A Clinical Study on the Use of Intraventricular Polymyxin B Supplemented by Continuous External Ventricular Drainage in the Treatment of Drug-Resistant Gram-Negative Bacilli Intracranial Infection
Received 25 May 2020
Accepted for publication 28 July 2020
Published 24 August 2020 Volume 2020:13 Pages 2963—2970
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 3
Editor who approved publication: Professor Suresh Antony
Hongwei Chen,1 Xiaochuan Guo,1 Dongcheng Xie,1 Xuanwei Dong,1 Jianxing Niu,1 Guoqiang Chen2
1Department of Neurosurgery for Cerebrospinal Fluid Diseases, Aviation General Hospital of China Medical University, Beijing 100012, People’s Republic of China; 2Department of Neurosurgery, Aviation General Hospital of China Medical University, Beijing 100012, People’s Republic of China
Correspondence: Guoqiang Chen
Department of Neurosurgery, Aviation General Hospital of China Medical University, No. 3 Anwai Beiyuan Street, Chaoyang District, Beijing 100012, People’s Republic of China
Tel/ Fax +86-010 59520008
Email [email protected]
Purpose: To investigate the clinical effect of ventricular polymyxin B supplemented by continuous external ventricular drainage in the treatment of intracranial infection with multidrug-resistant (MDR) or extensively drug-resistant (XDR) Gram-negative (G-) bacilli following neurosurgery.
Patients and Methods: A retrospective analysis was performed on 28 patients who had G-bacilli intracranial infection following neurosurgery in our department between January 2017 and December 2019. The patients were treated with intraventricular polymyxin B supplemented by continuous external ventricular drainage. The clinical characteristics, treatment process, cerebrospinal-fluid-related indicators, results and prognosis were analysed.
Results: All of 28 patients developed an infection subsequent to neurosurgery, and cerebrospinal fluid (CSF) cultures demonstrated MDR/XDR G- bacilli, including Acinetobacter baumannii in 14 cases, Klebsiella pneumoniae in 9 cases, Pseudomonas aeruginosa in 3 cases, and Enterobacter cloacae in 2 cases. The ventricular drainage tube remained unobstructed in all patients during treatment, and intraventricular polymyxin B combined with intravenous antibiotics were administered each day. The duration of treatment with intraventricular polymyxin B was 14.96± 4.28 days, and the time required to obtain a negative CSF culture was 8.23± 4.02 days. The bacterial clearance rate from cerebrospinal fluid was 92.9% (26/28), and the clinical cure rate was 82.1% (23/28). Among them, 18 patients underwent ventriculoperitoneal shunt insertion for hydrocephalus 82.5 (59.5,114.75) days after the infection was cured, and the mortality rate was 17.6% (5/28). There was no significant change in patient blood creatinine levels before and after treatment. Cured patients were followed up for 4 months to 3 years, and no recurrences were observed.
Conclusion: Treatment of intracranial infection with MDR/XDR G- bacilli using early intraventricular polymyxin B supplemented by continuous external ventricular drainage treatment may be a safe and effective treatment strategy.
Keywords: intracranial infection, drug-resistant, Gram-negative(G-)bacilli, intraventricular polymyxin B, continuous external ventricular drainage
In recent years, due to the abuse of broad-spectrum antibiotics, intracranial infections caused by multidrug-resistant (MDR) or extensively drug-resistant (XDR) Gram-negative (G-) bacilli such as Acinetobacter baumannii, Pseudomonas aeruginosa, Klebsiella pneumoniae, Enterobacter cloacae and Escherichia coli, are increasing year by year,1 and have become one of the biggest challenges in the clinical management of microbial infections. Effective antibacterial drugs currently available for treating infections caused by these “superbugs” are limited. Studies have demonstrated that polymyxin is a polypeptide antibiotic isolated from Bacillus polymyxa.2,3 It was abandoned as a treatment in the past due to reports of strong nephrotoxicity, but has been reintroduced into clinical practice to target drug-resistant gram-negative bacteria. Many studies have shown that polymyxin does not easily penetrate the blood-brain barrier to produce anti-infective activity,4,5 so intraventricular (IVT) and/or intrathecal (ITH) administration may be effective methods for treating G-bacilli intracranial infection. Therefore, the purpose of this study was to retrospectively analyze the clinical efficacy and safety of the treatment based on intraventricular polymyxin B and continuous ventricular drainage in 28 patients with MDR/XDR G- bacillus intracranial infection. The report is as follows.
