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Efficacies of minimally invasive puncture and small bone window craniotomy for hypertensive intracerebral hemorrhage, evaluation of motor‑evoked potentials and comparison of postoperative rehemorrhage between the two methods

  • Authors:
    • Lei Luan
    • Maolei Li
    • Hang Sui
    • Guoliang Li
    • Wenyong Pan
  • View Affiliations

  • Published online on: December 13, 2018     https://doi.org/10.3892/etm.2018.7094
  • Pages: 1256-1261
  • Copyright: © Luan et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

Application value of the minimally invasive puncture and small bone window craniotomy in hypertensive intracerebral hemorrhage was investigated to explore the effects of the above treatment methods on motor‑evoked potentials (MEPs) and postoperative rehemorrhage. Patients with hypertensive intracerebral hemorrhage who were admitted to Chengyang People's Hospital from March 2016 to December 2017 were selected and randomly divided into the minimally invasive group (n=40) and the craniotomy group (n=40). The minimally invasive group was treated with minimally invasive puncture and drainage for hematomas, while the craniotomy group received small bone window craniotomy for evacuation of hematomas. The clinical efficacy was compared between the two groups. At 28 days after operation, the Chinese scale of clinical neurological deficit of stroke patients (CSS) score in the minimally invasive group was lower than that in the craniotomy group (p<0.05). At 28 days after operation, the S‑100β level in the minimally invasive group was lower than that in the craniotomy group (p<0.05). At 1 week after operation, 35 patients in the minimally invasive group were able to elicit MEP waveforms, and only 7 patients in the craniotomy group were able to elicit positive waveforms. At 2 weeks after operation, 40 patients in the minimally invasive group and 20 patients in the craniotomy group could elicit MEP waveforms, and the incubation period, central motor conduction time and amplitude in the former were significantly better than those in the latter (p<0.05). The operation time and length of hospital stay were shorter with more total expenses of hospitalization in the minimally invasive group compared to those in the craniotomy group (p<0.05). Compared with small bone window craniotomy, minimally invasive puncture can reduce serum S‑100β level. Its advantages are obvious, so it is worthy of promotion and application.

Introduction

Hypertensive intracerebral hemorrhage is a non-traumatic brain parenchymal hemorrhage disease with the highest incidence rate in the cold season. Since the cold climate induces contraction of blood vessels in the human body, blood pressure fluctuates greatly, which easily causes blood vessel rupture resulting in hemorrhage (1). However, the pathological mechanism of hypertensive intracerebral hemorrhage is more complicated, which is related not only to the cold climate factors, but also to the formation of intracranial microaneurysms, intracranial arterial wall degeneration and necrosis and cerebrovascular amyloidosis (2). The disability and mortality rates of hypertensive intracerebral hemorrhage are high, so the improvement of clinical efficacy of these methods has become a research hotspot in recent years (3). At present, minimally invasive puncture and small bone window craniotomy are the main treatment methods for hypertensive intracerebral hemorrhage, but their advantages and disadvantages are not yet clear (4). In particular, there are few studies and reports on the effects of the two surgical methods on postoperative motor-evoked potentials (MEPs) of patients (5). This study compared the efficacy between minimally invasive puncture and small bone window craniotomy in the treatment of hypertensive intracerebral hemorrhage, and explored the effects of the above treatment methods on MEPs and postoperative rehemorrhage, so as to provide a basis for treating hypertensive intracerebral hemorrhage.

Patients and methods

General data

A total of 80 patients with hypertensive intracerebral hemorrhage admitted and treated in Chengyang People's Hospital (Qingdao, China) from March 2016 to December 2017 were selected for the study. Inclusion criteria: i) patients definitely diagnosed with hypertensive intracerebral hemorrhage (6); and ⅱ) patients undergoing surgical treatment within 72 h of onset with postoperative follow-up period ≥3 months. Exclusion criteria: i) patients with cerebral hemorrhage caused by trauma or other non-hypertensive factors; ⅱ) patients who were in critical condition with no time for surgical treatment; ⅲ) patients with diseases in the liver, kidney or other important organs; ⅳ) psychopaths; or v) women in the gestation period. These 80 patients were randomly divided into the minimally invasive group (n=40) and the craniotomy group (n=40). Comparisons of general data between the two groups of patients are shown in Table I.

