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Predicting clinical entry point for thoracic epidural catheter insertion during paramedian approach: A prospective observational study. 预测胸腔硬膜外导管在辅助入路时的临床插入点:前瞻性观察研究。
IF 1.5 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2024-04-26 DOI: 10.4103/joacp.joacp_448_22
Bhakti Y Deshmukh, Madhavi G Shetmahajan, Sumitra G Bakshi, Parmanand Jain

Background and aims: Thoracic epidural insertion has high failure rates in the mid-thoracic region due to steep angulation of oblique bending of spinous processes. The preferred skin puncture point for epidural needle insertion in the paramedian sagittal plane with respect to the superior/inferior tip of spinous process or inter-spinous cleft in the mid-thoracic region (T5-8) is not standard. The primary objective of this prospective observational study was to find the skin puncture point which had the best success rate for a successful epidural catheterization. Secondary objectives were to study the number of attempts and passes required to locate epidural space, incidence of failed epidural, and its relationship with patient characteristics and demographics.

Material and methods: After informed consent, 155 patients planned for general anesthesia with epidural analgesia in the mid-thoracic region were included in the trial. Patient demographics, the details of epidural attempts with respect to anatomical landmarks, distance from the midline, and number of passes in each attempt were noted. Epidural catheterization was considered successful after demonstrating dermatomal band of sensory blockade.

Results: The success rate at different skin puncture sites was not statistically significant (P = 0.58). We found a failure rate of 12.9%. Failed epidural catheterization was significantly high in the age group >56 years (n = 62 and P = 0.007).

Conclusion: In our study, none of the skin puncture points had a significant association with successful epidural insertion in mid-thoracic segments using a para-median approach.

背景和目的:由于脊柱棘突斜弯角度陡峭,胸椎硬膜外针插入中胸椎区域的失败率很高。在胸椎中段(T5-8)脊柱棘突上/下端或棘突间隙的矢状面旁侧,硬膜外穿刺针首选的皮肤穿刺点并不标准。这项前瞻性观察研究的主要目的是找到硬膜外导管插入成功率最高的皮肤穿刺点。次要目标是研究定位硬膜外腔所需的尝试和穿刺次数、硬膜外腔穿刺失败的发生率及其与患者特征和人口统计学的关系:经知情同意后,155 名计划在中胸段进行硬膜外镇痛的全身麻醉患者被纳入试验。试验中记录了患者的人口统计学特征、硬膜外尝试的解剖标志细节、与中线的距离以及每次尝试的次数。硬膜外导管插入术在显示皮肤感觉阻滞带后即为成功:不同皮肤穿刺部位的成功率无统计学意义(P = 0.58)。我们发现失败率为 12.9%。硬膜外导管穿刺失败率在年龄大于 56 岁的人群中明显偏高(n = 62,P = 0.007):结论:在我们的研究中,没有一个皮肤穿刺点与使用副中线方法在中胸段成功插入硬膜外导管有明显关系。
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引用次数: 0
"Burnout syndrome" in anesthesiologists and remedial measures- A narrative review. 麻醉师的“职业倦怠综合征”及其补救措施-述评
IF 1.5 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2023-07-07 DOI: 10.4103/joacp.joacp_322_22
Mridul M Panditrao, Minnu M Panditrao

Anesthesiology, as an occupation, has its own unique sets of challenges, problems, issues, and circumstances, all leading to "occupational stress," which by now should be unequivocally accepted as a well-established fact. It is futile to continue pursuing research questions like, if there "really" is stress existing among practicing anesthesiologists/trainees, by conducting questionnaire-based surveys and doing meta-analyses. A significantly high incidence of existence of occupational stress in anesthesiologists is an undisputable and practical reality, which, when longstanding, gets culminated into "burnout syndrome" with its disastrous outcomes. Rather than pursuing the often-trodden path of finding the incidence, sources, and other superficial issues, an in-depth study of available literary evidence in relation to burnout has been carried out. Objectifying it as a "syndrome," its etiopathogenesis, pathophysiology inclusive of the prevalent theories of its causality, typology, and progression into various stages of/continuum of the process as an evolving clinical entity have been described. The preventive measures and "coping strategies" have been discussed at length in the end. It is the fervent hope and the desire of the authors that this discourse will sensitize all anesthesiologists, especially the younger and upcoming future generation, and help them avoid becoming a prey to this dreadful entity!

