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[Summary of the best evidence for early rehabilitation of ICU-acquired swallowing dysfunction]. [重症监护下获得性吞咽功能障碍早期康复的最佳证据摘要]。
Q3 Medicine Pub Date : 2025-08-01 DOI: 10.3760/cma.j.cn121430-20250319-00276
Qianqian Peng, Ruixiang Sun, Xiaopan Xu, Ke Fang, Haijiao Jiang, Xiancui Zhang

Objective: To systematically search and integrate the best evidence for early rehabilitation of ICU-acquired swallowing dysfunction (ICU-ASD) using evidence-based medicine methods, providing high-quality evidence-based support for intensive care unit (ICU) healthcare professionals in implementing early rehabilitation assessment and intervention strategies for ICU-ASD.

Methods: The systematic search was conducted according to the "6S" pyramid evidence model. Multiple authoritative databases and resources were comprehensively searched, including: National Guideline Clearinghouse (NGC), National Institute for Health and Care Excellence (NICE), Canadian Medical Association Clinical Practice Guidelines Library (CMACPGL), New Zealand Guidelines Group (NZGG), Guidelines International Network (GIN), Registered Nurses' Association of Ontario (RNAO), Scottish Intercollegiate Guidelines Network (SIGN), PubMed/Medline, Cochrane Library, Embase, Cumulative Index to Nursing and Allied Health Literature (CINAHL), Web of Science, JBI Evidence-Based Health Care Database, Physiotherapy Evidence Database (PEDro), Chinese Medical Pulse Guidelines Website, SinoMed, CNKI, Wanfang Data, UpToDate, BMJ Best Practice, and professional association websites. The search encompassed guidelines, expert consensus statements, original studies [including cohort studies, quasi-experimental studies, and randomized controlled trials (RCT)], systematic reviews, and evidence summaries related to the prevention and management of ICU-ASD. The search period was limited from the inception of each database to November 30, 2024. The best evidence for early rehabilitation of ICU-ASD was summarized. The quality assessment of the literature and the extraction and synthesis of evidence were independently performed by two researchers with expertise in evidence-based medicine methodology.

Results: A total of 16 articles were included, consisting of 1 clinical decision-making study, 1 cohort study, 2 guidelines, 2 RCTs, 6 systematic reviews, 1 evidence summary, 2 expert consensuses, and 1 expert opinion. Following quality assessment, all 16 articles were incorporated into the analysis. For the early rehabilitation of ICU-ASD, five major themes were ultimately identified and 25 best evidence items were summarized, focusing on: multidisciplinary collaboration, swallowing screening and assessment, rehabilitation interventions, dietary and nutritional management, and oral hygiene.

Conclusions: The evidence summary provides individualized rehabilitation strategies for ICU-ASD patients, but their implementation still needs to be adapted to China's clinical practice context and patient preferences.

目的:应用循证医学方法系统检索和整合ICU-获得性吞咽功能障碍(ICU- asd)早期康复的最佳证据,为ICU医护人员实施ICU- asd早期康复评估和干预策略提供高质量的循证支持。方法:根据“6S”金字塔证据模型进行系统检索。全面检索多个权威数据库和资源,包括:国家指南信息中心(NGC)、国家健康与护理卓越研究所(NICE)、加拿大医学协会临床实践指南图书馆(CMACPGL)、新西兰指南小组(NZGG)、指南国际网络(GIN)、安大略省注册护士协会(RNAO)、苏格兰校际指南网络(SIGN)、PubMed/Medline、Cochrane图书馆、Embase、护理和联合健康文献累积索引(CINAHL)、科学网、JBI循证卫生保健数据库、物理治疗循证数据库(PEDro)、中医脉脉指南网、中国医学信息网、中国知网、万方数据、UpToDate、BMJ最佳实践、专业协会网站等。检索包括指南、专家共识声明、原始研究[包括队列研究、准实验研究和随机对照试验(RCT)]、系统评价和与ICU-ASD预防和管理相关的证据摘要。搜索周期从每个数据库建立之初到2024年11月30日。总结了ICU-ASD早期康复的最佳证据。文献的质量评估以及证据的提取和合成由两位具有循证医学方法学专业知识的研究人员独立完成。结果:共纳入文献16篇,包括1篇临床决策研究、1篇队列研究、2篇指南、2篇随机对照试验、6篇系统综述、1篇证据总结、2篇专家共识、1篇专家意见。在质量评估之后,所有16篇文章被纳入分析。对于ICU-ASD的早期康复,最终确定了5个主要主题,并总结了25个最佳证据项,重点是:多学科合作、吞咽筛查和评估、康复干预、饮食和营养管理、口腔卫生。结论:证据总结为ICU-ASD患者提供了个性化的康复策略,但其实施仍需根据中国的临床实践背景和患者偏好进行调整。
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引用次数: 0
[The advances in the application of peripheral perfusion index in patients with septic shock]. 外周血灌注指数在感染性休克患者中的应用进展
Q3 Medicine Pub Date : 2025-08-01 DOI: 10.3760/cma.j.cn121430-20250322-00287
Jiapan An, Xinqi Xu, Tingyu Yang, Bin Li, Zhimin Dou

