Efficacy of different doses of sugammadex after continuous infusion of rocuronium

AIM: To evaluate the effects of two different doses of sugammadex after maintenance anesthesia with sevofluorane and remifentanil and deep rocuroniuminduced neuromuscular blockade(NMB).METHODS: Patients between 20 and 65 years of age, with American Society of Anesthesiologists physical status classification Ⅰ-Ⅱ, undergoing gynecological surgery were included in a prospective, comparative and randomized study. NMB was induced with an injection of 0.6 mg/kg of rocuronium followed by continuous infusion of 0.3-0.6 mg/kg per hour to maintain a deep block. Anesthesia was maintained with sevofluorane and remifentanil. Finally, when surgery was finished, a bolus of 2 mg/kg(group A) or 4 mg/kg(group B) of sugammadex was applied when the NMB first response in the train-of-four was reached. The primary clinical endpoint was time to recovery to a train-of-four ratio of 0.9. Other variables recorded were the time until recovery of train-of-four ratio of 0.7, 0.8, hemodynamic variables(arterial blood pressure and heart rate at baseline, starting sugammadex, and minutes 2, 5 and 10) and adverse events were presented after one hour in the post-anesthesia care unit.RESULTS: Thirty-two patients were included in the study: 16 patients in group A and 16 patients in group B. Only 14 patients each group were recorded because arterial pressure values were lost in two patients from each group in minute 10. The two groups were comparable. Median recovery time from starting of sugammadex administration to a train-of-four ratio of 0.9 in group A and B was 129 and 110 s, respectively.The estimated difference in recovery time between groups was 24 s(95%CI: 0 to 45 s, Hodges-Lehmann estimator), entirely within the predefined equivalence interval. Times to recovery to train-of-four ratios of 0.8(group A: 101 s; group B: 82.5 s) and 0.7(group A: 90 s; group B: 65 s) from start of sugammadex administration were not equivalent between groups. There was not a significant variation in the arterial pressure and heart rate values between the two groups and none of the patients showed any clinical evidence of residual or recurrent NMB. CONCLUSION: A dose of 2 mg/kg of sugammadex after continuous rocuronium infusion is enough to reverse the NMB when first response in the Train-OfFour is reached.

Dose requirements of continuous infusion of rocuronium and atracurium throughout orthotopic liver transplantation in humans

Objective： To compare the dose requirements of continuous infusion of rocuronium and atracurium throughout orthotopic liver transplantation （OLT） in humans. Methods： Twenty male patients undergoing liver transplantation were randomly assigned to two comparable groups of 10 patients each to receive a continuous infusion of rocuronium or atracurium under intravenous balanced anesthesia. The response of adductor pollicis to train-of-four （TOF） stimulation of unlar nerve was monitored. The infusion rates of rocuronium and atracurium were adjusted to maintain Tl/Tc ratio of 2%-10%. The total dose of each drug given during each of the three phases of OLT was recorded. Results： Rocuronium requirement, which were （0.468±0.167）mg/（kg·h） during the paleohepatic phase, decreased significantly during the anhepatic phase to （0.303±0.134）mg/（kg·h） and returned to the initial values at the neohepatic period （（0.429±0.130） mg/（kg·h））; whereas atracuruim requirements remained unchanged during orthotopic liver transplantation. Conclusions： This study showed that the exclusion of the liver from the circulation results in the significantly reduced requirement of rocuronium while the requirement of atracurium was not changed, which suggests that the liver is of major importance in the clearance of rocuronium. A continuous infusion of atracurium with constant rate can provide stable neuromuscular blockade during the three stages of OLT.

Unexpected delayed reversal of rocuronium-induced neuromuscular blockade by sugammadex:A case report and review of literature

