首页 > 最新文献

Zhonghua yi xue za zhi最新文献

英文 中文
[Expert consensus on the clinical application of oxycodone injection (2025 edition)]. 【羟考酮注射液临床应用专家共识(2025年版)】。
Q3 Medicine Pub Date : 2025-12-02 DOI: 10.3760/cma.j.cn112137-20250903-02286

Oxycodone is an agonist of μ-and κ-opioid receptors which has been commonly used for the management of moderate to severe pain attributing to its distinct pharmacological properties. Due to the lack of unified medication guidance, significant variations exist in the clinical application of oxycodone injection among different medical institutions and healthcare providers, aggravating the standardization and homogenization of pain management. To solve this problem, the Pain Group of the Chinese Society of Anesthesiology has organized a multidisciplinary panel of experts to develop this consensus focusing on 15 key clinical questions. Based on systematic literature review and evidence evaluation, the consensus establishes 15 recommendations covering general anesthesia induction, preventive medication, postoperative analgesia, post-thoracic/abdominal surgery analgesia, epidural anesthesia, procedural sedation and analgesia, special patient use etc. This consensus aims to standardize clinical application and optimize pain management outcomes by providing evidence-based guidance on oxycodone injection.

羟考酮是一种μ- κ-阿片受体激动剂,由于其独特的药理特性,已被广泛用于中重度疼痛的治疗。由于缺乏统一的用药指导,不同医疗机构和医疗服务提供者对羟考酮注射液的临床应用存在较大差异,加剧了疼痛管理的规范化和同质化。为了解决这一问题,中国麻醉学会疼痛组组织了一个多学科专家小组,就15个关键临床问题达成共识。在系统文献回顾和证据评价的基础上,共识建立了全麻诱导、预防用药、术后镇痛、胸/腹术后镇痛、硬膜外麻醉、程序性镇静镇痛、特殊患者使用等15项建议。本共识旨在为羟考酮注射提供循证指导,规范临床应用,优化疼痛管理效果。
{"title":"[Expert consensus on the clinical application of oxycodone injection (2025 edition)].","authors":"","doi":"10.3760/cma.j.cn112137-20250903-02286","DOIUrl":"10.3760/cma.j.cn112137-20250903-02286","url":null,"abstract":"<p><p>Oxycodone is an agonist of μ-and κ-opioid receptors which has been commonly used for the management of moderate to severe pain attributing to its distinct pharmacological properties. Due to the lack of unified medication guidance, significant variations exist in the clinical application of oxycodone injection among different medical institutions and healthcare providers, aggravating the standardization and homogenization of pain management. To solve this problem, the Pain Group of the Chinese Society of Anesthesiology has organized a multidisciplinary panel of experts to develop this consensus focusing on 15 key clinical questions. Based on systematic literature review and evidence evaluation, the consensus establishes 15 recommendations covering general anesthesia induction, preventive medication, postoperative analgesia, post-thoracic/abdominal surgery analgesia, epidural anesthesia, procedural sedation and analgesia, special patient use etc. This consensus aims to standardize clinical application and optimize pain management outcomes by providing evidence-based guidance on oxycodone injection.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 ","pages":"4024-4040"},"PeriodicalIF":0.0,"publicationDate":"2025-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145597688","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
[Construction and validation of a prognostic model of chemotherapy combined with immunotherapy for advanced lung squamous cell carcinoma based on quantitative CT image features]. [基于定量CT影像特征的化疗联合免疫治疗晚期肺鳞状细胞癌预后模型的构建与验证]。