Septic shock, a prevalent critical condition in intensive care units (ICU) and a major cause of patient mortality, is fundamentally attributed to microcirculatory dysfunction. Traditional macrocirculatory parameters are often insufficiently sensitive to reflect microcirculatory status. Consequently monitoring peripheral microcirculatory function holds crucial significance for assessing disease progression and evaluating therapeutic efficacy in septic shock. The peripheral perfusion index (PPI), obtained from a standard pulse oximeter, is based on photoplethysmography (PPG). It calculates the differential absorption of red and infrared light emitted by the sensor between pulsatile arterial blood and non-pulsatile tissue, enabling real-time reflection of peripheral perfusion and thus providing non-invasive, continuous monitoring of microcirculatory function. Although often overlooked compared to other ICU monitoring parameters, PPI has demonstrated notable clinical advances in septic shock management. Specifically, in early identification, PPI combined with sequential organ failure assessment (SOFA) predicts disease progression, with its dynamic changes further aiding prognosis assessment. During fluid resuscitation, it guides fluid responsiveness evaluation and serves as a therapeutic target to optimize strategies. In circulatory support, it assists in determining vasoactive drug initiation timing and dosage titration. Additionally, PPI aids mechanical ventilation weaning and organ dysfunction evaluation. This article reviews the principles, influencing factors, and clinical application advances of PPI in septic shock, aiming to provide clinicians with a basis for individualized intervention, improved patient outcomes, and the advancement of precision medicine in septic shock management.

感染性休克是重症监护病房(ICU)常见的危重疾病,也是患者死亡的主要原因,其主要原因是微循环功能障碍。传统的大循环参数往往不够灵敏,不能反映微循环状态。因此,监测外周微循环功能对评估感染性休克的病情进展和疗效具有重要意义。外周灌注指数(PPI),由标准脉搏血氧计获得,是基于光容积脉搏波描记(PPG)。它计算传感器发出的红光和红外光在脉动动脉血和非脉动组织之间的差异吸收,从而实时反映外周灌注,从而提供无创、连续的微循环功能监测。虽然与其他ICU监测参数相比,PPI经常被忽视,但PPI在感染性休克管理中显示出显着的临床进展。具体而言,在早期诊断中,PPI联合序贯器官衰竭评估(SOFA)预测疾病进展,其动态变化进一步有助于预后评估。在液体复苏过程中,它指导液体反应性评估,并作为优化策略的治疗靶点。在循环支持方面,它有助于确定血管活性药物的起始时间和剂量滴定。此外,PPI有助于机械通气脱机和器官功能障碍评估。本文就感染性休克中PPI的原理、影响因素及临床应用进展进行综述,旨在为临床医生进行个体化干预,改善患者预后,推进精准医学在感染性休克治疗中的应用提供依据。
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引用次数: 0
[Clinical applications and research progress of muscle ultrasound in critically ill patients]. [肌肉超声在危重患者中的临床应用及研究进展]。
Q3 Medicine Pub Date : 2025-08-01 DOI: 10.3760/cma.j.cn121430-20250307-00224
Ling Lei, Jun Qiu, Tongjuan Zou, Yi Li, Ran Zhou, Yao Qin, Wanhong Yin

Critically ill patients often experience significant skeletal muscle wasting due to prolonged bed rest, metabolic disorders, inflammatory responses and malnutrition, which affects the patient's mobility and may also lead to increased mortality. Timely and accurate assessment of muscle status is important for optimizing treatment strategies and improving patient prognosis. There are various limitations in the current methods of assessing muscle mass, and muscle ultrasound, as a noninvasive, convenient, low-cost and suitable technique for bedside monitoring, has received increasing attention for its application in muscle assessment of critically ill patients. However, there are still a number of challenges in its practical application, such as the lack of uniform standards for the measurement method, the high dependence on the operation, and the reproducibility of the data that needs to be optimized, and so on. The aim of this article is to systematize the research progress of muscle ultrasound in muscle assessment of critically ill patients, and to discuss the advantages and limitations of its clinical application, in order to provide a scientific basis for future research and clinical practice.

由于长时间卧床休息、代谢紊乱、炎症反应和营养不良,危重患者经常出现明显的骨骼肌萎缩,这影响了患者的活动能力,也可能导致死亡率增加。及时准确地评估肌肉状态对优化治疗策略和改善患者预后具有重要意义。现有的肌肉质量评估方法存在诸多局限性,而肌肉超声作为一种无创、方便、低成本、适合床边监测的技术,在危重患者肌肉质量评估中的应用越来越受到重视。但其在实际应用中仍面临诸多挑战,如测量方法缺乏统一的标准,对操作的依赖性高,数据的再现性需要优化等。本文旨在对肌肉超声在危重病人肌肉评估中的研究进展进行系统梳理,并探讨其临床应用的优势与局限性,以期为今后的研究和临床实践提供科学依据。
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引用次数: 0
[Dynamics of histone acetylation modification in sepsis]. [脓毒症中组蛋白乙酰化修饰的动力学]。
Q3 Medicine Pub Date : 2025-08-01 DOI: 10.3760/cma.j.cn121430-20241113-00931
Ruxin Liu, Yujiao Tang, Xue Bai, Mengfei Chen, Ling Zhang

Sepsis is a life-threatening organ dysfunction caused by the host's dysregulated response to infection, with a complex pathogenesis and high mortality rate. Currently, there are no clear and effective treatment drugs available. Epigenetic modification serves as a major mechanism regulating gene expression under pathological and physiological conditions, and it has been shown to play a critical role in regulating the occurrence and development of sepsis. Histone acetylation modification, as a sophisticated epigenetic modification mechanism, plays a crucial regulatory role in many aspects of life. It can jointly regulate the acetylation status of histones through histone acetyltransferase (HAT) and histone deacetylase (HDAC), thereby changing DNA expression and dynamically regulating sepsis related gene expression at the epigenetic level. Previous studies have shown that histone acetylation can participate in the progression of sepsis by regulating inflammatory mediators, nuclear factor-ΚB (NF-ΚB) signaling pathway, autophagy, efferocytosis, ferroptosis, pyroptosis. These mechanisms are promising targets for novel sepsis treatments. In addition, with the deepening of research, it has been found that various selective/non selective histone deacetylase inhibitors (HDACI) can regulate histone acetylation status by acting on different HDAC targets, which has been shown to alleviate organ damage caused by sepsis and improve prognosis in septic animal models. This article further summarizes the role and potential applications of histone acetylation in sepsis, providing new ideas for the treatment of sepsis.

