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Institutional Experience Introducing Portable Capnography Intrahospital Transport of Ventilated Patients With Congenital Heart Disease. 先心病通气患者院内输送便携式血管造影的机构经验。
Pub Date : 2026-01-14 DOI: 10.1213/ane.0000000000007940
Morgan L Brown,David Whiting,James A DiNardo,Viviane G Nasr
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引用次数: 0
Site-Specific Blockade of LPA-TRPV1 Interaction at K710 Residue Influences on Myocardial Ischemia/Reperfusion Injury in Ex Vivo Mouse Hearts. LPA-TRPV1位点特异性阻断K710残基相互作用对离体小鼠心脏缺血/再灌注损伤的影响
Pub Date : 2026-01-14 DOI: 10.1213/ane.0000000000007907
Muge Qile,Zhaofei Luo,Chao Wu,Xueying Cheng,Yu Zhang,Liu Liu,Qingtong Wang,Ye Zhang,Eric R Gross,Shufang He
BACKGROUNDMyocardial ischemia/reperfusion (I/R) injury commonly occurs in patients undergoing cardiac or noncardiac surgeries, increasing perioperative mortality risk. Although numerous endogenous mediators released during I/R contribute to myocardial damage, their mechanisms require further elucidation. We investigated whether lysophosphatidic acid (LPA), a bioactive phospholipid, mediates myocardial I/R injury by interacting with cardiac transient receptor potential vanilloid 1 (TRPV1).METHODSA TRPV1K710N knock-in mouse model was generated by CRISPR/Cas9, introducing a point mutation at K710, the known LPA-binding site on TRPV1. Langendorff perfused isolated hearts from TRPV1K710N and wild-type (WT) mice underwent global I/R injury with or without exogenous LPA (10 μM). Myocardial infarct size, coronary effluent LDH levels, and mitochondrial ultrastructure/function were assessed. Additionally, H9c2 cardiomyocytes were transfected with a pCMV6-entry plasmid carrying TRPV1-K710N or TRPV1-WT for mitochondrial calcium influx and cell viability assays. The V1-Cal peptide (1μM), targeting the K710 region, was applied ex vivo and in vitro to block LPA-TRPV1 interaction.RESULTSTRPV1K710N hearts exhibited resistance to global I/R injury versus WT hearts, with reduced infarct size (28.3 ± 2.4% vs 39.9 ±2.3%, respectively, P= 0006), lower LDH levels, and attenuated mitochondrial damage. Exogenous LPA exacerbated I/R injury in WT hearts, increasing infarct size (63.7 ± 1.2% vs vehicle: 38.4 ± 2.4%; P <.0001), LDH release, and mitochondrial damage. TRPV1K710N hearts were resistant to LPA-induced injury, with no significant increase in infarct size after LPA treatment. Exogenous LPA induced pronounced swelling in mitochondria isolated from WT hearts, while mitochondria from TRPV1K710N hearts showed resistance to LPA challenge. In H9c2 cells, LPA significantly decreased viability in rTRPV1-WT cells and elevated mitochondrial calcium influx relative to rTRPV1-K710N cells. V1-Cal peptide attenuated LPA-mediated myocardial injury in WT hearts and reduced mitochondrial calcium overload in H9c2 cells.CONCLUSIONSBlockade of the TRPV1 K710 site by K710N mutation or V1-Cal peptide mitigates LPA-mediated myocardial injury and mitochondrial damage/dysfunction in isolated mouse hearts. Targeting the cardiac LPA-TRPV1 interaction represents a promising therapeutic strategy against perioperative myocardial injury.
