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1.
摘要 目的:对比七氟烷与丙泊酚维持麻醉对合并冠心病腹腔镜胆囊切除术(LC)患者心功能、氧化应激和术后认知功能的影响。方法:选取2020年3月~2022年4月在吉林大学第一医院乐群院区麻醉科行全麻下LC的98例合并冠心病的患者,按照随机数字表法将患者分为A组(n=49,丙泊酚维持麻醉)和B组(n=49,七氟烷维持麻醉)。对比两组麻醉效果、血流动力学相关指标[心率(HR)、平均动脉压(MAP)、血氧饱和度(SpO2)]、认知功能情况[简易智能精神状态量表(MMSE)评分]、心功能指标[心输出量(CO)、心脏指数(CI)、左室射血分数(LVEF)]、氧化应激指标[超氧化物歧化酶(SOD)、丙二醛(MDA)、总抗氧化能力(T-AOC)]和不良反应发生率。结果:B组的恢复自主呼吸时间、睁眼时间、拔管时间、定向力恢复时间均短于A组(P<0.05)。B组气腹后5 min、手术结束时SpO2、HR、MAP高于A组(P<0.05)。B组术后1 d、术后3 d MMSE评分高于A组(P<0.05)。B组术后1 d CO、CI、LVEF高于A组(P<0.05)。B组术后1d SOD高于A组,MDA、T-AOC低于A组(P<0.05)。两组不良反应发生率组间比较无统计学差异(P>0.05)。结论:与丙泊酚维持麻醉相比,七氟烷用于合并冠心病LC患者,有利于维持血流动力学稳定,减轻心功能、氧化应激损伤和术后认知功能障碍。  相似文献   

2.
摘要 目的:探讨不同麻醉方法对行腹腔镜子宫全切2型糖尿病(T2DM)患者血流动力学、血糖水平及补体C3、C4的影响。方法:前瞻性选择2016年1月至2019年1月期间我院收治的120例拟行腹腔镜子宫全切术的T2DM患者,采用随机数字表法将患者分为两组,A组(60例)采用靶控输注丙泊酚、瑞芬太尼全麻,B组(60例)采用靶控输注丙泊酚、瑞芬太尼复合吸入七氟醚全麻。观察两组围手术期血流动力学、血糖、胰岛素、胰高血糖素、C肽及补体C3、C4水平变化和差异,对比两组麻醉效果。结果:B组苏醒时间、拔管时间短于A 组(P<0.05),苏醒后视觉模拟评分法(VAS)评分低于A组(P<0.05)。B组建立气腹前(T1)、建立气腹后1.5 h(T2)、手术结束时(T3)、苏醒时(T4) 观测点平均动脉压(MAP)高于A组(P<0.05)。建立气腹前(M1)、建立气腹后1.5 h(M2)、术后第1 d(M3)、术后第3 d(M4)观测点胰岛素、C肽水平低于A组(P<0.05)。M1-M4观测点血糖高于A组(P<0.05),M2-M4观测点胰高血糖素水平高于A组(P<0.05)。M1-M4观测点补体C3、C4水平高于A组(P<0.05)。结论:靶控输注丙泊酚、瑞芬太尼复合七氟醚全麻麻醉效果更好,且有助于维持腹腔镜子宫全切T2DM患者血流动力学稳定,改善补体C3、C4水平,而靶控输注丙泊酚、瑞芬太尼全麻可维持血糖水平稳定,临床应根据患者情况选择合适的麻醉方案。  相似文献   

3.
摘要 目的:探讨连续胸椎旁神经阻滞(TPVB)联合全身麻醉对乳腺癌根治手术患者血流动力学、应激反应及生存质量的影响。方法:选择2017年2月~2019年8月期间于我院行乳腺癌根治手术的乳腺癌患者125例,按照随机数字表法分为A组62例和B组63例,A组给予全身麻醉,B组给予TPVB联合全身麻醉,对比两组血流动力学、应激反应、生存质量、疼痛及不良反应。结果:两组插管前(T1)~拔管时(T4)时间点平均动脉压(MAP)、心率(HR)均较麻醉前(T0)升高,但B组T1~T4时间点MAP、HR低于A组(P<0.05)。B组术后1 d肾上腺素、血糖、去甲肾上腺素及多巴胺水平低于A组(P<0.05)。两组术后6个月躯体角色、躯体功能、情感角色、社会功能、躯体疼痛、总体健康、活力以及心理健康评分均较术前升高(P<0.05)。B组术后4 h、术后12 h、术后24 h安静时视觉模拟评分法(VAS)评分 、运动时VAS评分低于A组(P<0.05)。两组不良反应总发生率对比未见统计学差异(P>0.05)。结论:TPVB联合全身麻醉应用于乳腺癌根治手术患者,可减轻机体应激反应,维持血流动力学平稳,减轻术后疼痛,且不增加不良反应发生率,对生存质量无显著影响。  相似文献   

