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1.
目的: 探讨银杏叶制剂联合地塞米松在老年突聋治疗中对血清炎症指标的影响。方法: 按随机数字表法将我院2016年7月-2021年7月收治的102例老年突聋患者分入两组(各51例)。对照组用地塞米松治疗,治疗组加用银杏叶制剂治疗。观察两组治疗前后纯音听阈和血管内皮功能指标[超氧化物歧化酶(SOD)、脂质过氧化物(LPO)、一氧化氮(NO)]、血清炎症指标[肿瘤坏死因子-α(TNF-α)、C反应蛋白(CRP)、白细胞介素-6(IL-6)],分析其疗效与不良反应。结果: 与对照组比较,治疗组总有效率更高(96.08%vs 82.35%)(χ2=4.993,P=0.025);两组治疗后各频率点阈值均下降,且相比对照组,治疗组治疗后各频率点阈值更低(P<0.05);治疗后两组SOD、NO水平均升高,LPO水平降低(P<0.05),且相比对照组,治疗组治疗后SOD、NO水平更高,LPO水平更低(P<0.05);治疗后两组血清TNF-α、CRP、IL-6水平降低,且相比对照组,治疗组TNF-α、CRP、IL-6水平更低(P<0.05);治疗组不良反应发生率5.88%,对照组为9.80%,两组比较差异无统计学意义(P=0.543,χ2=0.461)。结论: 银杏叶制剂联合地塞米松治疗老年突聋患者疗效理想,能恢复各频率点听力,安全可靠,推测改善患者血管内皮功能和炎症因子水平是其重要作用机制。  相似文献   
2.
《Molecular therapy》2022,30(5):1952-1965
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Survivors of childhood acute lymphoblastic leukemia (ALL) treated with chemotherapy only are at risk for neurocognitive impairment. Regions of interest were identified a priori based on glucocorticoid receptor distribution, and sex‐stratified multivariable linear regression models were used to test associations between brain MRI morphology and total number of intrathecal injections, and serum concentration of dexamethasone and methotrexate. Compared with controls, ALL survivors have persistently smaller volumes in the bilateral cerebellum (P < 0.005), hippocampal subregions (P < 0.03), temporal lobe regions (P < 0.03), frontal lobe regions (P < 0.04), and parietal lobe regions (precuneus; P < 0.002). Long‐term problems with learning may be related to residual posttreatment brain differences.  相似文献   
5.
目的:评价地塞米松不同给药途径(冠周局部注射和口服)在预防下颌阻生第三磨牙拔除术后肿胀、疼痛及张口受限中的疗效。方法:对480例患者的下颌阻生第三磨牙根据阻生类型进行分组(高位、中位、低位),每组中再分为实验组(拔牙术后局部注射地塞米松)和对照组(拔牙术后口服地塞米松),对患者术后第1、3、7天进行随访分析,对患者肿胀指数、疼痛程度和张口受限程度进行统计分析。结果:在拔牙术后第1天和第7天,高位组、中位组和低位组中的实验组与对照组在肿胀指数、疼痛程度和张口受限程度方面比较差异无统计学意义(P>0.05);术后第3天,高位组和中位组中的实验组与对照组在肿胀指数、疼痛程度和张口受限程度差异无统计学意义(P>0.05),低位组中的实验组与对照组相比,在肿胀反应中具有更好的预防效果(P<0.05),在疼痛程度和张口受限程度中具有一定的缓解效果(P>0.05)。结论:下颌阻生第三磨牙拔除术后,冠周局部给予地塞米松能够防治和减轻术后肿胀、疼痛以及张口受限的发生。  相似文献   
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Background

The efficacy of dexamethasone in extending the duration of local anaesthetic block is uncertain. In a randomised controlled triple blind crossover study in volunteers, we tested the hypothesis that neither i.v. nor perineurally administered dexamethasone prolongs the sensory block achieved with ropivacaine.