BACKGROUND Rocuronium,a nondepolarizing muscle relaxant,is usually administered during general anesthesia to facilitate endotracheal intubation and keep patients immobile during the surgery.Sugammadex,the selective reversal agent of rocuronium,fully reverses the neuromuscular blockade(NMB)at the end of surgery.Most reports show that sugammadex rapidly achieves a ratio of train-offour(TOF),a quantitative method of neuromuscular monitoring,of 0.9 which ensures adequate recovery for safe extubation.However,very rare patients with neuromuscular diseases may respond poorly to sugammadex.CASE SUMMARY A 69-year-old female presented with abdominal fullness and nausea,and was diagnosed with gastroparesis.She underwent gastric peroral endoscopic myotomy under general anesthesia with rocuronium(0.7 mg/kg).At the end of surgery,sugammadex 3.6 mg/kg was administered when TOF showed 2 counts.Afterward,the TOF ratio recovered to 0.65 in 30 min.She was awake but could not fully open her eyelids.The tidal volume during spontaneous breathing was low.After additional doses of sugammadex(up to 7.3 mg/kg)in the following 3 h,the TOF ratio was 0.9,and the endotracheal tube was smoothly removed.After excluding possible mechanisms underlying the prolonged recovery course,we speculated our patient may have had an undiagnosed neuromuscular disease,hinted by her involuntary movement of the tongue and mouth.Furthermore,her poor renal function and history of delayed recovery from general anesthesia may be related to the long duration of rocuronium.CONCLUSION In our case,both prolonged rocuronium-induced NMB and poor response to sugammadex were noted.To optimize the dose of rocuronium,perioperative TOF combined with other neuromuscular monitoring is suggested.

Continuous Rocuronium Administration Method Based on Pharmacokinetic/Pharmacodynamics Model during Propofol, Sevoflurane, and Desflurane Anesthesia

Purpose: Although rocuronium bromide (Rb) is suitable for continuous administration use, determination of optimal continuous doses is difficult due to individual differences. This study examines the efficacy of a continuous Rb administration method based on effect-site concentrations calculated by a pharmacokinetic/pharmacodynamics model during propofol, sevoflurane, and desflurane anesthesia. Methods: The 36 enrolled patients were equally divided into three groups (P;propofol, S;sevoflurane, and D;desflurane groups). After induction and administration of Rb 0.6 mg/kg, we calculated the simulated effect-site concentration at the point which the first twitch (%T1) recovered to > 0% and defined this as the Rb recovery concentration (Rbr.c.) level appropriate for continuous rocuronium administration. The continuous administration doses of Rb were adjusted to maintain Rbr.c. during surgery. The Rbr.c. and the recovery time at %T1 > 25% were recorded for each type of anesthesia. Results: Rbr.c. (μg/mL) for the P, S, and D groups were 1.54 ± 0.2, 1.24 ± 0.2, and 1.09 ± 0.2, respectively. Continuous administration doses (μg/kg/min) in the P, S, and D group were 6.7 ± 0.9, 5.2 ± 1.0, and 4.5 ± 0.8, respectively. Rbr.c. and continuous doses in the S and D groups were lower than the P group. Neuromuscular relaxations during surgery in the S and D groups were more strongly maintained than for the P group. There was also a significantly prolonged recovery duration for the %T1 > 25% in the D versus the other two groups (P < 0.05). Conclusion: Results showed that our continuous administration method was effective for maintaining sufficient muscle relaxation without excessively prolonged recovery effects for both sevoflurane and desflurane as well as propofol anesthesia.

Effective Use of Sugammadex for Incomplete Pyridostigmine Reversal of Muscle Relaxation by Rocuronium: A Case Report

Anticholinesterase does not allow adequate reversal of the deep neuromuscular blockade (NMB) achieved using high doses of relaxants. A 71-year-old female patient (weight 70 kg, height 169 cm) was scheduled for a transurethral resection of a bladder tumor under general anesthesia. We administered rocuronium 30 mg (0.43 mg/kg) for tracheal intubation due to an estimated short surgical time. During the operation, an additional rocuronium 10 mg was injected. The surgical procedure ended abruptly 10 minutes after receiving the last dose of rocuronium. At the end of surgery, the patient received pyridostigmine as a reversal. However, residual NMB persisted, and neuromuscular monitoring did not show the expected degree of recovery. Sugammadex 2 mg/kg was used, and the patient experienced complete reversal from NMB in just 2 min.

