Over the years, Acinetobacter baumannii, which is associated with post-neurosurgical meningitis and ventriculitis, has increasingly been regarded as an important nosocomially acquired pathogen [1, 3]. Statistical data showed that 3.6–11.2% of post-neurosurgical meningitis cases are caused by A. baumannii [2, 4]. Antimicrobial-resistant A. baumannii are divided into three categories: multidrug-resistant (MDR), extensively drug-resistant (XDR) and pandrug-resistant (PDR). XDR is defined as non-susceptibility to all penicillins and cephalosporins (including inhibitor combinations), fluroquinolones, aminoglycosides, and carbapenems. [5]. In the present case, XDR A. baumannii that was susceptible only to polymyxin and tigecycline was cultured from the cerebral spinal fluid (CSF) and sputum. As a result of the poor blood-brain barrier penetration, intraventricular (IVT) therapy polymyxin B was used through the external ventricular derivation (EVD).
Emerging evidence has indicated that intrathecal (IT) or IVT colistin administration is a safe and effective treatment for XDR A. baumannii meningitis [6]. Karaiskos et al. [2]. summarized 36 studies and a total of 81 patients who were diagnosed with meningitis secondary to neurosurgical procedures. A total of 89% (72/81) of the cases treated with IVT/ITH colistin were eventually cured, and the median time to achieve sterilization of the CSF was 4 days. De Bonis et al. [3]. compared the outcomes of the XDR A. baumannii ventriculomeningitis patients treated with intravenous (IV) colistin or IV plus IVT colistin. Compared with 33.3% of the cases in the IV alone group, 100% of the cases achieved CSF sterilization (a negative CSF culture result) in the IV + IVT group. The results showed that IVT colistin administration is significantly more effective than IV colistin alone [3]. To the best of our knowledge, polymyxin B and colistin (polymyxin E) were regarded as equivalent because of their similar chemical structures and their activity spectra [7]. However, compared to colistin, there is limited clinical data for the use of polymyxin B in ventriculitis treatment. Piparsania et al [8]. showed successful treatment of multidrug-resistant A. baumannii neonatal meningo-ventriculitis with IVT polymyxin B in combination with IV netilmicin and polymyxin B. IVT polymyxin B (40,000 units per dose) was given alternate day for four weeks. In the present case, sterilization of CSF was detected 5 days after the IVT polymyxin B administration. Hence, we speculate that IVT polymyxin B administration could be as effective as IVT colistin administration.
In the present case, tigecycline was used intravenously. Tigecycline, which belongs to a new class of antibiotics known as the glycylcyclines [9], has demonstrated excellent activity against Acinetobacter strains [10]. Pallotto et al. [11] showed the weak penetration of tigecycline to the CSF in a patient with ventriculo-atrial shunt infection. The average CSF concentration of tigecycline equals to 7.9% of the serum concentration. That is the reason why tigecycline is not currently recommended for Acinetobacter ventriculitis. Recently, Lauretti et al. reported a successful case of the IVT tigecycline use to treat PDR A. baumannii meningitis [12].
Potential toxicity is a concern associated with local administration of polymyxins. Chemical ventriculitis and meningitis which usually cause fever and altered mental state, are the most severe adverse effects reported with IVT/ITH polymyxin treatment. Karaiskos reviewed the literature and found that out of 81 patients with IVT/ITH colistin administration, chemical meningitis and chemical ventriculitis were diagnosed in 3 (3.7%) and 2 (2.4%) cases, respectively [2]. A recent retrospective study showed that out of 9 patients with IVT colistin administration, no cases of chemical meningitis were encountered [3]. However, to the best of our knowledge, limited reports on the adverse effects of IVT/ITH polymyxin B were published.
In the treatment process, two observations were noted. First, the transient ventricular adhesion due to the IVT polymyxin B administration was observed from the CT scan (Fig. 1). Initially, the IVT polymyxin B was administered through the right EVD. However, decreased CSF drainage and a contractible right ventricle were detected after the IVT polymyxin B administration. Six days later, when the left EVD were used for the polymyxin B administration, left ventricle shrinkage was observed. These phenomena indicate that there is a direct correlation between polymyxin B usage and ventricular adhesion. Second, at the 6-month follow-up, the neurological conditions of the patients had not improved, and the patient was still in a comatose status.
Therefore, we conclude that IVT and intravenous polymyxin B combined with intravenous tigecycline could be an effective therapeutic option in the treatment of XDR A. baumannii ventriculitis. Currently, IVT administration of antibiotics with favorable outcomes is widely reported. However, multicenter randomized studies are still needed to demonstrate the efficacy and safety of intraventricular administration on these patients.