Materials and Methods
Patients treated for G-bacilli intracranial infection at the Cerebrospinal Fluid (CSF) Diagnosis and Treatment Center of Beijing Aviation General Hospital of China Medical University from January 2017 to December 2019 were selected. The study was approved by the Medical Science Ethics Committee of the Aviation General Hospital (HK2017-01-04). The Committee waived signature of informed consents by the patients whose records were retrospectively reviewed, as this was a noninterventional, retrospective study with data management processed anonymously. Clinical diagnosis and treatment were collected in the medical records, except patients’ names. We have confidential measures for the privacy of patients. This study was conducted in accordance with the Declaration of Helsinki.
Inclusion Criteria and Exclusion Criteria
Inclusion criteria: 1) Age >18 years; 2) CSF culture results showing MDR/XDR G- bacilli;3 3) Fulfilment of the criteria for intracranial infection established by the Neurosurgery Branch of the Chinese Medical Association.6
Exclusion criteria: 1) Possible colonization or contamination with G- bacilli; 2) A history of intracranial infection before craniotomy; 3) Having received polymyxin B treatment due to intracranial infection or infection at other positions recently (in the past three months); 4) Pregnancy or concurrent malignant tumor in an area other than the central nervous system.
After admission, if the patients presented with clinical symptoms of infection and the bacterial culture of CSF indicated MDR/XDR G- bacilli; then, intravenous delivery of antibiotics was performed according to the results of the drug-sensitivity test. If three consecutive bacterial cultures of CSF after admission indicated the same results of MDR/XDR G- bacilli or if MDR/XDR G- bacilli were confirmed as pathogens at other hospitals and the first bacterial culture of CSF at our hospital after admission had the same result as that at another hospital; then, intracerebroventricular delivery of polymyxin B was performed. Intraventricular administration method: first, 5mL of cerebrospinal fluid was withdrawn and discarded, and 5mg polymyxin B was dissolved in 5mL normal saline and injected, after which the tube was clamped for 2 hours. This was done every 24 hours.
To monitor adverse events related to antibiotic therapy, any changes in clinical signs and symptoms that occurred after starting antibiotic therapy and any fluctuations in laboratory findings were recorded.
Testing for CSF Indicators
The Hitachi LABOSPECT 008 AS fully automated biochemical analyzer was used for biochemical analysis of cerebrospinal fluid, mainly including CSF glucose, CSF protein, and CSF chloride. Sysmex XN2000 was used for routine analysis of cerebrospinal fluid. The strain identification and drug susceptibility tests were carried out using the French Biomerieux VITEK 2 Compact fully automated microbiological analysis system. Drug sensitivity results were interpreted according to the 2019 version of the American Clinical and Laboratory Standardization Committee (CLSI) standard M100-S25. The polymyxin sensitivity standards were based on the US Food and Drug Administration (FDA) standards.
A retrospective case investigation method was used to collect clinical data on patients, including age, gender, main diagnosis, pre-infection craniocerebral surgery, main systemic antibiotics, CSF bacterial culture results, and clinical outcomes. Laboratory test data before and after treatment with intraventricular polymyxin B were collected, including CSF white blood cell count, CSF red blood cells, CSF glucose, CSF chloride, CSF protein levels, as well as liver function and kidney function tests.
Follow-Up and Evaluation Indicators
Clinical cure criteria: 1) Body temperature is normal for more than 3 consecutive days; 2) Improvement or resolution of the original clinical symptoms (meningeal irritation, consciousness); 3) CSF glucose above 2.2 mmol/L on 3 consecutive measurements, white blood cells:red blood cells <1:500; 4) Three consecutive negative CSF bacterial cultures.
SPSS v.23.0 software was used for statistical analysis. Measurement data that conformed to the normal distribution were expressed as mean ± standard deviation, and statistical analysis was performed using a paired t-test. Measurement data that did not conform to the normal distribution were calculated as the median (quartile interval), and the Wilcoxon test was used for statistical analysis. The count data were expressed as a percentage, and comparisons were carried out using the χ2 test. P <0.05 was considered statistically significant.