脓毒症是由宿主对感染反应失调引起的危及生命的器官功能障碍,其发病机制复杂,死亡率高。目前,还没有明确有效的治疗药物。表观遗传修饰是病理生理条件下调控基因表达的主要机制,在脓毒症的发生发展中起着至关重要的调节作用。组蛋白乙酰化修饰作为一种复杂的表观遗传修饰机制,在生命的许多方面起着至关重要的调节作用。它可以通过组蛋白乙酰转移酶(histone acetyltransferase, HAT)和组蛋白去乙酰化酶(histone deacetylase, HDAC)共同调节组蛋白的乙酰化状态,从而在表观遗传水平上改变DNA表达,动态调节脓毒症相关基因表达。既往研究表明,组蛋白乙酰化可通过调节炎症介质、核因子-ΚB (NF-ΚB)信号通路、自噬、efferocytosis、铁亡、焦亡参与脓毒症的进展。这些机制是新的脓毒症治疗的有希望的靶点。此外,随着研究的深入,发现各种选择性/非选择性组蛋白去乙酰化酶抑制剂(HDACI)可通过作用于不同的HDAC靶点调节组蛋白乙酰化状态,在脓毒症动物模型中已被证明可减轻脓毒症引起的器官损伤,改善预后。本文进一步总结组蛋白乙酰化在脓毒症中的作用及潜在应用,为脓毒症的治疗提供新的思路。
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引用次数: 0
[Design and application of a nasogastric tube auxiliary pushing device and intubation kit]. 一种鼻胃管辅助推管装置及插管套件的设计与应用。
Q3 Medicine Pub Date : 2025-08-01 DOI: 10.3760/cma.j.cn121430-20250510-00451
Qiao He, Xiaoyun Zhang, Yinfen Xiao, Hua Huang, Junyao Fan

As a common clinical treatment technique, nasogastric tube insertion plays an important role in assisting in disease diagnosis and treatment, and promoting patient recovery. Nasogastric tubes currently used in clinical practice are packaged individually without accompanying sterile materials, hence additional materials need to be prepared before operation, which is complicated and prone to omission, consumes clinical manpower, and increases the proportion of departmental consumption. The operator needs to hold the nasogastric tube with one hand and place it with the other hand during operation, the lack of auxiliary tool for uniformly controlling the placement of gastric tubes may easily lead to tube failure due to patient intolerance, agitation, or uneven force exerted by the operator, and improper force may even result in violent tube placement, leading to adverse outcomes such as mucosal bleeding and aspiration into the airway. Medical staff of intensive care unit of department of infectious diseases of Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology have designed a nasogastric tube auxiliary pushing device and an intubation kit to overcome the above problems, and obtaining National Utility Model Patent of China (patent number: ZL 2024 2 0300856.X). The device consists of two parts: a nasogastric tube auxiliary pushing device and a nasogastric tube insertion kit. Nasogastric tube auxiliary pushing device mainly consists of a nasogastric tube with guide wire, a circular wire harness, and a booster base with a pushing element. The tube insertion kit includes sterile treatment trays, main placement slots, and other operational accessory slots. The new nasogastric tube auxiliary pushing device and tube insertion kit integrates packaging and portable design, providing stable and uniform assistance for safe insertion of nasogastric tubes by a single person, which is able to reduce the occurrence of complications, ensure patient safety, improve patient comfort, and reduce occupational exposure risks, making it suitable for clinical promotion.

