Abstract
Nocardia species, which are ubiquitous in the environment, form lesions primarily in immunocompromised patients via oral or cutaneous infection. Some of these Nocardia species, such as N. farcinica, also infect the central nervous system via hematogenous dissemination, which rarely results in brain abscesses. Notably, N. farcinica is resistant to numerous antimicrobial drugs used in empirical therapy, necessitating the intervention of an infectious disease specialist. To date, no case of antimicrobial stewardship teams (ASTs) playing a central role in community hospitals without an infectious disease specialist has been reported. Here, we describe a case of N. farcinica-associated brain abscess in a small-to-medium-sized hospital with no infectious disease department or specialist, in which the AST assisted in the identification of the causative organism and in selecting appropriate therapeutic agents, ultimately leading to a cure.
The patient was an 88-year-old man with a high fever. He had been taking prednisolone (10-15 mg/day) for approximately 1 year for pemphigoid. Considering the possibility of fever owing to bacteremia of cutaneous origin, ampicillin/sulbactam antimicrobial therapy at 6 g/day was initiated. A subsequent close examination led to the diagnosis of a brain abscess. Emergency abscess drainage was performed by a neurosurgeon, and postoperative antimicrobial combination therapy comprising ceftriaxone (4 g/day), vancomycin (2 g/day), and metronidazole (1,500 mg/day) was commenced. The AST suspected Nocardia infection earlier, but further testing was difficult to perform at this facility. Therefore, by requesting assistance from Nagoya University Hospital, we performed early bacterial identification by mass spectrometry and appropriate antimicrobial susceptibility testing by a custom panel on day 11. The patient was non-responsive to all the previously used antibiotics at the time of admission. On day 13 after admission, the patient was successfully treated with trimethoprim-sulfamethoxazole (TMP-SMX) and imipenem/cilastatin sodium, and the patient was cured.
The AST can be as effective as an infectious disease specialist when a strong working relationship is established between the team and clinicians. Further, the activities of the AST can improve patient survival via active medical support in collaboration with attending physicians.
Keywords: microbiological technologist, diagnosis, pharmacist, nocardia farcinica, brain abscess, antimicrobial stewardship team
Introduction
Nocardia is a common genus found in fresh and saltwater and the soil, caves, dust, decaying plants, and animal feces [1,2]. It has a characteristic beaded branching cell morphology and is gram-positive, aerobic, partially acid-fast, lysozyme-resistant, and catalase-positive. Currently, 109 Nocardia species, of which approximately half are considered clinically relevant, have been identified, and some of these species were initially isolated from human sources [2]. Further, Nocardia species infect humans via two main routes: respiratory tract infection through direct or indirect inhalation of cells and the skin following surgical procedures or traumatic skin injury. Nocardia species are also known to cause hematogenous dissemination from the lungs and skin to the brain, as well as pseudotumor lesions in the abdomen, eyes, and joints [3]. Infection of the central nervous system (CNS) due to hematogenous dissemination is observed in one-third of cases, while brain abscesses occur in approximately 9% of cases [4].
Nocardia farcinica is a highly invasive species with a strong tendency to infect the CNS and cause brain abscesses [5]. According to a systematic review, it accounts for 39.6% of all Nocardia cases [6]. It is also the most common strain in Japan and primarily infects individuals aged 60-80 years, with men reported to be three times more likely to be infected than women [7]. Further, Nocardia species can grow on blood agar and other media used in routine culture tests. However, its growth is slow and, in many cases, can be overlooked [1]. This makes their identification in general laboratories challenging. Therefore, 16S ribosomal RNA analysis and mass spectrometry using Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry (MALDI-TOF MS) are often applied in this regard.
The activities of Antimicrobial Stewardship Teams (ASTs) include recommending appropriate specimen collection methods, selecting optimal antimicrobial agents based on the results of microbiological tests, and establishing the treatment administration period to ensure the prevention of recurrence. Thus, they play an important role in the rapid treatment of patients after diagnosis.
Here, we report a case of N. farcinica-associated brain abscess in a small-to-medium-sized hospital (255 beds) with no infectious disease department or specialist, in which the AST contributed to the early identification of the pathogenic microorganism and helped in the diagnosis, steps that ultimately led to the patient being cured.
