首页 > 最新文献

Anesthesia, Essays and Researches最新文献

英文 中文
A Comparative Study of Intrathecal Hyperbaric Bupivacaine 0.5% with Morphine and Dexmedetomidine in Lower Limb Orthopedic Surgeries: A Double-Blind Randomized Clinical Trial. 0.5%鞘内高压布比卡因与吗啡和右美托咪定在下肢骨科手术中的比较研究:一项双盲随机临床试验。
Pub Date : 2022-07-01 Epub Date: 2022-11-15 DOI: 10.4103/aer.aer_116_22
Shadab Ashfi, Azizul Haque, Mukesh Kumar, Ladhu Lakra

Background: Pain and its alleviation have been a challenge for humans for centuries. Sub arachnoid block is most commonly practiced method for anaesthesia for lower limb surgeries. Adjuvants like opioids and alpha 2 agonists have proven benefits in augmentation of effects of local anaesthetics for spinal anesthesia. The aim of this study was to compare the effects of morphine and dexmedetomidine for sub arachnoid block in lower limb orthopaedic surgeries.

Material and methods: This is a prospective randomised controlled trial done in 120 patients who were posted for lower limb orthopaedic surgery. Along with bupivacaine, Group A received intrathecal dexmedetomidine while group B received intrathecal morphine.

Results: the demographic profile was comparable in both the groups. The mean duration of motor block in Group A was 359.33 ± 34.4 and in Group B was 265.71 ± 28.47. The duration of rescue analgesia was almost double in Group A as compared to Group B with P < 0.0001 (CL 95%).

Conclusion: Intrathecal dexmedetomidine and morphine both provided good postoperative analgesia. Dexmedetomidine provided a longer duration of analgesia than morphine, thereby increasing the time for first rescue analgesia, but at the cost of greater side effects.

背景:几个世纪以来,疼痛及其缓解一直是人类面临的挑战。蛛网膜下腔阻滞是下肢手术中最常用的麻醉方法。阿片类药物和α2激动剂等佐剂已被证明在增强局部麻醉剂对脊柱麻醉的效果方面具有益处。本研究的目的是比较吗啡和右美托咪定在下肢整形外科治疗蛛网膜下腔阻滞的效果。材料和方法:这是一项前瞻性随机对照试验,对120名接受下肢整形外科手术的患者进行了研究。A组与布比卡因一起鞘内注射右美托咪定,B组鞘内注射吗啡。结果:两组的人口统计学特征具有可比性。A组运动阻滞的平均持续时间为359.33±34.4,B组为265.71±28.47。与B组相比,A组的抢救镇痛持续时间几乎是B组的两倍,P<0.0001(CL 95%)。结论:鞘内右美托咪定和吗啡均能提供良好的术后镇痛效果。右美托咪定提供的镇痛持续时间比吗啡更长,从而增加了首次抢救镇痛的时间,但代价是副作用更大。
{"title":"A Comparative Study of Intrathecal Hyperbaric Bupivacaine 0.5% with Morphine and Dexmedetomidine in Lower Limb Orthopedic Surgeries: A Double-Blind Randomized Clinical Trial.","authors":"Shadab Ashfi,&nbsp;Azizul Haque,&nbsp;Mukesh Kumar,&nbsp;Ladhu Lakra","doi":"10.4103/aer.aer_116_22","DOIUrl":"10.4103/aer.aer_116_22","url":null,"abstract":"<p><strong>Background: </strong>Pain and its alleviation have been a challenge for humans for centuries. Sub arachnoid block is most commonly practiced method for anaesthesia for lower limb surgeries. Adjuvants like opioids and alpha 2 agonists have proven benefits in augmentation of effects of local anaesthetics for spinal anesthesia. The aim of this study was to compare the effects of morphine and dexmedetomidine for sub arachnoid block in lower limb orthopaedic surgeries.</p><p><strong>Material and methods: </strong>This is a prospective randomised controlled trial done in 120 patients who were posted for lower limb orthopaedic surgery. Along with bupivacaine, Group A received intrathecal dexmedetomidine while group B received intrathecal morphine.</p><p><strong>Results: </strong>the demographic profile was comparable in both the groups. The mean duration of motor block in Group A was 359.33 ± 34.4 and in Group B was 265.71 ± 28.47. The duration of rescue analgesia was almost double in Group A as compared to Group B with <i>P</i> < 0.0001 (CL 95%).</p><p><strong>Conclusion: </strong>Intrathecal dexmedetomidine and morphine both provided good postoperative analgesia. Dexmedetomidine provided a longer duration of analgesia than morphine, thereby increasing the time for first rescue analgesia, but at the cost of greater side effects.</p>","PeriodicalId":7798,"journal":{"name":"Anesthesia, Essays and Researches","volume":"16 3","pages":"373-377"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813983/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10508709","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Perioperative Challenges in the Management of Rhino-Orbital Cerebral Mucormycosis: An Observational Study from a Tertiary Care Hospital. 鼻眶脑毛霉菌病围手术期治疗的挑战:一项来自三级护理医院的观察研究。
Pub Date : 2022-07-01 Epub Date: 2022-12-09 DOI: 10.4103/aer.aer_83_22
Pradnya Milind Bhalerao, Shital Mahendra Kuttarmare, Shweta Joshi, Sanyogita Vijay Naik

Background: Coronavirus disease 2019 (COVID-19) pandemic is the biggest threat of the century. Associated with this disease, are a number of rhino orbital cerebral mucormycosis cases seen as post COVID sequelae. Amphotericin B and surgical debridement are the treatment modalities.

Aims: This study aimed to describe the clinical characteristics and perioperative outcomes of patients with ROCM.

Settings and design: This was a prospective, observational study.

Materials and methods: We carried out a study of 238 patients with confirmed ROCM posted for functional endoscopic sinus surgery, craniotomies, maxillofacial surgeries, and orbital exenteration under general anesthesia and the perioperative challenges therein.

Statistical analysis used: Data were entered in the excel sheet. Descriptive statistics were used to summarize the data. Analysis was done using the Statistical Package for the Social Sciences (SPSS) version 27:0. Categorical variables were expressed as counts and percentages.

Results: 78% had diabetes mellitus, 64% had received steroids, 59% had a preoperative oxygen saturation of less than 90%, 86% had a 4-6 zone involvement on chest radiograph, and more than 50% had an anticipated difficult airway. Postsurgery, 13% of patients required intensive care. The 15-day mortality rate was 3% among the operated cases.

Conclusion: Post-COVID ROCM is challenging in terms of preoperative poor general condition, difficult airway, intraoperative concerns due to pathophysiology of the disease and its effect on organ systems, and the requirement of postoperative vigilant monitoring.