Analysis of incidence of residue neuromuscular blockade for rocuronium and cisatracurium

Objective:To observe the incidence of residual neuromuscular blockade at the end of operation and during tracheal extubation, and analyze the risk factors causing residual neuromuscular blockade by judging the degree of muscle relaxation according to clinical signs when after using rocuronium or cis-atracurium in general anesthesia.Methods: 500 adults were implemented with propofol-remifentanil intravenous anesthesia or sevoflurane inhalation anesthesia. Rocuronium and cis-atracurium were given, respectively. The TOFr was observed with blind method by TOF Watch SX monitor during anesthesia.Results: The mean TOFr=0.53±0.38 at the end of operation,including 275 cases of 0<TOFr<0.9 and 112 cases of TOFr=0. The mean TOFr=0.97±0.12 at extubation, including 60 cases of TOFr<0.9. The incidence of residual neuromuscular blockade at extubation showed an increasing trend with the increase of age or body mass index. The average TOFr value at extubation, which interval time over 10 min after neostigmine administration to extubation was significant higher than that of interval time less than 10 min.Conclusions:There has 12% patients with TOFr<0.9 when extubation by estimating rocuronium and cis-atracurium effect with clinical signs and experience, it has a hidden danger of residual neuromuscular blockade. The main risk factors to increasing the incidence of residual neuromuscular blockade are growing old and the short time of administrating muscle relaxants or neostigmine to extubation.

Suspected Anaphylactic Shock Associated with Rocuronium in an Infant: A Case Report

We report a case of severe anaphylactic shock in a 5-month-old infant who was scheduled to undergo an external inguinal hernia repair under general anesthesia. Rocuronium used for anesthesia induction was the most likely cause of anaphylaxis. High levels of serum tryptase and histamine detected in the blood sample collected during the anaphylactic reaction confirmed the diagnosis of anaphylactic shock. The patient’s clinical status improved within 90 min of intervention by the intravenous injection of vasopressors and a steroid. Surgery was canceled, and the patient stayed in the pediatric intensive care unit (PICU) under artificial ventilation for 5 h before safe extubation. The patient achieved full recovery the next day, without any sequelae. The rescheduled surgery was successfully completed 5 months later under general anesthesia without the use of neuromuscular blocking agents.

Sugammadex in the Management of Sinus Tachycardia after Rocuronium Administration: A Case Report

In rare cases, rocuronium has been associated with dose-related tachycardia, probably by a cardiac muscarinic M2 receptor blockade mechanism. We report the case of a 30-year-old female who underwent excision of a branchial cyst under general anesthesia. This patient presented an episode of sinus tachycardia (130 bpm) shortly after anesthesia induction with propofol, sufentanyl, and rocuronium. Tachycardia could not be explained by any cause other than the use of rocuronium, which was reverted with sugammadex. Two minutes after sugammadex administration, heart rate normalized, corroborating our hypothesis that rocuronium induced the sinus tachycardia observed in our patient. The patient recovered well from the anesthetic-surgical procedure and showed no further cardiovascular, ventilatory, or neurological changes, being transferred to the post-anesthesia care unit, and finally discharged to the ward.

Effectiveness and safety of rocuronium or nitroglycerin plus ropivacaine on pain during intravenous regional anesthesia:A double-blind randomized controlled trial

Objective:To compare the effects of adding rocuronium and nitroglycerin to ropivacaine in intravenous regional anesthesia(IVRA)on pain and hemodynamic parameters.Methods:This randomized controlled trial was done in 2023.Participants were 177 candidates for forearm operation surgery under IVRA selected from Valiasr Hospital,Arak,Iran.They were allocated by block randomization to three different groups,namely nitroglycerin group,rocuronium group and control group.Hemodynamic parameters were recorded before tourniquet application up to postoperative recovery time.Sensory block and motor block onset and duration and pain were also evaluated.The data analysis was carried out by IMB SPSS software 20.0.Results:177 Eligible patients were included in study,with 59 in each group.Time to sensory and motor block onset in the nitroglycerin group was significantly less than the other groups and the time of motor block in the rocuronium group was statistically higher than the control and the nitroglycerin groups(P<0.001).Seven participants in the nitroglycerin group experienced headache and three from the rocuronium group experienced dizziness.The side effects occurrence in the nitroglycerin group was more prevalent than in the control and rocuronium groups(P=0.009).Conclusions:Nitroglycerin significantly reduces the time to sensory and motor block onset,while rocuronium is more effective in prolonging the time of motor block.Although there is no difference between nitroglycerin and rocuronium respecting the pain score and opioid need administration,nitroglycerin is associated with a higher prevalence of medication side effects.Therefore,both nitroglycerin and rocuronium can be used as adjuvant for IVRA.The final choice relies on patients’conditions and anesthesiologists’judgment.

