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Central sensitisation in chronic low back pain: A cross-sectional study. 慢性腰痛的中枢致敏:一项横断面研究。
IF 1.9 Q1 ANESTHESIOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-05 DOI: 10.4103/ija.ija_433_25
Nagma Sheenam, Ravi Gaur, Nitesh Manohar Gonnade, T K Abins, Arindam Ghosh, Rejuwan Hussain

Background and aims: Central sensitisation (CS) is a key mechanism contributing to chronic low back pain (CLBP), influenced by demographic, metabolic, and psychological factors. This study aimed to evaluate the association between CS and variables such as age, gender, body mass index (BMI), vitamin D levels, psychological distress (anxiety, depression, kinesiophobia), and pain intensity in individuals with CLBP.

Methods: A cross-sectional observational study was conducted at a tertiary care centre between January and December 2023. Adults aged 18 years or older with CLBP (lasting at least 3 months) were included. Participants were assessed using the Central Sensitisation Inventory (CSI), Numerical Rating Scale (NRS), Tampa Scale for Kinesiophobia, BMI, and serum vitamin D levels. Individuals with neurological or psychiatric disorders or those on medications affecting pain modulation were excluded. Statistical analysis was performed using non-parametric tests and Spearman's correlation to explore associations between CSI scores and demographic, metabolic, and psychological variables. P value < 0.05 was considered statistically significant.

Results: The mean age of participants was 41.3 years. Females had significantly higher CSI scores than males (P < 0.001). CSI scores differed significantly across age groups (P = 0.024), with the highest scores observed in participants under 20 years of age. Weak correlations were observed between CSI scores and both BMI and vitamin D levels. BMI showed a weak positive correlation with CSI scores (ρ = 0.182, P = 0.036), while vitamin D levels showed a weak negative correlation with CSI scores (ρ = -0.181, P = 0.038). No significant associations were found between CSI scores and anxiety, depression, kinesiophobia, or pain intensity.

Conclusion: CS in CLBP is associated with age, gender, BMI, and vitamin D levels, but not psychological distress or pain intensity. These findings highlight the importance of personalised, multidimensional pain assessment and management approaches.

背景和目的:中枢致敏(CS)是导致慢性腰痛(CLBP)的关键机制,受人口统计学、代谢和心理因素的影响。本研究旨在评估CS与CLBP患者的年龄、性别、体重指数(BMI)、维生素D水平、心理困扰(焦虑、抑郁、运动恐惧症)和疼痛强度等变量之间的关系。方法:于2023年1月至12月在一家三级保健中心进行横断面观察研究。18岁或以上CLBP患者(持续至少3个月)被纳入研究对象。使用中枢致敏量表(CSI)、数值评定量表(NRS)、坦帕运动恐惧症量表、BMI和血清维生素D水平对参与者进行评估。排除了患有神经或精神疾病或正在服用影响疼痛调节药物的个体。采用非参数检验和Spearman相关进行统计分析,探讨CSI得分与人口统计学、代谢和心理变量之间的关系。P值< 0.05为差异有统计学意义。结果:参与者平均年龄为41.3岁。女性的CSI得分明显高于男性(P < 0.001)。不同年龄组的CSI得分差异显著(P = 0.024), 20岁以下的参与者得分最高。在CSI得分与BMI和维生素D水平之间观察到弱相关性。BMI与CSI评分呈弱正相关(ρ = 0.182, P = 0.036),维生素D水平与CSI评分呈弱负相关(ρ = -0.181, P = 0.038)。未发现CSI评分与焦虑、抑郁、运动恐惧症或疼痛强度之间存在显著关联。结论:CLBP患者CS与年龄、性别、BMI和维生素D水平有关,但与心理困扰或疼痛强度无关。这些发现强调了个性化、多维度疼痛评估和管理方法的重要性。
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引用次数: 0
Analgesic efficacy of ultrasound-guided modified thoracoabdominal nerve block in paediatric upper abdominal surgery: A randomised controlled trial. 超声引导改良胸腹神经阻滞在小儿上腹部手术中的镇痛效果:一项随机对照试验。
IF 1.9 Q1 ANESTHESIOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-05 DOI: 10.4103/ija.ija_357_25
Athira Jayan, Amarjeet Kumar, Chandni Sinha, Ajeet Kumar, Poonam Kumari, Amit K Sinha