4.
摘要 目的:探讨利多卡因咽喉表面麻醉对腹腔镜胆囊切除术(LC)患者应激反应、血流动力学及恢复质量的影响。方法:采用随机数字表法将长沙市第一医院2019年4月-2021年6月期间收治的80例行LC患者分为对照组(40例,接受全身麻醉)和观察组(40例,对照组的基础上接受利多卡因咽喉表面麻醉)。对比两组血流动力学指标、应激反应指标、呛咳和躁动的发生情况、疼痛情况及生活质量。结果:观察组气管插管即刻(T1)~手术结束时(T4)收缩压(SBP)、舒张压(DBP)和心率(HR)低于对照组同期(P<0.05)。观察组术后即刻皮质醇(Cor)、促肾上腺皮质激素(ACTH)低于对照组(P<0.05)。观察组的呛咳发生率、躁动发生率以及总发生率明显低于对照组(P<0.05)。观察组术后6 h、术后12 h、术后24 h疼痛视觉模拟评分法(VAS)评分低于对照组同期(P<0.05)。观察组术后1个月活力、躯体疼痛、社会功能、生理功能、总体健康、精神健康、生理职能、情感职能评分高于对照组(P<0.05)。结论:利多卡因咽喉表面麻醉用于LC患者,可发挥气道保护作用,减轻患者的应激反应,维持患者血流的动力平衡,提高恢复质量。  相似文献   

5.
摘要 目的:探讨老年直肠癌根治术患者麻醉中使用右美托咪定联合依托咪酯,机体血液微转移、胃肠功能恢复和认知功能的变化情况。方法:根据随机数字表法将我院2020年4月~2022年2月期间收治的112例老年直肠癌根治术患者分为对照组(n=56,依托咪酯麻醉)和研究组(n=56,右美托咪定联合依托咪酯麻醉)。对比两组血液微转移情况、血流动力学、麻醉效果、胃肠功能恢复情况和认知功能情况,统计两组不良反应发生情况。结果:两组术后24 h角蛋白20(CK20)阳性表达率均降低,且研究组低于对照组(P<0.05)。两组不良反应发生率组间对比无差异(P>0.05)。研究组插管即刻、术毕即刻、拔管即刻心率(HR)、平均动脉压(MAP)均高于对照组(P<0.05)。两组气管拔管时间、呼吸恢复时间、麻醉苏醒时间组间对比差异不明显(P>0.05)。研究组进食时间、首次排气时间、肠鸣音恢复时间均较对照组更短(P<0.05)。研究组术后1 d、术后3 d简易精神状态检查量表(MMSE)评分高于对照组,术后认知功能障碍(POCD)发生率低于对照组(P<0.05)。结论:依托咪酯联合右美托咪定用于老年直肠癌根治术患者,麻醉效果较好,可维持血流动力学稳定,降低血液微转移,改善胃肠功能和认知功能。  相似文献   

6.
摘要 目的:探讨不同浓度七氟烷吸入麻醉对非体外循环冠脉搭桥手术(OPCABG)患者苏醒质量、心肾功能和认知功能的影响。方法:选取我院2018年5月~2021年3月期间收治的行OPCABG患者93例,采用随机数字表法将受试对象随机分为A组(舒芬太尼、丙泊酚,31例)、B组(舒芬太尼、丙泊酚、0.5 MAC七氟烷,31例)和C组(舒芬太尼、丙泊酚、1.0 MAC七氟烷,31例)。观察三组患者血流动力学[心率(HR)和平均动脉压(MAP)]、苏醒质量、心肾功能[心肌肌钙蛋白I(cTnI)、肌酸激酶(CK-MB)/肌酐(Scr)、尿素氮(BUN)]和认知功能[简易精神状态测量量表(MMSE)、蒙特利尔认知功能评估量表(MoCA)评分]的变化,记录三组不良反应发生情况。结果:三组术后即刻(T1)~术后24h(T3)时间点HR升高后下降,MAP下降后升高(P<0.05);B组T1、术后6 h(T2)时间点HR低于A组、C组,MAP高于A组、C组(P<0.05);A组与C组T1、T2时间HR、MAP组间对比无显著性差异(P>0.05)。三组苏醒期躁动发生率组间对比无统计学差异(P>0.05);B组术后苏醒时间短于A组、C组(P<0.05);A组与C组术后苏醒时间组间对比无显著性差异(P>0.05)。三组的cTnI、CK-MB、Scr、BUN水平相较于麻醉开始前(T0)时间点均升高(P>0.05);B组T3时间点cTnI、CK-MB、Scr、BUN水平低于A组、C组(P<0.05)。B组术后第3 d MMSE、MoCA评分高于A组、C组(P<0.05)。三组不良反应发生率对比无差异(P>0.05)。结论:OPCABG患者在舒芬太尼、丙泊酚麻醉的基础上结合七氟烷吸入麻醉,可更好的稳定血流动力学,减轻对机体心肾功能和认知功能的影响,提高苏醒质量,且以0.5 MAC浓度的七氟烷综合效果最佳。  相似文献   