麻醉学作为一种职业,有其独特的挑战、问题、问题和环境,所有这些都会导致“职业压力”,到目前为止,这应该是一个明确的公认事实。继续进行问卷调查和荟萃分析等研究问题是徒劳的,例如,执业麻醉师/受训者是否“真的”存在压力。麻醉师职业压力的高发率是一个无可争议的现实,如果长期存在,最终会导致“职业倦怠综合症”,并带来灾难性的后果。与寻找倦怠的发生率、来源和其他表面问题的常见途径不同,本文对现有的与倦怠有关的文献证据进行了深入研究。将其客观化为一种“综合征”,其发病机制,病理生理学包括其因果关系,类型和作为一个不断发展的临床实体的过程的各个阶段/连续体的进展的流行理论已经被描述。最后详细讨论了预防措施和“应对策略”。这是作者的热切希望和愿望,这篇文章将敏感所有麻醉师,特别是年轻的和即将到来的下一代,并帮助他们避免成为这个可怕的实体的猎物!
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引用次数: 0
Post-operative vomiting after pediatric strabismus surgery: A comparison of propofol versus sevoflurane anaesthesia. 小儿斜视手术后的术后呕吐:异丙酚与七氟醚麻醉的比较。
IF 1.5 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2024-05-16 DOI: 10.4103/joacp.joacp_363_22
Shalini Subramanian, Deepa Shetty, Poornima Shivanna, Priyanka Das, Medha Phadke

Background and aims: Squint surgery is a risk factor for postoperative vomiting (POV) in children. This study was designed to compare the incidence of POV in children undergoing strabismus surgery under balanced anesthesia with sevoflurane versus intravenous anesthesia with propofol.

Material and methods: In this prospective randomized controlled study conducted in a tertiary care ophthalmology hospital, 70 ASA I-II children aged 1-12 years undergoing strabismus surgery were randomized to two groups -Group S (sevoflurane-based anesthesia) and Group P (propofol-based anesthesia) for maintenance. The surgical details, intraoperative hemodynamic parameters, recovery characteristics, and emergence delirium were recorded. Any episode of postoperative vomiting in the 0-2 hours, 2-6 hours, and 6-24 hours period was noted. Rescue antiemetic was administered if there was more than one episode of vomiting.

Results: Both the groups were similar with respect to demographic and surgical details. The average duration of surgery was 118.2 ± 41.88 min in group S and 137.32 ± 39.09 min in group P (P = .05). Four children in group S (11.4%) and one child in group P (2.9%) had POV in the first 24 hours but this was not statistically significant (P = .36). The median time to discharge from post anesthesia care unit was significantly less (P = .02) in the P group (50 min) than in the S group (60 min).

Conclusion: Propofol-based anesthesia does not offer advantage over sevoflurane, in reducing POV after squint surgery, when dual prophylaxis with dexamethasone and ondansetron is administered. It, however, reduces the duration of stay in the post anesthesia care unit.

背景和目的:斜视手术是儿童术后呕吐(POV)的一个危险因素。本研究旨在比较七氟醚平衡麻醉与丙泊酚静脉麻醉下斜视手术患儿术后呕吐的发生率:这项前瞻性随机对照研究在一家三级眼科医院进行,70名年龄在1-12岁接受斜视手术的ASA I-II级儿童被随机分为两组--S组(七氟烷麻醉)和P组(丙泊酚麻醉)。手术细节、术中血流动力学参数、术后恢复特征和术后谵妄均被记录在案。记录术后 0-2 小时、2-6 小时和 6-24 小时内的任何呕吐情况。如果呕吐不止一次,则进行补救性止吐:两组患者在人口统计学和手术细节方面相似。S组的平均手术时间为(118.2 ± 41.88)分钟,P组为(137.32 ± 39.09)分钟(P = .05)。S组有4名患儿(11.4%)和P组有1名患儿(2.9%)在术后24小时内出现POV,但无统计学意义(P = .36)。从麻醉后监护室出院的中位时间,P 组(50 分钟)明显少于 S 组(60 分钟)(P = .02):结论:在使用地塞米松和昂丹司琼双重预防措施的情况下,丙泊酚麻醉在减少斜视手术后POV方面与七氟醚相比没有优势。不过,它可以缩短在麻醉后护理病房的住院时间。
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引用次数: 0
Comparison of midpoint transverse process to pleura (MTP) block and erector spinae plane block (ESP) for postoperative analgesia in modified radical mastectomy patients: A double-blinded, randomized control trial. 改良根治性乳房切除术患者术后镇痛中点横突至胸膜(MTP)阻滞与竖脊平面阻滞(ESP)的比较:双盲随机对照试验。
IF 1.5 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2024-05-16 DOI: 10.4103/joacp.joacp_429_22
Priyanka Sethi, Manbir Kaur, Pradeep K Bhatia, Shilpa Goyal, Ankur Sharma, Shipra Roy, Narender Kaloria

