右美托咪定复合丙泊酚全麻对腰椎手术患者镇痛效果及术后恢复的影响

目的:探讨右美托咪定复合丙泊酚全麻对腰椎手术患者镇痛效果及术后恢复的影响。方法:选择我院于2015年10月~2016年10月择期行腰椎全麻手术患者92例,经随机数字表法分为观察组及对照组各46例,两组麻醉诱导方案相同,于麻醉诱导前给予观察组静脉泵入右美托咪啶,给予对照组静脉泵入生理盐水。术后均采用经静脉自控镇痛。记录两组患者麻醉诱导前(T0)、插管1 min(T1)、插管5 min(T2)、拔管后1 h(T3)及术毕(T4)的收缩压(SBP)、舒张压(DBP)、血氧饱和度(SPO_2)和心率(HR)。比较两组患者拔管后即刻疼痛及镇静情况。记录两组患者定向力恢复时间、苏醒时间、拔管时间以及吗啡使用剂量。统计两组患者不良反应情况。结果:两组患者T1时刻SBP、DBP水平较T0明显下降,对照组T3时刻SBP水平高于T0,差异有统计学意义(P0.05);观察组T1时刻DBP、SBP水平高于对照组,T3时刻SBP水平低于对照组,差异均有统计学意义(P0.05);T1、T2、T3、T4时刻观察组HR水平明显高于对照组,差异均有统计学意义(P0.05);拔管后观察组视觉模拟评分(VAS)低于对照组,而Ramasy评分高于对照组,差异有统计学意义(P0.05)。观察组吗啡使用剂量明显低于对照组,差异有统计学意义(P0.05),两组苏醒时间、定向力恢复时间以及拔管时间差异均无统计学意义(P0.05),两组不良反应发生率差异无统计学意义(P0.05)。结论:采用右美托咪定复合丙泊酚全麻对腰椎手术患者血流动力学的影响小,镇痛、镇静效果显著,术后镇痛药物使用量减少,值得临床推广。     

右美托咪定联合丙泊酚用于老年患者无痛肠镜的临床观察

目的:探讨右美托咪定联合丙泊酚用于老年患者无痛纤维结肠镜检查术的麻醉效果及安全性。方法:选择ASA 1-II级择期行无痛肠镜检查术的86例患者随机分为两组,即右美托咪定联合丙泊酚(实验组)和丙泊酚和芬太尼组(对照组),每组各43例。实验组先于10 min内缓解静脉输入右美托咪定0.5μg/kg,对照组同样时间内静脉输入1μg/kg芬太尼。两组均静脉给予丙泊酚1.5 mg/kg,必要时追加丙泊酚。观察两组患者注药前(T0)、注药镜检前(T1)、过脾曲时(T2)、过肝曲时(T3)、退镜时(T4)的心率(HR)、收缩压(SBP)、血氧饱和度(Sp O2)的变化,镇痛效果(VAS评分)、丙泊酚用量、苏醒时间及麻醉后不良反应发生情况。结果:实验组丙泊酚用量和苏醒时间明显短于对照组(P0.05),但两组VAS评分无统计学差异。实验组在T1-T4时间的HR和SBP显著低于对照组(P0.05),实验组Sp O2在T2-T3时间显著高于对照组(P0.05)。观察组低血压、呼吸抑制、不良体动均显著低于对照组(P0.05)。两组嗜睡、头晕、恶心呕吐发生率无统计学差异。结论:右美托咪定联合丙泊酚用于老年患者无痛肠镜检查麻醉效果确切,相对丙泊酚联合芬太尼,可以减少丙泊酚用量,不良反应少,值得临床推广。     

