Endoscopic Evacuation of Supratentorial Hematoma: a Hemostatic Strategy for Surgeons | Research Square window.SnipcartSettings = { analytics: { enabled: false } }; (function() { var accessVector = localStorage.getItem('access_vector') || ''; window.dataLayer = window.dataLayer || []; if (accessVector) { window.dataLayer.push({ user: { profile: { profileInfo: { snid: accessVector } } } }); } })(); (function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src='https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);})(window,document,'script','dataLayer','GTM-K279D39R'); Browse Preprints In Review Journals COVID-19 Preprints AJE Video Bytes Research Tools Research Promotion AJE Professional Editing AJE Rubriq About Preprint Platform In Review Editorial Policies Our Team Advisory Board Help Center Sign In Submit a Preprint Cite Share Download PDF Article Endoscopic Evacuation of Supratentorial Hematoma: a Hemostatic Strategy for Surgeons tiancai lan, changjin yang, yuanliang ye, jiale zhu, ruixiang wei, and 2 more This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-3984616/v1 This work is licensed under a CC BY 4.0 License Status: Posted Version 1 posted You are reading this latest preprint version Abstract Endoscopic hematoma evacuation has become well received for its high evacuation rate in patients with intracerebral hematoma. Effective hemostatic procedure is the key to the success of the procedure. Any single method cannot solve all kinds of intraoperative bleeding. The key to hemostasis is to identify the type of bleeding and take the best hemostasis method during endoscopic surgery. In our study, sixty-two intracerebral hemorrhage patients who underwent endoscopic hematoma evacuations were analyzed. Intraoperative bleeding was graded as Grades 0, 1, 2 and 3 based on characteristics of bleeding. A hemostatic strategy was created from the grading system. The efficiency was evaluated by operation time, evacuation rate, and re-bleeding rate after surgery. Procedure safety was evaluated by mortality rate and postoperative complications. We found that endoscopic removal of putamen hematoma was more prone to intraoperative bleeding (p = 0.00). Active bleeding occurred in early operative stage and errhysis happen in later stage (p = 0.00). Average evacuation rate was 95.61% and the mortality rate was 3.23%. The mean Glasgow outcome scale (GOS) score at 6-month follow-up was 3.77 ± 1.12. No patient experienced postoperative re-bleeding. These findings indicated that most patients will experience different degrees of intraoperative bleeding during endoscopic hematoma evacuation. A hemostatic strategy based on intraoperative bleeding grade resulted in efficiency and safety. Health sciences/Neurology/Neurological disorders/Neurovascular disorders/Stroke Health sciences/Diseases/Neurological disorders/Cerebrovascular disorders/Stroke Endoscopic surgery Intracerebral hemorrhage Hemostatic strategy Mortality Figures Figure 1 Figure 2 Figure 3 Introduction A spontaneous intracerebral hematoma (ICH) is one of the most deadly forms of stroke with extremely high mortality rate 1–5 . Only 20% of patients can survive in 6 months and the cost of survival is a great economic burden to everyone 6,7 . Endoscopic hematoma evacuation is an effective and safe minimal invasive technique for ICH 8–11 . Compare with craniotomy, endoscopic hematoma evacuation obtain higher evacuation rate and lower complications 11–13 . In an operation, a transparent plastic sheath is inserted into the hematoma, and the hematoma is gradually evacuated by manipulating the suction through the working space within the sheath 14,15 . However, even a careful atraumatic evacuation can result in intraoperative hemorrhage. Steep learning curve, active bleeding and limited surgical exposure are limitations of this procedure, especially for junior surgeons 14 . The incidence rate of postoperative re-bleeding can be 0–20% 15–18 . In order to prevent intraoperative bleeding, the hard blood clot adhering to hematoma cavity should not be removed with force, but leaving partial hard blood clot remain in brain may reduce the hematoma evacuation rate. Some hemostatic methods, including irrigation 19 , hemostatic matrix application 17 , compression with cotton, 15 and coagulation with bipolar 20–22 or monopolar 23 , were used to deal with intraoperative bleeding during endoscopic or microscopic hematoma evacuation. However, any single method cannot solve all kinds of intraoperative bleeding. Some bleeding may hide in normal brain tissue and can be coagulated by bipolar or monopolar, making it difficult for removal simultaneously. Moreover, unreasonable hemostatic methods can result in iatrogenic normal brain tissue injury, postoperative brain edema, and even re-bleeding. In this retrospective study, we analyzed the characteristics of intraoperative bleeding and established a hemostatic strategy based on intraoperative bleeding grade during endoscopic hematoma evacuation. We also evaluate the effectiveness and safety of this hemostatic strategy. Materials and methods Patients This study included 62 patients with supratentorial intracerebral hematoma (ICH) between January 2015 and July 2022 at the Neurosurgery Department of the Liuzhou People’s Hospital affiliated to Guangxi Medical University (Fig. 1 )..All patients underwent endoscopic hematoma evacuation with or without decompressive craniectomy. To observe the characteristics of intraoperative bleeding, the entire operative video of each patient was reviewed in detail. All methods were performed in accordance with the relevant guidelines. The study was approved by the ethics committee of the Liuzhou people’s Hospital. The need for individual consent was waived by the committee because of the retrospective nature of the study. Inclusion and Exclusion Criteria Patient selection for endoscopic evacuation of haematomas: 1) a putamen ICH with a hematoma volume greater than 30 ml; 2) a subcortical hemorrhage greater than 30 ml with significant mass effect (midline shift greater than 5 mm and compression of mesencephalic cistern) and neurological deterioration; 3) a thalamic ICH with a hematoma volume greater than 20ml and intraventricular hemorrhage (IVH) with acute hydrocephalus; 4) Hematoma removal after ruptured aneurysm embolization. Patient deselection for endoscopic evacuation of haematomas: 1) ICH caused by trauma, tumor, coagulopathy, or arteriovenous malformation; 2) patients taking antiplatelet or anticoagulation medications; 3) Hematomas was scattered, involving multiple cerebral cortex; Exclusion Criteria :1) patients who did not have operative video and without a follow-up CT scan within 3 days after surgery; 2) the patient’s family or legal representative didn’t consent to surgical treatment. Surgical Procedures For putamen ICH, we used transfrontal or transtemporal approach for hematoma evacuation. For patients with cortical hemorrhage, we used transcortical approach through the corridor that traverses the shortest distance to the center of hematoma (determined by preoperative CT scan). In patients with a thalamic ICH and IVH, we used the ipsilateral Kocher point as our entry point with free-hand technique to evacuate the blood. The surgical procedure was performed with the patient in the supine or lateral position. A single curved 4-cm skin incision was made on the entry site. A small craniotomy was widened to 20–25 mm in diameter, dura mater was incised and opened, a small sized pial incision on the cortex was performed, and then the transparent plastic sheath was inserted to the core of the hematoma (the distance based on the preoperative CT scan). The rigid endoscope measuring 0 degrees and 4 mm in diameter (Karl Storz, German) was held in left hand, while a suction cannula was held in right hand. While the assistant holding the sheath, the rigid endoscope and suction cannula were introduced into the hematoma cavity through the endoscopic corridor. The most distal part of the hematoma was evacuated first via suction. As the sheath was gradually withdrawn the residual hematoma was removed. Sometimes the hematoma was hard and was removed by forceps. When an intraoperative bleeding occurs, we adopted our hemostatic strategy based on the intraoperative bleeding grading system below. With meticulous hemostasis, a drainage tube was not routinely set into the hematoma cavity. An ICP monitor may be inserted as needed. Relationship between culprit vessels and hematoma We distinguished surrounding penetrating arteries from the bleeding vessels that caused hematoma based on their anatomic characteristics. The bleeding vessels could be inside (Fig. 2 :Type 1,a) or passed through the hematoma (Fig. 2 :Type 2,b), supplied normal brain tissues. Other kind of normal vessels were located at the edge of hematoma (Fig. 2 :Type 3,c) and adhere tightly . Grading system of intraoperative bleeding and hemostasis Table 1 presents the hemostatic strategy based on intraoperative bleeding grade intraoperative bleeding grading system used in this study. This grading system is based on bleeding speed and vessels. Grade 0 means no bleeding, water in transparent plastic sheath was clear and the scale of the sheath wall was clearly visible; Grade 1 means Errhysis, the water in the sheath was cloudy, bleeding vessels were not seen but the scale of the sheath wall was seen vaguely. Grade 2 indicates active bleeding, bleeding vessels were seen and bleeding site was located in distal segment of the vessel. Grade 3 also indicates active bleeding, bleeding site was located in junction between brain tissue and vessels. The hemostatic strategy was based on this grading system. Apply only collagen sponge or nothing at all for grade 0 bleeding (Fig. 2 :d,e); Locate and compress bleeding area for a few minutes with a hemostatic material (Absorbable oxidized regenerated cellulose Hemostat; Johnson & Johnson, Inc., Somerville, USA), and with repeated irrigation for grade 1 bleeding (Fig. 2 : f,g); Apply repeated irrigation-suction coagulation technique to found bleeding vessels for grade 2 bleeding (Fig. 2 :h,i). Hemostasis with monopolar and bipolar (after bleeding reduction) in turn and press hemostatic material at the end to found bleeding area and with repeated irrigation for grade 3 bleeding (Fig. 2 : j-m). Table 1 Grading system of intraoperative bleeding and hemostasis during endoscopic hematoma evacuation Grade Characteristics of intraoperative bleeding Hemostatic strategy Type of culprit vessels 0 No bleeding, water and mark(cotton) in transparent plastic sheath was clear only collagen sponge or nothing at all Not found 1 Errhysis, the water and mark (cotton) in the sheath was cloudy and vague, bleeding vessels can’t be seen compress bleeding area for a few minutes with a hemostatic material and with repeated irrigation Not found 2 Active bleeding, bleeding vessels were seen and bleeding site was located in distal segment of vessels. irrigation-suction coagulation technique The bleeding vessels could be inside (Type 1) or passed through the hematoma (Type 2) 3 Active bleeding, bleeding site was located in junction between brain tissue and vessels Hemostasis with monopolar and bipolar in turn and press hemostatic material with repeated irrigation The bleeding vessels were located at the edge of hematoma and adhere tightly(Type 3) Clinical and Radiological Follow-up All patients underwent a follow-up CT scan within 3 days after surgery (Fig. 2 :n-q). Endoscopic operation time, numbers of hemostasis in different grade, stage of appearance in different grade during operation-time, morbidity and mortality were recorded. Hematoma volume was measured by Slicer software and hematoma evacuation rate calculated as follows: [preoperative hematoma volume - postoperative hematoma volume]/preoperative hematoma volume × 100%. The 6-month mortality and long-term modified Rankin Scale