Background and aims: Modified radical mastectomy (MRM) is associated with moderate severity of postoperative pain. Besides intravenous (IV) analgesics, various nerve blocks are being described for pain relief of MRM patients. We compared erector spinae plane (ESP) block with midpoint transverse process to pleura (MTP) block in these patients for postoperative analgesia.

Material and methods: After receiving ethical committee approval from the institutional ethics committee (AIIMS, Jodhpur) and written informed consent from study participants, 66 patients who were assigned American Society of Anesthesiologists (ASA) physical status I and II, aged 18-75 years, and were scheduled to undergo MRM were enrolled and randomly allocated into two groups. Unilateral block was given before surgery at T3 or T4 level and with 15 ml of 0.5% ropivacaine in both the groups. Infusion of 0.5% ropivacaine (Neon laboratories limited, Mumbai, India) and 0.2% ropivacaine at a rate of 5 ml/h was maintained intraoperatively and postoperatively, respectively. Pain was assessed using the Visual Analogue Scale (VAS) for the next 24 hours. The total number of patients needing rescue analgesia, the total amount of rescue analgesics consumed in the next 24 hours, and patient satisfaction score were also compared between groups.

Results: Demographics and baseline vitals were comparable in the groups. On comparing VAS scores in both the groups during rest and movement at different time intervals, there was no difference in pain scores during the initial two hours. From the third hour, there was a statistically significant difference (P < 0.001) in pain VAS scores in both groups. The ESP group had lower VAS scores compared to the MTP group when followed for the next 24 hours. There was a statistically significant difference in patient satisfaction.

Conclusion: ESP block is more efficacious when compared to MTP block for postoperative analgesia in MRM patients.

背景和目的:改良根治性乳房切除术(MRM)会导致中等程度的术后疼痛。除了静脉注射(IV)镇痛药外,还有各种神经阻滞疗法用于缓解 MRM 患者的疼痛。我们比较了竖脊面(ESP)阻滞和胸膜横突中点(MTP)阻滞对这些患者术后镇痛的效果:在获得机构伦理委员会(AIIMS,焦特普尔)的批准和研究参与者的书面知情同意后,66 名美国麻醉医师协会(ASA)身体状况为 I 级和 II 级、年龄在 18-75 岁之间、计划接受 MRM 的患者被纳入研究,并随机分配到两组。两组患者均在手术前于 T3 或 T4 水平进行单侧阻滞,使用 15 毫升 0.5% 罗哌卡因。术中和术后分别以 5 毫升/小时的速度输注 0.5% 罗哌卡因(印度孟买 Neon Laboratories 有限公司)和 0.2% 罗哌卡因。在接下来的 24 小时内,使用视觉模拟量表(VAS)对疼痛进行评估。此外,还比较了两组患者需要镇痛抢救的总人数、接下来 24 小时内镇痛抢救的总用量以及患者满意度评分:结果:两组患者的人口统计学和基线生命体征相当。比较两组患者在休息和运动时不同时间间隔的 VAS 评分,最初两小时的疼痛评分没有差异。从第三小时开始,两组的疼痛 VAS 评分有显著的统计学差异(P < 0.001)。在接下来的 24 小时内,ESP 组的 VAS 评分低于 MTP 组。结论:ESP阻滞与MTP阻滞相比更有效:结论:在 MRM 患者的术后镇痛中,ESP 阻滞比 MTP 阻滞更有效。
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引用次数: 0
Comparison of neuraxial acoustic target window of the spine among rider sitting, cross leg, hamstring stretch, and classical sitting position: An observational study. 骑手坐姿、交叉腿、腿筋拉伸和传统坐姿的脊柱神经声学目标窗口比较:观察研究
IF 1.5 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2024-05-16 DOI: 10.4103/joacp.joacp_450_22
Govind Singh, Priyanka Sethi, Manbir Kaur, Pradeep Bhatia, Pawan K Garg, Kamlesh Kumari, Pawan K Dixit