Table I.

Comparison of general data between the two groups of patients.

Table I.

Comparison of general data between the two groups of patients.

VariablesMinimally invasive group (n=40)Craniotomy group (n=40)t/χ2P-value
Age (years)56.35±3.2157.41±4.080.6820.095
Sex (n)
  Male21221.0740.083
  Female1918
Body mass index (kg/m2)25.13±1.7325.15±2.410.5210.166
Volume of hematoma (ml)42.56±4.3143.06±5.080.7850.103
Glasgow Coma Scale score (points)10.11±1.5410.24±1.691.0920.065
Operation timing (n)
  At 12 h after onset20211.3360.072
  At 12–24 h after onset1615
  At 24–72 h after onset  4  4

This study was approved by the Ethics Committee of Chengyang People's Hospital. Signed informed consents were obtained from the patients or the guardians.

Treatment methods

The minimally invasive group was treated with minimally invasive puncture and drainage for hematoma: hematoma lesions were found by computed tomography (CT) before operation, minimally invasive puncture points were marked on the patient's scalp, and the direction and depth of minimally invasive needle insertion were scientifically evaluated. The patients were locally hypodermically injected with 1.0% lidocaine according to a method described in a previous study (7). Electric drill was applied to gradually insert the puncture needle into the patient's intracranial hematoma lesions. After the needle was pulled out, the hematoma aspiration was performed. When the hematoma volume reached ~50%, the aspiration was stopped.

The craniotomy group underwent small bone marrow craniotomy: the patients were generally anesthetized using the procedure and were examined via CT before operation in order to view the lesions that were away from important blood vessels and functional areas of the brain. Generally, bone windows with a diameter of ≤4 cm were selected at the closest point near the hematoma lesions. After the patient's endocranium was incised, the hematomas were aspirated with aspiration volume of 60–92%. After hemostasis, a drainage tube was placed on the patient's hematoma cavity. Urokinases were injected into the patient's hematoma cavity postoperatively, and if there were no symptoms of intracranial hypertension, open drainage was conducted 4 h after injection once a day. The patients were subjected to regular cranium CT re-examination after operation. If the hematoma volume was <10 ml, the drainage tube could be removed. Both groups of patients were treated with routine treatments such as anti-infective and neurotrophic treatments after operation.

Observation indexes
Operation-related indexes

The operation time, drainage tube removal time, length of hospital stay and the total expenses of hospitalization of patients were recorded and compared.

Neurological function

Before operation and at 28 days after operation, the Chinese scale of clinical neurological deficit of stroke patients (CSS) (8) was adopted to evaluate the neurological deficit scores of the two groups of patients.

Ability to daily living activities

Barthel index (9) was employed to assess the ability to daily living activities of the two groups of patients at 3 months after operation.

MEPs

Neurotic electrophysiology was utilized to detect MEPs in the two groups of patients (10).

Serum S-100β

Changes in the level of serum S-100β in the two groups of patients before operation and at 1, 3, 7, 14, 21 and 28 days after operation were determined via the enzyme-linked immunosorbent assay (ELISA).

Complications

After 3 months of follow-up, postoperative complications such as postoperative rehemorrhage or new intracranial hemorrhage, multiple organ failure and pulmonary embolism were observed and recorded.

Statistical analysis

Statistical Product and Service Solutions (SPSS) 21.0 software was used for data analysis. Enumeration data were also expressed as percentage (%). Chi-square test was used for intergroup comparisons. Measurement data were expressed as mean ± standard deviation (SD), and the t-test was applied for intragroup and intragroup comparisons. P<0.05 was considered to indicate a statistically significant difference.

Results

Comparison of postoperative complications

After 3 months of follow-up, there were no significant differences in the incidence rate of postoperative complications such as rehemorrhage or new intracranial hemorrhage and mortality rate (p>0.05) (Table II).

Table II.

Comparison of postoperative complications between the two groups [n (%)].

Table II.

Comparison of postoperative complications between the two groups [n (%)].