Case presentation
The patient was an 88-year-old man with a chief complaint being high fever. He had been taking prednisolone (10-15 mg/day) for approximately 1 year for pemphigoid, had a history of shingles and scabies, and had a pruritic rash on his trunk and lower extremities. He underwent surgery for lumbar spinal canal stenosis 12 years earlier. He had incontinence 10 days prior to admission and 6 days prior to admission, he was unable to stand up appropriately. Thus, he visited his local doctor for an examination.
On admission, the vital signs of this patient were as follows: body temperature, 39.0 °C; blood pressure, 133/82 mmHg; sinus rhythm pulse, 100 beats/min; respiratory rate, 18 breaths/min; oxygen saturation, 89% (room air), and Glasgow Coma Scale, 13/15 (E4V4M5). Further, his white blood cell count, neutrophil rate, and C-reactive protein (CRP) concentration were 13,100/µL (reference range: 3,300-8,600/µL), 83.5%, and 8.58 mg/dL (reference range: <0.14 mg/dL), respectively. The patient showed no symptoms of headache or vomiting, and at the time of admission, he was disorientated but was able to respond when spoken to. His chest and abdomen computed tomography (CT) images showed emphysema and a mass image on the mediastinal side of the lower middle lobe; however, there was no obvious pneumonia or active inflammation of his abdomen (Figure 1).
Figure 1. Chest CT showed a mass image on the mediastinal side of the lower middle lobe (red arrow) and no obvious pneumonia.
Since the source of the fever could not be determined on admission, ampicillin/sulbactam therapy (6 g/day) was initiated after considering the possibility of bacteremia of cutaneous origin owing to the numerous rashes and scratches observed on his skin. Further, given that the patient was hospitalized on the weekend, his head CT scan was performed the following week, on the fourth day of hospitalization. Notably, two space-occupying lesions with edema were observed in his right frontal lobe. Brain magnetic resonance imaging (MRI) further showed a hyperintense polycystic lesion on T2- and diffusion-weighted images (Figure 2a).
Figure 2. MRI scans obtained on different days after admission.
(a) Day 4: a polycystic lesion in the right frontal lobe of the patient’s brain with high intensity on the T2-weighted image (T2WI) and diffusion-WI. (b) Day 11: shrinkage of the brain lesion. (c) Day 39: fluid re-accumulation in the lesion space after drainage. On the right side is a gadolinium-enhanced T1 weighted-image (T1Gd). (d) Day 193: shrinkage of lesion and non-recurrence of the abscess.
The patient was referred to the neurosurgery department, where emergency abscess drainage was performed. Thereafter, 15 mL of the cream-colored abscess was cultured, while postoperative antimicrobial combination treatment, comprising ceftriaxone (CTRX; 4 g/day), vancomycin (VCM; 2 g/day), and metronidazole (MNZ; 1,500 mg/day), was commenced.
The AST microbiological technologist performed Gram staining on the bacilli on day 5 after admission and observed branched gram-positive rods. Further, Kinyoun staining showed weak anti-acidity, indicating the possibility of Nocardia (Figure 3). However, identifying the specific Nocardia species at our facility was challenging. Thus, these samples were sent to Nagoya University Hospital for further analysis.
Figure 3. (a) Colonies on Sheep Blood Agar, (b) Gram-stained (× 1,000), and (c) Kinyoun-stained (× 1,000) image of brain abscess.
The AST pharmacist took steps to quickly purchase trimethoprim-sulfamethoxazole (TMP-SMX) and imipenem/cilastatin sodium (IPM/CS), two intravenous antimicrobial agents, which were not in stock at our hospital given that they are not generally used at our hospital. Screening for human immunodeficiency virus infections recommended by the AST pharmacist was negative.
At Nagoya University Hospital, the bacteria were identified as N. farcinica via mass spectrometry (VITEK® MS; BIOMÉRIEUX, Tokyo, Japan) performed on day 8 after admission (99.8 confidence level). Based on the criteria set forth by the Clinical and Laboratory Standards Institute (CLSI), drug susceptibility testing performed on day 11 after admission revealed that the patient was resistant to all three drugs used for postoperative infection prevention (Table 1). Therefore, we decided to replace the combination therapy with TMP (720 mg/day) and SMX (3,600 mg/day) plus IPM/CS (1.5 g/day) on day 13 after admission. Before the change in the antimicrobial agents, the patient was referred to the Respiratory Medicine department for bronchoscopic alveolar lavage fluid examination in detail of the mass lesions in the lungs; N. farcinica was not detected in the collected lavage fluid or sputum. Two sets of blood cultures taken on admission were negative, and although the culture period was extended to three weeks, they were ultimately negative.