Background and aims: Adequate pain management is crucial for postoperative recovery in paediatric patients. This study aimed to evaluate the analgesic efficacy of ultrasound (US)-guided modified thoracoabdominal nerve block through perichondrial approach (mTAPA) block in paediatric patients undergoing upper abdominal surgeries.

Methods: This randomised controlled trial included 40 paediatric patients aged between 2 and 8 years scheduled for unilateral upper abdominal surgeries. Patients were randomised into two groups: Group I received general anaesthesia (GA) with US-guided mTAPA block (0.5 mL/kg of 0.2% ropivacaine), while Group II received GA only. Intravenous fentanyl 0.5 µg/kg was utilised for perioperative pain management. The primary outcome was to assess intraoperative opioid consumption, whereas secondary outcomes were postoperative pain scores, 24-h opioid consumption, and adverse effects such as nausea and vomiting. The independent Student t-test compared quantitative, normally distributed data, while the Mann-Whitney U test compared quantitative, discrete data. A P value of <0.05 was considered statistically significant.

Results: Patients in Group I had a statistically lower intraoperative median fentanyl consumption of 10.0 µg [range: 0-20, interquartile range (IQR): 0-10] versus 20 µg (range: 5-48, IQR: 20-27) in Group II (P = 0.001). There was a significant reduction in the number of patients requiring rescue opioid top-ups (32.5% vs 50%) and postoperative pain scores (till 16 hours) in Group I. The median time to rescue analgesia was significantly higher in Group I than Group II (P = 0.001). No significant side effects were observed in either group.

Conclusion: Ultrasound-guided modified thoracoabdominal nerve block through perichondrial approach as an adjunct to general anaesthesia provides effective analgesia by significantly reducing opioid consumption in paediatric patients undergoing upper abdominal surgeries through a unilateral subcostal incision.

背景和目的:适当的疼痛管理对儿科患者术后恢复至关重要。本研究旨在评价超声(US)引导下经软骨膜外入路改良胸腹神经阻滞(mTAPA)在小儿上腹部手术患者中的镇痛效果。方法:本随机对照试验纳入40例年龄在2至8岁之间的儿童,计划进行单侧上腹部手术。患者被随机分为两组:第一组接受全身麻醉(GA),使用美国引导的mTAPA阻滞(0.5 mL/kg 0.2%罗哌卡因),而第二组只接受全身麻醉。静脉注射芬太尼0.5µg/kg用于围手术期疼痛管理。主要结局是评估术中阿片类药物的消耗,而次要结局是术后疼痛评分、24小时阿片类药物的消耗以及恶心和呕吐等不良反应。独立学生t检验比较定量的、正态分布的数据,而Mann-Whitney U检验比较定量的、离散的数据。结果:组患者术中芬太尼用量中位数10.0µg[范围:0-20,四分位数间距(IQR): 0-10]低于组患者20µg(范围:5-48,IQR: 20-27),差异有统计学意义(P = 0.001)。I组需要阿片类药物补剂的患者数量(32.5% vs 50%)和术后疼痛评分(至16小时)均显著减少。I组恢复镇痛的中位时间显著高于II组(P = 0.001)。两组均未观察到明显的副作用。结论:超声引导下经软膜下入路改良胸腹神经阻滞作为全身麻醉的辅助,可显著减少经单侧肋下切口行上腹部手术的儿科患者阿片类药物的消耗,从而提供有效的镇痛效果。
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引用次数: 0
Author Reply to Comments on "Association between preoperative frailty and postoperative delirium and cognitive dysfunction in elderly patients undergoing surgery under general anaesthesia". 作者回复“老年全麻手术患者术前虚弱与术后谵妄及认知功能障碍的关系”
IF 1.9 Q1 ANESTHESIOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-05 DOI: 10.4103/ija.ija_995_25
K Anjaleekrishna, Dalim Kumar Baidya, Rohit Verma, Bikash Ranjan Ray, Rahul Kumar Anand, Akhil Kant Singh, Souvik Maitra, Puneet Khanna
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引用次数: 0
Analgesic efficacy of ultrasound-guided genicular nerve block in combination with adductor canal block in total knee arthroplasty: A randomised, double-blind, placebo-controlled trial. 超声引导下膝神经阻滞联合内收管阻滞在全膝关节置换术中的镇痛效果:一项随机、双盲、安慰剂对照试验。
IF 1.9 Q1 ANESTHESIOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-05 DOI: 10.4103/ija.ija_486_25
Rajendra K Sahoo, Laxman K Senapati, Prateek Mitra, Ganesh C Satapathy, Abhijit S Nair, Priyadarsini Samanta

