Effects of dexmedetomidine combined with sodium creatine phosphate on inflammation, oxidative stress, and neurological function recovery in patients undergoing intracranial hematoma evacuation: study protocol for a multi-center, prospective randomized parallel-cohort controlled trial
Chao-liang Tang1, Juan Li2, Bo Zhao3, Si Shi3, Hao Shen2, Zhong-yuan Xia3
1 Department of Anesthesiology, Renmin Hospital of Wuhan University, Wuhan, Hubei Province; Department of Anesthesiology, Anhui Provincial Hospital, Hefei, Anhui Province, China
2 Department of Anesthesiology, Anhui Provincial Hospital, Hefei, Anhui Province, China
3 Department of Anesthesiology, Renmin Hospital of Wuhan University, Wuhan, Hubei Province, China
|Date of Web Publication||30-Jan-2017|
Department of Anesthesiology, Renmin Hospital of Wuhan University, Wuhan, Hubei Province
Source of Support: None, Conflict of Interest: None
Background: In treating intracranial hematoma, dexmedetomidine (Dex) exhibits neuroprotective effects by preventing cognitive decline, and sodium creatine phosphate (SCP) exhibits neuroprotective effects by reducing cell death, maintaining the blood-brain barrier and improving interstitial cerebral edema. Few studies have examined the effects of Dex combined with SCP on perioperative inflammation and oxidative stress response, or recovery of neurological function.
Methods/Design: Here we propose a multi-center, prospective randomized parallel-cohort controlled trial, to be performed at Anhui Provincial Hospital and Renmin Hospital of Wuhan University, China. After screening against inclusion and exclusion criteria, 80 patients scheduled to receive intracranial hematoma evacuation will be randomly divided into control, Dex, SCP, and Dex + SCP groups, with 20 patients per group. Under general anesthesia, all patients will undergo craniotomy for hematoma removal. In the Dex and Dex + SCP groups, an intravenous bolus of Dex (0.6 μg/kg) will be administered 10 minutes before anesthesia induction and thereafter intravenous administration of Dex (0.4 μg/kg/h) will be given. In the SCP, and Dex + SCP groups, 1.0 g SCP will be administered 10 minutes before anesthesia induction. The primary outcome measure is the difference in postoperative 72-hour Glasgow Coma Scale (GCS) score and postoperative 12-hour GCS score. The secondary outcome measures include differences in postoperative 48-hour and 24-hour GCS scores and postoperative 12-hour GCS score; plasma levels of inflammatory and oxidative stress markers, and pathological changes in brain tissue before anesthesia induction and at the end of surgery; and physiological indices during surgery.
Discussion: We evaluate whether results from the proposed study protocol will provide evidence that the use of Dex combined with SCP in patients undergoing intracranial hematoma evacuation is feasible.
Trial registration: The study protocol was registered at Chinese Clinical Trial Registry (http://www.chictr.org.cn/) on 11 December 2014 (registration number: ChiCTR-IPR-14005656).
Ethics: The study protocol was approved by Ethics Committee, Anhui Provincial Hospital, China on 25 November 2014 (approval No. 2014-ethics-39) and will be performed in accordance with the Declaration of Helsinki formulated by the World Medical Association.
Informed consent: Written informed consent will be obtained from patient's guardians or clients prior to enrollment in the clinical trial.