背景:2019冠状病毒病(新冠肺炎)大流行是本世纪最大的威胁。与这种疾病相关的是一些被视为新冠肺炎后遗症的鼻眶脑毛霉菌病病例。两性霉素B和外科清创术是治疗方式。目的:本研究旨在描述ROCM患者的临床特征和围手术期结果。设置和设计:这是一项前瞻性观察性研究。材料和方法:我们对238名确诊ROCM的患者进行了研究,这些患者在全身麻醉下接受了功能性内窥镜鼻窦手术、开颅手术、颌面外科手术和眼眶摘除术,以及围手术期的挑战。使用的统计分析:数据输入excel表中。描述性统计被用来总结数据。使用社会科学统计软件包(SPSS)版本27:0进行分析。分类变量用计数和百分比表示。结果:78%的患者患有糖尿病,64%的患者服用了类固醇,59%的患者术前血氧饱和度低于90%,86%的患者在胸部X线片上有4-6区受累,超过50%的患者预计会出现气道困难。术后,13%的患者需要重症监护。术后15天死亡率为3%。结论:COVID后ROCM在术前总体状况不佳、气道困难、由于疾病的病理生理学及其对器官系统的影响而引起的术中担忧以及术后警惕性监测的要求方面具有挑战性。
{"title":"Perioperative Challenges in the Management of Rhino-Orbital Cerebral Mucormycosis: An Observational Study from a Tertiary Care Hospital.","authors":"Pradnya Milind Bhalerao,&nbsp;Shital Mahendra Kuttarmare,&nbsp;Shweta Joshi,&nbsp;Sanyogita Vijay Naik","doi":"10.4103/aer.aer_83_22","DOIUrl":"10.4103/aer.aer_83_22","url":null,"abstract":"<p><strong>Background: </strong>Coronavirus disease 2019 (COVID-19) pandemic is the biggest threat of the century. Associated with this disease, are a number of rhino orbital cerebral mucormycosis cases seen as post COVID sequelae. Amphotericin B and surgical debridement are the treatment modalities.</p><p><strong>Aims: </strong>This study aimed to describe the clinical characteristics and perioperative outcomes of patients with ROCM.</p><p><strong>Settings and design: </strong>This was a prospective, observational study.</p><p><strong>Materials and methods: </strong>We carried out a study of 238 patients with confirmed ROCM posted for functional endoscopic sinus surgery, craniotomies, maxillofacial surgeries, and orbital exenteration under general anesthesia and the perioperative challenges therein.</p><p><strong>Statistical analysis used: </strong>Data were entered in the excel sheet. Descriptive statistics were used to summarize the data. Analysis was done using the Statistical Package for the Social Sciences (SPSS) version 27:0. Categorical variables were expressed as counts and percentages.</p><p><strong>Results: </strong>78% had diabetes mellitus, 64% had received steroids, 59% had a preoperative oxygen saturation of less than 90%, 86% had a 4-6 zone involvement on chest radiograph, and more than 50% had an anticipated difficult airway. Postsurgery, 13% of patients required intensive care. The 15-day mortality rate was 3% among the operated cases.</p><p><strong>Conclusion: </strong>Post-COVID ROCM is challenging in terms of preoperative poor general condition, difficult airway, intraoperative concerns due to pathophysiology of the disease and its effect on organ systems, and the requirement of postoperative vigilant monitoring.</p>","PeriodicalId":7798,"journal":{"name":"Anesthesia, Essays and Researches","volume":"16 3","pages":"331-335"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814004/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10508702","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Effectiveness of Three Regimens of Sedation for Children Undergoing Magnetic Resonance Imaging: A Clinical Study. 三种镇静方式对儿童磁共振成像效果的临床研究。
Pub Date : 2022-07-01 Epub Date: 2022-12-09 DOI: 10.4103/aer.aer_45_22
Shwethashri Kondavagilu Ramaprasannakumar, Varadarajan Bhadrinarayan, Sudhir Venkataramaiah

Background: Magnetic resonance imaging (MRI) under sedation requires faster recovery for early discharge and feeding resumption in children with neuropsychiatric disorders. The use of dexmedetomidine alone results in delayed recovery. Propofol, when used alone, can cause hypotension and respiratory depression. A new regimen for sedation was evaluated by exploiting the properties of these drugs, to allow faster recovery with minimal adverse events.

Materials and methods: One hundred and fifty children aged 2-12 years requiring MRI were randomly allocated to these three groups. Group P (n = 50) received propofol bolus at 2 mg.kg-1 over 10 min followed by infusion at 100 μg.kg-1.min-1. Group D (n = 50) received dexmedetomidine bolus of 2 μg.kg-1 over 10 min followed by infusion at 1 μg.kg-1.h-1. Group PD (n = 50) received propofol bolus at 2 mg.kg-1 over 10 min followed by dexmedetomidine infusion at 1 μg.kg-1.h-1. Recovery characteristics were noted.

Results: Recovery following sedation in Group PD (15 ± 7.0 min) and Group P (17.35 ± 7.4 min) were comparable and significantly (P = 0.03) lesser than Group D (27.58 ± 8.09 min). Emergence delirium scores were significantly less in Group PD (5 ± 1.08) and Group D (5.6 ± 2.4), unlike scores in Group P (9 ± 2.43). About 79.5% (39/49) of children in Group P, 88.2% (45/51) of children in Group D, and 86% (43/50) of children in Group PD completed MRI without any movement. Seven (14.58%) in Group P, 2 (4%) in Group D, and 5 (10.20%) in Group PD required rescue sedation.

Conclusion: The regimen with propofol bolus and dexmedetomidine infusion provided adequate sedation and better recovery characteristics in children aged 2-12 years without systemic complications, as compared to the use of either agent alone.

