Case Report
A 48-year-old male patient presented to the Emergency Department of the Clinical Hospital of Infectious Diseases with fever, profuse sweating, vomiting, and sudden-onset severe headache, which began one day prior to admission.
The patient’s medical history is relevant for a hemorrhagic stroke in the left cerebellar hemisphere within the past three months. He underwent surgical evacuation of an intraparenchymal hematoma in the posterior cranial fossa, followed by a slowly favorable postoperative course. During his hospitalization in the Intensive Care Unit, the patient developed aspiration bronchopneumonia caused by Acinetobacter baumannii.
At the time of admission, the patient was afebrile but in a generally altered condition, conscious yet poorly cooperative, with a Glasgow Coma Scale score of 13, he exhibited neck stiffness and left-sided hemiparesis. Imaging studies and lumbar puncture supported the presumptive diagnosis of bacterial meningitis. Cerebrospinal fluid (CSF) analysis revealed 10713 leukocytes/mm3 (87.2% neutrophils), marked hypoglycorrhachia, and hyperproteinorrachia, consistent with bacterial meningitis. Microbiological examination of the CSF identified A. baumannii.
Empirical therapy was initiated with meropenem 2 g every 8 h and vancomycin 1 g every 12 h, in conjunction with corticosteroid therapy with dexamethasone, cerebral depletive measures, diuretics, and intravenous fluids for hydroelectrolytic rebalancing for 2 days, until the antibiotic susceptibility results were confirmed.
Once the presence of Acinetobacter baumannii complex in the CSF was confirmed, showing extensive drug resistance and susceptibility only to colistin and cefiderocol, antibiotic therapy was escalated to cefiderocol 2 g every 8 h in combination with colistin 5,000,000 IU every 12 h, corticosteroid therapy with dexamethasone and cerebral depletive for 14 days.
Dynamic follow-up included imaging studies and control lumbar punctures. Brain magnetic resonance imaging (MRI) at admission revealed findings consistent with occipital craniectomy, extensive postoperative occipital extracranial meningocele, a lesion in the left cerebellar hemisphere compatible with an abscess (25 × 10 mm), and chronic inflammatory changes of the bilateral maxillary sinuses (
Figure 1).
Given the poor penetration of antibiotics across the blood-brain barrier and the complexity of the case, MDR bacterial meningitis with a probable brain abscess, the decision was made to insert an intrathecal catheter for colistin administration, in collaboration with the Neurosurgery Department. The catheter was placed in the operating room, and colistin was administered intrathecally at a dose of 300,000 IU/day, after first withdrawing an equal volume of CSF.
Due to the location of the lesion in a region requiring a high-risk neurosurgical approach, which could significantly impact the patient’s quality of life, conservative management of the cerebellar abscess was chosen. This included intravenous and intrathecal antibiotic therapy, cerebral depletive measures, and corticosteroid therapy, resulting in a slowly favorable course with progressive reduction of the abscess.
Following the 14-day course of intravenous and intrathecal cefiderocol and colistin, therapy was de-escalated to ampicillin/sulbactam 6 g every 8 h, colistin 5000000 IU every 12 h IV, and oral minocycline 200 mg every 12 h. This regimen was administered in combination with dexamethasone corticosteroid therapy, cerebral anti-depletive measures, loop diuretics, hepatoprotective and gastric protective agents, and intravenous fluids for hydroelectrolytic rebalancing for an additional 21 days. The dynamics of inflammatory markers and CSF examination are presented in
Table 1 and
Table 2.
One week before discharge, the brain MRI (
Figure 2) showed a postoperative meningocele unchanged compared to the previous examination, occipital craniectomy, and a lesion in the left cerebellar hemisphere, imaging-compatible with an abscess, relatively stable in size compared to the prior study, with chronic inflammatory changes in the bilateral maxillary sinuses.
After 41 days of hospitalization in Infectious Diseases Department the patient was transferred to the Neurosurgery Department for re-evaluation of the possibility of surgical management of the cerebellar abscess. At the time of transfer from our clinic, the patient exhibited no signs of meningeal irritation, was conscious, cooperative, afebrile, with a Glasgow Coma Scale score of 15, and stable cardiorespiratory and digestive status.
Discussion
Multidrug-resistant (MDR) and extensively drug-resistant (XDR)
Acinetobacter baumannii represent a growing challenge in neurosurgical and critical care settings. These pathogens are predominantly associated with post-neurosurgical infections or infections related to ventricular devices. Their high potential for multidrug resistance, reported in over 50% of clinical isolates, severely limits therapeutic options. The treatment of
A. baumannii meningitis is particularly difficult due to the poor penetration of most antibiotics across the blood-brain barrier. Conventional intravenous therapy often fails to achieve bactericidal concentrations in the CSF, necessitating consideration of intrathecal or intraventricular routes for effective management. In the absence of standardized treatment protocols, individualized approaches based on antimicrobial susceptibility, clinical status, and drug availability are recommended, in accordance with IDSA guidelines [
3].
In this case, the patient developed MDR
A. baumannii meningitis and a probable cerebellar abscess following neurosurgical intervention for a hemorrhagic stroke. Initial empirical therapy with meropenem and vancomycin was chosen pending microbiological confirmation. Once the pathogen was identified as extensively drug-resistant and susceptible only to colistin and cefiderocol, therapy was escalated to intravenous cefiderocol and colistin. Given the limited CSF penetration of intravenous antibiotics and the complexity of the CNS infection, an intrathecal catheter was placed for colistin administration, following IDSA dosage recommendations [
4].
Surgical intervention for the cerebellar abscess was deferred due to its high-risk location and potential impact on the patient’s quality of life. Instead, conservative management was employed, combining intravenous and intrathecal antibiotics, corticosteroids, cerebral depletive measures, and supportive care. Dynamic imaging and serial lumbar punctures guided therapy and allowed progressive reduction of the abscess. After 14 days of intensive therapy, a de-escalation regimen with ampicillin/sulbactam, oral minocycline, and continued colistin was implemented for an additional 21 days, ensuring continued pathogen suppression while minimizing toxicity.
This case illustrates the necessity of an interdisciplinary approach, integrating infectious disease specialists, neurologists, neurosurgeons, and intensive care teams, to optimize outcomes in complex MDR CNS infections [
5].
It also highlights the importance of individualized therapy based on microbiological data, drug pharmacokinetics, and patient-specific surgical risk considerations.