Case report | Volume 39, Article 208, 22 Jul 2021 | 10.11604/pamj.2021.39.208.30565

Catheter-related bloodstream infection due to Acinetobacter ursingii in a hemodialysis patient: case report and literature review

Arsanios Martin Daniel, Diana Garzón, Andrés Vivas, Tíjaro Merchán Viviana, Diego Alejandro Cubides-Diaz, Yesid Mantilla Fabian

Corresponding author: Tíjaro Merchán Viviana, Faculty of Medicine, Fundación Universitaria Juan N Corpas, Bogotá, Colombia

Received: 28 Jun 2021 - Accepted: 12 Jul 2021 - Published: 22 Jul 2021

Domain: Infectious disease

Keywords: Acinetobacter infection, bacteremia, hemodialysis, catheter related infection, case report

©Arsanios Martin Daniel et al. Pan African Medical Journal (ISSN: 1937-8688). This is an Open Access article distributed under the terms of the Creative Commons Attribution International 4.0 License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Cite this article: Arsanios Martin Daniel et al. Catheter-related bloodstream infection due to Acinetobacter ursingii in a hemodialysis patient: case report and literature review. Pan African Medical Journal. 2021;39:208. [doi: 10.11604/pamj.2021.39.208.30565]

Available online at: https://www.panafrican-med-journal.com/content/article/39/208/full

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Case report

Catheter-related bloodstream infection due to Acinetobacter ursingii in a hemodialysis patient: case report and literature review

Catheter-related bloodstream infection due to Acinetobacter ursingii in a hemodialysis patient: case report and literature review

Arsanios Martin Daniel1, Diana Garzón2, Andrés Vivas2, Tíĵaro Merchán Viviana3,&, Diego Alejandro Cubides-Diaz1, Yesid Mantilla Fabian1

 

1Department of Internal Medicine, Universidad de la Sabana, Chía, Colombia, 2Faculty of Medicine, Universidad de la Sabana, Chía, Colombia, 3Faculty of Medicine, Fundación Universitaria Juan N Corpas, Bogotá, Colombia

 

 

&Corresponding author
Tíjaro Merchán Viviana, Faculty of Medicine, Fundación Universitaria Juan N Corpas, Bogotá, Colombia

 

 

Abstract

Acinetobacter ursingii is an anaerobic gram negative opportunistic coccobacillus, rarely isolated in bacteremic patients. It is mainly found in immunocompromised and severely ill patients with no identifiable source of infection. When isolated into the bloodstream, it usually displays resistance to at least two antimicrobial agents. To date only seven cases of bacteremia due to this microorganism have been reported in adults, of which, this accounts for the second one associated to renal replacement therapy and the first case of a documented catheter-related bloodstream infection (CRBSI) in a patient with a hemodialysis catheter. A 78-year-old male presented into the emergency department with acute kidney injury requiring hemodialysis, later developing bacteremia due to Acinetobacter ursingii.

 

 

Introduction    Down

The genus Acinetobacter comprises a group of gram-negative coccobacillus, aerobic, opportunistic, non-fermenter and oxidase-negative bacteria; frequently found in humid environments. Acinetobacter ursingii can be found within its genomic species [1]. We present a case of a 78-year-old patient who attended the emergency department for respiratory distress secondary to a blunt chest trauma, with progresive organ dysfunction requiring invasive mechanical ventilation and hemodialysis. After the instauration of renal replacement therapy, the patient presented signs of systemic inflammatory response, with posterior isolation of A. ursingii in peripheral blood and catheter-tip cultures.

 

 

Patient and observation Up    Down

Patient information: a 78-year-old male patient, with smoking history for 30 years and arterial hypertension presented in the emergency department due to acute blunt chest trauma.

 

Clinical findings: he was in bad-looking shape, with respiratory distress and altered level of consciousness. Vital signs were as follows: blood pressure 80/62 mmHg, heart rate 120 bpm, respiratory rate 28 bpm, oxygen saturation 70% on room air, and a Glasgow coma scale of 6. At physical examination he presented with generalized paleness, multiple abrasions on the anterior thorax, thoracoabdominal dissociation and bilateral decrease in breath sounds.

 

Timeline of current episode: orotracheal intubation was performed, with a later discovery of a hemopneumothorax requiring closed thoracostomy and red blood cell transfusion. Laboratory findings on admission and during hospitalization are presented in Table 1. The patient presented torpid evolution and multiorgan dysfunction, with hemorrhagic shock, acute liver and renal injury and respiratory distress. Acute physiology and cronic health evaluation (APACHE) and sepsis related organ failure assessment (SOFA) scores were 16 and 11 respectively. At day three of admission renal replacement therapy was initiated under continuous venovenous hemofiltration modality, but five days later the patient presented clinical deterioration with tachycardia, leukocytosis, neutrophilia, lactic acidosis and requirement of increasing doses of vasopressors.

 

Diagnostic assessment: antibiotic therapy was started with meropenem and vancomycin, and cultures were taken, two from peripheral blood and one from the hemodialysis-catheter tip, with isolation of A. ursingii on the three of them (Figure 1).

 

Diagnosis: the antibiotic susceptibility pattern is described in Table 2.

 

Therapeutic interventions: based on the results, vancomycin was suspended and antibiotic treatment was continued with meropenem.