背景:镇静状态下的磁共振成像(MRI)需要更快的恢复,才能使患有神经精神障碍的儿童尽早出院和恢复进食。单独使用右美托咪定会导致恢复延迟。单独使用异丙酚会引起低血压和呼吸抑制。通过利用这些药物的特性,对一种新的镇静方案进行了评估,以使其能够在最小的不良事件下更快地恢复。材料和方法:150名2-12岁需要MRI检查的儿童被随机分为这三组。P组(n=50)以2mg.kg-1的丙泊酚推注10分钟,然后以100μg.kg-1输注。D组(n=50)接受右美托咪定2μg.kg-1推注10分钟,然后以1μg.kg-1.h-1输注。PD组(n=50)接受丙泊酚2mg.kg-1推注10分钟,然后输注右美托咪定1μg.kg-1。注意到回收特征。结果:PD组(15±7.0分钟)和P组(17.35±7.4分钟)镇静后的恢复情况相当,且显著(P=0.03)低于D组(27.58±8.09分钟)。与P组(9±2.43)的评分不同,PD组(5±1.08)和D组(5.6±2.4)的突发性谵妄评分显著降低。P组约79.5%(39/49)的儿童、D组约88.2%(45/51)的儿童和PD组约86%(43/50)的儿童在没有任何运动的情况下完成了MRI检查。P组7例(14.58%),D组2例(4%),PD组5例(10.20%)需要抢救性镇静。结论:与单独使用这两种药物相比,丙泊酚推注和右美托咪定输注方案为2-12岁的儿童提供了足够的镇静和更好的恢复特性,没有系统性并发症。
{"title":"The Effectiveness of Three Regimens of Sedation for Children Undergoing Magnetic Resonance Imaging: A Clinical Study.","authors":"Shwethashri Kondavagilu Ramaprasannakumar,&nbsp;Varadarajan Bhadrinarayan,&nbsp;Sudhir Venkataramaiah","doi":"10.4103/aer.aer_45_22","DOIUrl":"10.4103/aer.aer_45_22","url":null,"abstract":"<p><strong>Background: </strong>Magnetic resonance imaging (MRI) under sedation requires faster recovery for early discharge and feeding resumption in children with neuropsychiatric disorders. The use of dexmedetomidine alone results in delayed recovery. Propofol, when used alone, can cause hypotension and respiratory depression. A new regimen for sedation was evaluated by exploiting the properties of these drugs, to allow faster recovery with minimal adverse events.</p><p><strong>Materials and methods: </strong>One hundred and fifty children aged 2-12 years requiring MRI were randomly allocated to these three groups. Group P (<i>n</i> = 50) received propofol bolus at 2 mg.kg<sup>-1</sup> over 10 min followed by infusion at 100 μg.kg<sup>-1</sup>.min<sup>-1</sup>. Group D (<i>n</i> = 50) received dexmedetomidine bolus of 2 μg.kg<sup>-1</sup> over 10 min followed by infusion at 1 μg.kg<sup>-1</sup>.h<sup>-1</sup>. Group PD (<i>n</i> = 50) received propofol bolus at 2 mg.kg<sup>-1</sup> over 10 min followed by dexmedetomidine infusion at 1 μg.kg<sup>-1</sup>.h<sup>-1</sup>. Recovery characteristics were noted.</p><p><strong>Results: </strong>Recovery following sedation in Group PD (15 ± 7.0 min) and Group P (17.35 ± 7.4 min) were comparable and significantly (<i>P</i> = 0.03) lesser than Group D (27.58 ± 8.09 min). Emergence delirium scores were significantly less in Group PD (5 ± 1.08) and Group D (5.6 ± 2.4), unlike scores in Group P (9 ± 2.43). About 79.5% (39/49) of children in Group P, 88.2% (45/51) of children in Group D, and 86% (43/50) of children in Group PD completed MRI without any movement. Seven (14.58%) in Group P, 2 (4%) in Group D, and 5 (10.20%) in Group PD required rescue sedation.</p><p><strong>Conclusion: </strong>The regimen with propofol bolus and dexmedetomidine infusion provided adequate sedation and better recovery characteristics in children aged 2-12 years without systemic complications, as compared to the use of either agent alone.</p>","PeriodicalId":7798,"journal":{"name":"Anesthesia, Essays and Researches","volume":"16 3","pages":"345-352"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813997/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10508703","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The Value of Routine Tests before Pediatric Eye Surgery: A 10-Year Experience at a Tertiary Care Hospital. 儿童眼科手术前常规检查的价值:在三级护理医院的10年经验。
Pub Date : 2022-07-01 Epub Date: 2022-12-09 DOI: 10.4103/aer.aer_112_22
Hideyo Horikawa, Mitsuhiro Matsuo, Mitsuaki Yamazaki

Background: Routine tests before ophthalmologic surgery in adult patients are no longer recommended. However, there are limited data on the utility of routine preoperative tests for children.

Aims: We aimed to describe the effect of routine preoperative tests on systemic perioperative complications by hospital discharge or by day 30 following eye surgery.

Settings and design: This was a single-center, observational, and descriptive study.

Subjects and methods: We examined all patients ≤ 17 years old for whom ophthalmologists consulted with anesthesiologists before eye surgery under general anesthesia in an academic teaching tertiary care hospital from January 2010 to December 2019.

Results: A total of 708 pediatric patients were analyzed. The mean patient age was 8.5 ± 4.6 years. The most frequently performed procedure was strabismus surgery in 433 patients (61.2%). Following anesthetic consultations, 15 patients (2.1%) underwent surgery postponed due to abnormalities at the physical examination. Routine tests identified that the two patients (0.3%) required additional evaluations due to elevated serum creatine kinase and electrocardiographic abnormalities. However, further examinations found that these abnormalities were unremarkable. The remaining 691 patients (97.6%) underwent surgery as scheduled. Substantial intraoperative blood loss was observed only in three patients with malignant tumors or trauma. The incidence of systemic complications was 0 (0%; 95% confidence interval, 0%-0.05%).

Conclusions: These data indicated that the development of systemic perioperative complications following pediatric ophthalmic surgery is rare. Preoperative tests should be requested only if they are clinically indicated or before potentially bleeding procedures, such as malignancy or trauma surgery.

背景:不再建议成人患者在眼科手术前进行常规检查。然而,关于儿童常规术前检查的实用性的数据有限。目的:我们旨在描述常规术前检查对出院或眼部手术后第30天系统围手术期并发症的影响。设置和设计:这是一项单中心、观察性和描述性研究。受试者和方法:我们检查了2010年1月至2019年12月在一家学术教学三级护理医院进行全身麻醉眼科手术前眼科医生咨询的所有≤17岁的患者。结果:共分析了708名儿科患者。患者平均年龄为8.5±4.6岁。最常见的手术是433名患者(61.2%)的斜视手术。在麻醉会诊后,15名患者(2.1%)因体检异常而推迟了手术。常规检查发现,由于血清肌酸激酶升高和心电图异常,两名患者(0.3%)需要进行额外评估。然而,进一步的检查发现这些异常并不明显。其余691名患者(97.6%)按计划接受了手术。仅在三名恶性肿瘤或创伤患者中观察到术中大量失血。系统性并发症的发生率为0(0%;95%置信区间,0%-0.05%)。结论:这些数据表明,儿童眼科手术后出现系统性围手术期并发症的情况很少见。只有在临床上有指示的情况下或在潜在出血程序(如恶性肿瘤或创伤手术)之前,才应要求进行术前检查。
{"title":"The Value of Routine Tests before Pediatric Eye Surgery: A 10-Year Experience at a Tertiary Care Hospital.","authors":"Hideyo Horikawa,&nbsp;Mitsuhiro Matsuo,&nbsp;Mitsuaki Yamazaki","doi":"10.4103/aer.aer_112_22","DOIUrl":"10.4103/aer.aer_112_22","url":null,"abstract":"<p><strong>Background: </strong>Routine tests before ophthalmologic surgery in adult patients are no longer recommended. However, there are limited data on the utility of routine preoperative tests for children.</p><p><strong>Aims: </strong>We aimed to describe the effect of routine preoperative tests on systemic perioperative complications by hospital discharge or by day 30 following eye surgery.</p><p><strong>Settings and design: </strong>This was a single-center, observational, and descriptive study.</p><p><strong>Subjects and methods: </strong>We examined all patients ≤ 17 years old for whom ophthalmologists consulted with anesthesiologists before eye surgery under general anesthesia in an academic teaching tertiary care hospital from January 2010 to December 2019.</p><p><strong>Results: </strong>A total of 708 pediatric patients were analyzed. The mean patient age was 8.5 ± 4.6 years. The most frequently performed procedure was strabismus surgery in 433 patients (61.2%). Following anesthetic consultations, 15 patients (2.1%) underwent surgery postponed due to abnormalities at the physical examination. Routine tests identified that the two patients (0.3%) required additional evaluations due to elevated serum creatine kinase and electrocardiographic abnormalities. However, further examinations found that these abnormalities were unremarkable. The remaining 691 patients (97.6%) underwent surgery as scheduled. Substantial intraoperative blood loss was observed only in three patients with malignant tumors or trauma. The incidence of systemic complications was 0 (0%; 95% confidence interval, 0%-0.05%).</p><p><strong>Conclusions: </strong>These data indicated that the development of systemic perioperative complications following pediatric ophthalmic surgery is rare. Preoperative tests should be requested only if they are clinically indicated or before potentially bleeding procedures, such as malignancy or trauma surgery.</p>","PeriodicalId":7798,"journal":{"name":"Anesthesia, Essays and Researches","volume":"16 3","pages":"392-396"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10499945","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Caudal Morphine in Pediatric Patients: A Comparison of Two Different Doses in Children Undergoing Infraumbilical Surgery - A Prospective, Randomized, Double-Blind Study. 儿童患者的尾部吗啡:接受脐下手术的儿童两种不同剂量的比较——一项前瞻性、随机、双盲研究。
Pub Date : 2022-07-01 Epub Date: 2022-12-09 DOI: 10.4103/aer.aer_120_22
Sushree Das, Ranjita Acharya, Madhusmita Patro, Nupur Moda, Gunde Mounika