Q3 Medicine Pub Date : 2025-12-02 DOI: 10.3760/cma.j.cn112137-20250619-01495
Y Y Hu, X Y Tan, L P Shi, H Xia, Y Q Cao, M J Yi, J J Xu, S J Zhang, X L Liu, W X Zhang, X Y Liang, X Y Song, S F Wang, Y Jin
<p><p><b>Objective:</b> To construct and validate a prognostic model for patients with advanced lung squamous cell carcinoma (LUSC) receiving chemotherapy combined with immunotherapy based on quantitative CT features. <b>Methods:</b> A total of 96 patients with advanced LUSC who received chemotherapy combined with immunotherapy at Union Hospital, Tongji Medical College, Huazhong University of Science and Technology from November 2020 to October 2023 were retrospectively included. They were randomly divided into a training set (<i>n</i>=72) and an internal validation set (<i>n</i>=24) at a ratio of 3∶1 (random sequence was generated by R Studio 4.4.2 software). Additionally, patients with advanced LUSC who visited Yichang Central People's Hospital from October 2020 to June 2024 were enrolled as the external validation set (<i>n</i>=58) according to the same criteria. Pretreatment chest CT images were obtained from patients, and quantitative CT features were extracted. Based on the training set data, LASSO regression and univariate and multivariate Cox regression models were used to screen the independent variables, and the model was constructed with the progression-free survival (PFS, progress=1, no progression=0) as the dependent variable. Taking the progression at 180 d as the outcome variable and the quantitative CT score as the evaluation index, the receiver operating characteristic (ROC) curve was drawn. The calibration curve and decision curve were used to evaluate the model efficacy. Based on the optimal cut-off value determined by the ROC curve, patients were divided into high-risk and low-risk groups, and the log-rank test was used to compare the survival differences between the two groups. <b>Results:</b> A total of 154 patients with LUSC were included, including 147 males and 7 females, with an age of (64.7±8.1) years; there were no statistically significant differences in demographic characteristics and TNM stage among the training set, internal validation set, and external validation set (all <i>P</i>>0.05). Four quantitative CT features were associated with PFS, including the percentage of low attenuation area with CT value < -910 HU in the whole lung (LAA%-910_lung) (<i>HR</i>=0.013, 95%<i>CI</i>: 0.002-0.313), the area percentage of low attenuation area with CT value < -950 HU in the right lower lung (LAA%-950_right_lower) (<i>HR</i>=0.011, 95%<i>CI</i>: 0.001-0.012), the minimum wall thickness of grade 2 airwall (minThicknessOfAirwall_2) (<i>HR</i>=0.117, 95%<i>CI</i>: 0.029-0.463) and the mean diameter of grade 1 airway (meanDiameterOfAirway_1) (<i>HR</i>=0.767, 95%<i>CI</i>: 0.687-0.857), which were used to construct the quantitative CT (QCT) score: QCTscore=-4.346×(LAA%-910_lung)-4.513×(LAA%-950_right_lower)-2.14×(minThicknessOfAirwall_2)-0.265×(meanDiameterOfAirway_1). The optimal cutoff value for the score was -9.45. The areas under the ROC curve (AUC) for predicting 180 d survival was 0.843 (95%<i>CI</i>: 0.773-0.952) in the