7.
摘要 目的:观察超声引导下髂筋膜神经阻滞联合全麻对老年股骨近端骨折患者术后血清疼痛介质前列腺素E2(PGE2)、P物质(SP)和认知功能及睡眠质量的影响。方法:选取2018年8月~2021年9月期间我院收治的择期行手术治疗的老年股骨近端骨折患者80例,根据随机数字表法分为对照组(40例,常规全麻方案)和观察组(40例,超声引导下髂筋膜神经阻滞联合全麻方案),对比两组麻醉效果、血流动力学、疼痛情况、认知功能和睡眠质量,观察不同模式麻醉下的安全性。结果:观察组的苏醒及拔管时间均短于对照组,丙泊酚使用量少于对照组(P<0.05)。两组置入喉罩时(T1)~术毕时(T3)心率(HR)先升高后下降,平均动脉压(MAP)先下降后升高(P<0.05);观察组T1~T3时点HR低于对照组,MAP高于对照组(P<0.05)。两组术后24 h血清PGE2、SP水平和视觉疼痛模拟量表(VAS)评分均升高,但观察组低于对照组(P<0.05)。两组术后1 d、2 d、3 d 蒙特利尔认知评估量表(MoCA)评分较术前先下降后升高(P<0.05);观察组术后2 d、3 d MoCA评分高于对照组(P<0.05)。两组术后1 d、2 d、3 d匹兹堡睡眠质量评估量表(PSQI)评分较术前先升高后下降(P<0.05);观察组术后1 d、2 d、3 d PSQI评分低于对照组(P<0.05)。两组不良反应发生率对比无差异(P>0.05)。结论:老年股骨近端骨折患者术中选用超声引导下髂筋膜神经阻滞联合全麻,镇痛效果显著,可稳定机体血流动力学,减少对认知功能和睡眠质量的影响,且安全性良好。  相似文献   

8.
IntroductionTakayasu arteritis (TA) and giant cell arteritis (GCA) are large vessel vasculitides (LVV) that usually present as granulomatous inflammation in arterial walls. High mobility group box 1 (HMGB1) is a nuclear protein that acts as an alarmin when released by dying or activated cells. This study aims to evaluate whether serum HMGB1 can be used as a biomarker in LVV.MethodsTwenty-nine consecutive TA patients with 29 healthy controls (HC) were evaluated in a cross-sectional study. Eighteen consecutive GCA patients with 16 HC were evaluated at the onset of disease and some of them during follow-up. Serum HMGB1 levels were measured by enzyme-linked immunosorbent assay.ResultsIn GCA patients at disease onset mean serum HMGB1 levels did not differ from HC (5.74 ± 4.19 ng/ml vs. 4.17 ± 3.14 ng/ml; p = 0.230). No differences in HMGB1 levels were found between GCA patients with and without polymyalgia rheumatica (p = 0.167), ischemic manifestations (p = 0.873), systemic manifestations (p = 0.474) or relapsing disease (p = 0.608). During follow-up, no significant fluctuations on serum HMGB1 levels were observed from baseline to 3 months (n = 13) (p = 0.075), 12 months (n = 6) (p = 0.093) and at the first relapse (n = 4) (p = 0.202). Serum HMGB1 levels did not differ between TA patients and HC [1.19 (0.45–2.10) ng/ml vs. 1.46 (0.89–3.34) ng/ml; p = 0.181] and no difference was found between TA patients with active disease and in remission [1.31 (0.63–2.16) ng/ml vs. 0.75 (0.39–2.05) ng/ml; p = 0.281]. HMGB1 levels were significantly lower in 16 TA patients on statins compared with 13 patients without statins [0.59 (0.29–1.46) ng/ml vs. 1.93 (0.88–3.34) ng/ml; p = 0.019]. Age was independently associated with higher HMGB1 levels regardless of LVV or control status.ConclusionsPatients with TA and GCA present similar serum HMGB1 levels compared with HC. Serum HMGB1 is not useful to discriminate between active disease and remission. In TA, use of statins was associated with lower HMGB1 levels. HMGB1 is not a biomarker for LVV.  相似文献   