score (mRS) were collected from patients’ medical records on re-admission, from the outpatient clinic records, or via telephone interviews. Statistical analysis All statistical analyses were performed using SPSS 22 for Windows ( SPSS Inc., Chicago, Illinois). Continuous variables were expressed as mean ± standard deviation. Categorical variables were expressed in frequency or as a percentage. Pearson’s Chisquare tests were used to determine any statistical difference about proportions. Continuous variables were compared using independent t-test or Mann–Whitney U test. A p-value of less than .05 was considered statistical significant. Results Baseline characteristics There were 62 patients enrolled in the study, including 42 cases of putamen hemorrhage, 9 cases of thalamic hemorrhage, 5 cases of intraventricular hemorrhage and 6 cases of lobar cerebral. Males and females represented 70.97% and 29.32% of patients, respectively. The mean age of the population was 53.32 ± 11.67 years. All patients underwent surgery within 24 hours of ictus. Forty-six patients underwent pure endoscopic hematoma evacuation, 16 patients were treated with hematoma evacuation and decompressive craniectomy (Table 2 ). Table 2. General data and clinical outcome of the 62 patients with spontaneous supratentorial ICH Variable Value Age(years) a 53.32 ± 11.67 Gender male female 44(70.96%) 18(29.32%) Location putamen thalamus ventricle lobar ICH volume (mL) a Pre Pro Operation time (min) a Endoscopic time Craniotomy time Blood loss a Medical morbidity Hypertension Renal insufficiency Diabetes mellitus; Entry point Transfrontal Transtemporal Transcortical Mortality rate(%) Postoperative rebleeding rate(%) a Pre-GCS Pro-GCS( 6 month) Pro-GOS( 6 month) Stage of bleeding appearance(%) a,b Grade 1 Grade 2 Grade 3 42 (67.74%) 9 (14.52%) 5 (8.06%) 6(9.68%) 53.68 ±18.90 3.19 ± 4.35 39.94±17.69 42.26±20.45 50.23±19.51 45(72.58%) 3(4.83%) 10(16.12%) 45(72.58%) 11(17.74%) 6(9.68%) 3.23 0 7.45±2.24 12.71±2.83 3.77±1.12 68.68±20.95 47.16±24.80 31.24±17.56 GCS Glasgow coma scale; GOS Glasgow outcome scale a Values are expressed as the mean ± SD; b Grade 3 bleeding occurred in early operative stage, with statistical significance(p=0.000) Intraoperative bleeding The numbers of hemostasis with patient in grade 1, 2 and 3 were 55, 18 and 24 respectively (p = 0.000) (Table 3 ). Compared with thalamic hematoma and lobar hematoma removal, endoscopic putamen hematoma removal was more prone to intraoperative bleeding (p = 0.038) (Table 3 ). When the endoscopic operating time was divided into one hundred equal parts, the average stage of bleeding appearance per patient in grade1, 2 and 3 were 68.68 ± 20.95, 47.16 ± 24.80 and 31.24 ± 17.56 respectively, these mean active bleeding occurred in early operative stage and errhysis happened later (p = 0.000) (Table 2 ). . Table 3 Characteristics of intraoperative bleeding with endoscopic hematoma evacuation Grade Operative stage Location of hematoma Early- stage Mid- stage Later-stage Putamen Thalamus Lobar 1 2(2.06) 11(11.34) 42(43.30) 37(38.14) 10(10.31) 8(8.25) 2 5(5.15) 10(10.30) 3(3.09) 30(30.93) 1(1.03) 2(2.06) 3 19(19.59) 4(4.12) 1(1.03) 22(22.68) 1(1.03) 1(1.03) χ 2 = 51.738 p = 0.000 χ 2 = 23.789 p = 0.000 Clinical outcome The mean preoperative hematoma volume was 53.68 ± 18.90 ml and the mean residual hematoma volume was 3.19 ± 4.35ml, representing an average evacuation rate of 95.61%. Endoscopic operating time was 39.94 ± 17.69 minutes (Fig. 3 ) and blood loss was 50.56 ± 20.19ml. No patient experienced postoperative re-bleeding. The mortality rate was 3.23% (2 of 62 patients), one died of renal failure, one from pneumonia and sepsis. Surgery-related morbidity wasn’t occurred in all patients. The mean preoperative Glasgow coma scale (GCS) score was 7.45 ± 2.24 and the mean GCS score 6 months after surgery was 12.71 ± 2.83. The mean GOS score at 6-month follow-up was 3.77 ± 1.12 (Table 2 ). Discussion Endoscopic surgery has been gaining popularity as a method for surgical intervention in ICH patients. Although the International Surgical Trial (STICH)in intracerebral hemorrhage study showed that emergency surgical hematoma evacuation failed to improve the outcome of ICH patient comparing with the same type of patients who received initial medical management without surgery, the STICH trial further clarify demonstrated improved outcomes with surgery for subgroups. A meta-analysis of 15 trials of surgery for ICH including STICH I and II with individual patient data showed a significant advantage for surgery. Compare with craniotomy, endoscopic hematoma evacuation obtain some advantage: (1)higher evacuation rate and lower complications;(2) exposure of deep structure and hemostasis under direct vision༛(3) maximum protection of normal brain tissue. Intraoperative bleeding during endoscopic hematoma removal is a stressful factor for surgeons. Even careful atraumatic evacuation of a hematoma can sometimes result in intraoperative hemorrhage. The principals for surgical hemostasis with intraparenchymal hematoma with endoscopic vs microscopic technique were not different. Also, whether surgery is performed through a tube (endoscopic visualization) or retractors (microscope for visualization) does not change principals of hemostasis. Some methods can be used to acquire secure hemostasis in endoscopic hematoma evacuation (Table 4 ). When an intraoperative hemorrhage occurs, the operating field was kept clear by irrigation and continuous suction. Hemorrhage from a small artery could be reduced with repeated irrigation in hematoma cavity. Another way was to compress the bleeding spot with cotton or hemostatic material for several minutes. Hemorrhage from a large artery can be stopped by coagulation with suction cannula or bipolar 10,15–17,19 . Table 4 Summary of the literature on hemostatic procedures for endoscopic evacuation of intracerebral hemorrhage Authors and years Surgical hemostatic procedures No. of pts Outcome Chad M Miller, et al. (2007) The hematoma cavity was irrigated with saline and hemostasis was inspected via endoscope 10 The re-bleeding rate was 20% and the mortality rate was 25%. Toru Nagasaka, et al. (2009) Handling of the multifunctional suction cannula and its application for balanced irrigation-suction 15 No surgical complications or re-bleeding occurred. Lu-Ting Kuo, et al. (2011) Most bleeding from these perforators stopped after gentle compression with cotton and irrigation for 2 minutes 68 The re-bleeding rate was 1.5% and the mortality rate was 5.9%. Hongwei Zhu, et al. (2012) Hemostasis was achieved by continuous saline irrigation, pressure packing and electrically coagulated with a suction cannula 28 The re-bleeding rate was 3.6% and the mortality rate was 7.1%. Wei-Hsin Wang, et al. (2015) Hemostasis was achieved by hemostatic agents or used bipolar forceps with the endoscope held by an assistant or holder 21 The re-bleeding rate was 9.52% and the mortality rate was 9.52%. Hui-Tzung Luh, et al. (2018) FloSeal Hemostatic Matrix was applied through a specialized 3-mm flexible catheter into the hematoma cavity. 42 The re-bleeding rate was 4.8% and the mortality rate was 7.1%. Present study Hemostatic strategy for endoscopic evacuation of intracerebral hematoma based on intraoperative bleeding grading system 62 No patient experienced postoperative re-bleeding and the mortality rate was 3.23% As we know, single or multiple branches of the penetrating arteries are responsible for cerebral bleeding. The causes of hemorrhages include arteriosclerosis, arterial dissection and micro-aneurysm formation, etc. 24–26 . The lenticulostriate arteries (LSA) represent one of the largest groups of perforating vessels in the brain and divided into two groups (medial and later) based on the originative location of the vessels 27 . The lenticulostriate arteries originate from the middle cerebral artery (MCA), and then turn sharply medial, make a loop, and penetrate anterior perforated substance into the brain 28 . Intracerebral segments of the LSA supply the Putamen, lateral segment of Globus Pallidus and internal capsule 29 . The diameter of lenticulostriate arteries vary from 0.7um to 2.2mm 30 . The intraoperative hemorrhage is often iatrogenic induce by injury of perforating vessels inside or outside the hematoma. Based on the anatomic characteristics of penetrating arteries, the relationship between the hematoma/brain tissue and the penetrating arteries can been speculated. For the intracerebral hematoma, the bleeding vessels can run inside or passed through the hematoma, supplying normal brain tissues. Other kind of normal vessels are located at the edge of hematoma and adhere tightly. When encountering intraoperative hemorrhage, the best choice of hemostatic method can be bewildered especially for inexperienced surgeons. It was invalid in active hemorrhage with the methods of observation and compression. Errhysis with coagulation would transfer to active hemorrhage because of brain tissue damage around small arteries. When active hemorrhage occurs, the operating field is filled with blood quickly, bipolar was difficult to use because of narrow corridor and visual control deteriorates. Based on intraventricular vision, some researches presented grading system and a step by step guide for the endoscopic management of intraoperative hemorrhages during intraventricular tumor surgery 31,32 . Based on the surgical sites, anatomical structure and bleeding vessels between the intraventricular surgery and intracerebral hematoma, we established a simple intraoperative bleeding grading system during endoscopic hematoma remove. This grading system can guide inexperienced surgeon to choose optimum hemostatic method and is safe and effective. The following points warrant attention with intraoperative bleeding grading system and hemostasis. First, to distinguish no bleeding, errhysis and active bleeding based on the characteristics of the water in transparent plastic sheath. No bleeding means clear water. Errhysis means light-red cloudy water and fuzzy reference (cotton or scale on the sheath). Active bleeding included red and muddy water, even malignant hemorrhage. Second, to find bleeding site or vessels through repeated irrigation and continuous suction, to coagulate the bleeder by touching the suction with appropriative power of monopolar. Third, to reduce the damage of normal brain tissue in Grade3 by using the outer wall of suction (not the tip) to touch the bleeding site. In our study, the concept of hematoma removal was to avoid following the brain parenchyma–hematoma junction during hematoma evacuation, therefore, the incidence of Grade3 was less than that of Grade1 and Grade2. The perforator vessels were located in the bottom of the hematoma and the lower part of the hematoma was removed first, so that the period in Grade3 was earlier than Grade1. Limitations The major strength of this study was to provide an alternative hemostatic strategy to neurosurgeons. A hemostatic strategy based on intraoperative bleeding grade resulted in efficiency and safety. The present study has some limitations. Firstly, evaluation of bleeding in endoscopy was largely subjective and likely to have interobserver variations. Secondly, the hemostatic strategy was dependent upon the intraoperative bleeding grading system, which could introduce a bias. In addition, more clinical experience was necessary to determine whether this strategy improves surgical outcomes. Conclusion Active bleeding occurs in early operative stage and errhysis happens in late stage. Hemostatic strategy based on intraoperative bleeding grading system can guide surgeon to choose the right hemostatic methods, shorten the operation time, and seems to be safe and effective, especially for inexperienced surgeons. Abbreviations ICH = intracerebral hematoma. Declarations Acknowledgements This work was supported by the key Clinical Research of Guangxi [Grant No. ], the Clinical Research of Liuzhou [Grant No.2021CBB0103], the Clinical Research of Liuzhou General Hospital [Grant No. LRYGCC202120] Authors' contributions Conception and design: TC Lan, CJ Yang. Acquisition of data: ST Liu, CM Wang Analysis and interpretation of data: JL Zhu, RX Wei. Drafting the article: YL Ye Critically revising the article: all authors. Reviewed submitted version of manuscript: all authors. Approved the final version of the manuscript on behalf of all authors: Statistical analysis: CM Wang. Study supervision: YL Ye, GR Ma. Competing interests The authors report no conflict of interest concerning the materials or methods used in this study or the findings specified in this paper. Data availability The datasets used and/or analysed during the current study available from the corresponding author on reasonable request. Ethics approval and consent to participate The study was approved by the ethics committee of the Liuzhou people’s Hospital. The need for individual consent was waived by the committee because of the retrospective nature of the study Authors' contributions Conception and design: TC Lan, CJ Yang. Acquisition of data: CM Wang. Analysis and interpretation of data: JL Zhu, RX Wei. Drafting the article: YL Ye Critically revising the article: all authors. Reviewed submitted version of manuscript: all authors. Approved the final version of the manuscript on behalf of all authors: Statistical analysis: CM Wang. Study supervision: YL Ye, GR Ma. References Adeeb, N. et al. The intracranial arachnoid mater : a comprehensive review of its history, anatomy, imaging, and pathology. Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 29 , 17–33, doi:10.1007/s00381-012-1910-x (2013). Hostettler, I. C., Seiffge, D. J. & Werring, D. J. Intracerebral hemorrhage: an update on diagnosis and treatment. Expert review of neurotherapeutics 19 , 679–694, doi:10.1080/14737175.2019.1623671 (2019). Malhotra, K. et al. Prevalence, Characteristics, and Outcomes of Undetermined Intracerebral Hemorrhage: A Systematic Review and Meta-Analysis. Stroke 52 , 3602–3612, doi:10.1161/strokeaha.120.031471 (2021). Hemphill, J. C., 3rd et al. Guidelines for the Management of Spontaneous Intracerebral Hemorrhage: A Guideline for Healthcare Professionals From the American Heart Association/American Stroke Association. Stroke 46 , 2032–2060, doi:10.1161/str.0000000000000069 (2015). Gross, B. A., Jankowitz, B. T. & Friedlander, R. M. Cerebral Intraparenchymal Hemorrhage: A Review. Jama 321 , 1295–1303, doi:10.1001/jama.2019.2413 (2019). Adeoye, O. & Broderick, J. P. Advances in the management of intracerebral hemorrhage. Nature reviews. Neurology 6 , 593–601, doi:10.1038/nrneurol.2010.146 (2010). Russell, M. W., Boulanger, L., Joshi, A. V., Neumann, P. J. & Menzin, J. The economic burden of intracerebral hemorrhage: evidence from managed care. Managed care interface 19 , 24–28, 34 (2006). Ye, Y., Wang, Q., Ou, W., He, J. & Zhao, Z. Endoscopic Surgery Without Decompressive Craniectomy in Large Putaminal Intracerebral Hemorrhage: Assessment of Efficacy and Safety. Neurocritical care 32 , 392–399, doi:10.1007/s12028-019-00880-8 (2020). Sun, G. C. et al. Image-guided endoscopic surgery for spontaneous supratentorial intracerebral hematoma. Journal of neurosurgery 127 , 537–542, doi:10.3171/2016.7.jns16932 (2017). Orakcioglu, B., Beynon, C., Bösel, J., Stock, C. & Unterberg, A. W. Minimally invasive endoscopic surgery for treatment of spontaneous intracerebral hematomas: a single-center analysis. Neurocritical care 21 , 407–416, doi:10.1007/s12028-014-9987-6 (2014). Kellner, C. P. et al. Time to Evacuation and Functional Outcome After Minimally Invasive Endoscopic Intracerebral Hemorrhage Evacuation. Stroke 52 , e536-e539, doi:10.1161/strokeaha.121.034392 (2021). Xu, X. et al. Effectiveness of endoscopic surgery for supratentorial hypertensive intracerebral hemorrhage: a comparison with craniotomy. Journal of neurosurgery 128 , 553–559, doi:10.3171/2016.10.jns161589 (2018). Sun, S. et al. Neuroendoscopic Surgery versus Craniotomy for Supratentorial Hypertensive Intracerebral Hemorrhage: A Systematic Review and Meta-Analysis. World neurosurgery 134 , 477–488, doi:10.1016/j.wneu.2019.10.115 (2020). Ma, L., Hou, Y., Zhu, R. & Chen, X. Endoscopic Evacuation of Basal Ganglia Hematoma: Surgical Technique, Outcome, and Learning Curve. World neurosurgery 101 , 57–68, doi:10.1016/j.wneu.2017.01.072 (2017). Kuo, L. T. et al. Early endoscope-assisted hematoma evacuation in patients with supratentorial intracerebral hemorrhage: case selection, surgical technique, and long-term results. Neurosurgical focus 30 , E9, doi:10.3171/2011.2.focus10313 (2011). Sadahiro, H. et al. Real-time ultrasound-guided endoscopic surgery for putaminal hemorrhage. Journal of neurosurgery 123 , 1151–1155, doi:10.3171/2014.11.Jns141508 (2015). Luh, H. T. et al. Local hemostatic matrix for endoscope-assisted removal of intracerebral hemorrhage is safe and effective. Journal of the Formosan Medical Association = Taiwan yi zhi 117 , 63–70, doi:10.1016/j.jfma.2017.02.016 (2018). Xu, X. et al. Comparison of endoscopic evacuation, stereotactic aspiration and craniotomy for the treatment of supratentorial hypertensive intracerebral haemorrhage: study protocol for a randomised controlled trial. Trials 18 , 296, doi:10.1186/s13063-017-2041-1 (2017). Nagasaka, T. et al. Balanced irrigation-suction technique with a multifunctional suction cannula and its application for intraoperative hemorrhage in endoscopic evacuation of intracerebral hematomas: technical note. Neurosurgery 65 , E826-827; discussion E827, doi:10.1227/01.Neu.0000350985.58062.3f (2009). Wang, W. H. et al. Endoscopic hematoma evacuation in patients with spontaneous supratentorial intracerebral hemorrhage. Journal of the Chinese Medical Association : JCMA 78 , 101–107, doi:10.1016/j.jcma.2014.08.013 (2015). Hsieh, P. C. Endoscopic removal of thalamic hematoma: a technical note. Minimally invasive neurosurgery : MIN 46 , 369–371, doi:10.1055/s-2003-812505 (2003). Angileri, F. F. et al. Fully Endoscopic Freehand Evacuation of Spontaneous Supratentorial Intraparenchymal Hemorrhage. World neurosurgery 94 , 268–272, doi:10.1016/j.wneu.2016.07.015 (2016). Nagasaka, T., Inao, S., Ikeda, H., Tsugeno, M. & Okamoto, T. Inflation-deflation method for endoscopic evacuation of intracerebral haematoma. Acta neurochirurgica 150 , 685–690; discussion 690, doi:10.1007/s00701-008-1561-6 (2008). Takebayashi, S. & Kaneko, M. Electron microscopic studies of ruptured arteries in hypertensive intracerebral hemorrhage. Stroke 14 , 28–36, doi:10.1161/01.str.14.1.28 (1983). Komiyama, M. et al. Simultaneous bleeding from multiple lenticulostriate arteries in hypertensive intracerebral haemorrhage. Neuroradiology 37 , 129–130, doi:10.1007/bf00588628 (1995). Mizutani, T., Kojima, H. & Miki, Y. Arterial dissections of penetrating cerebral arteries causing hypertension-induced cerebral hemorrhage. Journal of neurosurgery 93 , 859–862, doi:10.3171/jns.2000.93.5.0859 (2000). Marinković, S. et al. Structure and immunohistochemistry of the human lenticulostriate arteries. Folia morphologica 72 , 210–216, doi:10.5603/fm.2013.0035 (2013). Djulejić, V. et al. Morphometric analysis, region of supply and microanatomy of the lenticulostriate arteries and their clinical significance. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 19 , 1416–1421, doi:10.1016/j.jocn.2011.10.025 (2012). Hu, R. & Feng, H. Lenticulostriate Artery and Lenticulostriate-artery Neural Complex: New Concept for Intracerebral Hemorrhage. Current pharmaceutical design 23 , 2206–2211, doi:10.2174/1381612823666170220163750 (2017). Seo, S. W. et al. Measurements of lenticulostriate arteries using 7T MRI: new imaging markers for subcortical vascular dementia. Journal of the neurological sciences 322 , 200–205, doi:10.1016/j.jns.2012.05.032 (2012). Oertel, J., Linsler, S., Csokonay, A., Schroeder, H. W. S. & Senger, S. Management of severe intraoperative hemorrhage during intraventricular neuroendoscopic procedures: the dry field technique. Journal of neurosurgery 131 , 931–935, doi:10.3171/2018.4.Jns172537 (2018). Oertel, J., Linsler, S., Strohm, L. & Senger, S. Management of severe intraoperative hemorrhage during intraventricular neuroendoscopic procedures: the dry field technique. Acta Neurochir (Wien) 164 , 2551–2557, doi:10.1007/s00701-022-05207-9 (2022). Additional Declarations No competing interests reported. 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Also discoverable on Platform About Our Team In Review Editorial Policies Advisory Board Help Center Resources Author Services Accessibility API Access RSS feed Manage Cookie Preferences © Research Square 2026 | ISSN 2693-5015 (online) Privacy Policy Terms of Service Do Not Sell My Personal Information {"props":{"pageProps":{"initialData":{"identity":"rs-3984616","acceptedTermsAndConditions":true,"allowDirectSubmit":true,"archivedVersions":[],"articleType":"Article","associatedPublications":[],"authors":[{"id":280956277,"identity":"fdf3e9f9-f499-4eb2-b39c-d774ae9813c8","order_by":0,"name":"tiancai lan","email":"","orcid":"","institution":"Liuzhou People’s Hospital","correspondingAuthor":false,"prefix":"","firstName":"tiancai","middleName":"","lastName":"lan","suffix":""},{"id":280956278,"identity":"d848ab0f-c5eb-4059-885b-71b80ad9a7c4","order_by":1,"name":"changjin yang","email":"","orcid":"","institution":"Liuzhou People’s Hospital","correspondingAuthor":false,"prefix":"","firstName":"changjin","middleName":"","lastName":"yang","suffix":""},{"id":280956279,"identity":"28ae4d03-a83f-4f6c-8cec-cf06cfe812ab","order_by":2,"name":"yuanliang ye","email":"","orcid":"","institution":"Liuzhou People’s Hospital","correspondingAuthor":false,"prefix":"","firstName":"yuanliang","middleName":"","lastName":"ye","suffix":""},{"id":280956280,"identity":"0fcafc60-9da4-4696-9e5e-c437a83440b0","order_by":3,"name":"jiale zhu","email":"","orcid":"","institution":"Liuzhou People’s Hospital","correspondingAuthor":false,"prefix":"","firstName":"jiale","middleName":"","lastName":"zhu","suffix":""},{"id":280956281,"identity":"78a3a81b-8311-4757-9345-4fffcc64c9e3","order_by":4,"name":"ruixiang wei","email":"","orcid":"","institution":"Liuzhou People’s Hospital","correspondingAuthor":false,"prefix":"","firstName":"ruixiang","middleName":"","lastName":"wei","suffix":""},{"id":280956282,"identity":"70a3ae2e-cc37-4c55-a2d0-f6202695820f","order_by":5,"name":"Chuanming Wang","email":"","orcid":"","institution":"University of Science and Technology Union Shenzhen Hospital","correspondingAuthor":false,"prefix":"","firstName":"Chuanming","middleName":"","lastName":"Wang","suffix":""},{"id":280956283,"identity":"83971ae7-94c9-42fa-951f-8716b0c7ae03","order_by":6,"name":"Guirong Ma","email":"data:image/png;base64,iVBORw0KGgoAAAANSUhEUgAAAZAAAAAyAQMAAABI0h/eAAAABlBMVEX///8AAABVwtN+AAAACXBIWXMAAA7EAAAOxAGVKw4bAAAAzElEQVRIiWNgGAWjYBAC+/bmA4YfKiTq+9kbiNRiwHMsoVjijAXjzJ4DxGqRyDH4wNtWwbjhRgKRWswlEgw3SLZJMBvcfLzxBkONTTRBLZY9D5INCs5JsEneTiu2YDiWlttAUM/xhGMGEmUSPHy3c8wkGBsOE6HlQGL7Dx42CQmGm2eI1GJwIhkYam0SBgI3eIjUItlzjMFY4oxEgmQP0C8JxPiFn73/AzAq6xL42Q9vvPGhxoYIvyA7UiKBFOUQLaTqGAWjYBSMgpEBAJBaQhDWNg1GAAAAAElFTkSuQmCC","orcid":"","institution":"Liuzhou People’s Hospital","correspondingAuthor":true,"prefix":"","firstName":"Guirong","middleName":"","lastName":"Ma","suffix":""}],"badges":[],"createdAt":"2024-02-24 10:14:28","currentVersionCode":1,"declarations":"","doi":"10.21203/rs.3.rs-3984616/v1","doiUrl":"https://doi.org/10.21203/rs.3.rs-3984616/v1","draftVersion":[],"editorialEvents":[],"editorialNote":"","failedWorkflow":false,"files":[{"id":53014649,"identity":"0c7e97ee-56c8-49c8-be93-8741592f7560","added_by":"auto","created_at":"2024-03-19 15:53:05","extension":"png","order_by":1,"title":"Figure 1","display":"","copyAsset":false,"role":"figure","size":194989,"visible":true,"origin":"","legend":"\u003cp\u003eSTROBE flowchart of Supratentorial Hematoma.