Keywords: clinical trial; intracranial hemorrhage; dexmedetomidine; sodium creatine phosphate; intracranial hematoma; inflammation response; oxidative stress; neurologic function; multi-center, prospective randomized parallel-cohort controlled trial
|How to cite this article:|
Tang Cl, Li J, Zhao B, Shi S, Shen H, Xia Zy. Effects of dexmedetomidine combined with sodium creatine phosphate on inflammation, oxidative stress, and neurological function recovery in patients undergoing intracranial hematoma evacuation: study protocol for a multi-center, prospective randomized parallel-cohort controlled trial. Asia Pac J Clin Trials Nerv Syst Dis 2017;2:1-8
|How to cite this URL:|
Tang Cl, Li J, Zhao B, Shi S, Shen H, Xia Zy. Effects of dexmedetomidine combined with sodium creatine phosphate on inflammation, oxidative stress, and neurological function recovery in patients undergoing intracranial hematoma evacuation: study protocol for a multi-center, prospective randomized parallel-cohort controlled trial. Asia Pac J Clin Trials Nerv Syst Dis [serial online] 2017 [cited 2019 Oct 15];2:1-8. Available from: http://www.actnjournal.com/text.asp?2017/2/1/1/198958
| Introduction|| |
History and current related studies
Cerebral hemorrhage is a common and severe type of stroke, with high prevalence, morbidity and mortality. However, with the exception of surgical removal of hematoma and lowering of intracranial pressure by dehydration, there are no effective methods for improving neurological impairment caused by cerebral hemorrhage. During the perioperative period, patients with cerebral hemorrhage often experience acute agitation due to pain (Rajan et al., 2014; Sriganesh et al., 2015). Pain caused by cerebral hemorrhage increases sympathetic activity and causes stress responses, leading to increased blood pressure, intracranial pressure and cerebral oxygen consumption. This can cause excessive release of a range of hormones and inflammatory factors, leading to secondary brain injury, and eventually resulting in severe postoperative complications, such as intracranial hemorrhage (Chi et al., 2011, 2014; Hancı et al., 2012). Dexmedetomidine (Dex) is a highly selective new α2-adrenoceptor agonist that regulates the release of catecholamines to control blood pressure via a sympathetic negative feedback mechanism. It also acts on postsynaptic membrane α2 receptors, hyperpolarizing postsynaptic cells and inhibiting the conduction of pain signals to the brain, exhibiting analgesic, sedative, anti-anxiety and anti-sympathetic effects. Dex, as an anesthetic adjuvant, can motorize the adrenergic receptors in the central and peripheral nervous systems, effectively decrease sympathetic activity, lower abnormally elevated blood pressure and heart rate under stress, maintain hemodynamic stability, and simultaneously reduce the necessary dosages of sedatives and analgesics (Yi et al., 2011). Similar to other α2-adrenoceptor agonists, Dex does not produce respiratory depression; it can greatly alleviate brain edema caused by acute craniocerebral injury (Benggon et al., 2012), exhibit neuroprotective effects and prevent cognitive impairment (Zhu et al., 2013). After cerebral hemorrhage, a strong stress response of the body is triggered, stimulating the excessive release of proinflammatory factors via inflammatory cells at the bleeding site, causing metabolic disorders in the brain tissue. In addition, compression of the hematoma to the adjacent brain tissue can aggravate ischemia/hypoxic brain injury in normal brain tissue. All of these processes can strongly influence the recovery of neurological function after surgery (Zhang et al., 2006). After cerebral hemorrhage, cerebral blood flow in the corresponding brain regions decreases, and the brain tissue rapidly enters the ischemic/hypoxic state, disrupting the energy metabolism of brain cells and leading to brain edema and necrosis of brain tissue (Fallon, 2008; Vallböhmer et al., 2008). Use of anesthetics and surgery can also cause hypotension and low perfusion, leading to ischemia/hypoxia of the brain cells and causing abnormal energy metabolism of brain cells (D'Angelo et al., 2008).
Creatine phosphate is an important component of the tissue antioxidant system and an important substance for cell energy metabolism. There is strong evidence that exogenous creatine phosphate can react with adenosine di-phosphate to generate creatine and adenosine tri-phosphate in the cytoplasmic membrane, cytoplasmic reticulum, mitochondrial membrane space and myofibrils under the catalysis of phosphocreatine creatine kinase (Green et al., 2007; Hazra and Dubinett, 2007; Pan and Takahashi, 2007). This can supplement for adenosine tri-phosphate deficiency caused by cerebral ischemia/hypoxia or glucose deprivation, greatly decreasing cell death. In addition, supplementation of creatine phosphate can increase the anti-hypoxic ability of nerve cells, accelerate the recovery of brain cell membranes, maintain the integrity of brain cells, and progressively maintain the integrity of functionalized vascular walls while strengthening the regulation of anterior sphincter of capillaries to local blood pressure. These processes are conducive to maintaining the blood-brain barrier, improving interstitial brain edema (Al-Joudi et al., 2007; Lu et al., 2008), and exhibiting neuroprotective effects (Samaka et al., 2006; Ducray et al., 2007; Pankova et al., 2007).
Based on previous research, the proposed study is designed to investigate the effects of Dex combined with sodium creatine phosphate (SCP) on perioperative inflammation, oxidative stress, and neurological function recovery in patients undergoing intracranial hematoma evacuation, which will provide clinical evidence for anesthetic use and neuroprotection during removal of intracranial hematoma.
