Clinical article
Yüklə 114,35 Kb. Pdf görüntüsü
|
- Bu səhifədəki naviqasiya:
- J Korean Neurosurg Soc 35
- Rev Neurol 32
- J Korean Neurosurg Soc 38
- J Korean Neurosurg Soc 43
- Neurol Med Chir (Tokyo) 41
- Surg Neurol 57
- Acta Neurochir (Wien) 147
- Acta Neurochir (Wien) 137
- Neurosurgery 63
- J Neurosurg 87
|
122 Copyright © 2012 Korean Neurotraumatology Society CLINICAL ARTICLE Korean J Neurotrauma 2012;8:122-127 ISSN 2234-8999
Chronic subdural hematoma (CSDH) is a relatively com- mon disease, especially in the geriatric population, frequent- ly encountered in neurosurgical practice. 4,7) Formation of the outer membrane with an interior containing hyperosmolar blood collection causes development of CSDH, and the out- er membrane has abnormally permeable microcapillaries leading to accumulation of exudation from the macrocap- illaries in the outer membrane, therefore enlarging the area of the subdural hematoma. 6,18,24,28,29) CSDHs have been re- ported to show good postoperative prognosis with relatively simple method of surgical treatment including burr hole tre- phination. 1,2,5,16) Traditionally, burr hole trephination and eva- cuation of hematoma with closed drainage system has been widely accepted as the optimal treatment for CSDH. 15,19,21,23)
It is agreeable that surgical decompression offers a dramat- ic improvement of symptoms, and the procedure is relative- ly noninvasive and safe with satisfactory postoperative out- come in the majority of patients with CSDH. However, con- siderable recurrence rates have been reported ranging from 3 to 20% following surgical management. 9,11,17,27,30) This clinical analysis evaluated the postoperative course of CSDH and the factors correlated with recurrence. Materials and Methods Retrospective analysis of 157 consecutive patients diag- nosed with CSDH who were surgically treated from Sep- tember 2005 to December 2011 was performed. 20 patients who were inadequately followed up and 1 patient in whom Factors Affecting Postoperative Recurrence of Chronic Subdural Hematoma Woo-Keun Kong, MD, Byong-Chul Kim, MD, Keun-Tae Cho, MD, PhD and Seung-Koan Hong, MD, PhD Department of Neurosurgery, Collge of Medicine, Dongguk University, Ilsan Hospital, Goyang, Korea
evacuation. The aim of this study was to determine the independent factors and features of CSDH that are associated with postoperative recurrence.
tember 2005 to December 2011 was performed. The demographic data, clinical characteristics, radiologic features were analyzed to clarify the correlation between independent variables and postoperative recurrence of CSDH.
(43.4%), and past 3 months in 14 patients (10.3%). A total of 12 patients (8.8%) experienced recurrence of CSDH, and re- operation was performed in all recurred cases. The average duration between initial surgery and reoperation was 20.1 days. Delayed resolution and recurrence were more commonly presented in bilateral CSDH, but this data was not statistically sig- nificant. Large hematomas with maximum thickness over 20 mm were significantly correlated with higher recurrence rates of CSDH (p=0.032). In addition, the incidence of recurrence was significantly higher in the cases with high-density and mixed- density hematomas according to brain computed tomography (CT) findings (p=0.0026).
Discerning these risk factors could be beneficial in predicting the postoperative recurrence of CSDH.