GroupnStress ulcerRehemorrhage or new intracranial hemorrhageMultiple organ failurePulmonary embolismMortality
Minimally invasive group403 (7.50)  3 (7.50)2 (5.00)1 (2.50)6 (15.00)
Craniotomy group402 (5.00)  3 (7.50)1 (2.50)1 (2.50)5 (12.50)
χ2 0.9620.8561.0081.1450.697
P-value 0.1540.0970.1330.0980.086
Comparison of the CSS score

Before operation, there was no significant difference in the CSS score between the two groups (p>0.05). At 28 days after operation, the CSS score in the minimally invasive group (20.04±3.51 points) was lower than that in the craniotomy group (22.63±4.77 points) (p<0.05) (Table III).

Table III.

Comparison of the CSS score between the two groups (mean ± SD, points).

Table III.

Comparison of the CSS score between the two groups (mean ± SD, points).

GroupNo. of survived casesBefore operationAt 28 days after operationtP-value
Minimally invasion group3440.96±6.1520.04±3.5121.095<0.001
Craniotomy group3540.87±5.3222.63±4.7717.126<0.001
t 1.0911.352
P-value 0.1740.026
Comparison of the Barthel score

At 3 months after operation, there were no significant differences in the scores of self-care ability, mild dysfunction, moderate dysfunction and severe dysfunction between the two groups (p>0.05) (Table IV).

Table IV.

Comparison of the Barthel score between the two groups at 3 months after operation [n (%)].

Table IV.

Comparison of the Barthel score between the two groups at 3 months after operation [n (%)].

GroupNo. of survived casesSelf-care ability (100 points)Mild dysfunction (60–99 points)Moderate dysfunction (41–60 points)Severe dysfunction (≤40 points)
Minimally invasion group346 (17.65)22 (64.71)5 (14.71)1 (2.94)
Craniotomy group357 (20.00)21 (60.00)5 (14.29)2 (5.71)
χ2 0.5410.7620.9940.805
P-value 0.3720.2480.1160.129
Comparison of serum S-100β

Through treatment, the levels of serum S-100β in both groups displayed a gradual decreasing trend. The level of S-100β in the minimally invasive group was remarkably lower than that in the craniotomy group at 28 days after operation (p<0.05) (Fig. 1).

Comparisons of various MEP indexes

At 1 week after operation, 35 patients in the minimally invasive group were able to elicit MEP waveforms, and only 7 patients in the craniotomy group were able to elicit positive waveforms. At 2 weeks after operation, 40 patients in the minimally invasive and 20 patients in the craniotomy group could elicit MEP waveforms. The incubation period, central motor conduction time, and amplitude in the former were significantly better than those in the latter (p<0.05) (Table V).

Table V.

Comparison of various MEP indexes between the two groups at 2 weeks after operation.

Table V.

Comparison of various MEP indexes between the two groups at 2 weeks after operation.

GroupNo. of survived casesIncubation period (msec)Central motor conduction time (msec)Amplitude (mV)
Minimally invasion group4021.74±2.68   8.78±1.359.68±5.44
Craniotomy group4042.15±3.2713.76±1.923.42±1.75
t 6.9415.4326.017
P-value 0.0240.0330.021

[i] MEP, motor-evoked potential.

Comparison of operation-related indexes

There was no significant difference in the drainage tube removal time between the two groups (p>0.05). The operation time and length of hospital stay were shorter with more total expenses of hospitalization in the minimally invasive group compared to those in the craniotomy group (p<0.05) (Table VI).

Table VI.

Comparison of operation-related indexes between the two groups (mean ± SD).

Table VI.

Comparison of operation-related indexes between the two groups (mean ± SD).