Background: One of the most feared symptoms of any disease is PAIN. It is a complex phenomenal experience, especially in children. Various methods and medications have been administered through different routes. Regional anesthesia produces marvelous postoperative analgesia and cessation of stress response in infants and children. Caudal epidural analgesia is the most acceptable and popular method of providing intra- and postoperative analgesia for abdominal, perineal, and lower limb surgeries in children. The use of preservative-free morphine as an adjunct to ropivacaine increases the quality and duration of analgesia despite the various side effects. Various articles use various doses of morphine as an adjuvant in caudal epidural analgesia. Hence, we conducted the study to compare the two dosages of morphine that is 20 μg.kg-1 and 30 μg.kg-1 of caudal epidural morphine for infraumblical surgeries with regard to its efficacy and safety and side effect profiles.

Materials and methods: The study is a prospective, randomized, double-blinded study. Sixty patients were divided into two groups. Group A: 20 μg.kg-1 of morphine was added to 0.2% ropivacaine 1 mL.kg-1 and the solution was made. Group B: 30 μg.kg-1 of morphine was added to 1 mL.kg-1 of 0.2% ropivacaine. Heart rate, systolic blood pressure, diastolic blood pressure, SPO2, pain score, and sedation score were recorded immediately, after 15 min, 30 min, 45 min, 1 h, 2 h, 4 h, 8 h, 12 h, 16 h, 18 h, and 24 h were recorded.

Results: The mean duration of analgesia is similar in both groups (P = 0.011). The mean duration was 20.517 ± 1.9143 h in Group A and 22.233 ± 1.6853 h in Group B. Children with the requirement of one dose of rescue analgesia in Group A was 83.3% which was higher than Group B being 66.7%. Children with no analgesic requirement were 16.7% in Group A and 33.3% in Group B. The incidence of side effects was more in Group B (8 [26.7%] children with nausea and vomiting; 1 [3.3%] children with urinary retention) than in Group A (2 [6.6%] children with nausea and vomiting.

Conclusion: From the above observations, it can be concluded that morphine of less dosage (20 μg.kg-1) when added to 0.2% ropivacaine for the caudal epidural block has better efficacy than morphine of higher dosage (30 μg.kg-1) as the duration of analgesia is similar with decreased incidence of side effects.

背景:任何疾病最可怕的症状之一就是疼痛。这是一种复杂而非凡的体验,尤其是在儿童身上。已经通过不同的途径给药了各种方法和药物。区域麻醉在婴儿和儿童中产生了极好的术后镇痛和停止应激反应。尾部硬膜外镇痛是为儿童腹部、会阴和下肢手术提供术中和术后镇痛的最可接受和最受欢迎的方法。使用不含防腐剂的吗啡作为罗哌卡因的辅助药物可以提高镇痛的质量和持续时间,尽管有各种副作用。各种文章使用不同剂量的吗啡作为硬膜外尾部镇痛的辅助药物。因此,我们进行了这项研究,以比较两种剂量的吗啡,即20μg.kg-1和尾侧硬膜外吗啡30μg.kg-1,用于脐下手术的疗效、安全性和副作用。材料和方法:本研究为前瞻性、随机、双盲研究。60名患者被分为两组。A组:在0.2%罗哌卡因1mL.kg-1中加入吗啡20μg.kg-1制成溶液。B组:在0.2%罗哌卡因1mL·kg~(-1)中加入吗啡30μg.kg~(-2)。在记录15分钟、30分钟、45分钟、1小时、2小时、4小时、8小时、12小时、16小时、18小时和24小时后,立即记录心率、收缩压、舒张压、SPO2、疼痛评分和镇静评分。结果:两组平均镇痛持续时间相似(P=0.011),A组平均为20.517±1.9143h,B组平均为22.233±1.6853h。A组需要一次镇痛的儿童为83.3%,高于B组的66.7%。无镇痛需求的儿童为16.7%,B组为33.3%。B组恶心呕吐患儿8例(26.7%),尿潴留患儿1例(3.3%),副作用发生率高于A组恶心呕吐儿2例(6.6%)高剂量(30μg.kg-1)与镇痛持续时间相似,副作用发生率降低。
{"title":"Caudal Morphine in Pediatric Patients: A Comparison of Two Different Doses in Children Undergoing Infraumbilical Surgery - A Prospective, Randomized, Double-Blind Study.","authors":"Sushree Das,&nbsp;Ranjita Acharya,&nbsp;Madhusmita Patro,&nbsp;Nupur Moda,&nbsp;Gunde Mounika","doi":"10.4103/aer.aer_120_22","DOIUrl":"10.4103/aer.aer_120_22","url":null,"abstract":"<p><strong>Background: </strong>One of the most feared symptoms of any disease is PAIN. It is a complex phenomenal experience, especially in children. Various methods and medications have been administered through different routes. Regional anesthesia produces marvelous postoperative analgesia and cessation of stress response in infants and children. Caudal epidural analgesia is the most acceptable and popular method of providing intra- and postoperative analgesia for abdominal, perineal, and lower limb surgeries in children. The use of preservative-free morphine as an adjunct to ropivacaine increases the quality and duration of analgesia despite the various side effects. Various articles use various doses of morphine as an adjuvant in caudal epidural analgesia. Hence, we conducted the study to compare the two dosages of morphine that is 20 μg.kg<sup>-1</sup> and 30 μg.kg<sup>-1</sup> of caudal epidural morphine for infraumblical surgeries with regard to its efficacy and safety and side effect profiles.</p><p><strong>Materials and methods: </strong>The study is a prospective, randomized, double-blinded study. Sixty patients were divided into two groups. Group A: 20 μg.kg<sup>-1</sup> of morphine was added to 0.2% ropivacaine 1 mL.kg<sup>-1</sup> and the solution was made. Group B: 30 μg.kg<sup>-1</sup> of morphine was added to 1 mL.kg<sup>-1</sup> of 0.2% ropivacaine. Heart rate, systolic blood pressure, diastolic blood pressure, SPO<sub>2</sub>, pain score, and sedation score were recorded immediately, after 15 min, 30 min, 45 min, 1 h, 2 h, 4 h, 8 h, 12 h, 16 h, 18 h, and 24 h were recorded.</p><p><strong>Results: </strong>The mean duration of analgesia is similar in both groups (<i>P</i> = 0.011). The mean duration was 20.517 ± 1.9143 h in Group A and 22.233 ± 1.6853 h in Group B. Children with the requirement of one dose of rescue analgesia in Group A was 83.3% which was higher than Group B being 66.7%. Children with no analgesic requirement were 16.7% in Group A and 33.3% in Group B. The incidence of side effects was more in Group B (8 [26.7%] children with nausea and vomiting; 1 [3.3%] children with urinary retention) than in Group A (2 [6.6%] children with nausea and vomiting.</p><p><strong>Conclusion: </strong>From the above observations, it can be concluded that morphine of less dosage (20 μg.kg<sup>-1</sup>) when added to 0.2% ropivacaine for the caudal epidural block has better efficacy than morphine of higher dosage (30 μg.kg<sup>-1</sup>) as the duration of analgesia is similar with decreased incidence of side effects.</p>","PeriodicalId":7798,"journal":{"name":"Anesthesia, Essays and Researches","volume":"16 3","pages":"360-365"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9814005/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10565490","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Comparison of Effectiveness of CE Technique and Jaw Thrust Technique for Mask Ventilation on Apneic Anesthetized Adults: A Randomized Controlled Trial. CE技术和Jaw Thrust技术对麻醉成人面罩通气效果的比较:一项随机对照试验。
Pub Date : 2022-07-01 Epub Date: 2022-12-09 DOI: 10.4103/aer.aer_110_22
Akshara Madhav, Leena Harshad Parate, Suresh Govindswamy

Background: The two most common techniques for mask ventilation are CE and jaw thrust (JT) technique. However, few studies have validated their efficiency in terms of tidal volume (TV).