(Korean J Neurotrauma 2012;8:122-127) KEY WORDS: Chronic subdural hematoma ㆍ Recurrence ㆍ Risk factors ㆍ Reoperation. Received: July 25, 2012 / Revised: September 10, 2012 Accepted: September 12, 2012 Address for correspondence: Keun-Tae Cho, MD, PhD Department of Neurosurgery, Collge of Medicine, Dongguk Uni- versity, Ilsan Hospital, 814 Siksa-dong, Ilsandong-gu, Goyang 410- 773, Korea Tel: +82-31-961-7322, Fax: +82-31-961-7327 E-mail: duihns@gmail.com online
ML
Comm www.neurotrauma.or.kr 123
Woo-Keun Kong, et al. organization of CSDH was accompanied by brain tumor were excluded from the study. Consequently, total of 136 pa- tients were included in the analysis. Diagnosis of CSDH was confirmed by brain computed tomography (CT) in all cas- es. The clinical features, brain CT findings, surgical results, and postoperative status of the patients were serially ana- lyzed. Initial neurological examination on admission was performed with the Glasgow Coma Scale (GCS) score, and thorough verification of clinical information of all patients was conducted. Single or two burr holes were trephined at the region of maximal hematoma thickness under general anesthesia. Subdural hematoma was evacuated and washed out by irri- gation with warm physiological saline solution. Closed- system drainage of the subdural hematoma cavity using soft silicon drain was performed in all cases for 1 to 5 days. Postoperative brain CT scans were obtained within 3 days following surgery. Subdural drainage catheter was removed following confirmation of near total removal of hematoma on postoperative brain CT findings and definite improve- ment of symptoms. Following surgery, all patients received adequate intravenous volume supplementation, and were educated to be cautious of head trauma and aggressive phys- ical activities. All patients included in this study were followed-up for more than 3 months postoperatively. Periodic brain CT scans were performed on 1 week basis until regression of subdural hematoma and recovery of pa- tients to premorbid functional status were presented. The re- currence of CSDH was defined as re-accumulation of the hematoma located within the operated hematoma cavity with effacement of the sulci markings on brain CT scans obtained within 3 months postoperatively along with the re- appearance of neurological symptoms including cognitive dysfunction, motor weakness, or dysphasia. 8,9,20)
Recurred CSDHs were surgically managed by drainage of hematoma using previously trephined burr hole. Patients who present- ed no remarkable neurological deficits or small amount of residual hematoma were observed and closely followed-up. Preoperative brain magnetic resonance imaging (MRI) was evaluated in 8 patients. Although the number of patients who underwent brain MRI study preoperatively was rela- tively small, characteristic findings were compared between patients without postoperative recurrence and patients who showed recurrence of CSDH. Independent variables evaluated in the analysis of factors associated with recurrence of CSDH included the following parameters: age and sex; history of seizure, head trauma; underlying diseases; associated cerebrovascular disease; car- diovascular disease; chronic alcohol intake; smoking histo- ry; laboratory findings (coagulopathy and liver function ab- normality); medication of antiplatelet or anticoagulant agents; initial and postoperative brain CT findings (hematoma thick- ness, density, laterality regarding ipsilateral or bilateral, de- gree of midline shift, cerebral atrophy, location of drainage catheter tip, and amount of postoperative pneumocephalus). Statistical analysis was conducted through Pearson’s chi- square test and the Student t-test with SPSS software (ver- sion 14.0; SPSS Institute, Inc., Chicago, IL). In all analyses, a p-value of less than 0.05 was considered as statistically significant.