GroupNo. of survived casesOperation time (min)Drainage tube removal time (days)Length of hospital stay (days)Total expenses of hospitalization (RMB ¥ × 104)
Minimally invasion group34   71.69±15.425.65±1.6420.57±4.3217.96±2.89
Craniotomy group35104.85±26.444.91±1.5325.34±5.4512.55±1.95
t 7.2761.3418.1257.954
P-value 0.0170.0880.0120.029

Discussion

The efficacy of conservative treatments for hypertensive intracerebral hemorrhage is currently not ideal, and surgical treatment is an important method to treat this kind of disease. Relevant data have indicated (11,12) that the application of traditional craniotomy evacuation of hematomas is limited in clinical practice due to iatrogenic injury. Small bone window craniotomy is an improved technique based on traditional craniotomy, which is currently applied in the treatment of intracranial superficial hematomas. However, hematomas in the deep site increase the damage to brain tissues and reduce the significance of cerebral hemorrhage treatment (13,14). In recent years, as the understanding of the minimally invasive techniques continues to deepen, the application of minimally invasive puncture and drainage for hematomas in the treatment of cerebral hemorrhage has gradually drawn attention (15). The principle of minimally invasive puncture and drainage for hematomas is to pierce a puncture needle into the patient's hematoma lesion via an electric drill to construct a channel for hematoma evacuation. Subsequently, the biochemical enzyme technique is adopted to liquefy and extract hematomas, thus achieving hematoma evacuation (16,17). The results of the present study manifested that at 28 days after operation, the CSS score was 20.04±3.51 points in the minimally invasive group, which was lower than that in the craniotomy group (22.63±4.77 points) (p<0.05), in consistency with other research findings (18).

After 3 months of follow-up, there were no significant differences in the incidence rate of postoperative complications such as rehemorrhage or new intracranial hemorrhage, the mortality rate, and the Barthel score (p>0.05), suggesting that the efficacies of the two treatment options were identical in the aspects of complications, mortality rate and the ability to daily living activities. The operation time and length of hospital stay were shorter with more total expenses of hospitalization in the minimally invasive group compared to those in the craniotomy group (p<0.05), which is in agreement with the literature (19) and may be related to factors such as the operation procedures and anesthetic methods of the above two operations.

According to relevant data (20), serum S-100β is involved in the occurrence and development of cerebral hemorrhage, and the prognosis of patients with cerebral hemorrhage can be evaluated by measuring the level of serum S-100β. This study revealed that the level of S-100β in the minimally invasive group was notably lower than that in the craniotomy group at 28 days after operation (p<0.05), suggesting that the minimally invasive puncture and drainage for hematomas can reduce more effectively the expression of serum S-100β than the small bone marrow craniotomy evacuation of hematomas. The reason may be that the minimally invasive puncture and drainage for hematomas does not aggravate brain and systemic injuries in patients. The evacuation of hematomas can reduce the mechanical compression of them in patients, and the inflammatory damage mediated by them can be decreased through reducing the content of serum S-100β.

Relevant data have manifested (21) that MEPs can be used to evaluate motor function (pyramidal beam function). Clinically, MEP is generally employed for the recovery of motor function after stroke. The results of this study demonstrated that at 1 week after operation, 35 patients in the minimally invasive group were able to elicit MEP waveforms, and only 7 patients in the craniotomy group were able to elicit positive waveforms. At 2 weeks after surgery, 40 patients in the minimally invasive group could elicit MEP waveforms, and 20 patients in the craniotomy group could elicit MEP waveforms. The incubation period, central motor conduction time and amplitude in the minimally invasive group were significantly better than those in the craniotomy group (p<0.05). In the craniotomy group, 20 patients were not able to elicit positive MEP waveforms at 2 weeks postoperatively, suggesting that the patient's motor center cannot produce nerve impulses at this time. It is worth mentioning that MEP can indicate the neurological function. Besides, the lack and absence of MEPs suggest that the neurological function may not be well restored (22). The above evaluation results of MEPs further suggest that the minimally invasive puncture and drainage for the clinical treatment of hypertensive cerebral hemorrhage has better clinical efficacy.

In summary, compared with the small bone window craniotomy, the minimally invasive puncture reduces the content of serum S-100β. Its advantages are obvious, so it is worthy of promotion and application.

Acknowledgements

Not applicable.

Funding

No funding was received.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors' contributions

LL wrote and revised the manuscript. LL, HS and ML treated the patients and were also involved in the conception of the study. LL and HS recorded and analyzed the operation-related indexes. GL interpreted the neurological function. WP was responsible for serum S-100β detection. All authors read and approved the final manuscript.

