|Year : 2019 | Volume
| Issue : 12 | Page : 2095-2103
Application of neuroendoscopic surgical techniques in the assessment and treatment of cerebral ventricular infection
Feng Guan1, Wei-Cheng Peng1, Hui Huang1, Zu-Yuan Ren2, Zhen-Yu Wang3, Ji-Di Fu4, Ying-Bin Li5, Feng-Qi Cui6, Bin Dai1, Guang-Tong Zhu1, Zhi-Yong Xiao1, Bei-Bei Mao1, Zhi-Qiang Hu MD 1
1 Department of Neurosurgery, Beijing Shijitan Hospital, Capital Medical University, Beijing, China
2 Department of Neurosurgery, Peking Union Medical College Hospital, Beijing, China
3 Department of Neurosurgery, Peking University Third Hospital, Peking University, Beijing, China
4 Department of Neurosurgery, Beijing Tongren Hospital, Capital Medical University, Beijing, China
5 Department of Neurosurgery, the Second Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu Province, China
6 Department of Neurosurgery, Beijing Liangxiang Hospital, Beijing, China
|Date of Submission||31-Jan-2019|
|Date of Acceptance||30-Apr-2019|
|Date of Web Publication||7-Aug-2019|
Department of Neurosurgery, Beijing Shijitan Hospital, Capital Medical University, Beijing
Source of Support: This work was supported by the Capital Health Research and Development of Special Funding Support of China, No. 2011-2008-06 (to
ZQH), Capital Characteristic Clinical Application Research of China, No. Z131107002213044 (to ZQH) and Beijing Municipal Administration
of Hospitals Incubating Program of China, No. PX2019026 (to FG), Conflict of Interest: None
Cerebral ventricular infection (CVI) is one of the most dangerous complications in neurosurgery because of its high mortality and disability rates. Few studies have examined the application of neuroendoscopic surgical techniques (NESTs) to assess and treat CVI. This multicenter, retrospective study was conducted using clinical data of 32 patients with CVI who were assessed and treated by NESTs in China. The patients included 20 men and 12 women with a mean age of 42.97 years. NESTs were used to obliterate intraventricular debris and pus, fenestrate or incise the intraventricular compartment and reconstruct cerebrospinal fluid circulation, and remove artificial material. Intraventricular irrigation with antibiotic saline was applied after neuroendoscopic surgery (NES). Secondary hydrocephalus was treated by endoscopic third ventriculostomy or a ventriculoperitoneal shunt. Neuroendoscopic findings of CVI were used to classify patients into Grade I (n = 3), Grade II (n = 13), Grade III (n = 10), and Grade IV (n = 6) CVI. The three patients with grade I CVI underwent one NES, the 23 patients with grade II/III CVI underwent two NESs, and patients with grade IV CVI underwent two (n = 3) or three (n = 3) NESs. The imaging features and grades of neuroendoscopy results were positively related to the number of neurosurgical endoscopic procedures. Two patients died of multiple organ failure and the other 30 patients fully recovered. Among the 26 patients with secondary hydrocephalus, 18 received ventriculoperitoneal shunt and 8 underwent endoscopic third ventriculostomy. There were no recurrences of CVI during the 6- to 76-month follow-up after NES. Application of NESTs is an innovative method to assess and treat CVI, and its neuroendoscopic classification provides an objective, comprehensive assessment of CVI. The study trial was approved by the Institutional Review Board of Beijing Shijitan Hospital, Capital Medical University, China.
Keywords: nerve regeneration; neuroendoscopy; surgery; cerebral ventricular infection; assessment; treatment; hydrocephalus; irrigation; neural regeneration
|How to cite this article:|
Guan F, Peng WC, Huang H, Ren ZY, Wang ZY, Fu JD, Li YB, Cui FQ, Dai B, Zhu GT, Xiao ZY, Mao BB, Hu ZQ. Application of neuroendoscopic surgical techniques in the assessment and treatment of cerebral ventricular infection. Neural Regen Res 2019;14:2095-103
|How to cite this URL:|
Guan F, Peng WC, Huang H, Ren ZY, Wang ZY, Fu JD, Li YB, Cui FQ, Dai B, Zhu GT, Xiao ZY, Mao BB, Hu ZQ. Application of neuroendoscopic surgical techniques in the assessment and treatment of cerebral ventricular infection. Neural Regen Res [serial online] 2019 [cited 2020 Feb 27];14:2095-103. Available from: http://www.nrronline.org/text.asp?2019/14/12/2095/262591
Chinese Library Classification No. R445; R459.9; R741
| Introduction|| |
Cerebral ventricular infection (CVI) is one of the most dangerous complications in neurosurgery because of its high mortality and disability rates (Boeer et al., 2011; Guanci, 2013; Davies et al., 2016). CVI is especially prevalent in patients who have undergone external ventricular drainage (EVD) or have an intraventricular stent in place (Sneh-Arbib et al., 2013). CVI can lead to a series of symptoms and side effects, including headaches, consciousness disorders, and even death if treatment is not prompt (Al Shirawi et al., 2006; Fiorella et al., 2015; Glimåker et al., 2015). Although similar conditions such as meningitis and encephalitis have been widely studied (Wang et al., 2014; Chen et al., 2015), there are few studies on CVI (Zheng et al., 2014), despite an urgent need to understand this disease. Currently, the standard assessment of CVI involves imaging (computed tomography [CT], magnetic resonance imaging [MRI]), blood tests, and cerebrospinal fluid (CSF) tests and cultures,. However, the ventricular situation of CVI has not been directly observed and assessed.
