza, RSV and other viruses were 3.09 (95% CI 2.22 to 4.30), 3.00 (95% CI 1.95 to 4.62) and 2.60 (95% CI 1.79 to 3.80) (online supplemental eTable 8). In analyses stratified by age, the 30-day mortality aHR for patients aged 70 years or older was 5.41 (95% CI 4.17 to 7.00), 4.93 (95% CI 3.37 to 7.23) and 5.03 (95% CI 3.61 to 7.01) in patients with SARS-CoV-2 compared with influenza, RSV and other viruses, respectively (online supplemental eTable 9). The corresponding aHR for patients aged 50–69 years were 2.16 (95% CI 1.31 to 3.57), 1.71 (95% CI 0.81 to 3.60) and 2.07 (95% CI 1.13 to 3.79). The excess mortality in patients with SARS-CoV-2 occurred in the first 30 days, and in adjusted analyses, there was no significantly increased mortality risk among patients with SARS-CoV-2 compared with the other virus groups from day 31 to day 90 (online supplemental eFigure 5).
Patients with SARS-CoV-2 had an increased risk of ICU admission as compared with influenza and other viruses (table 3). The ICU LOS was longer, and the 30-day mortality after ICU admission was higher for patients with SARS-CoV-2 compared with all other virus groups. SARS-CoV-2 was associated with an increased risk of pulmonary embolism, adjusted ORs 5.26 (95% CI 3.34 to 8.28), 6.23 (95% CI 2.82 to 13.76) and 3.34 (95% CI 2.06 to 5.40) compared with influenza, RSV and other viruses, respectively, and also AMI compared with influenza and RSV, aHR 1.42 (95% CI 1.18 to 1.71) and 1.58 (95% CI 1.19 to 2.09), respectively. A decreased risk of AKI was observed for SARS-CoV-2 compared with influenza. For HOB, no significant risk differences were observed in adjusted analyses. The increased SARS-CoV-2 HR for mortality and ICU admission were consistent across sensitivity analyses (online supplemental eTable 8), but with more favourable outcomes for the SARS-CoV-2 cohort admitted from May to September 2020 as compared with February–April 2020. Adjusted mortality HRs were similar for analyses based on complete cases and multiple imputed data, and no significant difference was observed in 30-day mortality, 90-day mortality or ICU admission between 2015–2020 and 2011–2014 for influenza, RSV as well as other viruses (online supplemental eTable 10 and eFigure 6).
This observational study of 12 700 adult and paediatric admissions to a University Hospital in Stockholm, Sweden, showed that although SARS-CoV-2 was associated with younger age in adults and an overall lower comorbidity burden, there was a marked increased risk of 30-day mortality, ICU admission, ICU mortality and pulmonary embolism compared with other respiratory viruses. The mortality increase was most pronounced among the elderly and was attenuated during the later part of the study period, possibly due to improved management of patients with SARS-CoV-2. These findings were consistent across sensitivity analyses, considering potential change over time in diagnostic procedures, patient management and clinical presentation at admission, which highlights important differences in healthcare demands between SARS-CoV-2 and other respiratory viruses.
Combined with data from others studies, our results indicate substantial differences in outcomes for patients with SARS-CoV-2 compared with other respiratory viruses. In a study from Denmark where SARS-CoV-2 positive patients were compared with influenza, the unadjusted 30-day mortality was three times higher for patients with SARS-CoV-2, and a study from the UK comparing two cohorts of ICU patients admitted with diagnostic codes of COVID-19 and other respiratory viruses reported an almost doubled mortality in the COVID-19 cohort.19 20 A French study based on diagnostic codes reported a three times increased in-hospital mortality in 89 530 patients with COVID-19 compared with 45 819 patients with influenza, with the risk increase being more pronounced for patients aged ≥60 years.21
A study based on data from the US Department of Veterans Affairs healthcare system, with 95% of patients being male, reported a five times higher mortality in patients with COVID-19 compared with influenza.22 These studies corroborate our findings of a threefold and fourfold increased 90-day and 30-day mortality in patients with SARS-CoV-2 compared with patients hospitalised with influenza or RSV.
Previous case series have demonstrated cardiac and circulatory complications in COVID-19, with reported acute myocardial injury incidence between 7% and 40% in hospitalised patients and 2%–9% developing pulmonary embolism.23–27 However, acute cardiovascular events have also been associated with influenza and RSV, and previous studies based on diagnostic codes reported higher proportion of influenza patients developing cardiovascular complications as compared with patients with COVID-19.21 28–30 In our study, SARS-CoV-2 was associated with an increased risk of troponin-defined acute myocardial injury compared with influenza and RSV, and there was a 3–5 fold increased risk of pulmonary embolism in patients with SARS-CoV-2 compared with the other virus groups. This is concordant with studies from Denmark, France and the USA that reported an increased risk of thromboembolic events in patients with SARS-CoV-2 compared with influenza.19 21 30 Yet, retrospective studies comparing thromboembolic and cardiac events in patients with COVID-19 compared with other viruses might suffer from bias since they rely on ICD-10 discharge codes as well as likely differential testing strategies in patients with COVID-19. In our study, troponin T was assessed in 65% of SARS-CoV-2 compared with 27% and 29% in influenza and RSV patients. Also, elevated troponin might indicate myocarditis that has been associated with COVID-19, rather than ischaemic heart disease.21
Male sex, overweight, obesity, diabetes and hypertension were more common in patients with SARS-CoV-2 compared with the other respiratory viruses, which strengthen evidence that these are risk factors for hospitalisation with COVID-19.5 6 31 32 Yet, the overall comorbidity burden of patients with SARS-CoV-2, as measured by CCI and ECI scores, were lower. Patients with SARS-CoV-2 in our study were somewhat younger than reported from other cohorts, which was adjusted for in the analyses.19 30 The younger age distribution could partly be explained by differences in the affected patient populations and hospitalisation patterns during the SARS-CoV-2 pandemic.