目的:建立并验证基于定量CT特征的晚期肺鳞状细胞癌(LUSC)化疗联合免疫治疗预后模型。方法:回顾性分析2020年11月至2023年10月华中科技大学同济医学院协和医院化疗联合免疫治疗的晚期LUSC患者96例。随机分为训练集(n=72)和内部验证集(n=24),比例为3∶1(随机序列由R Studio 4.4.2软件生成)。选取2020年10月至2024年6月在宜昌市中心人民医院就诊的晚期LUSC患者作为外部验证集(n=58)。获取患者胸部CT预处理图像,提取定量CT特征。以训练集数据为基础,采用LASSO回归、单变量和多变量Cox回归模型筛选自变量,以无进展生存期(PFS,进展=1,无进展=0)为因变量构建模型。以180 d病程为结局变量,定量CT评分为评价指标,绘制受试者工作特征(ROC)曲线。采用标定曲线和决策曲线评价模型的有效性。根据ROC曲线确定的最佳截断值,将患者分为高危组和低危组,采用log-rank检验比较两组患者的生存差异。结果:共纳入154例LUSC患者,其中男性147例,女性7例,年龄(64.7±8.1)岁;训练集、内部验证集和外部验证集的人口学特征和TNM分期差异无统计学意义(P < 0.05)。4项定量CT特征与PFS相关,包括全肺CT值< -910 HU的低衰减区百分比(LAA%-910_lung) (HR=0.013, 95%CI: 0.002 ~ 0.313)、右下肺CT值< -950 HU的低衰减区面积百分比(LAA%-950_right_lower) (HR=0.011, 95%CI: 0.001 ~ 0.012)、2级气壁最小壁厚(minThicknessOfAirwall_2) (HR=0.117, 95%CI:0.029-0.463)和1级气道平均直径(meanDiameterOfAirway_1) (HR=0.767, 95%CI: 0.687-0.857),用于构建定量CT (QCT)评分:QCT评分=-4.346×(LAA%-910_lung)-4.513×(LAA%-950_right_lower)-2.14×(minThicknessOfAirwall_2)-0.265×(meanDiameterOfAirway_1)。得分的最佳临界值为-9.45。预测180 d生存的ROC曲线下面积(AUC)在训练集中为0.843 (95%CI: 0.773-0.952),在内部测试集中为0.778 (95%CI: 0.527-0.999),在外部测试集中为0.762 (95%CI: 0.615-0.921)。Hosmer-Lemeshow优度拟合检验结果表明,模型拟合效果较好(训练集:χ2=8.058, P=0.428;内部验证集:χ2=12.883, P=0.116;内部验证集:χ2=3.141, P=0.925)。决策曲线显示,当训练集的风险阈值为0 ~ 79%,内部验证集的风险阈值为0 ~ 81%,独立验证集的风险阈值为0 ~ 82%时,预测模型具有临床净效益。3组数据中,高危组(QCT评分≥-9.45)180 d PFS率低于低危组(QCT评分< -9.45)(训练组:5.1% vs 66.7%;内部验证组:180 d无进展生存率12.5% vs 75%;外部验证组:180 d无进展生存率68.6% vs 100.0%,均P0.05)。结论:基于QCT图像特征,构建了LUSC化疗联合免疫治疗的预后预测模型,为预测LUSC患者化疗联合免疫治疗的疗效提供了有效手段。
{"title":"[Construction and validation of a prognostic model of chemotherapy combined with immunotherapy for advanced lung squamous cell carcinoma based on quantitative CT image features].","authors":"Y Y Hu, X Y Tan, L P Shi, H Xia, Y Q Cao, M J Yi, J J Xu, S J Zhang, X L Liu, W X Zhang, X Y Liang, X Y Song, S F Wang, Y Jin","doi":"10.3760/cma.j.cn112137-20250619-01495","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250619-01495","url":null,"abstract":"&lt;p&gt;&lt;p&gt;&lt;b&gt;Objective:&lt;/b&gt; To construct and validate a prognostic model for patients with advanced lung squamous cell carcinoma (LUSC) receiving chemotherapy combined with immunotherapy based on quantitative CT features. &lt;b&gt;Methods:&lt;/b&gt; A total of 96 patients with advanced LUSC who received chemotherapy combined with immunotherapy at Union Hospital, Tongji Medical College, Huazhong University of Science and Technology from November 2020 to October 2023 were retrospectively included. They were randomly divided into a training set (&lt;i&gt;n&lt;/i&gt;=72) and an internal validation set (&lt;i&gt;n&lt;/i&gt;=24) at a ratio of 3∶1 (random sequence was generated by R Studio 4.4.2 software). Additionally, patients with advanced LUSC who visited Yichang Central People's Hospital from October 2020 to June 2024 were enrolled as the external validation set (&lt;i&gt;n&lt;/i&gt;=58) according to the same criteria. Pretreatment chest CT images were obtained from patients, and quantitative CT features were extracted. Based on the training set data, LASSO regression and univariate and multivariate Cox regression models were used to screen the independent variables, and the model was constructed with the progression-free survival (PFS, progress=1, no progression=0) as the dependent variable. Taking the progression at 180 d as the outcome variable and the quantitative CT score as the evaluation index, the receiver operating characteristic (ROC) curve was drawn. The calibration curve and decision curve were used to evaluate the model efficacy. Based on the optimal cut-off value determined by the ROC curve, patients were divided into high-risk and low-risk groups, and the log-rank test was used to compare the survival differences between the two