Aims: This study aimed to compare the effectiveness of the CE technique and JT technique during pressure-controlled ventilation (PCV) by the mean of returned TV on apneic anesthetized adults.

Design: This was a prospective, randomized cross over study.

Settings: This study was conducted in a tertiary care hospital.

Methods: Ethical Committee approval from our institution was taken (ss-1/EC 049/2017) and was registered in Clinical Trials Registry of India (CTRI/2018/04/012958). Sixty-five American Society of Anesthesiologists Physical Status classes I and II adult patients were enrolled in the study. After induction and muscle relaxation, mask ventilation was performed with CE and JT technique on PCV mode (Pinsp 15 cm H2O, respiratory rate 15) for 1 min each. The mean of returned TV of last 12 breaths, gastric insufflation, audible mask leak, and operator comfort in each technique were compared.

Statistical analysis: Statistical software namely IBM SPSS 22.0 and R environment version 3.2.2 (IBM Corp. SPSS Statistics for Windows, Version 22.0. Armonk, NY, USA) were used for data analysis. Microsoft Excel was used to generate graphs and tables. Data were expressed as mean ± standard deviation for continuous variables and number (%) for categorical variables. Student's t-test (two tailed, independent) was used to find the significance of the study parameters on a continuous scale. Chi-square/Fisher's exact test was used to find the significance of the study parameters on a categorical scale between two or more groups.

Results: There was a significant increase in mean TV generated by JT technique over CE technique (591.46 ± 140.27 mL vs. 544.59 ± 159.08 mL; P < 0.001). Gastric insufflation (12.9% vs. 14.5%) and mask leak (11.3% vs. 38.7%) were more in CE technique. Operator comfort (79% vs. 19.4%) was more in JT technique.

Conclusion: A two-handed JT technique is more effective than a one-handed CE technique for mask ventilation in apneic anesthetized adults.

背景:面罩通气最常见的两种技术是CE和下颌推压(JT)技术。然而,很少有研究证实其在潮气量(TV)方面的有效性。目的:本研究旨在通过对呼吸暂停麻醉的成年人返回TV的平均值,比较CE技术和JT技术在压力控制通气(PCV)过程中的效果。设计:这是一项前瞻性随机交叉研究。背景:本研究在一家三级护理医院进行。方法:获得我机构伦理委员会的批准(ss-1/EC 049/2017),并在印度临床试验注册中心注册(CTRI/2018/04/012958)。65名美国麻醉师学会一级和二级成年患者参加了这项研究。诱导和肌肉放松后,用CE和JT技术在PCV模式(Pinsp 15 cm H2O,呼吸频率15)下分别进行面罩通气1分钟。比较了每种技术中最后12次呼吸的返回电视、胃吹入、可听见的面罩泄漏和操作者舒适度的平均值。统计分析:统计软件,即IBM SPSS 22.0和R环境版本3.2.2(IBM Corp.SPSS Statistics for Windows,版本22.0。Armonk,NY,USA)进行数据分析。使用Microsoft Excel生成图表。数据表示为连续变量的平均值±标准差,分类变量的数值(%)。学生t检验(双尾,独立)用于在连续量表上发现研究参数的显著性。卡方/Fisher精确检验用于在两组或两组以上的分类量表上发现研究参数的显著性。结果:与CE技术相比,JT技术产生的平均TV显著增加(591.46±140.27 mL vs.544.59±159.08 mL;P<0.001)。CE技术产生的胃充气(12.9%vs.14.5%)和面罩渗漏(11.3%vs.38.7%)更多。JT技术的操作者舒适度(79%对19.4%)更高。结论:在呼吸暂停麻醉的成人中,双手JT技术比单手CE技术更有效。
{"title":"Comparison of Effectiveness of CE Technique and Jaw Thrust Technique for Mask Ventilation on Apneic Anesthetized Adults: A Randomized Controlled Trial.","authors":"Akshara Madhav,&nbsp;Leena Harshad Parate,&nbsp;Suresh Govindswamy","doi":"10.4103/aer.aer_110_22","DOIUrl":"10.4103/aer.aer_110_22","url":null,"abstract":"<p><strong>Background: </strong>The two most common techniques for mask ventilation are CE and jaw thrust (JT) technique. However, few studies have validated their efficiency in terms of tidal volume (TV).</p><p><strong>Aims: </strong>This study aimed to compare the effectiveness of the CE technique and JT technique during pressure-controlled ventilation (PCV) by the mean of returned TV on apneic anesthetized adults.</p><p><strong>Design: </strong>This was a prospective, randomized cross over study.</p><p><strong>Settings: </strong>This study was conducted in a tertiary care hospital.</p><p><strong>Methods: </strong>Ethical Committee approval from our institution was taken (ss-1/EC 049/2017) and was registered in Clinical Trials Registry of India (CTRI/2018/04/012958). Sixty-five American Society of Anesthesiologists Physical Status classes I and II adult patients were enrolled in the study. After induction and muscle relaxation, mask ventilation was performed with CE and JT technique on PCV mode (Pinsp 15 cm H<sub>2</sub>O, respiratory rate 15) for 1 min each. The mean of returned TV of last 12 breaths, gastric insufflation, audible mask leak, and operator comfort in each technique were compared.</p><p><strong>Statistical analysis: </strong>Statistical software namely IBM SPSS 22.0 and R environment version 3.2.2 (IBM Corp. SPSS Statistics for Windows, Version 22.0. Armonk, NY, USA) were used for data analysis. Microsoft Excel was used to generate graphs and tables. Data were expressed as mean ± standard deviation for continuous variables and number (%) for categorical variables. Student's <i>t</i>-test (two tailed, independent) was used to find the significance of the study parameters on a continuous scale. Chi-square/Fisher's exact test was used to find the significance of the study parameters on a categorical scale between two or more groups.</p><p><strong>Results: </strong>There was a significant increase in mean TV generated by JT technique over CE technique (591.46 ± 140.27 mL vs. 544.59 ± 159.08 mL; <i>P</i> < 0.001). Gastric insufflation (12.9% vs. 14.5%) and mask leak (11.3% vs. 38.7%) were more in CE technique. Operator comfort (79% vs. 19.4%) was more in JT technique.</p><p><strong>Conclusion: </strong>A two-handed JT technique is more effective than a one-handed CE technique for mask ventilation in apneic anesthetized adults.</p>","PeriodicalId":7798,"journal":{"name":"Anesthesia, Essays and Researches","volume":"16 3","pages":"386-391"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813989/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10513874","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comparing Efficacy of Intravenous Dexmedetomidine and Lidocaine on Perioperative Analgesic Consumption in Patients Undergoing Laparoscopic Surgery. 静脉注射右美托咪定和利多卡因对腹腔镜手术患者围术期镇痛药物消耗的疗效比较。
Pub Date : 2022-07-01 Epub Date: 2022-12-09 DOI: 10.4103/aer.aer_121_22
Vishwadeep Singh, Akhilesh Pahade, Ashita Mowar

Background: Perioperative pain management is a major challenge for anaesthesiologists. IV lidocaine and dexmedetomidine have been utilised for peri-operative pain management.