Population pharmacokinetics of rocuronium delivered by target-controlled infusion in adult patients

Background Target-controlled infusion （TCI） has been recently developed and successfully implemented in clinical practice. The current study was to estimate the population pharmacokinetics of rocuronium TCI in adult patients using nonlinear mixed-effects model （NONMEM）, and to investigate the influence of relevant factors in adult patients. Methods Fourteen ASA Ⅰ-Ⅱ patients undergoing elective laparoscopy operation with general anesthesia were included. After induction, all patients received rocuronium by TCI system. The beginning target plasma concentration （Cpt） was 2.0 μg/ml, then increased Cpt according to the neuromuscular transmission monitoring. The endpoint of Cpt was determined when the T1 scale was blocked by 90%-95%. TCI rocuronium was stopped 30 minutes before the end of the operation. Arterial blood was drawn before anesthesia at 0, 2, 4, 6, 8, 10, 15, 20, 30, 45, 60, 120, 180, 240 and 360 minutes after the infusion of rocuronium was stopped for the analysis of plasma concentrations of rocuronium by liquid chromatography-mass spectrometry/mass spectrometry （LC-MS/MS）. The population pharmacokinetics analysis was performed using NONMEM program. Results The pharmacokinetics of TCI rocuronium in adult patients was best described by a three-comparment model. Pharmacokintic parameters were clearance （CL）1=0.205 L/min, CL2=0.324 L/min, CL3=0.0292 L/min, volumes of distribution （V）1=4.00 L, V2=2.28 L, V3=4.26 L, Vdss=10.54 L. Both age and weight as covariates affected the pharmacokinetic parameters. V1 and CL1 were negatively correlated with patient age. CL1 was positively correlated with weight. Conclusions No pharmacokinetic change was noted when rocuronium was administered via TCI. Both age and weight as covariates affected the pharmacokinetic parameters.

Different sensitivities to rocuronium of the neuromuscular junctions innervated by normal/damaged facial nerves and somatic nerve in rats： the role of the presynaptic acetylcholine quantal release

Background Muscles present different responses to muscle relaxants, a mechanism of importance in surgeries requiring facial nerve evoked electromyography under general anaesthesia. The non-depolarizing muscle relaxants have multiple reaction formats in the neuromuscular junction, in which pre-synaptic quantal release of acetylcholine was one of the important mechanisms. This study was to compare the pre-synaptic quantal release of acetylcholine from the neuromuscular junctions innervated by normal/damaged facial nerves and somatic nerve under the effect of rocuronium in rats in vitro. Methods Acute right-sided facial nerve injury was induced by nerve crush axotomies. Both sided facial nerve connected orbicularis oris strips and tibial nerve connected gastrocnemius strips were isolated to measure endplate potentials （EPP） and miniature endplate potentials （MEPP） using an intracellular microelectrode gauge under different rocuronium concentrations. Then, the pre-synaptic quantal releases of acetylcholine were calculated by the ratios of the EPPs and the MEPPs, and compared among the damaged or normal facial nerve innervated orbicularis oris and tibial nerve innervated gastrocnemius. Results The EPP/MEPP ratios of the three neuromuscular junctions decreased in a dose dependent manner with the increase of the rocuronium concentration. With the concentrations of rocuronium being 5 pg/ml, 7.5 IJg/ml and 10 pg/ml, the decrease of the EPP/MEPP ratio in the damaged facial nerve group was greater than that in the normal facial nerve group. The decrease in the somatic nerve group was the biggest, with significant differences. Conclusions Rocuronium presented different levels of inhibition on the pre-synaptic quantal release of acetylcholine in the three groups of neuromuscular junctions. The levels of the inhibition showed the following sequence： somatic nerve 〉 damaged facial nerve 〉 normal facial nerve. The difference may be one of the reasons causing the different sensitivities to rocuronium among the muscles innervated by the normal/injured facial nerves and the somatic nerve. The results may provide some information for the proper usage of muscle relaxants in surgeries requiring electromyographic monitoring for the pre-surgically impaired facial nerves.