右美托咪定复合丙泊酚全麻在腰椎管减压、椎弓根钉内固定植骨、融合术中的应用

目的:观察右美托咪定复合丙泊酚全麻在腰椎管减压、椎弓根钉内固定植骨融合术中的应用价值。方法:将2015年7月至2019年8月于我院手术治疗84例腰椎退行性疾病患者按随机数字表法分为观察组和对照组,每组42例。观察组于麻醉诱导前静脉泵入0.5μg/kg右美托咪定并在术中以0.2μg/kg·h麻醉维持,对照组于麻醉诱导前静脉泵入生理盐水。对比两组麻醉诱导前(T0)、诱导后(T1)、插管后1 min(T2)和5 min(T3)、拔管1 min(T4)和5 min(T5)的心率(HR)、收缩压(SBP)及舒张压(DBP)的数值,同时记录患者的手术时间、苏醒时间、瑞芬太尼用量及12 h内吗啡用量。比较各时间点VAS评分及不良反应的发生率。结果:与T0比较,两组患者T1时HR、SBP、DBP均显著降低(P<0.05),与T1比较,两组患者T2、T3和T4时HR、SBP、DBP均显著升高(P<0.05),观察组在T3、T4和T5时HR、SBP、DBP均显著降低(P<0.05)。观察组患者各时间点VAS评分及瑞芬太尼用量和24 h吗啡用量均显著低于对照组(P<0.05),观察组患者不良反应发生率显著低于对照组(P<0.05)。结论:右美托咪定复合丙泊酚全麻能够维持术中血液动力学稳定,减少术中麻醉药物和术后镇痛药物用量,改善术后镇痛效果,且不良反应少。     

右美托咪定联合七氟烷对心脑血管介入患者血液动力学及苏醒影响

目的:探究右美托咪定联合七氟烷对心脑血管介入治疗患者血液动力学影响,并分析药物对患者苏醒干预效果。方法:选择2015年3月至2019年3月于我院均接受介入治疗的心脑血管系统疾病92例,按照随机数字表法将其均分为研究组与对照组(各46例),对照组采用七氟烷麻醉并以生理盐水进行连续泵注,研究组采用七氟烷联合右美托咪定的方式实施麻醉,对比两组T_0(麻醉诱导前)、T_1(气管插管后)、T_2(手术结束时)、S_1(苏醒即刻)、S_2(指令配合)、S_3(气管拔除)时的心率(Heart rate,HR)、平均动脉压(Mean arterial pressure,MAP),对比两组苏醒时Riker镇静和躁动评分(Riker sedation and agitation score,SAS)及拔管时间。结果:(1)对比显示,T_0时,两组患者HR与MAP对比差异不具有统计学意义(P0.05),T_1及T_2时刻研究组HR及MAP均明显低于对照组(P0.05);(2)S_1时刻两组HR及MAP对比差异不具有统计学意义(P0.05),S_2及S_3时刻研究组HR及MAP均明显低于对照组(P0.05);(3)研究组苏醒时其SAS评分低于对照组,拔管时间短于对照组(P0.05);(4)观察组随访期间心脑血管事件的发生率为10.87%,显著低于对照组的28.26%(P0.05)。同时,两组随访期间各死亡1例。结论:心脑血管疾病行介入治疗患者应用右美托咪定联合七氟烷干预能够显著稳定患者血液动力学,同时还能够改善患者苏醒状态,缓解患者随麻醉作用减弱而出现的应激反应,减少心脑血管事件的发生,改善预后。     

