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Correction: A quasi-experimental evaluation of the association between implementation of Quality-Based Procedures funding for hip fractures and improvements in processes and outcomes for hip fracture patients in Ontario: an interrupted time series analysis. 更正:对安大略省髋部骨折 "质量为本程序 "资助的实施与髋部骨折患者的治疗过程和结果改善之间关系的准实验性评估:间断时间序列分析。
IF 3.4 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2024-09-01 DOI: 10.1007/s12630-024-02808-z
Hui Yu Zhang, Reva R Ramlogan, Robert Talarico, George Grammatopoulos, Steven Papp, Daniel I McIsaac
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引用次数: 0
The correlation between quality of recovery and parturient outcomes after Cesarean delivery: a cohort study. 剖腹产后恢复质量与产妇预后之间的相关性:一项队列研究。
IF 3.4 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2024-09-01 Epub Date: 2024-08-12 DOI: 10.1007/s12630-024-02799-x
Hon Sen Tan, Chin Wen Tan, Rehena Sultana, Lu Yang, May U S Mok, Ban Leong Sng

Purpose: Recent studies have reported the use of the obstetric-specific quality of recovery tool (ObsQoR-10) to assess the quality of recovery in parturients after childbirth; however, the correlation between ObsQoR-10 scores and important postpartum outcomes are unclear. The primary aim of the present study was to investigate the correlations between ObsQoR-10 scores at 24 hr after Cesarean delivery and breastfeeding, depressive symptomatology, overall health, and pain at seven days postpartum.

Methods: We recruited parturients who underwent elective Cesarean delivery at KK Hospital in Singapore. Parturients provided responses to post-Cesarean questionnaires at 1) 24 hr (ObsQoR-10, EuroQol EQ-Visual Analogue Scale, Edinburgh Postnatal Depression Scale), 2) 48 hr (ObsQoR-10, EQ-Visual Analogue Scale), and 3) seven days after Cesarean delivery (ObsQoR-10, Breastfeeding Self-Efficacy Scale-Short form, EQ-Visual Analogue Scale, Edinburgh Postnatal Depression Scale, pain survey).

Results: We enrolled 222 participants, 200 (90%) of whom completed the seven-day follow-up between September 2022 and April 2023. There was limited correlation between ObsQoR-10 at 24 hr with the Edinburgh Postnatal Depression Scale (r = 0.135), EQ-Visual Analogue Scale (r = 0.158), Breastfeeding Self-Efficacy Scale-Short form (r = 0.225), and averaged pain scores (r = -0.107) at seven days postpartum. ObsQoR-10 breastfeeding sub-score at 24 hr was weakly correlated with Breastfeeding Self-Efficacy Scale-Short form at seven days postpartum (r = 0.307).

Conclusion: ObsQoR-10 at 24 hr postpartum had limited correlation with breastfeeding, depressive symptomatology, overall health, and pain at seven days.

Study registration: ClinicalTrials.gov ( NCT04989894 ); first submitted 4 July 2021.

研究目的最近有研究报告称,产科专用恢复质量工具(ObsQoR-10)可用于评估产妇的产后恢复质量;然而,ObsQoR-10评分与重要产后结果之间的相关性尚不清楚。本研究的主要目的是调查剖宫产后 24 小时的 ObsQoR-10 评分与产后七天的母乳喂养、抑郁症状、整体健康和疼痛之间的相关性:我们招募了在新加坡 KK 医院接受择期剖宫产的产妇。产妇在剖宫产后 1) 24 小时内(ObsQoR-10、EuroQol 情商-视觉模拟量表、爱丁堡产后抑郁量表)、2) 48 小时内(ObsQoR-10、情商-视觉模拟量表)和 3) 7 天内(ObsQoR-10、母乳喂养自我效能量表-简表、情商-视觉模拟量表、爱丁堡产后抑郁量表、疼痛调查)回答了调查问卷:我们共招募了 222 名参与者,其中 200 人(90%)在 2022 年 9 月至 2023 年 4 月期间完成了为期七天的随访。产后 24 小时的 ObsQoR-10 与爱丁堡产后抑郁量表(r = 0.135)、EQ-视觉模拟量表(r = 0.158)、母乳喂养自我效能量表-简表(r = 0.225)以及产后七天的平均疼痛评分(r = -0.107)之间存在有限的相关性。产后七天时,24 小时内的 ObsQoR-10 母乳喂养子分数与母乳喂养自我效能感量表短表(r = 0.307)呈弱相关:产后24小时的ObsQoR-10与产后七天的母乳喂养、抑郁症状、整体健康和疼痛的相关性有限:研究注册:ClinicalTrials.gov(NCT04989894);2021 年 7 月 4 日首次提交。
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引用次数: 0
Prevention of hypotension after induction of general anesthesia using point-of-care ultrasound to guide fluid management: a randomized controlled trial. 利用护理点超声波指导液体管理,预防全身麻醉诱导后的低血压:随机对照试验。
IF 3.4 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2024-09-01 Epub Date: 2024-03-13 DOI: 10.1007/s12630-024-02748-8
Elad Dana, Cristian Arzola, James S Khan