鼻胃管置入术作为临床常用的治疗技术,在辅助疾病诊断和治疗、促进患者康复等方面发挥着重要作用。目前临床上使用的鼻胃管都是单件包装,没有附带无菌材料,手术前需要准备额外材料,操作复杂,容易遗漏,消耗临床人力,增加科室消耗比例。操作时,操作者需要一手握住鼻胃管,另一手放置,缺乏辅助工具统一控制胃管的放置,容易因患者不耐受、激动或操作者施力不均匀而导致管失效,施力不当甚至可能导致猛烈置管,导致粘膜出血、误吸入气道等不良后果。华中科技大学同济医学院同济医院传染病科重症监护室医护人员针对上述问题,设计了一种鼻胃管辅助推管装置和插管套件,并获得了中国国家实用新型专利(专利号:ZL 2024 2 0300856.X)。该装置由鼻胃管辅助推入装置和鼻胃管插入套件两部分组成。鼻胃管辅助推进装置主要由带导丝的鼻胃管、圆形线束、带推进元件的助力底座组成。管插入套件包括无菌处理托盘,主要放置槽,和其他操作附件槽。新型鼻胃管辅助推入装置及置管套件集成了包装和便携设计,可为一人安全置管提供稳定、均匀的辅助,减少并发症的发生,保证患者安全,提高患者舒适度,降低职业暴露风险,适合临床推广。
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引用次数: 0
[Proteomics reveals biomarkers for sepsis-associated acute kidney injury: a prospective multicenter cohort study]. 蛋白质组学揭示了脓毒症相关急性肾损伤的生物标志物:一项前瞻性多中心队列研究。
Q3 Medicine Pub Date : 2025-08-01 DOI: 10.3760/cma.j.cn121430-20250317-00253
Weimin Zhu, Nanjin Chen, Hanzhi Dai, Cuicui Dong, Yubin Xu, Qi Chen, Fangyu Yu, Cheng Zheng, Chao Zhang, Sheng Zhang, Yinghe Xu, Yongpo Jiang
<p><strong>Objective: </strong>To identify and validate novel biomarkers for the early diagnosis of sepsis-associated acute kidney injury (SA-AKI) and precise continuous renal replacement therapy (CRRT) using proteomics.</p><p><strong>Methods: </strong>A prospective multicenter cohort study was conducted. Patients with sepsis admitted to five hospitals in Taizhou City of Zhejiang Province from April 2019 to December 2021 were continuously enrolled, based on the occurrence of acute kidney injury (AKI). Sepsis patients were divided into SA-AKI group and non-SA-AKI group, and healthy individuals who underwent physical examinations during the same period were used as control (NC group). Peripheral blood samples from participants were collected for protein mass spectrometry analysis. Differentially expressed proteins were identified, and functional enrichment analysis was conducted on these proteins. The levels of target proteins were detected by enzyme linked immunosorbent assay (ELISA), and the predictive value of target protein for SA-AKI were evaluated by receiver operator characteristic curve (ROC curve). Additionally, sepsis patients and healthy individuals were selected from one hospital to externally verify the expression level of the target protein and its predictive value for SA-AKI, as well as the accuracy of CRRT treatment.</p><p><strong>Results: </strong>A total of 37 patients with sepsis (including 19 with AKI and 18 without AKI) and 31 healthy individuals were enrolled for proteomic analysis. Seven proteins were identified with significantly differential expression between the SA-AKI group and non-SA-AKI group: namely cystatin C (CST3), β <sub>2</sub>-microglobulin (β <sub>2</sub>M), insulin-like growth factor-binding protein 4 (IGFBP4), complement factor I (CFI), complement factor D (CFD), CD59, and glycoprotein prostaglandin D2 synthase (PTGDS). Functional enrichment analysis revealed that these proteins were involved in immune response, complement activation, coagulation cascade, and neutrophil degranulation. ELISA results demonstrated specific expression of each target protein in the SA-AKI group. Additionally, 65 patients with sepsis (38 with AKI and 27 without AKI) and 20 healthy individuals were selected for external validation of the 7 target proteins. ELISA results showed that there were statistically significant differences in the expression levels of CST3, β <sub>2</sub>M, IGFBP4, CFD, and CD59 between the SA-AKI group and non-SA-AKI group. ROC curve analysis indicated that the area under the curve (AUC) values of CST3, β <sub>2</sub>M, IGFBP4, CFD, and CD59 for predicting SA-AKI were 0.788, 0.723, 0.723, 0.795, and 0.836, respectively, all exceeding 0.7. Further analysis of patients who underwent CRRT or not revealed that IGFBP4 had a good predictive value, with an AUC of 0.84.</p><p><strong>Conclusions: </strong>Based on proteomic analysis, CST3, β <sub>2</sub>M, IGFBP4, CFD, and CD59 may serve as potential biomarkers for t
目的:利用蛋白质组学技术鉴定和验证脓毒症相关急性肾损伤(SA-AKI)的早期诊断和精确持续肾替代治疗(CRRT)的新生物标志物。方法:采用前瞻性多中心队列研究。根据急性肾损伤(AKI)的发生情况,连续纳入2019年4月至2021年12月在浙江省台州市五家医院住院的脓毒症患者。脓毒症患者分为SA-AKI组和非SA-AKI组,同期体检的健康人作为对照组(NC组)。收集参与者外周血样本进行蛋白质质谱分析。鉴定出差异表达蛋白,并对其进行功能富集分析。采用酶联免疫吸附试验(ELISA)检测靶蛋白水平,采用受试者操作特征曲线(ROC曲线)评价靶蛋白对SA-AKI的预测价值。另外,选择一家医院的脓毒症患者和健康个体,从外部验证靶蛋白表达水平及其对SA-AKI的预测价值,以及CRRT治疗的准确性。结果:共纳入37例脓毒症患者(其中19例合并AKI, 18例未合并AKI)和31例健康个体进行蛋白质组学分析。SA-AKI组与非SA-AKI组有7个蛋白表达差异显著,分别是胱抑素C (CST3)、β 2-微球蛋白(β 2M)、胰岛素样生长因子结合蛋白4 (IGFBP4)、补体因子I (CFI)、补体因子D (CFD)、CD59和糖蛋白前列腺素D2合成酶(PTGDS)。功能富集分析显示,这些蛋白参与免疫应答、补体激活、凝血级联和中性粒细胞脱粒。ELISA结果显示SA-AKI组各靶蛋白均有特异性表达。此外,选择65例脓毒症患者(38例合并AKI, 27例未合并AKI)和20名健康个体对这7种靶蛋白进行外部验证。ELISA结果显示,SA-AKI组与非SA-AKI组CST3、β 2M、IGFBP4、CFD、CD59表达水平差异均有统计学意义。ROC曲线分析显示,CST3、β 2M、IGFBP4、CFD、CD59预测SA-AKI的曲线下面积(AUC)值分别为0.788、0.723、0.723、0.795、0.836,均超过0.7。对接受或未接受CRRT的患者的进一步分析显示,IGFBP4具有良好的预测价值,AUC为0.84。结论:基于蛋白质组学分析,CST3、β 2M、IGFBP4、CFD和CD59可能是SA-AKI诊断的潜在生物标志物,其中IGFBP4可能是预测SA-AKI患者是否需要CRRT的潜在生物标志物。然而,需要进一步的临床验证。
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引用次数: 0
[Development and validation of a predictive model for acute respiratory distress syndrome in geriatric patients following gastrointestinal perforation surgery]. [胃肠穿孔手术后老年患者急性呼吸窘迫综合征预测模型的建立和验证]。
Q3 Medicine Pub Date : 2025-08-01 DOI: 10.3760/cma.j.cn121430-20250409-00345
Ze Zhang, You Fu, Jing Yuan, Quansheng Du
<p><strong>Objective: </strong>To identify the risk factors for acute respiratory distress syndrome (ARDS) in geriatric patients following gastrointestinal perforation surgery, and constructed a model to validate its predictive value.</p><p><strong>Methods: </strong>A retrospective analysis was conducted. The clinical data of geriatric patients (aged ≥ 60 years) after gastrointestinal perforation surgery admitted to the intensive care unit (ICU) of Hebei General Hospital from October 2017 to October 2024 were enrolled. Two groups were divided according to whether ARDS occurred postoperatively, and the differences in each index between the groups were compared. Lasso regression and multifactorial Logistic regression analyses were used to identify independent risk factors for the development of ARDS, and a prediction model was constructed based on these, which was presented using a nomogram. The receiver operator characteristic curve (ROC curve), calibration curve, and decision curve analysis (DCA) were plotted to evaluate the discrimination, accuracy, and clinical practicability of the model.