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The role of intraoperative ultrasound in gross total resection of brain mass lesions and outcome
The Egyptian Journal of Neurology, Psychiatry and Neurosurgery volume 55, Article number: 73 (2019)
Surgical resection of brain mass lesion mandates safety and the best outcome for the patient.
The aim of this study was the evaluation of intraoperative ultrasound (IOUS) in gross total resection of brain mass lesions and patients’ safety in comparison to conventional surgery.
Materials and methods
In total, 632 patients were operated for brain mass lesion resection at Neurosurgery Department, Zagazig University Hospitals, during the period from January 2011 to October 2018 and divided randomly into two groups, IOUS group and conventional group, for the detection value of IOUS in resection, safety, and outcome after 3 months follow-up.
The IOUS group showed statistically significant gross total resection regardless to pathology, location, size, age, and sex in favor of IOUS use, and also, there were significantly less complications and better outcome after 3 months follow-up with the IOUS group. Significantly better outcome was found with gross total resection in total surgeries.
The use of IOUS during brain mass lesion surgery is safe and can assist the surgeon in gross total resection with better outcome.
The use of ultrasound in brain mass lesion resection is a real-time capability of this imaging. Ultrasound may provide an alternative tool to intraoperative magnetic resonance imaging (MRI) for delineating tumor tissues and improving the chances of gross total resection . The purpose of brain tumor removal is maximal resection while sparing healthy tissues. The extent of resection is a key prognostic factor in survival time, functional recovery, and tumor recurrence rates . The optimal results of brain lesion surgery may be achieved by maximal surgical resection without disturbance of neurological functions . Due to the imprecise correlation between preoperative images, intraoperative anatomy, and also poor differentiation of some tumors from a normal tissue, substantial tumor volume may remain postoperatively which may lead to rapid disease recurrence. To avoid these, better delineation of normal from tumor tissue intraoperatively could improve clinical outcome as increasing chance of total resection and decreasing normal tissue damage . Intraoperative imaging technology increases the extent of tumor resection and patients’ outcome including survival time. MRI systems are time-consuming and of high cost. Computed tomography (CT) usually is not of choice as ionizing radiation and limited mass delineation. Several researches have demonstrated that the image quality of ultrasound has improved enough to visualize and guide tumor resection [1, 5]. The most important disadvantage of neuronavigation is the inconsistency with preoperative images from changes of the lesion and critical anatomic structures associated with brain shift as intraoperative tumor resection or cerebrospinal fluid drainage. This creates the need for updating the preoperative image with the intraoperative image .
The ultrasonography can assist the surgeon to solve the common problem of brain shift, and any tumor residual can be spotted by ultrasound and removed .
The aim of this study was the evaluation of intraoperative ultrasound in gross total resection of brain mass lesions and patients’ safety in comparison to conventional surgery.
Patients and methods
Since 2007, the intraoperative ultrasound has been used during brain and spinal cord surgeries at Neurosurgery Department, Zagazig University Hospitals, but not routinely in all surgeries.
In total, 632 patients were operated for brain mass lesion resection at Neurosurgery Department, Zagazig University Hospitals, during the period from January 2011 to October 2018 and divided randomly into two groups: IOUS group and conventional group. All surgeries were done under general anesthesia. Ultrasound IBE-2500D, a digital scanner with endocavitary transducer 5, 6.5, and 8 MHZ of footprint 1.8 × 0.8 cm which is used in most operative works and electronic convex array transducer 2.5, 3.5, and 5 MHZ of footprint 5 × 1.2 cm which is used to examine deep details especially with large craniotomy, is known as the reverse relation between frequency and both of depth and resolution; low-frequency waves offer low image spatial resolution but can penetrate deeper as low degree of waves of attenuation. The probe was covered by a sterile glove filled with the acoustic gel. For delineating the best image spatial resolution of the brain and the mass lesion, the following factors must be applied: The first factor is the position of the patient’s head must allow the lesion and the resection cavity to be upward to permit saline to stay in the resection cavity and prevent air artifact. In posterior fossa surgery in sitting position, elongated glove finger gel pad technique was used to fill the surgical cavity. The second factor is selecting the proper ultrasound probe regarding size and frequencies. The third factor is the gel connection without air bubbles inside the glove. The fourth factor is adjusting the scanner brightness, depth, gain compensation, focus, and frequency for best images. The fifth factor is cottonoid and spatula should be removed, and blood washing by saline during imaging.