groups. &lt;b&gt;Results:&lt;/b&gt; A total of 154 patients with LUSC were included, including 147 males and 7 females, with an age of (64.7±8.1) years; there were no statistically significant differences in demographic characteristics and TNM stage among the training set, internal validation set, and external validation set (all &lt;i&gt;P&lt;/i&gt;&gt;0.05). Four quantitative CT features were associated with PFS, including the percentage of low attenuation area with CT value &lt; -910 HU in the whole lung (LAA%-910_lung) (&lt;i&gt;HR&lt;/i&gt;=0.013, 95%&lt;i&gt;CI&lt;/i&gt;: 0.002-0.313), the area percentage of low attenuation area with CT value &lt; -950 HU in the right lower lung (LAA%-950_right_lower) (&lt;i&gt;HR&lt;/i&gt;=0.011, 95%&lt;i&gt;CI&lt;/i&gt;: 0.001-0.012), the minimum wall thickness of grade 2 airwall (minThicknessOfAirwall_2) (&lt;i&gt;HR&lt;/i&gt;=0.117, 95%&lt;i&gt;CI&lt;/i&gt;: 0.029-0.463) and the mean diameter of grade 1 airway (meanDiameterOfAirway_1) (&lt;i&gt;HR&lt;/i&gt;=0.767, 95%&lt;i&gt;CI&lt;/i&gt;: 0.687-0.857), which were used to construct the quantitative CT (QCT) score: QCTscore=-4.346×(LAA%-910_lung)-4.513×(LAA%-950_right_lower)-2.14×(minThicknessOfAirwall_2)-0.265×(meanDiameterOfAirway_1). The optimal cutoff value for the score was -9.45. The areas under the ROC curve (AUC) for predicting 180 d survival was 0.843 (95%&lt;i&gt;CI&lt;/i&gt;: 0.773-0.952) in the","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 44","pages":"4056-4064"},"PeriodicalIF":0.0,"publicationDate":"2025-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145649445","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
[Clinical prognostic prediction research: a technical roadmap]. 【临床预后预测研究:技术路线图】。
Q3 Medicine Pub Date : 2025-12-02 DOI: 10.3760/cma.j.cn112137-20250703-01615
Y M Zhao, N Li, W W Li

In recent years, the number of research papers on building disease prognosis prediction models (referred to as modeling) has rapidly increased, but clinical applications are rare, and a vast array of studies and papers failed to improve clinical practice. The reasons for this are worthy of attention. The author proposes that modeling research is a systematic engineering, and the current "one-step" technical approach is the main reason for the above phenomenon. Modeling research can be divided into four stages: topic selection, preliminary preparation, modeling, promotion and application, and re-evaluation. Each stage has a series of clinical and scientific questions that need to be answered, and should be gradually promoted. The paper clarifies from a methodological perspective that modeling research should be guided by clinical problems and needs, and form a series of studies based on clear clinical application scenarios and subsequent solutions. The paper analyzes the objectives and tasks of each research, available research plans, key points and difficulties to be noted, and milestone achievements of each stage. Meanwhile, it is suggested to strive to incorporate modeling research into the framework of scientific community behavior, and empower evidence-based medicine with research results and their promotion and application. Finally, the author points out that modeling research and its subsequent clinical applications face legal, ethical, and management (including potential conflict of interest risks) issues and challenges that need to be addressed through further research.

