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Case Report

Multiple Secondary Healthcare-Associated Infections Due to Carbapenem-Resistant Organisms in a Critically Ill COVID-19 Patient on Extensively Prolonged Venovenous Extracorporeal Membrane Oxygenation Support—A Case Report

by
Hiroaki Baba
1,2,*,†,
Hajime Kanamori
1,2,3,†,
Issei Seike
1,
Ikumi Niitsuma-Sugaya
1,
Kentaro Takei
1,
Kengo Oshima
1,2,
Yudai Iwasaki
4,
Yuko Ogata
4,
Hirona Nishimaki
4,
Daisuke Konno
4,
Takuya Shiga
4,
Koji Saito
4,
Koichi Tokuda
1,2,3 and
Tetsuji Aoyagi
1,2
1
Department of Infectious Diseases, Internal Medicine, Tohoku University Graduate School of Medicine, 2-1 Seiryo machi, Aoba-ku, Sendai 980-8575, Japan
2
Department of Intelligent Network for Infection Control, Tohoku University Graduate School of Medicine, 2-1 Seiryo machi, Aoba-ku, Sendai 980-8575, Japan
3
Division of Infection Control, Tohoku University Hospital, 1-1 Seiryo machi, Aoba-ku, Sendai 980-8574, Japan
4
Intensive Care Unit, Tohoku University Hospital, 1-1 Seiryo machi, Aoba-ku, Sendai 980-8574, Japan
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Microorganisms 2022, 10(1), 19; https://doi.org/10.3390/microorganisms10010019
Submission received: 30 November 2021 / Revised: 21 December 2021 / Accepted: 21 December 2021 / Published: 23 December 2021
(This article belongs to the Special Issue Infections in Intensive Care Units)
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Abstract

:
Patients with severe Coronavirus disease 2019 (COVID-19) are at high risk for secondary infection with multidrug-resistant organisms (MDROs). Secondary infections contribute to a more severe clinical course and longer intensive care unit (ICU) stays in patients with COVID-19. A man in his 60s was admitted to the ICU at a university hospital for severe COVID-19 pneumonia requiring mechanical ventilation. His respiratory condition worsened further due to persistent bacteremia caused by imipenem-non-susceptible Klebsiella aerogenes and he required VV-ECMO. Subsequently, he developed a catheter-related bloodstream infection (CRBSI) due to Candida albicans, ventilator-associated pneumonia (VAP) due to multidrug-resistant Pseudomonas aeruginosa (MDRP), and a perianal abscess due to carbapenem-resistant K. aerogenes despite infection control procedures that maximized contact precautions and the absence of MDRO contamination in the patient’s room environment. He was decannulated from VV-ECMO after a total of 72 days of ECMO support, and was eventually weaned off ventilator support and discharged from the ICU on day 138. This case highlights the challenges of preventing, diagnosing, and treating multidrug-resistant organisms and healthcare-associated infections (HAIs) in the critical care management of severe COVID-19. In addition to the stringent implementation of infection prevention measures, a high index of suspicion and a careful evaluation of HAIs are required in such patients.

1. Introduction

Coronavirus disease 2019 (COVID-19) has a wide spectrum of severity ranging from mild illness that does not require treatment to severe illness that requires an intensive care unit (ICU) level of care, including intensive ventilation and extracorporeal membrane oxygenation (ECMO) [1]. Patients with severe COVID-19 are at high risk for secondary infections with multidrug-resistant organisms (MDROs) [2,3]. Secondary infections contribute to a more severe clinical course and longer ICU stays in patients with COVID-19 [2]. Secondary infection is a common complication of ECMO; however, few publications have described such infection in patients with severe COVID-19 receiving ECMO. Here, we report on multiple secondary healthcare-associated infections (HAIs) due to carbapenem-resistant organisms in a patient with severe COVID-19 on prolonged venovenous extracorporeal membrane oxygenation (VV-ECMO).