Purpose: Hypotension after induction of general anesthesia (GAIH) is common and is associated with postoperative complications including increased mortality. Collapsibility of the inferior vena cava (IVC) has good performance in predicting GAIH; however, there is limited evidence whether a preoperative fluid bolus in patients with a collapsible IVC can prevent this drop in blood pressure.

Methods: We conducted a single-centre randomized controlled trial with adult patients scheduled to undergo elective noncardiac surgery under general anesthesia (GA). Patients underwent a preoperative point-of-care ultrasound scan (POCUS) to identify those with a collapsible IVC (IVC collapsibility index ≥ 43%). Individuals with a collapsible IVC were randomized to receive a preoperative 500 mL fluid bolus or routine care (control group). Surgical and anesthesia teams were blinded to the results of the scan and group allocation. Hypotension after induction of GA was defined as the use of vasopressors/inotropes or a decrease in mean arterial pressure < 65 mm Hg or > 25% from baseline within 20 min of induction of GA.

Results: Forty patients (20 in each group) were included. The rate of hypotension after induction of GA was significantly reduced in those receiving preoperative fluids (9/20, 45% vs 17/20, 85%; relative risk, 0.53; 95% confidence interval, 0.32 to 0.89; P = 0.02). The mean (standard deviation) time to complete POCUS was 4 (2) min, and the duration of fluid bolus administration was 14 (5) min. Neither surgical delays nor adverse events occurred as a result of the study intervention.

Conclusion: A preoperative fluid bolus in patients with a collapsible IVC reduced the incidence of GAIH without associated adverse effects.

Study registration: ClinicalTrials.gov (NCT05424510); first submitted 15 June 2022.

目的:全身麻醉诱导(GAIH)后出现低血压很常见,并且与包括死亡率增加在内的术后并发症有关。下腔静脉(IVC)的塌陷性在预测 GAIH 方面表现良好;然而,对于 IVC 塌陷的患者,术前注射液体是否能防止血压下降,目前证据有限:我们对计划在全身麻醉(GA)下接受择期非心脏手术的成年患者进行了一项单中心随机对照试验。患者在术前接受护理点超声波扫描(POCUS),以确定哪些患者存在可塌陷的 IVC(IVC 可塌陷指数≥ 43%)。患有塌陷性 IVC 的患者被随机分为接受术前 500 mL 液体栓塞或常规护理(对照组)两组。手术团队和麻醉团队对扫描结果和组别分配实行盲法。诱导 GA 后的低血压定义为使用血管加压药/肌注药或诱导 GA 后 20 分钟内平均动脉压比基线下降 25%:共纳入 40 例患者(每组 20 例)。接受术前输液的患者在诱导 GA 后发生低血压的比例明显降低(9/20,45% vs 17/20,85%;相对风险,0.53;95% 置信区间,0.32 至 0.89;P = 0.02)。完成 POCUS 的平均(标准差)时间为 4 (2) 分钟,给药时间为 14 (5) 分钟。研究干预既没有导致手术延迟,也没有发生不良事件:结论:可塌陷 IVC 患者术前注射液体可降低 GAIH 的发生率,且无相关不良反应:研究注册:ClinicalTrials.gov(NCT05424510);2022年6月15日首次提交。
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引用次数: 0
YouTube as a source of education in perioperative anesthesia for patients and trainees: a systematic review. 将 YouTube 作为围术期麻醉患者和受训人员的教育来源:系统综述。
IF 3.4 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2024-09-01 Epub Date: 2024-06-20 DOI: 10.1007/s12630-024-02791-5
Matthew W Nelms, Arshia Javidan, Ki Jinn Chin, Muralie Vignarajah, Fangwen Zhou, Chenchen Tian, Yung Lee, Ahmed Kayssi, Faysal Naji, Mandeep Singh

Background: Online video sharing platforms like YouTube (Google LLC, San Bruno, CA, USA) have become a substantial source of health information. We sought to conduct a systematic review of studies assessing the overall quality of perioperative anesthesia videos on YouTube.