9.
摘要 目的:探究艾司氯胺酮联合舒芬太尼对剖宫产围手术期镇痛、应激指标及抑郁评分的影响。方法:选取2021年1月~2021年10月期间我院收治的行剖宫产手术的180例产妇,采用随机数字表法分为A组、B组、C组各60例。A组胎儿娩出后即刻静脉输注艾司氯胺酮,术后艾司氯胺酮联合舒芬太尼静脉自控镇痛;B组和C组胎儿娩出后不给予艾司氯胺酮,用生理盐水代替;B组术后静脉自控镇痛与A组相同,C组术后给予舒芬太尼静脉自控镇痛。比较三组产妇术后4 h(T1)、8 h(T2)、12 h(T3)、24 h(T4)、48 h(T5)疼痛程度[简化McGill疼痛问卷(SF-MPQ)评分]、镇静程度(Ramsay镇静评分),记录三组术前1 d和术后1 d的应激指标[去甲肾上腺素(NE)、皮质醇(Cor)、促肾上腺皮质激素(ACTH)]水平,比较三组术前1 d和术后3、7 d抑郁程度[爱丁堡产后抑郁量表(EPDS)],比较三组不良反应发生情况。结果:T1、T2、T3时A组视觉模拟评分(VAS)明显低于B、C组(P均<0.05),T1、T2时A组痛分级指数(PRI)感觉分明显低于B、C组(P均<0.05),T1、T2、T3、T4、T5时A组PRI情感分明显低于B、C组(P均<0.05),T1时A组现时疼痛强度(PPI)评分明显低于B、C组(P均<0.05)。T1、T2、T3、T4、T5时,三组Ramsay镇静评分比较差异均无统计学意义(P均>0.05)。术后1 d,三组NE、Cor、ACTH水平均较术前1 d显著升高(P均<0.05),术前1 d和术后1 d,三组NE、Cor、ACTH水平比较差异均无统计学意义(P均>0.05);术后3、7 d时A组EPDS评分明显低于术前1 d和同时间B、C组(P均<0.05);三组不良反应发生情况对比无显著性差异(P均>0.05)。结论:艾司氯胺酮联合舒芬太尼在剖宫产围术期镇痛中应用效果良好,能够减轻产妇术后早期抑郁程度。  相似文献   

10.
BackgroundSeveral lines of preclinical studies have shown promising antidiabetic effects of the aqueous leaves extract of Coccinia grandis (Linn.) Voigt (Cucurbitaceae) in vivo and in vitro.Purpose: The present study was conducted to evaluate the efficacy and safety of a newly developed herbal formulation of C. grandis in newly diagnosed patients with type 2 diabetes mellitus (T2DM).Study design: A three months long, randomized, double blind, placebo controlled clinical trial in patients with newly diagnosed T2DM.Method: Based on fasting plasma glucose (FPG) concentration, a total number of 158 newly diagnosed patients with T2DM (45 ± 15 years age) were recruited for the present trial from the University Medical Clinic, Teaching Hospital, Karapitiya, Galle, Sri Lanka. They were randomly assigned to the test or placebo group to receive 500 mg of herbal drug (n = 79) or placebo drug (n = 79) once daily for three months. Patients and investigators were blinded for the treatment. Percentage of glycated hemoglobin (HbA1C %), insulin and lipid profile parameters were estimated at the base line and at the end of the intervention. Serum concentration of fructosamine was assessed at every other visit of the trial. The homeostatic model assessment for insulin resistance (HOMA-IR), atherogenic index (AI), cardio-protective index (CPI) and coronary risk index (CRI) were calculated. Furthermore, fasting plasma glucose concentration, renal and liver toxicity parameters, hematological parameters, blood pressure (BP) were assessed throughout the study in two weekly intervals till the end of three months.Results: Out of 158, a total number of 145 patients completed the entire clinical trial period successfully. Mean (SD) changes of variables from the baseline to the end of the intervention in test and placebo groups were 0.65 (0.54) and 0.08 (0.66) for HbA1C % (p < 0.001), 1.91 (3.07) and -1.28 (9.77) for insulin (p < 0.001), 0.02 (0.03) and -0.01 (0.04) for frucosamine (p < 0.001), 1.51 (0.49) and 0.05 (0.50) for FPG (p < 0.001), 1.73 (1.36) and -0.37 (3.38) for HOMA-IR (p < 0.001), 0.16 (0.18) and -0.04 (0.42) for TG (p < 0.001), 0.07 (0.08) and -0.02 (0.19) for VLDL-C (p < 0.001), respectively. However, the herbal drug of C. grandis was unable to change other outcome variables significantly when compared to the placebo (p > 0.05). All the renal, liver and toxicity parameters, hematological parameters and BP were within the normal physiological reference ranges at each visit.Conclusion: Treatment with herbal drug of C. grandis (500 mg per day) for three months for patients with newly diagnosed T2DM significantly improved their glycemic and selected lipid profile parameters with well tolerated safety.  相似文献   