2. Case Presentation

A man in his 60s who smokes and has type 2 diabetes presented with fever and shortness of breath, and was admitted to an isolation unit at a university hospital for severe COVID-19 pneumonia. Despite treatment with dexamethasone and remdesivir, his condition deteriorated rapidly and he required endotracheal intubation and mechanical ventilation; therefore, he was transferred to the ICU on day two of admission. He was put on airborne, droplet, and contact precautions in a single, airborne infection isolation room, with negative pressure and an anteroom. However, on day 18 he developed a fever greater than 38.0 °C and his respiratory condition worsened further. He presented severe respiratory failure with a partial pressure of oxygen (PaO2) of 51 mmHg on day 21 while on the following ventilator settings: fraction of inspired oxygen (FiO2) of 1.0, pressure support (PS) of 17 cmH2O, and a positive end-expiratory pressure (PEEP) of 12 cmH2O; and required VV-ECMO (Figure 1). Culture from blood and the tip of the central venous catheter (CVC) were positive for Klebsiella aerogenes (Isolate ID: KE-1) that was not susceptible to imipenem but was susceptible to piperacillin-tazobactam, meropenem, and amikacin (Table 1). Sputum cultures were positive for Citrobacter koseri and Pseudomonas aeruginosa (Table 1) but negative for K. aerogenes. Urine analysis showed no pyuria (<5 white blood cells per high power field), and urine culture was negative. A blood test showed elevated serum C-reactive protein (CRP) (>10.0 mg/L; reference range, <0.3 mg/L) but low procalcitonin (PCT) (0.11 ng/mL; reference range, <0.05 ng/mL). Liver and renal functions were normal. Tests for serum 1,3-β-D-glucan, the cytomegalovirus (CMV) pp65 antigenemia assay, and stool Clostridioides difficile toxins were negative. Whole-body enhanced computed tomography (CT) on day 18 showed diffuse ground-glass opacities in both lung fields (Figure 2) but no other abnormal findings, including venous thromboembolism, deep abscess, and sinusitis. Despite treatment with piperacillin-tazobactam 4.5 g once every 6 h (q6h) to treat the catheter-related bloodstream infection (CRBSI), the fever persisted. Blood cultures remained positive for K. aerogenes 3 days after the initiation of piperacillin-tazobactam treatment, despite the removal of the CVC and exchange of the ECMO oxygenator and pump. Because of the suspected bacterial colonization of the ECMO cannulas, the antimicrobial regimen was switched from piperacillin-tazobactam to a combination of short infusion (30 min) of meropenem 2 g q8h plus amikacin 5 mg/kg q12h on day 23; however, blood culture still remained positive for K. aerogenes on day 26, so the short infusion of meropenem was switched to an extended infusion (3 h) [4]. Subsequently, the patient’s condition improved, and blood culture became negative for K. aerogenes on day 32.
Although airborne precautions were lifted on day 24 after SARS-CoV-2 reverse transcription polymerase chain reaction tests of two consecutive nasopharyngeal samples taken 24 h apart were negative, single room isolation and contact precautions were continued because of the earlier detection of imipenem-non-susceptible K. aerogenes (Figure 1). On day 40, respiratory function was improved such that the patient could be weaned off ECMO. However, he deteriorated again because of CRBSI due to Candida albicans on day 38, and ventilator-associated pneumonia (VAP) due to multidrug-resistant Pseudomonas aeruginosa (MDRP) on day 45 (Table 1), and required a second course of ECMO due to his worsening oxygenation (PaO2 of 52 mmHg with FiO2 of 1.0, PS of 15 cmH2O, and a PEEP of 12 cmH2O) on day 47 (Figure 1).
On day 64, he suddenly developed fever, hypotension, and tachycardia. Enhanced CT revealed a perianal horseshoe abscess that was not apparent on physical examination (Figure 3). The abscess was successfully drained, and the culture showed non-carbapenemase-producing, carbapenem-resistant K. aerogenes (Isolate ID: KE-2) (Table 1). The patient recovered and, after a total of 72 days of ECMO support, was decannulated from VV-ECMO on day 93, although mechanical ventilation was continued. Subsequently, the patient had two more episodes of MDRP-VAP that were successfully treated with colistin plus extended infusion meropenem and aerosolized tobramycin 90 mg q8hr in combination with intravenous piperacillin-tazobactam, respectively (Figure 1). He was eventually weaned off ventilator support and discharged from the ICU on day 138. At the time of writing this paper, on day 228, the patient is undergoing rehabilitation on a general ward, whereby continuous contact precautions are being continued because MDRP was detected in sputum. Although chest CT on day 228 shows persistent interstitial changes distributed throughout the entire lung fields (Figure 2), the patient is in a good clinical condition without respiratory support, and his neurological and nutritional status is normal.
We tested the ICU room for contamination with carbapenem-resistant organisms on day 24. We collected a total of 10 samples from 10 sites, including eight high-touch surfaces and medical devices (bed rail, bedside table, vital signs monitor, infusion pump control panel, ventilator monitor/tube, venovenous extracorporeal membrane oxygenation monitor, ultrasound imaging system probe/keyboard, and computer keyboard), the sink surface/drain, and the floor surface (Supplementary Method S1). As a result, no bacterial growth was detected in all the samples.
Both K. aerogenes isolates KE-1 and KE-2 were confirmed to be negative for carbapenemase genes of blaIMP-1, blaIMP-6, blaVIM, blaGES, blaKPC, blaNDM, and blaOXA-48 groups (Supplementary Method S2). Whole genome sequencing (WGS)-based phylogenetic analysis revealed isolates KE-1 and KE-2 were genetically separated (Supplementary Method S3, Supplementary Dataset).