The demographic data and clinical characteristics of 136 consecutive patients are summarized in Table 1. There were 98 male (72.1%) and 38 female (27.9%) patients with male to female ratio of 2.6 : 1. The range of age was from 43 to 97 years with an average of 64.3 years. The initial neuro- logical status of patients presented by GCS score on admis- sion showed mean value of 12.4. Arterial hypertension was the most common underlying disease presented in 41 pa- tients (30.1%). Five patients (3.7%) had history of seizure, among them 1 patient presented recurrence of CSDH. How- ever, these clinical findings were not significantly correlat- ed with the postoperative recurrence of CSDH (p＞0.05). The risk factors with comparison between recurred CSDH and patients without recurrence are summarized in Table 2. Resolution of CSDH was achieved within 1 month fol- TABLE 1. Demographic characteristics and clinical findings of the patients in the recurred group and the group with no recurrence Variables Number of patients (%) p value RG NRG Total Gender
Male Female 0 7 (58.3)
0 5 (41.7)
0 91 (73.4) 0 33 (26.6) 0 98 (72.1) 0 38 (27.9) 0.794 Mean age (years) 62.3 67.1
64.3 0.912
Mental status Alert
Confused Drowsy Stuporous Comatose 0 7 (58.3)
0 2 (16.7)
0 2 (16.7)
0 1 (8.3)
0 0 (0.0)
0 85 (68.6) 0 20 (16.2) 0 14 (11.6) 00 4 (3.4)
00 1 (0.2)
0 92 (67.6) 0 22 (16.2) 0 16 (11.8) 00 5 (3.7)
00 1 (0.7)
0.371 History of head 0.469
Present Absent 10 (83.3) 0 2 (16.7) 0 95 (76.6) 0 29 (23.4) 105 (77.2) 0 31 (22.8) History of seizure Present Absent 0 1 (8.3) 11 (91.7) 00 4 (3.2) 120 (96.8) 00 5 (3.7) 131 (96.3) 0.702
RG: recurrence group, NRG: nonrecurrence group 124 Korean J Neurotrauma 2012;8:122-127 Postoperative Recurrence of Chronic Subdural Hematoma lowing surgery in 51 patients (37.5%), between 1 to 3 months in 59 patients (43.4%), and past 3 months postoperatively in 14 patients (10.3%). The recurrence of CSDH occurred in 12 patients (8.8%). There were 7 male (58.3%) and 5 female (41.7%) patients with recurrence of CSDH ranging in age from 62 to 85 years. Reoperation of recurred CSDH was per- formed in all 12 patients. The average interval between ini- tial surgery and reoperation was 20.1 days. Following initial surgery, the recurrence of CSDH occurred within 1 week in 1 patient (8.3%), between 1 to 2 weeks in 5 patients (41.7%), between 2 to 3 weeks in 2 patients (16.7%), between 3 to 4 weeks in 1 patient (8.3%), and over 4 weeks in 2 patients (16.7%).
The recurrence of CSDH occurred on right cerebral con- vexity in 3 patients (25.0%), left in 7 patients (58.3%), and bilateral in 2 patients (16.7%). In regard with the laterality of hematoma, delayed resolution and recurrence were more commonly presented in bilateral CSDH. However, this data of difference was not statistically significant (p=0.453). Re- currence of CSDH was significantly more common in pa- tients with hematomas with maximum thickness over 20 mm (p=0.032). The density of the hematomas according to brain CT findings were classified into high-density, mixed- density, iso-density, and low-density. The incidence of re- currence was significantly higher in the cases with high- density and mixed-density hematomas (p=0.0026) (Table 3). The recurrence of CSDH was relatively higher in the cases with midline shift over 10 mm. However, this differ- ence was not statistically significant (p=0.765). There was no significant correlation between the recurrence of CSDH and the severity of cerebral atrophy (p=0.960). Among the 8 patients evaluated preoperatively with brain MRI, 3 patients presented recurrence of CSDH. Signal in- tensity of CSDH on preoperative T1-weighted MRI was analyzed. 