</p><p><strong>Results: </strong>A total of 155 geriatric patients following gastrointestinal perforation surgery were ultimately included in the analysis, among whom 43 developed ARDS, with an incidence rate of 27.7%. There were significantly differences in age, body mass index (BMI), acute kidney injury comorbidity, heart rate, onset time, the duration of surgery, the site of perforation, seroperitoneum, amount of bleeding, shock comorbidity, central venous pressure (CVP), C-reactive protein, and albumin between ARDS and non-ARDS groups. Lasso regression identified nine significant predictors: age, BMI, acute kidney injury comorbidity, onset time, seroperitoneum, shock comorbidity, CVP, hemoglobin, and albumin. Multivariate Logistic regression analysis identified BMI [odds ratio (OR) = 1.310, P < 0.001], hemoglobin (OR = 1.019, P = 0.045), seroperitoneum (OR = 1.001, P = 0.017), and albumin (OR = 0.871, P < 0.001) as independent risk factors for the occurrence of ARDS. A prediction model was constructed based on the above four independent risk factors, and the ROC curve showed that the area under the curve (AUC) of the model for predicting the occurrence of ARDS was 0.885 [95% confidence interval (95%CI) was 0.824-0.946], and internal validation was performed using bootstrap resampling (Bootstrap 500 times), which showed that the AUC value of the model was 0.886 (95%CI was 0.883-0.889). Calibration curves revealed excellent concordance between observed outcomes and model predictions. DCA indicated a high net benefit value for the model, which has good clinical utility.</p><p><strong>Conclusions: </strong>BMI, hemoglobin, seroperitoneum, and albumin were identified as independent risk factors for ARDS in geriatric patients following gastrointestinal perforation surgery. The prediction model constructed using these four indicators facilitates early identificat
目的:探讨老年患者胃肠道穿孔术后急性呼吸窘迫综合征(ARDS)发生的危险因素,并构建模型验证其预测价值。方法:回顾性分析。选取2017年10月至2024年10月河北省总医院重症监护病房(ICU)住院的胃肠穿孔术后老年患者(年龄≥60岁)的临床资料。根据术后是否发生ARDS分为两组,比较两组间各项指标的差异。采用Lasso回归和多因素Logistic回归分析确定ARDS发展的独立危险因素,并在此基础上构建预测模型。绘制受试者特征曲线(ROC曲线)、校正曲线和决策曲线分析(DCA),评价模型的辨别性、准确性和临床实用性。结果:155例胃肠穿孔手术后的老年患者最终纳入分析,其中43例发生ARDS,发生率为27.7%。ARDS组与非ARDS组在年龄、体重指数(BMI)、急性肾损伤合并症、心率、发病时间、手术时间、穿孔部位、浆膜、出血量、休克合并症、中心静脉压(CVP)、c反应蛋白、白蛋白等方面存在显著差异。Lasso回归确定了9个显著的预测因子:年龄、BMI、急性肾损伤合并症、发病时间、血清腹膜、休克合并症、CVP、血红蛋白和白蛋白。多因素Logistic回归分析发现,BMI[比值比(OR) = 1.310, P < 0.001]、血红蛋白(OR = 1.019, P = 0.045)、血清腹膜(OR = 1.001, P = 0.017)、白蛋白(OR = 0.871, P < 0.001)是ARDS发生的独立危险因素。基于以上4个独立危险因素构建预测模型,ROC曲线显示模型预测ARDS发生的曲线下面积(AUC)为0.885[95%可信区间(95% ci)为0.824-0.946],采用bootstrap重采样(bootstrap 500次)进行内部验证,模型的AUC值为0.886 (95% ci为0.883-0.889)。校准曲线显示观测结果与模型预测之间具有良好的一致性。DCA显示该模型具有较高的净效益值,具有良好的临床应用价值。结论:BMI、血红蛋白、血清腹膜和白蛋白被确定为胃肠道穿孔手术后老年患者ARDS的独立危险因素。利用这四个指标构建的预测模型有助于临床医生早期识别高危人群。
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引用次数: 0
[Construction of a risk prediction model for the timing of extracorporeal membrane oxygenation initiation]. [体外膜氧合起始时间风险预测模型的构建]。
Q3 Medicine Pub Date : 2025-08-01 DOI: 10.3760/cma.j.cn121430-20241129-00971
Dehua Zeng, Xifeng Liu, Zhibiao He, Aiqun Zhu
<p><strong>Objective: </strong>To identify the risk factors related to the timing of patients receiving extracorporeal membrane oxygenation (ECMO) initiation and construct a risk prediction model for ECMO initiation timing.</p><p><strong>Methods: </strong>Patients who received ECMO admitted to the Second Xiangya Hospital of Central South University from January 2020 to January 2024 were retrospectively collected. The case data mainly included physiological and biochemical indicators 1 hour before ECMO initiation. According to the outcome of the patients, they were divided into survival group and death group. Univariate and multivariate Logistic regression analysis were used to analyze the predictors of mortality risk in patients with ECMO, and a nomogram prediction model was constructed. The discrimination, calibration accuracy, and goodness of the model were evaluated by the receiver operator characteristic curve (ROC curve), calibration curve, and the Hosmer-Lemeshow test, respectively. Decision curve analysis (DCA) evaluated the clinical net benefit rate of the model.</p><p><strong>Results: </strong>A total of 81 ECMO patients were included, including 59 males and 22 females; age range from 16 to 61 years old, with a median age of 56.0 (39.5, 61.5) years old; 20 patients received veno-arterial (V-A) ECMO, and 61 patients received veno-venous (V-V) ECMO; 23 patients ultimately survived and 58 patients died. Univariate analysis showed that age, blood urea nitrogen, serum creatinine, D-dimer, arterial blood carbon dioxide partial pressure, and prothrombin time of the death group were all higher than those of the survival group, while albumin was slightly lower than that of the survival group. There was a statistically significant difference in the direct cause of ECMO initiation between the two groups. Multivariate Logistic regression analysis showed that age [odds ratio (OR) = 1.069, 95% confidence interval (95%CI) was 1.015-1.125, P = 0.012], direct cause of ECMO initiation [with heart failure as the reference, return of spontaneous circulation (ROSC) after cardiopulmonary support (OR = 30.672, 95%CI was 1.265-743.638, P = 0.035), novel coronavirus infection (OR = 8.666, 95%CI was 0.818-91.761, P = 0.073), other severe pneumonia (OR = 4.997, 95%CI was 0.558-44.765, P = 0.150)], pre-ECMO serum creatinine (OR = 1.008, 95%CI was 1.000-1.016, P = 0.044), prothrombin time (OR = 1.078, 95%CI was 0.948-1.226, P = 0.252), and D-dimer (OR = 1.135, 95%CI was 1.047-1.231, P = 0.002) were entered into the final regression equation. A nomogram prediction model was developed based on these five factors. The area under the ROC curve (AUC) of the model was 0.889 (95%CI was 0.819-0.959), higher than the AUC of the sequential organ failure assessment (SOFA; AUC = 0.604, 95%CI was 0.467-0.742). The calibration curve showed good consistency between the model predictions and the observed results. The Hosmer-Lemeshow goodness-of-fit test showed that χ <sup>2</sup> =