\u003c/p\u003e","description":"","filename":"OnlineFigure1.png","url":"https://assets-eu.researchsquare.com/files/rs-3984616/v1/eff8d2300683885a2e0063bc.png"},{"id":53014648,"identity":"de9125ba-5fbf-409f-a801-8cb7a6de0c4c","added_by":"auto","created_at":"2024-03-19 15:53:05","extension":"jpg","order_by":2,"title":"Figure 2","display":"","copyAsset":false,"role":"figure","size":2398954,"visible":true,"origin":"","legend":"\u003cp\u003eSchematic diagram illustrating the intraoperative culprit vessels, grading system of intraoperative bleeding and clinical outcome. The bleeding vessels could be inside (Type 1, a) or passing through (Type 2,b) or at the edge of the hematoma (Type 3,c). Grading system based on bleeding speed and vessels: grade 0, no bleeding with collagen sponge only (d.e); grade 1, active bleeding with the hemostatic material (f,g); grade 2, active bleeding site located in distal segment of vessel, hemostasis with irrigation-suction coagulation technique (h,i); grade 3, active bleeding site located in junction between brain tissue and vessels, hemostasis with monopolar coagulation, bipolar and pressure hemostatic material at last (j-m) . Clinical cases with no re-bleeding after surgery (n-q).\u003c/p\u003e","description":"","filename":"Figure2.jpg","url":"https://assets-eu.researchsquare.com/files/rs-3984616/v1/9857072c09ec26a179613774.jpg"},{"id":53014647,"identity":"1a7025ff-4dbd-46c4-8e23-25457d354339","added_by":"auto","created_at":"2024-03-19 15:53:05","extension":"png","order_by":3,"title":"Figure 3","display":"","copyAsset":false,"role":"figure","size":131469,"visible":true,"origin":"","legend":"\u003cp\u003eComparing with Hsieh PC\u003cem\u003e etal\u003c/em\u003e\u003csup\u003e2\u003c/sup\u003e\u003cem\u003e \u003c/em\u003eand Ma LC\u003cem\u003e etal\u003c/em\u003e\u003csup\u003e14\u003c/sup\u003e, Endoscopic surgery for \u0026nbsp;intracerebral hemorrhage with grading system of intraoperative bleeding and hemostasis required shorter operation time.\u003c/p\u003e","description":"","filename":"OnlineFigure3.png","url":"https://assets-eu.researchsquare.com/files/rs-3984616/v1/215f8229ca80b12a6b7d670a.png"},{"id":54814304,"identity":"86fc9304-2921-4cdf-8aa2-d484e74bf362","added_by":"auto","created_at":"2024-04-17 07:00:44","extension":"pdf","order_by":0,"title":"","display":"","copyAsset":false,"role":"manuscript-pdf","size":694441,"visible":true,"origin":"","legend":"","description":"","filename":"manuscript.pdf","url":"https://assets-eu.researchsquare.com/files/rs-3984616/v1/93fde83b-2dfe-4a59-aa88-2ec37ea96002.pdf"}],"financialInterests":"No competing interests reported.","formattedTitle":"Endoscopic Evacuation of Supratentorial Hematoma: a Hemostatic Strategy for Surgeons","fulltext":[{"header":"Introduction","content":"\u003cp\u003eA spontaneous intracerebral hematoma (ICH) is one of the most deadly forms of stroke with extremely high mortality rate \u003csup\u003e1\u0026ndash;5\u003c/sup\u003e. Only 20% of patients can survive in 6 months and the cost of survival is a great economic burden to everyone \u003csup\u003e6,7\u003c/sup\u003e. Endoscopic hematoma evacuation is an effective and safe minimal invasive technique for ICH \u003csup\u003e8\u0026ndash;11\u003c/sup\u003e. Compare with craniotomy, endoscopic hematoma evacuation obtain higher evacuation rate and lower complications \u003csup\u003e11\u0026ndash;13\u003c/sup\u003e.\u003c/p\u003e \u003cp\u003eIn an operation, a transparent plastic sheath is inserted into the hematoma, and the hematoma is gradually evacuated by manipulating the suction through the working space within the sheath \u003csup\u003e14,15\u003c/sup\u003e. However, even a careful atraumatic evacuation can result in intraoperative hemorrhage. Steep learning curve, active bleeding and limited surgical exposure are limitations of this procedure, especially for junior surgeons \u003csup\u003e14\u003c/sup\u003e. The incidence rate of postoperative re-bleeding can be 0\u0026ndash;20% \u003csup\u003e15\u0026ndash;18\u003c/sup\u003e.\u003c/p\u003e \u003cp\u003eIn order to prevent intraoperative bleeding, the hard blood clot adhering to hematoma cavity should not be removed with force, but leaving partial hard blood clot remain in brain may reduce the hematoma evacuation rate. Some hemostatic methods, including irrigation \u003csup\u003e19\u003c/sup\u003e, hemostatic matrix application \u003csup\u003e17\u003c/sup\u003e, compression with cotton, \u003csup\u003e15\u003c/sup\u003e and coagulation with bipolar \u003csup\u003e20\u0026ndash;22\u003c/sup\u003e or monopolar \u003csup\u003e23\u003c/sup\u003e, were used to deal with intraoperative bleeding during endoscopic or microscopic hematoma evacuation. However, any single method cannot solve all kinds of intraoperative bleeding. Some bleeding may hide in normal brain tissue and can be coagulated by bipolar or monopolar, making it difficult for removal simultaneously. Moreover, unreasonable hemostatic methods can result in iatrogenic normal brain tissue injury, postoperative brain edema, and even re-bleeding.\u003c/p\u003e \u003cp\u003eIn this retrospective study, we analyzed the characteristics of intraoperative bleeding and established a hemostatic strategy based on intraoperative bleeding grade during endoscopic hematoma evacuation. We also evaluate the effectiveness and safety of this hemostatic strategy.\u003c/p\u003e"},{"header":"Materials and methods","content":"\u003cp\u003ePatients\u003c/p\u003e \u003cp\u003eThis study included 62 patients with supratentorial intracerebral hematoma (ICH) between January 2015 and July 2022 at the Neurosurgery Department of the Liuzhou People\u0026rsquo;s Hospital affiliated to Guangxi Medical University (Fig.\u0026nbsp;\u003cspan refid=\"Fig1\" class=\"InternalRef\"\u003e1\u003c/span\u003e)..All patients underwent endoscopic hematoma evacuation with or without decompressive craniectomy. To observe the characteristics of intraoperative bleeding, the entire operative video of each patient was reviewed in detail. All methods were performed in accordance with the relevant guidelines. The study was approved by the ethics committee of the Liuzhou people\u0026rsquo;s Hospital. The need for individual consent was waived by the committee because of the retrospective nature of the study.\u003c/p\u003e \u003cp\u003e \u003c/p\u003e \u003cp\u003eInclusion and Exclusion Criteria\u003c/p\u003e \u003cp\u003ePatient selection for endoscopic evacuation of haematomas: 1) a putamen ICH with a hematoma volume greater than 30 ml; 2) a subcortical hemorrhage greater than 30 ml with significant mass effect (midline shift greater than 5 mm and compression of mesencephalic cistern) and neurological deterioration; 3) a thalamic ICH with a hematoma volume greater than 20ml and intraventricular hemorrhage (IVH) with acute hydrocephalus; 4) Hematoma removal after ruptured aneurysm embolization. Patient deselection for endoscopic evacuation of haematomas: 1) ICH caused by trauma, tumor, coagulopathy, or arteriovenous malformation; 2) patients taking antiplatelet or anticoagulation medications; 3) Hematomas was scattered, involving multiple cerebral cortex; Exclusion Criteria :1) patients who did not have operative video and without a follow-up CT scan within 3 days after surgery; 2) the patient\u0026rsquo;s family or legal representative didn\u0026rsquo;t consent to surgical treatment.\u003c/p\u003e \u003cp\u003eSurgical Procedures\u003c/p\u003e \u003cp\u003eFor putamen ICH, we used transfrontal or transtemporal approach for hematoma evacuation. For patients with cortical hemorrhage, we used transcortical approach through the corridor that traverses the shortest distance to the center of hematoma (determined by preoperative CT scan). In patients with a thalamic ICH and IVH, we used the ipsilateral Kocher point as our entry point with free-hand technique to evacuate the blood. The surgical procedure was performed with the patient in the supine or lateral position. A single curved 4-cm skin incision was made on the entry site. A small craniotomy was widened to 20\u0026ndash;25 mm in diameter, dura mater was incised and opened, a small sized pial incision on the cortex was performed, and then the transparent plastic sheath was inserted to the core of the hematoma (the distance based on the preoperative CT scan). The rigid endoscope measuring 0 degrees and 4 mm in diameter (Karl Storz, German) was held in left hand, while a suction cannula was held in right hand. While the assistant holding the sheath, the rigid endoscope and suction cannula were introduced into the hematoma cavity through the endoscopic corridor. The most distal part of the hematoma was evacuated first via suction. As the sheath was gradually withdrawn the residual hematoma was removed. Sometimes the hematoma was hard and was removed by forceps. When an intraoperative bleeding occurs, we adopted our hemostatic strategy based on the intraoperative bleeding grading system below. With meticulous hemostasis, a drainage tube was not routinely set into the hematoma cavity. An ICP monitor may be inserted as needed.\u003c/p\u003e \u003cp\u003eRelationship between culprit vessels and hematoma\u003c/p\u003e \u003cp\u003eWe distinguished surrounding penetrating arteries from the bleeding vessels that caused hematoma based on their anatomic characteristics. The bleeding vessels could be inside (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003e:Type 1,a) or passed through the hematoma (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003e:Type 2,b), supplied normal brain tissues. Other kind of normal vessels were located at the edge of hematoma (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003e:Type 3,c) and adhere tightly .\u003c/p\u003e \u003cp\u003e \u003c/p\u003e \u003cp\u003eGrading system of intraoperative bleeding and hemostasis\u003c/p\u003e \u003cp\u003eTable\u0026nbsp;\u003cspan refid=\"Tab1\" class=\"InternalRef\"\u003e1\u003c/span\u003e presents the hemostatic strategy based on intraoperative bleeding grade intraoperative bleeding grading system used in this study. This grading system is based on bleeding speed and vessels. Grade 0 means no bleeding, water in transparent plastic sheath was clear and the scale of the sheath wall was clearly visible; Grade 1 means Errhysis, the water in the sheath was cloudy, bleeding vessels were not seen but the scale of the sheath wall was seen vaguely. Grade 2 indicates active bleeding, bleeding vessels were seen and bleeding site was located in distal segment of the vessel. Grade 3 also indicates active bleeding, bleeding site was located in junction between brain tissue and vessels. The hemostatic strategy was based on this grading system. Apply only collagen sponge or nothing at all for grade 0 bleeding (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003e:d,e); Locate and compress bleeding area for a few minutes with a hemostatic material (Absorbable oxidized regenerated cellulose Hemostat; Johnson \u0026amp; Johnson, Inc., Somerville, USA), and with repeated irrigation for grade 1 bleeding (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003e: f,g); Apply repeated irrigation-suction coagulation technique to found bleeding vessels for grade 2 bleeding (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003e :h,i). Hemostasis with monopolar and bipolar (after bleeding reduction) in turn and press hemostatic material at the end to found bleeding area and with repeated irrigation for grade 3 bleeding (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003e: j-m).