11.
Silver nanoparticles (AgNano) are known for their unique physical, chemical and biological properties, enabling cell penetration and anti-inflammatory response. In Experiment 1, the effect of an in ovo administration of AgNano (15 µg/egg; = 360) at different incubation times (d 7 and d 18) on hatchability parameters was explored. In Experiment 2, post-hatch performance of broilers (42 d, = 250) was studied after in ovo AgNano administration: Group T1 remained un-injected, Group T2 was the sham control and Groups T3, T4 and T5 were injected with 12.5, 25 and 50 µg AgNano, respectively, at 18 d of incubation. Chick weight, chick to egg weight ratio and hatchability as well average daily gain, average daily feed intake and feed conversion ratio were similar in all treatment groups. No variation was seen in the weight of thymus; however, the bursa and spleen weight was increased (p < 0.05) in Groups T4 and T5 in comparison to Group T1. The in vivo immune response to phytohaemagglutinin-P was increased in Group T3 in comparison to Groups T1 and T2 (p < 0.05), while the response to sheep red blood cells was increased in all AgNano-treated groups in comparison with Group T1 (p < 0.01). The expression of toll-like receptors 2 and 4 genes was up-regulated in AgNano groups in comparison with Groups T1 and T2 (p < 0.01). In summary, an in ovo supplementation of AgNano carried out at d 18 of incubation is effective and modulates the post-hatch immune response without affecting the hatchability, growth and other performance parameters in broilers.  相似文献   

12.
BackgroundGeohelminths are parasites that stand out for their prevalence and wide distribution, depending on the soil for their transmission.AimsThe aim of this work was to evaluate the predatory capacity of the fungal isolate of the genus Duddingtonia (CG768) on third stage larvae (L3) of Ancylostoma spp. in beach sand under laboratory conditions.MethodsIn the assay A five treatment groups and 1 control group were formed. The treatment groups contained 5000, 10,000, 15,000, 20,000 or 25,000 chlamydospores of the fungal isolate and 1000 Ancylostoma spp. L3 in pots containing 30 g of sand. The control group (without fungus) contained only 1000 Ancylostoma spp. L3 and distilled water in pots with 30 g of sand.ResultsEvidence of predatory activity was observed at the end of 15 days, where we observed the following percentages of reduction of L3: Group 1 (4.5%); Group 2 (24.5%); Group 3 (59.2%); Group 4 (58.8%); Group 5 (63%). However, difference was noted (p < 0.01) only at concentrations 15,000, 20,000 and 25,000 in relation to control group. In the assay B two groups were formed in Petri dishes of 9 cm in diameter containing agar water 2% medium. In the treated group, each Petri dish contained 500 Ancylostoma spp. L3 and 5 g of sand containing the isolate CG 768 at a concentration of 25,000 chlamydospores/g of sand, and the control group (without fungus) contained only 500 L3. At the end of 7 days the non-predation L3 of Petri dishes using the method of Baermann were recovered. Difference (p < 0.01) between groups on reducing the average number of Ancylostoma spp. L3 (percent reduction of 84%) was observed.ConclusionsThe results of this study confirm earlier work on the efficiency of the Duddingtonia genus in the control of Ancylostoma spp. infective larvae.  相似文献   