Background and aims: Distal motor-sparing nerve blocks are increasingly popular for knee arthroplasty pain. Genicular nerve ablation, initially proposed for knee osteoarthritis, is also currently used for postoperative pain management. We hypothesised that superior postoperative analgesia can be achieved by combining genicular nerve block with adductor canal block (ACB) by reducing 24-hour opioid consumption.

Methods: Fifty patients were assigned to Group I (ultrasound-guided ACB with 20 mL of 0.25% ropivacaine and 4 mg dexamethasone and ultrasound-guided superomedial (SM), superolateral (SL), and inferomedial (IM) GNB with 5 mL of 0.25% ropivacaine and 2 mg of dexamethasone at each location and Group II (ultrasound-guided ACB with 20 mL of 0.25% ropivacaine, 4 mg dexamethasone, and ultrasound-guided three-location GNB with 15 mL of 0.9% saline). The outcomes measured were 24-hour morphine consumption, pain scores over 24 hours, and the time to rescue analgesia. The continuous data were analysed using an unpaired t-test or the Mann-Whitney U test, and the Chi-square test was used to analyse the categorical variables.

Results: The mean total consumption of morphine (mg) was 5.96 [standard deviation (SD): 2.73] in Group I and 15.52 (SD: 2.67) in Group II, with a mean difference of 9.56 [95% confidence interval (CI): -4.66, -2.39] (P < 0.001, Cohen's d = 3.54). In Group II, the mean time for first rescue analgesia was 20.73 (SD: 7.28) hours, whereas it was 24.00 (SD: 0.00) hours in Group I, with a mean difference of -3.27 (95% CI: -11.33, 4.783) (P = 0.034, Cohen's d = 0.45). Pain severity at rest was substantially lower in Group I at 6 hours (P = 0.020), 12 hours (P = 0.003), and 24 hours (P = 0.002). Pain score with movement in Group I was considerably lower at 6 hours (P = 0.008) and 12 hours (P < 0.001).

Conclusion: Combining genicular block with ACB provided superior postoperative analgesia and reduced opioid consumption compared to ACB alone.