\u003c/p\u003e \u003cp\u003e \u003cdiv class=\"gridtable\"\u003e\u003ctable float=\"Yes\" id=\"Tab1\" border=\"1\"\u003e \u003ccaption language=\"En\"\u003e \u003cdiv class=\"CaptionNumber\"\u003eTable 1\u003c/div\u003e \u003cdiv class=\"CaptionContent\"\u003e \u003cp\u003eGrading system of intraoperative bleeding and hemostasis during endoscopic hematoma evacuation\u003c/p\u003e \u003c/div\u003e \u003c/caption\u003e \u003ccolgroup cols=\"4\"\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c1\" colnum=\"1\"\u003e\u003c/div\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c2\" colnum=\"2\"\u003e\u003c/div\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c3\" colnum=\"3\"\u003e\u003c/div\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c4\" colnum=\"4\"\u003e\u003c/div\u003e \u003cthead\u003e \u003ctr\u003e \u003cth align=\"left\" colname=\"c1\"\u003e \u003cp\u003eGrade\u003c/p\u003e \u003c/th\u003e \u003cth align=\"left\" colname=\"c2\"\u003e \u003cp\u003eCharacteristics of intraoperative bleeding\u003c/p\u003e \u003c/th\u003e \u003cth align=\"left\" colname=\"c3\"\u003e \u003cp\u003eHemostatic strategy\u003c/p\u003e \u003c/th\u003e \u003cth align=\"left\" colname=\"c4\"\u003e \u003cp\u003eType of culprit vessels\u003c/p\u003e \u003c/th\u003e \u003c/tr\u003e \u003c/thead\u003e \u003ctbody\u003e \u003ctr\u003e \u003ctd align=\"left\" colname=\"c1\"\u003e \u003cp\u003e0\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c2\"\u003e \u003cp\u003eNo bleeding, water and mark(cotton) in transparent plastic sheath was clear\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c3\"\u003e \u003cp\u003eonly collagen sponge or nothing at all\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c4\"\u003e \u003cp\u003eNot found\u003c/p\u003e \u003c/td\u003e \u003c/tr\u003e \u003ctr\u003e \u003ctd align=\"left\" colname=\"c1\"\u003e \u003cp\u003e1\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c2\"\u003e \u003cp\u003eErrhysis, the water and mark (cotton) in the sheath was cloudy and vague, bleeding vessels can\u0026rsquo;t be seen\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c3\"\u003e \u003cp\u003ecompress bleeding area for a few minutes with a hemostatic material and with repeated irrigation\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c4\"\u003e \u003cp\u003eNot found\u003c/p\u003e \u003c/td\u003e \u003c/tr\u003e \u003ctr\u003e \u003ctd align=\"left\" colname=\"c1\"\u003e \u003cp\u003e2\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c2\"\u003e \u003cp\u003eActive bleeding, bleeding vessels were seen and bleeding site was located in distal segment of vessels.\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c3\"\u003e \u003cp\u003eirrigation-suction coagulation technique\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c4\"\u003e \u003cp\u003eThe bleeding vessels could be inside (Type 1) or passed through the hematoma (Type 2)\u003c/p\u003e \u003c/td\u003e \u003c/tr\u003e \u003ctr\u003e \u003ctd align=\"left\" colname=\"c1\"\u003e \u003cp\u003e3\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c2\"\u003e \u003cp\u003eActive bleeding, bleeding site was located in junction between brain tissue and vessels\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c3\"\u003e \u003cp\u003eHemostasis with monopolar and bipolar in turn and press hemostatic material with repeated irrigation\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c4\"\u003e \u003cp\u003eThe bleeding vessels were located at the edge of hematoma and adhere tightly(Type 3)\u003c/p\u003e \u003c/td\u003e \u003c/tr\u003e \u003c/tbody\u003e \u003c/colgroup\u003e \u003c/table\u003e\u003c/div\u003e \u003c/p\u003e \u003cp\u003eClinical and Radiological Follow-up\u003c/p\u003e \u003cp\u003eAll patients underwent a follow-up CT scan within 3 days after surgery (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003e:n-q). Endoscopic operation time, numbers of hemostasis in different grade, stage of appearance in different grade during operation-time, morbidity and mortality were recorded. Hematoma volume was measured by Slicer software and hematoma evacuation rate calculated as follows: [preoperative hematoma volume - postoperative hematoma volume]/preoperative hematoma volume \u0026times; 100%. The 6-month mortality and long-term modified Rankin Scale score (mRS) were collected from patients\u0026rsquo; medical records on re-admission, from the outpatient clinic records, or via telephone interviews.\u003c/p\u003e \u003cdiv id=\"Sec3\" class=\"Section2\"\u003e \u003ch2\u003eStatistical analysis\u003c/h2\u003e \u003cp\u003eAll statistical analyses were performed using \u003cem\u003eSPSS\u003c/em\u003e 22 for Windows (\u003cem\u003eSPSS\u003c/em\u003e Inc., Chicago, Illinois). Continuous variables were expressed as mean\u0026thinsp;\u0026plusmn;\u0026thinsp;standard deviation. Categorical variables were expressed in frequency or as a percentage. Pearson\u0026rsquo;s Chisquare tests were used to determine any statistical difference about proportions. Continuous variables were compared using independent t-test or Mann\u0026ndash;Whitney U test. A p-value of less than .05 was considered statistical significant.\u003c/p\u003e \u003c/div\u003e"},{"header":"Results","content":"\u003cp\u003eBaseline characteristics\u003c/p\u003e \u003cp\u003eThere were 62 patients enrolled in the study, including 42 cases of putamen hemorrhage, 9 cases of thalamic hemorrhage, 5 cases of intraventricular hemorrhage and 6 cases of lobar cerebral. Males and females represented 70.97% and 29.32% of patients, respectively. The mean age of the population was 53.32\u0026thinsp;\u0026plusmn;\u0026thinsp;11.67 years. All patients underwent surgery within 24 hours of ictus. Forty-six patients underwent pure endoscopic hematoma evacuation, 16 patients were treated with hematoma evacuation and decompressive craniectomy (Table\u0026nbsp;\u003cspan refid=\"Tab2\" class=\"InternalRef\"\u003e2\u003c/span\u003e).\u003c/p\u003e \u003cp\u003e\u003cstrong\u003eTable 2.\u0026nbsp;\u003c/strong\u003eGeneral data and clinical outcome of the 62 patients with\u0026nbsp;spontaneous supratentorial ICH\u003c/p\u003e\n\u003ctable border=\"1\" cellspacing=\"0\" cellpadding=\"0\"\u003e\n \u003ctbody\u003e\n \u003ctr\u003e\n \u003ctd width=\"61.023622047244096%\" valign=\"top\"\u003e\n \u003cp\u003eVariable\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"38.976377952755904%\" valign=\"top\"\u003e\n \u003cp\u003eValue\u003c/p\u003e\n \u003c/td\u003e\n \u003c/tr\u003e\n \u003ctr\u003e\n \u003ctd width=\"61.023622047244096%\" valign=\"top\"\u003e\n \u003cp\u003eAge(years)\u003csup\u003ea\u0026nbsp;\u003c/sup\u003e\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"38.976377952755904%\" valign=\"top\"\u003e\n \u003cp\u003e53.32 \u0026plusmn; 11.67\u003c/p\u003e\n \u003c/td\u003e\n \u003c/tr\u003e\n \u003ctr\u003e\n \u003ctd width=\"61.023622047244096%\" valign=\"top\"\u003e\n \u003cp\u003eGender\u003c/p\u003e\n \u003cp\u003e\u0026nbsp; male \u0026nbsp; \u0026nbsp; \u0026nbsp; \u0026nbsp; \u0026nbsp; \u0026nbsp; \u0026nbsp; \u0026nbsp; \u0026nbsp; \u0026nbsp; \u0026nbsp; \u0026nbsp;\u003c/p\u003e\n \u003cp\u003e\u0026nbsp; female\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"38.976377952755904%\" valign=\"top\"\u003e\n \u003cp\u003e\u0026nbsp;\u003c/p\u003e\n \u003cp\u003e44(70.96%)\u003c/p\u003e\n \u003cp\u003e18(29.32%)\u003c/p\u003e\n \u003c/td\u003e\n \u003c/tr\u003e\n \u003ctr\u003e\n \u003ctd width=\"61.023622047244096%\" valign=\"top\"\u003e\n \u003cp\u003eLocation\u003c/p\u003e\n \u003cp\u003e\u0026nbsp;\u0026nbsp;putamen\u003c/p\u003e\n \u003cp\u003e\u0026nbsp; thalamus\u003c/p\u003e\n \u003cp\u003e\u0026nbsp; ventricle\u003c/p\u003e\n \u003cp\u003e\u0026nbsp; lobar\u003c/p\u003e\n \u003cp\u003eICH volume (mL)\u003csup\u003e\u0026nbsp;a\u003c/sup\u003e\u003c/p\u003e\n \u003cp\u003e\u0026nbsp; Pre\u003c/p\u003e\n \u003cp\u003e\u0026nbsp; Pro\u003c/p\u003e\n \u003cp\u003eOperation time (min)\u003csup\u003e\u0026nbsp;a\u003c/sup\u003e\u003c/p\u003e\n \u003cp\u003eEndoscopic time\u003c/p\u003e\n \u003cp\u003e\u0026nbsp;\u0026nbsp;Craniotomy time\u0026nbsp;\u0026nbsp;\u003c/p\u003e\n \u003cp\u003eBlood loss\u003csup\u003e\u0026nbsp;a\u003c/sup\u003e\u003c/p\u003e\n \u003cp\u003eMedical morbidity\u003c/p\u003e\n \u003cp\u003eHypertension\u003c/p\u003e\n \u003cp\u003eRenal insufficiency\u003c/p\u003e\n \u003cp\u003eDiabetes mellitus;\u003c/p\u003e\n \u003cp\u003eEntry point\u003c/p\u003e\n \u003cp\u003eTransfrontal\u0026nbsp;\u003c/p\u003e\n \u003cp\u003eTranstemporal\u003c/p\u003e\n \u003cp\u003eTranscortical\u003c/p\u003e\n \u003cp\u003eMortality rate(%)\u003c/p\u003e\n \u003cp\u003ePostoperative rebleeding rate(%)\u003csup\u003ea\u003c/sup\u003e\u003c/p\u003e\n \u003cp\u003ePre-GCS\u003c/p\u003e\n \u003cp\u003ePro-GCS( 6 month)\u003c/p\u003e\n \u003cp\u003ePro-GOS( 6 month)\u003c/p\u003e\n \u003cp\u003eStage of bleeding appearance(%)\u003csup\u003ea,b\u003c/sup\u003e\u003c/p\u003e\n \u003cp\u003eGrade 1\u003c/p\u003e\n \u003cp\u003eGrade 2\u003c/p\u003e\n \u003cp\u003eGrade 3\u003c/p\u003e\n \u003c/td\u003e\n \u003ctd width=\"38.976377952755904%\" valign=\"top\"\u003e\n \u003cp\u003e\u0026nbsp;\u003c/p\u003e\n \u003cp\u003e42 (67.74%)\u003c/p\u003e\n \u003cp\u003e9 (14.52%)\u003c/p\u003e\n \u003cp\u003e5 (8.06%)\u003c/p\u003e\n \u003cp\u003e6(9.68%)\u003c/p\u003e\n \u003cp\u003e\u0026nbsp;\u003c/p\u003e\n \u003cp\u003e53.68\u0026nbsp;\u0026plusmn;18.90\u003c/p\u003e\n \u003cp\u003e3.19 \u0026plusmn; 4.35\u003c/p\u003e\n \u003cp\u003e\u0026nbsp;\u003c/p\u003e\n \u003cp\u003e39.94\u0026plusmn;17.69\u003c/p\u003e\n \u003cp\u003e42.26\u0026plusmn;20.45\u003c/p\u003e\n \u003cp\u003e50.23\u0026plusmn;19.51\u003c/p\u003e\n \u003cp\u003e\u0026nbsp;\u003c/p\u003e\n \u003cp\u003e45(72.58%)\u003c/p\u003e\n \u003cp\u003e3(4.83%)\u003c/p\u003e\n \u003cp\u003e10(16.12%)\u003c/p\u003e\n \u003cp\u003e\u0026nbsp;\u003c/p\u003e\n \u003cp\u003e45(72.58%)\u003c/p\u003e\n \u003cp\u003e11(17.74%)\u003c/p\u003e\n \u003cp\u003e6(9.68%)\u003c/p\u003e\n \u003cp\u003e3.23\u003c/p\u003e\n \u003cp\u003e0\u003c/p\u003e\n \u003cp\u003e7.45\u0026plusmn;2.24\u003c/p\u003e\n \u003cp\u003e12.71\u0026plusmn;2.83\u003c/p\u003e\n \u003cp\u003e3.77\u0026plusmn;1.12\u003c/p\u003e\n \u003cp\u003e\u0026nbsp;\u003c/p\u003e\n \u003cp\u003e68.68\u0026plusmn;20.95\u003c/p\u003e\n \u003cp\u003e47.16\u0026plusmn;24.80\u003c/p\u003e\n \u003cp\u003e31.24\u0026plusmn;17.56\u003c/p\u003e\n \u003c/td\u003e\n \u003c/tr\u003e\n \u003c/tbody\u003e\n\u003c/table\u003e\n\u003cp\u003e\u003cem\u003eGCS\u0026nbsp;\u003c/em\u003eGlasgow coma scale; \u003cem\u003eGOS\u003c/em\u003e Glasgow outcome scale\u003c/p\u003e\n\u003cp\u003e\u003csup\u003ea\u003c/sup\u003e Values are expressed as the mean \u0026plusmn; SD;\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003e\u003csup\u003eb\u003c/sup\u003e\u003c/strong\u003e\u003cstrong\u003e\u0026nbsp;\u003c/strong\u003eGrade 3 bleeding occurred in early operative stage, with statistical significance(p=0.000)\u003c/p\u003e\u003cp\u003eIntraoperative bleeding\u003c/p\u003e \u003cp\u003eThe numbers of hemostasis with patient in grade 1, 2 and 3 were 55, 18 and 24 respectively (p\u0026thinsp;=\u0026thinsp;0.000) (Table\u0026nbsp;\u003cspan refid=\"Tab3\" class=\"InternalRef\"\u003e3\u003c/span\u003e). Compared with thalamic hematoma and lobar hematoma removal, endoscopic putamen hematoma removal was more prone to intraoperative bleeding (p\u0026thinsp;=\u0026thinsp;0.038) (Table\u0026nbsp;\u003cspan refid=\"Tab3\" class=\"InternalRef\"\u003e3\u003c/span\u003e). When the endoscopic operating time was divided into one hundred equal parts, the average stage of bleeding appearance per patient in grade1, 2 and 3 were 68.68\u0026thinsp;\u0026plusmn;\u0026thinsp;20.95, 47.16\u0026thinsp;\u0026plusmn;\u0026thinsp;24.80 and 31.24\u0026thinsp;\u0026plusmn;\u0026thinsp;17.56 respectively, these mean active bleeding occurred in early operative stage and errhysis happened later (p\u0026thinsp;=\u0026thinsp;0.000) (Table\u0026nbsp;\u003cspan refid=\"Tab2\" class=\"InternalRef\"\u003e2\u003c/span\u003e). .