近年来,建立疾病预后预测模型(简称建模)的研究论文数量迅速增加,但临床应用较少,大量的研究和论文未能改善临床实践。其原因值得注意。笔者认为建模研究是一项系统工程,目前的“一步法”技术方法是造成上述现象的主要原因。建模研究可分为选题、前期准备、建模、推广应用、再评估四个阶段。每个阶段都有一系列临床和科学问题需要回答,并应逐步推进。本文从方法学角度明确了建模研究应以临床问题和需求为导向,形成基于明确临床应用场景和后续解决方案的系列研究。分析了各阶段的研究目标和任务,现有的研究计划,需要注意的重点和难点,以及各阶段的里程碑式成果。同时,建议努力将建模研究纳入科学共同体行为的框架,以研究成果和推广应用赋予循证医学以力量。最后,作者指出,建模研究及其后续临床应用面临法律、伦理和管理(包括潜在的利益冲突风险)等问题和挑战,需要通过进一步的研究来解决。
{"title":"[Clinical prognostic prediction research: a technical roadmap].","authors":"Y M Zhao, N Li, W W Li","doi":"10.3760/cma.j.cn112137-20250703-01615","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250703-01615","url":null,"abstract":"<p><p>In recent years, the number of research papers on building disease prognosis prediction models (referred to as modeling) has rapidly increased, but clinical applications are rare, and a vast array of studies and papers failed to improve clinical practice. The reasons for this are worthy of attention. The author proposes that modeling research is a systematic engineering, and the current \"one-step\" technical approach is the main reason for the above phenomenon. Modeling research can be divided into four stages: topic selection, preliminary preparation, modeling, promotion and application, and re-evaluation. Each stage has a series of clinical and scientific questions that need to be answered, and should be gradually promoted. The paper clarifies from a methodological perspective that modeling research should be guided by clinical problems and needs, and form a series of studies based on clear clinical application scenarios and subsequent solutions. The paper analyzes the objectives and tasks of each research, available research plans, key points and difficulties to be noted, and milestone achievements of each stage. Meanwhile, it is suggested to strive to incorporate modeling research into the framework of scientific community behavior, and empower evidence-based medicine with research results and their promotion and application. Finally, the author points out that modeling research and its subsequent clinical applications face legal, ethical, and management (including potential conflict of interest risks) issues and challenges that need to be addressed through further research.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 44","pages":"4019-4023"},"PeriodicalIF":0.0,"publicationDate":"2025-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145649335","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
[Effectiveness and safety of anlotinib combination regimens in patients with previously immunotherapy treated advanced non-small cell lung cancer]. [安洛替尼联合方案在既往免疫治疗晚期非小细胞肺癌患者中的有效性和安全性]。
Q3 Medicine Pub Date : 2025-12-02 DOI: 10.3760/cma.j.cn112137-20250405-00836
R R Cheng, G W Zhang, C Huang, X J Song, H X Jia
<p><p><b>Objective:</b> To explore the effectiveness and safety of anlotinib combination regimens in patients with previously immunotherapy treated advanced non-small cell lung cancer (NSCLC). <b>Methods:</b> This study retrospectively included 85 patients with previously immunotherapy treated advanced NSCLC who received anlotinib combination regimens or single-agent chemotherapy in the First Affiliated Hospital of Zhengzhou University from October 2018 to October 2023. The observation group was consisted of 43 patients who received anlotinib combination regimens, and the control group was consisted of 42 patients who received single-agent chemotherapy. Observation group received anlotinib combined with chemotherapy and anlotinib combined with immunotherapy, while control group received single-agent chemotherapy. The follow-up period ended on May 25, 2024. The baseline characteristics, recent effectiveness, prognosis, and adverse reactions were compared between the observation group and the control group. Survival curves were plotted using the Kaplan-Meier method, and the log-rank test was used to compare the differences. <b>Results:</b> In observation group, there were 29 males and 14 females with a median age [<i>M</i> (<i>Q</i><sub>1</sub>, <i>Q</i><sub>3</sub>)] of 63 (27, 73) years; in control group, there were 27 males and 