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Antibiotic Use, Bacterial Co-Infection, and Antimicrobial Resistance in Adults Hospitalized with COVID-19, Influenza,
Florina Cristiana Lucaciu1,2,3, Ovidiu Rosca2,3, Ana Maria Mihai1,2,3
1Doctoral School, "Victor Babes" University of Medicine and Pharmacy, 2 Eftimie Murgu Square, 300041 Timisoara, Romania.
Background:
Adults hospitalized with COVID-19, influenza A/B, or respiratory syncytial virus (RSV) frequently receive empirical antibiotics, but antibiotic prescribing, confirmed bacterial co-infection, antimicrobial resistance (AMR), and outcomes have not been jointly synthesized across these infections.
Methods:
We conducted a PRISMA 2020 systematic review and meta-analysis of 39 studies including 839,531 hospitalized adults. Random-effects models with Freeman-Tukey double-arcsine transformation pooled prevalence estimates; sensitivity and publication-bias analyses were performed where appropriate.
Results:
Pooled antibiotic use was 62.56% (95% CI, 53.75-70.97%) for COVID-19, 57.48% (25.76-86.09%) for influenza A/B, and 76.03% (67.62-83.53%) for RSV, with very high heterogeneity. Confirmed bacterial co-infection was lower: 5.31% (3.43-7.56%), 18.66% (9.98-29.30%), and 24.36% (18.53-30.70%), respectively. Prescribing-to-confirmed infection ratios ranged from 3.0 to 46.2. AMR evidence was restricted to COVID-19 studies and was dominated by carbapenem-resistant Gram-negative organisms, mainly in secondary, ICU-associated, or healthcare-associated infections. Confirmed bacterial complications were associated with ICU admission, longer hospitalization, and higher mortality.
Conclusions:
Antibiotic prescribing exceeded confirmed bacterial infection across all viral groups, but estimates require cautious interpretation due to heterogeneity, diagnostic uncertainty, observational evidence, and the absence of low-risk-of-bias studies. The evidence base was dominated by COVID-19 cohorts, while influenza A/B and RSV data, especially virus-specific AMR evidence, remain limited. COVID-19-specific AMR findings should not be generalized to influenza A/B or RSV. Virus-specific stewardship should prioritize rapid diagnostics, systematic sampling, reassessment, and de-escalation when bacterial infection is not confirmed.
Insights
Antibiotic prescribing for COVID-19, influenza, and RSV often exceeds confirmed bacterial infections. Virus-specific stewardship and rapid diagnostics are crucial for appropriate antimicrobial use and combating resistance.
Area of Science:
- Infectious Diseases
- Public Health
- Clinical Medicine
Background:
- Hospitalized adults with COVID-19, influenza, or RSV frequently receive empirical antibiotics.
- Limited synthesis exists on antibiotic prescribing, bacterial co-infection, antimicrobial resistance (AMR), and outcomes across these viral respiratory infections.
Purpose of the Study:
- To systematically review and synthesize data on antibiotic use, bacterial co-infections, AMR, and outcomes in hospitalized adults with COVID-19, influenza A/B, or RSV.
Main Methods:
- A PRISMA 2020 systematic review and meta-analysis of 39 studies involving 839,531 hospitalized adults.
- Random-effects models were used to pool prevalence estimates, with sensitivity and publication-bias analyses.
Main Results:
- Pooled antibiotic use was high: 62.56% for COVID-19, 57.48% for influenza A/B, and 76.03% for RSV, with significant heterogeneity.
- Confirmed bacterial co-infection prevalence was lower (5.31% COVID-19, 18.66% influenza, 24.36% RSV), leading to high prescribing-to-infection ratios.
- AMR data was limited to COVID-19, dominated by carbapenem-resistant Gram-negative organisms; bacterial complications correlated with ICU admission, longer hospitalization, and mortality.
Conclusions:
- Antibiotic prescribing surpassed confirmed bacterial infections across all viral respiratory illnesses studied.
- Findings necessitate cautious interpretation due to heterogeneity and diagnostic limitations; COVID-19 AMR data cannot be generalized to influenza or RSV.
- Virus-specific antimicrobial stewardship should emphasize rapid diagnostics, systematic sampling, reassessment, and de-escalation when bacterial infection is ruled out.
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