背景和目的:远端保留运动神经阻滞治疗膝关节置换术疼痛越来越受欢迎。膝神经消融术,最初建议用于膝关节骨关节炎,目前也用于术后疼痛管理。我们假设通过膝神经阻滞和内收管阻滞(ACB)联合减少24小时阿片类药物的消耗,可以实现更好的术后镇痛。方法:50例患者分为超声引导ACB组(0.25%罗哌卡因+ 4 mg)和超声引导上内侧(SM)、上外侧(SL)、内侧间(IM) GNB组(5ml 0.25%罗哌卡因+ 2 mg地塞米松)和超声引导ACB组(0.25%罗哌卡因+ 4 mg地塞米松+ 20 mL超声引导三部位GNB + 15 mL 0.9%生理盐水)。测量结果为24小时吗啡用量、24小时疼痛评分和镇痛恢复时间。连续资料分析采用非配对t检验或Mann-Whitney U检验,分类变量分析采用卡方检验。结果:ⅰ组和ⅱ组吗啡平均总用量(mg)分别为5.96和15.52 mg (SD: 2.67),平均差异为9.56 mg[95%可信区间(CI): -4.66, -2.39] (P < 0.001, Cohen’SD = 3.54)。II组患者首次抢救镇痛平均时间为20.73 (SD: 7.28)小时,而I组患者首次抢救镇痛平均时间为24.00 (SD: 0.00)小时,平均差异为-3.27 (95% CI: -11.33, 4.783) (P = 0.034, Cohen’SD = 0.45)。静息疼痛严重程度在6小时(P = 0.020)、12小时(P = 0.003)和24小时(P = 0.002)时显著降低。第1组在6小时(P = 0.008)和12小时(P < 0.001)时疼痛随运动评分明显降低。结论:与单独ACB相比,膝阻滞联合ACB具有更好的术后镇痛效果,并减少阿片类药物的消耗。
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引用次数: 0
Comparison of partial pressure of oxygen between compression-only CPR and standard CPR in simulated adult cardiac arrest - A manikin-based clinical modelling. 模拟成人心脏骤停时,单纯按压CPR和标准CPR的氧分压比较——基于人体模型的临床模型。
IF 1.9 Q1 ANESTHESIOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-05 DOI: 10.4103/ija.ija_495_25
Pankaj Kundra, Stalin Vinayagam, Anusha Cherian, Balakrishnan Ashokka

Background and aims: Compression-only cardiopulmonary resuscitation (CPR) has been shown to be as effective as conventional CPR, and oxygen supplementation during compression-only CPR may be beneficial. The study aimed to compare the arterial oxygen levels achieved while supplementing oxygen through high flow nasal cannula (HFNC) during compression-only CPR and bag-mask ventilation (BMV) during conventional CPR in simulated cardiac arrest scenarios on a high-fidelity simulator.

Methods: The study included a simulated cardiac arrest created on a human patient simulator (HPS). The simulation included two sets of scenarios. In Simulation A, cardiac arrest was simulated on HPS, and compression-only CPR was provided by AutoPulse, and oxygen supplementation was provided using HFNC. In Simulation B, chest compression was provided by AutoPulse, and BMV was supplemented with oxygen at 15 L/min at a compression-to-ventilation ratio of 30:2. Both simulation scenarios were evaluated for three different starting PaO2 values: 100 mmHg, 80 mmHg, and 60 mmHg. The change in PaO2 and PAO2 values was recorded every minute for 6 minutes. Statistical analysis was conducted using SPSS Statistics (Version 24.0; IBM, Armonk, NY), and P < 0.05 was considered statistically significant.

Results: In Simulation A, at a starting PaO2 of 100 mmHg, there was an increase in the PaO2 at the 2nd minute, which was sustained till the 6th minute. PaO2 values were persistently higher at all time points as compared to Simulation B (P < 0.001). At a starting PaO2 of 80 mmHg, there was no change in PaO2 in Simulation A as compared to a sustained fall in Simulation B (P < 0.001). At the starting PaO2 of 60 mmHg, a decrease in PaO2 was observed in both Simulation A and Simulation B (P = 0.57).

Conclusion: In a simulated setting, compression-only CPR with HFNC results in better PaO2 levels compared to conventional CPR with BMV.