Novelty of this study
Previously reported studies have mainly focused on the neuroprotective effects of Dex or SCP on intracranial hematoma ([Table 1]). Few studies have examined the effects of Dex combined with SCP on perioperative inflammation and oxidative stress as well as recovery of neurological function in patients with intracranial hematoma.
|Table 1: Previous studies on the neuroprotective effects of dexmedetomidine (Dex) or sodium creatine phosphate (SCP) in patients with intracranial hematoma |
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| Methods/Design|| |
This is a multi-center, prospective randomized parallel-cohort controlled trial, which will be performed at Anhui Provincial Hospital and Renmin Hospital of Wuhan University, China. Eighty patients scheduled to receive intracranial hematoma evacuation will be randomly divided into control, Dex, SCP, and Dex + SCP groups.
In the Dex and Dex + SCP groups, an intravenous bolus of Dex (0.6 μg/kg) will be administered 10 minutes before anesthesia induction, followed by intravenous Dex (0.4 μg/kg/h) administration. In the SCP and Dex + SCP groups, 1.0 g SCP will be administered 10 minutes before anesthesia induction. Under general anesthesia, all patients will undergo craniotomy for hematoma removal. The primary outcome measure is the difference of postoperative 72-hour Glasgow Coma Scale (GCS) score and postoperative 12-hour GCS score. The secondary outcome measures include the differences in postoperative 48-hour and 24-hour GCS scores and postoperative 12-hour GCS score; plasma levels of inflammatory and oxidative stress markers, and pathological changes in brain tissue before anesthesia induction and at the end of surgery; and measurements of physiological indices during surgery. Other outcome measures include dosages of propofol and remifentanil, amount of drainage, operation time, and anesthesia time.
The flowchart of study protocol is shown in [Figure 1].
|Figure 1: The flowchart of study protocol. |
Note: Dex: Dexmedetomidine; SCP: sodium creatine phosphate; GCS: Glasgow Coma Scale
Click here to view
Patients with intracranial hemorrhage scheduled for craniotomy for hematoma removal in the Anhui Provincial Hospital and Renmin Hospital of Wuhan University, China will be considered for admission to this study after screening against the inclusion and exclusion criteria described below.
Patients meeting all of the following criteria will be considered for admission to this study:
- Patients with intracranial hemorrhage confirmed by computed tomography (CT) or magnetic resonance imaging (MRI) findings who need surgery: (1) Hypertensive cerebral hemorrhage: a) lobar hemorrhage ≥ 30 mL; b) basal ganglia hemorrhage ≥ 30 mL; c) thalamic hemorrhage ≥ 10 mL; d) cerebellar hemorrhage ≥ 10 mL; e) intraventricular hemorrhage, causing obstructive hydrocephalus or molded intraventricular hemorrhage; f) intracranial hemorrhage volumes do not meet the indications for surgery, but patients have severe neurological disorders; (2) traumatic intracranial hemorrhage: a) acute epidural, subdural hematoma, amount of supratentorial hematoma ≥ 30 mL, amount of subtentorial hematoma ≥ 10 mL, unstable disease condition; b) subacute chronic subdural hematoma; c) intracranial hematoma referencing to hypertension indications; d) brain injury complicated by intraventricular hemorrhage and obstructive hydrocephalus (Rao and Wang, 2014)
- Mode of surgery: craniotomy for hematoma removal
- Age 18-70 years of age
- American Society of Anesthesiologists (ASA) grade I-IV
Patients presenting with one or more of the following conditions will be excluded from this study:
- Coagulation disorder
- Identified aneurysm or arterial malformation caused by hematoma
- Previous drug allergy
- Drug (alcohol, opioids or tranquilizers) addiction
- Complication with other severe diseases, such as severe hypertension, cardiovascular disease, malignant tumor, autoimmune diseases, mental disorders and patients with diabetes who have poor blood glucose control
- Liver and kidney dysfunction
- Long-term use of opioids
- Advanced brain herniation or brain death
- Evidence of infection before suffering from cerebral hemorrhage
- Currently lactating
In accord with previous studies (Xu et al., 2011; Yu et al., 2012; Bishnoi et al., 2016; Wang et al., 2016), there will be 20 patients per group. Thus, 80 patients will be included in this study. Data analysis will follow the intention-to-treat principle.
The baseline information is shown in [Table 2].
