Dear Editor,
The recently published article by Lansbury L et al. showed that a low proportion of COVID-19 patients have a bacterial co-infection.1 However, Huttner B et al. recommended antibiotics for most severe COVID-19 presentations.2 Rawson TM et al. described a widespread use of broad-spectrum antibacterials in 72% (1450 out of 2010) COVID-19 patients, despite a paucity of evidence for bacterial co-infection.3 COVID-19 may mimic bacterial pneumonia2 , 4 and, therefore, antibiotics for possible bacterial coinfection are frequently administered. We conducted a retrospective analysis aimed at describing the impact of early antibiotic therapy (i.e., before intensive care unit [ICU] admission) on mortality and delayed severe healthcare-associated infections in the ICU.
From 9th April to 20th May 2020 we retrospectively reviewed all medical charts of intubated ICU patients admitted to a community hospital dedicated to the care of COVID-19 patients in the Southern part of Switzerland. This hospital served as a reference center for a population of 350’000 inhabitants (seven public hospitals).
We described patients who received antibiotics (versus no antibiotics) before ICU stay and we analyzed differences in mortality, ventilator-associated pneumonia (VAP), catheter-related bloodstream infections (CRBSIs), urinary tract infections (UTIs) and candidemias (i.e., outcomes) between both groups. Importantly, antibiotics before ICU admission were administered at the discretion of the attending physician and this variable was routinely collected. Characteristics of patients were described as count (percent) or median (interquartile range) for qualitative and quantitative variables, respectively, and were compared between groups using Chi-square, Fisher or Mann–Whitney tests, as appropriate. The study was approved by the regional Ethics Committee (number: 2020-01216 CE 36641).
We included 48 ICU patients with COVID-19. The median age was 66.5 (interquartile range [IQR] 60 -71) and 33% (n=11) were female. Antibiotics before ICU admission were administered in 40% (n=19) of cases, in all cases the clinical indication was a suspected bacterial co-infection. The most frequently used antibiotic was amoxicillin/clavulanate (68%, n=13). Characteristics of patients with or without antibiotics are reported in the Table 1 . In general, patients’ characteristics in both group swere similar. In patients without antibiotics cardiovascular disease was more frequently observed (38% versus 16% in patients with antibiotics, p=0.12); whereas women (32% versus 17% in patients without antibiotics, p=0.25) and antivirals (68% versus 48%, p=0.17) were more frequently observed in the group with antibiotics. Mortality was similar between the two groups (24% without antibiotics versus 26% with antibiotics, p=0.86). Interestingly, no difference in the number of delayed healthcare-associated infections during ICU stay was observed between groups. UTI tended to be more frequent in the group without antibiotic, whereas candidemias appeared to be more frequent in the antibiotic group. The low number of patients included in our analysis did not allow a firm conclusion. However, our preliminary results illustrate that early administered antibiotics do not appear to significantly impact mortality or delayed hospital-acquired infections in critically ill patients and call into question the utility of early treatment of a presumptive bacterial superinfection in COVID-19 patients. Large multi-centric studies are urgently needed5 to investigate the impact of early antibiotics therapy on1 mortality,2 subsequent healthcare associated infections and3 ICU complications (i.e., duration of mechanical ventilation).
Table 1.
Without antibiotics (n=29) | With antibiotics (n=19) | p-value | |
---|---|---|---|
Age, median (IQR) | 66 [60; 71] | 67 [60; 72] | 0.74 |
Sex, female | 5 (17.2) | 6 (31.6) | 0.25 |
≥1 comorbidity | 22 (75.9) | 16 (84.2) | 0.49 |
Cardiovascular disease | 11 (37.9) | 3 (15.8) | 0.12 |
Diabetes mellitus | 7 (24.1) | 6 (31.6) | 0.57 |
Hypertension | 16 (55.2) | 8 (42.1) | 0.38 |
Lymphopenia at admission, median (IQR) | 0.7 [0.6; 0.9] | 0.7 [0.4; 0.9] | 0.33 |
CRP at admission, median (IQR) | 128 [57; 206] | 83 [47; 132] | 0.29 |
Creatinin at admission, median (IQR) | 95 [84; 118] | 98 [81; 128] | 0.92 |
Lymphopenia duration, median (IQR) | 23 [16; 31] | 25 [23; 35] | 0.11 |
SAPS at ICU admission, median (IQR) | 45 [40; 65] | 47 [37; 55] | 0.79 |
Corticosteroids during ICU stay | 15 (51.7) | 10 (52.6) | 0.95 |
Antivirals* | 14 (48.3) | 13 (68.4) | 0.17 |
Tocilizumab | 3 (10.3) | 2 (10.5) | 0.99 |
Healthcare-associated infections during ICU stay | |||
Infection number per patient, median (IQR) | 1 [1; 2] | 1 [1; 2] | 0.98 |
VAP | 19 (65.5) | 14 (73.7) | 0.55 |
UTI | 8 (27.6) | 2 (10.5) | 0.28 |
CRBSI | 7 (24.1) | 5 (26.3) | 0.86 |
Colitis | 0 (0) | 1 (5.3) | 0.39 |
Candidemia | 2 (6.9) | 3 (15.8) | 0.37 |
Mortality | 7 (24.1) | 5 (26.3) | 0.86 |
Legends. *Antivirals commonly administered at our institution were: hydroxychloroquin, lopinavir/ritonavir and remdesivir. IQR: interquartile range. CRP: C-reactive protein. SAPS: Simplified Acute Physiology Score. ICU: Intensive care unit. VAP: Ventilator-associated pneumonia. UTI: Urinary tract infection. CRBSI: Catheter-related bloodstream infection.
Declaration of Competing Interest
None.
Acknowledgements
Funding. NB is currently receiving a Post.doc Mobility grant from the Swiss National Science Foundation (grant number: P400PM_183865) and a grant from the Bangerter-Rhyner Foundation.
References
- 1.Lansbury L, Lim B, Baskaran V, Lim WS. Co-infections in people with COVID-19: a systematic review and meta-analysis. The Journal of infection. 2020 doi: 10.1016/j.jinf.2020.05.046. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Huttner BD, Catho G, Pano-Pardo JR, Pulcini C, Schouten J. COVID-19: don't neglect antimicrobial stewardship principles! Clin Microbiol Infect. 2020 doi: 10.1016/j.cmi.2020.04.024. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Rawson TM, Moore LSP, Zhu N, Ranganathan N, Skolimowska K, Gilchrist M. Bacterial and fungal co-infection in individuals with coronavirus: A rapid review to support COVID-19 antimicrobial prescribing. Clin Infect Dis. 2020 doi: 10.1093/cid/ciaa530. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Shi H, Han X, Jiang N, Cao Y, Alwalid O, Gu J. Radiological findings from 81 patients with COVID-19 pneumonia in Wuhan. China: a descriptive study. The Lancet infectious diseases. 2020;20(4):425–434. doi: 10.1016/S1473-3099(20)30086-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Clancy CJ, Nguyen MH. COVID-19, superinfections and antimicrobial development: What can we expect? Clin Infect Dis. 2020 doi: 10.1093/cid/ciaa524. [DOI] [PMC free article] [PubMed] [Google Scholar]