背景和目的:单纯按压心肺复苏(CPR)已被证明与常规CPR一样有效,在单纯按压心肺复苏期间补充氧气可能是有益的。该研究旨在比较在高保真模拟器上模拟心脏骤停情景时,在纯按压心肺复苏期间通过高流量鼻插管(HFNC)补充氧气和在常规心肺复苏期间通过气囊面罩通气(BMV)补充氧气所达到的动脉氧水平。方法:研究包括在人体病人模拟器(HPS)上模拟心脏骤停。模拟包括两组场景。在模拟A中,在HPS上模拟心脏骤停,由autoppulse提供单纯按压式CPR,并使用HFNC进行补氧。在模拟B中,胸腔按压由autoppulse提供,BMV以15l /min的速度补充氧气,压通比为30:2。在这两种模拟场景中,分别对三种不同的起始PaO2值进行了评估:100 mmHg、80 mmHg和60 mmHg。每分钟记录一次PaO2和PaO2值的变化,持续6分钟。统计学分析采用SPSS Statistics (Version 24.0; IBM, Armonk, NY),以P < 0.05为差异有统计学意义。结果:在模拟A中,在起始PaO2为100 mmHg时,PaO2在第2分钟升高,并持续至第6分钟。与模拟B相比,PaO2值在所有时间点持续升高(P < 0.001)。在起始PaO2为80 mmHg时,与模拟B的持续下降相比,模拟a的PaO2没有变化(P < 0.001)。在起始PaO2为60 mmHg时,模拟a和模拟B的PaO2均下降(P = 0.57)。结论:在模拟环境中,与BMV常规CPR相比,HFNC单纯按压CPR的PaO2水平更好。
{"title":"Comparison of partial pressure of oxygen between compression-only CPR and standard CPR in simulated adult cardiac arrest - A manikin-based clinical modelling.","authors":"Pankaj Kundra, Stalin Vinayagam, Anusha Cherian, Balakrishnan Ashokka","doi":"10.4103/ija.ija_495_25","DOIUrl":"10.4103/ija.ija_495_25","url":null,"abstract":"<p><strong>Background and aims: </strong>Compression-only cardiopulmonary resuscitation (CPR) has been shown to be as effective as conventional CPR, and oxygen supplementation during compression-only CPR may be beneficial. The study aimed to compare the arterial oxygen levels achieved while supplementing oxygen through high flow nasal cannula (HFNC) during compression-only CPR and bag-mask ventilation (BMV) during conventional CPR in simulated cardiac arrest scenarios on a high-fidelity simulator.</p><p><strong>Methods: </strong>The study included a simulated cardiac arrest created on a human patient simulator (HPS). The simulation included two sets of scenarios. In Simulation A, cardiac arrest was simulated on HPS, and compression-only CPR was provided by AutoPulse, and oxygen supplementation was provided using HFNC. In Simulation B, chest compression was provided by AutoPulse, and BMV was supplemented with oxygen at 15 L/min at a compression-to-ventilation ratio of 30:2. Both simulation scenarios were evaluated for three different starting PaO<sub>2</sub> values: 100 mmHg, 80 mmHg, and 60 mmHg. The change in PaO<sub>2</sub> and PAO<sub>2</sub> values was recorded every minute for 6 minutes. Statistical analysis was conducted using SPSS Statistics (Version 24.0; IBM, Armonk, NY), and <i>P</i> < 0.05 was considered statistically significant.</p><p><strong>Results: </strong>In Simulation A, at a starting PaO<sub>2</sub> of 100 mmHg, there was an increase in the PaO<sub>2</sub> at the 2<sup>nd</sup> minute, which was sustained till the 6<sup>th</sup> minute. PaO<sub>2</sub> values were persistently higher at all time points as compared to Simulation B (<i>P</i> < 0.001). At a starting PaO<sub>2</sub> of 80 mmHg, there was no change in PaO<sub>2</sub> in Simulation A as compared to a sustained fall in Simulation B (<i>P</i> < 0.001). At the starting PaO<sub>2</sub> of 60 mmHg, a decrease in PaO<sub>2</sub> was observed in both Simulation A and Simulation B (<i>P</i> = 0.57).</p><p><strong>Conclusion: </strong>In a simulated setting, compression-only CPR with HFNC results in better PaO<sub>2</sub> levels compared to conventional CPR with BMV.</p>","PeriodicalId":13339,"journal":{"name":"Indian Journal of Anaesthesia","volume":"69 10","pages":"1055-1060"},"PeriodicalIF":1.9,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12445773/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145112908","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
Perineural fresh frozen plasma with local anaesthetics in coagulopathic patients undergoing peripheral nerve blocks: A clinical case series. 周围神经阻滞治疗凝血障碍患者的神经周围新鲜冷冻血浆局部麻醉:临床病例系列。
IF 1.9 Q1 ANESTHESIOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-05 DOI: 10.4103/ija.ija_476_25
Sandeep Diwan, Archana Areti, Nitin Gawai, Parag Sancheti