Table 1. Antimicrobial susceptibility of N. farcinica (Clinical and Laboratory Standards Institute susceptibility standard M62-1st).
MIC: minimum inhibitory concentration; S: susceptible; R: resistant; I: intermediate
| Antimicrobial agent | MIC (μg/mL) | Interpretation |
| Amoxicillin-clavulanate | 4 | S |
| Ceftriaxone | >32 | R |
| Imipenem | 1 | S |
| Amikacin | ≤8 | S |
| Clarithromycin | >16 | R |
| Doxycycline | >1 | I or R |
| Minocycline | ≤1 | S |
| Ciprofloxacin | ≤1 | S |
| Moxifloxacin | ≤1 | S |
| Sulfamethoxazole-trimethoprim | 2 | S |
The patient was monitored via blood tests and imaging evaluations regularly, and an MRI on day 39 after admission showed fluid accumulation in his brain, where the first drainage was performed (Figure 2b, 2c). Further, the patient had a mild fever (37.7 °C). Even though the fever was previously resolved, the CRP increased from 0.19 to 4.09 mg/dL. On day 42, after admission, a second abscess drainage was performed, and 7 mL of cream-colored purulent fluid was collected and examined. Analysis in this regard showed that the drained pus cultures did not contain microorganisms, including N. farcinica. The patient showed good progress after this second surgery, and on day 57 after admission, he was placed on an oral TMP-SMX (320 mg/1,600 mg) monotherapy twice daily. In accordance with a previous report that the duration of antimicrobial therapy should be 4-8 weeks for intravenous administration and at least 6 months for long-term oral administration [5,8], we administered the drug intravenously for 6 weeks before reducing the dose by two-thirds for oral administration. At 111 days after admission, he was discharged from the hospital and was continued on oral medications. He received outpatient medical therapy and follow-up imaging, and an MRI performed on day 193 after admission showed that the lesion had shrunk and had not recurred (Figure 2d). The duration of treatment was initially planned to be 12 months, but since prednisolone was still being administered, the duration of administration was further extended. The administration was terminated after an MRI on day 473 confirmed the disappearance of the abscess.
Discussion
In this report, we present a case of a brain abscess owing to an N. farcinica infection identified by a well-functioning AST at a small-to-medium-sized hospital established in 2017. To date, no reports have been published on AST interventions with respect to diagnostic and therapeutic support. Only a few cases of brain abscesses are present at our hospital each year, and this was the first case of a Nocardia-associated brain abscess in 35 years since the hospital was opened.
Brain abscesses caused by Nocardia species, which account for only 2% of all intracranial abscesses [9,10], are frequently overlooked during initial diagnosis. Further, N. farcinica infection is lethal in 55% of immunocompromised and 20% of immunocompetent patients and has a poor prognosis in more than 30% of patients who receive inadequate empirical antimicrobial therapy [3,11]. Furthermore, N. farcinica can be isolated from clinical specimens, such as pus, sputum, bronchial secretions, and skin [12]. However, the identification of Nocardia species may be challenging in some cases, given that they grow slowly and require weeks to form colonies [2].
For our patient, smear findings provided a very important clue that allowed the AST microbiological technologist to make an early assumption of Nocardia. In general, identifying bacterial species is often challenging for hospitals that are not well equipped. Further, given that a considerable amount of time is required for analysis and that testing at a specialized institution is often necessary, we requested an examination at the Nagoya University Hospital. Further, the AST pharmacists demonstrated their true worth by obtaining and selecting the necessary antimicrobial agents and establishing dose regimes. With the exception of amikacin (AMK), N. farcinica is resistant to ampicillin, broad-spectrum cephalosporins, clarithromycin, and aminoglycosides. In general, bacteria-induced brain abscesses are treated empirically using third-generation cephalosporins, MNZ, and VCM before susceptibility test results are available [13]. Nocardia species are typically resistant to these agents. Thus, triple therapy using TMP-SMX, AMK, and CTRX or IPM/CS is recommended [1,14]. CTRX monotherapy is rarely effective against N. farcinica [15,16]. Many small and medium-sized hospitals have access to only one agent of carbapenems; at our hospital, the AST could use only meropenem, which shows activity against N. farcinica [1]. However, for the treatment of this patient, we considered another carbapenem, IPM/CS, which had sufficient evidence in the literature but had not been previously used at our hospital [8]. Intravenous infusion of TMP-SMX had also not been previously adopted; therefore, we adopted it as we did IPM/CS. TMP-SMX is the first-line drug in standard therapy for N. farcinica, given that it crosses the blood-brain barrier, shows excellent tissue migration ability, and has been used in several cases in the past. Even though there has been some debate regarding N. farcinica showing TMP-SMX resistance, no substantial evidence exists in this regard [2].
