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1.
目的 评价右美托咪定对丙泊酚复合瑞芬太尼麻醉下脑功能区手术患者唤醒试验质量的影响.方法 拟行术中唤醒的脑功能区手术患者27例,性别不限,年龄17 ~ 43岁,BMI 20~ 24kg/m2,ASA分级Ⅰ或Ⅱ级,采用随机数字表法,将患者随机分为2组∶对照组(C组,n=13)和右美托咪定组(D组,n=14).麻醉诱导后气管插管,麻醉维持:2组均靶控输注丙泊酚和瑞芬太尼,丙泊酚血浆靶浓度3 ~5 μg/ml,调整丙泊酚血浆靶浓度维持BIS值55 ~ 65,瑞芬太尼效应室靶浓度2~6ng/ml.打开硬脑膜后,D组停止输注丙泊酚和瑞芬太尼,经15 min静脉输注右美托咪定负荷量0.3μg/kg,随后以0.2 μg-1·kg·h-1速率维持;C组打开硬脑膜后15 min将丙泊酚血浆靶浓度降至0.5μg/ml,将瑞芬太尼效应室靶浓度降至0.5 ng/ml.记录唤醒时间、唤醒试验期间心血管事件、头痛、躁动、谵妄和术中知晓等的发生情况.结果 所有患者均成功实施唤醒,并顺利完成手术.与C组比较,D组唤醒试验期间高血压、心动过速、头痛和术中知晓的发生率均降低(P<0.05),唤醒时间差异无统计学意义(P>0.05),2组未见躁动和谵妄的发生.结论 右美托咪定可提高丙泊酚复合瑞芬太尼麻醉下脑功能区手术患者唤醒试验的质量.  相似文献   

2.
目的 观察术前给予右美托咪定对气管异物取出术患儿气管拔管的镇静效果.方法 气管异物取出术患儿60例,随机均分为两组,分别在全麻诱导前10 min内静脉输注右美托咪定0.5 μg/kg(D组)或生理盐水(C组).术中丙泊酚2mg·kg-1·h-1、瑞芬太尼0.1μg·kg-1·h-1维持麻醉.记录拔管前1 min、拔管时、拔管后1、5min时的HR、MAP、RR、Ramsay镇静评分的变化,以及拔管期间呛咳和躁动情况.结果 D组HR、RR、MAP、呛咳评分和躁动评分低于C组(P<0.05),Ramsay镇静评分高于C组(P<0.05).结论 术前给予右美托咪定可为气管异物患儿苏醒期提供较好的镇静,减少拔管期间躁动和呛咳.  相似文献   

3.
目的评价右美托咪定对丙泊酚联合瑞芬太尼全麻下脑功能区肿瘤切除术患者唤醒试验中应激反应的影响。方法拟行术中唤醒试验的脑功能区肿瘤切除术患者48例,随机均分为右美托咪定组和对照组,右美托咪定组麻醉诱导前10min将负荷量0.8μg/kg右美托咪定进行静脉输注,继以0.4μg·kg-1·h-1进行维持;对照组采用等量生理盐水进行静脉输注。丙泊酚和瑞芬太尼靶控输注进行麻醉诱导与维持,于唤醒试验前30min停用丙泊酚和肌松药,调整瑞芬太尼血浆浓度为1ng/ml,右美托咪定组输注速率0.1μg·kg-1·h-1。记录两组患者唤醒前麻醉时间、麻醉药用量和唤醒时间,分别于唤醒前30min(T1)、唤醒时(T2)、唤醒后5min(T3)和研究结束后加深麻醉10min(T4)时,记录两组患者MAP、HR和BIS值,及血浆中去甲肾上腺素(NE)和肾上腺素(E)浓度,记录两组患者唤醒期间不良反应发生情况。结果两组患者唤醒时间、唤醒前麻醉时间和顺阿曲库铵用量差异无统计学意义。与对照组比较,右美托咪定组患者唤醒前丙泊酚和瑞芬太尼用量明显减少(P0.05)。与T1时比较,T2和T3时两组患者MAP和BIS均明显升高、HR明显增快(P0.05)。与对照组比较,T2和T3时右美托咪定组MAP明显降低(P0.05),T1~T4时HR明显减慢(P0.05),T1~T4时右美托咪定组患者NE和E浓度明显降低(P0.05),右美托咪定组患者躁动、心动过速、呛咳和高血压发生率均明显降低(P0.05)。各时点两组BIS值差异无统计学意义。结论右美托咪定对丙泊酚联合瑞芬太尼全麻下脑功能区肿瘤切除术唤醒试验中应激反应有较好的抑制作用,能够降低血浆NE和E浓度,对血流动力学影响较小,不良反应发生率降低。  相似文献   