3. Discussion

In our case, multiple secondary HAIs occurred despite infection control procedures that maximized contact precautions and despite the absence of MDRO contamination in the patient’s room environment, which is an important reservoir of MDROs [5]. Patients with severe COVID-19 tend to require ECMO for longer than patients with conventional acute respiratory distress syndrome and are commonly treated with empiric, broad-spectrum antibiotic therapy, which puts them at high risk of acquiring MDROs [1,2]. In patients undergoing ECMO, acquisition of MDROs significantly increases the risk for subsequent VAP and CRBSI, both of which are associated with an increased risk of death [6]. Therefore, early detection and preventive strategies for HAIs and antimicrobial stewardship programs adapted to patients with severe COVID-19 receiving ECMO are needed.
Determining the cause of fever in patients with severe COVID-19 receiving ECMO is challenging because fever can be caused by many infectious conditions, including VAP, CRBSI, catheter-associated urinary tract infection, ECMO device-related infection, Clostridioides difficile infection, other bacterial infections (e.g., meningitis, sinusitis, biliary tract infections, and deep abscesses), non-bacterial infections (e.g., aspergillosis, CMV infection); non-infectious conditions (e.g., cerebral infarction/hemorrhage, venous thromboembolism, adrenal insufficiency, crystal arthritis, and drug fever), and COVID-19 recurrence [2,7,8,9,10]. The accurate diagnosis of HAIs is often hampered by difficulties distinguishing HAIs from other infections and non-infectious conditions. For example, ECMO frequently masks the signs and symptoms of infections [11]. Patients with severe COVID-19 usually present diffuse bilateral lung infiltrates on chest imaging that are difficult to distinguish from signs of other respiratory infections, including VAP, pulmonary aspergillosis, and CMV pneumonia [7]. Extensive airspace opacification due to lung-protective lung strategies makes interpretation of chest radiographic findings more difficult [11]. Clinical biomarkers of inflammation, including CRP and PCT, are not specific to infections, and the inflammatory response can be caused by the host response to the ECMO circuit itself [12]. A deep abscess is often hard to diagnose, particularly in patients under general anesthesia, which masks pain [13]. A perianal abscess, which is typically caused by Enterobacterales and anaerobic bacteria, can be fatal and requires urgent drainage [14,15], as seen in our case. In the absence of visible signs in patients with COVID-19 sepsis, particularly in those with risk factors such as male sex, smoking, and diabetes (which are also risk factors for severe COVID-19) [13,16], physicians should consider examining the anorectal region by enhanced CT or transperineal ultrasonography [17].
To the best of our knowledge, this case represents the longest reported ECMO runtime with a successful recovery [18]. Some studies showed promising outcomes of prolonged ECMO treatment (>28 days) in patients with severe COVID-19, although the data are limited [1,18]. Survival after prolonged ECMO has improved remarkably in recent years because of technological advances and prevention and management of complications [18]; however, HAIs are still one of the most difficult challenges for healthcare professionals applying ECMO. Bacterial colonization of ECMO cannulas should be considered in patients on ECMO with persistent bacteremia of unknown origin that does not improve with removal of the CVC and exchange of the oxygenator and pump [19,20]; however, changing the cannulas is highly problematic because of the high risk of potentially lethal complications and limited vascular access [21]. Furthermore, robust data are lacking on the optimal antibiotic dose for patients on ECMO [22]. Ideally, therapeutic drug monitoring (TDM) is necessary because circuit drug loss and enlarged volume of distribution have previously been reported [22,23]; however, TDM of meropenem is not yet common practice. If this method is not available, extended infusion of meropenem and combination therapy with aminoglycosides for synergistic effects are reasonable therapeutic options for patients on ECMO with refractory meropenem-susceptible, non-carbapenemase-producing-carbapenem-resistant Enterobacterales bacteremia [24,25].