术中不同速率输注右美托咪定在全凭静脉麻醉中的量效关系研究

目的:以脑电双频指数(bispectral index,BIS)作为麻醉镇静程度指标,探讨不同速率输注右美托咪定(dexmedetomidine,DEX)对全凭静脉麻醉中丙泊酚用量,术中重要时点血液动力学及麻醉恢复质量的影响。方法:选择拟于全麻下行妇科腹腔镜手术的患者60例(ASA I~II级),根据DEX输注速率不同随机分为四组,即D1、D2、D3和D4组,每组15例,麻醉诱导前四组均给予负荷剂量DEX0.5μg·kg-1,10 min输注完毕,继而四组分别以0.2、0.4、0.6和0.8μg·kg-1·h-1输注速度持续输注至冲洗腹腔。四组麻醉诱导方法相同,术中以BIS作为麻醉深度指标,根据BIS值调节丙泊酚血浆靶浓度维持麻醉。记录入室用药前(T0)、DEX负荷量输注后(T1)、气腹即刻(T2)、气腹后5 min(T3)、气腹后30 min(T4)、解除气腹后5 min(T5)、拔喉罩即刻(T6)、拔喉罩后1 min(T7)时收缩压(SBP)、舒张压(DBP)、心率(HR)、丙泊酚平均用量、苏醒时间、拔喉罩时间、拔喉罩后15 min OAA/S评分、术中及术后24小时内不良反应的发生情况。结果:①D2、D3、D4组丙泊酚平均用量较D1组明显减少(P0.05),D3、D4组丙泊酚平均用量较D2组明显减少(P0.05),D3、D4组间差异无统计学意义(P0.05)。②与T0比较,T1~T2时四组SBP、DBP、HR降低(P0.05),T3~T4时D3、D4组SBP、DBP、HR降低(P0.05),D1、D2组SBP、DBP无明显变化(P0.05),T5~T7时四组SBP、DBP、HR降低(P0.05);D3、D4组在T3~T5时SBP、DBP较D1、D2组明显降低(P0.05),D1、D2两组间差异无统计学意义(P0.05),D3、D4两组间差异无统计学意义(P0.05)。③D4组苏醒时间、拔喉罩时间、较D1~3组明显延长(P0.05),D4组OAA/S评分较D1~3组明显降低(P0.05)。④D4组使用阿托品次数较D1~3组明显增多(P0.05),四组术中使用麻黄碱次数和术后24小时内恶心、呕吐、寒战差异无统计学差异(P0.05)。结论:在妇科腹腔镜手术中,DEX作为全身麻醉辅助用药,负荷剂量0.5μg·kg-1,术中持续输注速率0.4μg·kg-1·h-1可以有效降低丙泊酚用量,使围手术期的血流动力学保持平稳,不延长苏醒时间和拔喉罩时间,且不良反应更少,值得临床推广应用。     

右旋美托咪啶用于食道癌手术麻醉的临床研究

目的：观察右旋美托咪啶用于食道癌手术麻醉的临床研究。方法：100例美国麻醉医师协会（ASA）Ⅰ-Ⅱ级择期行食道癌手术患者,随机分为生理盐水组（A组）和右旋美托咪啶组（B组）（n=50）,麻醉诱导前10min分别静脉注射右旋美托咪啶1μg／kg、生理盐水10ml后,两组麻醉诱导和维持相同。随后持续注射右旋美托咪啶0．4μg／kg·h直至手术结束前30min,观察与记录麻醉诱导前（T0）、插管即刻（T1）、拔管后1min（T2）、5min（T3）、10min（T4）平均动脉压（MAP）、心率（HR）、血氧饱和度（SaO2）、中心静脉压（CVP）、丙泊酚用量、芬太尼用量及不良反应。结果：T0、T1、T2,T3、T4A组与B组比较,MAP明显下降、HR明显减慢（P〈0．05）,丙泊酚和芬太尼用药量B组显著少于A组（P〈0．05）。B组术后咽喉疼痛、呛咳躁动发生率也明显低于A组（P〈0．05）。结论：右旋美托咪啶可减轻食道癌手术气管插管与拔管的心血管反应、减少麻醉药用量,减少胸科手术后咽喉疼痛、呛咳躁动的发生率。     

喉上神经阻滞复合瑞芬太尼和右美托咪定用于经皮气管切开术的临床效果

目的:探讨喉上神经阻滞复合瑞芬太尼和右美托咪定应用于经皮气管切开术(PT)的临床效果。方法:将60例因呼吸困难行PT的患者随机分为两组。所有患者均喉上神经阻滞,对照组(30例)采用丙泊酚复合瑞芬太尼,实验组(30例)采用右美托咪定复合瑞芬太尼。观察并比较两组患者术前(T1)、麻醉药物注射结束后(T2)、气管切开置入套管时(T3)、手术结束时(T4)收缩压(SBP)、舒张压(DBP)、心率(HR)、血氧饱和度(SpO_2)及平均动脉压(MAP)、警觉/镇静(OAA/S)评分的变化及术中并发症的发生情况。结果:对照组T3、T4时刻SBP、DBP、HR、MAP均较T1时明显升高,且明显高于实验组同时点(P0.05),而实验组T2、T3、T4时SBP、DBP、HR、MAP与T1时刻比较差异无明显统计学意义(P0.05)。实验组术中呛咳、呼吸抑制的发生率显著低于对照组(P0.05)。两组T2～T4时刻OAA/S评分均明显低于T1时刻,且实验组OAA/S评分均明显低于对照组同时刻(P0.05)。结论:喉上神经阻滞复合右美托咪啶和瑞舒芬太尼应用于PT中可维持血流动力学的稳定,减少应激反应,降低术中并发症的发生率。     