3 patients (37.5%) showed high signal intensity, and 5 patients (62.5%) revealed iso-signal intensity or low signal intensity on brain MRI. From the 3 patients with high signal intensity, 1 patient (33.3%) presented recurrence of CSDH, and out of the 5 patients who revealed iso-signal in- tensity or low signal intensity, 2 patients (40.0%) showed re- currence. Although this data was not statistically significant (p=0.492), the recurrence rate of CSDHs that exhibited iso- signal or low signal intensity on T1-weighted MRI was high- er than in patients who showed homogenous high signal in- tensity on T1-weighted MRI. Out of 136 patients, 32 patients (23.5%) underwent surgery with single burr hole trephination, and 104 patients (76.5%) with two burr hole trephination. The recurrence rates of CSDH in patients operated by single burr hole trephina- tion and two burr hole trephination were 3.1% (n=1) and 10.6% (n=11), respectively presenting higher incidence of recurrence in surgeries with two burr hole trephination. However, this difference was not statistically significant (p=0.175) (Table 4). The mean duration of indwelling state of subdural drainage catheter was 4.8 days in patients with TABLE 2. The risk factors in 136 patients with chronic subdural hematoma
Risk factor Number of patients (%) p value RG NRG Total Chronic alcoholism Absent 0 7 (58.3)
0 5 (41.7)
0 46 (37.1) 0 78 (62.9) 0 53 (38.9) 0 83 (61.1) 0.274 Smoking
Present Absent 0 3 (25.0)
0 9 (75.0)
0 41 (33.1) 0 83 (66.9) 0 44 (32.4) 0 92 (67.6) 0.713 Hypertension Present Absent 0 4 (33.3)
0 8 (66.7)
0 43 (34.7) 0 81 (65.3) 0 47 (34.6) 0 89 (65.4) 0.625 Cardiovascular 0.742
Present Absent 0 2 (16.7)
10 (83.3) 0 15 (12.1) 109 (87.9) 0 17 (12.5) 119 (87.5) Cerebrovascular disease 0.216
Present Absent 0 3 (25.0)
0 9 (75.0)
0 23 (18.5) 101 (81.5) 0 26 (19.1) 110 (80.9) Prolongation of PT INR or aPTT 0.721
Present Absent 0 2 (16.7)
10 (83.3) 0 16 (12.9) 108 (87.1) 0 18 (13.2) 118 (86.8) Antiplatelet or 0.758
On medication Not on medication 1 (8.3)
11 (91.7) 0 14 (11.3) 110 (88.7) 0 15 (11.0) 121 (89.0) RG: recurrence group, NRG: nonrecurrence group TABLE 3. Preoperative radiologic features of chronic subdural hematoma on brain computed tomography Radiologic features
Number of patients (%) p value RG NRG Total Laterality Right Left
Bilateral 3 (25.0)
7 (58.3) 2 (16.7)
37 (29.8) 68 (54.8) 19 (15.4) 40 (29.4) 75 (55.1) 21 (15.4) 0.453 0
＜ 20 mm
≥ 20 mm
4 (33.3) 8 (66.7)
76 (61.3) 48 (38.7) 80 (58.8) 56 (41.2) 0.032 0
High Mixed
Iso Low
4 (33.3) 5 (41.7)
2 (16.7) 1 (8.3)
0 11 (8.9)
0 24 (19.4) 61 (19.2) 28 (22.5) 15 (11.0) 29 (21.3) 63 (46.3) 29 (21.3) 0.0026 RG: recurrence group, NRG: nonrecurrence group www.neurotrauma.or.kr 125
Woo-Keun Kong, et al. no recurrence, and 5.3 days in cases of recurred CSDH. There was no statistically significant correlation between the duration of subdural drainage catheter indwelling state and recurrence of CSDH (p=0.356).