Treatment of CVI is also challenging. Currently, the most common treatment of CVI involves an antibiotic treatment that targets the infection (Ng et al., 2014). However, the most effective antibiotics and the optimal treatment strategy remain controversial. In fact, there is evidence that the blood-brain barrier may limit the ability of antibiotics to enter CSF (Warf, 2005). Other factors can influence the efficacy of CVI treatment. Intraventricular and intrathecal medications can be interrupted by subarachnoid adhesion, the intraventricular compartment, an abscess, and artificial implants (Warf et al., 2012). Furthermore, acute CVI that has not been effectively treated may transform into chronic inflammation, thus reducing the optimal treatment window (Gathura et al., 2010; Kulkarni et al., 2010).
Neuroendoscopic surgical techniques (NESTs) are performed using an endoscope, which is a small telescope-like device equipped with a high-resolution video camera on the end to allow the neurosurgeon to navigate and access the lesion (Du et al., 2018). The advantages of NESTs include less complications and a faster recovery than traditional surgery and minimal scarring. Only a few studies have examined the application of NESTs to assess and treat CVI (Chang et al., 2007; Fehrenbach et al., 2016). Nevertheless, neuroendoscopic surgery (NES) may be an effective approach to provide a panoramic intraventricular view and visual assessment of CVI. Therefore, in the present study, we examined the efficacy of NESTs in assessing and treating CVI in patients who had received NES.
| Materials and Methods|| |
This multicenter, retrospective study was conducted in accordance with the Helsinki Declaration of 1975, as revised in 2000. The study has been approved by the Institutional Review Board of Beijing Shijitan Hospital, Capital Medical University, China (Additional file 1). All patients or their legal guaidians in this study authorized the release of their medical records and information.
This study included the clinical data of 20 men and 12 women (mean age: 42.97 years, range: 24–60 years) who presented with CVI in six hospitals in China from March 2010 to December 2017 (Additional Table 1). These hospitals included the Beijing Shijitan Hospital of Capital Medical University, Peking Union Medical College Hospital, Peking University Third Hospital, Beijing Tongren Hospital of Capital Medical University, the Second Affiliated Hospital of Nanjing Medical University, and Beijing Liangxiang Hospital. The same chief neurosurgeon performed all surgeries in all centers.
All eligible patients enrolled in this study met the following criteria: (1) history of a neurosurgical operation; (2) symptoms of fever, headache, neck/upper back pain, epilepsy, or consciousness disorder; (3) positive meningeal irritation sign; (4) increased leukocytes in the CSF; (5) positive CSF culture; (6) linear enhancement of the ventricular walls and/or intraventricular debris, the intraventricular compartment, or abscesses diagnosed by CT and/or MRI; and (7) intravenous and/or intrathecal antibiotic treatment for 2–4 weeks, but with no improvement.
All cases of CVI were treated by an intravascular approach with/without intrathecal antibiotics for 4 weeks to 6 months before NES. However, the outcomes of these patients were poor. The initiating factors for development of CVI were open surgery (n = 5), endoscopic third ventriculostomy (ETV; n = 5), EVD (n = 7), ventriculoperitoneal (VP) shunt (n = 13), repeated Ommaya taps (n = 1), and pituitary tumor resection by an endoscopic endonasal approach (n = 1). Clinical manifestations included fever (range, 37.5–42°C; n = 32), headache (n = 29), neck/upper back pain (n = 16), dizziness (n = 14), slurred speech (n = 9), intracranial hypertension (n = 21), epilepsy (n = 18), consciousness disorder (n = 8), and meningeal irritation sign (n = 26).
A blood examination showed increased leukocytes (1.51 ± 0.39 × 109/L; n = 29), increased procalcitonin levels (10.61 ± 3.61 µg/L; n = 30), and increased C-reactive protein levels (122.15 ± 21.42 mg/L; n = 32). CSF examination showed abnormal (n = 28) and normal CSF appearance (n = 4), positive Pan reaction (n = 32), increased leukocytes (1.63 ± 0.65 × 106/L; n = 32), increased protein levels (1.31 ± 0.47 g/L; n = 28), decreased glucose levels (1.58 ± 0.56 mM; n = 29), and decreased chloride levels (68.71 ± 19.74 mM; n = 27).
CSF bacterial culture showed that results were positive in all cases. Pathogens included Staphylococcus epidermidis (n = 14), Staphylococcus aureus (n = 6), Enterococcus faecium (n = 8), Pseudomonas aeruginosa (n = 10), Klebsiellap-neumoniae (n = 5), Enterobacter cloacae (n = 3), and mixed pathogens (n = 14) (Additional Table 1).
CT and MRI were performed in all cases before NES. We observed linear ependymal enhancement (n = 32), ventricular dilation (n = 21), intraventricular debris (n = 25), the intraventricular compartment (n = 17), and intraventricular abscesses (n = 6). A single-photon emission CT examination was performed in cases of secondary hydrocephalus as-sociated with CVI (n = 26). The results showed 18 cases of non-obstructive hydrocephalus and eight cases of obstructive hydrocephalus.
The MINOP ® Modular Neuroendoscopy System (Aesculap, Tuttlingen, Germany) includes a trocar and InVent trocar.
- The MINOP trocar with a 6-mm outer diameter and 4 channels: scope channel, 2.8-mm diameter; working channel, 2.2-mm diameter; irrigation channel, 1.4-mm diameter; overflow channel, 1.4-mm diameter. MINOP endoscope with 0° and 30° view directions, a 2.7-mm shaft diameter, and a 180-mm shaft length.
- The MINOP InVent trocar with an 8.3-mm outer diameter and 3/4 channels: scope channel, 2.8-mm diameter; irrigation channel, 1.0-mm diameter; two merging channels with a large working/overflow channel of 3.7 × 6.5 mm and a small working/overflow channel of 2.2-mm diameter. MINOP InVent endoscope with 0° and 30° view directions, a 2.7-mm shaft diameter, and a 180-mm shaft length.