不同剂量盐酸羟考酮复合右美托咪定对开腹手术患者镇痛效应及血流动力学的影响

目的:探讨不同剂量盐酸羟考酮复合右美托咪定对开腹手术患者镇痛效应及血流动力学的影响。方法:选择从2015年3月到2017年3月期间在我院接受开腹手术治疗的患者100例进行研究。根据随机数字表法对患者进行分组,A组(应用1.0 mg/kg的盐酸羟考酮及2.5μg/kg的右美托咪定麻醉)、B组(应用0.75 mg/kg的盐酸羟考酮及2.5μg/kg的右美托咪定麻醉)、C组(应用0.5 mg/kg的盐酸羟考酮及2.5μg/kg的右美托咪定麻醉)和D组(应用1.0 mg/kg的盐酸羟考酮麻醉),每组各25例。对比各组镇痛效应满意度以及麻醉诱导前(T0)、插管即刻(T1)、插管后5 min(T2)时的血流动力学指标,并统计各组不良反应情况。结果:A、B、C三组的镇痛效应满意度均分别明显高于D组,差异均有统计学意义(均P0.05),A、B、C三组的镇痛效应满意度对比差异无统计学意义(P0.05)。A、B组T1时的收缩压(SBP)、舒张压(DBP)、平均动脉压(MAP)及心率(HR)水平均分别高于C、D组,差异有统计学意义(P0.05);T0和T2时,各组的SBP、DBP、MAP及HR水平相比差异均无统计学意义(均P0.05)。各组T1时SBP、DBP、MAP及HR水平与T0时相比明显上升,而T2时又明显下降,差异均有统计学意义(P0.05)。B组不良反应总发生率为12.00%,明显低于A组的36.00%、C组的44.00%及D组的40.00%,差异均有统计学意义(均P0.05)。结论:不同剂量的盐酸羟考酮与右美托咪定复合麻醉对开腹手术患者的镇痛效应较好,并对患者的血流动力学水平均造成一定影响,但随着时间的延长而逐渐减弱,2.5μg/kg的右美托咪定以及0.75 mg/kg的盐酸羟考酮复合麻醉的安全性较高,值得在临床上推广应用。     

丙泊酚靶控输注麻醉维持对老年胃癌根治术患者血流动力学 及苏醒质量的影响

目的:探讨丙泊酚靶控输注麻醉维持对老年胃癌根治术患者血流动力学以及术后苏醒质量的影响.方法:ASAI～Ⅱ级行胃癌根治术的60例患者随机分为A组和B组.两组使用靶控输注麻醉诱导,起始血浆靶浓度为1μg·ml-1 1％丙泊酚泵注,A组采用靶控输注丙泊酚维持麻醉,B组采用七氟烷吸入维持麻醉.记录麻醉前(T0)、切皮后5min(T1)、手术开始30 rmin(T2)、手术开始60min(T3)、停药时(T4)、出室时(T5)各时间点的血流动力学指标的变化.记录患者术后睁眼时间、拔管时间、定向力恢复时间.结果:两组血流动力学指标(SBP、DBP、HR)在T1～T3时点迅速下降,与T0比较均有显著性差异(P＜0.05),T4时血流动力学指标(SBP、DBP、HR)开始上升,至T5时基本达到基线水平,与T0比较差异无统计学意义(P＞0.05).血流动力学指标(SBP、DBP、HR)在组间比较差异均无统计学意义(P＞0.05).两组术后睁眼时间比较差异无统计学意义(P＞0.05),A组术后拔管时间、定向力恢复时间均低于B组,相比较有显著性差异(P＜0.05).结论:丙泊酚靶控输注麻醉维持对老年胃癌根治术患者血流动力学影响小,患者术后苏醒质量高,是老年胃癌根治术患者理想的麻醉方法.     

