ICU-Acquired Colonization and Infection in COVID-19 Patients: History
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Contributor:
Alexandre Gaudet
,
Louis Kreitmann
,
Saad Nseir

A large proportion of ICU-acquired infections are related to multidrug-resistant bacteria (MDR). Infections caused by these bacteria are associated with increased mortality, and prolonged duration of mechanical ventilation and ICU stay.  Although a huge amount of literature is available on COVID-19 and MDR bacteria, only a few clinical trials have properly evaluated the association between them using a non-COVID-19 control group and accurate design and statistical methods. The results of these studies suggest that COVID-19 patients are at a similar risk of ICU-acquired MDR colonization compared to non-COVID-19 controls. However, a higher risk of ICU-acquired infection related to MDR bacteria has been reported in several studies, mainly ventilator-associated pneumonia and bloodstream infection. Several potential explanations could be provided for the high incidence of ICU-acquired infections related to MDR. Immunomodulatory treatments, such as corticosteroids, JAK2 inhibitors, and IL-6 receptor antagonist, might play a role in the pathogenesis of these infections. Additionally, a longer stay in the ICU was reported in COVID-19 patients, resulting in higher exposure to well-known risk factors for ICU-acquired MDR infections, such as invasive procedures and antimicrobial treatment. Another possible explanation is the surge during successive COVID-19 waves, with excessive workload and low compliance with preventive measures. Further studies should evaluate the evolution of the incidence of ICU-acquired infections related to MDR bacteria, given the change in COVID-19 patient profiles. A better understanding of the immune status of critically ill COVID-19 patients is required to move to personalized treatment and reduce the risk of ICU-acquired infections. The role of specific preventive measures, such as targeted immunomodulation, should be investigated.

  • antimicrobial resistance
  • multidrug resistance
  • cross-infection

1. Introduction

Patients affected by the most severe form of coronavirus disease 2019 (COVID-19) pneumonia develop acute respiratory distress syndrome (ARDS), characterized by profound and life-threatening hypoxemia. These patients often have a prolonged intensive care unit (ICU) stay and require an extended duration of invasive mechanical ventilation (IMV) [1]. Several studies have shown that critically ill COVID-19 patients present a higher incidence of ICU-acquired infections than non-COVID-19 controls, especially hospital- and ventilator-associated pneumonia (HAP and VAP, respectively) [2] and bloodstream infections (BSI) [3]. They are exposed to broad-spectrum antimicrobials [4], which leads to a sustained antibiotic selection pressure. Consequently, there have been major concerns about the potential impact of the COVID-19 pandemic on the emergence and spread of antimicrobial resistance (AMR) [5].
AMR is an important concern in ICUs, where a significant proportion of secondary infections are attributed to multidrug-resistant (MDR) bacteria [6]. In studies conducted prior to the pandemic, ICU-acquired colonization with MDR bacteria was linked to a longer ICU length-of-stay [7], and ICU-acquired infection with MDR bacteria was associated with a longer duration of IMV [8] and higher mortality [6][9].
Several studies have investigated the burden of AMR among COVID-19 patients (see reviews in [10][11][12][13][14][15]), but most presented important methodological limitations. These include a limited sample size, a retrospective and/or monocentric design, the inclusion of both ICU and non-ICU patients, the absence of a control group of non-COVID-19 patients, and the failure to use appropriate statistical methods to account for important confounding factors.