Randomization and blinding
Eighty patients will be randomly divided into four groups, with 20 patients per group according to a random digital table, carried out by a statistician blinded to the study protocol. Patients and results evaluators will be blinded to grouping.
Venous access will be established for monitoring the patients' vital signs. Under local anesthesia with 0.5 mL 2% lidocaine, radial artery puncture will be performed for direct arterial pressure monitoring. During the surgery, Lactated Ringer's Injection will be administered into the patients according to a 4-2-1 principle (i.e., 4 mL/kg for < body mass < 10 kg, 2 mL/kg for the second 10 kg and 1 mL/kg for the next).
In the Dex and Dex + SCP groups, an intravenous bolus of Dex (0.6 μg/kg; China National Medicines Guorui Pharmaceutical Co., Ltd., China) will be administered 10 minutes before anesthesia induction, followed by intravenous Dex (0.4 μg/kg/h) administration. In the SCP and Dex + SCP groups, 1.0 g SCP (dissolved in 100 mL normal saline; Haikou Kellett Pharmaceutical Co., Ltd., China) will be administered, starting from 10 minutes before anesthesia induction for 30 minutes.
Anesthesia induction: Three minutes after intravenous administration of sufentanil (0.5 μg/kg), atracurium (0.2 mg/kg) and propofol (2 mg/kg), tracheal intubation will be terminated. Anesthesia will be maintained by target-controlled infusion with remifentanil (predicted concentration (Cp) 3.0-4.0 ng/mL) and propofol (Cp 3.0-4.0 μg/mL). Dosages of remifentanil and propofol will be adjusted in accord with changes in the bispectral index. The bispectral index value will be maintained between 45-55. Dex administration will not be terminated until 10 minutes prior to the completion of the surgery. Remifentanil and propofol a dministration will not be terminated until completion of the surgery.
Primary outcome measure
- Difference of postoperative 72-hour GCS (Teasdale and Jennett, 1974) score and postoperative 12-hour GCS score.
- GCS is composed of three tests: eye, verbal and motor responses with scores ranging from 3-15. The GCS is the most widely used assessment of disturbance of consciousness. It is used for evaluation of coma after traumatic brain injury causing various types of impairment in a range of types of consciousness (details of the GCS are shown in Additional file 1 [Additional file 1]).
Secondary outcome measures
- Differences in postoperative 48-hour and 24-hour GCS scores and postoperative 12-hour GCS score.
- Plasma levels of inflammatory markers: Prior to anesthesia induction and at the end of the surgery, 3 mL of peripheral venous blood will be collected then preserved at −80°C. Plasma levels of interleukin-6, -8 and -10 and tumor necrosis factor-α will be measured using the enzyme-linked immunosorbent assay (ELISA) method (Welch et al., 2016).
- Plasma levels of oxidative stress markers: Prior to anesthesia induction and at the end of the surgery, 3 mL of peripheral venous blood will be collected for measurement of plasma levels of malondialdehyde, superoxide dismutase, 4-hydroxynonenal, neurotensin and 8-hydroxydeoxyguanosine. Malondialdehyde is a commonly used peroxidation index for membrane lipids (Gerritsen et al., 2006) and it is determined using the thiobarbituric acid method. Superoxide dismutase is the major antioxidant enzyme produced by the mitochondria (Washio et al., 2008) and is determined with the xanthine oxidase method. 4-Hydroxynonenal is a highly active, diffusible lipid peroxide (Chen and Ran, 2006) determined with the ELISA method. Neurotensin is a biomarker of nitrated protein (Ceriello et al., 2001). 8-Hydroxydeoxyguanosine is a specific product of DNA oxidative damage (Gao et al., 2012) and is a recognized biomarker of oxidative damage to DNA by both endogenous and exogenous factors. Both nitrotyrosine and 8-hydroxydeoxyguanosine are tested with the ELISA method (Welch et al., 2016).
- Pathological changes of brain tissue: Neuronal specific enolase and CD31 expression will be detected with immunohistochemical staining in the brain tissue surrounding the hematoma of patients to investigate neuronal damage and angiogenesis.
- Physiological indices: Patient's systolic blood pressure, diastolic blood pressure, and heart rate will be measured at the time of patients entering the operating room, prior to anesthesia induction, 1 minute after tracheal intubation, at the beginning of operation, after removal of the bone flap, after dura mater opening, at the end of surgery and after extubation.
Other outcome measures
The dosages of propofol and remifentanil, amount of drainage, operation time, and anesthesia time will also be recorded.