丙泊酚联合右美托咪啶对肺癌根治术患者镇痛及应激反应的影响

目的:研究丙泊酚联合右美托咪啶用于肺癌根治术患者中的镇痛效果及对应激反应的影响。方法:选取2014年8月至2016年7月本院收治的肺癌根治术患者78例,根据患者入院顺序分为观察组和对照组,39例每组。对照组采取咪达唑仑联合右美托咪啶进行麻醉,观察组采取丙泊酚联合右美托咪啶进行麻醉,两组均复合使用瑞芬太尼维持。比较两组患者镇痛效果、平均动脉压、心率、血糖、血清白介素-6(IL-6)、白介素-10(IL-10)、肿瘤坏死因子-α(TNF-α)及白细胞总数(WBC)水平。结果:观察组患者在苏醒即刻、苏醒后10 min、苏醒后30 min的视觉模拟(VAS)评分显著低于对照组(P0.05),治疗后24小时血清IL-6、TNF-α、WBC、心率、平均动脉压、血糖水平均显著低于对照组(P0.05),血清白介素(IL-10)水平显著高于对照组(P0.05)。观察组和对照组的不良反应发生率比较差异无统计学意义(P0.05)。结论:丙泊酚联合右美托咪啶用于肺癌根治术患者中具有较好的镇痛效果,并能有效抑制应激反应,安全性高。     

白蚁与动物及微生物的共生类型及其机制

综述了白蚁螱客的主要种类、共生关系及相关机制的研究进展。白蚁螱客中,已报道的动物种类达170种。在与动物的共生关系中存在偏利共生（宾主共栖和异种共栖）、互利共生和无关共生三种;在与微生物的共生关系中,存在与内生菌（原生动物、细菌、真菌和放线菌）和外生菌（蚁巢伞菌等）间的互利关系。指出了白蚁与螱客研究中存在的问题,给出了解决方案,并提出了今后可能的研究热点或方向,为白蚁的综合利用（如纤维素酶）及今后研究物种间的协同进化提供了基础资料。     

New amino-dithiaphospholanes and phosphoramidodithioites and their rhodium and iridium complexes

New sulfur derivatives of phosphoramidite ligands were synthesized and the impact of the sulfur unit on the spectroscopic properties of their rhodium and iridium complexes was investigated. The new ligands Bn₂NPSCH₂CH₂S^a(P-S^a) (Bn = benzyl, 4), Bn₂NPSCHCHS^a(CH₂)₃C^aH₂(P-S^a)(C^a-S^a) (6) and Bn₂NP(4-XC₆H₄OMe)₂ (X = S, 7a; X = O, 7b) were converted to the rhodium and iridium complexes trans-[Rh(CO)Cl(L)₂] (L = 4, 6, 7), [RhCl(COD)(L)] (L = 4, 6, 7), [IrCl(COD)(7a)] and [IrCl₂Cp∗(6)]. For comparison, some phosphoramidite complexes of these formulations also were synthesized. The new metal complexes were spectroscopically analyzed. For the carbonyl complexes, the ν_CO IR stretching frequencies were lower than for the corresponding phosphite and phosphoramidite ligands. The ¹J_PRh coupling constants for the rhodium complexes with the new ligands were also smaller than for the respective phosphoramidite and phosphite complexes. Finally, the ¹J_PSe coupling constants of the selenides of the new ligands were lower than those of the phosphoramidite ligands but higher than for PPh₃. The spectroscopic data reveal that the new thio ligands 4, 6 and 7a are more electron donating than phosphites and phosphoramidites but less electron donating than PPh₃.     

Astrocytes and Synaptosomes Transport and Metabolize Lactate and Acetate Differently

Astrocytes transport the monocarboxylate acetate, but synaptosomes do not. The reason for this is unknown, because both preparations express monocarboxylate transporters (MCT). The transport and metabolism of lactate, another monocarboxylate, was examined in these two preparations, and the results were compared to those for acetate. Lactate transport is more rapid in astrocytes than in synaptosomes, but of lower affinity (Kms of 17 and 4 mM, respectively). Lactate (0.2 mM) is metabolized to CO2 more rapidly in synaptosomes than in astrocytes (rates of 0.37 and 0.07 nmol x mg protein(-1) x min(-1), respectively). The reason for this is unclear, but cellular differences in lactate dehydrogenase isotype expression may be involved. Acetate is metabolized to CO2 more rapidly in astrocytes than in synaptosomes (rates of 0.43 and 0.02 nmol x mg protein(-1) x min(-1), respectively). This is likely due to cellular differences in the expression of monocarboxylate transporter subtypes.     