Background and aims: To compare ultra-sonographic dimensions of acoustic target window of the spine in the participants at four different sitting positions namely cross leg sitting (CLP), hamstring stretch (HSP), classical sitting (CSP) and riders sitting position (RSP). The primary objective of this study was to measure the neuraxial acoustic target window (defined as interlaminar distance between L3-L4 lamina). The secondary objective was to compare ultra-sonographic measurements of the depth of ligamentum flavum from the skin, and to compare the diameter of intrathecal space and comfort score in the four different sitting positions.

Material and methods: This study is a prospective observational study. Eighty participants were included and positioned in four different sitting positions to perform an ultra-sonographic scan and measure various parameters of the acoustic neuraxial window. The interlaminar distance, the distance of skin from the ligamentum flavum, and the diameter of the spinal canal or intrathecal space was measured in the L3-L4 intervertebral space in different positions.

Results: The mean value of interlaminar distance among four sitting positions was ranging from 1.40 cm to 1.44 cm (P value 0.725.) The distance of ligamentum flavum from skin and diameter of intrathecal space was also comparable in all the groups. The comfort score in CSP was significantly better when compared to other groups with a median score of 4 (P value < 0.001).

Conclusions: There is no statistically significant difference in interlaminar distance in various sitting positions. All four positions are equally effective and can be used as an alternative to spinal/epidural intervention, but the CSP came out to be the most comfortable and more emphasis should be given to the comfort as it increases the chance of success rate of the procedure.

背景和目的:比较参与者在四种不同坐姿(即交叉腿坐(CLP)、腿筋拉伸(HSP)、传统坐姿(CSP)和骑手坐姿(RSP))下脊柱声学目标窗的超声学尺寸。本研究的主要目的是测量神经轴声学目标窗口(定义为 L3-L4 椎板之间的层间距离)。次要目的是比较黄韧带距皮肤深度的超声学测量值,并比较四种不同坐姿下的椎管内空间直径和舒适度评分:本研究是一项前瞻性观察研究。材料:本研究是一项前瞻性观察研究。80 名参与者被纳入研究中,以四种不同的坐姿进行超声纳扫描,并测量神经听诊窗的各种参数。在不同体位下测量 L3-L4 椎间隙的层间距离、皮肤与黄韧带的距离以及椎管或椎管内间隙的直径:四种坐姿的层间距离平均值为 1.40 厘米至 1.44 厘米(P 值为 0.725),各组的黄韧带与皮肤的距离和椎间隙直径也相当。CSP组的舒适度评分明显优于其他组,中位数为4分(P值<0.001):各种坐姿下的层间距离没有明显的统计学差异。所有四种体位都同样有效,可作为脊柱/硬膜外介入治疗的替代体位,但 CSP 最为舒适,应更加重视舒适度,因为舒适度可提高手术的成功率。
{"title":"Comparison of neuraxial acoustic target window of the spine among rider sitting, cross leg, hamstring stretch, and classical sitting position: An observational study.","authors":"Govind Singh, Priyanka Sethi, Manbir Kaur, Pradeep Bhatia, Pawan K Garg, Kamlesh Kumari, Pawan K Dixit","doi":"10.4103/joacp.joacp_450_22","DOIUrl":"10.4103/joacp.joacp_450_22","url":null,"abstract":"<p><strong>Background and aims: </strong>To compare ultra-sonographic dimensions of acoustic target window of the spine in the participants at four different sitting positions namely cross leg sitting (CLP), hamstring stretch (HSP), classical sitting (CSP) and riders sitting position (RSP). The primary objective of this study was to measure the neuraxial acoustic target window (defined as interlaminar distance between L3-L4 lamina). The secondary objective was to compare ultra-sonographic measurements of the depth of ligamentum flavum from the skin, and to compare the diameter of intrathecal space and comfort score in the four different sitting positions.</p><p><strong>Material and methods: </strong>This study is a prospective observational study. Eighty participants were included and positioned in four different sitting positions to perform an ultra-sonographic scan and measure various parameters of the acoustic neuraxial window. The interlaminar distance, the distance of skin from the ligamentum flavum, and the diameter of the spinal canal or intrathecal space was measured in the L3-L4 intervertebral space in different positions.</p><p><strong>Results: </strong>The mean value of interlaminar distance among four sitting positions was ranging from 1.40 cm to 1.44 cm (<i>P</i> value 0.725.) The distance of ligamentum flavum from skin and diameter of intrathecal space was also comparable in all the groups. The comfort score in CSP was significantly better when compared to other groups with a median score of 4 (<i>P</i> value < 0.001).</p><p><strong>Conclusions: </strong>There is no statistically significant difference in interlaminar distance in various sitting positions. All four positions are equally effective and can be used as an alternative to spinal/epidural intervention, but the CSP came out to be the most comfortable and more emphasis should be given to the comfort as it increases the chance of success rate of the procedure.</p>","PeriodicalId":14946,"journal":{"name":"Journal of Anaesthesiology, Clinical Pharmacology","volume":"40 2","pages":"318-323"},"PeriodicalIF":1.5,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11196033/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141450546","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
Evaluation of risk factors for postoperative neurologic intensive care admission after brain tumor craniotomy: A single-center longitudinal study. 脑肿瘤开颅手术后入住神经重症监护病房的风险因素评估:单中心纵向研究。
IF 1.5 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2024-05-16 DOI: 10.4103/joacp.joacp_323_22
Konish Biswas, Sanjay Agrawal, Priyanka Gupta, Rajnish Arora