General Information Regarding the Patients
A total of 28 patients were enrolled in this study, including 23 males and 5 females; the average age was 44.64±17.42 years (range, 16–71 years). All patients were transferred to our hospital following infection at another hospital, and all had undergone neurosurgery before infection. The primary diseases and surgical methods are shown in Table 1.
Table 1 Demographics of the Patients
Surgical Treatment and Intraventricular Administration for the Patients
Surgical treatment principles, including the existing external ventricular drainage tube for drainage, were kept in place or reinserted, the external lumbar cistern drainage from the previous hospital, the ventriculoperitoneal shunt, the skull repair material, and blocked external ventricular drainage tubes were removed, as shown in Table 2. Intraventricular administration: all patients were given intraventricular polymyxin B 5mg/d, with an average administration time of 14.96±4.28 days (range, 9–23). Table 2
Table 2 Surgical Treatment and Local Administration of Intracranial Infection
Bacterial results and Systemic Medication
All CSF cultures demonstrated MDR/XDR G- bacilli, including 14 cases of Acinetobacter baumannii, 9 cases of Klebsiella pneumoniae, 3 cases of Pseudomonas aeruginosa, and 2 cases of Enterobacter cloacae. The drug resistance analysis of CSF pathogens is shown in Table 3. All patients were treated with systemic antibiotics (based on drug sensitivity results), including tigecycline (n = 7), tigecycline – cefoperazone sodium and sulbactam sodium (n = 7), polymyxin-sulperazon (n = 3), Tigecycline-polymyxin (n = 2), amikacin (n = 2), tigecycline-amikacin (n = 1), tigecycline-gentamicin (n = 1), polymyxin-meropenem (n = 1), levofloxacin and sodium chloride – cefoperazone sodium and sulbactam sodium (n = 1), ceftazidime (n = 1), ceftazidime-etimicin (n = 1), Ceftazidime – levofloxacin and sodium chloride (n = 1).
Table 3 Analysis of Cerebrospinal Fluid Pathogenic Bacteria and Drug Resistance in 28 Patients with Intracranial Infection by G-Bacilli
Methods of systemic antibiotics use, including polymyxin B: 50 mg intravenous infusion, once every 12 hours; tigecycline: first dose of 100 mg, then 50 mg intravenous infusion every 12 hours; cefoperazone sodium and sulbactam sodium: 3g intravenous infusion every 8 hours; Amikacin 0.6g intravenous infusion every 12 hours; Meropenem 2g intravenous infusion every 8 hours; Levofloxacin and sodium chloride 0.6g intravenous infusion, once every 12 hours; ceftazidime 2g intravenous infusion, once every 8 hours; etimicin sulfate 150mg, once every 12 hours. Systemic antibiotic treatment lasted for an average of 47.25±20.86 days (range, 19–85 days).
Clinical Symptoms and CSF Laboratory Data for the Patients Before and After Treatment
See Table 4 for details.
Table 4 Clinical Symptoms and Laboratory Data in Patients
Treatment Results and Complications
The CSF bacterial clearance rate in the 28 patients was 92.9% (26/28), and the average time from application of IVT polymyxin B to negative CSF culture was 8.23±4.02 days (range, 3–16 days). Twenty-three cases were clinically cured, and the cure rate was 82.1% (23/28), of which 18 cases (64.3%) underwent ventriculoperitoneal shunt due to the presence of hydrocephalus 82.5 (59.5,114.75) days after infection had been controlled. The overall mortality rate was 17.6% (5/28), and the mortality rate due to infection was 7.1% (2/28). Analysis of causes, including 2 patients had purulent CSF with multiple brain abscesses at the time of admission, suggesting extensive brain parenchymal infection. After intraventricular polymyxin B treatment, intraventricular CSF culture was negative, but the drainage fluid of the abscess cavity remained culture positive. One case died in the hospital, and 1 case died after giving up treatment and returning home; 2 cases suffered spontaneous ventricular hemorrhage after a negative CSF result and, as their condition worsened, the 2 patients gave up treatment and died after returning home; 1 case had a massive secondary cerebral infarction after a negative CSF and died after giving up treatment and returning home. All cured patients were followed up for 4 months to 3 years, and no recurrences were noted. See Table 5 for details.