Peripheral nerve blocks (PNBs) in coagulopathic patients are typically avoided due to the risks of bleeding and potential nerve compression. This case series explores the use of perineural fresh frozen plasma (FFP) to enhance local haemostasis in such settings. Five patients with an international normalised ratio of > 1.8, requiring urgent surgery, received PNBs with perineural FFP after haematology consultation. Seven ultrasound-guided blocks were performed, with FFP injected perineurally and along the needle tract, followed by systemic FFP 20 minutes later. All procedures were completed under PNB without conversion or need for additional analgesia. One patient developed a localised haematoma post-supraclavicular block, resolving after perineural FFP. No neurological deficits, major bleeding, or infections were observed. These preliminary results suggest that perineural FFP may reduce bleeding complications in high-risk patients, though further research is needed. Until validated, its use should remain investigational and be undertaken with multidisciplinary oversight and strict adherence to aseptic technique and ultrasound guidance.

由于出血和潜在的神经压迫风险,凝血病患者通常避免周围神经阻滞(PNBs)。本病例系列探讨了在这种情况下使用神经周围新鲜冷冻血浆(FFP)来增强局部止血。5例国际正常化比值为bbb1.8,需要紧急手术的患者在血液学会诊后接受pnb伴神经周围FFP。超声引导阻滞7次,沿神经周和针道注射FFP, 20分钟后全身注射FFP。所有手术均在PNB下完成,没有转换或需要额外的镇痛。一名患者在锁骨上阻滞后出现局部血肿,在神经周围FFP后消退。没有观察到神经功能缺损、大出血或感染。这些初步结果表明,神经周围FFP可以减少高危患者的出血并发症,但还需要进一步的研究。在验证之前,它的使用应保持研究性,并在多学科监督下进行,严格遵守无菌技术和超声指导。
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引用次数: 0
Application efficacy of dural puncture epidural versus traditional combined spinal epidural for labour analgesia: A systematic review and meta-analysis with trial sequential analysis. 硬膜穿刺硬膜外镇痛与传统脊髓硬膜外联合镇痛在分娩中的应用效果:一项系统综述和荟萃分析。
IF 1.9 Q1 ANESTHESIOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-05 DOI: 10.4103/ija.ija_802_25
Junjun Qin, Weili Zhou, Zhengwei Chen, Changlin He, Jiasen Ma

Background and aims: This study aimed to systematically evaluate the effectiveness and safety of dural puncture epidural (DPE) and combined spinal epidural (CSE) for labour analgesia in parturients.

Methods: Searches were performed in PubMed, Embase, Web of Science, Cochrane Library, CNKI, Wanfang Database, VIP Database, and CBM Database up to June 2025 to identify randomised controlled trials (RCTs) investigating the application of DPE and CSE techniques for labour analgesia in parturients. Data from eligible studies were pooled to calculate the combined standardised mean difference (SMD) or risk ratio (RR).