4.
目的研究在熵指数指导下右美托咪定、丙泊酚及依托咪酯用于脑功能区手术术中唤醒的有效性及安全性。方法选择择期行脑功能区手术且需术中唤醒患者60例,随机分为右美托咪定组(D组)、丙泊酚组(P组)和依托咪酯组(E组),每组20例。手术过程中调整右美托咪定、丙泊酚或依托咪酯的泵注剂量使反应熵(RE)维持在40~60。记录唤醒时间、唤醒质量、唤醒期间不良反应的发生情况。结果 D组唤醒时间明显短于P、E两组(P0.05);D组唤醒质量明显优于P、E两组(P0.05),P组唤醒质量明显优于E组(P0.05)。D组不良反应总发生率明显低于P、E两组(P0.05)。结论在熵指数指导下,右美托咪定、丙泊酚和依托咪酯联合瑞芬太尼麻醉用于脑功能区手术术中唤醒均是安全且有效的,但右美托咪定的唤醒质量最高,唤醒期间不良反应发生率最低。  相似文献   

5.
目的 观察右美托咪定复合瑞芬太尼用于困难气道患者纤维支气管镜引导下经鼻清醒气管插管中的安全性及有效性.方法 选择择期手术的困难气道患者40例,随机均分为:右美托咪定复合瑞芬太尼组(D组)和丙泊酚复合瑞芬太尼组(P组).D组给予右美托咪定1μg/kg静脉泵注15 min,同时给予瑞芬太尼0.5 μg/kg静脉泵注3 min;P组给予丙泊酚1.5 mg/kg静脉推注3 min和瑞芬太尼0.5 μg/kg静脉泵注3 min后纤支镜下经鼻插入气管导管.观察并比较两组患者入室时(T0)、给药前(T1)、给药后10 min(T2)、给药结束时(T3)、插管前(T4)、插管时(T5)、插管完成时(T6)、插管完成后1 min(T7)、5 min(T8)的HR、MAP、SpO2和RR;并记录患者插管过程中呛咳、恶心及躁动等不良反应和知晓情况.结果 与T0、T1时比较,T2~T8时两组HR、P组RR均明显减慢(P<0.05);两组MAP、SpO2明显降低(P<0.05).与P组比较,T2~T4、T8时D组HR明显减慢(P<0.05);T2~T7时MAP明显升高(P<0.05);T2、T3和Ts~T7时SpO2明显升高(P<0.05);T2~T8时RR明显增快(P<0.01).D组呛咳、恶心、躁动、插管知晓及SpO2下降发生率明显低于P组(P<0.05).结论 右美托咪定复合瑞芬太尼或丙泊酚复合瑞芬太尼在纤维支气管镜引导下经鼻清醒气管插管都是安全有效的.与丙泊酚复合瑞芬太尼相比,右美托咪定复合瑞芬太尼可提供更稳定的血流动力学且不良反应发生率低.  相似文献   

6.
目的 评价右美托咪定对脊柱侧弯矫形术患者术中唤醒试验的影响.方法 选择拟行脊柱侧弯矫形术患者60例,年龄13~ 18岁,ASA分级Ⅰ级.采用随机数字表法,将患者随机分为2组(n=30)∶舒芬太尼组(S组)和右美托咪定+舒芬太尼组(DS组).两组均采用舒芬太尼、依托咪酯、顺阿曲库铵麻醉诱导,气管插管后机械通气,靶控吸入七氟醚复合靶控输注舒芬太尼维持麻醉.DS组麻醉诱导后静脉输注右美托咪定0.2 μg·kg-1·h-1至术毕,S组以等容量生理盐水替代.唤醒试验前停止输注顺阿曲库铵,下调七氟醚呼气末靶浓度至0;S组、DS组分别下调舒芬太尼Ce至0.1、0.08ng/ml.5 min后开始唤醒试验.记录唤醒时间、唤醒期间呛咳/躁动和心血管事件的发生情况.术后随访患者,记录术中知晓的发生情况.结果 DS组唤醒时无心血管事件发生.与S组比较,DS组唤醒时间缩短,心血管事件、呛咳/躁动的发生率降低(P<0.05).术后随访无一例发生术中知晓.结论 右美托咪定可用于脊柱侧弯矫形术患者术中唤醒试验,唤醒时间短,血液动力学平稳,不良反应少.  相似文献   