Table 5 Outcomes and Complications
The blood creatinine of patients before and after intraventricular polymyxin was (44.75±16.68) μmol/L and (48.64±13.01) μmol/L, and the differences were not statistically significant (P = 0.115). Renal function was not impaired. No epileptic seizures, neurotoxicity or neuromuscular block occurred during intraventricular administration or within 2 hours of administration.
Intracranial infection is a serious complication with a high rate of disability and mortality after neurosurgery.9,10 The incidence rate is 1–10%.11 In recent years, the incidence of G-bacilli intracranial infections, with Acinetobacter baumannii and Klebsiella pneumoniae in particular, has significantly increased,12,13 accounting for more than 30% of cases.12 Furthermore, drug resistance rates are gradually increasing,1 resulting in extreme difficulties for clinical treatment. In terms of treatment of G-bacilli intracranial infection, carbapenem antibiotics are usually preferred, especially high-dose meropenem as the initial treatment, but the current rate of resistance of G- bacilli to carbapenems has been increasing yearly.14 In this study, the rate of resistance of the bacteria identified the CSF test to carbapenems was as high as 89.3% (25/28) when the patients were admitted to our hospital. The reason for such a high rate may be related to the fact that this group of patients had received large doses of high-grade antibiotics in the previous hospital based on prior experience, which may have caused drug resistance. Due to the high degree of resistance, treatment of MDR and even XDR G-bacilli is fraught with challenges and the prognosis is poor. This requires a clinical search for an antibiotic that is not drug-resistant for treatments to be completed.
Polymyxin B, as a drug with rapid bactericidal activity, has good activity against most G- bacteria,15 which is consistent with the results of this study. Many studies have shown that polymyxin B has a significant effect on various serious nosocomial infections caused by MDR G- bacilli such as bacteremia, urinary tract infections, abdominal infections and wound infections.14,16,17 However, due to various reasons, such as its large molecular weight and difficulty in penetrating the blood-brain barrier to achieve effective bacteriostatic concentrations in CSF, there is limited research on the application of polymyxin B in the treatment of intracranial infections in China and globally.
The 2017 guidelines of the American Society for Infectious Diseases (IDSA) recommended that IVT and/or ITH therapy is a treatment for intracranial infections, especially when systemic intravenous medication is not effective.18 Because this route of administration can bypass the blood-brain barrier and directly act on the site of infection, the effect is more direct and precise, and at the same time, the toxic reactions of systemic drugs can be avoided.19 However, many antibiotics are currently not approved for intraventricular and/or intrathecal use, such as meropenem, ceftazidime and tigecycline. Therefore, the intracerebroventricular and/or intrathecal use of these antibiotics is off-label use and involves safety issues. Polymyxin B is an antibiotic whose official instructions clearly state that it can be used for IVT/ITH administration. Moreover, Polymyxin B, compared to Polymyxin E, shows superior PK characteristics in the human body, reducing the potential for nephrotoxicity. Therefore, this study used only polymyxin B in the ventricles. Studies have shown that polymyxin B alone is less effective in treating G- bacilli,20 and when combined with other antibiotics, its efficacy can be significantly enhanced.21 At present, there is no uniform standard for the clinical treatment cycle of severe intracranial infection, but generally, the course of treatment is relatively long, often requiring 4–8 weeks. A total of 28 patients with MDR/XDR G- bacilli intracranial infection after neurosurgery were included in this group. Intraventricular polymyxin B was used for 14.96±4.28 (range, 9–23) days, supplemented with intravenous administration of various sensitive antibiotics for 47.25±20.86 (range, 19–85) days, the CSF bacterial clearance rate was as high as 92.9% (26/28), and the clinical cure rate was 82.1% (23/28). The results showed that intraventricular polymyxin B can effectively remove MDR/XDR G- bacilli in the CSF, but, even though the effects are clear, intravenous antibiotics may have played a synergistic role. Recently, Shang et al reported that intraventricular lavage combined with daily polymyxin E can effectively improve the neurological symptoms and CSF laboratory indicators in patients with severe ventricular inflammation.22 In this study, intraventricular polymyxin B has also been used to achieve the same effect.