Results: Eleven studies with 1461 parturients were included. DPE had higher visual analogue scale (VAS) pain scores at 10 min [SMD: 0.60; 95% confidence interval (CI): 0.24, 0.95; P = 0.001; I 2 = 76%] compared to CSE but fewer parturients requiring physician top-up boluses (RR = 0.64; 95% CI: 0.46, 0.88; P = 0.006; I 2 = 11%). It also showed significantly lower incidences of abnormal foetal heart rate patterns (RR = 0.27; 95% CI: 0.16, 0.44; P < 0.001; I 2 = 0%), pruritus (RR = 0.27; 95% CI: 0.14, 0.53; P < 0.001; I 2 = 54%), and maternal hypotension (RR = 0.36; 95% CI: 0.15, 0.89; P = 0.030; I 2 = 74%). No significant intergroup differences were found in first-stage labour duration, neonatal Apgar scores, or adverse reactions. The trial sequential analysis suggested the need for further data.

Conclusion: Compared with CSE, although DPE has a slower onset of analgesia, it may provide more reliable analgesic effects and result in lower incidence rates of adverse reactions in both parturients and foetuses. Substantial heterogeneity in some outcomes, driven by clinical heterogeneity including dose variations and limited studies, warrants cautious interpretation.

背景与目的:本研究旨在系统评价硬膜穿刺硬膜外麻醉(DPE)和脊髓硬膜外联合麻醉(CSE)用于分娩镇痛的有效性和安全性。方法:检索PubMed、Embase、Web of Science、Cochrane Library、中国知网、万方数据库、VIP数据库和CBM数据库,检索到2025年6月前调查DPE和CSE技术在分娩镇痛中的应用的随机对照试验(RCTs)。纳入符合条件的研究数据,计算标准化平均差(SMD)或风险比(RR)。结果:纳入11项研究,1461例产妇。DPE在10 min时具有更高的视觉模拟评分(VAS)疼痛评分[SMD: 0.60;95%置信区间(CI): 0.24, 0.95;P = 0.001;[I 2 = 76%]与CSE相比,但需要医生补充药物的产妇较少(RR = 0.64; 95% CI: 0.46, 0.88; P = 0.006; I 2 = 11%)。胎儿心率异常(RR = 0.27; 95% CI: 0.16, 0.44; P < 0.001; i2 = 0%)、瘙痒(RR = 0.27; 95% CI: 0.14, 0.53; P < 0.001; i2 = 54%)和母体低血压(RR = 0.36; 95% CI: 0.15, 0.89; P = 0.030; i2 = 74%)的发生率也显著降低。在第一产程、新生儿Apgar评分或不良反应方面,组间无显著差异。试验序列分析表明需要进一步的数据。结论:与CSE相比,DPE虽然镇痛起效较慢,但其镇痛效果更可靠,产妇和胎儿不良反应发生率更低。由于临床异质性(包括剂量变化和有限的研究),一些结果存在实质性异质性,因此需要谨慎解释。
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引用次数: 0
Confidence interval reporting in randomised controlled trials: A critical analysis of IJA publications. 随机对照试验中的可信区间报告:IJA出版物的关键分析。
IF 1.9 Q1 ANESTHESIOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-05 DOI: 10.4103/ija.ija_811_25
Lalit Gupta, Kapil Chaudhary, Devang Bharti
{"title":"Confidence interval reporting in randomised controlled trials: A critical analysis of IJA publications.","authors":"Lalit Gupta, Kapil Chaudhary, Devang Bharti","doi":"10.4103/ija.ija_811_25","DOIUrl":"10.4103/ija.ija_811_25","url":null,"abstract":"","PeriodicalId":13339,"journal":{"name":"Indian Journal of Anaesthesia","volume":"69 10","pages":"1069-1072"},"PeriodicalIF":1.9,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12445755/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145112871","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
Revisiting the deep rectus sheath block: An anatomical mismatch for optimal analgesia. 重新审视深直肌鞘阻滞:最佳镇痛的解剖学不匹配。
IF 1.9 Q1 ANESTHESIOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-05 DOI: 10.4103/ija.ija_534_25
Kartik Sonawane, Namburi R Naveena, Tuhin Mistry
{"title":"Revisiting the deep rectus sheath block: An anatomical mismatch for optimal analgesia.","authors":"Kartik Sonawane, Namburi R Naveena, Tuhin Mistry","doi":"10.4103/ija.ija_534_25","DOIUrl":"10.4103/ija.ija_534_25","url":null,"abstract":"","PeriodicalId":13339,"journal":{"name":"Indian Journal of Anaesthesia","volume":"69 10","pages":"1078-1081"},"PeriodicalIF":1.9,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12445759/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145112953","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
Imputation of arterial oxygen partial pressures using pulse oximetry in surgical patients under general anaesthesia: A prospective cohort study. 在全麻手术患者中应用脉搏血氧仪测量动脉氧分压:一项前瞻性队列研究。
IF 1.9 Q1 ANESTHESIOLOGY Pub Date : 2025-10-01 Epub Date: 2025-09-05 DOI: 10.4103/ija.ija_153_25
Mohamad F El-Khatib, Marwan Rizk, Amro Khalili, Thuraya HajAli, Ibrahim El Mallah, Rasha Shreim, Carine Zeeni