7.
目的 评价不同剂量右美托咪定对丙泊酚复合瑞芬太尼用于整形外科手术患者麻醉效果的影响.方法 择期行大面积皮肤瘢痕切除和进行皮瓣转移的手术患者60例,性别不限,年龄18~64岁,体重45 ~ 75 kg,ASA分级Ⅰ或Ⅱ级,采用随机数字表法,将患者分为3组(n=20):对照组(C组)、低剂量负荷量右美托咪定组(D1组)和高剂量负荷量右美托咪定组(D2组),D1组和D2组分别于麻醉诱导前10 min静脉输注右美托咪定0.6、1.0μg/kg负荷量,随后以0.4 μg· kg-1·h-1速率静脉输注至手术结束前30 min.麻醉诱导:靶控输注丙泊酚(血浆靶浓度4.0μg/ml)和瑞芬太尼(效应室靶浓度2.0 ng/ml),患者意识消失后静脉注射罗库溴铵0.6 mg/kg,气管插管后,机械通气,麻醉维持:靶控输注丙泊酚(血浆靶浓度2.0 ~ 3.5 μg/ml)和瑞芬太尼(效应室靶浓度1.5 ~ 2.5 ng/ml),维持Narcotrend指数为D级.分别于麻醉前、右美托咪定输注10 min、气管插管前即刻、气管插管后1 min、气管插管后5 min、停止输注右美托咪定、拔除气管导管前即刻、拔除气管导管后1 min、拔除气管导管后5min时记录Narcotrend指数、收缩压(SP)、舒张压(DP)和HR.记录麻醉诱导时间、丙泊酚和瑞芬太尼的用量,记录自主呼吸、定向力恢复和拔除气管导管的时间.拔除气管导管后10 min时行镇静-躁动评分,记录术中窦性心动过缓和麻醉恢复期不良事件的发生情况.结果 与C组比较,D1组和D2组丙泊酚、瑞芬太尼的总用量和拔除气管导管后10 min时镇静-躁动评分、麻醉恢复期恶心、呛咳和躁动的发生率降低,右美托咪定输注10 min时Narcotrend指数和HR降低,D2组麻醉诱导时间缩短(P<0.05或0.01),D2组术中窦性心动过缓发生率高于C组和D1组(P<0.05),3组间自主呼吸恢复时间、定向力恢复时间和拔除气管导管时间差异无统计学意义(P>0.05).D1组和D2组气管插管前后和拔除气管导管前后SP、DP和HR差异无统计学意义(P>0.05).结论 对于整形外科手术患者,麻醉诱导前静脉输注右美托咪定负荷量0.6 μg/kg,随后以0.4 μg·kg-1 ·h-1速率输注可缩短麻醉诱导时间,减少丙泊酚和瑞芬太尼用量,有效地抑制气管插管和拔除气管导管时的应激反应,降低了不良反应的发生.  相似文献   

8.
目的观察右美托咪定复合丙泊酚与瑞芬太尼对脑动脉瘤夹闭术患者的麻醉效果。方法选取64例脑动脉瘤夹闭术患者,按照麻醉方法不同分为2组,各32例。观察组麻醉诱导前给予右美托咪定1.0μg/kg,并以0.4μg/(kg·h)右美托咪定维持至拔除气管导管。对照组给予等容量0.9%的氯化钠注射液。2组均采用丙泊酚、瑞芬太尼与罗库溴铵进行麻醉诱导,对比2组麻醉效果。结果观察组T_1、T_2、T_3时点的HR、DBP、SBP低于对照组,不良反应发生率低于对照组,差异具有统计学意义(P0.05)。结论右美托咪定复合丙泊酚与瑞芬太尼对脑动脉瘤夹闭术患者血流动力学影响较小,具有较高的安全性和应用价值。  相似文献   