Background and aims: Perioperative variable parameters can be significant risk factors for postoperative intensive care unit (ICU) admission after elective craniotomy for intracranial neoplasm, as assessed by various scoring systems such as Cranio Score. This observational study evaluates the relationship between these factors and early postoperative neurological complications necessitating ICU admission.

Material and methods: In total, 119 patients, aged 18 years and above, of either sex, American Society of Anesthesiologists (ASA) grades I-III, scheduled for elective craniotomy and tumor excision were included. The primary objective was to evaluate the relationship between perioperative risk factors and the incidence of early postoperative complications as a means of validation of the Cranio Score. The secondary outcomes studied were 30-day postoperative morbidity/mortality and the association with patient-related risk factors.

Results: Forty-five of 119 patients (37.82%) required postoperative ICU care with the mean duration of ICU stay being 1.92 ± 4.91 days. Tumor location (frontal/infratemporal region), preoperative deglutition disorder, Glasgow Coma Scale (GCS) less than 15, motor deficit, cerebellar deficit, midline shift >3 mm, mass effect, tumor size, use of blood products, lateral position, inotropic support, elevated systolic/mean arterial pressures, and duration of anesthesia/surgery were associated with a higher incidence of ICU care. Maximum (P = 0.035, AOR = 1.130) and minimum systolic arterial pressures (P = 0.022, Adjusted Odds Ratio (AOR) = 0.861) were the only independent risk factors. Cranio Score was found to be an accurate predictor of complications at a cut-off point of >10.52%. The preoperative motor deficit was the only independent risk factor associated with 30-day morbidity (AOR = 4.66).

Conclusion: Perioperative hemodynamic effects are an independent predictor of postoperative ICU requirement. Further Cranio Score is shown to be a good scoring system for postoperative complications.

