Duration and recovery profile of cisatracurium after succinylcholine during propofol or isoflurane anesthesia

Study Objective: To determine the duration and recovery profile of maintenance doses of cisatracurium besylate following succinylcholine, and during propofol or isoflurane anesthesia.

Design: Randomized, open-label study.

Setting: Operating suite of a university-affiliated medical center.

Patients: Forty ASA physical status I and II adult patients having elective surgery with general anesthesia lasting longer than 90 minutes.

Interventions: Following a standardized induction sequence, a baseline electromyogram (EMG) was obtained. An intubating dose of intravenous (IV) succinylcholine 1.0 mg/kg was administered. Ventilation was maintained with a face mask until the first twitch (T₁) of the evoked train-of-four (TOF) reached 10% of control when tracheal intubation was performed. Spontaneous recovery from neuromuscular blockade was allowed to occur until the first twitch returned to 25% of control. Patients then were randomized to receive cisatracurium as follows. Group 1: 0.025 mg/kg [0.5 × 95% effective dose (ED₉₅)]; Group 2: 0.05 mg/kg (ED₉₅); Group 3: 0.05 mg/kg (ED₉₅); and Group 4: 0.1 mg/kg (2×ED₉₅). Anesthesia for Groups 1 and 2 were maintained with isoflurane 1% to 2%, 66% nitrous oxide (N₂O) in oxygen (O₂), and in Groups 3 and 4, anesthesia was maintained with propofol 80 to 160 μg/kg/min, 66% N₂O in O₂. The TOF-evoked EMG was recorded at 10-second intervals. The time for the evoked EMG to spontaneously return to 25%, 50%, and 75% of the original baseline was recorded.

Measurements and Main Results: There were 10 patients in each of the four groups. The duration of action of cisatracurium 0.05 mg/kg (ED₉₅) after an intubating dose of succinylcholine is 24.5 ± 10 minutes and 21.3 ± 9 minutes during anesthesia maintained with isoflurane and propofol, respectively. Doubling the dose of cisatracurium resulted in approximately twice the duration of action (40.2 ± 7 min) during propofol anesthesia. Following a dose of cisatracurium 0.025 mg/kg (0.5×ED₉₅), the T₁ of the EMG-evoked response did not decrease below 25% in 7 of 10 patients.

Conclusion: Following succinylcholine, the duration of action of a single dose of cisatracurium 0.05 mg/kg is 20 to 25 minutes during anesthesia maintained with propofol or isoflurane. The duration and recovery profile of cisatracurium is dose dependent during propofol and isoflurane anesthetics. Cisatracurium 0.025 mg/kg is an inadequate maintenance dose following recovery from succinylcholine and it fails to provide adequate surgical relaxation.     

晚期肺癌73例外科治疗分析

目的 总结近９ａ实施的肺癌手术２０３例,其中属于Ⅲｂ或Ⅳ期的晚期肺癌７３例,旨在讨论晚期肺癌的手术指征,手术操作要点。方法 行全肺切除１８例（左肺１５例,右肺３例）,肺叶切除５４例,肺癌切除后复发余肺切除１例,经心包内处理肺血管１７例,合并民房部分切除２例;支气管成形术１３敢管隆凸成形术１例。结果 除１例因急性呼吸功能衰竭导致死亡外,其余均临床治愈,术后生存率１ａ内为９５％,１ａ以不足２ａ为８０％     

双上斜肌麻痹的临床特征与治疗

双眼上斜肌同时麻痹称为双上斜肌麻痹,近年来受到国内外眼科学者的重视。本文报告13例,均是我科近年来手术治疗并在术后观察3个月以上者。13例病人都无明显外伤史,发病在出生时及出生后早期,为先天性病变。手术次数1～2次。临床特征:不对称病变以单眼上斜视,代偿头位为主要表现,其中有一部分病人为潜在型双侧病变。对称型以两侧同向注视时的反向上斜视为主要表现,双侧Bielschowsky征为阳性。不少病人同时有V型斜视。需要手术治疗的病人一般应做双眼手术。可根据病情决定是同时做双侧手术,还是分次做,以及术式、术量。术后大部分病人能获得满意的头位及眼位。     

川芎嗪对缺氧缺糖损伤的血管内皮细胞周期和前列环素的影响

目的：研究在缺氧缺糖条件下，血管内皮细胞活性、前列环素生成和细胞周期的变化及川芎嗪对它们的影响。方法：缺氧缺糖诱导血管内皮细胞损伤，MTT比色法、流式细胞仪观察川芎嗪对血管内皮细胞作用及细胞周期的影响，放射免疫法测定细胞培养液中前列环素含量。结果：川芎嗪抑制缺氧缺糖引起的血管内皮细胞减少，其作用主要使S期和G2M期细胞比率增加，促进损伤的血管内皮细胞释放前列环素。结论：川芎嗪具有保护缺氧缺糖诱导血管内皮细胞损伤，其作用主要是通过增加S期和G2M期细胞和前列环素的水平。     