CSDH generally develops in geriatric patients usually ca- used by relatively mild head trauma. 8) Diverse methods of managements including conservative and surgical treatment through burr hole trephination and conduction of closed drainage system have been performed. In general, majority of previously reported literatures support surgical treatment of CSDH, proposing that burr hole trephination is a rela- tively simple and safe technique with reliable morbidity of 0 to 9%. 3,5,12,20) Postoperative recurrence of CSDH is not rare. Previous studies reported recurrence rates ranging from 9.2 to 26.5%, and in this study, recurrence rate was 8.8%. 1,9,16)
Various risk factors for recurrence of CSDH have been reported in pre- vious studies, including advanced age, cerebral atrophy, bleed- ing tendency, chronic alcohol intake, bilateral location of he- matoma, and postoperative pneumocephalus. 2,13,14)
However, these previously reported results have occasionally presented inconsistency. In this study, although older patients present- ed a higher tendency of recurrence, advanced age was not sig- nificantly correlated with the recurrence of CSDH. Atrophy of cerebral parenchyma is a sequel of cerebro- vascular accidents. Relatively small volume of cerebral pa- renchyma leads to enlargement of subarachnoid space, and thus, causing injuries induced by stretching of the bridging veins. This condition impedes postoperative brain expan- sion, and sustained rebleeding into the subdural hematoma cavity could act as a factor for recurrence of CSDH. 27,28,30)
In conclusion, hematomas with greater thickness may pres- ent higher rates of recurrence since postoperative subdural space is larger than in smaller hematomas. 2,10,17) Yamamoto et al. 30)
proposed that larger hematomas present greater ten- dency of recurrence since subdural space following surgical evacuation is larger than in smaller hematomas. In this study, although cerebral atrophy did not present statistically sig- nificant correlation with recurrence, large hematomas were significantly correlated with higher recurrence rates. Previous studies propose higher recurrence rates in bilat- eral CSDH. 1,9,27,30) However, this correlation was not statis- tically significant in our study. Even with statistical insignif- icance, bilateral CSDH could present rapid and progressive aggravation with increased intracranial pressure, and thus, surgical treatment should be considered earlier if indicat- ed. 13,14)
Although the statistical significance was not evident, pa- tients operated with two burr holes showed relatively high- er recurrence rates than those with one burr hole. Accord- ing to results reported by previous studies, saline irrigation via two burr holes, which is generally considered more ef- ficient in evacuating hematoma, may lead to accumulation of larger amount of postoperative subdural air, and act as a factor for recurrence of CSDH. 2,19,26) The density of subdural hematoma on brain CT scans was classified into 4 categories as high-density, mixed- density, iso-density, and low-density. In this study, signifi- cant correlation was evident between high and mixed den- sity and the recurrence of CSDH. The density of hematoma on CT scan represents the proportion of fresh blood clots in hematoma cavity. Greater proportion of these fresh blood clots signifies active growth of vessels into the hematoma membrane and rebleeding into the hematoma cavity. 10,17,22)
According to previous study by Nomura et al., 18) CSDH was classified into five categories in regard with brain CT find- ings as low-density, isodense, high-density, mixed-density, and layered types. They reported that the high-density and isodense types presented similarity in rebleeding present- ing higher recurrence rates than the low-density types. The signal intensity of subdural hematoma on brain MRI revealed characteristic finding suggesting that the recur- rence of CSDH presented higher tendency in patients with iso-signal to low signal intensity on T1-weighted MRI. However, this data was not statistically significant. Tsutsumi et al. 28)