Impairment of recovery of muscle function by residual rocuronium after re-transfusion of intraoperative salvaged blood

Background Recurarization has previously been described in the context of acute normovolemic hemodilution.The aim of this study was to investigate the impairment of recovery of neuromuscular function after re-transfusion of intraoperative salvaged blood in patients treated with rocuronium.Methods We enrolled 50 patients undergoing general anesthesia for lumbar surgery.Intraoperative blood salvage （IBS） was used in 30 patients （group Ⅰ）; the remaining 20 comprised a control group （group C）.Anesthesia was induced with fentanyl,midazolam,propofol and rocuronium.Rocuronium was infused to maintain neuromuscular blockade during surgery.Blood was collected from the operative field and re-transfused in the post-anesthesia care unit （PACU）.Neuromuscular function was monitored using the train-of-four ratio （TOFr）.Once the train-of-four ratio exceeded 90 in the PACU,neuromuscular function was evaluated every 5 minutes for 30 minutes.The TOFr and incremental recovery of TOFr from baseline were recorded.Salvaged blood was re-transfused at the beginning of the evaluation for patients in group Ⅰ,and afterwards for patients in group C.Blood gas analysis was assessed before anesthesia and in the PACU.Results Incremental recovery of TOFr from baseline was significantly less in group Ⅰ than controls at 25 minutes （6.1±3.2vs.9.1±3.2,respectively; P=0.001） and 30 minutes （7.1±3.2 vs.10.0±2.2,respectively; P=-0.001）.There were no significant differences in gas exchange between the groups.Conclusions In patients who had received a rocuronium infusion during anesthesia,re-transfusion of salvaged blood significantly impaired recovery of neuromuscular function recovery in the PACU,but without significant impairment of respiratory function.

A comparative study of the dose response and time course of recovery of atracurium and rocuronium

To compare the characteristics of the dose response relationship and the time course of action between atracurium and rocuronium in adult patients anesthetized with N 2O O 2 fentanyl thiopene Methods Sixty patients, ASA grade Ⅰ, aged 18-50 years, scheduled for elective plastic surgery were studied All patients were randomly divided into either the atracurium or rocuronium group General anesthesia was maintained with 60% nitrous oxide and 40% oxygen, thiopentone, and fentanyl Neuromuscular function was assessed using an accelograph with train of four (TOF) stimulation at the wrist every 12 seconds The percentage depression of the first twitch (T 1) was used as the study parameter The dose response relationship of atracurium and rocuronium was determined by the cumulative dose response technique Results According to the dose response curves established by a least squares linear regression, the potency ratio of atracurium to rocuronium was 1∶1 2 There were significant differences in the ED 50 , ED 90 , and ED 95 between the two drugs After the intravenous administration of equipotent doses of both drugs (1 5×ED 95 ), the duration of peak effect, clinical duration, and total duration were significantly different between the two drugs, but their recovery indexes were similar Conclusions Atracurium and rocuronium are low potency nondepolarizing relaxants with intermediate duration As compared to atracurium, the neuromuscular blocking effect of rocuronium was about 20% less potent and its duration of action was shorter

Anesthesia with propofol-remifentanil combined with rocuronium for bronchial foreign body removal in children: Experience of 2886 cases

Importance: The appropriate anesthetic method can reduce the complications of children with tracheal foreign body and reduce the mortality rate of children. What kind of anesthetic method to choose has always been the focus of debate. Purpose: To evaluate the efficacy and safety of anesthesia with propofol-remifentanil combined with rocuronium for foreign body aspiration (FBA) removal with the positive-pressure ventilation technique. Methods: Medical records of patients who underwent bronchoscopy for evaluation of FBA in our unit from January 2015 to January 2018 were retrospectively reviewed. Demographic data (age and sex), nature of foreign body and location, complications, length of hospital stay and outcome were analyzed. Results: A total of 2886 children were included in this study. The median age was 24 months (8 months to 10 years). FBA was detected and removed in 95.6％ of patients. The average operation time was 17 ± 5 min and average length of hospital stay was 2 days. Observed peri-interventional complications included desaturation (n = 66), laryngospasm (n = 19), laryngeal or subglottic edema (n = 15), irritating cough (n = 3), body movement (n = 76) and pneumonia (n = 206). No deaths occurred during hospitalization or follow-up in this series. Interpretation: Anesthesia with propofol-remifentanil combined with rocuronium under positive-pressure ventilation is an effective and safe technique during FBA removal in children.