According to reports, the mortality rate associated with intracranial infections caused by MDR/XDR G- bacilli is as high as 26–71%.22–24 The total mortality rate in this study was 17.6% (5/28), and the mortality rate directly caused by infection was 7.1% (2/28), which was lower than that reported in the literature. This may be related to the timely use of intraventricular polymyxin B following the identification of MDR/XDR G- bacilli in the patients in this study. In the past, intraventricular administration has been considered an alternative option when intravenous treatment was ineffective. Two patients in this group were given high-dose intravenous antibiotics in the hospital where they had received treatment previously and no effects were observed, and they already had severe diffuse infection of the brain parenchyma when they were admitted to our hospital. Although they were treated with intraventricular polymyxin B, their infection could not be controlled in the end. Wang et al also showed that timely and effective IVT treatment may improve the cure rate of intracranial infection after neurosurgery.23
According to reports, polymyxin has strong side effects such as nephrotoxicity, neurotoxicity and neuromuscular blockage. However, recent studies have confirmed that the incidence and severity of nephrotoxicity are rare and mild,25 and are reversible after the drug is withdrawn.26 In addition, the neurotoxic effects caused by polymyxin B are generally mild and can be resolved once drug treatment is stopped. Recent studies have shown that patients with renal insufficiency do not need drug dose adjustment when using polymyxin B.27 Other studies have shown that intraventricular antibiotic treatment may cause seizures.28 None of the above-mentioned adverse reactions occurred during treatment in this group of patients, which suggests that intraventricular polymyxin B is adequately safe in the treatment of MDR/XDR G- bacilli intracranial infection.
Studies have shown that artificial materials related to infections should be completely removed as soon as possible during intracranial infections.6,18 In addition, smooth and continuous CSF drainage is essential for the treatment of severe intracranial infection,22 usually using external ventricular drainage or lumbar cistern drainage. Most researchers believe that lumbar cistern drainage is more effective at reducing the recurrence of intracranial infections. However, as MDR/XDR G- bacteria CSF is mostly cloudy, turbid, and even purulent, the drainage tube outside the lumbar cistern can be easily blocked, leading to a higher possibility of infection. In this study, unobstructed external ventricular drainage tubes were used for the treatment of inflammatory CSF and intraventricular drug delivery. The lumbar cistern drainage tube from previous hospitals, ventriculoperitoneal shunt and skull repair materials were removed, but the external ventricular drainage tube from previous hospitals was not removed due to its unobstructed flow. It is suggested that during the treatment of intracranial infection, continuous and unobstructed cerebrospinal fluid drainage can effectively drain CSF with bacteria to the outside of the body, and there is no need to replace it prematurely or too frequently, which can help avoid secondary damage to brain tissues and the nervous system, and any intracranial bleeding that may occur as a result.
The mortality rate of hydrocephalus caused by intracranial infection is as high as 50%, and the prognosis is poor in 70% patients,29,30 which is mainly due to the fact that white blood cells, protein and other indicators in CSF cannot return to their normal value within a short time after the bacteria in CSF are cleared, and shunting treatment performed at this moment probably fails, so the final shunt operation cannot be performed. For such patients, continuous CSF drainage technology can be used to continue drainage and purify inflammatory CSF. This method can effectively extend the time of tube placement, reducing the possibility of intracranial infection.31 During drainage, patients should undergo weekly cerebrospinal fluid routine tests, biochemical tests and bacterial cultures. After three consecutive satisfactory CSF results, the ventriculoperitoneal shunt is placed. In this study, 18 cases had hydrocephalus, after CSF bacteria were cleared, and they were switched to continuous drainage of CSF. Postoperative drainage was performed by intraventricular shunt for 47.25±20.86 days. There was no further infection during drainage. They were followed up for 4 months to 3 years, and no cases of recurrence were noted.
In cases of MDR/XDR G- bacilli intracranial infection, early intraventricular polymyxin B supplemented by continuous ventricular drainage treatment has a clinical cure rate of 82.1%, with no change in renal function post-treatment, and is thus a safe and effective treatment strategy. However, these findings are yet to be confirmed by large-scale research.
This study also has the following limitations: (1) The number of cases is relatively small. (2) This study was a single-center retrospective design, which lacked a simple intravenous infusion control. There existed certain limitations in proving or disproving the efficacy or safety of any intervention. A multi-center randomized controlled trial is required to verify the findings of the present study in the future. (3) This study did not comprehensively investigate important characteristics such as CSF drug concentrations and optimal dosage of polymyxin B.