15 females, with a median age of 64 (28, 73) years. Objective response rates for the observation group and control group were 23.3% (10/43) and 14.3% (6/42), respectively, with no statistically significant difference (<i>P</i>=0.290). Disease control rates were 83.7% (36/43) and 57.1% (24/42) for the observation and the control groups, respectively, with a statistically significant difference (<i>P</i>=0.007). The median follow-up duration for the observation group and the control group was 14.2 and 9.6 months, respectively. Prognosis results indicated that the median PFS for the observation group and the control group were 6.1 (95%<i>CI</i>: 2.41-9.79) and 2.9 months (95%<i>CI</i>: 2.59-3.21), respectively. The observation group was significantly higher than the control group (<i>P</i>=0.009). The median OS were 15.5 (95%<i>CI</i>: 8.99-22.01) and 10.3 months (95%<i>CI</i>: 7.87-12.74), respectively. The observation group was also significantly higher than the control group (<i>P</i>=0.016). Safety analysis results exhibited that the incidence of adverse reactions of different grades in the observation group and control groups were 88.4% (38/43) and 81.0% (34/42), respectively; The grade ≥3 adverse reactions occurred in 41.9% (18/43) and 33.3% (14/42), respectively, with no statistically significant difference (both <i>P</i>>0.05). The grade≥3 adverse reactions were controlled through dose adjustment and symptomatic treatment. <b>Conclusion:</b> In patients with previously immunotherapy treated advanced NSCLC, anlotinib combination regimens demonstrates preliminary efficacy and tolerable safety profile compared to single
目的:探讨安洛替尼联合治疗方案在已接受免疫治疗的晚期非小细胞肺癌(NSCLC)患者中的有效性和安全性。方法:本研究回顾性纳入2018年10月至2023年10月在郑州大学第一附属医院接受过免疫治疗的85例晚期NSCLC患者,这些患者接受过安洛替尼联合方案或单药化疗。观察组43例患者接受安洛替尼联合方案治疗,对照组42例患者接受单药化疗。观察组采用安洛替尼联合化疗和安洛替尼联合免疫治疗,对照组采用单药化疗。随访期于2024年5月25日结束。比较观察组和对照组患者的基线特征、近期疗效、预后及不良反应。采用Kaplan-Meier法绘制生存曲线,采用log-rank检验比较差异。结果:观察组患者男性29例,女性14例,中位年龄[M (Q1, Q3)] 63(27,73)岁;对照组男性27例,女性15例,中位年龄64(28,73)岁。观察组和对照组客观有效率分别为23.3%(10/43)和14.3%(6/42),差异无统计学意义(P=0.290)。观察组和对照组的疾病控制率分别为83.7%(36/43)和57.1%(24/42),差异有统计学意义(P=0.007)。观察组和对照组的中位随访时间分别为14.2个月和9.6个月。预后结果显示,观察组和对照组的中位PFS分别为6.1个月(95%CI: 2.41 ~ 9.79)和2.9个月(95%CI: 2.59 ~ 3.21)。观察组显著高于对照组(P=0.009)。中位OS分别为15.5个月(95%CI: 8.99 ~ 22.01)和10.3个月(95%CI: 7.87 ~ 12.74)。观察组也显著高于对照组(P=0.016)。安全性分析结果显示,观察组和对照组不同程度不良反应发生率分别为88.4%(38/43)和81.0% (34/42);3级以上不良反应发生率分别为41.9%(18/43)和33.3%(14/42),差异无统计学意义(P < 0.05)。通过调整剂量和对症治疗,控制≥3级不良反应。结论:在先前接受免疫治疗的晚期NSCLC患者中,与单药化疗相比,安洛替尼联合方案显示出初步的有效性和可耐受的安全性。
{"title":"[Effectiveness and safety of anlotinib combination regimens in patients with previously immunotherapy treated advanced non-small cell lung cancer].","authors":"R R Cheng, G W Zhang, C Huang, X J Song, H X Jia","doi":"10.3760/cma.j.cn112137-20250405-00836","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250405-00836","url":null,"abstract":"&lt;p&gt;&lt;p&gt;&lt;b&gt;Objective:&lt;/b&gt; To explore the effectiveness and safety of anlotinib combination regimens in patients with previously immunotherapy treated advanced non-small cell lung cancer (NSCLC). &lt;b&gt;Methods:&lt;/b&gt; This study retrospectively included 85 patients with previously immunotherapy treated advanced NSCLC who received anlotinib combination regimens or single-agent chemotherapy in the First Affiliated Hospital of Zhengzhou University from October 2018 to October 2023. The observation group was consisted of 43 patients who received anlotinib combination regimens, and the control group was consisted of 42 patients who received single-agent chemotherapy. Observation group received anlotinib combined with chemotherapy and anlotinib combined with immunotherapy, while control group received single-agent chemotherapy. The follow-up period ended on May 25, 2024. The baseline characteristics, recent effectiveness, prognosis, and adverse reactions were compared between the observation group and the control group. Survival curves were plotted using the Kaplan-Meier method, and the log-rank test was used to compare the differences. &lt;b&gt;Results:&lt;/b&gt; In observation group, there were 