Background and aims: Monitoring oxygen saturation (SpO2) during general anaesthesia using pulse oximetry is mandatory, though it may not always reflect the actual oxygenation status. Arterial blood gas (ABG) analysis remains the gold standard for measuring the partial pressure of oxygen (PaO2), but it is invasive and limited by complications. This study aims to validate five existing equations for predicting PaO2 from SpO2 and, if applicable, to derive and validate a new equation in adult patients undergoing surgeries under general anaesthesia.

Methods: A prospective cohort study was conducted on adult patients undergoing general anaesthesia and requiring ABG measurements at several time points intraoperatively. Using SPSS software, a Bland-Altman analysis was performed to assess the agreement between derived and measured PaO2 values using five existing equations. Regression analysis was then performed to develop a new equation for predicting PaO2, which was validated in a second cohort.

Results: During the initial phase, 150 ABG samples were collected from 83 patients. Bland-Altman analysis revealed weak agreements with all existing equations. A new logarithmic equation, El-Khatib's equation (PaO2 = 10-25.6 × SpO2 13.9), was derived. The validation phase involved 150 ABG samples from 65 patients, demonstrating strong agreement with El-Khatib's equation (systematic bias of 13 mmHg, limits of agreement: -189 to 214 mmHg).

Conclusion: Five existing equations for predicting PaO2 from SpO2 revealed weak agreement in adult patients under general anaesthesia. El-Khatib's equation demonstrated strong potential for predicting PaO2, providing a reliable non-invasive alternative for determining PaO2 in clinical practice.

背景和目的:在全身麻醉期间使用脉搏血氧仪监测血氧饱和度(SpO2)是强制性的,尽管它可能并不总是反映实际的氧合状态。动脉血气(ABG)分析仍然是测量氧分压(PaO2)的金标准,但它具有侵入性,并受到并发症的限制。本研究旨在验证从SpO2预测PaO2的五个现有方程,如果适用,在全麻醉下接受手术的成人患者中推导并验证一个新的方程。方法:一项前瞻性队列研究对接受全身麻醉并在术中几个时间点需要测量ABG的成年患者进行了研究。使用SPSS软件进行Bland-Altman分析,以评估使用五个现有方程得出的PaO2值与测量值之间的一致性。然后进行回归分析,建立预测PaO2的新方程,并在第二组队列中进行验证。结果:在初始阶段,从83例患者中收集了150份ABG样本。Bland-Altman分析揭示了与所有现有方程的弱一致性。导出了新的对数方程El-Khatib方程(PaO2 = 10-25.6 × SpO2 13.9)。验证阶段涉及来自65名患者的150份ABG样本,证明与El-Khatib方程(系统偏倚为13 mmHg,一致性限:-189至214 mmHg)非常吻合。结论:用SpO2预测PaO2的现有5个方程在全麻成人患者中一致性较弱。El-Khatib的公式显示了预测PaO2的强大潜力,为临床实践中确定PaO2提供了可靠的非侵入性替代方法。
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Indian Journal of Anaesthesia
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