13.
摘要 目的:探究右美托咪定联合去甲肾上腺素在全麻下腰椎手术中对患者围术期循环指标及术后恢复指标的影响。方法:选择2019年1月至2020年12月于我院接受治疗的68例行全麻下腰椎手术患者为研究对象,按照随机、双盲、对照的方式区分为研究组与对照组(每组各34例患者),对照组患者术中应用右美托咪定,研究组患者在对照组基础上加用去甲肾上腺素,对比两组患者围术期血流动力学(血压、心率)变化、术中出血量、手术时间、麻醉时间、术后疼痛度、苏醒指标的影响。结果:比较显示术前(T0)、插管时(T1)两组患者的平均动脉压(Mean arterial pressure,MAP)与心率(heart rate,HR)组间差异不大(P>0.05),但手术30 min(T2)、手术60 min(T3)、手术结束拔管(T4)时研究组MAP和HR均高于对照组(P<0.05);研究组患者术中出血量与对照组比较无明显差异(P>0.05),研究组患者麻醉时间低于对照组患者(P<0.05);研究组患者苏醒躁动评分以及术后6 h疼痛度评分均低于对照组(P<0.05)。结论:全麻下腰椎手术患者联用右美托咪定与去甲肾上腺素能够显著稳定患者围术期血流动力学,缩短麻醉苏醒时间,且不增加术中出血量,不增加患者术后苏醒躁动及应激性疼痛现象,值得临床推广应用。  相似文献   

14.
BackgroundTreatments for coronavirus disease 2019 (COVID-19) are limited by suboptimal efficacy.MethodsFrom January 30, 2020 to March 23, 2020, we conducted a non-randomised controlled trial, in which all adult patients with laboratory-confirmed COVID-19 were assigned to three groups non-randomly and given supportive treatments: Group A, Lopinavir-Ritonavir; Group B, Huashi Baidu Formula (a Chinese medicineformula made by the China Academy of Chinese Medical Sciences to treat COVID-19, which is now in the clinical trial period) and Lopinavir-Ritonavir; and Group C, Huashi Baidu Formula. The use of antibiotics, antiviruses, and corticosteroids was permitted in Group A and B. Traditional Chinese medicine injections were permitted in Group C. The primary outcomes were clinical remission time (interval from admission to the first time the patient tested negatively for novel coronavirus or an obvious improvement was observed from chest CT) and clinical remission rate (number of patients whose clinical time was within 16 days/total number of patients).ResultsA total of 60 adult patients with COVID-19 were enrolled at sites in Wuhan, China, and the sample size of each group was 20. In Groups A, B and C, the clinical remission rates were 95.0%%(19/20), 100.0%%(20/20) and 100.0%%(20/20), respectively. Compared with Groups A and B, the clinical remission time of Group C was significantly shorter (5.9 days vs. 10.8 days, p < 0.05; 5.9 days vs. 9.7 days, p < 0.05). There was no significant difference among Groups A, B, and C in terms of the time taken to be released from quarantine. The clinical biochemical indicators and safety indexes showed no significant differences among the three groups.ConclusionsOur findings suggest that Lopinavir-Ritonavir has some efficacy in the treatment of COVID-19, and the Huashi Baidu Formula might enhance this effect to an extent. In addition, superiority was displayed in the treatment of COVID-19 through a combination of the Huashi Baidu Formula and traditional Chinese medicine injection. In future, well-designed prospective double-blinded randomised control trials are required to confirm our findings.  相似文献   

15.
目的:探讨不同麻醉方式对骨科手术患者血流动力学、术后精神状态及认知功能的影响。方法:选取2016年1月~2018年12月期间我院收治的89例骨科手术患者,根据数字表法将患者随机分为对照组(n=44)和研究组(n=45),对照组给予全身麻醉,研究组给予硬膜外麻醉,比较两组患者围术期指标情况,比较两组患者不同时间点血流动力学、术后精神状态及术后认知功能障碍(POCD)发生率。结果:两组患者术中麻醉时间、术中出血量比较,差异无统计学意义(P0.05);研究组麻醉药物使用量少于对照组,苏醒时间、语言恢复时间短于对照组(P0.05)。两组患者麻醉后术前(T2)时间点平均动脉压(MAP)、心率(HR)均较麻醉前(T1)时间点降低,两组患者手术30 min(T3)、手术结束时(T4)时间点MAP、HR均较T2时间点升高(P0.05),但两组患者T1~T4时间点MAP、HR比较,差异无统计学意义(P0.05)。对照组术后6 h(T5)~术后72 h(T8)时间点、研究组T5~术后24 h(T7)时间点MMSE评分低于T1时间点(P0.05),而研究组T8时间点MMSE评分与T1时间点比较,差异无统计学意义(P0.05);研究组T7、T8时间点MMSE评分高于对照组(P0.05)。研究组T5、术后12 h(T6)时间点POCD发生率均低于对照组(P0.05),两组T7、T8时间点POCD发生率比较,差异无统计学意义(P0.05)。结论:两种麻醉方式均可对骨科手术患者血流动力学、术后精神状态造成一定影响,但硬膜外麻醉对术后精神状态的影响程度相对更轻,同时还可降低POCD发生率,改善围术期部分指标。  相似文献   