- Intermittent or continuous hyperthermia, CSF white blood cell count ≥ 10 × 106/L, and positive result of CSF culture through intravenous and/or intrathecal antibiotics for 2–4 weeks (for all patients); (2) imaging data showed obvious ependymal enhancement and/or substantial inflammatory debris on diffusion-weighted imaging (for all patients); (3) imaging data showed intraventricular compartments (optional); (4) imaging data showed intraventricular abscess (for all patients); (5) if EVD was necessary because of CVI secondary to hydrocephalus leading to increased intracranial pressure, neuroendoscopic assessment and treatment were performed according to intraventricular condition during the EVD procedure (for all patients).
Neuroendoscopic classification of CVI
Neuroendoscopic classification of CVI (Grade I–IV) was used for the assessment of CVI in the study. Grade I (early) was classified as clear or yellowish CSF, granular ependymitis, little debris, little pseudomembrane on the ventricular wall, identifiable anatomical landmarks, pink or whitish choroid plexus, a patent foramen of Monro, and a normal third ventricular floor [Figure 1]IA–D. Grade II (aggressive) was classified as yellowish or light turbid CSF, granular ependymitis, moderate debris, moderate pseudomembrane and pus, identifiable anatomical landmarks, whitish or yellowish choroid plexus, a patent and enlarged foramen of Monro, and a thickened third ventricular floor [Figure 1]IIA–D. Grade III (severe) was classified as turbid CSF, granular ependymitis, excessive debris and pus, intra-ventricular compartments, difficult to identify anatomical landmarks, membrane-obscured choroid plexus, an enlarged or closed foramen of Monro, a thickened, opaque third ventricular floor, and secondary hydrocephalus [Figure 1]IIIA–D. Grade IV (excessive) was classified as was Grade III, but was accompanied by an intraventricular abscess [Figure 1]IVA–D and [Table 1]).
|Figure 1: Neuroendoscopic classification of cerebral ventricular infection. |
(IA–D) Grade I: Clear or yellowish cerebrospinal fluid (CSF), granular ependymitis, identifiable anatomical landmarks. (IIA–D) Grade II: Yellowish or light, turbid CSF, granular ependymitis, moderate debris and pus, moderate pseudomembrane on the ventricular wall, patent and enlarged foramen of Monro, identifiable anatomical landmarks, and thickened third ventricular floor. (IIIA–D) Grade III: Turbid CSF, granular ependymitis, excessive debris and pus, compartments, difficulty in identifying anatomical landmarks, enlarged or closed foramen of Monro, and thickened and opaque third ventricular floor. (IVA–D) Grade IV: The same as grade III, but accompanied by intraventricular abscesses (red arrows).
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|Table 1: Neuroendoscopic classification of cerebral ventricular infection (CVI) (Grades I–IV)|
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Treatment for cerebral ventricular infection
The neuroendoscopic bilateral frontal or unilateral frontal approach with septostomy under general anesthesia was performed in all patients. The purpose of NES was to obliterate intraventricular debris and pus, fenestrate or incise the intraventricular compartment and reconstruct the CSF circulation, remove artificial implant material, and resect or externally drain intraventricular abscesses. Intraventricular irrigation with antibiotic saline (IVIAS) was applied after NES. ETV or VP shunt was performed for secondary hydrocephalus resulting from CVI.
The standard procedure included four or more of the following steps. Neuroendoscopic IVIAS was performed during NES (for all patients). The severity of the ventricular situation with NESTs was assessed [Figure 1]; for all patients). Debris, sediments, pus, and blood clots were obliterated in the ventricle [Figure 2]A, [Figure 2]B, [Figure 2]C, [Figure 2]D; for all patients). The intra-ventricular compartments were fenestrated or incised [Figure 2]E & [Figure 2]F; optional). If the aqueduct of the midbrain was enlarged, the neuroendoscope was placed into the fourth ventricle to assess and treat CVI [Figure 2]G, [Figure 2]H, [Figure 2]I, [Figure 2]J; optional). The intra-endoscopic technique was converted into an extra-endoscopic technique to obliterate a large amount of intra-ventricular debris, pus, and clots with an aspirator [Figure 2]K & [Figure 2]L; optional). All intraventricular artificial implants were dissociated and removed [Figure 2]M; for all patients). The ventricular abscess was resected or drained (optional). The EVD catheter was placed in an optimal site, such as the foramen of Monro or occipital horn, with neuroendoscopic guidance for IVIAS [Figure 2]N; for all patients). Neuroendoscopic biopsy specimens that were obtained from the debris and pus were detected by hematoxylin-eosin staining.
|Figure 2: Application of neuroendoscopic surgical techniques to treat cerebral ventricular infection.|
(A, B) Before (A) and after (B) obliteration of blood clots in the right occipital horn of the lateral ventricle. (C, D) Before (C) and after (D) obliteration of debris and pus in the right lateral ventricle. (E, F) Before (E) and after (F) fenestration of the membrane over the foramen of Monro. (G-J) The enlarged aqueduct of the midbrain (G), assessment of the infection state in the fourth ventricle (H), before (I) and after (J) obliteration of debris and pus in the fourth ventricle. (K, L) Conversion of the intra-endoscopic technique to the extra-endoscopic technique to obliterate a large amount of intraventricular debris, pus, and clots with an aspirator. (M) Dissociation of artificial implants attached to the ventricular wall. (N) To place the external ventricular drainage catheter at the optimal location by neuroendoscopic guidance. (O, P) Intraventricular views before (O) and after (P) intraventricular irrigation with antibiotic saline. Two weeks after intraventricular irrigation with antibiotic saline, blood vessels on the ventricular wall were obviously dilated and hyperemic.