Ethics approval and consent to participate

This study was approved by the Ethics Committee of Chengyang People's Hospital (Qingdao, China). Patients who participated in this research had complete clinical data. Signed informed consents were obtained from the patients or the guardians.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

References

1 

Chen G, Ping L, Zhou S, Liu W, Liu L, Zhang D, Li Z, Tian Y and Chen Z: Early prediction of death in acute hypertensive intracerebral hemorrhage. Exp Ther Med. 11:83–88. 2016. View Article : Google Scholar : PubMed/NCBI

2 

Doden T, Sato H, Sasahara E, Murata T, Yako T, Kitazawa K, Higuchi K, Kobayashi S and Hashimoto T: Clinico-radiological characteristics and pathological diagnosis of cerebral amyloid angiopathy-related intracerebral hemorrhage. J Stroke Cerebrovasc Dis. 25:1736–1745. 2016. View Article : Google Scholar : PubMed/NCBI

3 

Fouda AY, Artham S, El-Remessy AB and Fagan SC: Renin-angiotensin system as a potential therapeutic target in stroke and retinopathy: Experimental and clinical evidence. Clin Sci (Lond). 130:221–238. 2016. View Article : Google Scholar : PubMed/NCBI

4 

Hu R and Feng H: Lenticulostriate artery and lenticulostriate-artery neural complex: New concept for intracerebral hemorrhage. Curr Pharm Des. 23:2206–2211. 2017. View Article : Google Scholar : PubMed/NCBI

5 

Matsumoto K, Sakaki S, Abekura M and Yoshimine T: Co-existence of unruptured cerebral aneurysms in patients with hypertensive intracerebral hemorrhage. Acta Neurochir (Wien). 146:1085–1089; discussion 1089. 2004. View Article : Google Scholar : PubMed/NCBI

6 

Tian X, Shu H, Zhang H, Wang H and Guo L: Intracranial hemorrhage due to rupture of an anterior communicating artery aneurysm in a patient with pituitary adenoma. J Craniofac Surg. 26:e154–e155. 2015. View Article : Google Scholar : PubMed/NCBI

7 

Yiannakopoulos CK: Carpal ligament decompression under local anaesthesia: The effect of lidocaine warming and alkalinisation on infiltration pain. J Hand Surg Br. 29:32–34. 2004. View Article : Google Scholar : PubMed/NCBI

8 

Zhang Y, Liu B, Liu Z, Wang Y, Zhao H, Zi M, Wang L, Liu H, Chen Z and Xie Y: Development of a disease-specific health-related quality of life questionnaire for patients with post-stroke spasticity. J Tradit Chin Med. 32:674–678. 2012. View Article : Google Scholar : PubMed/NCBI

9 

Lue YJ, Lin RF, Chen SS and Lu YM: Measurement of the functional status of patients with different types of muscular dystrophy. Kaohsiung J Med Sci. 25:325–333. 2009. View Article : Google Scholar : PubMed/NCBI

10 

Kenning TJ, Dalfino JC, German JW, Drazin D and Adamo MA: Analysis of the subdural evacuating port system for the treatment of subacute and chronic subdural hematomas. J Neurosurg. 113:1004–1010. 2010. View Article : Google Scholar : PubMed/NCBI

11 

Southwell DG, Hervey-Jumper SL, Perry DW and Berger MS: Intraoperative mapping during repeat awake craniotomy reveals the functional plasticity of adult cortex. J Neurosurg. 124:1460–1469. 2016. View Article : Google Scholar : PubMed/NCBI

12 

Velnar T and Bunc G: Iatrogenic metastasis of a benign meningioma to the periosteum at the site of previous craniotomy: A case report. Wien Klin Wochenschr. 120:766–769. 2008. View Article : Google Scholar : PubMed/NCBI

13 

Chi FL, Lang TC, Sun SJ, Tang XJ, Xu SY, Zheng HB and Zhao HS: Relationship between different surgical methods, hemorrhage position, hemorrhage volume, surgical timing, and treatment outcome of hypertensive intracerebral hemorrhage. World J Emerg Med. 5:203–208. 2014. View Article : Google Scholar : PubMed/NCBI

14 

Morotti A, Paciaroni M, Zini A, Silvestrelli G, Del Zotto E, Caso V, Dell'Acqua ML, Simone AM, Lanari A, Costa P, et al: Risk profile of symptomatic lacunar stroke versus nonlobar intracerebral hemorrhage. Stroke. 47:2141–2143. 2016. View Article : Google Scholar : PubMed/NCBI