The ultrasound was used before dural opening for delineation of the mass lesion, after dural opening for tailoring the site and direction of surgical corridor, and during resection for determining the process of surgery. The ultrasound probe can be used to identify the best site for cortical incision, taking into account the shorter path to the middle of the lesion, and avoidance of eloquent cortex according to preoperative imaging data. In cases with remnants detected by ultrasound in the eloquent area, the operation was ended without gross total resection. The surgeon or the assistant is well trained for ultrasound usage either machine work, image reading, or tissue manipulation.
CT or MRI of the brain was done during the first 48 h after surgery for assessing the extent of resection. Gross total resection (GTR) was considered when no visible mass in postoperative imaging, subtotal resection (STR) when > 50% resection, and partial (p) resection when less 50% resection. The calculation of mass residual in most cases was done according to the method of Bergsneider and colleagues , which depends on early postoperative MRI (within 48 h of surgery); in cases of contrast-enhancing lesions, the residual was defined as enhancing axial T1 tissues after excluding spontaneously hyper-intense T1 tissues, e.g., blood products identified on pre-contrast T1. For non-enhancing tumor regions, the residual was delineated as remaining areas of T2 of preoperative imaging taking into account postoperative changes.
All patients studied preoperatively by imaging, laboratory investigations, and clinically for general, and neurological status, and then after surgery for at least three months for detecting the extent of resection, and the neurological status for comparing the two groups of patients with, and without intraoperative ultrasound usage. Karnofsky  performance score was used to assess the condition of the patients preoperatively, and during follow up for comparison. Patients with meningiomas, recurrent tumors, or incomplete data were excluded from this study. Informed consents were obtained for the procedures with approval from the Zagazig University Institutional Review Board (Zu-IRB).
The collected data were coded, processed, and analyzed using the SPSS (Statistical Package for Social Sciences) version 20 Windows (SPSS Inc., 2012-013, IBM, USA). Quantitative data was presented as number and percent. Comparison between groups was done by chi-square test. Student’s t test was used to compare between the two groups. p < 0.05 was considered to be statistically significant.
In this study, 632 patients were operated for brain mass lesion resection, divided randomly into two groups, IOUS group and conventional group. The two groups’ population criteria (Table 1) showed no significant difference regarding the number of patients, age, sex, pathology of lesions, location of lesions to tentorium cerebelli and cortex, and maximal mass diameter, but the IOUS group showed significantly more metastatic tumors. Table 2 showed the significant difference between the two groups regarding the extent of mass resection according to pathology, mass location, size, age, and sex in favor to IOUS use.
The main concern of the surgeon is the patients’ safety during and after surgery. Tables 3 and 4 showed the role of IOUS use in patients’ safety and outcomes; the IOUS group showed statistically significantly less complications and better outcome.
The value of gross total resection of brain mass lesion appeared in Table 5 as there was significantly better outcome with gross total resection in comparison to subtotal and partial resections.
Several studies showed the benefits of intraoperative ultrasound for achieving maximal safe resection in brain tumor surgery .
In this study, the IOUS group showed statistically significantly better gross total resection of brain mass lesions whatever the pathology of masses, location of masses, size of masses, age of patients, and sex of patients in comparison to the conventional group. Total resections were achieved in 253/332 (76%) patient with brain mass lesions, in 179/238 (75%) patients with brain tumors, in 111/154 (72%) patients with gliomas, in 73% of high-grade gliomas, 69% of low-grade gliomas, 86% of metastatic tumors, 82% of medulloblastoma, 80% of brain hematomas, and 76% of brain abscesses in the IOUS group. By IOUS, gross total resection of infratentorial lesions ( Figs 1, 2) were acheived in 72% and in 80% of supratentorial lesions (Figs 3, 4, 5, 6, 7, 8, 9 and 10).
The role of IOUS in gross total resection was addressed in many studies on brain tumors and other lesions.