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Repeated NES criterion
Repeated NES was performed when IVIAS after NES had been performed for 2 weeks but the patient still exhibited the following: (1) Intermittent or continuous hyperthermia (≥ 37.5°C); (2) CSF white blood cell count ≥ 10 × 106/L; (3) positive result of CSF culture; and (4) linear enhancement of the ventricular walls and/or intraventricular debris, pus, or compartment confirmed by CT and/or MRI.
Intraventricular irrigation with antibiotic saline after NES
IVIAS was applied either intermittently (Grade I) or continuously (Grade II–IV). IVIAS was applied for 2–6 weeks after NES. Antibiotic saline for irrigating the ventricle was prepared and replaced according to the half-life of the antibiotic. The intraventricular medication included Vancomycin, Gentamicin, and Amicacin (Additional Table 1). The intraventricular antibiotic dose was 5–10% of that provided intravenously. Neuroendoscopic intraventricular views were observed before and after IVIAS ([Figure 2]O & [Figure 2]P; optional).
Discharge and follow-up evaluation
The modified Rankin Scale (mRS) (Reponen et al., 2016; Wilson et al., 2017) was used to evaluate outcomes at dis-charge and during follow-up. Outpatient follow-up visits were scheduled for the following 6–76 months. An MRI (diffusion weighted imaging sequence and contrast-enhanced) follow-up scan was arranged. Complications associated with surgery and persistence of symptoms during the follow-up period were noted.
Descriptive of patients’ characters and clinical data were summarized, and continuous variables are presented as the mean ± standard deviation (SD). Association of neuroendoscopic classification with imaging features of cerebral ven-tricular infection was performed under generalized linear regression, in which t-tests and F-tests were done under a 0.05 statistical significance. All data were analyzed using SPSS version 19.0 statistical software (IBM Corp., Armonk, NY, USA).
| Results|| |
Clinical data of patients with CVI that received neuroendoscopic surgical treatment
Two patients (6%) had severe lung infection caused by A baumannii. Both patients were treated with antibacterial and mechanical ventilation, but the efficacy was poor. Ultimately, these two patients died of respiratory failure, 6 weeks and 4 weeks after NES. The other 30 (94%) patients were completely cured. Intracranial hypertension was normalized in 21 patients, disturbance of consciousness was significantly diminished in 5 patients, and meningeal irritation signs disappeared in 26 patients. Among the 26 patients with secondary hydrocephalus, 18 underwent a VP shunt and 8 underwent ETV. ETV failed in one patient and was replaced with a VP shunt. After surgery, cerebral ventricular dilation was normalized in 12 patients, reduced in 5, and unchanged in 4. Among the 32 patients who showed CT/MRI-detected line enhancement of the ventricular wall, 26 showed the disappearance of enhancement and the 6 other patients showed reduced enhancement. Among the 6 patients with an intraventricular abscess, the abscess dis-appeared in 5 patients, and showed linear enhancement with contrast-enhanced CT and MRI in one patient.
Laboratory examinations after NES
Blood examination showed that leukocytes, procalcitonin levels, and C-reactive protein levels were normalized in all patients. CSF appeared normal (n = 24) or light yellow (n = 8). The Pan reaction was negative in all patients (n = 32). The CSF leukocyte count ranged from 0 to 11 × 106/L. CSF chemistry tests showed that total protein levels ranged from 0 to 46 mg/L, glucose levels ranged from 21 to 50 mM, and chloride levels ranged from 110 to 140 mM. CSF culture was negative in all patients.
Association of neuroendoscopic classification with imaging features of CVI
The neuroendoscopic bilateral frontal approach was used in 29 patients (Grades II–IV), and the unilateral frontal ap-proach with septostomy was used in 3 patients (grade I). Classification of CVI by NESTs showed 3 Grade I cases, 13 grade II cases, 10 grade III cases, and 6 Grade IV cases. Of these, the 3 patients with Grade I CVI underwent one NES, the 23 patients with Grade II/III underwent two NESs, and patients with Grade IV underwent two (n = 3) or three (n = 3) NESs (Additional Table 2). Linear regression analysis showed that the number of NESs significantly increased with an increase in CVI Grade (P = 0.000, Additional Table 3). Neuronavigation was applied to 9 Grade II patients, 8 Grade III patients, and 5 Grade IV patients.
For linear regression analysis, four CVI imaging features of ependymal enhancement, intraventricular debris, intra-ventricular compartments, and intraventricular abscess were used as the dependent variables, and neuroendoscopic CVI classification was used as the independent variable. The F-test results showed that the associations between imaging features and grades of neuroendoscopic CVI classification were statistically significant (F = 33.146, P = 0.000). Thus, the higher the grade of neuroendoscopic classification of CVI, the more likely it was that a patient would present with imaging features of intraventricular debris, intraventricular compartments, and intraventricular abscess [Table 2] and [Table 3].
|Table 2: Association between neuroendoscopic classification and imaging features of cerebral ventricular infection|
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|Table 3: Regression analysis on imaging features and neuroendoscopic classification of cerebral ventricular infection|
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Pathological findings of a biopsy specimen of material lining the ventricular wall
Neuroendoscopic biopsy specimens that were obtained from the debris and pus in the ventricle showed edematous changes with scattered hemorrhage and necrosis by hematoxylin-eosin staining. We also observed gliosis, inflammatory cells, proliferation of epithelioid cells, and ependymal thickening [Figure 3].
|Figure 3: Hematoxylin-eosin staining of a biopsy specimen of material lining the ventricular wall.|
(A, B) The edematous changes with scattered hemorrhage and gliosis (red arrows), necrosis (black arrows), inflammatory cells, proliferation of epithelioid cells, and ependymal thickening can be seen (original magnification, A, 100×; B, 200×). Scale bars: 100 μm.