A new and efficient method for the synthesis of rocuronium bromide

Rocuronium bromide has been used as an aminosteroid non-depolarizing neuromuscular blocker and muscle relaxant.In this work,a new and efficient route for preparing a key intermediate 2β-（4-morpholinyl）-16β-（1-pyrrolidinyl）-5α-androstan-3α,17β-diol（6） was developed through a ring-opening of epoxide followed by introducing and pyrrolidine.Compound 6 can easily provide rocuronium bromide and the overall yield of compound 6 in 5 steps increased to 57.8%,which was higher than currently reported methods.Extraordinarily,this method would avoid the generation of disubstituted impurities E and F which are difficult to remove.

罗库溴铵用于帕金森病患者的神经肌肉阻滞效应

目的观察帕金森病(Parkinson's disease,PD)与非PD患者罗库溴铵的神经肌肉阻滞效应。方法纳入年龄18~65岁,美国麻醉医师协会(American Society of Anesthesiologists,ASA)Ⅰ~Ⅲ,接受丘脑底核-脑深部电刺激手术的PD患者(PD组)31例和行面神经减压的非PD患者(non-PD组)24例为研究对象。麻醉诱导单次给予罗库溴铵(0.6 mg/kg),采用四个成串刺激(train-of-four,TOF)监测肌松,记录罗库溴铵体内作用时间(the duration of 90%recovery of TOF,DURTOF 90%)、起效时间、临床作用时间、恢复指数和术毕2 h内严重呼吸系统并发症发生情况。结果与non-PD组比较,PD组DURTOF 90%和临床作用时间均显著延长,差异有统计学意义(P<0.05);2组患者的起效时间差异无统计学意义(P>0.05)。PD患者的罗库溴铵DURTOF 90%与病程相关,病程越长,DURTOF 90%越长。2组患者术后均无严重呼吸系统并发症发生。结论PD患者应用罗库溴铵的DURTOF 90%和临床作用时间明显延长,且DURTOF 90%与病程呈正相关。

罗库溴铵引起围手术期寂静肺1例分析

围手术期发生的寂静肺具有起病急、进展迅速及死亡率高等特点。本文报道1例62岁左下肺结节患者在胸腔镜下接受下肺段切除术,手术中使用罗库溴铵辅助气管插管。首次给药后21 min,患者出现气道压增高、通气困难及“铁肺”手感,表现出类似于寂静肺的症状。随后追加静脉注射甲泼尼龙80 mg和肾上腺素50μg(分次),但未见明显缓解,血氧饱和度降至38%,再次给予肾上腺素1 mg后,气道压逐渐降至33 cmH_(2)O,血氧饱和度也逐步回升。考虑到气道痉挛可能由多次插管刺激引起,再次追加罗库溴铵以便进行再插管,然而插管前患者再次出现气道压增高与通气困难。对本次不良事件与可疑药物罗库溴铵进行关联性评价,结果为可能有关。本文对罗库溴铵引发寂静肺的机制、相应的预防与救治进行了探讨,提示术前应进行充分的麻醉评估,制定适宜的麻醉诱导方案,一旦发生不良事件,应及时识别救治。