Methods: We searched Embase, MEDLINE, and Ovid for articles published from database inception to 1 May 2023. We included primary studies evaluating YouTube videos as a source of information regarding perioperative anesthesia. We excluded studies not published in English and studies assessing acute or chronic pain. Studies were screened and data were extracted in duplicate by two reviewers. We appraised the quality of studies according to the social media framework published in the literature. We used descriptive statistics to report the results using mean, standard deviation, range, and n/total N (%).

Results: Among 8,908 citations, we identified 14 studies that examined 796 videos with 59.7 hr of content and 47.5 million views. Among the 14 studies that evaluated the video content quality, 17 different quality assessment tools were used, only three of which were externally validated (Global Quality Score, modified DISCERN score, and JAMA score). Per global assessment rating of video quality, 11/13 (85%) studies concluded the overall video quality as poor.

Conclusions: Overall, the educational content quality of YouTube videos evaluated in the literature accessible as an educational resource regarding perioperative anesthesia was poor. While these videos are in demand, their impact on patient and trainee education remains unclear. A standardized methodology for evaluating online videos is merited to improve future reporting. A peer-reviewed approach to online open-access videos is needed to support patient and trainee education in anesthesia.

Study registration: Open Science Framework ( https://osf.io/ajse9 ); first posted, 1 May 2023.

背景:YouTube(谷歌有限责任公司,美国加利福尼亚州圣布鲁诺)等在线视频共享平台已成为健康信息的重要来源。我们试图对评估 YouTube 上围术期麻醉视频整体质量的研究进行系统性回顾:我们检索了 Embase、MEDLINE 和 Ovid 数据库中从数据库开始到 2023 年 5 月 1 日发表的文章。我们纳入了将 YouTube 视频作为围术期麻醉信息来源进行评估的主要研究。我们排除了非英文发表的研究以及评估急性或慢性疼痛的研究。由两名审稿人对研究进行筛选并提取一式两份的数据。我们根据文献中发表的社交媒体框架对研究质量进行了评估。我们采用了描述性统计方法,以平均值、标准差、范围和 n/ 总 N (%) 来报告结果:在 8908 篇引用文献中,我们发现了 14 项研究,这些研究共研究了 796 个视频,内容长达 59.7 小时,观看次数达 4750 万次。在这 14 项评估视频内容质量的研究中,共使用了 17 种不同的质量评估工具,其中只有三种工具经过外部验证(全球质量评分、修改后的 DISCERN 评分和 JAMA 评分)。根据视频质量的总体评估评级,11/13(85%)项研究认为视频的总体质量较差:总体而言,作为围术期麻醉教育资源的YouTube视频的教育内容质量较差。虽然这些视频需求量很大,但它们对患者和受训人员教育的影响仍不明确。为了改进未来的报告,我们需要一种标准化的方法来评估在线视频。需要对在线开放视频进行同行评审,以支持麻醉领域的患者和受训人员教育:开放科学框架 ( https://osf.io/ajse9 ); 首次发布,2023 年 5 月 1 日。
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引用次数: 0
Assessing the accuracy of data reporting in erector spinae plane block clinical trials: a Granularity-Related Inconsistency of Means test analysis. 评估竖脊肌平面阻滞临床试验中数据报告的准确性:与粒度相关的均值不一致测试分析。
IF 3.4 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2024-09-01 Epub Date: 2024-06-03 DOI: 10.1007/s12630-024-02772-8
Alessandro De Cassai, Sofia Gazzea, Annalisa Boscolo, Tommaso Pettenuzzo, Paolo Navalesi
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引用次数: 0
Correction: Prevention of hypotension after induction of general anesthesia using point-of-care ultrasound to guide fluid management: a randomized controlled trial. 更正:利用护理点超声波指导液体管理,预防全身麻醉诱导后的低血压:随机对照试验。
IF 3.4 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2024-09-01 DOI: 10.1007/s12630-024-02779-1
Elad Dana, Cristian Arzola, James S Khan
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引用次数: 0
Is constant vigilance a realistic expectation for anesthesiologists? 对麻醉医生来说,时刻保持警惕是否是一种现实的期望?
IF 3.4 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2024-09-01 Epub Date: 2024-06-25 DOI: 10.1007/s12630-024-02787-1
Yuqi Gu, M Dylan Bould
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引用次数: 0
Blood loss measurement in liver transplantation: validation of an estimating equation. 肝脏移植中的失血量测量:估算方程的验证。
IF 3.4 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2024-09-01 Epub Date: 2024-08-27 DOI: 10.1007/s12630-024-02820-3
François M Carrier, Éva Amzallag, Martin Girard, Emmanuelle Fortin, Émilie Marceau, Helen Trottier, Michaël Chassé
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引用次数: 0
Channelled versus nonchannelled Macintosh videolaryngoscope blades in patients with a cervical collar: a randomized controlled noninferiority trial. 在佩戴颈圈的患者中使用有通道与无通道 Macintosh 视频喉镜刀片:随机对照非劣效性试验。
IF 3.4 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2024-09-01 Epub Date: 2024-05-22 DOI: 10.1007/s12630-024-02769-3
Kyung Won Shin, Sang Phil Lee, Taeyup Kim, Seungeun Choi, Yoon Jung Kim, Hee-Pyoung Park, Hyongmin Oh