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Complications of neuroendoscopic surgical treatment in patients with CVI
Two patients died of multiple organ failure. Less serious complications included seizures (n = 5), subcutaneous effusion (n = 4), subdural effusion (n = 6), intracranial pneumatosis (n = 8), pneumonia (n = 4), and slight intraventricular hemorrhage (n = 5). There were no incision infections, CSF leakages, serious complications associated with ETV, obstructions, infections with rejection of a VP shunt, or ventricular fungal infections.
Follow-up analysis of patients with cerebral ventricular infection that received neuroendoscopic surgical treatment
At discharge, the median mRS score was 3 (range, 0–6). During the 6–76 months of follow-up, there was no recurrence of CVI, and the surgical results for hydrocephalus were satisfactory. The median mRS follow-up score was 2 (range, 0–6).
Case report of cerebral ventricular abscess with neuroendoscopic surgical treatment
A 35-year-old man had an 11-month history of intermittent fever (range, 37–42°C) after undergoing endoscopic endonasal approach for a pituitary tumor. The patient was treated intermittently with intravenous antibiotics (Ceftriaxone sodium and Vancomycin) for approximately 10 months, but with minimal effect. The Glasgow Coma Scale score on admission was 10. The meningeal irritation sign was positive. The pathogen in CSF culture was identified as Pseudomonas Aeruginosa. Sensitive antibiotics were Gentamicin and Amicacin. The patient was treated with IVIAS (Amicacin) after NES for 4 weeks.
Contrast-enhanced MRI showed an annular enhancement signal in the aqueduct and a linear enhancement signal in the fourth ventricle [Figure 4]A, [Figure 4]B, [Figure 4]C. The patient was diagnosed with CVI, intraventricular abscess, and obstructive hydro-cephalus. During NES, we found yellow tissue deposited at the foramen of the aqueduct [Figure 4]D. A biopsy specimen of the yellow tissue showed inflammatory cellular infiltration. An external catheter for draining the abscess was placed into the third ventricle through the foramen of Monro, and then inserted into the abscess cavity with navigation guidance [Figure 4]E & [Figure 4]F. T2-weighted MRI showed that the drainage catheter was inserted into the abscess cavity through the foramen of the aqueduct [Figure 4]G. Three-dimensional CT reconstruction of the skull showed the drainage catheter in the abscess, as well as the left and right EVD catheters [Figure 4]H, [Figure 4]I, [Figure 4]J.
|Figure 4: Medical images and scenarios of neuroendoscopic surgery (NES) for cerebral ventricular infection.|
(A–C) Contrast-enhanced magnetic resonance imaging (MRI) shows an enhanced annular signal in the aqueduct (red arrow) and an en-hanced linear signal in the fourth ventricle. (D) During NES, yellow tissue (red arrow) was deposited at the foramen of the aqueduct. (E) The catheter used for external drainage of the abscess was placed in the third ventricle through the foramen of Monro. (F) An external drainage catheter was inserted into the abscess cavity. (G) T2-weighted MRI showed that the catheter was in the abscess cavity. (H–J) Three-dimensional computed tomography reconstruction of the skull shows the drainage catheter in the abscess, as well as the left and right external ventricular drainage catheters. (K–M) Contrast-enhanced MRI showed that the previous annular enhanced signal had disappeared and been replaced by point-and-line signals in the aqueduct and fourth ventricle 4 weeks after NES. (N–P) Contrast-enhanced MRI at one year of follow-up. A: Anterior; P: posterior; R: right; L: left.
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After 4 weeks of IVIAS following NES, contrast MRI showed that the previous annular enhancement signal of the aqueduct had disappeared and transformed into point-and-line enhanced signals [Figure 4]K, [Figure 4]L, [Figure 4]M. His temperature had returned to the normal range. Blood and CSF tests were normalized, and CSF cultures after NES were negative. The patient was discharged with a favorable outcome after the VP shunt. The follow-up was 54 months, and the patient fully recovered with an mRS score of 0 [Figure 4]N, [Figure 4]O, [Figure 4]P.
| Discussion|| |
Efficacy of neuroendoscopic surgical techniques in assessment and treatment of CVI
In the present study, the cure rate (> 90%) and the death rate (6%) of CVI was compared with the cure rate (about 80%) and the death rate (10–30%) of CVI by the treatment of only intravenous and intrathecal antibiotics reported in previous studies (Park et al., 2006; Mori, 2007; Rath et al., 2012; Ziaka et al., 2013; Kumar et al., 2015, 2016; Terada et al., 2016; Satyarthee, 2017; Mahoney et al., 2018; Shang et al., 2018; Yuen et al., 2018). This comparison indicates a satisfactory neural function recovery and regeneration of NEST for CVI. All grade I patients underwent one NES and intermittent IVIAS. Patients with grade II–IV underwent two or three NESs and continuous IVIAS. Linear regression analysis showed that the number of NESs significantly increased with an increase in CVI grade. This indicates that a higher CVI classification is associated with multiple operations. Therefore, the surgical procedure should be rationally designed for higher CVI grades before the first NES, such as incision and unilateral or bilateral approach, to avoid incisional CSF leakage. F-test of regression analysis on the associations between imaging features and grades of neuroendoscopic CVI classification also confirmed that the higher the grade of neuroendoscopic classi-fication of CVI, the more likely a patient was to present with imaging features of intraventricular debris, intraventricular compartments, and intraventricular abscess. An important consideration regarding NEST treatment of CVI is that NES with neuronavigation should be applied in cases of abnormal intraventricular structures identified by CT and MRI. This may avoid injury caused by blind grasping, fistulas, and suction. Because of gravity and positioning, the debris, pus, and blood clots are often deposited in the third ventricle, occipital areas, and temporal horn of the lateral ventricle. These areas may be assessed and cleared during NES (Mori, 2007). Application of NESTs may also be used to reconstruct the CSF circulation, which is beneficial for IVIAS after NES. Furthermore, artificial implants are usually surrounded by bacteria and adhere to the ventricular wall or choroid plexus. During NES, artificial implants can be identified visually and removed to avoid secondary intracranial hemorrhage. With endoscopic guidance, a 14 Fr EVD catheter for IVIAS can be placed at the ideal site (e.g., foramen of Monro, the occipital horn of the lateral ventricle) to avoid adhesion to the choroid plexus and ventricular wall. During NES, two methods may be applied to treat an intraventricular abscess, as follows: (1) complete removal of the abscess when it is around the shunt or in a non-essential functional area; and (2) draining of the abscess when it is in close proximity to an important anatomical structure (e.g., the brainstem), or when the cyst of the abscess cannot be completely removed.