2. Epidemiology

The majority of these studies presented important methodological limitations, mainly related to a retrospective (n = 21) or single-centered (n = 15) design. Most studies compared COVID-19 ICU patients with a control group of non-COVID-19 ICU patients enrolled before the onset of the pandemic. Most studies (n = 22) focused on ICU-acquired infections, and eight also evaluated ICU-acquired colonization with resistant bacteria. The assessment of antibiotic resistance relied on classical microbiology criteria, but the definitions used to classify bacteria as “difficult-to-treat” or “multidrug-resistant” varied across studies.
Finally, several studies have mostly reported bacteriological data and have failed to provide a clear link between bacteriology (e.g., the result of a blood or tracheal aspirate culture) and patient-related data (infection vs. colonization status, clinical variables, etc.), making any attempt to precisely evaluate the incidence, risk factors, and prognostic impact of ICU-acquired MDR colonization/infection impossible. In line with this, only eight studies have adjusted statistical analyses on patient-level factors known to be associated with the occurrence of ICU-acquired infection/colonization with resistant bacteria.
Regarding the incidence of VAP related to MDR bacteria, in the COVAPID study, a retrospective multicenter study (36 ICUs) comparing 568 COVID-19 patients with 1008 controls, the incidence of VAP was significantly higher in COVID-19 patients (36.1%) than in patients with flu (22.2%) or no viral infection (16.5%), but the frequency of MDR strains was lower in COVID-19 patients (23.3%) than in patients with flu (38.4%) and no viral infection (33.8%) [2][16]. Data can be used to provide estimates of the cumulative incidence of VAP related to MDR bacteria in all three groups (11.8% in COVID-19 patients, 11.6% in flu patients, and 8.6% in patients with no viral infection), which does not suggest that this incidence might be higher among COVID-19 patients (contrarily to the COVID-BMR study [17]). However, in a retrospective multicenter study on 1879 COVID-19 patients and 1879 controls in 94 ICUs, the incidence of a first episode of VAP was higher in COVID-19 patients (adjusted sHR 1.68, 95% CI 1.45–1.96), with a similar frequency of MDR pathogens (except for a lower frequency of MRSA), which would suggest a higher incidence of VAP episodes related to MDR bacteria in the COVID-19 group [18] (in line with the COVID-BMR study [17]). Similarly, in a retrospective monocentric study, COVID-19 patients (n = 90) had a higher incidence of VAP (sHR 1.72, 95% CI 1.14–2.57), including MDR VAP (23% vs. 11%, p = 0.03), than non-COVID-19 controls (n = 82; in line with the COVID-BMR study [17]). Finally, using the REA-REZO surveillance network database, a large retrospective study in France found a higher incidence of VAP [19] among 1687 COVID-19 patients than controls (72,258 non-COVID-19 ICU patients recruited before and during the pandemic), with similar proportions of resistant strains among isolated bacteria, again suggesting that the incidence of ICU-acquired infections related to MDR bacteria might be higher among COVID-19 patients. In conclusion, even if no study has been designed to specifically assess this endpoint, the existing literature suggests that COVID-19 patients may have a higher incidence of VAP related to MDR bacteria than controls, mostly linked to a higher incidence of VAP (related to non-MDR and MDR strains altogether) [13].
Regarding the incidence of BSI related to MDR bacteria, a retrospective monocentric study on 497 COVID-19 patients and 823 controls reported that COVID-19 patients had a higher incidence of BSI related to MDR bacteria [20] (adjusted cause-specific HR (cHR) 2.65, 95% CI 1.25–5.59, in line with the COVID-BMR study [17]). Similarly, a retrospective international study in 53 ICUs found an increased incidence of hospital-acquired BSI related to difficult-to-treat Gram-negative bacteria in COVID-19 (n = 252) vs. controls (n = 577; 19.4% vs. 13%, p = 0.017) [21]. Finally, a large retrospective study in France found a higher incidence of VAP and BSI related to MDR bacteria in COVID-19 patients [22]. In conclusion, the existing literature suggests that COVID-19 patients may have a higher incidence of BSI related to MDR bacteria than controls.
The occurrence of ICU-acquired infections with MDR bacteria is influenced by several factors, but is preceded by colonization in the majority of cases. In the COVID-BMR study, there was no significant difference in the cumulative incidence of ICU-acquired MDR colonization between COVID-19 patients and controls (34.1% vs. 27.9%, adjusted sHR 1.27, 95% CI 0.85–1.88) [17]. These estimates were in line with a monocentric retrospective study where the cumulative incidence of ICU-acquired colonization with MDR bacteria was not statistically different in COVID-19 patients when compared with matched controls (respectively 33% vs. 21% sHR 1.71, 95% CI 0.93–3.12) [23]. Among the studies, two monocentric retrospective studies reported a similar incidence of ICU-acquired colonization with MDR bacteria in COVID-19 patients vs. controls [24][25]; a monocentric retrospective found a lower incidence of ICU-acquired MDR colonization in COVID-19 vs. control patients (47.4% vs. 81.4%, p = 0.005) [26]; and a multicenter retrospective study found decreased rates of MRSA, VRE, CRE and CRAB in systematic screening samples from COVID-19 in comparison with non-COVID-19 patients [27]. In conclusion, the existing literature suggests that the incidence of ICU-acquired colonization with MDR bacteria is similar or potentially lower in COVID-19 patients vs. controls.
As discussed in the COVID-BMR study, assessing ICU-acquired MDR colonization and infection separately enables a more precise investigation of the mechanisms leading to the emergence and spread of AMR among COVID-19 ICU patients [17]. As ICU-acquired MDR colonization could be related to the cross-transmission of MDR strains across patients through direct contact with healthcare workers, findings would suggest that organizational changes triggered by the COVID-19 pandemic—such as the cohorting of patients in dedicated COVID-19 units with strict enforcement of infection prevention and control (IPC) policies, enhanced hand hygiene, use of protective personal equipment (PPE), and efforts to decrease patient contacts—might have had a positive impact on this phenomenon. Second, findings also suggest that COVID-19 patients might harbor distinct characteristics that make them more susceptible than controls to developing ICU-acquired MDR infections once colonized with a given MDR strain; these factors will be discussed in more detail in paragraph 4 related to pathophysiology.