9.
《中华麻醉学杂志》2022,(4):426-429
目的从术后转归角度, 评价复合右美托咪定全身麻醉用于老年患者腹腔镜结直肠癌根治术的优化效应。方法择期全身麻醉下行腹腔镜结直肠癌根治术老年患者112例, 性别不限, ASA分级Ⅱ或Ⅲ级。采用随机数字表法分为2组(n=56):常规全身麻醉组(C组)和复合右美托咪定全身麻醉组(D组)。D组于麻醉诱导开始时经10 min静脉输注右美托咪定0.5 μg/kg, 随后依次静脉注射咪达唑仑、舒芬太尼、依托咪酯和苯磺顺阿曲库铵;麻醉维持使用七氟烷、瑞芬太尼和丙泊酚, 静脉输注右美托咪定0.5 μg·kg-1·h-1至术毕前30 min;C组以等量生理盐水代替右美托咪定用药, 余同D组。于术前1 d、术后2、7 d时采集静脉血样检测血常规, 计算中性粒细胞计数/淋巴细胞计数比值(NLR)。记录术中麻醉药物用量、术后麻醉相关并发症发生情况及术后首次排气时间和排便时间。结果与C组比较, D组术中丙泊酚及瑞芬太尼用量减少, 术后2、7 d时NLR降低, 术后谵妄及术后恶心呕吐发生率降低, 术后首次排气时间及排便时间缩短(P<0.05)。结论复合右美托咪定全身麻醉用于腹腔镜结直肠癌根治术老年患者, 较常规...  相似文献   

10.
目的 比较瑞芬太尼复合丙泊酚或不同剂量右美托咪定在清醒气管插管中的安全性和有效性.方法 择期全麻手术患者60例,以随机数字表法分为三组:瑞芬太尼+丙泊酚2mg· kg-1·h-1组(P组)、瑞芬太尼+0.5 μg/kg右美托咪定组(D1组)和瑞芬太尼+1 μg/kg右美托咪定组(D2组),每组20例.入室后三组患者均以0.25 μg.kg-1· min-1泵注瑞芬太尼,同时泵注不同镇静药,给药后5 min,2%利多卡因进行气管内表面麻醉,给药后10 min行可视喉镜下气管插管.记录插管成功率、插管时间,并记录给药前(T0)、插管前(T1)、插管成功即刻(T2)及插管后3min(T3)时的MAP、HR、SpO2;记录T0~T2时RR及PETCO2;同时记录患者呼吸抑制、呛咳及插管知晓等不良反应.结果 P组、D1和D2组一次插管成功率分别为80%、85%和90%.与T0时比较,T1时D1、D2组HR均明显减慢(P<0.01),而D2组MAP明显升高(P<0.01);T2时P、D1组HR明显增快(P<0.01),三组MAP均明显升高(P<0.01);T3时P组MAP明显降低,且明显低于D1、D2两组(P<0.01).与T0时比较,T1、T2时三组患者RR均明显减慢,PET CO2明显升高(P<0.01),其中D1组RR明显快于,PET CO2明显低于P组和D2组(P<0.05).P组患者呼吸抑制、呛咳及插管知晓等不良反应的发生率明显高于D1、D2组(P<0.05或P<0.01).结论 瑞芬太尼复合右美托咪定可安全地用于清醒气管插管,在维持血压稳定及减少不良反应方面优于复合丙泊酚.瑞芬太尼复合小剂量右美托咪定对呼吸抑制轻微,安全性较高.  相似文献   