We acknowledge the support received from Scientific Research Project of Aviation General Hospital of Beijing (No. YJ202021).
The authors report no conflicts of interest in this work.
1. Kim BN, Peleg AY, Lodise TP, et al. Management of meningitis due to antibiotic-resistant Acinetobacter species. Lancet Infect Dis. 2009;9(4):245–255. doi:10.1016/S1473-3099(09)70055-6
2. Giamarellou H, Antoniadou A, Kanellakopoulou K. Acinetobacter baumannii: a universal threat to public health? Int J Antimicrob Agents. 2008;32(2):106–119. doi:10.1016/j.ijantimicag.2008.02.013
3. Magiorakos AP, Srinivasan A, Carey RB, et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect. 2012;18(3):268–281. doi:10.1111/j.1469-0691.2011.03570.x
4. Markantonis SL, Markou N, Fousteri M, et al. Penetration of colistin into cerebrospinal fluid. Antimicrob Agents Chemother. 2009;53(11):4907–4910. doi:10.1128/AAC.00345-09
5. Antachopoulos C, Karvanen M, Iosifidis E, et al. Serum and cerebrospinal fluid levels of colistin in pediatric patients. Antimicrob Agents Chemother. 2010;54(9):3985–3987. doi:10.1128/AAC.01799-09
6. Chinese neurosurgery society, Chinese neurosurgical critical management collaboration group. Consensus of experts in the diagnosis and treatment of infection in Chinese neurosurgical critical patients 1(2017). Natl Med J China. 2017;97(21):1607–1613.
7. Pan S, Huang X, Wang Y, et al. Efficacy of intravenous plus intrathecal/intracerebral ventricle injection of polymyxin B for post-neurosurgical intracranial infections due to MDR/XDR Acinectobacter baumannii: a retrospective cohort study. Antimicrob Resist Infect Control. 2018;7(1):1–9. doi:10.1186/s13756-018-0305-5
8. Lihong Z, Yaping S, Jin L. Efficacy of polymyxin B in treating intracranial Klebsiella pneumoniae infection with pan-drug resistance. Chin J Antibiot. 2019;44(12):1414–1418.
9. Golan E, Wong K, Alahmadi H, et al. Endoscopic sphenoid sinus drainage in Lemierre syndrome. J Clin Neurosci. 2014;21(2):346–348. doi:10.1016/j.jocn.2013.02.020
10. Moazzam AA, Rajagopal SM, Sedghizadeh PP, Zada G, Habibian M. Intracranial bacterial infections of oral origin. J Clin Neurosci. 2015;22(5):800–806. doi:10.1016/j.jocn.2014.11.015
11. Reichert MC, Medeiros EA, Ferraz FA. Hospital-acquired meningitis in patients undergoing craniotomy: incidence, evolution, and risk factors. Am J Infect Control. 2002;30(3):158–164. doi:10.1067/mic.2002.119925
12. Srinivas D, Veena Kumari HB, Somanna S, Bhagavatula I, Anandappa CB. The incidence of postoperative meningitis in neurosurgery: an institutional experience. Neurol India. 2011;59(2):195–198. doi:10.4103/0028-3886.79136
13. van de Beek D, Cabellos C, Dzupova O, et al. ESCMID guideline: diagnosis and treatment of acute bacterial meningitis. Clin Microbiol Infect. 2016;22(Suppl 3):S37–62. doi:10.1016/j.cmi.2016.01.007
14. Teng CB, Koh PT, Lye DC, Ang BS. Continuous versus intermittent infusion of polymyxin B in the treatment of infections caused by multidrug-resistant Gram-negative bacteria. Int J Antimicrob Agents. 2008;31(1):80–82. doi:10.1016/j.ijantimicag.2007.08.004
15. Neiva LB, Borges FT, Watanabe M, Pessoa Ede A, Barbosa DA, Vattimo Mde F. Nephrotoxicity of polymyxin B: experimental study in cells and implications for nursing practice. Rev Esc Enferm USP. 2014;48(2):272–277. doi:10.1590/S0080-6234201400002000011
16. Ouderkirk JP, Nord JA, Turett GS, Kislak JW. Polymyxin B nephrotoxicity and efficacy against nosocomial infections caused by multiresistant gram-negative bacteria. Antimicrob Agents Chemother. 2003;47(8):2659–2662. doi:10.1128/AAC.47.8.2659-2662.2003