Purpose: Channelled blades have the advantage of avoiding stylet use and potential airway injury during videolaryngoscopic intubation. Nevertheless, the effectiveness of channelled Macintosh-type blades has not yet been fully established. We sought to assess the utility of channelled Macintosh-type blades for videolaryngoscopic intubation under cervical spine immobilization.

Methods: We conducted a randomized controlled noninferiority trial in neurosurgical patients with a difficult airway simulated by a cervical collar. Videolaryngoscopic intubation with a reinforced tracheal tube was performed using a channelled Macintosh-type blade without a stylet (channelled group, n = 130) or a nonchannelled Macintosh-type blade with a stylet (nonchannelled group, n = 131). The primary outcome was intubation success rate. Secondary outcomes included time to intubation and incidence or severity of intubation-related complications (subglottic, lingual, and dental injuries; bleeding; sore throat; and hoarseness).

Results: The initial intubation success rate was 98% and 99% in the channelled and nonchannelled groups, respectively, showing the noninferiority of the channelled group (difference in proportions -0.8%; 95% confidence interval [CI], -4.8% to 2.9%; predefined noninferiority margin, -5%; P = 0.62). Fewer participants in the channelled group had subglottic injuries than in the nonchannelled group (32% [32/100] vs 57% [54/95]; difference in proportions, -25%; 95% CI, -39% to -11%; P < 0.001). There were no significant differences between the two groups in the overall intubation success rate, time to intubation, and incidence or severity of other intubation-related complications.

Conclusions: For videolaryngoscopic intubation in patients with a cervical collar, channelled Macintosh-type blades are an alternative to nonchannelled Macintosh-type blades, with a noninferior initial intubation success rate and a lower incidence of subglottic injury.

Study registration: CRIS.nih.go.kr ( KCT0005186 ); first submitted 29 June 2020.

目的:导管刀片的优点是在视频喉镜插管过程中避免使用支架和潜在的气道损伤。然而,Macintosh 型导流刀片的有效性尚未完全确定。我们试图评估在颈椎固定的情况下视频咽喉镜插管时使用导流式 Macintosh 型刀片的效用:我们在神经外科患者中进行了一项随机对照非劣效性试验,患者使用颈椎项圈模拟困难气道。使用不带支架的Macintosh型通道式刀片(通道式组,n = 130)或带支架的Macintosh型非通道式刀片(非通道式组,n = 131),用加强型气管导管进行视频喉镜插管。主要结果是插管成功率。次要结果包括插管时间和插管相关并发症的发生率或严重程度(声门下、舌部和牙齿损伤;出血;咽喉痛;声音嘶哑):导管组和非导管组的初始插管成功率分别为 98% 和 99%,显示出导管组的非劣效性(比例差异 -0.8%;95% 置信区间 [CI],-4.8% 至 2.9%;预定义非劣效差值,-5%;P = 0.62)。与非通道组相比,通道组出现声门下损伤的人数更少(32% [32/100] vs 57% [54/95];比例差异,-25%;95% 置信区间 [CI],-39% 至 -11%;P 结论:视频喉镜插管术与非通道组相比,其效果更佳:对于有颈椎项圈的患者进行视频喉镜插管,带导管的Macintosh型刀片是非带导管Macintosh型刀片的替代品,其初始插管成功率和声门下损伤发生率均低于非带导管Macintosh型刀片:研究注册:CRIS.nih.go.kr ( KCT0005186 ); 2020年6月29日首次提交。
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引用次数: 0
Association of pain assessment method and postepidural pain levels in labouring patients with limited English proficiency. 英语水平有限的产妇疼痛评估方法与硬膜外麻醉后疼痛程度的关系。
IF 3.4 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2024-09-01 Epub Date: 2024-07-29 DOI: 10.1007/s12630-024-02802-5
Won Lee, Ronald B George, Alicia Fernandez
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引用次数: 0
期刊
Canadian Journal of Anesthesia-Journal Canadien D Anesthesie
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