Patil and colleagues  studied 192 patients with intracranial masses which were operated upon with IOUS. Supratentorial lesions found in 71%, brain abscesses in 14 cases, metastases 10 cases, glioma 83 cases, and other lesions 85 cases. Male to female ratio was 51:45, the youngest was 6 years old, and the oldest was 73 years. Gross total resection was achieved in 70%, subtotal in 19%, and biopsy in 11% of supratentorial lesions, while among the infratentorial group, gross total resection was achieved in 89%, subtotal in 7%, and biopsy in 3.6%. Moiyadi and colleagues  reported gross total resection in 55% of brain tumors by IOUS, and Erdogan and colleagues  reported 19/32 (59%) gross total resection. Wang and colleagues , in their study on IOUS use, concluded that all lesions were identified and located with accuracy 100%. Total resection was achieved in 70/98 (70%) patients. IOUS facilitates total removal while protecting brain tissue and neurological symptoms improved in 80/98 (82%) patients and unchanged in 18 patients. Picarelli and colleagues , in their study on brain metastases surgery by IOUS, the total resection was achieved in 100%, and surgical morbidity and mortality were 3% and 5%, respectively. In my study, the total resection by IOUS was achieved in 86% of metastatic brain tumors. Goren and colleagues  mentioned intracranial hemorrhage can be evacuated safely by IOUS as surgeon can assess dimensions, brain structures, and the shortest point to the clot. Tang and colleagues  in their study on meningioma by IOUS recorded the total resection in 19/20 patients (Simpson grades I and II). No deaths and all patients improved except one.
In this study, gross total resection of brain mass lesions in children by IOUS was 63/84 (75%) which was statistically significantly better than the conventional group.
Studies on childhood brain lesions documented the value of IOUS. Roth and colleagues  had achieved gross total resection in 14/16 (88%) patients. El Beltagy and colleagues  reported gross total resection in 14/25 (56%) patients, Ulrich and colleagues  reported 82% gross total resection, and Moiyadi and colleagues  had achieved 80% gross total resection.
Studies on intraoperative neuronavigator, CT, MRI, 5 ALA (aminolevulinic acid) addressed great fallacies which had been avoided with IOUS as brain shift during neuronavigation, radiation exposure with CT, high cost and long operative time of MRI, and inability of 5 ALA to stain low-grade tumors [13, 24, 25]. Roder and colleagues  in their study on 117 patients with brain tumors showed the total resection in 74% with intraoperative MRI, 46% with 5 ALA, and 13% with conventional surgery. In my study, gross total resections of brain tumors were achieved in 30% with conventional surgery. Mahboob and Eljamel  stated that literature review demonstrated gross total resection of glioma by neuronavigator in 31–36%, by 5 ALA in 69.1%, by intraoperative MRI in 70%, and by intraoperative ultrasound in 73.4%. Belsuzarri and colleagues  mentioned gross total resection increased from 36% to 65% by using 5 ALA with glioblastoma but was useless with low-grade glioma as low vascularity of such tumors affects 5 ALA staining.
Regarding postoperative complications in this study, operative mortality in the first postoperative month was 15/632 (2.4%), 3 (1%) in IOUS group and 12 (4%) in the conventional group. The IOUS group showed statistically significantly less complication than the conventional group. Also, there were statistically significantly better outcome 3 months after surgery in the IOUS group as shown by postoperative Karnofsky score improvement, Karnofsky functional outcome, and postoperative complication improvement in comparison to the conventional group.
Moiyadi and colleagues , in their study on IOUS, concluded that the extent of resection is a great prognostic marker and IOUS is a cost-effective alternative to intraoperative MRI. They recorded postoperative morbidity in only one case (1/20 patients 5%) in their study on 16 supratentorial and 4 infratentorial tumors in children (5–18 years old) and four patients showed improvement in the early postoperative period. Wang and colleagues  studied on small subcortical lesions including tumors, abscesses, and other lesion, they completely resected all lesions by IOUS, and all original symptoms significantly alleviated. Wang and colleagues  studied on 113 lesions (cranial and spinal); they stated that no IOUS complications and ultrasound ensure safety by minimizing injury to neural tissues and shortening the time of surgery. Bernstein and colleagues  stated that ultrasonography leads to a safe and wider resection. Cheon  stated that the goal of cerebral glioma removal is not only maximal but also safe removal which was achieved by IOUS. Wang and colleagues  reported that IOUS can facilitate total lesion resection while protecting neurological function, reduce complication, and prevent mechanical injury to intracerebral blood vessels. The extent of resection is associated with survival [18, 31, 32].
Brain surgeries aim to eliminate the pathological process without damage to brain tissues. The neurosurgeon reviews and assesses preoperative diagnostic information and intraoperative tools to make a decision including orientation and delineation of the pathological mass throughout the surgery. Intraoperative ultrasound is an available cheap tool which provides intraoperative safety and confidence to the surgeon for achieving total brain mass lesions resection. This study encourages to use IOUS.