目的:探讨影响患者接受体外膜氧合(ECMO)启动时间的危险因素,构建ECMO启动时间的风险预测模型。方法:回顾性收集2020年1月至2024年1月在中南大学湘雅第二医院接受ECMO的患者。病例资料主要包括ECMO启动前1小时的生理生化指标。根据患者预后情况分为生存组和死亡组。采用单因素和多因素Logistic回归分析对ECMO患者死亡风险的预测因素进行分析,并构建nomogram预测模型。采用受试者特征曲线(ROC曲线)、校正曲线和Hosmer-Lemeshow检验分别评价模型的判别性、校正精度和优度。决策曲线分析(Decision curve analysis, DCA)评价模型的临床净效益率。结果:共纳入ECMO患者81例,其中男性59例,女性22例;年龄16 ~ 61岁,中位年龄56.0(39.5,61.5)岁;静脉-动脉(V-A) ECMO 20例,静脉-静脉(V-V) ECMO 61例;23名患者最终存活,58名患者死亡。单因素分析显示,死亡组的年龄、血尿素氮、血清肌酐、d -二聚体、动脉血二氧化碳分压、凝血酶原时间均高于生存组,白蛋白略低于生存组。两组ECMO启动的直接原因有统计学差异。多因素Logistic回归分析显示,年龄[优势比(OR) = 1.069, 95%可信区间(95% ci)为1.015 ~ 1.125,P = 0.012]、启动ECMO的直接原因[以心力衰竭为参照,心肺支持后自主循环恢复(ROSC) (OR = 30.672, 95% ci为1.265 ~ 743.638,P = 0.035)、新型冠状病毒感染(OR = 8.666, 95% ci为0.818 ~ 91.761,P = 0.073)、其他重症肺炎(OR = 4.997, 95% ci为0.558 ~ 44.765,P = 0.150)]、将ecmo前血清肌酐(OR = 1.008, 95%CI为1.000 ~ 1.016,P = 0.044)、凝血酶原时间(OR = 1.078, 95%CI为0.948 ~ 1.226,P = 0.252)、d -二聚体(OR = 1.135, 95%CI为1.047 ~ 1.231,P = 0.002)纳入最终回归方程。基于这五个因素,建立了一种nomogram预测模型。模型的ROC曲线下面积(AUC)为0.889 (95%CI为0.819 ~ 0.959),高于序贯器官衰竭评价的AUC (SOFA; AUC = 0.604, 95%CI为0.467 ~ 0.742)。校正曲线显示,模型预测值与观测结果具有较好的一致性。Hosmer-Lemeshow拟合优度检验显示χ 2 = 4.668, P = 0.792。DCA分析显示,当风险阈值为0-0.8时,净效益率大于0,显著优于SOFA评分。结论:采用年龄、ECMO启动的直接原因、凝血酶时间、血清肌酐、d -二聚体等5个因素构建的ECMO启动时间风险预测模型具有良好的判别性和校准性。它可以作为启动前评估工具来识别和预测ECMO患者启动后的死亡风险。
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引用次数: 0
[A randomized controlled trial on light music therapy for preventing intensive care unit delirium in patients undergoing invasive mechanical ventilation]. [轻音乐治疗预防重症监护病房有创机械通气患者谵妄的随机对照试验]。
Q3 Medicine Pub Date : 2025-08-01 DOI: 10.3760/cma.j.cn121430-20250302-00200
Xiaqin Liu, Li'an Tang, Caihong Wang, Debin Huang
<p><strong>Objective: </strong>To explore the effect of light music therapy on delirium in intensive care unit (ICU) patients undergoing invasive mechanical ventilation, and provide evidence-based support for clinical prevention of delirium.</p><p><strong>Methods: </strong>A prospective randomized controlled trial was conducted. 140 patients with invasive mechanical ventilation admitted to the department of respiratory and critical care medicine of First Affiliated Hospital of Guangxi Medical University from January 2024 to January 2025 were enrolled. The patients were divided into intervention group and control group using a random number table method. The control group received routine treatment and nursing care, while the intervention group received light music therapy three times a day for 30 minutes each time for 7 consecutive days. The confusion assessment method-ICU (CAM-ICU) was used to evaluate delirium, and the incidence of delirium within 7 days was statistically analyzed. Richmond agitation-sedation score (RASS), critical care pain observation tool (CPOT) score, mechanical ventilation duration, the length of ICU stay, and ICU stay expenses were record.</p><p><strong>Results: </strong>129 cases were ultimately included, including 64 cases in the control group and 65 cases in the intervention group. There was no statistically significant difference in baseline data between the two groups, indicating comparability. The incidence of delirium in the intervention group was significantly lower than that in the control group (27.7% vs. 51.6%, χ <sup>2</sup> = 7.687, P = 0.006). There was no significantly difference in RASS score between the two groups before enrollment (P = 0.840). After intervention, the RASS score in the intervention group significantly decreased, from 2.00 points on the 1st day of enrollment to 0.00 points on the 7th day, while the control group only decreased from 2.00 points to 1.50 points. The decreasing trend of the intervention group was more pronounced, especially on the 3rd day (P = 0.047) and the 7th day (P =0.005), with significant differences between the groups. The time effect (F = 18.929, P < 0.001), group effect (F = 6.655, P = 0.011), and time group interaction effect (F = 7.372, P < 0.001) of the two groups of RASS score were significant, suggesting that light music therapy has better timeliness and sustainability in improving patients' sedation status. There was no significantly difference in CPOT score between the two groups before enrollment (P = 0.902). After intervention, the CPOT score in the intervention group rapidly decreased from 3.00 points before enrollment to 1.00 points on the 1st day, and continued until the 7th day, while the control group showed a slower decrease from 2.50 points to 2.00 points and only dropped to 1.00 points on the 7th day. There were significant differences on 1st day and 3rd day between two groups (both P < 0.05). The time effect (F = 28.125, P < 0.001), group effect (F =
目的:探讨轻音乐治疗对重症监护病房(ICU)有创机械通气患者谵妄的影响,为临床预防谵妄提供循证支持。方法:采用前瞻性随机对照试验。选取2024年1月至2025年1月广西医科大学第一附属医院呼吸与重症医学科收治的140例有创机械通气患者。采用随机数字表法将患者分为干预组和对照组。对照组接受常规治疗及护理,干预组接受轻音乐治疗,每天3次,每次30分钟,连续7天。采用神志不清评价法- icu (CAM-ICU)评价谵妄,统计分析7 d内谵妄的发生率。记录患者的Richmond激动镇静评分(RASS)、重症监护疼痛观察工具评分(CPOT)、机械通气时间、ICU住院时间、ICU住院费用。结果:最终纳入129例,其中对照组64例,干预组65例。两组基线数据无统计学差异,具有可比性。干预组谵妄发生率显著低于对照组(27.7% vs. 51.6%, χ 2 = 7.687, P = 0.006)。两组患者入组前RASS评分差异无统计学意义(P = 0.840)。干预后,干预组RASS评分从入组第1天的2.00分显著下降到第7天的0.00分,而对照组仅从2.00分下降到1.50分。干预组下降趋势更为明显,特别是在第3天(P = 0.047)和第7天(P =0.005),组间差异有统计学意义。两组RASS评分的时间效应(F = 18.929, P < 0.001)、组效应(F = 6.655, P = 0.011)、时间组交互效应(F = 7.372, P < 0.001)均显著,提示轻音乐治疗在改善患者镇静状态方面具有较好的时效性和可持续性。两组患者入组前CPOT评分差异无统计学意义(P = 0.902)。干预后,干预组的CPOT评分从入组前的3.00分迅速下降到第1天的1.00分,并持续到第7天,而对照组的CPOT评分从2.50分下降到2.00分,下降速度较慢,到第7天仅下降到1.00分。第1天、第3天两组比较差异均有统计学意义(P < 0.05)。时间效应(F = 28.125, P < 0.001),组效应(F = 11.580, P = 0.001),和时间组交互作用(F = 4.048, P = 0.020) CPOT两组的得分显著,表明光音乐疗法有更好的疼痛控制,但交互效应较低,表明干预CPOT分数的影响主要集中在早期阶段(1 - 3天),和长期影响可能会受到其他因素的影响。与对照组比较,干预组机械通气时间(10.57±2.94天∶11.95±3.74天,P = 0.021)和ICU住院时间(14.91±4.37天∶17.53±4.83天,P = 0.002)显著减少。干预组ICU住院费用略低于对照组[万元:22.431(12.473,28.489)比29.362(11.996,41.389)],但差异无统计学意义(P = 0.086)。结论:轻音乐治疗可有效降低有创机械通气患者谵妄的发生率,改善意识和疼痛感知,缩短机械通气时间和住院时间,具有重要的临床推广价值。
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引用次数: 0
[Association between fluid balance trajectory and 28-day mortality and continuous renal replacement therapy in patients with severe acute pancreatitis]. [重症急性胰腺炎患者体液平衡轨迹与28天死亡率和持续肾脏替代治疗的关系]。
Q3 Medicine Pub Date : 2025-08-01 DOI: 10.3760/cma.j.cn121430-20250427-00399
Songxun Tang, Jiong Xiong, Fangqi Wu, Fuyu Deng, Tingting Li, Xu Liu, Yan Tang, Feng Shen