15 

Han WY, Tao YQ, Xu F, Zhang YQ, Li ZY and Liang GB: The short- and long-term efficacy analysis of stereotactic surgery combined external ventricular drainage in the treatment of the secondary intraventricular hemorrhage. Brain Behav. 7:e008642017. View Article : Google Scholar : PubMed/NCBI

16 

Guldberg-Kjär T and Johansson B: ADHD symptoms across the lifespan: A comparison of symptoms captured by the Wender and Barkley Scales and DSM-IV criteria in a population-based Swedish sample aged 65 to 80. J Atten Disord. 19:390–404. 2015. View Article : Google Scholar : PubMed/NCBI

17 

Sonni S, Lioutas VA and Selim MH: New avenues for treatment of intracranial hemorrhage. Curr Treat Options Cardiovasc Med. 16:2772014. View Article : Google Scholar : PubMed/NCBI

18 

Wang WZ, Jiang B, Liu HM, Li D, Lu CZ, Zhao YD and Sander JW: Minimally invasive craniopuncture therapy vs. conservative treatment for spontaneous intracerebral hemorrhage: Results from a randomized clinical trial in China. Int J Stroke. 4:11–16. 2009. View Article : Google Scholar : PubMed/NCBI

19 

James ML, Blessing R, Phillips-Bute BG, Bennett E and Laskowitz DT: S100B and brain natriuretic peptide predict functional neurological outcome after intracerebral haemorrhage. Biomarkers. 14:388–394. 2009. View Article : Google Scholar : PubMed/NCBI

20 

Ikedo T, Nakamura K, Sano N, Nagata M, Okada Y, Terakawa Y and Murata T: Intraoperative transcranial motor-evoked potentials predict motor function outcome in intracerebral hemorrhage surgery. World Neurosurg. 90:518–523. 2016. View Article : Google Scholar : PubMed/NCBI

21 

Voulgaris S, Karagiorgiadis D, Alexiou GA, Mihos E, Zigouris A, Fotakopoulos G, Drosos D and Pahaturidis D: Continuous intraoperative electromyographic and transcranial motor evoked potential recordings in spinal stenosis surgery. J Clin Neurosci. 17:274–276. 2010. View Article : Google Scholar : PubMed/NCBI

22 

Bestmann S and Krakauer JW: The uses and interpretations of the motor-evoked potential for understanding behaviour. Exp Brain Res. 233:679–689. 2015. View Article : Google Scholar : PubMed/NCBI

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Spandidos Publications style
Luan L, Li M, Sui H, Li G and Pan W: Efficacies of minimally invasive puncture and small bone window craniotomy for hypertensive intracerebral hemorrhage, evaluation of motor‑evoked potentials and comparison of postoperative rehemorrhage between the two methods. Exp Ther Med 17: 1256-1261, 2019
APA
Luan, L., Li, M., Sui, H., Li, G., & Pan, W. (2019). Efficacies of minimally invasive puncture and small bone window craniotomy for hypertensive intracerebral hemorrhage, evaluation of motor‑evoked potentials and comparison of postoperative rehemorrhage between the two methods. Experimental and Therapeutic Medicine, 17, 1256-1261. https://doi.org/10.3892/etm.2018.7094
MLA
Luan, L., Li, M., Sui, H., Li, G., Pan, W."Efficacies of minimally invasive puncture and small bone window craniotomy for hypertensive intracerebral hemorrhage, evaluation of motor‑evoked potentials and comparison of postoperative rehemorrhage between the two methods". Experimental and Therapeutic Medicine 17.2 (2019): 1256-1261.
Chicago
Luan, L., Li, M., Sui, H., Li, G., Pan, W."Efficacies of minimally invasive puncture and small bone window craniotomy for hypertensive intracerebral hemorrhage, evaluation of motor‑evoked potentials and comparison of postoperative rehemorrhage between the two methods". Experimental and Therapeutic Medicine 17, no. 2 (2019): 1256-1261. https://doi.org/10.3892/etm.2018.7094