Availability of data and materials
All data that support the findings of this study are available from the neurosurgery department Zagazig University Hospital. Data are however available from the author when requested with permission.
Gross total resection
Magnetic resonance imaging
Unsgaard G, Ommendal S, Muller T, Gronningsaeter A, Hernes TAN. Neuronavigation by intraoperative three-dimensional ultrasound: initial experience during brain tumor resection. Neurosurgery. 2002;50(4):804–12.
Almenawer SA, Badhiwala JH, Alhazzani W, Greenspoon J, Farrokhyar F, Yarascavitch B, et al. Biopsy versus partial versus gross total resection in older patients with high-grade glioma: a systematic review and meta-analysis. Neuro Oncol. 2015;17(6):868–81.
Elserry TH, Anwer H, Radwan HA. Introduction of vaginal probe for intraoperative ultrasound of intra-axial brain lesions. Egyp J Neurosurg. 2013;28(4):5–12.
Zhang ZZ, Shield LBE, Sun DA, Zhang YP, Hunt MA, Christopher BS. The art of intraoperative glioma identification. Front Oncol. 2015;5(175):1–7.
Gronningsaeter A, Kleven A, Ommedal S, Aarseth TE, Lie T, Lindseth F, Lango T, Unsgaard G. Sono Wand, an ultrasound-based neuronavigation system. Neurosurgery. 2000;47(6):1373–80.
Tümtürk A, Kucuk AO, Ulutabanca H, Menkü A, Gergin S, Oral S. The impact of the use of neuronavigation together with intraoperative ultrasonography in minimally invasive intracranial cavernous hemangioma surgery. Erciyes Med J. 2015;36(4):161–5. https://doi.org/10.5152/etd.2014.8462.
Giovani A, Brehar F, Bucur N, Martin D, Gorgan RM. Intraoperative neuronavigation integrated high resolution 3D ultrasound for brain shift and tumor resection control. Romanian Neurosurg. 2015;XXIX2:141–9.
Bergsneider M, Sehati N, Villablanca P, McArthur DL, Donald P. Extent of glioma resection using low-field (0.2 T) versus high-field (1.5 T) intraoperative MRI, and image-guided frameless neuronavigation. Clin Neurosurg. 2005;52:389–99.
Karnofsky DA, Burchenal J. The clinical evaluation of chemotherapeutic agents in cancer. New York: Columbia University Press; 1949. p. 191–205.
Camp S, Apostolopoulos V, Raptopoulos V, Nandi D. Objective image analysis of real-time three-dimensional intraoperative ultrasound for intrinsic brain tumor surgery. J Therapeutic Ultrasound. 2017;5:2–4.
Patil D, Sharma V, Tiwari VDP. Intraoperative ultrasound in intracranial space occupying lesions. World J Surg Med Radiat Oncol. 2013;8:1–5.
Moiyadi AV, Shetty PM, Mahajan A, Udare A, Sridhar E. Usefulness of three-dimensional navigable intraoperative ultrasound in resection of brain tumors with a special emphasis on malignant glioma. Acta Neurochir (Wien). 2013;155(12):2217–25.
Erdogan N, Tucer B, Mavili E, Menku A, Kurtsoy A. Ultrasound guidance in intracranial tumor resection: correlation with postoperative magnetic resonance findings. Acta Radiologica. 2005;46(7):743–9.
Wang J, Liu X, Hou WH, Dong G, Wei Z, Zhou H, Duan YY. The relationship between intraoperative ultrasonography and pathological grade in cerebral glioma. J Int Med Res. 2008;36:1426–34.
Picarelli H, Oliveira ML, Bor-Seng-Shu E, Ribas ESC, Santos AM, Teixeira MJ. Intraoperative ultrasonography for presumed brain metastasis: a case series study. Arq Neuro-psiquiatr. 2012;70(10):793–8.
Goren O, Monteith SJ, Hadani M, Bakon M, Harnof S. Modern intraoperative imaging modalities for the vascular neurosurgeon treating intracerebral hemorrhage. Neurosurg Focus. 2013;34(5):1–13.