背景心肌缺血/再灌注(I/R)损伤常见于心脏或非心脏手术患者,增加围手术期死亡风险。虽然在I/R过程中释放的许多内源性介质有助于心肌损伤,但其机制有待进一步阐明。我们研究了溶血磷脂酸(LPA)是否通过与心脏瞬时受体电位香草蛋白1 (TRPV1)相互作用介导心肌I/R损伤。方法利用CRISPR/Cas9技术建立TRPV1K710N敲入小鼠模型,在TRPV1上已知的lpa结合位点K710上引入点突变。Langendorff灌注TRPV1K710N和野生型(WT)小鼠的离体心脏,在有或没有外源性LPA (10 μM)的情况下进行全局I/R损伤。评估心肌梗死面积、冠状动脉流出液LDH水平和线粒体超微结构/功能。此外,用携带TRPV1-K710N或TRPV1-WT的pcmv6进入质粒转染H9c2心肌细胞,进行线粒体钙内流和细胞活力测定。针对K710区域的V1-Cal肽(1μM)在体内和体外应用阻断LPA-TRPV1相互作用。结果与WT相比,strpv1k710n心脏表现出对全局I/R损伤的抵抗,梗死面积减小(分别为28.3±2.4%和39.9±2.3%,P= 0006), LDH水平降低,线粒体损伤减轻。外源性LPA加重了WT心脏的I/R损伤,增加了梗死面积(63.7±1.2% vs .对照组:38.4±2.4%;P < 0.0001)、LDH释放和线粒体损伤。TRPV1K710N心脏对LPA诱导的损伤有抵抗性,LPA治疗后梗死面积无显著增加。外源性LPA诱导WT心脏分离的线粒体明显肿胀,而TRPV1K710N心脏的线粒体对LPA的攻击表现出抵抗性。在H9c2细胞中,与rTRPV1-K710N细胞相比,LPA显著降低了rTRPV1-WT细胞的活力,增加了线粒体钙内流。V1-Cal肽可减轻lpa介导的WT心脏心肌损伤,减少H9c2细胞线粒体钙超载。结论通过K710N突变或V1-Cal肽阻断TRPV1 K710位点可减轻lpa介导的离体小鼠心脏心肌损伤和线粒体损伤/功能障碍。靶向心脏LPA-TRPV1相互作用是一种很有前途的治疗围手术期心肌损伤的策略。
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引用次数: 0
Risk Factors and Prediction of Chronic Postsurgical Pain Among Patients With Distal Lower Extremity Fracture: Cohort Analysis. 下肢远端骨折患者术后慢性疼痛的危险因素及预测:队列分析。
Pub Date : 2026-01-14 DOI: 10.1213/ane.0000000000007902
Yangzi Zhu,Ying Wu,Kailun Gao,Yuning Sun,Junfeng Hu,Liwei Wang,Jun-Li Cao
BACKGROUNDThe surgical interventions aimed at fracture repair are often accompanied by chronic postsurgical pain (CPSP), which is associated with depression, impaired quality of life, and increased societal burden. This phenomenon is particularly understudied in young patients with distal lower extremity fracture. Developing a scalable and accurate predictive model could improve postoperative care by enabling early detection of high-risk patients and guiding personalized pain management strategies.METHODSThis study collected in-hospital medical records and conducted follow-up for all patients over a 1-year period. We developed a predictive model through a 3-stage approach involving Least Absolute Shrinkage and Selection Operator (LASSO) regression, information gain analysis, and multivariable logistic regression, followed by model validation. Using the Shinyapps.io platform to build a webpage risk calculator for the final prediction model.RESULTSThe final cohort included 818 patients: 38.4% of whom experienced CPSP, and 18.2% of patients with CPSP developed neuropathic pain. There are 6 independent variables associated with CPSP: postoperative analgesic technique, fixation type, preoperative clinical management, and numerical rating scale (NRS) score on the day of the visit and postoperative day 1. The optimism-corrected area under the receiver operating curve for the development cohort and validation cohort were 0.872 and 0.838, respectively, and this model demonstrated good calibration and clinical utility. A web-based predictive nomogram was established by integrating machine learning-based big data variable screening with the interpretability of traditional logistic regression.CONCLUSIONSThis study demonstrates that pain management strategies, surgical approaches, and patient psychological factors collectively influence the development of CPSP. By integrating machine learning-based big data variable screening with the interpretability of traditional logistic regression, we developed a web-based predictive nomogram capable of identifying early CPSP risk at hospital discharge, thereby improving accessibility to transitional pain care interventions.