reported that the principal cause of recur- rence of CSDH is likely to be the repetitive microhemor- rhages from microvessels of the hematoma membrane. In cases of rebleeding, the fresh component of subdural he- matoma is demonstrated as iso or low signal intensity on T1-weighted MRI. In this stage, microvessels of the hema- toma membrane tends to easily rebleed, and be more vul- nerable to recurrence of CSDH. Although our data was not statistically significant, CSDH presenting iso or low signal intensity on T1-weighted MRI may be more prone to re- currence. From the 12 cases of re-operation due to recurrence of CSDH, 4 patients (33.3%) presented multilayered hemato- ma. There was a limitation regarding the fact that since brain TABLE 4. Comparison of recurrence rates in patients treated with one burr hole vs. two burr holes Factors OBH
TBH p value No. of patients 32 (23.5%) 104 (76.5%) Recurrence 0 1 (3.1%) 0 0 11 (10.6%) 0.175 OBH: one burr hole, TBH: two burr holes 126 Korean J Neurotrauma 2012;8:122-127 Postoperative Recurrence of Chronic Subdural Hematoma MRI scans were not perfor-med in all patients, clear distinc- tion between monolayered and multilayered hematoma was difficult to conclude. Previous studies reported that multilayered structure of CSDH is significantly correlated with higher recurrence rates, and certain articles supported conduction of craniotomy and complete removal of CSDH including hematoma membranes. 15,16,28) Tanikawa et al. 25) re-
ported that CSDH with large amount of intrahematomal mem- branes presents higher recurrence rates, and that resection of the multilayered membranes, formation of a connection with all other compartments of CSDH, and evacuation of the he- matoma could promote resorption of subdural fluid, lead- ing to prevention of rebleeding. However, this proposal re- mains controversial. This study was a retrospective and non-randomized study, and imposes certain limitations. Therefore, it is potentially subject to diverse biases and variations. Further analyses with larger size of samples would be necessary to clarify the definite risk factors for recurrence of CSDH. Conclusion Considerable proportion of patients treated surgically for CSDH presented postoperative recurrence. Certain risk factors influencing postoperative recurrence of CSDH were articulated in the present study. Large amount of hemato- ma evaluated by maximum thickness, and higher density on CT scans were significantly correlated with higher recur- rence rates of CSDH. Discerning these risk factors could be beneficial in predicting the recurrence of CSDH following surgical treatment. ■ The authors have no financial conflicts of interest.
1) Amirjamshidi A, Abouzari M, Eftekhar B, Rashidi A, Rezaii J, Es- fandiari K, et al. Outcomes and recurrence rates in chronic subdu- ral haematoma. Br J Neurosurg 21:272-275, 2007 2) Choi CH, Moon BG, Kang HI, Lee SJ, Kim JS. Factors affecting the reaccumulation of chronic subdural hematoma after burr-hole trephination and closed-system drainage. J Korean Neurosurg Soc 35:192-198, 2004 3) Choi WW, Kim KH. Prognostic factors of chronic subdural hema- toma.
4) Cousseau DH, Echevarría Martín G, Gaspari M, Gonorazky SE. [Chronic and subacute subdural haematoma. An epidemiological study in a captive population]. Rev Neurol 32:821-824, 2001 5) El-Kadi H, Miele VJ, Kaufman HH. Prognosis of chronic subdural hematomas.
6) Friede RL, Schachenmayr W. The origin ofsubdural neomembranes. II. Fine structural of neomembranes.
7) Jeong CA, Kim TW, Park KH, Chi MP, Kim JO, Kim JC. Retro- spective analysis of re-operated patients after chronic subdural he- matoma surgery. J Korean Neurosurg Soc 38:116-120, 2005 8) Jeong JE, Kim GK, Park JT, Lim YJ, Kim TS, Rhee BA, et al. A clinical analysis of chronic subdural hematoma according to age fac- tor.
J Korean Neurosurg Soc 29:748-753, 2000 9) Kang MS, Koh HS, Kwon HJ, Choi SW, Kim SH, Youm JY. Factors influencing recurrent chronic subdural hematoma after surgery.
10) Kim HY, Kwon SC, Kim TH, Shin HS, Hwang YS, Park SK. Anal- ysis of management according to CT findings in chronic subdural hematoma. J Korean Neurosurg Soc 37:96-100, 2005 11) Ko BS, Lee JK, Seo BR, Moon SJ, Kim JH, Kim SH. Clinical analy- sis of risk factors related to recurrent chronic subdural hematoma.
12) Kravtchouk AD, Likhterman LB, Potapov AA, El-Kadi H. Post- operative complications of chronic subdural hematomas: preven- tion and treatment. Neurosurg Clin N Am 11:547-552, 2000 13) Kurokawa Y, Ishizaki E, Inaba K. Bilateral chronic subdural he- matoma cases showing rapid and progressive aggravation.