\u003c/p\u003e \u003cp\u003e \u003cdiv class=\"gridtable\"\u003e\u003ctable float=\"Yes\" id=\"Tab3\" border=\"1\"\u003e \u003ccaption language=\"En\"\u003e \u003cdiv class=\"CaptionNumber\"\u003eTable 3\u003c/div\u003e \u003cdiv class=\"CaptionContent\"\u003e \u003cp\u003eCharacteristics of intraoperative bleeding with endoscopic hematoma evacuation\u003c/p\u003e \u003c/div\u003e \u003c/caption\u003e \u003ccolgroup cols=\"8\"\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c1\" colnum=\"1\"\u003e\u003c/div\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c2\" colnum=\"2\"\u003e\u003c/div\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c3\" colnum=\"3\"\u003e\u003c/div\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c4\" colnum=\"4\"\u003e\u003c/div\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c5\" colnum=\"5\"\u003e\u003c/div\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c6\" colnum=\"6\"\u003e\u003c/div\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c7\" colnum=\"7\"\u003e\u003c/div\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c8\" colnum=\"8\"\u003e\u003c/div\u003e \u003cthead\u003e \u003ctr\u003e \u003cth align=\"left\" colname=\"c1\" morerows=\"1\" rowspan=\"2\"\u003e \u003cp\u003eGrade\u003c/p\u003e \u003c/th\u003e \u003cth align=\"left\" colspan=\"3\" nameend=\"c4\" namest=\"c2\"\u003e \u003cp\u003eOperative stage\u003c/p\u003e \u003c/th\u003e \u003cth align=\"left\" colname=\"c5\" morerows=\"1\" rowspan=\"2\"\u003e\u0026nbsp;\u003c/th\u003e \u003cth align=\"left\" colspan=\"3\" nameend=\"c8\" namest=\"c6\"\u003e \u003cp\u003eLocation of hematoma\u003c/p\u003e \u003c/th\u003e \u003c/tr\u003e \u003ctr\u003e \u003cth align=\"left\" colname=\"c2\"\u003e \u003cp\u003eEarly- stage\u003c/p\u003e \u003c/th\u003e \u003cth align=\"left\" colname=\"c3\"\u003e \u003cp\u003eMid- stage\u003c/p\u003e \u003c/th\u003e \u003cth align=\"left\" colname=\"c4\"\u003e \u003cp\u003eLater-stage\u003c/p\u003e \u003c/th\u003e \u003cth align=\"left\" colname=\"c6\"\u003e \u003cp\u003ePutamen\u003c/p\u003e \u003c/th\u003e \u003cth align=\"left\" colname=\"c7\"\u003e \u003cp\u003eThalamus\u003c/p\u003e \u003c/th\u003e \u003cth align=\"left\" colname=\"c8\"\u003e \u003cp\u003eLobar\u003c/p\u003e \u003c/th\u003e \u003c/tr\u003e \u003c/thead\u003e \u003ctbody\u003e \u003ctr\u003e \u003ctd align=\"left\" colname=\"c1\"\u003e \u003cp\u003e1\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c2\"\u003e \u003cp\u003e2(2.06)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c3\"\u003e \u003cp\u003e11(11.34)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c4\"\u003e \u003cp\u003e42(43.30)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c5\"\u003e\u0026nbsp;\u003c/td\u003e \u003ctd align=\"left\" colname=\"c6\"\u003e \u003cp\u003e37(38.14)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c7\"\u003e \u003cp\u003e10(10.31)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c8\"\u003e \u003cp\u003e8(8.25)\u003c/p\u003e \u003c/td\u003e \u003c/tr\u003e \u003ctr\u003e \u003ctd align=\"left\" colname=\"c1\"\u003e \u003cp\u003e2\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c2\"\u003e \u003cp\u003e5(5.15)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c3\"\u003e \u003cp\u003e10(10.30)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c4\"\u003e \u003cp\u003e3(3.09)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c5\"\u003e\u0026nbsp;\u003c/td\u003e \u003ctd align=\"left\" colname=\"c6\"\u003e \u003cp\u003e30(30.93)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c7\"\u003e \u003cp\u003e1(1.03)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c8\"\u003e \u003cp\u003e2(2.06)\u003c/p\u003e \u003c/td\u003e \u003c/tr\u003e \u003ctr\u003e \u003ctd align=\"left\" colname=\"c1\"\u003e \u003cp\u003e3\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c2\"\u003e \u003cp\u003e19(19.59)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c3\"\u003e \u003cp\u003e4(4.12)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c4\"\u003e \u003cp\u003e1(1.03)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c5\"\u003e\u0026nbsp;\u003c/td\u003e \u003ctd align=\"left\" colname=\"c6\"\u003e \u003cp\u003e22(22.68)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c7\"\u003e \u003cp\u003e1(1.03)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c8\"\u003e \u003cp\u003e1(1.03)\u003c/p\u003e \u003c/td\u003e \u003c/tr\u003e \u003ctr\u003e \u003ctd align=\"left\" colname=\"c1\"\u003e\u0026nbsp;\u003c/td\u003e \u003ctd align=\"left\" colspan=\"3\" nameend=\"c4\" namest=\"c2\"\u003e \u003cp\u003eχ\u003csup\u003e2\u003c/sup\u003e\u0026thinsp;=\u0026thinsp;51.738\u003c/p\u003e \u003cp\u003ep\u0026thinsp;=\u0026thinsp;0.000\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c5\"\u003e\u0026nbsp;\u003c/td\u003e \u003ctd align=\"left\" colspan=\"3\" nameend=\"c8\" namest=\"c6\"\u003e \u003cp\u003eχ\u003csup\u003e2\u003c/sup\u003e\u0026thinsp;=\u0026thinsp;23.789\u003c/p\u003e \u003cp\u003ep\u0026thinsp;=\u0026thinsp;0.000\u003c/p\u003e \u003c/td\u003e \u003c/tr\u003e \u003c/tbody\u003e \u003c/colgroup\u003e \u003c/table\u003e\u003c/div\u003e \u003c/p\u003e \u003cp\u003eClinical outcome\u003c/p\u003e \u003cp\u003eThe mean preoperative hematoma volume was 53.68\u0026thinsp;\u0026plusmn;\u0026thinsp;18.90 ml and the mean residual hematoma volume was 3.19\u0026thinsp;\u0026plusmn;\u0026thinsp;4.35ml, representing an average evacuation rate of 95.61%. Endoscopic operating time was 39.94\u0026thinsp;\u0026plusmn;\u0026thinsp;17.69 minutes (Fig.\u0026nbsp;\u003cspan refid=\"Fig3\" class=\"InternalRef\"\u003e3\u003c/span\u003e) and blood loss was 50.56\u0026thinsp;\u0026plusmn;\u0026thinsp;20.19ml. No patient experienced postoperative re-bleeding. The mortality rate was 3.23% (2 of 62 patients), one died of renal failure, one from pneumonia and sepsis. Surgery-related morbidity wasn\u0026rsquo;t occurred in all patients. The mean preoperative Glasgow coma scale (GCS) score was 7.45\u0026thinsp;\u0026plusmn;\u0026thinsp;2.24 and the mean GCS score 6 months after surgery was 12.71\u0026thinsp;\u0026plusmn;\u0026thinsp;2.83. The mean GOS score at 6-month follow-up was 3.77\u0026thinsp;\u0026plusmn;\u0026thinsp;1.12 (Table\u0026nbsp;\u003cspan refid=\"Tab2\" class=\"InternalRef\"\u003e2\u003c/span\u003e).\u003c/p\u003e \u003cp\u003e \u003c/p\u003e"},{"header":"Discussion","content":"\u003cp\u003eEndoscopic surgery has been gaining popularity as a method for surgical intervention in ICH patients. Although the International Surgical Trial (STICH)in intracerebral hemorrhage study showed that emergency surgical hematoma evacuation failed to improve the outcome of ICH patient comparing with the same type of patients who received initial medical management without surgery, the STICH trial further clarify demonstrated improved outcomes with surgery for subgroups. A meta-analysis of 15 trials of surgery for ICH including STICH I and II with individual patient data showed a significant advantage for surgery. Compare with craniotomy, endoscopic hematoma evacuation obtain some advantage: (1)higher evacuation rate and lower complications;(2) exposure of deep structure and hemostasis under direct vision༛(3) maximum protection of normal brain tissue.\u003c/p\u003e \u003cp\u003eIntraoperative bleeding during endoscopic hematoma removal is a stressful factor for surgeons. Even careful atraumatic evacuation of a hematoma can sometimes result in intraoperative hemorrhage. The principals for surgical hemostasis with intraparenchymal hematoma with endoscopic vs microscopic technique were not different. Also, whether surgery is performed through a tube (endoscopic visualization) or retractors (microscope for visualization) does not change principals of hemostasis. Some methods can be used to acquire secure hemostasis in endoscopic hematoma evacuation (Table\u0026nbsp;\u003cspan refid=\"Tab4\" class=\"InternalRef\"\u003e4\u003c/span\u003e). When an intraoperative hemorrhage occurs, the operating field was kept clear by irrigation and continuous suction. Hemorrhage from a small artery could be reduced with repeated irrigation in hematoma cavity. Another way was to compress the bleeding spot with cotton or hemostatic material for several minutes. Hemorrhage from a large artery can be stopped by coagulation with suction cannula or bipolar \u003csup\u003e10,15\u0026ndash;17,19\u003c/sup\u003e.\u003c/p\u003e \u003cp\u003e \u003cdiv class=\"gridtable\"\u003e\u003ctable float=\"Yes\" id=\"Tab4\" border=\"1\"\u003e \u003ccaption language=\"En\"\u003e \u003cdiv class=\"CaptionNumber\"\u003eTable 4\u003c/div\u003e \u003cdiv class=\"CaptionContent\"\u003e \u003cp\u003eSummary of the literature on hemostatic procedures for endoscopic evacuation of intracerebral hemorrhage\u003c/p\u003e \u003c/div\u003e \u003c/caption\u003e \u003ccolgroup cols=\"4\"\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c1\" colnum=\"1\"\u003e\u003c/div\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c2\" colnum=\"2\"\u003e\u003c/div\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c3\" colnum=\"3\"\u003e\u003c/div\u003e \u003cdiv align=\"left\" class=\"colspec\" colname=\"c4\" colnum=\"4\"\u003e\u003c/div\u003e \u003cthead\u003e \u003ctr\u003e \u003cth align=\"left\" colname=\"c1\"\u003e \u003cp\u003eAuthors and years\u003c/p\u003e \u003c/th\u003e \u003cth align=\"left\" colname=\"c2\"\u003e \u003cp\u003eSurgical hemostatic procedures\u003c/p\u003e \u003c/th\u003e \u003cth align=\"left\" colname=\"c3\"\u003e \u003cp\u003eNo. of pts\u003c/p\u003e \u003c/th\u003e \u003cth align=\"left\" colname=\"c4\"\u003e \u003cp\u003eOutcome\u003c/p\u003e \u003c/th\u003e \u003c/tr\u003e \u003c/thead\u003e \u003ctbody\u003e \u003ctr\u003e \u003ctd align=\"left\" colname=\"c1\"\u003e \u003cp\u003eChad M Miller, et al. (2007)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c2\"\u003e \u003cp\u003eThe hematoma cavity was irrigated with saline and hemostasis was inspected via endoscope\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c3\"\u003e \u003cp\u003e10\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c4\"\u003e \u003cp\u003eThe re-bleeding rate was 20% and the mortality rate was 25%.\u003c/p\u003e \u003c/td\u003e \u003c/tr\u003e \u003ctr\u003e \u003ctd align=\"left\" colname=\"c1\"\u003e \u003cp\u003eToru Nagasaka, et al. (2009)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c2\"\u003e \u003cp\u003eHandling of the multifunctional suction cannula and its application for balanced irrigation-suction\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c3\"\u003e \u003cp\u003e15\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c4\"\u003e \u003cp\u003eNo surgical complications or re-bleeding occurred.\u003c/p\u003e \u003c/td\u003e \u003c/tr\u003e \u003ctr\u003e \u003ctd align=\"left\" colname=\"c1\"\u003e \u003cp\u003eLu-Ting Kuo, et al. (2011)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c2\"\u003e \u003cp\u003eMost bleeding from these perforators stopped after gentle compression with cotton and irrigation for 2 minutes\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c3\"\u003e \u003cp\u003e68\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c4\"\u003e \u003cp\u003eThe re-bleeding rate was 1.5% and the mortality rate was 5.9%.\u003c/p\u003e \u003c/td\u003e \u003c/tr\u003e \u003ctr\u003e \u003ctd align=\"left\" colname=\"c1\"\u003e \u003cp\u003eHongwei Zhu, et al. (2012)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c2\"\u003e \u003cp\u003eHemostasis was achieved by continuous saline irrigation, pressure packing and electrically coagulated with a suction cannula\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c3\"\u003e \u003cp\u003e28\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c4\"\u003e \u003cp\u003eThe re-bleeding rate was 3.6% and the mortality rate was 7.1%.