The schedule of primary and secondary outcome measures is shown in [Table 3].
The case report forms will be filled out by the investigators accurately, completely and in time. The written records will be transferred to an electronic format by professional staff using a double-data entry strategy.
All observations and findings in clinical trials will be verified to ensure data reliability, to ensure that the conclusions from clinical trials are derived from the original data, and to ensure that the database is locked by the primary investigator. All relevant data will be stored by Anhui Provincial Hospital and Renmin Hospital of Wuhan University of China.
All data will be statistically analyzed by professional statisticians and anonymized trial data will be published at www.figshare.com.
All data will be statistically analyzed using SPSS 23.0 software (IBM, Armonk, NY, USA). Data analysis will follow the intention-to-treat principle. All data will be expressed as the mean ± SD. Independent-sample t-tests will be used for comparison of normally distributed data. Nonparametric two-sample tests (Wilcoxon signed-rank tests) will be used for comparison of non-normally distributed data. A level of P < 0.05 will be considered statistically significant.
Possible sources of bias include: (1) diagnosis bias (the choice of criteria for inclusion); (2) admission bias (the tendency to choose hospitalized patients to reduce the lost to follow-up rate and increase compliance); (3) no-response bias (patients failing to respond to the survey, or providing false responses); (4) measurement bias (possible errors because of poor staff performance); (5) confounding bias (sex, age).
Measures that will be taken to control bias include: (1) unified training of investigators; (2) strict inclusion and exclusion criteria; (3) ensuring sample independence; (4) avoiding additional harm to patients in the trial process, increasing the likelihood of compliance; (5) reducing the number of withdrawn cases, and follow-up with withdrawn patients; (6) curative effect evaluation will be performed by designated persons before and after treatment to avoid measurement bias; (7) confounding factors (such as etiology, course of disease and sex) likely to influence the curative effects will be treated as independent variables in a multivariate analysis; (8) to reduce the loss of data, data from withdrawn patients will also be included in an intention-to-treat analysis.
The results and relevant data from this study will be owned and used without charge by Renmin Hospital of Wuhan University and Anhui Provincial Hospital, China. Patient's baseline information will be password-protected by the Anhui Provincial Hospital, China. Patient identity will not be divulged unless required by law. The findings from this study will be published for scientific purposes without disclosing the patient's identity.
| Trial Status|| |
Patient recruitment is currently underway.
| Discussion|| |
Significance of this study
Dex, as a promising neurosurgical anesthetic, has unique sedative and analgesic effects, does not produce respiratory depression, has stable hemodynamics, exhibits neuroprotective effects on postoperative re-hemorrhage and promotes the recovery of neurological function. Dex in combination with systemic anesthetics for craniotomy for removal of intracranial hematoma has been found to maintain hemodynamic stability during surgery (Benggon et al., 2012). SCP is an important substance for cell energy metabolism. It can provide energy under conditions of insufficient energy, and protects important organs. Dex in combination with SCP may exhibit stronger neuroprotective effects during the removal of intracranial hematoma in patients with cerebral hemorrhage than monotherapy.
Strengths and limitations of this study
In this study, the addition of Dex and SCP, which are commonly used in the clinic, to conventional systemic anesthetics for craniotomy for removal of intracranial hematoma is a simple and feasible method. In addition, the hospitals at which surgery will be performed are equipped with the relevant capability and equipment. Moreover, the experimental processes will not cause additional harm to patients, increasing the likelihood of compliance. All of these characteristics are likely to facilitate success in surgery. Nevertheless, differences in etiology, disease course and sex exist between the patients with cerebral hemorrhage that will be included in this study. In addition, the included patients are likely to have a history of hypertension. Thus, discrepancies regarding category, usage and dosage of blood pressure-lowering drugs may exist between patients. These limitations should be taken into consideration in future studies.
Evidence for contribution to future studies
The proposed study is designed to provide clinical evidence for the use of Dex in combination with SCP in craniotomy for the removal of intracranial hematoma, enabling new treatment options for improving inflammation, oxidative stress and neurological function recovery in patients with cerebral hemorrhage.
Additional file 1: Glasgow Coma Scale.
| References|| |
Al-Joudi FS, Iskandar ZA, Hasnan J, Rusli J, Kamal Y, Imran AK, Ahmed M, Zakaria J (2007) Expression of survivin and its clinicopathological correlations in invasive ductal carcinoma of the breast. Singapore Med J 48:607-614.