Therapeutic options for meropenem-resistant Enterobacterales and MDRP infections are very limited in Japan, where the new first-line drugs for these MDROs (i.e., ceftazidime-avibactam, meropenem-vaborbactam, imipenem-cilastatin-relebactam, and ceftolozane-tazobactam) are not available at the time of writing [24,26]. Under these conditions, combination therapy (i.e., β-lactam agent plus aminoglycoside or polymyxins) remains an important therapeutic option for severe cases, even when considering adverse effects such as nephrotoxicity and ototoxicity [25]. In this context, aerosolized tobramycin is also a promising option for treatment of MDRP-VAP [27].
Although we have presented a single case report, it nevertheless highlights the significant diagnostic and therapeutic challenges of HAIs in patients with COVID-19 receiving long-term ECMO. Previous studies demonstrated a significant reduction in the incidence of exogenous HAIs due to the stringent infection prevention and control (IPC) measures implemented during the COVID-19 pandemic [28,29]. However, preventing the development of secondary endogenous infections in patients requiring prolonged multidisciplinary treatment in the ICU remains challenging, as in this case. In addition to adequate IPC measures, a high index of suspicion and careful evaluation of HAIs are required in such patients because clinical signs and symptoms, laboratory findings, and imaging features of HAIs are usually unremarkable and non-specific, and a wide range of other infectious and non-infectious conditions need to be differentiated. Infectious diseases specialists play a crucial role in preventing and managing HAIs and in addressing antimicrobial resistance by implementing antimicrobial stewardship to provide the best care for patients with severe COVID-19.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/microorganisms10010019/s1. Supplementary Method S1: We collected environmental samples with eSwab 480 CE (Copan, Brescia, Italy) and incubated them with 10 mL of Mueller–Hinton broth at 37 °C for 48 h for pre-enrichment. Then, we placed 100 µL of the broth on the CHROMagarTM mSuper CARBA (Nippon Becton Dickinson, Tokyo, Japan) and incubated the sample at 37 °C for 48 h. Supplementary Method S2: Both Klebsiella aerogenes isolates KE-1 and KE-2 were confirmed to be negative for carbapenemase genes of blaIMP-1, blaIMP-6, blaVIM, blaGES, blaKPC, blaNDM, and blaOXA-48 groups by using Cica geneusR Carbapenemase Genotype detection kit 2 (Kanto Chemical CO., Inc., Tokyo, Japan). Supplementary Method S3: Whole genome sequencing (WGS) was performed on both Klebsiella aerogenes isolates KE-1 and KE-2 as follows: bacterial DNA was extracted with the QIAmp DNA Mini GIAcube Kit (Quiagen, Hilden, Germany) according to the manufacturer’s instructions, and a DNA library was prepared from each sample with a Nextera XT DNA Sample Prep Kit (Illumina, San Diego, CA, USA) according to the manufacturer’s instructions. For sequencing, a Miseq (Illumina, San Diego, CA, USA) was used to generate paired-end 300 bp reads. Both samples showed an average of 150-fold coverage (Supplementary Dataset). Phylogeny based on WGS-based core-genome multi-locus sequence typing (cgMLST) was performed with SeqSphere + version 6.0.2 (Ridom GmbH, Münster, Germany) by using an ad hoc scheme comprising 4466 target loci based on the KCTC2190 genome (NC_015663.1) (Jünemann S et al., Nat Biotechnol 2013; Seth-Smith HMB et al., Front Public Health 2019). The K. aerogenes isolates KE-1 and KE-2 were genetically separated by 71 cgMLST allele differences (Weber DJ et al., Curr Opin Infect Dis 2013). Supplementary Dataset: Total numbers of contigs, total length, N50 length, average coverage, and accession numbers for Klebsiella aerogenes isolates KE-1 from blood culture and KE-2 from perianal abscess drainage culture analyzed with whole-genome sequencing. Both samples showed an average of 150-fold coverage. The sequence data have been deposited in the DDBJ/EMBL/GenBank Sequence Read Archive under accession numbers DRX279247 and DRX279248.