Aims and objectives: To analyse the effects of intraoperative intravenous lignocaine/dexmedetomidine on pain relief, opioid consumption, peri-operative hemodynamic and side-effect profiles/unique interactions in patients undergoing laparoscopic surgeries.

Materials and methods: Prospective, interventional, single-centric, double-blind, randomised, active-controlled, Helsinki protocol-compliant clinical study was conducted on 90 ASA I/II class patients aged 18-60 yrs. This Patients were block-randomised to Group-L (2% Lignocaine), Group-D (dexmedetomidine) and Group C (Control/Placebo/0.9% normal saline). Hemodynamic were noted at pre-defined time frames intra-/post-operatively. Post-operative VAS score and Richmond Agitation Sedation Score monitoring was done.

Results: Demographic parameters of were comparable. Mean intra-operative fentanyl consumption amongst the three groups were 20.5 ± 20.05 mcg, 26.5 ± 17.57 mcg and 46.83 + 21.31 mcg (Group-L, Group-D, Group-C; P value Group-L vs Group-D:0.22, Group L/D vs Group C: <0.0001). Group-D exhibited the lower heart rates and MAP (P < 0.05). Extubation- First rescue analgesic phase was comparable for the Group-C and Group-L (59.17 ± 46.224 min vs 61.64 ± 53.819 min) and significantly greater in Group-D (136.07 + 55.350 min; P < 0.0001).

Conclusion: Both Dexmedetomidine and lignocaine can be useful intra-operative pain relief adjuncts. Dexmedetomidine delayed First rescue analgesic and total analgesic consumption more than lignocaine. Dexmedetomidine patients exhibited bradycardia intraoperatively more than the other groups. we recommend, Dexmedetomidine in the intra-operative phase and lignocaine in the post-operative phase can be an alternative in patients who are poor candidates for post-operative opioids/sedation/contraindicated regional anaesthesia regimes.

背景:围手术期疼痛管理是麻醉师面临的主要挑战。静脉注射利多卡因和右美托咪定已用于围手术期疼痛管理。目的和目的:分析术中静脉注射利多卡因/右美托咪定对腹腔镜手术患者的疼痛缓解、阿片类药物消耗、围手术期血液动力学和副作用/独特相互作用的影响。材料和方法:对90名年龄在18-60岁的ASA I/II级患者进行前瞻性、介入性、单中心、双盲、随机、主动对照、符合赫尔辛基方案的临床研究。这些患者被分为L组(2%利多卡因)、D组(右美托咪定)和C组(对照/安慰剂/0.9%生理盐水)。术中/术后在预先定义的时间范围内记录血液动力学。术后VAS评分和Richmond激动镇静评分监测。结果:的人口学参数具有可比性。三组术中芬太尼平均消耗量为20.5±20.05 mcg,26.5±17.57 mcg和46.83±21.31 mcg(L组、D组、C组;P值L组与D组:0.22,L/D组与C组:P<0.05)。C组和L组的拔管-第一次抢救镇痛阶段具有可比性(59.17±46.224 min与61.64±53.819 min),D组显著更高(136.07±55.350 min;P<0.0001)。结论:地塞米松和利多卡因都是有用的术中镇痛辅助药物。右美托咪定比利多卡因更延迟急救镇痛和总镇痛消耗。右美托咪定患者在术中表现出的心动过缓多于其他组。我们建议,术中阶段的右美托咪定和术后阶段的利多卡因可以作为术后阿片类药物/镇静/禁忌症区域麻醉方案的替代方案。
{"title":"Comparing Efficacy of Intravenous Dexmedetomidine and Lidocaine on Perioperative Analgesic Consumption in Patients Undergoing Laparoscopic Surgery.","authors":"Vishwadeep Singh,&nbsp;Akhilesh Pahade,&nbsp;Ashita Mowar","doi":"10.4103/aer.aer_121_22","DOIUrl":"10.4103/aer.aer_121_22","url":null,"abstract":"<p><strong>Background: </strong>Perioperative pain management is a major challenge for anaesthesiologists. IV lidocaine and dexmedetomidine have been utilised for peri-operative pain management.</p><p><strong>Aims and objectives: </strong>To analyse the effects of intraoperative intravenous lignocaine/dexmedetomidine on pain relief, opioid consumption, peri-operative hemodynamic and side-effect profiles/unique interactions in patients undergoing laparoscopic surgeries.</p><p><strong>Materials and methods: </strong>Prospective, interventional, single-centric, double-blind, randomised, active-controlled, Helsinki protocol-compliant clinical study was conducted on 90 ASA I/II class patients aged 18-60 yrs. This Patients were block-randomised to Group-L (2% Lignocaine), Group-D (dexmedetomidine) and Group C (Control/Placebo/0.9% normal saline). Hemodynamic were noted at pre-defined time frames intra-/post-operatively. Post-operative VAS score and Richmond Agitation Sedation Score monitoring was done.</p><p><strong>Results: </strong>Demographic parameters of were comparable. Mean intra-operative fentanyl consumption amongst the three groups were 20.5 ± 20.05 mcg, 26.5 ± 17.57 mcg and 46.83 + 21.31 mcg (Group-L, Group-D, Group-C; <i>P</i> value Group-L vs Group-D:0.22, Group L/D vs Group C: <0.0001). Group-D exhibited the lower heart rates and MAP (<i>P</i> < 0.05). Extubation- First rescue analgesic phase was comparable for the Group-C and Group-L (59.17 ± 46.224 min vs 61.64 ± 53.819 min) and significantly greater in Group-D (136.07 + 55.350 min; <i>P</i> < 0.0001).</p><p><strong>Conclusion: </strong>Both Dexmedetomidine and lignocaine can be useful intra-operative pain relief adjuncts. Dexmedetomidine delayed First rescue analgesic and total analgesic consumption more than lignocaine. Dexmedetomidine patients exhibited bradycardia intraoperatively more than the other groups. we recommend, Dexmedetomidine in the intra-operative phase and lignocaine in the post-operative phase can be an alternative in patients who are poor candidates for post-operative opioids/sedation/contraindicated regional anaesthesia regimes.</p>","PeriodicalId":7798,"journal":{"name":"Anesthesia, Essays and Researches","volume":"16 3","pages":"353-359"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813992/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10508705","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A Single-Level Epidural Blood Patch for Multiple Cerebrospinal Fluid Leaks: How it Works. 用于多发性脑脊液渗漏的单水平硬膜外血液贴剂:其工作原理。
Pub Date : 2022-07-01 Epub Date: 2022-12-09 DOI: 10.4103/aer.aer_131_22
Amlan Swain, Seelora Sahu, Rashmi Kumari, Manjul Tripathi

Spontaneous intracranial hypotension caused by cerebrospinal fluid (CSF) leak is a rarely encountered cause of persistent postural headaches in the absence of trauma or dural puncture. It presents with postural headache and is characterized by radiological findings of spinal CSF leak. The mainstay of management is an epidural patch with the patient's own blood (epidural blood patch [EBP]) and/or a fibrin glue product. We report here a case of spontaneous intracranial hemorrhage presenting with persistent headaches and bilateral subdural hematomas secondary to CSF leaks at multiple levels along the spinal cord, which was successfully managed with a single lumbar EBP.