急性中毒并多器官功能失常综合征61例临床分析

目的调查急性中毒并多器官功能失常综合征(MODS)的发病情况和转归。方法回顾性分析300例急性中毒患者,其中61例并发MODS。结果61例并发MODS中,死亡14例,病死率22.9％。发生2、3、4、5或5个以上器官功能失常病死率分别为4.7％、15.7％、37.5％、80％。受累器官个数在死亡组和存活组的比较差异显著。结论 不同中毒致MODS的病死率不同,随器官功能失常数目的增加而升高。     

香菇多糖对巨噬细胞一氧化氮和一氧化氮合酶活性的影响

目的研究香菇多糖(LTN)诱导巨噬细胞的一氧化氮(NO)生成和一氧化氮合酶(iNOS)的活性,探讨LTN的免疫调节作用机理.方法采用Griess反应和荧光法测定不同剂量的LTN作用小鼠腹腔巨噬细胞后NO的生成量和iNOS活性.观察mRNA转录抑制剂、蛋白质合成抑制剂和iNOS抑制剂对巨噬细胞NO的生成和iNOS活性的影响.结果LTN能使小鼠腹腔巨噬细胞NO生成增加,iNOS活性增高,并呈作用剂量依赖关系.3种抑制剂均能抑制LTN诱导的小鼠腹腔巨噬细胞N0的生成和iNOS活性.结论LTN能刺激小鼠腹腔巨噬细胞提高iNOS活性和NO的生成.提示LTN的免疫调节作用机制可能与LTN刺激巨噬细胞NO生成有关.     

The conduct of in vitro and in vivo drug-drug interaction studies: a Pharmaceutical Research and Manufacturers of America (PhRMA) perspective.

Current regulatory guidances do not address specific study designs for in vitro and in vivo drug-drug interaction studies. There is a common desire by regulatory authorities and by industry sponsors to harmonize approaches, to allow for a better assessment of the significance of findings across different studies and drugs. There is also a growing consensus for the standardization of cytochrome P450 (P450) probe substrates, inhibitors and inducers and for the development of classification systems to improve the communication of risk to health care providers and to patients. While existing guidances cover mainly P450-mediated drug interactions, the importance of other mechanisms, such as transporters, has been recognized more recently, and should also be addressed. This article was prepared by the Pharmaceutical Research and Manufacturers of America (PhRMA) Drug Metabolism and Clinical Pharmacology Technical Working Groups and represents the current industry position. The intent is to define a minimal best practice for in vitro and in vivo pharmacokinetic drug-drug interaction studies targeted to development (not discovery support) and to define a data package that can be expected by regulatory agencies in compound registration dossiers.     

《医话选粹》自序

医话是医业的小品文,不拘形式,不拘框架,与文学小品文唯一不同的是专谈医生的事务。因此,它自然是医生写的、讲的,是医生读的、听的。其中大至民族民生的卫生大事,小至日常卫生的琐事,只要是健康卫生范围内的事,都可秉笔而书。但有一点是主要的,那就是必须使读者在业务方面有所收获,此有别于茶余饭后的闲话聊天,读过、阅过、听过之后,读(听)者脑子里一无所得。是古人所谓“开卷有益”。     

克隆病与副结核杆菌

分支杆菌、尤其是副结核杆菌长期被疑为克隆病的致病菌。采用聚合酶链反应（ＰＣＲ）技术对手术及内镜活检的７４例石蜡包埋组织（３６例克隆病、１８例溃疡性结肠炎和２０例非炎性肠病对照组织）中的副结核杆菌ＤＮＡ进行检测。扩增的靶ＤＮＡ为副结核杆菌染色体特异重复插入序列ＩＳ９００上４００ｂｐ的片段。其产物特异性通过生物素标记的副结核杆菌全染色体探针Ｓｏｕｔｈｅｒｎ杂交证实。结果显示：４７．２％的克隆病、１１．１％的溃疡性结肠炎和１５．０％的非炎性肠病对照组织中检出了副结核杆菌ＤＮＡ，并发现克隆病组织中副结核杆菌的检出率与其病变部位和是否存在肉芽肿病变无关。提示部分克隆病组织中确有副结核杆菌存在，且后者与克隆病间可能存在特殊相关性。     

实验性偏头痛动物模型c-fos、c-jun基因表达

目的　复制实验性偏头痛动物模型并探讨其c -fos、c -jun基因表达。方法　采用CristinaTassorelli硝酸甘油法复制大鼠实验性偏头痛模型。免疫组化ABC法研究偏头痛大鼠脑组织即刻早期基因c -fos、c -jun的表达。结果　硝酸甘油型实验性偏头痛大鼠出现双耳发红、甩头、前肢频繁搔头 ,活动增加等外在表现 ,脑组织c -fos、c -jun基因表达阳性细胞数增加 ,基因表达阳性细胞的面积扩大、灰度降低或变化不大。结论　硝酸甘油型实验偏头痛大鼠模型复制方法简单、重复性较好、脑组织c -fos和c -jun基因异常表达明显 ,可以作为偏头痛治疗药物筛选、药效评价和发病机理研究的动物模型。