\u003c/p\u003e \u003c/td\u003e \u003c/tr\u003e \u003ctr\u003e \u003ctd align=\"left\" colname=\"c1\"\u003e \u003cp\u003eWei-Hsin Wang, et al. (2015)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c2\"\u003e \u003cp\u003eHemostasis was achieved by hemostatic agents or used bipolar forceps with the endoscope held by an assistant or holder\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c3\"\u003e \u003cp\u003e21\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c4\"\u003e \u003cp\u003eThe re-bleeding rate was 9.52% and the mortality rate was 9.52%.\u003c/p\u003e \u003c/td\u003e \u003c/tr\u003e \u003ctr\u003e \u003ctd align=\"left\" colname=\"c1\"\u003e \u003cp\u003eHui-Tzung Luh, et al. (2018)\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c2\"\u003e \u003cp\u003eFloSeal Hemostatic Matrix was applied through a specialized 3-mm flexible catheter into the hematoma cavity.\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c3\"\u003e \u003cp\u003e42\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c4\"\u003e \u003cp\u003eThe re-bleeding rate was 4.8% and the mortality rate was 7.1%.\u003c/p\u003e \u003c/td\u003e \u003c/tr\u003e \u003ctr\u003e \u003ctd align=\"left\" colname=\"c1\"\u003e \u003cp\u003ePresent study\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c2\"\u003e \u003cp\u003eHemostatic strategy for endoscopic evacuation of intracerebral hematoma based on intraoperative bleeding grading system\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c3\"\u003e \u003cp\u003e62\u003c/p\u003e \u003c/td\u003e \u003ctd align=\"left\" colname=\"c4\"\u003e \u003cp\u003eNo patient experienced postoperative re-bleeding and the mortality rate was 3.23%\u003c/p\u003e \u003c/td\u003e \u003c/tr\u003e \u003c/tbody\u003e \u003c/colgroup\u003e \u003c/table\u003e\u003c/div\u003e \u003c/p\u003e \u003cp\u003eAs we know, single or multiple branches of the penetrating arteries are responsible for cerebral bleeding. The causes of hemorrhages include arteriosclerosis, arterial dissection and micro-aneurysm formation, etc. \u003csup\u003e24\u0026ndash;26\u003c/sup\u003e. The lenticulostriate arteries (LSA) represent one of the largest groups of perforating vessels in the brain and divided into two groups (medial and later) based on the originative location of the vessels \u003csup\u003e27\u003c/sup\u003e. The lenticulostriate arteries originate from the middle cerebral artery (MCA), and then turn sharply medial, make a loop, and penetrate anterior perforated substance into the brain \u003csup\u003e28\u003c/sup\u003e. Intracerebral segments of the LSA supply the Putamen, lateral segment of Globus Pallidus and internal capsule \u003csup\u003e29\u003c/sup\u003e. The diameter of lenticulostriate arteries vary from 0.7um to 2.2mm \u003csup\u003e30\u003c/sup\u003e. The intraoperative hemorrhage is often iatrogenic induce by injury of perforating vessels inside or outside the hematoma. Based on the anatomic characteristics of penetrating arteries, the relationship between the hematoma/brain tissue and the penetrating arteries can been speculated. For the intracerebral hematoma, the bleeding vessels can run inside or passed through the hematoma, supplying normal brain tissues. Other kind of normal vessels are located at the edge of hematoma and adhere tightly.\u003c/p\u003e \u003cp\u003eWhen encountering intraoperative hemorrhage, the best choice of hemostatic method can be bewildered especially for inexperienced surgeons. It was invalid in active hemorrhage with the methods of observation and compression. Errhysis with coagulation would transfer to active hemorrhage because of brain tissue damage around small arteries. When active hemorrhage occurs, the operating field is filled with blood quickly, bipolar was difficult to use because of narrow corridor and visual control deteriorates. Based on intraventricular vision, some researches presented grading system and a step by step guide for the endoscopic management of intraoperative hemorrhages during intraventricular tumor surgery\u003csup\u003e31,32\u003c/sup\u003e. Based on the surgical sites, anatomical structure and bleeding vessels between the intraventricular surgery and intracerebral hematoma, we established a simple intraoperative bleeding grading system during endoscopic hematoma remove. This grading system can guide inexperienced surgeon to choose optimum hemostatic method and is safe and effective.\u003c/p\u003e \u003cp\u003eThe following points warrant attention with intraoperative bleeding grading system and hemostasis. First, to distinguish no bleeding, errhysis and active bleeding based on the characteristics of the water in transparent plastic sheath. No bleeding means clear water. Errhysis means light-red cloudy water and fuzzy reference (cotton or scale on the sheath). Active bleeding included red and muddy water, even malignant hemorrhage. Second, to find bleeding site or vessels through repeated irrigation and continuous suction, to coagulate the bleeder by touching the suction with appropriative power of monopolar. Third, to reduce the damage of normal brain tissue in Grade3 by using the outer wall of suction (not the tip) to touch the bleeding site.\u003c/p\u003e \u003cp\u003eIn our study, the concept of hematoma removal was to avoid following the brain parenchyma\u0026ndash;hematoma junction during hematoma evacuation, therefore, the incidence of Grade3 was less than that of Grade1 and Grade2. The perforator vessels were located in the bottom of the hematoma and the lower part of the hematoma was removed first, so that the period in Grade3 was earlier than Grade1.\u003c/p\u003e \u003cp\u003eLimitations\u003c/p\u003e \u003cp\u003eThe major strength of this study was to provide an alternative hemostatic strategy to neurosurgeons. A hemostatic strategy based on intraoperative bleeding grade resulted in efficiency and safety. The present study has some limitations. Firstly, evaluation of bleeding in endoscopy was largely subjective and likely to have interobserver variations. Secondly, the hemostatic strategy was dependent upon the intraoperative bleeding grading system, which could introduce a bias. In addition, more clinical experience was necessary to determine whether this strategy improves surgical outcomes.\u003c/p\u003e"},{"header":"Conclusion","content":"\u003cp\u003eActive bleeding occurs in early operative stage and errhysis happens in late stage. Hemostatic strategy based on intraoperative bleeding grading system can guide surgeon to choose the right hemostatic methods, shorten the operation time, and seems to be safe and effective, especially for inexperienced surgeons.\u003c/p\u003e"},{"header":"Abbreviations","content":"\u003cp\u003eICH = intracerebral hematoma.\u003c/p\u003e"},{"header":"Declarations","content":"\u003cp\u003e\u003cstrong\u003eAcknowledgements\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eThis work was supported by the key Clinical Research of Guangxi [Grant No. \u0026nbsp; \u0026nbsp;], the Clinical Research of Liuzhou [Grant No.2021CBB0103], the Clinical Research of Liuzhou General Hospital [Grant No. LRYGCC202120]\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eAuthors\u0026apos; contributions\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eConception and design: TC Lan, CJ Yang. Acquisition of data: ST Liu, CM Wang Analysis and interpretation of data: JL Zhu, RX Wei. Drafting the article: YL Ye Critically revising the article: all authors. Reviewed submitted version of manuscript: all authors. Approved the final version of the manuscript on behalf of all authors: Statistical analysis: CM Wang. Study supervision: YL Ye, GR Ma.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eCompeting interests\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eThe authors report no conflict of interest concerning the materials or methods\u003c/p\u003e\n\u003cp\u003eused in this study or the findings specified in this paper.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eData availability\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eThe datasets used and/or analysed during the current study available from the corresponding author on reasonable request.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eEthics approval and consent to participate\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eThe study was approved by the ethics committee of the Liuzhou people\u0026rsquo;s Hospital. The need for individual consent was waived by the committee because of the retrospective nature of the study\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eAuthors\u0026apos; contributions\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eConception and design: TC Lan, CJ Yang. Acquisition of data: CM Wang. Analysis and interpretation of data: JL Zhu, RX Wei. Drafting the article: YL Ye Critically revising the article: all authors. Reviewed submitted version of manuscript: all authors. Approved the final version of the manuscript on behalf of all authors: Statistical analysis: CM Wang. Study supervision: YL Ye, GR Ma.\u003c/p\u003e"},{"header":"References","content":"\u003col\u003e\n \u003cli\u003e\u003cspan\u003eAdeeb, N. \u003cem\u003eet al.\u003c/em\u003e The intracranial arachnoid mater : a comprehensive review of its history, anatomy, imaging, and pathology. \u003cem\u003eChild\u0026apos;s nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery\u003c/em\u003e \u003cstrong\u003e29\u003c/strong\u003e, 17\u0026ndash;33, doi:10.1007/s00381-012-1910-x (2013).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eHostettler, I. C., Seiffge, D. J. \u0026amp; Werring, D. J. Intracerebral hemorrhage: an update on diagnosis and treatment. \u003cem\u003eExpert review of neurotherapeutics\u003c/em\u003e \u003cstrong\u003e19\u003c/strong\u003e, 679\u0026ndash;694, doi:10.1080/14737175.2019.1623671 (2019).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eMalhotra, K. \u003cem\u003eet al.\u003c/em\u003e Prevalence, Characteristics, and Outcomes of Undetermined Intracerebral Hemorrhage: A Systematic Review and Meta-Analysis. \u003cem\u003eStroke\u003c/em\u003e \u003cstrong\u003e52\u003c/strong\u003e, 3602\u0026ndash;3612, doi:10.1161/strokeaha.120.031471 (2021).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eHemphill, J. C., 3rd \u003cem\u003eet al.\u003c/em\u003e Guidelines for the Management of Spontaneous Intracerebral Hemorrhage: A Guideline for Healthcare Professionals From the American Heart Association/American Stroke Association. \u003cem\u003eStroke\u003c/em\u003e \u003cstrong\u003e46\u003c/strong\u003e, 2032\u0026ndash;2060, doi:10.1161/str.0000000000000069 (2015).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eGross, B. A., Jankowitz, B. T. \u0026amp; Friedlander, R. M. Cerebral Intraparenchymal Hemorrhage: A Review. \u003cem\u003eJama\u003c/em\u003e \u003cstrong\u003e321\u003c/strong\u003e, 1295\u0026ndash;1303, doi:10.1001/jama.2019.2413 (2019).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eAdeoye, O. \u0026amp; Broderick, J. P. Advances in the management of intracerebral hemorrhage. \u003cem\u003eNature reviews. Neurology\u003c/em\u003e \u003cstrong\u003e6\u003c/strong\u003e, 593\u0026ndash;601, doi:10.1038/nrneurol.2010.146 (2010).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eRussell, M. W., Boulanger, L., Joshi, A. V., Neumann, P. J. \u0026amp; Menzin, J. The economic burden of intracerebral hemorrhage: evidence from managed care. \u003cem\u003eManaged care interface\u003c/em\u003e \u003cstrong\u003e19\u003c/strong\u003e, 24\u0026ndash;28, 34 (2006).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eYe, Y., Wang, Q., Ou, W., He, J. \u0026amp; Zhao, Z. Endoscopic Surgery Without Decompressive Craniectomy in Large Putaminal Intracerebral Hemorrhage: Assessment of Efficacy and Safety. \u003cem\u003eNeurocritical care\u003c/em\u003e \u003cstrong\u003e32\u003c/strong\u003e, 392\u0026ndash;399, doi:10.1007/s12028-019-00880-8 (2020).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eSun, G. C. \u003cem\u003eet al.