背景和目的:根据各种评分系统(如颅骨评分)的评估,围手术期变量参数可能是颅内肿瘤择期开颅术后入住重症监护病房(ICU)的重要风险因素。这项观察性研究评估了这些因素与需要入住重症监护室的术后早期神经并发症之间的关系:本研究共纳入 119 名计划接受择期开颅手术和肿瘤切除术的患者,年龄均在 18 岁及以上,性别不限,美国麻醉医师协会(ASA)分级为 I-III 级。主要目的是评估围手术期风险因素与术后早期并发症发生率之间的关系,以此验证开颅评分。研究的次要结果是术后 30 天的发病率/死亡率以及与患者相关风险因素的关系:119例患者中有45例(37.82%)需要术后重症监护室护理,重症监护室平均住院时间为(1.92 ± 4.91)天。肿瘤位置(额叶/颞下区)、术前吞咽障碍、格拉斯哥昏迷量表(GCS)小于15、运动障碍、小脑功能障碍、中线移位>3毫米、肿块效应、肿瘤大小、使用血液制品、侧卧位、肌力支持、收缩压/平均动脉压升高以及麻醉/手术持续时间与较高的重症监护室护理发生率相关。最大收缩压(P = 0.035,AOR = 1.130)和最小收缩压(P = 0.022,调整比值比 (AOR) = 0.861)是唯一独立的风险因素。在分界点大于 10.52% 时,Cranio Score 可准确预测并发症。术前运动障碍是与 30 天发病率相关的唯一独立风险因素(AOR = 4.66):结论:围手术期血流动力学影响是术后需要入住重症监护室的独立预测因素。结论:围手术期血流动力学影响是术后需要入住重症监护室的独立预测因素,而 Cranio Score 则是术后并发症的良好评分系统。
{"title":"Evaluation of risk factors for postoperative neurologic intensive care admission after brain tumor craniotomy: A single-center longitudinal study.","authors":"Konish Biswas, Sanjay Agrawal, Priyanka Gupta, Rajnish Arora","doi":"10.4103/joacp.joacp_323_22","DOIUrl":"10.4103/joacp.joacp_323_22","url":null,"abstract":"<p><strong>Background and aims: </strong>Perioperative variable parameters can be significant risk factors for postoperative intensive care unit (ICU) admission after elective craniotomy for intracranial neoplasm, as assessed by various scoring systems such as Cranio Score. This observational study evaluates the relationship between these factors and early postoperative neurological complications necessitating ICU admission.</p><p><strong>Material and methods: </strong>In total, 119 patients, aged 18 years and above, of either sex, American Society of Anesthesiologists (ASA) grades I-III, scheduled for elective craniotomy and tumor excision were included. The primary objective was to evaluate the relationship between perioperative risk factors and the incidence of early postoperative complications as a means of validation of the Cranio Score. The secondary outcomes studied were 30-day postoperative morbidity/mortality and the association with patient-related risk factors.</p><p><strong>Results: </strong>Forty-five of 119 patients (37.82%) required postoperative ICU care with the mean duration of ICU stay being 1.92 ± 4.91 days. Tumor location (frontal/infratemporal region), preoperative deglutition disorder, Glasgow Coma Scale (GCS) less than 15, motor deficit, cerebellar deficit, midline shift >3 mm, mass effect, tumor size, use of blood products, lateral position, inotropic support, elevated systolic/mean arterial pressures, and duration of anesthesia/surgery were associated with a higher incidence of ICU care. Maximum (<i>P</i> = 0.035, AOR = 1.130) and minimum systolic arterial pressures (<i>P</i> = 0.022, Adjusted Odds Ratio (AOR) = 0.861) were the only independent risk factors. Cranio Score was found to be an accurate predictor of complications at a cut-off point of >10.52%. The preoperative motor deficit was the only independent risk factor associated with 30-day morbidity (AOR = 4.66).</p><p><strong>Conclusion: </strong>Perioperative hemodynamic effects are an independent predictor of postoperative ICU requirement. Further Cranio Score is shown to be a good scoring system for postoperative complications.</p>","PeriodicalId":14946,"journal":{"name":"Journal of Anaesthesiology, Clinical Pharmacology","volume":"40 2","pages":"217-227"},"PeriodicalIF":1.5,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11196047/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141450550","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
Efficacy of lignocaine nebulization in patients with COVID-19 respiratory infection: An exploratory randomized double-blinded controlled trial. COVID-19呼吸道感染患者雾化吸入木质素的疗效:一项探索性随机双盲对照试验。
IF 1.5 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2024-05-16 DOI: 10.4103/joacp.joacp_205_22
Praveen Talawar, Debendra Kumar Tripathy, Ashutosh Kaushal, Mridul Dhar, Adabala Vijaybabu, Praik Tuppad, Sangadala Priyanka, Deepak Kumar, Ruhi Sharma, Sumedha Suresh Kumar

Background and aims: Coronavirus disease (COVID-19)-related pneumonia is proposed to be an inflammatory process. The treatment currently includes supportive therapy and low-dose steroids. Anti-inflammatory drugs have been proposed to prevent cytokine storms and improve oxygenation in such cases. The study aimed to assess the efficacy of nebulized lignocaine in COVID-19 patients with pneumonia.