背景:针对骨折修复的手术干预通常伴随着慢性术后疼痛(CPSP),这与抑郁、生活质量下降和社会负担增加有关。在下肢远端骨折的年轻患者中,这种现象的研究尤其不足。开发可扩展和准确的预测模型可以通过早期发现高危患者和指导个性化疼痛管理策略来改善术后护理。方法收集住院病历,随访1年以上。我们通过最小绝对收缩和选择算子(LASSO)回归、信息增益分析和多变量逻辑回归三阶段方法建立了预测模型,然后进行模型验证。使用Shinyapps。IO平台构建网页风险计算器,进行最终预测模型。结果最终纳入818例患者,其中38.4%的患者发生CPSP, 18.2%的患者发生神经性疼痛。与CPSP相关的自变量有6个:术后镇痛技术、固定方式、术前临床管理、就诊当日及术后第1天的数值评定量表(NRS)评分。开发组和验证组受试者工作曲线下的乐观校正面积分别为0.872和0.838,该模型具有良好的校准性和临床实用性。将基于机器学习的大数据变量筛选与传统逻辑回归的可解释性相结合,建立了基于网络的预测模态图。结论疼痛管理策略、手术方式和患者心理因素共同影响CPSP的发展。通过将基于机器学习的大数据变量筛选与传统逻辑回归的可解释性相结合,我们开发了一个基于网络的预测nomogram,能够在出院时识别早期CPSP风险,从而提高过渡性疼痛护理干预的可及性。
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引用次数: 0
Whole Blood versus Components for Transfusion in Trauma and Life-Threatening Hemorrhage-Unresolved Issues. 全血与输血成分在创伤和危及生命的出血-未解决的问题。
Pub Date : 2026-01-13 DOI: 10.1213/ane.0000000000007923
Phuong-Lan Thi Nguyen,Catherine Marcucci,Majed Refaai,Akua Asante,Nicholas Tong,Neil Blumberg
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引用次数: 0
LEMONS: Incorporating Stiffness of Submental/Submandibular Space into Difficult Airway Assessment. 柠檬:将颏下/下颌下间隙的硬度纳入困难气道评估。
Pub Date : 2026-01-13 DOI: 10.1213/ane.0000000000007896
Chen-Hwan Cherng
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引用次数: 0
Medical Society Guideline Writing: The Why and How. 医学学会指南写作:为什么和如何。
Pub Date : 2026-01-13 DOI: 10.1213/ane.0000000000007903
Craig S Jabaley,Mark E Nunnally,Brigid C Flynn
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引用次数: 0
Prolonged Fasting and Patient-Centered Outcomes: When Science Meets Common Sense. 延长禁食和以病人为中心的结果:当科学遇到常识。
Pub Date : 2026-01-13 DOI: 10.1213/ane.0000000000007935
Alexander Nagrebetsky,Girish P Joshi
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引用次数: 0
Does a Research Paper Always Need a Hypothesis? 研究论文总是需要假设吗?
Pub Date : 2026-01-13 DOI: 10.1213/ane.0000000000007932
Jean Charchaflieh,Avery Tung
{"title":"Does a Research Paper Always Need a Hypothesis?","authors":"Jean Charchaflieh,Avery Tung","doi":"10.1213/ane.0000000000007932","DOIUrl":"https://doi.org/10.1213/ane.0000000000007932","url":null,"abstract":"","PeriodicalId":7799,"journal":{"name":"Anesthesia & Analgesia","volume":"216 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145961590","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Billing Follow-Up for Single-Shot Nerve Blocks: A Documentation Solution to Preserve Patient Oversight and Revenue. 单针神经阻滞的账单跟踪:保存患者监督和收入的文档解决方案。
Pub Date : 2026-01-13 DOI: 10.1213/ane.0000000000007937
Veena Graff,Allen Yang,Jacklynn Sztain,Engy Said
{"title":"Billing Follow-Up for Single-Shot Nerve Blocks: A Documentation Solution to Preserve Patient Oversight and Revenue.","authors":"Veena Graff,Allen Yang,Jacklynn Sztain,Engy Said","doi":"10.1213/ane.0000000000007937","DOIUrl":"https://doi.org/10.1213/ane.0000000000007937","url":null,"abstract":"","PeriodicalId":7799,"journal":{"name":"Anesthesia & Analgesia","volume":"68 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145961592","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Detecting Early Oxygenator Failure During Cardiopulmonary Bypass: An Evaluation of Uncalibrated Measurements of In-Line Po2. 体外循环过程中早期氧合器衰竭的检测:在线Po2未校准测量的评估。
Pub Date : 2026-01-13 DOI: 10.1213/ane.0000000000007933
Micheal W Vespe,Ronald A Kahn
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引用次数: 0
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Anesthesia & Analgesia
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