Benggon M, Chen H, Applegate R, Martin R, Zhang JH (2012) Effect of dexmedetomidine on brain edema and neurological outcomes in surgical brain injury in rats. Anesth Analg 115:154-159.
Bishnoi V, Kumar B, Bhagat H, Salunke P, Bishnoi S (2016) Comparison of dexmedetomidine versus midazolam-fentanyl combination for monitored anesthesia care during burr-hole surgery for chronic subdural hematoma. J Neurosurg Anesthesiol 28:141-146.
Ceriello A, Mercuri F, Quagliaro L, Assaloni R, Motz E, Tonutti L, Taboga C (2001) Detection of nitrotyrosine in the diabetic plasma: evidence of oxidative stress. Diabetologia 44:834-838.
Chen J, Ran PX (2006) Role of 4-hydroxynonenal in pathophysiological process. Guoji Huxi Zazhi 26:821-824.
Chi FL, Lang TC, Sun SJ, Tang XJ, Xu SY, Zheng HB, Zhao HS (2014) 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.
Chi OZ, Hunter C, Liu X, Weiss HR (2011) The effects of dexmedetomidine on regional cerebral blood flow and oxygen consumption during severe hemorrhagic hypotension in rats. Anesth Analg 113:349-355.
D′Angelo C, Mirijello A, Leggio L, Ferrulli A, Carotenuto V, Icolaro N, Miceli A, D′Angelo V, Gasbarrini G, Addolorato G (2008) State and trait anxiety and depression in patients with primary brain tumors before and after surgery: 1-year longitudinal study. J Neurosurg 108:281-286.
Drummond JC, Sturaitis MK (2010) Brain tissue oxygenation during dexmedetomidine administration in surgical patients with neurovascular injuries. J Neurosurg Anesthesiol 22:336-341.
Ducray AD, Schläppi JA, Qualls R, Andres RH, Seiler RW, Schlattner U, Wallimann T, Widmer HR (2007) Creatine treatment promotes differentiation of GABA-ergic neuronal precursors in cultured fetal rat spinal cord. J Neurosci Res 85:1863-1875.
Fallon KE (2008) The clinical utility of screening of biochemical parameters in elite athletes: analysis of 100 cases. Br J Sports Med 42:334-337.
Fitz-Henry J (2011) The ASA classification and peri-operative risk. Ann R Coll Surg Engl 93:185-187.
Gao YN, Yang J, Song QX, Li BG, Chen GH, Ding L (2012) Application of 8-hydroxydeoxyguanosine as a biomarker of oxidative damage in diagnosis. Yaoxue yu Linchuang Yanjiu 20:223-228.
Gerritsen WB, van Boven WJ, Boss DS, Haas FJ, van Dongen EP, Aarts LP (2006) Malondialdehyde in plasma, a biomarker of global oxidative stress during mini-CABG compared to on- and off-pump CABG surgery: a pilot study. Interact Cardiovasc Thorac Surg 5:27-31.
Green HJ, Ball-Burnett M, Jones S, Farrance B (2007) Mechanical and metabolic responses with exercise and dietary carbohydrate manipulation. Med Sci Sports Exerc 39:139-148.
Hancý V, Yurdakan G, Yurtlu S, Turan IÖ, Sipahi EY (2012) Protective effect of dexmedetomidine in a rat model of α-naphthylthiourea-induced acute lung injury. J Surg Res 178:424-430.
Hazra S, Dubinett SM (2007) Ciglitazone mediates COX-2 dependent suppression of PGE2 in human non-small cell lung cancer cells. Prostaglandins Leukot Essent Fatty Acids 77:51-58.
Lu M, Strohecker A, Chen F, Kwan T, Bosman J, Jordan VC, Cryns VL (2008) Aspirin sensitizes cancer cells to TRAIL-induced apoptosis by reducing survivin levels. Clin Cancer Res 14:3168-3176.
Pan JW, Takahashi K (2007) Cerebral energetic effects of creatine supplementation in humans. Am J Physiol Regul Integr Comp Physiol 292:R1745-R1750.
Pankova TM, Starostina MV, Shtark MB, Epstein OI (2007) Neuroprotective effect of ultra-low doses of antibodies against S100 protein in neuroblastoma culture during oxygen and glucose deprivation. Bull Exp Biol Med 144:288-290.