Material and methods: This was an exploratory randomized double-blinded control trial conducted in COVID-19 patients with respiratory failure requiring oxygen therapy either by face mask or non-invasive mechanical ventilation. Patients included were of the age of more than 18 years of either gender. The patients were randomized to receive either lignocaine or distilled water nebulization. The outcomes assessed were PaO2/FiO2 ratio, hemodynamics, respiratory parameters, and sequential organ failure score (SOFA).

Results: The two groups were comparable concerning demographic variables. The PaO2/FiO2 were significantly higher in the lignocaine group from day 2 onward. The SPO2 was significantly higher on day 3 in the lignocaine group and thereafter there was no significant difference. Other hemodynamic, respiratory parameters, and SOFA scores showed no difference in both the groups.

Conclusion: Lignocaine nebulization improved oxygenation in COVID-19 patients and can be used as adjunctive therapy along with other supportive medications.

背景和目的:冠状病毒病(COVID-19)相关肺炎被认为是一种炎症过程。目前的治疗方法包括支持疗法和小剂量类固醇。有人建议使用抗炎药物来防止细胞因子风暴并改善此类病例的氧合。本研究旨在评估雾化木质素对 COVID-19 肺炎患者的疗效:这是一项探索性随机双盲对照试验,针对 COVID-19 呼吸衰竭患者进行,患者需要使用面罩或无创机械通气进行吸氧治疗。患者年龄在 18 岁以上,性别不限。患者被随机分配接受木质素或蒸馏水雾化吸入。评估结果包括PaO2/FiO2比值、血液动力学、呼吸参数和序贯器官衰竭评分(SOFA):结果:两组在人口统计学变量方面具有可比性。结果:两组在人口统计学变量方面具有可比性,从第 2 天起,木质素组的 PaO2/FiO2 明显更高。木质素组的 SPO2 在第 3 天明显升高,此后无明显差异。两组的其他血液动力学、呼吸参数和 SOFA 评分均无差异:结论:雾化吸入木质素可改善 COVID-19 患者的氧合状况,可与其他辅助药物一起作为辅助疗法使用。
{"title":"Efficacy of lignocaine nebulization in patients with COVID-19 respiratory infection: An exploratory randomized double-blinded controlled trial.","authors":"Praveen Talawar, Debendra Kumar Tripathy, Ashutosh Kaushal, Mridul Dhar, Adabala Vijaybabu, Praik Tuppad, Sangadala Priyanka, Deepak Kumar, Ruhi Sharma, Sumedha Suresh Kumar","doi":"10.4103/joacp.joacp_205_22","DOIUrl":"10.4103/joacp.joacp_205_22","url":null,"abstract":"<p><strong>Background and aims: </strong>Coronavirus disease (COVID-19)-related pneumonia is proposed to be an inflammatory process. The treatment currently includes supportive therapy and low-dose steroids. Anti-inflammatory drugs have been proposed to prevent cytokine storms and improve oxygenation in such cases. The study aimed to assess the efficacy of nebulized lignocaine in COVID-19 patients with pneumonia.</p><p><strong>Material and methods: </strong>This was an exploratory randomized double-blinded control trial conducted in COVID-19 patients with respiratory failure requiring oxygen therapy either by face mask or non-invasive mechanical ventilation. Patients included were of the age of more than 18 years of either gender. The patients were randomized to receive either lignocaine or distilled water nebulization. The outcomes assessed were PaO<sub>2</sub>/FiO<sub>2</sub> ratio, hemodynamics, respiratory parameters, and sequential organ failure score (SOFA).</p><p><strong>Results: </strong>The two groups were comparable concerning demographic variables. The PaO<sub>2</sub>/FiO<sub>2</sub> were significantly higher in the lignocaine group from day 2 onward. The SPO<sub>2</sub> was significantly higher on day 3 in the lignocaine group and thereafter there was no significant difference. Other hemodynamic, respiratory parameters, and SOFA scores showed no difference in both the groups.</p><p><strong>Conclusion: </strong>Lignocaine nebulization improved oxygenation in COVID-19 patients and can be used as adjunctive therapy along with other supportive medications.</p>","PeriodicalId":14946,"journal":{"name":"Journal of Anaesthesiology, Clinical Pharmacology","volume":"40 2","pages":"271-275"},"PeriodicalIF":1.5,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11196040/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141450547","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
'Ten'der points of perioperative analgesia research. 围术期镇痛研究的十个要点。
IF 1.5 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2024-05-16 DOI: 10.4103/joacp.joacp_39_24
Varun Suresh, Rohan Magoon
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引用次数: 0
Can the preuse check of epidural set detect all manufacturing defects? 硬膜外装置的使用前检查能否检测出所有制造缺陷?
IF 1.5 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2024-05-16 DOI: 10.4103/joacp.joacp_389_22
Raksha Vyas, Sadik Mohammed, Priyabrat Karan, Rakesh Kumar
{"title":"Can the preuse check of epidural set detect all manufacturing defects?","authors":"Raksha Vyas, Sadik Mohammed, Priyabrat Karan, Rakesh Kumar","doi":"10.4103/joacp.joacp_389_22","DOIUrl":"10.4103/joacp.joacp_389_22","url":null,"abstract":"","PeriodicalId":14946,"journal":{"name":"Journal of Anaesthesiology, Clinical Pharmacology","volume":"40 2","pages":"351-352"},"PeriodicalIF":1.5,"publicationDate":"2024-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11196053/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141450543","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
Comparison of human cadaver and blue phantom for teaching ultrasound-guided regional anesthesia to novice postgraduate students of anesthesiology: A randomized controlled trial. 在向麻醉学研究生新手教授超声引导区域麻醉时,比较人体尸体和蓝色模型:随机对照试验。
IF 1.5 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-04-01 Epub Date: 2024-05-16 DOI: 10.4103/joacp.joacp_234_22
Deepanshu Dang, Manoj Kamal, Mritunjay Kumar, Bharat Paliwal, Ashish Nayyar, Pradeep Bhatia, Geeta Singariya