17. Sobieszczyk ME, Furuya EY, Hay CM, et al. Combination therapy with polymyxin B for the treatment of multidrug-resistant Gram-negative respiratory tract infections. J Antimicrob Chemother. 2004;54(2):566–569. doi:10.1093/jac/dkh369
18. Tunkel AR, Hasbun R, Bhimraj A, et al. 2017 infectious diseases society of America’s clinical practice guidelines for healthcare-associated ventriculitis and meningitis. Clin Infect Dis. 2017;64(6):e34–e65. doi:10.1093/cid/ciw861
19. Wen DY, Bottini AG, Hall WA, Haines SJ. Infections in neurologic surgery. The intraventricular use of antibiotics. Neurosurg Clin N Am. 1992;3(2):343–354. doi:10.1016/S1042-3680(18)30666-1
20. Nadkarni AS, Schliep T, Khan L, Zeana CB. Cluster of bloodstream infections caused by KPC-2 carbapenemase-producing Klebsiella pneumoniae in Manhattan. Am J Infect Control. 2009;37(2):121–126. doi:10.1016/j.ajic.2007.10.013
21. Cai B, Cai Y, Liew YX, et al. Clinical efficacy of polymyxin monotherapy versus nonvalidated polymyxin combination therapy versus validated polymyxin combination therapy in extensively drug-resistant gram-negative bacillus infections. Antimicrob Agents Chemother. 2016;60(7):4013–4022. doi:10.1128/AAC.03064-15
22. Shang F, Xu Y, Wang N, Cheng W, Chen W, Duan W. Diagnosis and treatment of severe neurosurgical patients with pyogenic ventriculitis caused by gram-negative bacteria. Neurol Sci. 2018;39(1):79–84. doi:10.1007/s10072-017-3146-8
23. Wang JH, Lin PC, Chou CH, et al. Intraventricular antimicrobial therapy in postneurosurgical Gram-negative bacillary meningitis or ventriculitis: a hospital-based retrospective study. J Microbiol Immunol Infect. 2014;47(3):204–210. doi:10.1016/j.jmii.2012.08.028
24. Kumar A, Agrawal D, Sharma BS. The role of endoscopic lavage in recalcitrant multidrug-resistant gram-negative ventriculitis among neurosurgical patients. World Neurosurg. 2016;93:315–323. doi:10.1016/j.wneu.2016.06.022
25. Shahbazi F, Dashti-Khavidaki S. Colistin: efficacy and safety in different populations. Expert Rev Clin Pharmacol. 2015;8(4):423–448. doi:10.1586/17512433.2015.1053390
26. Nelson BC, Eiras DP, Gomez-Simmonds A, et al. Clinical outcomes associated with polymyxin B dose in patients with bloodstream infections due to carbapenem-resistant Gram-negative rods. Antimicrob Agents Chemother. 2015;59(11):7000–7006. doi:10.1128/AAC.00844-15
27. Peyko V, Cohen H. A comparison of adjusted versus unadjusted doses of polymyxin B based on renal function and incidence of acute kidney injury. J Pharm Pract. 2018;897190018798881.
28. Ziai WC, Lewin JJ. Improving the role of intraventricular antimicrobial agents in the management of meningitis. Curr Opin Neurol. 2009;22(3):277–282. doi:10.1097/WCO.0b013e32832c1396
29. Kasanmoentalib ES, Brouwer MC, van der Ende A, van de Beek D. Hydrocephalus in adults with community-acquired bacterial meningitis. Neurology. 2010;75(10):918–923. doi:10.1212/WNL.0b013e3181f11e10
30. Wang KW, Chang WN, Chang HW, Wang HC, Lu CH. Clinical relevance of hydrocephalus in bacterial meningitis in adults. Surg Neurol. 2005;64(1):
31. George T, Moorthy RK, Rajshekhar V. Long tunnel external ventricular drain: an adjunct in the management of patients with infection associated hydrocephalus. Br J Neurosurg. 2019;33(6):659–663. doi:10.1080/02688697.2019.1667483
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