16.
摘要 目的:研究贮存式自体成分输血对胃肠肿瘤根治术患者T淋巴细胞亚群、血液流变学以及预后的影响。方法:选取2016年12月~2017年12月我院收治的95例行胃肠肿瘤根治术的胃肠肿瘤早期患者作为研究对象。按随机数表法分为A组(n=47,贮存式自体成分输血)和B组(n=48,异体成分输血)。比较两组患者血常规指标[红细胞计数(RBC)、血红蛋白(Hb)、血细胞比容(Hct)]、免疫功能指标(CD3+、CD4+、CD8+、CD4+/CD8+)、血液流变学指标[红细胞沉降率、平均血液黏度、红细胞刚性指数及红细胞变形指数]的变化。随访患者2年,采用Kaplan-Meier曲线分析两组预后情况。结果:术前至术后7 d 时间段A组的CD3+、CD4+水平及CD4+/CD8+呈先降低后升高趋势,且术后7 d已恢复至术前水平;B组术后1 d、3 d、7 d的CD3+、CD4+水平及CD4+/CD8+明显低于A组(P<0.05),两组CD8+水平相比无差异(P>0.05) 。两组术后7 d的RBC、Hct、Hb分别较输血前下降(P<0.05),但两组间比较差异无统计学意义(P>0.05);两组患者术后7 d的红细胞沉降率均升高,但A组低于B组(P<0.05) ,两组患者术后的红细胞变形指数、平均血液黏度和红细胞刚性指数比较无差异 (P>0.05) 。Kaplan-Meier检验结果显示,A组较B组生存率明显升高(P<0.05)。结论:贮存式自体成分输血对胃肠肿瘤根治术患者红细胞沉降率、细胞免疫功能的影响程度较异体成分输血减轻,且贮存式自体成分输血可以明显提高患者的术后生存率。  相似文献   

17.
摘要 目的:观察老年腹腔镜胃肠肿瘤切除术患者使用七氟醚联合右美托咪定复合麻醉后,机体应激反应和脑氧代谢的变化情况。方法:将我院2020年1月至2020年12月期间收治的100例老年腹腔镜胃肠肿瘤切除术患者根据随机数字表法分为对照组(n=50,七氟醚麻醉)和研究组(n=50,右美托咪定联合七氟醚麻醉)。观察两组血流动力学、应激反应、脑氧代谢、认知功能和不良反应。结果:两组手术60 min(T1)~手术后30 min(T3)时间点较麻醉诱导前(T0)时间点心率(HR)先下降后升高,平均动脉压(MAP)先升高后下降(P<0.05)。研究组T1~T3时间点HR及MAP低于对照组(P<0.05)。两组术后3 d多巴胺(DA)、肾上腺素(AD)、去甲肾上腺素(NE)水平升高,但研究组低于对照组(P<0.05)。两组术后3 d血氧含量差(DajvO2)和脑氧摄取率(CERO2)下降,且研究组低于对照组(P<0.05)。研究组术后6 h、术后1 d、术后3 d简易精神状态检查量表(MMSE)评分高于对照组(P<0.05)。两组不良反应发生率,对比无显著性差异(P>0.05)。结论:七氟醚联合右美托咪定应用于老年腹腔镜胃肠肿瘤切除术患者,可有效减轻机体应激反应,减轻机体认知功能损伤,维持血流动力学稳定和脑氧代谢。  相似文献   