 

Follow-up and outcome of interventions: eight days later the patient presented sudden refractory hypotension, bradycardia, cardiac arrest and death.

 

Patient perspective: the patient could not share their perspective.

 

Informed consent: written informed consent was obtained from the patient to publish this paper.

 

 

Discussion Up    Down

Acinetobacter ursingii is a gram-negative coccobacillus, non-motile, non-fermenter, catalase and oxidase negative; frequently found in humid environments [1], its name comes from the microbiologist and taxonomist Jan Ursing, who first described it in 1989 [2]. Until the year 2021 there has been reported only 7 cases of bacteremia due to this microorganism in adults. The main characteristics of these cases, including ours, are presented in Table 3.

 

All of the reported patients had comorbidities (specially tumoral), were hospitalized, with severe disease courses and most of them were immunosuppressed [3]. Two of the cases had multi-organic dysfunction, however, only the reported by Endo et al. [4] presented renal dysfunction just like our case. In a retrospective study, where 456 cultures of Acinetobacter spp were analyzed, the patients with A. ursingii infections had prolonged intensive care unit (ICU) stays, were immunocompromised, underwent several invasive procedures or had multiple invasive devices, specially central venous catheters [5]. It has been demonstrated that Acinetobacter spp have the ability to invade skin and intravascular catheters [6,7], nonetheless, the great majority of the cases presented primary bacteremia without an identifiable source of infection or dissemination. Atas DB et al. reported the only case where infection was directly associated with renal replacement therapy, but the modality was intraperitoneal dialysis in a patient with chronic kidney disease presenting catheter-related peritonitis [8].

 

The association between acute kidney injury requiring hemodialysis and infection due to A. ursingii had not been described previously in the literature and its early identification might be of great clinical and epidemiological relevance. Since it is an opportunistic nosocomial microorganism with a long lasting survival on surfaces, its dissemination between patients is easy [9], increasing the risk of outbreaks in hospital environments and high circulation areas like renal units. Regarding its antimicrobial treatment, the isolations described so far are a 100% resistant to third and fourth generation cephalosporins and 80% sensitive to imipenem, levofloxacin, amikacin, gentamicin and colistin; which is consistent with the findings presented by Laurent Dortet et al. and Chao et al. [5,10], and the ones described in our patient. Nonetheless, due to the low frequency of its isolations and the limited clinical trials published so far, the full mechanisms behind its antimicrobial resistance are yet to be described.

 

 

Conclusion Up    Down

Bacteremia secondary to A. ursingii in hemodialysis patients is a rare cause of mortality. This would be the first reported case in the literature of a CRBSI due to this microorganism in a patient with hemodialysis. It is not possible to determine a strong association between infection and risk factors due to the rarity of this microorganism. It seems to be more frequent in severely ill patients with multiple comorbidities and invasive devices, so awareness should be taken in these kinds of patients in order to decrease the probability for A. ursingii infections.

 

 

Competing interests Up    Down

The authors declare no competing interests.

 

 

Authors' contributions Up    Down

All authors contributed to this work. They have also read and agreed to the final manuscript.

 

 

Tables and figure Up    Down

Table 1: laboratory findings on admission and during hospitalization

Table 2: antibiogram and resistance profile of A. ursingii isolated in hemodialysis-catheter tip culture

Table 3: clinical characteristics of Acinetobacter ursingii infections

Figure 1: A) blood agar showing white mucoid colonies consistent with Acinetobacter ursingii; B) gram stain of blood culture with gram negative coccobacillary forms

 

 

References Up    Down

  1. Chew KL, Chew KL. Acinetobacter ursingii masquerading as Gram-positive cocci. Clin Microbiol Infect. 2018 Aug;24(8):856-857. PubMed | Google Scholar

  2. Romero-Gómez MP, Sundlov A, Sáez-Nieto JA, Alvarezc D, Peña P. Bacteriemia por Acinetobacter. Enferm Infecc Microbiol Clin. 2006 Oct;24(8):535-6. PubMed

  3. Chiu CH, Lee Y-T, Wang YC, Yin T, Kuo SC, Yang Y-S et al. A retrospective study of the incidence, clinical characteristics, identification and antimicrobial susceptibility of bacteremic isolates of Acinetobacter ursingii. BMC Infect Dis. 2015;15(1):400. PubMed | Google Scholar

  4. Endo S, Sasano M, Yano H, Inomata S, Ishibashi N, Aoyagi T et al. IMP-1-producing carbapenem-resistant Acinetobacter ursingii from Japan. J Antimicrob Chemother. 2012;67(10):2533-4. PubMed | Google Scholar

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  8. Atas DB, Velioglu A, Asicioglu E, Tigen E. Peritoneal dialysis-related peritonitis with acinetobacter ursingii. Ther Apher Dial. 2016;20(2):205-6. PubMed | Google Scholar

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Case report

Catheter-related bloodstream infection due to Acinetobacter ursingii in a hemodialysis patient: case report and literature review

Case report

Catheter-related bloodstream infection due to Acinetobacter ursingii in a hemodialysis patient: case report and literature review

Case report

Catheter-related bloodstream infection due to Acinetobacter ursingii in a hemodialysis patient: case report and literature review