Background and aims: Simulation is increasingly used in medical teaching. Various studies have evaluated different simulation models for training of regional anesthesia (RA). We compared the use of human cadaver and blue phantom models for training of regional anesthesia to novice postgraduate students of anesthesiology.

Material and methods: Fifty students were taught knobology of the ultrasonography (USG) machine. They were divided into two equal groups by computer-generated random number table, and the groups assigned were kept in sealed envelopes. In group BP, students were trained on a blue phantom model, and in group HC, students were trained on human cadaver. After training, a didactic video of sonoanatomy of the supraclavicular block was shown to all participants. The block performance was then judged on patients requiring supraclavicular block. The primary objective of the study was to compare the block performance time, and secondary objectives were the quality of image acquired, orientation of transducer to the target, identification of ultrasound artifacts, errors committed, complications, and success rate.

Results: The mean block performance time was shorter in group HC compared to group BP (451.96 ± 50.25 and 526.48 ± 43.486 s, respectively; P < 0.001). The image quality score, transducer orientation to the target, and identification of USG artifacts were better in group HC compared to group BP, with lesser number of needle passes.

Conclusion: Cadaver-based training produced better results compared to blue phantom simulator model for teaching of ultrasound-guided RA to novice postgraduate trainees of anesthesiology.

背景和目的:模拟在医学教学中的应用越来越广泛。多项研究评估了用于区域麻醉(RA)培训的不同模拟模型。我们比较了使用人体尸体模型和蓝色幻影模型对麻醉学研究生新手进行区域麻醉培训的情况:我们向 50 名学生传授了超声造影机(USG)的操作技巧。通过计算机生成的随机数字表将他们平均分成两组,并将分配到的组别装在密封的信封中。在 BP 组,学生在蓝色幻影模型上接受培训;在 HC 组,学生在人体尸体上接受培训。训练结束后,向所有参与者播放锁骨上阻滞的声波解剖教学视频。然后对需要锁骨上阻滞的患者的阻滞表现进行评判。研究的首要目标是比较阻滞时间,次要目标是获取图像的质量、换能器对目标的定位、识别超声伪影、所犯错误、并发症和成功率:结果:与 BP 组相比,HC 组的平均阻滞时间更短(分别为 451.96 ± 50.25 秒和 526.48 ± 43.486 秒;P < 0.001)。与 BP 组相比,HC 组的图像质量评分、探头对目标的定位以及 USG 伪影的识别都更好,而且穿刺针的次数更少:结论:在对麻醉学研究生新手进行超声引导 RA 教学时,基于尸体的培训与蓝色幻影模拟器模型相比效果更好。
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Journal of Anaesthesiology, Clinical Pharmacology
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