Rapporteur report: Basics and technology and metrology and standards

The first and second sessions of the Workshop focussed on the basics of ultrasound and infrasound, their applications in both industry and medicine, and metrology and protection standards for ultrasound applications.     

Relative and combined effects of ethanol and protein deficiency on strontium and barium bone content and fecal and urinary excretion

To elucidate accumulation of minerals in human iliac arteries with aging, the content of minerals was analyzed by inductively coupled plasma atomic emission spectrometry. Bilateral common, internal, and external iliac arteries of 16 men and 8 women, ranging ages from 65 to 93 yr, were examined. It was found that an extremely high accumulation of calcium and phosphorus occurred in the common iliac artery at old age, being higher than that of the internal and external iliac arteries. It should be noted that the accumulation of calcium and phosphorus is the highest in the common iliac artery among the human arteries examined to date. Regarding sexual differences, the content of calcium and phosphorus in the common and internal iliac arteries was higher in women than in men, whereas their content in the external iliac artery was lower in women than in men.     

Prostaglandin and thromboxane production by human and guinea-pig macrophages and leucocytes

The ability of partially purified human and guinea-pig haematogenous cell populations, when cultured in vitro, to metabolise arachidonic acid (AA) has been studied. Supernatants from 24 hour cell culture have been subjected to analysis for products of AA metabolism by gas chromatography with electron-capture detection.The cell types studied were human peripheral blood monocytes (both glass adherent and non-adherent), neutrophils, eosinophils and leukemic leucocytes; thoracic duct lymphocytes and lung alveolar macrophages. From the guinea-pig, induced and non-induced macrophage or neutrophil enriched peritoneal exudate populations, lymph node cells, peritoneal eosinophils and peripheral blood platelets were examined. Supernatants were assayed for the presence of PGE₂, PGD₂, PGF_2α, TXB₂ and 6-keto-PGF_1α. In all types studied PGE₂ and TXB₂ were the major products formed. The identification of PGE₂ and TXB₂ was confirmed by GC/MS with multiple ion monitoring.The results have been compared with other reports and their possible significance discussed in relation to the proposed role of prostaglandins as mediators and modulators in immunopathology.     

Chemokines and cytokines: axis and allies in asthma and allergy

Allergic asthma can be precipitated by many factors. For the atopic person, fungus, pollen, dust mites, cockroach antigens, and diesel exhaust are all agents that may trigger an allergic attack. Cytokines and chemokines are integral mediators of fungal asthma. From the earliest time points, they recruit and activate the cells required for the clearance of fungus as well as being critical factors involved in the immunopathology of this disease. In the final analysis, it is clear that these mediators can act to the benefit or the detriment of the host.     

Oxidation and nitration of ribonuclease and lysozyme by peroxynitrite and myeloperoxidase

In spite of the many studies on protein modifications by reactive species, knowledge about the products resulting from the oxidation of protein-aromatic residues, including protein-derived radicals and their stable products, remains limited. Here, we compared the oxidative modifications promoted by peroxynitrite and myeloperoxidase/hydrogen peroxide/nitrite in two model proteins, ribonuclease (6Tyr) and lysozyme (3Tyr/6Trp). The formation of protein-derived radicals and products was higher at pH 5.4 and 7.4 for myeloperoxidase and peroxynitrite, respectively. The main product was 3-nitro-Tyr for both proteins and oxidants. Lysozyme rendered similar yields of nitro-Trp, particularly when oxidized by peroxynitrite. Hydroxylated and dimerized products of Trp and Tyr were also produced, but in lower yields. Localization of the main modified residues indicates that peroxynitrite decomposes to radicals within the proteins behaving less specifically than myeloperoxidase. Nitrogen dioxide is emphasized as an important protein modifier.