Finally, when there is excessive intraventricular debris, pus, and abscesses, the intra-endoscopic technique may be converted to an extra-endoscopic technique, which can effectively accelerate the surgical process and ensure the safety and efficacy of NES. Our specific procedure was as follows. First, the neuroendoscope was placed into the lateral ventricle via the neuroendoscopic access or cortical fistula as an observation tool. A closed adjustable pressure aspirator was placed into the lateral ventricle via the neuroendoscopic access or cortical fistula. When the aspirator was near debris, sediments, and pus, the aspirator was opened to remove the inflammatory substances. The depth and direction of the aspirator were controlled by the surgeon, and the intensity of the aspirator was adjusted according to the quantity of the inflammatory substances.
Role of intraventricular irrigation with antibiotic saline after NE
Although intraventricular debris and pus are removed by NESTs, ependymitis is not fundamentally cured. Therefore, IVIAS is applied after NES to consolidate the NES (Terada et al., 2016; Yuen et al., 2018). In our study, intermittent IVIAS was conducted in patients with Grade I CVI (early stage), whereas continuous IVIAS was applied in patients with Grade II–IV CVI (aggressive, severe, and excessive stages, respectively). Kumar et al. (2015, 2016) reported that endoscopic lavage may be helpful in improving the outcome of CVI patients. In any patient with ventriculitis, if CSF sterilization is not achieved within 7–14 days of intravenous and/or intrathecal antibiotics, endoscopic lavage (2 weeks or longer) must be seriously considered because it may help to expedite the clearance of infection. Compared with the intravascular and intrathecal route, antibiotics can be applied directly to the ventricle by IVIAS (Terada et al., 2016; Yuen et al., 2018). IVIAS also maintains a stable concentration of medication in the CSF, which provides a reasonable and effective sterilization level that can cure CVI. Additionally, IVIAS replaces inflammatory or hemorrhagic CSF, debris, and inflammatory mediators in the ventricle. Nevertheless, in our study, obviously dilated, hyperemic blood vessels were found in the ventricular wall during IVIAS in 8 patients (which indicated a potential risk of intra-ventricular bleeding.
There are several important considerations that should be made when using IVIAS. An antibiotic should be selected according to evidence-based medicine and the susceptibility of the bacteriological culture. If a patient had NES treatment and 2 weeks of IVIAS, after which their temperature was still > 37.5°C and they had abnormal CSF test results, the location of EVD catheter needed to be changed for continued IVIAS. Furthermore, during the procedure, neuroendoscopic inspection was used to evaluate the therapeutic effect of CVI, and relict sediment or inflammatory deposits can be cleaned up. The drainage catheter must also be fluent during IVIAS, and the temperature of the antibiotic saline should be consistent with body temperature (36–37°C) to avoid chills. Finally, drugs (Depakine, 20–30 mg/kg per day) are required to prevent epilepsy.
Strategies for treating secondary hydrocephalus associated with CVI
CVI can easily cause midbrain aqueduct adhesion, stenosis or atresia, and obstruction of the fourth ventricle outlet leading to obstructive hydrocephalus. ETV is feasible for treating secondary obstructive hydrocephalus associated with CVI if the imaging data confirms obstruction of the CSF pathway (Mohan et al., 2012). ETV should be performed after CVI is completely cured so that the CVI cannot spread to the cerebral and spinal subarachnoid spaces. There are also some considerations that should be made for CVI during ETV. First, CVI usually leads to abnormal intraventricular anatomical structures, which makes it difficult to identify anatomical landmarks (Wang et al., 2017). In the present study, we found inflammatory thickening of the third ventricular floor in five cases. Application of neuronavigation is strongly recommended to ensure the safety and efficacy of ETV. Second, a stoma should be shaped to avoid closure. Finally, the basilar cistern should be further observed and assessed through the stoma of the third ventricular floor.
However, in some patients, CVI with obstructive hydrocephalus is also accompanied by communicating hydrocephalus. In the present study, ETV failed in one patient with midbrain aqueduct atresia, and it was replaced with a VP shunt. The reason for ETV failure was that CVI caused CSF absorption dysfunction, which led to communicating hydrocephalus. Therefore, if the imaging data confirm that the ventricular system is dilated and there is no specific CSF pathway obstruction, a VP shunt should be performed as soon as possible. A VP shunt is an optimal choice for non-obstructive hydrocephalus. When the CSF culture is continuously negative (at least 3 consecutive times), and the patient’s temperature and blood and CSF leukocyte and protein levels are normalized after ceasing IVIAS, a VP shunt should be considered. We suggest that subsequent intravascular antibiotic treatment should been performed for 1–2 weeks after the VP shunt (Husain et al., 2007; Wang et al., 2017). In our study, CVI and secondary hydrocephalus were cured and there was no recurrence.