3. Pathophysiology

Recent epidemiological data have brought to light a notable increase in the risk of MDR infections among patients hospitalized in ICUs with severe COVID-19. This increased susceptibility to MDR infections can be attributed to several factors. Primarily, the administration of immunomodulatory treatments in the management of critically ill COVID-19 patients in ICUs plays a significant role. These treatments encompass various modalities, including, but not limited to, the widespread use of dexamethasone along with potential adjunctive therapies, such as JAK2 inhibitors and IL-6 receptor antagonists. Thus, in the COVID-BMR study, treatment with steroids was found in 75% of COVID-19 patients, vs. 22% of non-COVID-19 patients [17]. The immunosuppressive effects resulting from these treatments may be contributory factors for the elevated incidence of infections, particularly MDR infections. Interestingly, according to findings from the COVID-BMR study, the increased risk of MDR infection among COVID-19 patients occurs as early as seven days following admission to the ICU [17]. Conversely, other data have identified a heightened risk of VAP occurring around three weeks after admission to the ICU in patients exposed to dexamethasone [28][29]. This apparent discrepancy in the timings of infection onset seems to indicate that other factors are likely to contribute to the higher incidence of MDR infections in critically ill COVID-19 patients.
Consistent data have shed light on the direct involvement of the SARS-CoV-2 virus in triggering post-aggressive immunoparalysis. Comparatively, the inflammatory response to COVID-19 appears to be generally of a more moderate intensity when compared with sepsis, with a prolonged state of immunoparalysis observed among severely ill COVID-19 patients. However, it is crucial to note that immune dysregulation in COVID-19 patients exhibits a heterogeneous pattern. Notably, there is a high incidence of lymphopenia affecting both B and T cell populations, with subsequent impacts on cellular and humoral responses. Furthermore, studies have also indicated the presence of monocyte dysfunction, whose intensity seemingly correlates with disease severity [30][31][32][33]. These immune alterations collectively contribute to the development of an immunodeficient state intrinsically linked to COVID-19, thereby rendering severe COVID-19 patients more susceptible to MDR infections.
Another potential explanation for the higher risk of MDR infections among severely ill COVID-19 patients is the increased likelihood of MDR emergence due to the selection pressure resulting from antibiotic use. Notably, exposure to antibiotics stands as one of the primary risk factors for the development of MDR in ICUs [34]. Furthermore, compelling evidence suggests an elevated frequency of antibiotic administration among severely ill COVID-19 patients, potentially resulting from relaxed antibiotic stewardship during the pandemic. Data from the ISARIC consortium, encompassing nearly 50,000 hospitalized COVID-19 patients, revealed that 37% of patients had been exposed to antibiotics prior to hospital admission. This exposure frequency further increased to over 85% during the initial phase of hospitalization, despite bacterial sampling being conducted in only 17% of patients, with positive bacterial cultures found in less than 3% of the total cohort [4][35]. Consequently, the low occurrence of bacterial coinfections is consistent with the findings from the extensive European study COVID-ICU, which reported a 7% frequency of bacterial coinfections upon admission to the ICU [1]. Similarly, a recent meta-analysis involving over 30,000 patients reported a frequency of confirmed bacterial coinfection during the initial phase of approximately 4%, while the rate of antibiotic administration was 60% [36]. These data highlight the significant disparity between the low occurrence of initial bacterial coinfections in severely ill hospitalized COVID-19 patients and the high frequency of antibiotic exposure.