11.
Background : We investigated the vasopressor hormone response following mesenteric traction (MT) with hypotension due to prostacyclin (PGI2) release in patients undergoing abdominal surgery with a combined general and epidural anesthesia. Methods : In a prospective, randomized, placebo-controlled study we administered 400 mg ibuprofen (i.v.) in 42 patients scheduled for abdominal surgery. General anesthesia was combined with epidural anesthesia (T4-L1). Before as well as 5, 15, 30, 45, and 90 min after MT we recorded plasma osmolality, hemodynamics and measured 6-keto-PGFlα (stabile metabolite of PGI2), TXB2 (stabile metabolite of thromboxane A2) active renin, and arginine vasopressin (AVP) plasma concentrations by radioimmunoassay. Catecholamine levels were assessed by high-pressure liquid chromatography (HPLC) with electrochemical detection. Results : Following MT, arterial hypotension occurred along with a substantial PGI2 release. This was completely abolished by ibuprofen administration. Although plasma levels of 6-keto-PGF (1133 (708) vs. 60 (3) ng/L, median (median absolute deviation), P=0.0001, placebo vs. ibuprofen) remained significantly elevated, blood pressure was restored within 30 min after MT in the placebo group. At the same point in time plasma concentrations of TXB2 (164 (87) vs. 58 (1) ng/L, P=0.0001), epinephrine (46 (33) vs. 14 (6) ng/L, P=0.001), AVP (41 ± (18) vs. 12 (7) ng/L, P=0.0004), and active renin (27 (12) vs. 12 (4) ng/L, P = 0.001) were significantly higher in placebo-treated patients. Conclusion : Under combined general and epidural anesthesia arterial hypotension following MT due to endogenous PGI2 release is associated with enhanced release of AVP, active renin, epinephrine and thromboxane A2, presumably contributing to hemodynamic stability within 30 min after MT.  相似文献   

12.
Don Dame 《Artificial organs》1996,20(5):613-617
Abstract: Virtually all blood pumps contain some kind of rubbing, sliding, closely moving machinery surfaces that are exposed to the blood being pumped. These valves, internal bearings, magnetic bearing position sensors, and shaft seals cause most of the problems with blood pumps. The original teaspoon pump design prevented the rubbing, sliding machinery surfaces from contacting the blood. However, the hydraulic efficiency was low because the blood was able to "slip around" the rotating impeller so that the blood itself never rotated fast enough to develop adequate pressure. An improved teaspoon blood pump has been designed and tested and has shown acceptable hydraulic performance and low hemolysis potential. The new pump uses a nonrotating "swinging" hose as the pump impeller. The fluid enters the pump through the center of the swinging hose; therefore, there can be no fluid slip between the revolving blood and the revolving impeller. The new pump uses an impeller that is comparable to a flexible garden hose. If the free end of the hose were swung around in a circle like half of a jump rope, the fluid inside the hose would rotate and develop pressure even though the hose impeller itself did not "rotate"; therefore, no rotating shaft seal or internal bearings are required.  相似文献   

13.
Abstract: A variety of protein-bound or hydrophobic substances, accumulating as a result of pathologic conditions such as exogenous or endogenous intoxications, are removed poorly by conventional detoxification methods because of low accessibility (hemodialysis), insufficient adsorption capabilities (hemosorption), low efficiency (peritoneal dialysis), or economic limitations (high-volume plasmapheresis). Combining advantages of existing methods with microspheric technology, a module-based system was designed. Major operating parameters of the latter can be modified to allow for adjustment to individual clinical situations. An extracorporeal blood circuit including a plasmafilter is combined with a secondary high-velocity plasma circuit driven by a centrifugal pump. Different microspheric adsorbers can be combined in one circuit or applied in sequence. Thus, a prolonged treatment can be tailored using specially designed selective adsorber materials. Comparing this system with existing methods (high-flux hemodialysis, molecular adsorbent recycling system), results from our in vitro studies and animal experiments demonstrate the superior efficiency of substance removal.  相似文献   

14.
Background : Our objective was to determine whether administration of propranolol or verapamil modifies the hemodynamic adaptation to continuous positive-pressure ventilation (CPPV), in particular the regional distribution of cardiac output (CO).
Methods : General hemodynamics and regional blood flows assessed by microsphere technique (15 (μm) were recorded in 16 anesthetized pigs during spontaneous breathing (SB) and CPPV with 8 cm H2O end-expiratory pressure (CPPV8) before and after intravenous administration of propranolol (0.3 mg · kg−1 followed by 0.15 mg · kg−1 · h−1, n=8) or verapamil (0.1 mg · kg−1 followed by 0.3 mg · kg−1 · h−1, n=8).
Results : CPPV8 depressed CO by 25% without shifts in its relative distribution with the exception of a noteworthy increase in adrenal perfusion. Propranolol increased arterial blood pressure, and due to a fall in heart rate, CO dropped by 25%. The kidneys and, to a lesser extent, the splanchic region and central nervous system received increased fractions of the remaining CO at the expense of skeletal muscle flow. Similar patterns were seen during SB and CPPV8 such that the combination of propranolol and CPPV8 depressed CO by 50%. The circulatory effects of verapamil were less evident but myocardial perfusion tended to increase.
Conclusions : The combination of propranolol or verapamil with CPPV does not result in any specific hemodynamic interaction in anesthetized pigs, except that the combined effect of propranolol and CPPV may severely reduce CO.  相似文献   