\u003c/em\u003e Image-guided endoscopic surgery for spontaneous supratentorial intracerebral hematoma. \u003cem\u003eJournal of neurosurgery\u003c/em\u003e \u003cstrong\u003e127\u003c/strong\u003e, 537\u0026ndash;542, doi:10.3171/2016.7.jns16932 (2017).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eOrakcioglu, B., Beynon, C., B\u0026ouml;sel, J., Stock, C. \u0026amp; Unterberg, A. W. Minimally invasive endoscopic surgery for treatment of spontaneous intracerebral hematomas: a single-center analysis. \u003cem\u003eNeurocritical care\u003c/em\u003e \u003cstrong\u003e21\u003c/strong\u003e, 407\u0026ndash;416, doi:10.1007/s12028-014-9987-6 (2014).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eKellner, C. P. \u003cem\u003eet al.\u003c/em\u003e Time to Evacuation and Functional Outcome After Minimally Invasive Endoscopic Intracerebral Hemorrhage Evacuation. \u003cem\u003eStroke\u003c/em\u003e \u003cstrong\u003e52\u003c/strong\u003e, e536-e539, doi:10.1161/strokeaha.121.034392 (2021).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eXu, X. \u003cem\u003eet al.\u003c/em\u003e Effectiveness of endoscopic surgery for supratentorial hypertensive intracerebral hemorrhage: a comparison with craniotomy. \u003cem\u003eJournal of neurosurgery\u003c/em\u003e \u003cstrong\u003e128\u003c/strong\u003e, 553\u0026ndash;559, doi:10.3171/2016.10.jns161589 (2018).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eSun, S. \u003cem\u003eet al.\u003c/em\u003e Neuroendoscopic Surgery versus Craniotomy for Supratentorial Hypertensive Intracerebral Hemorrhage: A Systematic Review and Meta-Analysis. \u003cem\u003eWorld neurosurgery\u003c/em\u003e \u003cstrong\u003e134\u003c/strong\u003e, 477\u0026ndash;488, doi:10.1016/j.wneu.2019.10.115 (2020).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eMa, L., Hou, Y., Zhu, R. \u0026amp; Chen, X. Endoscopic Evacuation of Basal Ganglia Hematoma: Surgical Technique, Outcome, and Learning Curve. \u003cem\u003eWorld neurosurgery\u003c/em\u003e \u003cstrong\u003e101\u003c/strong\u003e, 57\u0026ndash;68, doi:10.1016/j.wneu.2017.01.072 (2017).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eKuo, L. T. \u003cem\u003eet al.\u003c/em\u003e Early endoscope-assisted hematoma evacuation in patients with supratentorial intracerebral hemorrhage: case selection, surgical technique, and long-term results. \u003cem\u003eNeurosurgical focus\u003c/em\u003e \u003cstrong\u003e30\u003c/strong\u003e, E9, doi:10.3171/2011.2.focus10313 (2011).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eSadahiro, H. \u003cem\u003eet al.\u003c/em\u003e Real-time ultrasound-guided endoscopic surgery for putaminal hemorrhage. \u003cem\u003eJournal of neurosurgery\u003c/em\u003e \u003cstrong\u003e123\u003c/strong\u003e, 1151\u0026ndash;1155, doi:10.3171/2014.11.Jns141508 (2015).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eLuh, H. T. \u003cem\u003eet al.\u003c/em\u003e Local hemostatic matrix for endoscope-assisted removal of intracerebral hemorrhage is safe and effective. \u003cem\u003eJournal of the Formosan Medical Association\u0026thinsp;=\u0026thinsp;Taiwan yi zhi\u003c/em\u003e \u003cstrong\u003e117\u003c/strong\u003e, 63\u0026ndash;70, doi:10.1016/j.jfma.2017.02.016 (2018).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eXu, X. \u003cem\u003eet al.\u003c/em\u003e Comparison of endoscopic evacuation, stereotactic aspiration and craniotomy for the treatment of supratentorial hypertensive intracerebral haemorrhage: study protocol for a randomised controlled trial. \u003cem\u003eTrials\u003c/em\u003e \u003cstrong\u003e18\u003c/strong\u003e, 296, doi:10.1186/s13063-017-2041-1 (2017).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eNagasaka, T. \u003cem\u003eet al.\u003c/em\u003e Balanced irrigation-suction technique with a multifunctional suction cannula and its application for intraoperative hemorrhage in endoscopic evacuation of intracerebral hematomas: technical note. \u003cem\u003eNeurosurgery\u003c/em\u003e \u003cstrong\u003e65\u003c/strong\u003e, E826-827; discussion E827, doi:10.1227/01.Neu.0000350985.58062.3f (2009).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eWang, W. H. \u003cem\u003eet al.\u003c/em\u003e Endoscopic hematoma evacuation in patients with spontaneous supratentorial intracerebral hemorrhage. \u003cem\u003eJournal of the Chinese Medical Association : JCMA\u003c/em\u003e \u003cstrong\u003e78\u003c/strong\u003e, 101\u0026ndash;107, doi:10.1016/j.jcma.2014.08.013 (2015).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eHsieh, P. C. Endoscopic removal of thalamic hematoma: a technical note. \u003cem\u003eMinimally invasive neurosurgery : MIN\u003c/em\u003e \u003cstrong\u003e46\u003c/strong\u003e, 369\u0026ndash;371, doi:10.1055/s-2003-812505 (2003).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eAngileri, F. F. \u003cem\u003eet al.\u003c/em\u003e Fully Endoscopic Freehand Evacuation of Spontaneous Supratentorial Intraparenchymal Hemorrhage. \u003cem\u003eWorld neurosurgery\u003c/em\u003e \u003cstrong\u003e94\u003c/strong\u003e, 268\u0026ndash;272, doi:10.1016/j.wneu.2016.07.015 (2016).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eNagasaka, T., Inao, S., Ikeda, H., Tsugeno, M. \u0026amp; Okamoto, T. Inflation-deflation method for endoscopic evacuation of intracerebral haematoma. \u003cem\u003eActa neurochirurgica\u003c/em\u003e \u003cstrong\u003e150\u003c/strong\u003e, 685\u0026ndash;690; discussion 690, doi:10.1007/s00701-008-1561-6 (2008).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eTakebayashi, S. \u0026amp; Kaneko, M. Electron microscopic studies of ruptured arteries in hypertensive intracerebral hemorrhage. \u003cem\u003eStroke\u003c/em\u003e \u003cstrong\u003e14\u003c/strong\u003e, 28\u0026ndash;36, doi:10.1161/01.str.14.1.28 (1983).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eKomiyama, M. \u003cem\u003eet al.\u003c/em\u003e Simultaneous bleeding from multiple lenticulostriate arteries in hypertensive intracerebral haemorrhage. \u003cem\u003eNeuroradiology\u003c/em\u003e \u003cstrong\u003e37\u003c/strong\u003e, 129\u0026ndash;130, doi:10.1007/bf00588628 (1995).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eMizutani, T., Kojima, H. \u0026amp; Miki, Y. Arterial dissections of penetrating cerebral arteries causing hypertension-induced cerebral hemorrhage. \u003cem\u003eJournal of neurosurgery\u003c/em\u003e \u003cstrong\u003e93\u003c/strong\u003e, 859\u0026ndash;862, doi:10.3171/jns.2000.93.5.0859 (2000).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eMarinković, S. \u003cem\u003eet al.\u003c/em\u003e Structure and immunohistochemistry of the human lenticulostriate arteries. \u003cem\u003eFolia morphologica\u003c/em\u003e \u003cstrong\u003e72\u003c/strong\u003e, 210\u0026ndash;216, doi:10.5603/fm.2013.0035 (2013).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eDjulejić, V. \u003cem\u003eet al.\u003c/em\u003e Morphometric analysis, region of supply and microanatomy of the lenticulostriate arteries and their clinical significance. \u003cem\u003eJournal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia\u003c/em\u003e \u003cstrong\u003e19\u003c/strong\u003e, 1416\u0026ndash;1421, doi:10.1016/j.jocn.2011.10.025 (2012).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eHu, R. \u0026amp; Feng, H. Lenticulostriate Artery and Lenticulostriate-artery Neural Complex: New Concept for Intracerebral Hemorrhage. \u003cem\u003eCurrent pharmaceutical design\u003c/em\u003e \u003cstrong\u003e23\u003c/strong\u003e, 2206\u0026ndash;2211, doi:10.2174/1381612823666170220163750 (2017).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eSeo, S. W. \u003cem\u003eet al.\u003c/em\u003e Measurements of lenticulostriate arteries using 7T MRI: new imaging markers for subcortical vascular dementia. \u003cem\u003eJournal of the neurological sciences\u003c/em\u003e \u003cstrong\u003e322\u003c/strong\u003e, 200\u0026ndash;205, doi:10.1016/j.jns.2012.05.032 (2012).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eOertel, J., Linsler, S., Csokonay, A., Schroeder, H. W. S. \u0026amp; Senger, S. Management of severe intraoperative hemorrhage during intraventricular neuroendoscopic procedures: the dry field technique. \u003cem\u003eJournal of neurosurgery\u003c/em\u003e \u003cstrong\u003e131\u003c/strong\u003e, 931\u0026ndash;935, doi:10.3171/2018.4.Jns172537 (2018).\u003c/span\u003e\u003c/li\u003e\n \u003cli\u003e\u003cspan\u003eOertel, J., Linsler, S., Strohm, L. \u0026amp; Senger, S. Management of severe intraoperative hemorrhage during intraventricular neuroendoscopic procedures: the dry field technique. \u003cem\u003eActa Neurochir (Wien)\u003c/em\u003e \u003cstrong\u003e164\u003c/strong\u003e, 2551\u0026ndash;2557, doi:10.1007/s00701-022-05207-9 (2022).\u003c/span\u003e\u003c/li\u003e\n\u003c/ol\u003e"}],"fulltextSource":"","fullText":"","funders":[],"hasAdminPriorityOnWorkflow":false,"hasManuscriptDocX":true,"hasOptedInToPreprint":true,"hasPassedJournalQc":"","hasAnyPriority":false,"hideJournal":true,"highlight":"","institution":"","isAcceptedByJournal":false,"isAuthorSuppliedPdf":false,"isDeskRejected":"","isHiddenFromSearch":false,"isInQc":false,"isInWorkflow":false,"isPdf":false,"isPdfUpToDate":true,"isWithdrawnOrRetracted":false,"journal":{"display":true,"email":"
[email protected]","identity":"researchsquare","isNatureJournal":false,"hasQc":true,"allowDirectSubmit":true,"externalIdentity":"","sideBox":"","snPcode":"","submissionUrl":"/submission","title":"Research Square","twitterHandle":"researchsquare","acdcEnabled":true,"dfaEnabled":false,"editorialSystem":"","reportingPortfolio":"","inReviewEnabled":false,"inReviewRevisionsEnabled":true},"keywords":"Endoscopic surgery, Intracerebral hemorrhage, Hemostatic strategy Mortality","lastPublishedDoi":"10.21203/rs.3.rs-3984616/v1","lastPublishedDoiUrl":"https://doi.org/10.21203/rs.3.rs-3984616/v1","license":{"name":"CC BY 4.0","url":"https://creativecommons.org/licenses/by/4.0/"},"manuscriptAbstract":"\u003cp\u003eEndoscopic hematoma evacuation has become well received for its high evacuation rate in patients with intracerebral hematoma. Effective hemostatic procedure is the key to the success of the procedure. Any single method cannot solve all kinds of intraoperative bleeding. The key to hemostasis is to identify the type of bleeding and take the best hemostasis method during endoscopic surgery. In our study, sixty-two intracerebral hemorrhage patients who underwent endoscopic hematoma evacuations were analyzed. Intraoperative bleeding was graded as Grades 0, 1, 2 and 3 based on characteristics of bleeding. A hemostatic strategy was created from the grading system. The efficiency was evaluated by operation time, evacuation rate, and re-bleeding rate after surgery. Procedure safety was evaluated by mortality rate and postoperative complications. We found that endoscopic removal of putamen hematoma was more prone to intraoperative bleeding (p\u0026thinsp;=\u0026thinsp;0.00). Active bleeding occurred in early operative stage and errhysis happen in later stage (p\u0026thinsp;=\u0026thinsp;0.00). Average evacuation rate was 95.61% and the mortality rate was 3.23%. The mean Glasgow outcome scale (GOS) score at 6-month follow-up was 3.77\u0026thinsp;\u0026plusmn;\u0026thinsp;1.12. No patient experienced postoperative re-bleeding. These findings indicated that most patients will experience different degrees of intraoperative bleeding during endoscopic hematoma evacuation. A hemostatic strategy based on intraoperative bleeding grade resulted in efficiency and safety.\u003c/p\u003e","manuscriptTitle":"Endoscopic Evacuation of Supratentorial Hematoma: a Hemostatic Strategy for Surgeons","msid":"","msnumber":"","nonDraftVersions":[{"code":1,"date":"2024-03-19 15:53:00","doi":"10.21203/rs.3.rs-3984616/v1","editorialEvents":[{"type":"communityComments","content":0}],"status":"published","journal":{"display":true,"email":"
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