Methods

Ultrasound-guided ulnar nerve blocks (ropivacaine 0.75% wt/vol, 3 ml, with saline 1 ml with or without dexamethasone 4 mg) were performed on three occasions in 24 male volunteers along with an i.v. injection of saline 1 ml with or without dexamethasone 4 mg. The combinations of saline and dexamethasone were as follows: control group, perineural and i.v. saline; perineural group, perineural dexamethasone and i.v. saline; i.v. group, perineural saline and i.v. dexamethasone. Sensory block was measured using a VAS in response to pinprick testing. The duration of sensory block was the primary outcome and time to onset of sensory block the secondary outcome.

Results

All 24 subjects completed the trial. The median [inter-quartile range (IQR)] duration of sensory block was 6.87 (5.85–7.62) h in the control group, 7.37 (5.78–7.93) h in the perineural group and 7.37 (6.10–7.97) h in the i.v. group (P=0.61). There was also no significant difference in block onset time between the three groups.

Conclusion

Dexamethasone 4 mg has no clinically relevant effect on the duration of sensory block provided by ropivacaine applied to the ulnar nerve.

Clinical trial registration

DRKS, 00014604; EudraCT, 2018-001221-98.  相似文献   
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Owing to the frequent incidence of blast-induced traumatic brain injury (bTBI) in recent military conflicts, there is an urgent need to develop effective therapies for bTBI-related pathologies. Blood-brain barrier (BBB) breakdown has been reported to occur after primary blast exposure, making restoration of BBB function and integrity a promising therapeutic target. We tested the hypothesis that treatment with dexamethasone (DEX) after primary blast injury potentiates recovery of an in vitro BBB model consisting of mouse brain endothelial cells (bEnd.3). DEX treatment resulted in complete recovery of transendothelial electrical resistance and hydraulic conductivity 1 day after injury, compared with 3 days for vehicle-treated injured cultures. Administration of RU486 (mifepristone) inhibited effects of DEX, confirming that barrier restoration was mediated by glucocorticoid receptor signaling. Potentiated recovery with DEX treatment was accompanied by stronger zonula occludens (ZO)-1 tight junction immunostaining and expression, suggesting that increased ZO-1 expression was a structural correlate to BBB recovery after blast. Interestingly, augmented ZO-1 protein expression was associated with specific upregulation of the α+ isoform but not the α isoform. This is the first study to provide a mechanistic basis for potentiated functional recovery of an in vitro BBB model because of glucocorticoid treatment after primary blast injury.  相似文献   
10.
《The Journal of arthroplasty》2022,37(10):1898-1905.e7
BackgroundCorticosteroids are commonly used intraoperatively to treat pain and reduce opioid consumption and nausea associated with primary total joint arthroplasty (TJA). The purpose of this study was to evaluate the efficacy and safety of corticosteroids in primary TJA to support the combined clinical practice guidelines of the American Association of Hip and Knee Surgeons, American Academy of Orthopaedic Surgeons, Hip Society, Knee Society, and the American Society of Regional Anesthesia and Pain Management.MethodsThe MEDLINE, Embase, and Cochrane Central Register of Controlled Trials databases were searched for studies published before February 2020 on corticosteroids in TJA. All included studies underwent qualitative and quantitative homogeneity testing followed by a systematic review and direct comparison meta-analysis to assess the efficacy and safety of corticosteroids.ResultsCritical appraisal of 1,581 publications revealed 23 studies regarded as the best available evidence for analysis. Intraoperative dexamethasone reduces postoperative pain, opioid consumption, and nausea and vomiting. Multiple doses lead to further reduction in pain, opioid consumption, nausea and vomiting. There is insufficient evidence on the risk of adverse events with perioperative dexamethasone in TJA.ConclusionStrong evidence supports the use of a single dose or multiple doses of intravenous dexamethasone to reduce postoperative pain, opioid consumption, nausea and vomiting after primary TJA. There is insufficient evidence on perioperative dexamethasone in primary TJA to determine the optimal dose, number of doses, or risk of postoperative adverse events.  相似文献   
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