Limitations Multicenter studies with more extended follow-up periods should be designed for further optimization of the neuro-endoscopic classification of CVI and identifying the safe and effective dose of IVIAS.
Conclusions Application of NESTs to assess and treat CVI is an innovative method. Neuroendoscopic classification of CVI (grades I–IV) provides an objective, comprehensive assessment of CVI. IVIAS is also a necessary procedure for the permanent cure of CVI. NESTs should be applied more extensively for assessing and treating CVI.
Author contributions: Study conception and design: FG, ZQH; neuroendoscopic surgical implementation: FG, HH, ZYR, ZYW, JDF, YBL, FQC, ZQH; data collection: WCP, GTZ, ZYX, BBM; data analysis: FG, WCP, ZQH; manuscript preparation: FG, WCP. All authors approved the final version of the paper.
Conflicts of interest: None declared.
Financial support: This work was supported by the Capital Health Research and Development of Special Funding Support of China, No. 2011-2008-06 (to ZQH), Capital Characteristic Clinical Application Research of China, No. Z131107002213044 (to ZQH) and Beijing Municipal Administration of Hospitals Incubating Program of China, No. PX2019026 (to FG). The funders had no involvement in study design; data collection, analysis, and interpretation; paper writing; or decision to submit the paper for publication.
Institutional review board statement: The study was approved by the Institutional Review Board of Beijing Shijitan Hospital, Capital Medical University, China. This study was performed in accordance with the relevant ethical requirement of the Declaration of Helsinki.
Informed consent statement: The authors certify that they have obtained all appropriate patient consent forms. In the forms the patients or their legal guardians have given their consent for patients’ images and other clinical information to be reported in the journal. The patients or their legal guardians understand that the patients’ names and initials will not be published and due efforts will be made to conceal their identity.
Reporting statement: This study followed the Recommendations for the Conduct, Reporting, Editing and Publication of Scholarly Work in Medical Journals developed by the International Committee of Medical Journal Editors.
Biostatistics statement: The statistical methods of this study were reviewed by the biostatistician of Beijing Shijitan Hospital, Capital Medical University.
Copyright license agreement: The Copyright License Agreement has been signed by all authors before publication.
Data sharing statement: Datasets analyzed during the current study are available from the corresponding author on reasonable request.
Plagiarism check: Checked twice by iThenticate.
Peer review: Externally peer reviewed.
Open peer reviewer: N. Scott Litofsky, University of Missouri-Columbia School of Medicine, USA.
Additional file 1: Ethics Approval Documentation (Chinese)[Additional file 1].
Additional file 2: Open peer review report 1[Additional file 2].
Additional Table 1: Patients’ characteristics and details[Additional file 3].
Additional Table 2: Relation between neuroendoscopic classification of cerebral ventricular infection and the number of neuroendoscopic surgeries[Additional file 4].
Additional Table 3: Linear regression analysis results of Additional [Table 2][Additional file 5].
Funding: This work was supported by the Capital Health Research and Development of Special Funding Support of China, No. 2011-2008-06 (to ZQH), Capital Characteristic Clinical Application Research of China, No. Z131107002213044 (to ZQH) and Beijing Municipal Administration of Hospitals Incubating Program of China, No. PX2019026 (to FG).
| References|| |
Al Shirawi N, Memish ZA, Cherfan A, Al Shimemeri A (2006) Post-neurosurgical meningitis due to multidrug-resistant Acinetobacter baumanii treated with intrathecal colistin: case report and review of the literature. J Chemother 18:554-558.
Boeer K, Vogelsang H, Deufel T, Pfister W, Kiehntopf M (2011) Immediate diagnosis of ventriculits: evaluation of parameters independent of microbiological culture. Acta Neurochir (Wien) 153:1797-1805.
Chang CW, Nagashima G, Fujimoto T, Suzuki R, Itokawa H, Endoh S, Noda M, Okuda M (2007) Conspicuous endoscopic appearance of ventriculitis caused by coagulase-negative staphylococci. J Infect Chemother 13:177-179.
Chen K, Wu Y, Wang Q, Wang J, Li X, Zhao Z, Zhou J (2015) The methodology and pharmacokinetics study of intraventricular administration of vancomycin in patients with intracranial infections after craniotomy. J Crit Care 30:218.e1-5.
Davies BM, Jones A, Patel HC (2016) Surgical-site infection surveillance in cranial neurosurgery. Br J Neurosurg 30:35-37.
Du B, Shan AJ, Zhang YJ, Wang J, Peng KW, Zhong XL, Peng YP (2018) The intra-neuroendoscopic technique: A new method for rapid removal of acute severe intraventricular hematoma. Neural Regen Res 13:999-1006.
Fehrenbach MK, Bernhard M, Siekmeyer M, Lippmann N, Kiess W, Nestler U, Meixensberger J, Preuss M (2016) VP-shunt dysfunction caused by malaria CNS infection. Childs Nerv Syst 32:759-760.
Fiorella D, Zuckerman SL, Khan IS, Ganesh Kumar N, Mocco J (2015) Intracerebral hemorrhage: a common and devastating disease in need of better treatment. World Neurosurg 84:1136-1141.
Gathura E, Poenaru D, Bransford R, Albright AL (2010) Outcomes of ventriculoperitoneal shunt insertion in Sub-Saharan Africa. J Neurosurg Pediatr 6:329-335.
Glimåker M, Johansson B, Grindborg Ö, Bottai M, Lindquist L, Sjölin J (2015) Adult bacterial meningitis: earlier treatment and improved outcome following guideline revision promoting prompt lumbar puncture. Clin Infect Dis 60:1162-1169.