在没有外伤或硬膜穿刺的情况下,由脑脊液(CSF)渗漏引起的自发性颅内低血压是持续性体位性头痛的罕见原因。它表现为体位性头痛,以脊髓CSF渗漏的放射学表现为特征。主要的治疗方法是使用患者自身血液的硬膜外补片(硬膜外血液补片[EBP])和/或纤维蛋白胶产品。我们在此报告了一例自发性颅内出血,表现为持续性头痛和双侧硬膜下血肿,继发于脊髓多个层面的脑脊液泄漏,单次腰椎EBP成功治疗。
{"title":"A Single-Level Epidural Blood Patch for Multiple Cerebrospinal Fluid Leaks: How it Works.","authors":"Amlan Swain,&nbsp;Seelora Sahu,&nbsp;Rashmi Kumari,&nbsp;Manjul Tripathi","doi":"10.4103/aer.aer_131_22","DOIUrl":"10.4103/aer.aer_131_22","url":null,"abstract":"<p><p>Spontaneous intracranial hypotension caused by cerebrospinal fluid (CSF) leak is a rarely encountered cause of persistent postural headaches in the absence of trauma or dural puncture. It presents with postural headache and is characterized by radiological findings of spinal CSF leak. The mainstay of management is an epidural patch with the patient's own blood (epidural blood patch [EBP]) and/or a fibrin glue product. We report here a case of spontaneous intracranial hemorrhage presenting with persistent headaches and bilateral subdural hematomas secondary to CSF leaks at multiple levels along the spinal cord, which was successfully managed with a single lumbar EBP.</p>","PeriodicalId":7798,"journal":{"name":"Anesthesia, Essays and Researches","volume":"16 3","pages":"416-418"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813988/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10508708","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
First-pass Success Rate and Number of Attempts Required for Intubation in Anticipated Difficult Airway: Comparison between Macintosh and Channeled King Vision Video Laryngoscopes. 首次通过成功率和预期困难气道插管所需的尝试次数:Macintosh和Channeled King Vision视频喉镜的比较。
Pub Date : 2022-07-01 Epub Date: 2022-10-31 DOI: 10.4103/aer.aer_68_22
Rameez Raja, Sunana Gupta, Nandita Mehta, Prerna Attal

Background and aims: Video laryngoscopy has been shown to improvise Cormack-Lehane grading and rate of successful tracheal intubation and is now incorporated in most of the difficult airway guidelines. Since there is scarce literature regarding the use of channeled blade of King Vision video laryngoscope (KVVL) in anticipated difficult intubation, we planned to undertake this randomized control trial to assess the performance of channeled blade of KVVL and Macintosh laryngoscope in patients with anticipated difficult intubation.

Design and setting: This prospective randomized study was conducted in a tertiary care hospital.

Materials and methods: Patients fulfilling the inclusion criteria were randomly assigned equally to the KVVL group or Macintosh group. The primary outcome of the study was intubation success in the first attempt and number of attempts required for intubation, and the secondary outcomes were Cormack-Lehane grading and time required to intubate in both the groups.

Results: The first-pass success of intubation was 88.6% in the KVVL group and 76.5% in the Macintosh group (P = 0.035). The second attempt of intubation was required in 11.4% and 20.6% of patients in the KVVL and Macintosh groups, respectively. Cormack Lehane Grade I was achieved in 100% of patients of the KVVL group as compared to 29.4% of patients in the Macintosh group. Moreover, the difference was statistically significant (P = 0.035). The mean duration of intubation was prolonged in the KVVL group as compared to the Macintosh group, and the difference was statistically significant (P = 0.04).

Conclusion: The channeled blade of KVVL had a higher first-pass success rate and required fewer attempts to intubate when used in patients with anticipated difficult intubation. Further, the KVVL was found to be significantly better than the Macintosh laryngoscope in terms of Cormack-Lehane grading, but the time taken to intubate the trachea was more in the KVVL group.

背景和目的:视频喉镜已被证明可以提高Cormack-Lehane分级和气管插管成功率,目前已被纳入大多数困难气道指南。由于关于在预期困难插管中使用King Vision视频喉镜(KVVL)通道刀片的文献很少,我们计划进行这项随机对照试验,以评估KVVL和Macintosh喉镜通道刀片在预期困难气管插管患者中的性能。设计和设置:这项前瞻性随机研究在一家三级护理医院进行。材料和方法:符合入选标准的患者被随机分为KVVL组或Macintosh组。该研究的主要结果是第一次插管成功率和插管所需的次数,次要结果是两组的Cormack-Lehane分级和插管所需要的时间。结果:KVVL组第一次插管成功率为88.6%,Macintosh组为76.5%(P=0.035)。KVVL和Macintosh组分别有11.4%和20.6%的患者需要第二次插管。KVVL组100%的患者达到Cormack-Lehane I级,而Macintosh组的患者达到了29.4%。此外,差异具有统计学意义(P=0.035)。KVVL组的平均插管时间比Macintosh组延长,结论:KVVL的通道刀片在预期插管困难的患者中使用时,首次通过成功率较高,插管次数较少。此外,在Cormack-Lehane分级方面,KVVL明显优于Macintosh喉镜,但KVVL组气管插管所需时间更长。
{"title":"First-pass Success Rate and Number of Attempts Required for Intubation in Anticipated Difficult Airway: Comparison between Macintosh and Channeled King Vision Video Laryngoscopes.","authors":"Rameez Raja,&nbsp;Sunana Gupta,&nbsp;Nandita Mehta,&nbsp;Prerna Attal","doi":"10.4103/aer.aer_68_22","DOIUrl":"10.4103/aer.aer_68_22","url":null,"abstract":"<p><strong>Background and aims: </strong>Video laryngoscopy has been shown to improvise Cormack-Lehane grading and rate of successful tracheal intubation and is now incorporated in most of the difficult airway guidelines. Since there is scarce literature regarding the use of channeled blade of King Vision video laryngoscope (KVVL) in anticipated difficult intubation, we planned to undertake this randomized control trial to assess the performance of channeled blade of KVVL and Macintosh laryngoscope in patients with anticipated difficult intubation.</p><p><strong>Design and setting: </strong>This prospective randomized study was conducted in a tertiary care hospital.</p><p><strong>Materials and methods: </strong>Patients fulfilling the inclusion criteria were randomly assigned equally to the KVVL group or Macintosh group. The primary outcome of the study was intubation success in the first attempt and number of attempts required for intubation, and the secondary outcomes were Cormack-Lehane grading and time required to intubate in both the groups.</p><p><strong>Results: </strong>The first-pass success of intubation was 88.6% in the KVVL group and 76.5% in the Macintosh group (<i>P</i> = 0.035). The second attempt of intubation was required in 11.4% and 20.6% of patients in the KVVL and Macintosh groups, respectively. Cormack Lehane Grade I was achieved in 100% of patients of the KVVL group as compared to 29.4% of patients in the Macintosh group. Moreover, the difference was statistically significant (<i>P</i> = 0.035). The mean duration of intubation was prolonged in the KVVL group as compared to the Macintosh group, and the difference was statistically significant (<i>P</i> = 0.04).</p><p><strong>Conclusion: </strong>The channeled blade of KVVL had a higher first-pass success rate and required fewer attempts to intubate when used in patients with anticipated difficult intubation. Further, the KVVL was found to be significantly better than the Macintosh laryngoscope in terms of Cormack-Lehane grading, but the time taken to intubate the trachea was more in the KVVL group.</p>","PeriodicalId":7798,"journal":{"name":"Anesthesia, Essays and Researches","volume":"16 3","pages":"340-344"},"PeriodicalIF":0.0,"publicationDate":"2022-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813986/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10513870","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comparative Evaluation of Intrathecal Dexmedetomidine and Fentanyl as an Adjuvant for Combined Spinal-Epidural Analgesia for Labor. 右美托咪定与芬太尼鞘内辅助脊髓-硬膜外联合分娩镇痛的比较评价。
Pub Date : 2022-04-01 Epub Date: 2022-08-19 DOI: 10.4103/aer.aer_73_22
Anshul Jain, Ashok Mittal, Sanjya Sharma, Akash Deep