术前急性高容量血液稀释对罗库溴铵量效关系及作用时间的影响

目的 探讨术前急性高容量血液稀释(acute hypervolaemic haemodilution,AHH)对罗库溴铵量效关系及作用时间的影响。方法 选取2022年4—10月首都医科大学附属北京朝阳医院怀柔医院需择期进行全麻手术的患者80例,随机分成AHH组和对照组,每组40例。AHH组麻醉30 min内静脉输注15 ml/kg 6%羟乙基淀粉,对照组30 min内缓慢滴注1~2 ml/kg 6%羟乙基淀粉。比较两组患者的一般情况,AHH前(t1)、AHH完成即刻(t2)、4个成串刺激(train of four,TOF)=0.9即刻(t3)的血液及尿液相关指标,罗库溴铵的绝对作用时间[自T1(第1个颤搐反应)=0至T1=1%所需时间]、临床作用时间(自T1=0至T1=25%所需时间)、体内作用时间(自T1=0至TOF=0.9所需时间)和恢复指数(T1从25%恢复至75%所需时间)。结果 80例患者中男50例、女30例;平均年龄(53.2±4.6)岁;平均身高(167.41±6.35)cm;平均体质量(67.88±6.38)kg。与t1相比,AHH组t2和t3的Hb、红细胞压积、TP、ALB、K^(+)、Mg^(2+)、Ca^(2+)、HR均降低;与对照组t2和t3相比,AHH组同时段的Hb、红细胞压积、TP、ALB、K^(+)、Ca^(2+)、Mg^(2+)、HR均较低,MAP和尿量均较高;差异均有统计学意义(P<0.05)。AHH组和对照组罗库溴铵的量效关系方程分别为y=105.7lgX-172.7和y=104.9lgX-169.0。两组罗库溴铵的ED_(50)、ED_(90)、ED_(95)、绝对作用时间、临床作用时间、体内作用时间和恢复指数方面的差异均无统计学意义(P> 0.05)。结论 15 ml/kg 6%羟乙基淀粉进行AHH不明显改变罗库溴铵的量效关系及作用时间。

两种不同的非去极化肌松剂复合瑞芬太尼用于支撑喉镜下声带息肉手术的比较

目的比较1倍ED 95罗库溴铵和顺式阿曲库铵复合瑞芬太尼麻醉在支撑喉镜下声带息肉手术的效果。方法选取三峡大学人民医院2019年1~11月在全身麻醉下行支撑喉镜声带息肉切除术的50例患者,采用随机数字表法分为罗库溴铵组(R组,n=25)、顺式阿曲库铵组(C组,n=25)。观察2组患者血流动力学指标、肌松作用时间、自主呼吸恢复时间、气管拔管时间。结果两组患者并发症发生率差异无统计学意义(P>0.05)。罗库溴铵组气管插管条件更佳、放置支撑喉镜时患者呛咳和体动的发生率更低、手术医生满意度更高、血流动力学指标更稳定、肌松作用时间更短、自主呼吸恢复和气管拔管时间更短(P<0.05)。结论1倍ED 95罗库溴铵复合瑞芬太尼麻醉在支撑喉镜下声带息肉手术的效果优于等效剂量的顺式阿曲库铵,有利于加快此类短小手术的周转。

不同剂量罗库溴铵对腔镜甲状腺切除术中喉返神经监测的影响

目的探讨不同剂量罗库溴铵对腔镜甲状腺切除术中喉返神经监测的影响。方法选择2021年10月至2022年10月行经乳晕入路腔镜甲状腺切除术的患者116例,男30例,女86例,年龄18~64岁,BMI 18.5~30.0 kg/m^(2),ASAⅠ或Ⅱ级。采用随机数字表法将患者分为三组:罗库溴铵0.30 mg/kg组(R1组,n=39)、罗库溴铵0.45 mg/kg(R2组,n=39)和罗库溴铵0.60 mg/kg(R3组,n=38)。麻醉诱导后,R1组、R2组和R3组分别静脉注射罗库溴铵0.30、0.45、0.60 mg/kg。当TOF值为0后插入神经监测气管导管,术中全程监测肌松,神经监测结束前不追加肌松药。记录首次出现喉返神经肌电图(EMG)时间及EMG振幅、插管时间及气管插管质量(Cooper’s评分法)。记录术中低血压、高血压、心动过缓、心动过速、体动的发生情况。记录术后咽痛、声音嘶哑、肌肉疼痛的发生情况。结果三组首次出现喉返神经EMG时间差异无统计学意义。与R1组比较,R2组和R3组首次出现喉返神经EMG振幅明显降低(P<0.05)。与R1组比较,R2组和R3组插管时间明显缩短(P<0.05)。与R2组比较,R3组插管时间明显缩短(P<0.05)。与R1组比较,R2组和R3组气管插管质量明显升高(P<0.05)。与R1组比较,R2组和R3组术中体动、术后咽痛发生率明显降低(P<0.05)。结论在腔镜甲状腺切除术中,与罗库溴铵0.30 mg/kg比较,罗库溴铵0.45和0.60 mg/kg既能提供良好的气管插管条件,又能监测到喉返神经肌电信号,罗库溴铵0.60 mg/kg插管时间更短。