Rajan S, Deogaonkar M, Kaw R, Nada EMS, Hernandez AV, Ebrahim Z, Avitsian R (2014) Factors predicting incremental administration of antihypertensive boluses during deep brain stimulator placement for Parkinson′s disease. J Clin Neurosci 21:1790-1795.
Rao ML, Wang WZ (2014) Minimally invasive puncture for removal of intracranial hematoma: technical specifications. Beijing: People′s Medical Publishing House.
Samaka RM, Abdou AG, Abd El-Wahed MM, Kandil MA, El-Kady NM (2006) Cyclooxygenase-2 expression in chronic gastritis and gastric carcinoma, correlation with prognostic parameters. J Egypt Natl Canc Inst 18:363-374.
Sato K, Kamii H, Shimizu H, Kato M (2006) Preoperative sedation with dexmedetomidine in patients with aneurysmal subarachnoid hemorrhage. Masui 55:51-54.
Sriganesh K, Reddy M, Jena S, Mittal M, Umamaheswara Rao GS (2015) A comparative study of dexmedetomidine and propofol as sole sedative agents for patients with aneurysmal subarachnoid hemorrhage undergoing diagnostic cerebral angiography. J Anesth 29:409-415.
Teasdale G, Jennett B (1974) Assessment of coma and impaired consciousness. A practical scale. Lancet 2:81-84.
Vallböhmer D, Kuhn E, Warnecke-Eberz U, Brabender J, Hoffmann AC, Metzger R, Baldus SE, Drebber U, Hoelscher AH, Schneider PM (2008) Failure in downregulation of intratumoral survivin expression following neoadjuvant chemoradiation in esophageal cancer. Pharmacogenomics 9:681-690.
Wang W, Chen Q, Qian YN, Yu WY (2016) Effect of creatine phosphate sodium on bispectral index and recovery quality during general anesthesia emergence period in elderly patients. Linchuang Mazui Xue Zazhi 32:563-566.
Washio K, Inagaki M, Tsuji M, Morio Y, Akiyama S, Gotoh H, Gotoh T, Gotoh Y, Oguchi K (2008) Oral vitamin C supplementation in hemodialysis patients and its effect on the plasma level of oxidized ascorbic acid and Cu/Zn superoxide dismutase, an oxidative stress marker. Nephron Clinical Practice 109:c49-c54.
Welch NG, Easton CD, Scoble JA, Williams CC, Pigram PJ, Muir BW (2016) A chemiluminescent sandwich ELISA enhancement method using a chromium (III) coordination complex. J Immunol Methods 438:59-66.
Xu KQ, Yang LX, Chen MY, Shao H, Zhang T (2011) Effects of creatine phosphate on cognitive dysfunction darly after neurosurgery in patients. Zhongguo Shiyong Yiyao 6:3-5.
Yi LD, Peng LB, Tan CQ, Cui W, Wan XM, Luo X, Cao JH, Zeng XH, Yang QF (2011) Dexmedetomidine: a new sedative and analgesic drug. Zhongguo Xinyao yu Linchuang Zazhi 30:5-10.
Yu MS, Zhang R, Fu MY, Wu XQ, Sun X, Wang J (2012) Clinical observation on patients with severe head injury combined with myocavdial damage treated by creatine phosphate. Xiandai Shengwu Yixue Jinzhan 12:3888-3890,3920.
Zhang YM, Qi ST, Fang LX, Qiu BH (2006) Clinical study of systemic inflammatory response syndrome after acute and severe craniocerebral trauma. Zhongguo Linchuang Shenjing Waike Zazhi 11:34.
Zhu YM, Wang CC, Chen L, Qian LB, Ma LL, Yu J, Zhu MH, Wen CY, Yu LN, Yan M (2013) Both PI3K/Akt and ERK1/2 pathways participate in the protection by dexmedetomidine against transient focal cerebral ischemia/reperfusion injury in rats. Brain Res 1494:1-8.
Declaration of patient consent
The authors certify that they will obtain all appropriate patient consent forms. In the form the patients will give their consent for their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Conflicts of interest
Conception and design of study protocol: CLT and ZYX; trial conduction: CLT, JL, BZ, SS and HS; data management and manuscript writing: CLT; manuscript authorization: ZYX. All authors approved the final version of this paper.
This paper was screened twice using CrossCheck to verify originality before publication.
This paper was double-blinded and stringently reviewed by international expert reviewers.
[Table 1], [Table 2], [Table 3]
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