14) Lee KS, Bae WK, Yoon SM, Doh JW, Bae HG, Yun IG. Location of the chronic subdural haematoma: role of the gravity and crani- al morphology. Brain Inj 15:47-52, 2001 15) Lind CR, Lind CJ, Mee EW. Reduction in the number of repeated operations for the treatment of subacute and chronic subdural he- matomas by placement of subdural drains. J Neurosurg 99:44-46, 2003
16) Mori K, Maeda M. Surgical treatment of chronic subdural hema- toma in 500 consecutive cases: clinical characteristics, surgical outcome, complications, and recurrence rate.
17) Nakaguchi H, Tanishima T, Yoshimasu N. Factors in the natural his- tory of chronic subdural hematomas that influence their postoper- ative recurrence. J Neurosurg 95:256-262, 2001 18) Nomura S, Kashiwagi S, Fujisawa H, Ito H, Nakamura K. Charac- terization of local hyperfibrinolysis in chronic subdural hematomas by SDS-PAGE and immunoblot. J Neurosurg 81:910-913, 1994 19) Okada Y, Akai T, Okamoto K, Iida T, Takata H, Iizuka H. A com- parative study of the treatment of chronic subdural hematoma--burr hole drainage versus burr hole irrigation. Surg Neurol 57:405-409; discussion 410, 2002 20) Ramachandran R, Hegde T. Chronic subdural hematomas--causes of morbidity and mortality. Surg Neurol 67:367-372; discussion 372- 373, 2007 21) Santarius T, Kirkpatrick PJ, Ganesan D, Chia HL, Jalloh I, Smielews- ki P, et al. Use of drains versus no drains after burr-hole evacua- tion of chronic subdural haematoma: a randomised controlled trial.
22) Son WS, Park SH, Kang DH, Park J, Sung JK, Hwang SK. Rela- tionship between the level of fibrinogen and the signal density on brain computed tomography in the chronic subdural hematoma. J Korean Neurotraumatol Soc 6:43-47, 2010 23) Stanisic M, Lund-Johansen M, Mahesparan R. Treatment of chron- ic subdural hematoma by burr-hole craniostomy in adults: influence of some factors on postoperative recurrence. Acta Neurochir (Wien) 147:1249-1256; discussion 1256-1257, 2005 24) Stroobandt G, Fransen P, Thauvoy C, Menard E. Pathogenetic fac- tors in chronic subdural haematoma and causes of recurrence after drainage. Acta Neurochir (Wien) 137:6-14, 1995 25) Tanikawa M, Mase M, Yamada K, Yamashita N, Matsumoto T, Banno T, et al. Surgical treatment of chronic subdural hematoma based on intrahematomal membrane structure on MRI. Acta Neurochir (Wien) 143:613-618; discussion 618-619, 2001 26) Taussky P, Fandino J, Landolt H. Number of burr holes as indepen- dent predictor of postoperative recurrence in chronic subdural hae- matoma.
Br J Neurosurg 22:279-282, 2008 www.neurotrauma.or.kr 127
Woo-Keun Kong, et al. 27) Torihashi K, Sadamasa N, Yoshida K, Narumi O, Chin M, Yamaga- ta S. Independent predictors for recurrence of chronic subdural he- matoma: a review of 343 consecutive surgical cases. Neurosurgery 63:1125-1129; discussion 1129, 2008 28) Tsutsumi K, Maeda K, Iijima A, Usui M, Okada Y, Kirino T. The relationship of preoperative magnetic resonance imaging findings and closed system drainage in the recurrence of chronic subdural hematoma.
29) Wilberger JE. Pathophysiology of evolution and recurrence of ch- ronic subdural hematoma.
30) Yamamoto H, Hirashima Y, Hamada H, Hayashi N, Origasa H, Endo S. Independent predictors of recurrence of chronic subdural hematoma: results of multivariate analysis performed using a logis- tic regression model. J Neurosurg 98:1217-1221, 2003 Yüklə 114,35 Kb. Dostları ilə paylaş:
|