Guanci MM (2013) Ventriculitis of the central nervous system. Crit Care Nurs Clin North Am 25:399-406.
Husain M, Jha DK, Rastogi M, Husain N, Gupta RK (2007) Neuro-endoscopic management of intraventricular neurocysticercosis (NCC). Acta Neurochir (Wien) 149:341-346.
Kulkarni AV, Drake JM, Kestle JR, Mallucci CL, Sgouros S, Constantini S (2010) Predicting who will benefit from endoscopic third ventriculostomy compared with shunt insertion in childhood hydrocephalus using the ETV Success Score. J Neurosurg Pediatr 6:310-315.
Kumar A, Agrawal D, Sharma BS (2016) The role of endoscopic lavage in recalcitrant multidrug-resistant gram-negative ventriculitis among neurosurgical patients. World Neurosurg 93:315-323.
Kumar A, Verma N, Agrawal D, Sharma BS (2015) Endoscopic lavage for antibiotic unresponsive severe Acinetobacter baumanii ventriculitis: an unexplored treatment option. Acta Neurochir (Wien) 157:1225-1227.
Mahoney D, Porter D, Albur M (2018) Successful treatment of multicompartmental cerebral ventriculitis caused by Acinetobacter baumanii. IDCases 11:1-2.
Mohan S, Jain KK, Arabi M, Shah GV (2012) Imaging of meningitis and ventriculitis. Neuroimaging Clin N
Mori T (2007) Endoscopic features of ventriculitis caused by coagulase-negative streptococci. J Infect Chemother 13:188.
Ng K, Mabasa VH, Chow I, Ensom MH (2014) Systematic review of efficacy, pharmacokinetics, and administration of intraventricular vancomycin in adults. Neurocrit Care 20:158-171.
Park SW, Yoon SH, Cho KG (2006) An endoscopically proven ventriculitis-type, cyst-like intraventricular primary lymphoma of the central nervous system. Acta Neurochir (Wien) 148:981-984.
Rath TJ, Hughes M, Arabi M, Shah GV (2012) Imaging of cerebritis, encephalitis, and brain abscess. Neuroimaging Clin N
Reponen E, Tuominen H, Hernesniemi J, Korja M (2016) Modified rankin scale and short-term outcome in cranial neurosurgery: a prospective and unselected cohort study. World Neurosurg 91:567-573.e7.
Satyarthee GD (2017) Expanding horizon of neuroendoscopic procedure from endoscopic-assisted tumor resection, vascular surgery, and management of hydrocephalus to diagnostic and therapeutic management of pyogenic ventriculitis. World Neurosurg 104:1024-1025.
Shang F, Xu Y, Wang N, Cheng W, Chen W, Duan W (2018) Diagnosis and treatment of severe neurosurgical patients with pyogenic ventriculitis caused by gram-negative bacteria. Neurol Sci 39:79-84.
Sneh-Arbib O, Shiferstein A, Dagan N, Fein S, Telem L, Muchtar E, Eliakim-Raz N, Rubinovitch B, Rubin G, Rappaport ZH, Paul M (2013) Surgical site infections following craniotomy focusing on possible post-operative acquisition of infection: prospective cohort study. Eur J Clin Microbiol Infect Dis 32:1511-1516.
Terada Y, Mineharu Y, Arakawa Y, Funaki T, Tanji M, Miyamoto S (2016) Effectiveness of neuroendoscopic ventricular irrigation for ventriculitis. Clin Neurol Neurosurg 146:147-151.
Wang F, Yao XY, Zou ZR, Yu HL, Sun T (2017) Management of pyogenic cerebral ventriculitis by neuroendoscopic surgery. World Neurosurg 98:6-13.
Wang JH, Lin PC, Chou CH, Ho CM, Lin KH, Tsai CT, Wang JH, Chi CY, Ho MW (2014) Intraventricular antimicrobial therapy in postneurosurgical Gram-negative bacillary meningitis or ventriculitis: a hospital-based retrospective study. J Microbiol Immunol Infect 47:204-210.
Warf BC (2005) Hydrocephalus in Uganda: the predominance of infectious origin and primary management with endoscopic third ventriculostomy. J Neurosurg 102:1-15.
Warf BC, Bhai S, Kulkarni AV, Mugamba J (2012) Shunt survival after failed endoscopic treatment of hydrocephalus. J Neurosurg Pediatr 10:463-470.
Wilson A, Bath PM, Berge E, Cadilhac DA, Cuche M, Ford GA, Macisaac R, Quinn TJ, Taylor M, Walters M, Wolff C, Lees KR; for the ESO-VISTA Health Economics Working Group (2017) Understanding the relationship between costs and the modified Rankin Scale: A systematic review, multidisciplinary consensus and recommendations for future studies. Eur Stroke J 2:3-12.
Yuen J, Chen B, Brent A, Plaha P
(2018) Endoscopic washout for medically refractory cerebral ventriculitis. J Neurosurg Sci 62:523-526.
Zheng SP, Li GP, You C (2014) Excessive external drainage of CSF might aggravate bacterial ventriculitis. Turk Neurosurg 24:108-110.
Ziaka M, Markantonis SL, Fousteri M, Zygoulis P, Panidis D, Karvouniaris M, Makris D, Zakynthinos E (2013) Combined intravenous and intraventricular administration of colistin methanesulfonate in critically ill patients with central nervous system infection. Antimicrob Agents Chemother 57:1938-1940.
P-Reviewer: Litofsky NS; C-Editor: Zhao M; S-Editors: Yu J, Li CH;L-Editors: Cason N, Yu J, Song LP; T-Editor: Jia Y
[Figure 1], [Figure 2], [Figure 3], [Figure 4]
[Table 1], [Table 2], [Table 3]