Author Contributions

Conceptualization, investigation, and writing—original draft preparation, H.B. and H.K.; review and editing, I.S., I.N.-S., K.T. (Kentaro Takei), K.O., Y.I., Y.O., H.N., D.K., T.S., K.S., K.T. (Koichi Tokuda) and T.A. All authors contributed to the clinical management of the patient. All authors have read and agreed to the published version of the manuscript.

Funding

The data analysis and the writing of the manuscript in this work were supported by JSPS KAKENHI (Grant Number JP18K16169).

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Ethics Committee of Tohoku University Graduate School of Medicine (code 2019-1-270, date of approval: 26 July 2019).

Informed Consent Statement

Written informed consent was obtained from the patient for publication of this case report.

Data Availability Statement

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Acknowledgments

We thank all the intensive care unit staff. The Department of Intelligent Network for Infection Control, Tohoku University Graduate School of Medicine, is an endowment department supported with an unrestricted grant from Kyosei Igaku Laboratory.

Conflicts of Interest

The authors declare no conflict of interest.

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Microorganisms 10 00019 g001 550
Figure 1. Clinical course and treatment of the present case: The patient had acquired multiple secondary infections requiring long-term broad-spectrum antibiotic use. Centers for Disease Control and Prevention criteria (https://www.cdc.gov/hai/index.html, accessed on 30 November 2021) for diagnosis of catheter-related bloodstream infection and ventilator-associated pneumonia were met. Abbreviations: CRBSI, catheter-related bloodstream infection; CRE, carbapenem-resistant Enterobacteriaceae; MDRP, multidrug-resistant Pseudomonas aeruginosa; CT, computed tomography; MV, mechanical ventilation; VV-ECMO, venovenous extracorporeal membrane oxygenation; RT-PCR, reverse transcription polymerase chain reaction.
Figure 1. Clinical course and treatment of the present case: The patient had acquired multiple secondary infections requiring long-term broad-spectrum antibiotic use. Centers for Disease Control and Prevention criteria (https://www.cdc.gov/hai/index.html, accessed on 30 November 2021) for diagnosis of catheter-related bloodstream infection and ventilator-associated pneumonia were met. Abbreviations: CRBSI, catheter-related bloodstream infection; CRE, carbapenem-resistant Enterobacteriaceae; MDRP, multidrug-resistant Pseudomonas aeruginosa; CT, computed tomography; MV, mechanical ventilation; VV-ECMO, venovenous extracorporeal membrane oxygenation; RT-PCR, reverse transcription polymerase chain reaction.
Microorganisms 10 00019 g001
Microorganisms 10 00019 g002 550
Figure 2. Chest computed tomography (CT) images of the present case: (A) CT on day 18 of admission (just before extracorporeal membrane oxygenation cannulation). Bilateral, peripheral, and basal predominant ground-glass opacities (GGOs) and consolidation were observed; (B) CT on day 228 (135 days post-decannulation). The CT shows significant improvement of GGOs and consolidation but persistent interstitial changes distributed throughout the entire lung fields.
Figure 2. Chest computed tomography (CT) images of the present case: (A) CT on day 18 of admission (just before extracorporeal membrane oxygenation cannulation). Bilateral, peripheral, and basal predominant ground-glass opacities (GGOs) and consolidation were observed; (B) CT on day 228 (135 days post-decannulation). The CT shows significant improvement of GGOs and consolidation but persistent interstitial changes distributed throughout the entire lung fields.
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Figure 3. Perianal abscess in a patient with severe coronavirus disease 2019: (A) enhanced computed tomography revealed a horseshoe-shaped collection of fluid, 35 mm in diameter, surrounding the anus; (B) appearance of perianal region after incision and drainage—external examination before drainage showed only a skin tag without swelling around the anus.
Figure 3. Perianal abscess in a patient with severe coronavirus disease 2019: (A) enhanced computed tomography revealed a horseshoe-shaped collection of fluid, 35 mm in diameter, surrounding the anus; (B) appearance of perianal region after incision and drainage—external examination before drainage showed only a skin tag without swelling around the anus.
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Table
Table 1. Antimicrobial susceptibility testing in detected bacterial isolates in the present case.
Table 1. Antimicrobial susceptibility testing in detected bacterial isolates in the present case.
MIC Value (µg/mL) and Interpretation
Organism Klebsiella aerogenes (KE-1) Klebsiella aerogenes (KE-2) Citrobacter koseriPseudomonas aeruginosa MDRP
Source Blood Drainage Culture Sputum Sputum Sputum
AntibioticsAmpicillin>16 R>16 R>16 R
Ampicillin-sulbactum>16 R>16 R≤4 S
Amoxicillin-clavulanate>16 R>16 R≤8 S
Piperacillin16 S64 I>64 R16 S32 I
Piperacillin-tazobactam8 S16 S8 S8 S32 I
Cefazolin>16 R>16 R≤1 S
Cefmetazole>32 R>32 R≤4 S
Ceftriaxone≤0.5 S>2 R≤0.5 S
Ceftazidime>8 R>8 R≤1 S4 S>16 R
Cefepime≤1 S8 S≤1 S8 S>16 R
Imipenem2 I>2 R≤0.5 S1 S>8 R
Meropenem≤0.25 S>2 R≤0.25 S≤0.5 S>8 R
Aztreonam≤1 S>8 R≤1 S>16 R>16 R
Amikacin≤8 S≤8 S≤8 S≤4 S32 I
Gentamicin≤2 S≤2 S≤2 S2 S8 I
Tobracin ≤1 S4 S
Minocycline>8 R>8 R4 S
Ciprofloxacin<0.25 S>2 R<0.5 S0.5 S>4 R
Levofloxacin1 S>4 R≤0.12 S2 S>8 R
Fosfomycin≤4 S>16 R≤4 S>16 R>16 R
Trimethoprim-sulfamethoxazole≤40 S≤40 S≤40 S
Bacteria and their antibiotic susceptibilities were determined by the VITEK-MS and VITEK-2 systems (Sysmex-bioMérieux Japan, Tokyo, Japan), respectively. Susceptibility results were interpreted according to available breakpoints set by Clinical and Laboratory Standards Institute (CLSI) guidelines (Performance Standards for Antimicrobial Susceptibility Testing. M100-S27. CLSI, Wayne, USA. 2018). Abbreviations: MIC, minimum inhibitory concentration; MDRP, multidrug-resistant Pseudomonas aeruginosa; R, resistant; I, intermediate; S, sensitive.
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Baba, H.; Kanamori, H.; Seike, I.; Niitsuma-Sugaya, I.; Takei, K.; Oshima, K.; Iwasaki, Y.; Ogata, Y.; Nishimaki, H.; Konno, D.; et al. Multiple Secondary Healthcare-Associated Infections Due to Carbapenem-Resistant Organisms in a Critically Ill COVID-19 Patient on Extensively Prolonged Venovenous Extracorporeal Membrane Oxygenation Support—A Case Report. Microorganisms 2022, 10, 19. https://doi.org/10.3390/microorganisms10010019