15.
Background: Obesity is increasing globallly, including in the formerly "Eastern Bloc" countries. Methods: A survey was made of obesity and bariatric surgery. Results: In the 8 East and Central European countries studied, with total population 300 million, roughly 43% of the population was overweight (BMI 25-30), 23% obese (BMI > 30), with about 15 million people morbidly obese (BMI > 40). From 0-10 morbidly obese individuals/100,000/year undergo bariatric surgery. Conclusion: Most countries were found to provide inadequate treatment for obesity.The majority of the morbidly obese are not treated effectively. However, health-care awareness of obesity and bariatric surgeons are slowly increasing.  相似文献   

16.
Background : Inhibitory effects of volatile anaesthetics on platelet aggregation have been demonstrated in several studies. However, the influence of volatile anaesthetics on intracoronary platelet adhesion has not been elucidated so far.
Methods : Isolated hearts of guinea pigs were perfused with buffer in the absence or presence of volatile anaesthetics (0.5 and 1 MAC) at constant coronary flow rates of 5 ml/min for 25 min, then 1 ml/min for 30 min and again 5 ml/min for 10 min. Before, during and after low-flow perfusion, a bolus of human platelets was applied into the coronary system. To simulate thrombogenic conditions, 0.3 U/ml human thrombin was infused during low-flow perfusion and reperfusion. The number of platelets sequestered to the endothelium was calculated from the difference between coronary in- and output of platelets. The myocardial production of lactate and consumption of pyruvate and coronary perfusion pressure were also determined.
Results : At a flow rate of 5 ml/min only about 3% of the applied platelets did not emerge from the coronary system, in any group. In contrast, 13.1±1.2% (mean±SEM) of infused platelets became adherent in low-flow perfusion in the control group without anaesthetic. The adherence was reduced with each 1 MAC isoflurane (to 6.2±1.2%), sevoflurane (to 4.4±0.9%) or halothane (to 3.2±1.5%) (each P <0.05 vs. control). Volatile anaesthetic, 0.5 MAC, did not inhibit platelet adhesion to a statistically significant extent in any case. Perfusion pressure and metabolic parameters were not statistically different between the control and the hearts exposed to anaesthetics.
Conclusion : Volatile anaesthetics in a concentration of 1 MAC can reduce the adhesion of platelets in the coronary system under reduced flow conditions. This action does not arise from vasodilation or inhibition of ischaemic stress.  相似文献   

17.
Background: It has been shown that the depressive effects of both propofol and midazolam on consciousness are synergistic with opioids, but the nature of their interactions on other physiological systems, e. g. respiration, has not been fully investigated. The present study examined the effect of propofol and midazolam alone and in combination with fentanyl on phrenic nerve activity (PNA) and whether such interactions are additive or synergistic. Methods: PNA was recorded in 27 anaesthetised and artificially ventilated rabbits. In three groups, propofol, fentanyl and midazolam were administered intravenously in incremental doses to construct dose-response curves for the depressant effects of each one on PNA. In another two groups, the effect of pretreatment with either fentanyl 1 μg · kg?1 i. v. or midazolam 0.05 mg · kg?1 i. v. on the effects of propofol and fentanyl respectively on PNA were studied. Results: Propofol and fentanyl caused a dose-dependent depression of PNA with complete abolition at the highest total doses of 16 mg · kg?1 i. v. and 32 μg · kg?1 i. v., respectively. In contrast, midazolam in incremental doses to a total of 0.8 mg · kg?1 reduced mean PNA by 63%, but approximately 12% of PNA remained at a total dose as high as 6.4 mg · kg?1. The mean ED50s, calculated from dose-response curves, were 5.4 mg · kg?1, 3.9 μg · kg?1 and 0.4 mg · kg?1 for propofol, fentanyl and midazolam, respectively. Initial doses of either fentanyl 1 μg · kg?1 i. v. or midazolam 0.05 mg · kg?1 i. v. acted synergistically with subsequent doses of either propofol or fentanyl to abolish PNA at total doses of 8 mg · kg?1 and 8 μg · kg?1, respectively. Conclusion: Fentanyl has a synergistic interaction with both propofol and midazolam on PNA and hence potentially on respiration.  相似文献   