Furthermore, other hypotheses regarding the characteristics of hospital stays can be postulated to explain the increased risk of MDR infections among patients admitted to the ICU for COVID-19. According to data from the COVID-BMR study, the median length of stay in the ICU for severely ill COVID-19 patients was found to be 15 days, compared with 10 days for patients admitted for other reasons [17]. Additionally, the authors noted increased exposure to invasive medical devices among COVID-19 patients compared with non-COVID-19 patients. This included a higher utilization of extracorporeal membrane oxygenation (ECMO), observed in over 9% of COVID-19 patients compared with 2% of non-COVID-19 patients, as well as arterial catheters, utilized in 97% of COVID-19 patients versus 83% of non-COVID-19 patients. Notably, the study also highlighted an extended duration of exposure to these invasive devices. As compared with non-COVID-19 cases, COVID-19 patients exhibited a median duration of exposure of 16 versus 11 days for central venous catheters, 14 versus 9 days for arterial catheters, and 15 versus 8 days for invasive mechanical ventilation. Consequently, the increased frequency of breaches in the anatomical barrier resulting from prolonged exposure to invasive devices likely contributed to the increased risk of infection among MDR-colonized patients, thereby amplifying the incidence of MDR infections among COVID-19 patients in ICUs.
Lastly, material and organizational factors, such as a surge in patient admissions to ICUs, may also participate in the increased risk of MDR infections among patients admitted for COVID-19. The relationship between the scarcity of ICU beds and the prognosis of hospitalized COVID-19 patients has been well-documented since the initial waves of the pandemic [37][38]. Several factors have been identified to explain this relationship, including a shortage of nursing staff leading to an excessive workload [39], which, in turn, may result in reduced adherence to individual protective measures. Similarly, the inadequate availability of personal protective equipment has also been identified as a contributing factor during the pandemic, potentially heightening the risk of MDR transmission [40].

4. Specific Preventive Measures

Several studies reported a higher incidence of ICU-acquired infections, including those related to MDR bacteria in COVID-19 patients [2][17]. Although this high incidence could be explained by exposure to well-known risk factors, such as invasive procedures and long ICU stays, the role of compliance with preventive measures during the surge was not evaluated. One could argue that general preventive measures should be strictly applied in COVID-19 patients, given the high incidence of ICU-acquired infections in these patients.
No randomized controlled study has evaluated the efficiency of measures aiming to prevent ICU-acquired infection in COVID-19 patients. Previous studies highlighted a link between microbiota alteration in COVID-19 patients and the severity of inflammation, persistence of ARDS, and mortality [41][42][43][44]. The role of digestive and pulmonary microbiota in the pathogenesis of ICU-acquired infections has also been suggested [45][46]. However, whether the alteration of microbiota results in different effects on ICU-acquired infection in COVID-19 patients, as compared with non-COVID-19 patients is still to be evaluated. In a recent pilot study performed in 17 COVID-19 patients, gut microbiota composition significantly differed between patients with ICU-acquired colonization related to MDR bacteria, compared with those with no MDR bacteria colonization [47]. Further studies are needed to confirm these findings.

This entry is adapted from the peer-reviewed paper 10.3390/antibiotics12091464

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