When N. farcinica was identified, the antimicrobial therapy was not changed. Rather, we prioritized the identification of pulmonary lesions, and after obtaining drug susceptibility results, we optimized the therapy using a combination of TMP-SMX and IPM/CS. The creatinine clearance in this case was > 50 mL/min, and AMK could be used while adjusting the dose with therapeutic drug monitoring. However, since this patient was very old, we excluded the use of AMK from the combination therapy in consideration of worsening renal function. Tetracycline is the drug of choice when TMP-SMX cannot be used owing to allergy. However, tetracycline was not selected in this case because the patient had no history of allergy. It is also worth emphasizing that doxycycline was not used as it is only effective against N. farcinica in 2% of patients [17]. Further, moxifloxacin, a fluoroquinolone, and linezolid, an oxazolidinone, are effective in vitro [18]; however, we retained them as second-line treatments owing to limited clinical experience with their use and the fact that the use of antimicrobial agents generally requires a lot of cautions. Even though the optimal treatment was delayed for approximately 3 days, the prognosis of the patient basically remained unaffected, given that the disease progressed at a slower rate than is generally observed for a bacterial infection-related brain abscess.
The activities of the AST, particularly those of the microbiological technologist and pharmacist, as well as the rapid surgical treatment after the diagnosis of the brain abscess, were crucial for the successful treatment of our patient. The AST, which can be involved in antimicrobial and diagnostic stewardship, is indispensable for community hospitals without infectious disease specialists [3]. Although the structural problem of insufficient staff is a disadvantage for AST activities in small and medium-sized hospitals, it is possible to fully take advantage of close proximity and easy communication among staff. AST pharmacists trained in infectious disease practice will be able to propose appropriate antibiotic dosing designs to many physicians, making full use of pharmacokinetics and pharmacodynamics parameters and therapeutic drug monitoring. By continuing to consult with physicians on a daily basis on all aspects of infectious disease care, and by treating them sincerely, you will earn the trust of physicians. Their activities in the current case included the early detection and identification of pathogenic microorganisms, recommendation of appropriate specimen collection, selection of the optimal antimicrobial agents based on the results of microbiological tests, and setting the treatment administration period to prevent recurrence.
For nocardiosis, the median time from admission to is 42 days (range, 9-120 days), with patients with underlying disease showing particularly longer treatment durations (up to 53.8 days) [19]. Although this report is limited to N. farcinica-associated brain abscesses, it can be said that the activities of the AST allowed for very early diagnosis compared to the time taken for diagnosis of brain abscesses reported in previous studies [5,19].
Conclusions
In this study, we report the case of an 88-year-old man who presented with high fever as the primary complaint and was diagnosed with an N. farcinica infection. This patient showed no response to various antimicrobial regiments, but owing to the activities of the AST, the Nocardia infection was diagnosed early, on day 13 of admission, and an optimal treatment dose and duration were proposed. Therefore, the AST can be as beneficial as an infectious disease specialist, and their activities, in collaboration with attending physicians, can lead to improved patient survival. Furthermore, we believe that the fusion of antimicrobial and diagnostic stewardship activities can contribute to improving the long-term survival rate.
Acknowledgments
We wish to acknowledge Mei Yamada, Yurie Otake, Yukari Osada, Tatsuya Hirano, and Seiji Sugiura, for their support and advice regarding patient treatment. We would like to thank Editage (www.editage.jp) for English language editing.
The authors have declared that no competing interests exist.
Author Contributions
Concept and design: Tetsushi Amano, Keisuke Oka
Acquisition, analysis, or interpretation of data: Tetsushi Amano, Keisuke Oka, Tomohide Nishikawa, Taro Shimizu, Kosei Ota
Drafting of the manuscript: Tetsushi Amano
Critical review of the manuscript for important intellectual content: Tetsushi Amano, Keisuke Oka, Tomohide Nishikawa, Taro Shimizu, Kosei Ota
Supervision: Keisuke Oka, Tomohide Nishikawa
Human Ethics
Consent was obtained or waived by all participants in this study
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