AMA Style

Baba H, Kanamori H, Seike I, Niitsuma-Sugaya I, Takei K, Oshima K, Iwasaki Y, Ogata Y, Nishimaki H, Konno D, et al. Multiple Secondary Healthcare-Associated Infections Due to Carbapenem-Resistant Organisms in a Critically Ill COVID-19 Patient on Extensively Prolonged Venovenous Extracorporeal Membrane Oxygenation Support—A Case Report. Microorganisms. 2022; 10(1):19. https://doi.org/10.3390/microorganisms10010019

Chicago/Turabian Style

Baba, Hiroaki, Hajime Kanamori, Issei Seike, Ikumi Niitsuma-Sugaya, Kentaro Takei, Kengo Oshima, Yudai Iwasaki, Yuko Ogata, Hirona Nishimaki, Daisuke Konno, and et al. 2022. "Multiple Secondary Healthcare-Associated Infections Due to Carbapenem-Resistant Organisms in a Critically Ill COVID-19 Patient on Extensively Prolonged Venovenous Extracorporeal Membrane Oxygenation Support—A Case Report" Microorganisms 10, no. 1: 19. https://doi.org/10.3390/microorganisms10010019

APA Style

Baba, H., Kanamori, H., Seike, I., Niitsuma-Sugaya, I., Takei, K., Oshima, K., Iwasaki, Y., Ogata, Y., Nishimaki, H., Konno, D., Shiga, T., Saito, K., Tokuda, K., & Aoyagi, T. (2022). Multiple Secondary Healthcare-Associated Infections Due to Carbapenem-Resistant Organisms in a Critically Ill COVID-19 Patient on Extensively Prolonged Venovenous Extracorporeal Membrane Oxygenation Support—A Case Report. Microorganisms, 10(1), 19. https://doi.org/10.3390/microorganisms10010019

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