Tang H, Sun H, Xie L, Tang Q, Gong Y, Mao Y, Xie Q, Zheng M, Wang D, Zhu H, Zhu J, Feng X, Yao Z, Chen X, Zhou L. Intraoperative ultrasound assistance in resection of intracranial meningiomas. Chin J Cancer Res. 2013;25(3):339–45.
Roth J, Biyani N, Beni-Adani CS. Real-time neuronavigation with high-quality 3D ultrasound SonoWand in pediatric neurosurgery. Pediatr Neurosurg. 2007;43(3):185–91.
El Beltagy MA, Aggag M, Kamal M. Role of intraoperative ultrasound in resection of pediatric brain tumors. Childs Nerv Syst. 2010;26(9):1189–93.
Ulrich NH, Burkhardt JK, Serra C, Bernays RL, Bozinov O. Resection of pediatric intra-cerebral tumors with the aid of intraoperative real-time 3-D ultrasound. Childs Nerv Syst. 2012;28(1):101–9.
Moiyadi AV, Shetty P, Degaonkar A. Resection of pediatric brain tumors: intraoperative ultrasound revisited. J Pediatr Neurosci. 2017;12(1):19–23.
Kanan A, Gasson B. Brain tumor resections guided by magnetic resonance imaging. AORN J. 2003;77(3):583–9.
Jani K. Intraoperative imaging-guided delineation and localization of regions of surgical interest: feasibility study. Acta Univ Oul D. 2012;1147:1–100.
Belsuzarri TAB, Sangenis RMA, Araujo JFM. Brain tumor surgery: supplemental intraoperative imaging techniques and future challenges. J Cancer Metastasis Treat. 2016;2:70–9.
Sasatry RA, Bi WL, Pieper S, Frisken SF, Kapur T, Wells WM, Golby AJ. Application of ultrasound in the resection of brain tumors. J Neuroimaging. 2017;27(1):5–15.
Roder C, Bisdas S, Ebner FH, Honegger J, Naegele T, Ernemann U, Tatagiba M. Maximizing the extent of resection and survival benefit of patients in glioblastoma surgery: high-field iMRI versus conventional, and 5-ALA- assisted surgery. Eur J Surg Oncol. 2014;40(3):297–304.
Mahboob SO, Eljamel M. Intraoperative image-guided surgery in neuro-oncology with specific focus on high-grade gliomas. Future Oncol. 2017;13(26):2349–61.
Wang J, Duan YY, Liu X, Wang Y, Gao GD, Qin HZ, Wang L. Application of intraoperative ultrasonography for guiding microneurosurgical resection of small subcortical lesions. Korean J Radiol. 2011;12(5):541–6.
Wang YI, Yong W, Dong YI, Yida W. The value of intraoperative ultrasound in neurosurgery. J Med Ultrasonic. 2006;33(1):61.
Bernstein EM, Gulati S, Solheim O, Kvistad KA, Torp SH, Selbekk T, Unsgard G, Haberg A. Functional magnetic resonance imaging and diffusion tensor tractography incorporated into 3-dimentional ultrasound based neuronavigation system: impact on therapeutic strategies, extent of resection, and clinical outcome. Neurosurgery. 2010;67(2):251–64.
Cheon JE. Intraoperative neurosonography revisited: Effective neuronavigation in pediatric neurosurgery. Ultrasonography. 2015;34(2):79–87.
Lam CH, Hall WA, Truwit CL, Liu H. Intraoperative MRI-guided approaches to pediatric posterior fossa tumors. Pediator Neurosurg. 2001;34:295–300.
It is lucky to work with the neurosurgery team at Zagazig University Hospital.
All patients operated at Zagazig university hospitals neurosurgery department for free.
Ethics approval and consent to participate
A research committee approval has been granted for this study by the medical ethics committee, Faculty of Medicine, Zagazig university at 5/1/ 2012. Informed consent according to the criteria set by the local research ethics committee in our center obtained in writing before surgery. If consent could not be obtained because the patient was in a coma or young age (< 16 years), consent was obtained from the legal guardian.
Consent for publication
Informed consents were obtained for all patients and no personal data included in this study.
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Elmesallamy, W.A.E.A. The role of intraoperative ultrasound in gross total resection of brain mass lesions and outcome. Egypt J Neurol Psychiatry Neurosurg 55, 73 (2019). https://doi.org/10.1186/s41983-019-0117-4
- Intraoperative ultrasound
- Brain mass lesions
- Gross total resection