18.
Background: Catecholaminergic support is often used to improve haemodynamics in patients undergoing major abdominal surgery. Dopexamine is a synthetic vasoactive catecholamine with beneficial microcirculatory properties. Methods: The influence of perioperative administration of dopexamine on cardiorespiratory data and important regulators of macro- and microcirculation were studied in 30 patients undergoing Whipple pancreaticduodenectomy. The patients received randomized and blinded either 2 μg · kg?1 · min?1 of dopexamine (n=15) or placebo (n=15, control group). The infusion was started after induction of anaesthesia and continued until the morning of the first postoperative day. Endothelin-1 (ET-1), vasopressin, atrial natriuretic peptide (ANP), and catecholamine plasma levels were measured from arterial blood samples. Measurements were carried out after induction of anaesthesia, 2 h after onset of surgery, at the end of surgery, 2 h after surgery, and on the morning of the first postoperative day. Results: Cardiac index (CI) increased significantly in the dopexamine group (from 2.61±0.41 to 4.57±0.78 1 · min?1 · m?2) and remained elevated until the morning of the first postoperative day. Oxygen delivery index (DO2I) and oxygen consumption index (VO2I) were also significantly increased in the dopexamine group (DO2I: from 416±91 to 717±110 ml/m2 · m2; VO2I: from 98±25 to 157±22 ml/m2 · m2), being significantly higher than in the control group. pHi remained stable only in the dopexamine patients, indicating adequate splanchnic perfusion. Vasopressive regulators of circulation increased significantly only in the untreated control patients (vasopressin: from 4.37±1.1 to 35.9±12.1 pg/ml; ET-1: from 2.88±0.91 to 6.91±1.20 pg/ml). Conclusion: Patients undergoing major abdominal surgery may profit from prophylactic perioperative administration of dopexamine hydrochloride in the form of improved haemodynamics and oxygenation as well as beneficial influence on important regulators of organ blood flow.  相似文献   

19.
A concept of balanced analgesia using nonsteroidal anti-inflammatory drugs (NSAIDs), paracetamol (acetaminophen), opioids, and corticosteroids can also be used in patients with pre-existing illnesses. NSAIDs are the most effective treatment for acute pain of moderate intensity in children; however, these drugs should be avoided in patients at increased risk for serious side effects, e.g. patients with renal impairment, bleeding tendency, or extreme prematurity. NSAIDs can be given with minimal risks to the younger child with mild to moderate asthma, and, in these patients, the use of steroids can be encouraged; in addition to their antiemetic and analgesic action, a beneficial effect on asthma symptoms can be expected. In the non-intubated child with cerebral trauma, exaggerated sedation caused by opioids and increased bleeding tendency caused by NSAIDs must be avoided. In neonates and small infants, the oral administration of sucrose or glucose is helpful to minimize pain reaction during short uncomfortable interventions.  相似文献   

20.
Background: Halothane inhibits in vitro and in vivo activity of cytochrome P-450 (CYP) 2E1. There are several fluorinated volatile anaesthetics besides halothane, and most of them are defluorinated by CYP2E1. It is unclear whether other fluorinated anaesthetics inhibit the in vivo activity of CYP2E1.
Methods: We compared the inhibitory effects of therapeutic concentrations of four inhalational anaesthetics, halothane, enflurane, isoflurane, and sevoflurane, on chlorzoxazone metabolism in rabbits receiving artificial ventilation.
Results: All four inhalational anaesthetics decreased arterial blood pressure and increased plasma chlorzoxazone concentration. However, no significant differences in the plasma chlorzoxazone concentration were found between the four anaesthetics. The estimated chlorzoxazone clearance increased after beginning inhalation with all four agents, but no significant difference in clearance was noted between agents.
Conclusions: At therapeutic concentrations, the in vivo inhibitory effect on chlorzoxazone metabolism was similar for all four inhalational anaesthetics examined, even though their chemical characteristics and extent of hepatic metabolism differ considerably.  相似文献   

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