Objective: To investigate the association between fluid balance trajectories within the first 3 days of intensive care unit (ICU) admission and 28-day mortality as well as the incidence of continuous renal replacement therapy (CRRT) in patients with severe acute pancreatitis (SAP).

Methods: Clinical data of SAP patients were extracted from the Medical Information Mart of Intensive Care-IV (MIMIC-IV). Group-based trajectory modeling (GBTM) was used to analyze the daily fluid balance of patients within 3 days of ICU admission, and grouping them accordingly. Univariate and multivariate Logistic regression analyses were performed to assess the association between fluid balance trajectory and 28-day mortality and ICU CRRT in SAP patients.

Results: A total of 251 SAP patients were included, with 33 deaths within 28 days, and a 28-day mortality of 13.15%; 49 patients (19.52%) continued to receive bedside CRRT after 3 days of ICU admission. The fluid balance on the 3rd day, cumulative fluid balance within 3 days of ICU admission, and incidence of CRRT in the death group were significantly higher than those in the survival group. According to GBTM groups, there were 127 cases in the moderate fluid resuscitation with rapid reduction (MF group), 44 cases in the large fluid resuscitation with rapid reduction (LF group), 20 cases in the moderate fluid resuscitation with slow reduction (MS group), and 60 cases in the small fluid resuscitation with slow reduction (SS group). The cumulative fluid balance within 3 days of ICU admission of the MF group, LF group, MS group, and SS group were 8.60% (5.15%, 11.70%), 16.70% (13.00%, 21.02%), 23.40% (19.38%, 25.45%), and 0.65% (-2.35%, 2.20%), respectively, and the incidence of CRRT during ICU hospitalization were 11.02%, 29.55%, 85.00%, and 8.33%, respectively, with statistically significant differences among the groups (both P < 0.05); the 28-day mortality were 11.02%, 18.18%, 20.00%, and 11.67%, respectively, with no statistically significant difference among the groups (P > 0.05). Kaplan-Meier survival curve analysis showed there was no statistically significant difference in 28-day cumulative survival rate among groups with different fluid balance trajectories (Log-rank test: χ 2 = 2.31, P = 0.509). Multivariate Logistic regression analysis showed that cumulative fluid balance within 3 days of ICU admission was an independent risk factor for 28-day mortality [odds ratio (OR) = 1.071, 95% confidence interval (95%CI) was 1.005-1.144, P = 0.040] and CRRT requirement (OR = 1.233, 95%CI was 1.125-1.372, P < 0.001); early aggressive fluid resuscitation on day 1 reduced CRRT risk (OR = 0.866, 95%CI was 0.756-0.978, P = 0.030).