Few studies have directly compared with what extent clinical presentation at admission can be used to differentiate SARS-CoV-2 from other respiratory viruses, and current evidence is based on studies of small sample sizes.4 5 33 34 Patients with SARS-CoV-2 more often presented with normal haemodynamic measurements, WCC, platelet count and creatinine values and were more often tachypnoeic. No clear difference was observed for saturation, measured as worst peripheral capillary oxygen saturation (SpO2), or when accounting for oxygen treatment using the SpO2/fraction of inspired oxygen (FiO2) ratio. Prediction models of increased complexity, although increasing in performance, demonstrated limited virus discriminating capability, for example, model 3 resulted in 60% sensitivity and 80% specificity to differentiate between SARS-CoV-2 and influenza. Future prospective studies should assess if symptoms and laboratory tests such as ferritin and interleukin-6 are associated with SARS-CoV-2 compared with other viruses.35
Among children, no difference in sex distribution was observed, whereas patients with SARS-CoV-2 were older compared with other respiratory viruses in line with a previous study that reported patients with COVID-19 to be older compared with patients with influenza.21 Paediatric patients with SARS-CoV-2 were more likely to present without an increased body temperature and dyspnoea, possibly due to more frequent screening of SARS-CoV-2 compared with other respiratory viruses. Paediatric patients with SARS-CoV-2 had a lower prevalence of chronic respiratory diseases and congenital malformations compared with other viruses. Severe outcomes were rare in the paediatric cohort.
Strengths of our study include the large study size, similar strict inclusion criteria regardless of viral infections and ample access to clinical data that enabled thorough analyses of clinical phenotype as well as adjustment for confounding. The strict virological inclusion criteria increased the internal validity of the study and reduced the risk of including patients transferred from other hospitals to the Karolinska University Hospital, which was more common during the SARS-CoV-2 epidemic. Even though the study population comprised a large portion of consecutively admitted patients with viral infections in the Stockholm region during a 9-year period, to verify generalisability, confirmation of the findings is warranted in patients from other geographical regions and hospitals. Data were collected from patient records, which depends on correct entry by healthcare staff. Yet, the risk of misclassification is likely independent of type of respiratory infections, and we restricted our analysis to routinely collected data. To increase internal validity, we restricted the analyses to episodes positive for only one virus, which might hamper the generalisability to all patients positive with respiratory virus. Yet, this would have minor impact on the results among adults since we only excluded 1.8% of admissions. Indications for SARS-CoV-2 testing might have differed compared with other respiratory viruses. Yet, the results were robust in sensitivity analyses restricting the study population to patients with fever, reduced oxygen saturation or increased respiratory rate at admission. However, the results for other viruses than SARS-CoV-2, influenza and RSV need to be interpreted with caution due to differential testing indications. Finally, due to the pandemic, hospitalisation patterns in different age groups, length of stay and ICU admission criteria might differ compared with the earlier study period.
SARS-CoV-2 is associated with an increased risk of mortality, ICU admission and pulmonary embolism in hospitalised patients compared with influenza, RSV and other respiratory viruses. Although SARS-CoV-2 is associated with specific patient and clinical characteristics at admission compared with other respiratory viruses, substantial overlap precludes discrimination based on these characteristics.
Data availability statement
No data are available. Data from deidentified electronic health records are not freely available due to protection of the personal integrity of the participants.
The study was approved by the Regional Ethical Review Board in Stockholm (Dnr 2018/1030-31, COVID-19 research amendment Dnr 2020–01385).
Contributors PH, HT and SvdW had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Study concept and design: PH, AF, MB, AT and PN. Acquisition, analysis or interpretation of data: PH, JKV, SvdW, HT, ARM, JM, RD and OH. Drafting of the manuscript: PH nd PN. Critical revision of the manuscript for important intellectual content: all authors. Statistical analysis: PH and FG. Additional contributions: none.
Funding The work was supported by grants from the Swedish Innovation Agency (Vinnova) and Region Stockholm. PH was supported by Karolinska Institutet (combined clinical studies and PhD training programme). JKV was supported by Region Stockholm (combined clinical residency and PhD training programme).
Disclaimer The funders had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review or approval of the manuscript; and decision to submit the manuscript for publication.
Competing interests None declared.
Provenance and peer review Not commissioned; externally peer reviewed.
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