Background: Combined spinal-epidural technique is a widely accepted and popular modality for labor analgesia. Opioids are being used as adjuvants since long time. Dexmedetomidine is a new drug that is being used as an intrathecal adjuvant.

Aim: The study aims to compare the safety and efficacy of fentanyl and dexmedetomidine as intrathecal adjuvants in labor analgesia.

Settings and design: This was a continuous, prospective, randomized controlled trial with 120 parturients.

Materials and methods: After ethical approval and written consent, participants were divided randomly into two groups: Group A - bupivacaine 2.5 mg (0.5 mL diluted to 2 mL) + 20 μg of dexmedetomidine in 1 mL saline intrathecally (total volume: 3 mL) and Group B - bupivacaine 2.5 mg (0.5 mL diluted to 2 mL) + 15 μg of fentanyl in 1 mL saline intrathecally (total volume: 3 mL). Primary outcomes were satisfactory analgesia, mode of delivery, and neonatal outcome. Participants were monitored for the onset and duration of analgesia, degree of motor block, and maternal and fetal side effects.

Results: A total of 108 parturients reported sufficient analgesia (Group A: 57; Group B: 51), and 74 patients delivered vaginally (Group A: 41; Group B: 44). The rates of normal vaginal delivery were higher in Group B. Group A reported earlier onset of analgesia (61.26 ± 18.23 s) that lasted for longer duration (124.16 ± 26.23 min) than in Group B. There were no serious side effects in any of the groups. Fetal ultrasound revealed attenuation of fetal heart rate variability. The heart rate of newborns was also found to be low in Group A.

Conclusion: Chances of vaginal delivery are higher with intrathecal fentanyl as an adjuvant. Intensity and duration of analgesia are better with intrathecal dexmedetomidine.

背景:脊髓-硬膜外联合技术是一种被广泛接受和流行的分娩镇痛方式。阿片类药物作为佐剂使用已久。右美托咪定是一种被用作鞘内佐剂的新药。目的:比较芬太尼和右美托咪定作为鞘内佐剂用于分娩镇痛的安全性和有效性。环境和设计:这是一项连续、前瞻性、随机对照试验,有120名产妇参加。材料与方法:经伦理批准并书面同意后,将受试者随机分为两组:A组布比卡因2.5 mg (0.5 mL稀释至2 mL) +右美托咪定20 μg鞘内盐水1 mL(总容量为3 mL); B组布比卡因2.5 mg (0.5 mL稀释至2 mL) +芬太尼15 μg鞘内盐水1 mL(总容量为3 mL)。主要结局是令人满意的镇痛、分娩方式和新生儿结局。监测参与者镇痛的开始和持续时间、运动阻滞的程度以及母体和胎儿的副作用。结果:共有108例产妇报告充分镇痛(A组:57例;B组51例),顺产74例(A组41例;B组:44)。b组阴道正常分娩率较高,A组镇痛起效时间较b组早(61.26±18.23 s),持续时间较b组长(124.16±26.23 min),两组均无严重副作用。胎儿超声显示胎儿心率变异性衰减。a组新生儿的心率也较低。结论:鞘内芬太尼作为辅助剂阴道分娩的几率更高。鞘内注射右美托咪定镇痛的强度和持续时间较好。
{"title":"Comparative Evaluation of Intrathecal Dexmedetomidine and Fentanyl as an Adjuvant for Combined Spinal-Epidural Analgesia for Labor.","authors":"Anshul Jain,&nbsp;Ashok Mittal,&nbsp;Sanjya Sharma,&nbsp;Akash Deep","doi":"10.4103/aer.aer_73_22","DOIUrl":"https://doi.org/10.4103/aer.aer_73_22","url":null,"abstract":"<p><strong>Background: </strong>Combined spinal-epidural technique is a widely accepted and popular modality for labor analgesia. Opioids are being used as adjuvants since long time. Dexmedetomidine is a new drug that is being used as an intrathecal adjuvant.</p><p><strong>Aim: </strong>The study aims to compare the safety and efficacy of fentanyl and dexmedetomidine as intrathecal adjuvants in labor analgesia.</p><p><strong>Settings and design: </strong>This was a continuous, prospective, randomized controlled trial with 120 parturients.</p><p><strong>Materials and methods: </strong>After ethical approval and written consent, participants were divided randomly into two groups: Group A - bupivacaine 2.5 mg (0.5 mL diluted to 2 mL) + 20 μg of dexmedetomidine in 1 mL saline intrathecally (total volume: 3 mL) and Group B - bupivacaine 2.5 mg (0.5 mL diluted to 2 mL) + 15 μg of fentanyl in 1 mL saline intrathecally (total volume: 3 mL). Primary outcomes were satisfactory analgesia, mode of delivery, and neonatal outcome. Participants were monitored for the onset and duration of analgesia, degree of motor block, and maternal and fetal side effects.</p><p><strong>Results: </strong>A total of 108 parturients reported sufficient analgesia (Group A: 57; Group B: 51), and 74 patients delivered vaginally (Group A: 41; Group B: 44). The rates of normal vaginal delivery were higher in Group B. Group A reported earlier onset of analgesia (61.26 ± 18.23 s) that lasted for longer duration (124.16 ± 26.23 min) than in Group B. There were no serious side effects in any of the groups. Fetal ultrasound revealed attenuation of fetal heart rate variability. The heart rate of newborns was also found to be low in Group A.</p><p><strong>Conclusion: </strong>Chances of vaginal delivery are higher with intrathecal fentanyl as an adjuvant. Intensity and duration of analgesia are better with intrathecal dexmedetomidine.</p>","PeriodicalId":7798,"journal":{"name":"Anesthesia, Essays and Researches","volume":"16 2","pages":"197-202"},"PeriodicalIF":0.0,"publicationDate":"2022-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9701333/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40503904","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
期刊
Anesthesia, Essays and Researches
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1