Conclusions: Dynamic fluid management is essential in SAP patients. While early aggressive fluid resuscitation may reduce CRRT demand, excessive cumulative fluid balance is associated with increased

目的:探讨重症监护病房(ICU)入院前3天液体平衡轨迹与重症重症胰腺炎(SAP)患者28天死亡率及持续肾替代治疗(CRRT)发生率的关系。方法:从重症监护医学信息市场- iv (MIMIC-IV)中提取SAP患者的临床资料。采用分组轨迹模型(Group-based trajectory modeling, GBTM)分析患者入院3 d内的每日体液平衡情况,并进行分组。采用单因素和多因素Logistic回归分析评估SAP患者体液平衡轨迹与28天死亡率和ICU CRRT之间的关系。结果:共纳入251例SAP患者,其中28天内死亡33例,28天死亡率为13.15%;49例(19.52%)患者在ICU入院3天后继续接受床边CRRT治疗。死亡组患者入院第3天体液平衡、入院第3天累积体液平衡、CRRT发生率均显著高于生存组。按GBTM组分,中度液体复苏快速复位(MF组)127例,重度液体复苏快速复位(LF组)44例,中度液体复苏缓慢复位(MS组)20例,轻度液体复苏缓慢复位(SS组)60例。MF组、LF组、MS组、SS组患者入院后3 d内累积体液平衡分别为8.60%(5.15%、11.70%)、16.70%(13.00%、21.02%)、23.40%(19.38%、25.45%)、0.65%(-2.35%、2.20%),住院期间CRRT发生率分别为11.02%、29.55%、85.00%、8.33%,组间差异均有统计学意义(P均< 0.05);28天死亡率分别为11.02%、18.18%、20.00%、11.67%,组间比较差异无统计学意义(P < 0.05)。Kaplan-Meier生存曲线分析显示,不同体液平衡轨迹组28天累积生存率差异无统计学意义(Log-rank检验:χ 2 = 2.31, P = 0.509)。多因素Logistic回归分析显示,ICU入院3 d内累积体液平衡是28天死亡率的独立危险因素[优势比(OR) = 1.071, 95%可信区间(95% ci)为1.005 ~ 1.144,P = 0.040]和CRRT要求(OR = 1.233, 95% ci为1.125 ~ 1.372,P < 0.001);第1天早期积极液体复苏降低CRRT风险(OR = 0.866, 95%CI为0.756 ~ 0.978,P = 0.030)。结论:动态体液管理对SAP患者至关重要。虽然早期积极的液体复苏可以减少CRRT的需求,但过度的累积液体平衡与28天死亡率和CRRT发生率增加有关。
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Zhonghua wei zhong bing ji jiu yi xue
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