18.
ObjectiveTo investigate how curcumin affects the glucose and lipid metabolism in type 2 diabetes mellitus (DM) rat models, and to explore its effect on the free fatty acid (FFA) and tumor necrosis factor α (TNF-α) in serum.MethodsSuccessfully established type 2 DM rats were divided into three groups, i.e. the normal control group, model group and curcumin group, and received the medication for consecutive 8 weeks. Thereafter, we detected the level of fasting blood glucose (FBG), and the blood glucose at 30 min, 60 min and 120 min; besides, we also carried out the insulin tolerance tests to measure the levels of fasting serum insulin (FINS) and blood glucose at 40 min and 90 min; additionally, we also detected the levels of TC, TG, HDL-C, LDL-C, FFA and TNF-α in serum. The results were expected to discover the mechanism of curcumin in decreasing the blood glucose level in DM rats.ResultsCompared with the model group, AUCs of FBG, blood glucose at 30 min, 60 min and 120 min, and glucose were decreased in varying degrees in the curcumin group, and the differences had statistical significance (p < .05). After subcutaneous injection of insulin, we found that the blood glucose at 40 min and 90 min in the curcumin group was decreased, while AUC of glucose level was also decreased (p < .05 or .01). Eight weeks after medication, compared with the rats in the normal group, the levels of HDL-C, LDL-C, TC and TG in rats of the model group and the curcumin group were obviously increased (p < .05). In comparison with the model group, the level of LDL-C in rats of the curcumin group was also decreased significantly (p < .05). In comparison with the normal control group in the same period, we found that the content of FFAs and TNF-α in serum of rats of the model group were elevated significantly, and the differences had statistical significance (p < .05 or .01); the levels in the curcumin group were significantly decreased in comparison with the model group in the same period, and the difference had statistical significance (p < .05 or .01).ConclusionTreatment with curcumin can significantly improve the metabolic disorder of glucose and lipid, enhance the sensitivity to the insulin, and ameliorate the resistance to insulin of the type II DM rats. Meanwhile, this treatment method can also significantly decrease the level of FFA and TNF-α in serum of type II DM rats. Thus, we inferred that the mechanism of curcumin to improve the insulin resistance might be correlated with the decreases of FFA and TNF-α in serum.  相似文献   

19.
摘要 目的:前瞻性研究术中肋间神经阻滞(IINB)对肋骨骨折(RF)患者机体应激反应、血流动力学及生活质量的影响。方法:选择2017年1月-2021年12月于成都医学院第一附属医院行胸腔镜手术治疗的RF患者70例,依据随机数字表法分为IINB组(n=35)与对照组(n=35)。对照组行静吸复合全麻,IINB组于对照组基础上行IINB。观察两组手术前(T0),手术开始5 min(T1)、15 min(T2)、30 min(T3)及手术结束时(T4)平均动脉压(MAP)、心率(HR)等血流动力学指标;术后恢复情况;术后6 h、12 h、24 h、48 h疼痛情况及镇痛补救率;术后1 d、3 d、7 d生存质量;术后3 d并发症等指标。结果:IINB组各时点MAP、HR均低于对照组(P<0.05)。IINB组进食恢复时间、首次下床活动时间、留置胸管时间、术后住院时间均短于对照组(P<0.05)。IINB组术后6 h、12 h、24 h、48 h VAS评分均低于对照组(P<0.05);IINB组镇痛补救率20.00%(7/35)低于对照组42.86%(15/35)(P<0.05)。IINB组术后1 d、3 d、7 d各项生存质量评分均高于对照组(P<0.05)。IINB组术后3 d并发症发生率2.86%(1/35)低于对照组22.86%(8/35)(P<0.05)。结论:IINB可有效缓解RF患者疼痛及机体应激反应,维持术中血流动力学的稳定性,有效缓解术后疼痛,促进患者术后恢复,提高其生活质量,减少术后并发症。  相似文献   

20.
目的:探讨全凭静脉麻醉(TIVA)对腔镜下甲状腺手术的苏醒躁动及术后镇痛效果的影响。方法:将74例接受腔镜下甲状腺手术的患者随机分为TIVA组与静吸复合麻醉(VICA)组,每组各37例。比较两组诱导麻醉前(T0)、切皮后1 min(T1)、手术开始后30 min(T3)、手术结束时(T3)及术后30 min(T4)血糖(GLU)、血清皮质醇(COR)、白介素(IL-6)水平的变化、麻醉药物用量、术后自主呼吸恢复时间、苏醒时间、拔管时间、苏醒期躁动及术后镇痛效果。结果:T1时刻,两组GLU、COR、IL-6水平均呈现出不同程度升高,而TIVA组T1~T4时刻各指标均较VICA组明显降低(P0.05)。与VICA组比较,TIVA组丙泊酚的术中使用量显著减少,术后自主呼吸恢复时间、苏醒时间及拔管时间均显著缩短(P0.05),苏醒期躁动的发生率及躁动程度均较VICA组明显降低(P0.05),术后12、24 h切口疼痛的VAS评分均明显高于VICA组(P0.05)。结论:TIVA应用于腔镜下甲状腺手术可减少机体的应激反应和全麻药剂量,改善苏醒期质量,但应根据患者的疼痛感受采取必要的镇痛措施。  相似文献   

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