29 males and 14 females with a median age [&lt;i&gt;M&lt;/i&gt; (&lt;i&gt;Q&lt;/i&gt;&lt;sub&gt;1&lt;/sub&gt;, &lt;i&gt;Q&lt;/i&gt;&lt;sub&gt;3&lt;/sub&gt;)] of 63 (27, 73) years; in control group, there were 27 males and 15 females, with a median age of 64 (28, 73) years. Objective response rates for the observation group and control group were 23.3% (10/43) and 14.3% (6/42), respectively, with no statistically significant difference (&lt;i&gt;P&lt;/i&gt;=0.290). Disease control rates were 83.7% (36/43) and 57.1% (24/42) for the observation and the control groups, respectively, with a statistically significant difference (&lt;i&gt;P&lt;/i&gt;=0.007). The median follow-up duration for the observation group and the control group was 14.2 and 9.6 months, respectively. Prognosis results indicated that the median PFS for the observation group and the control group were 6.1 (95%&lt;i&gt;CI&lt;/i&gt;: 2.41-9.79) and 2.9 months (95%&lt;i&gt;CI&lt;/i&gt;: 2.59-3.21), respectively. The observation group was significantly higher than the control group (&lt;i&gt;P&lt;/i&gt;=0.009). The median OS were 15.5 (95%&lt;i&gt;CI&lt;/i&gt;: 8.99-22.01) and 10.3 months (95%&lt;i&gt;CI&lt;/i&gt;: 7.87-12.74), respectively. The observation group was also significantly higher than the control group (&lt;i&gt;P&lt;/i&gt;=0.016). Safety analysis results exhibited that the incidence of adverse reactions of different grades in the observation group and control groups were 88.4% (38/43) and 81.0% (34/42), respectively; The grade ≥3 adverse reactions occurred in 41.9% (18/43) and 33.3% (14/42), respectively, with no statistically significant difference (both &lt;i&gt;P&lt;/i&gt;&gt;0.05). The grade≥3 adverse reactions were controlled through dose adjustment and symptomatic treatment. &lt;b&gt;Conclusion:&lt;/b&gt; In patients with previously immunotherapy treated advanced NSCLC, anlotinib combination regimens demonstrates preliminary efficacy and tolerable safety profile compared to single","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 44","pages":"4041-4047"},"PeriodicalIF":0.0,"publicationDate":"2025-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145649469","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
[AI-assisted transformation from single imaging to multi-omics data analysis enhances the precision diagnosis and treatment of lung cancer/lung nodules]. [人工智能辅助从单一影像到多组学数据分析的转化,提高了肺癌/肺结节的精准诊断和治疗]。
Q3 Medicine Pub Date : 2025-12-02 DOI: 10.3760/cma.j.cn112137-20250602-01355
J J Xu, D Lyu, L P Shi, Q Tan, S F Wang, M Zhou, G H Yang, Y Jin

Conventional radiomics approaches are constrained by suboptimal diagnostic performance, limited capacity to characterize molecular heterogeneity within the tumor microenvironment, and insufficient capture of critical biological information regarding host immune responses. In response, AI-augmented multi-omics analytics have emerged as a core component throughout the management of lung cancer and pulmonary nodules, decoding intricate tumor biological landscapes to deliver novel dimensions for precision diagnosis and treatment, thereby establishing a foundational component of their comprehensive disease management. This cross-dimensional data synthesis not only transcends the informational limitations inherent in unimodal methodologies but also enables integrative profiling spanning anatomical architecture to molecular mechanisms, thereby substantially propelling the advancement of precision diagnosis and treatment of lung cancer and pulmonary nodules. Nevertheless, persistent challenges including inadequate data standardization and limited model interpretability remain to be addressed. The translational pathway is further impeded by delayed clinical validation and technical complexities in multi-omics data integration. Future research endeavors should prioritize the implementation of prospective trials and the development of novel AI technologies to overcome these obstacles, ultimately enabling early detection and personalized therapeutic interventions for lung cancer and pulmonary nodules.

传统的放射组学方法受到以下因素的限制:诊断性能欠佳,表征肿瘤微环境中分子异质性的能力有限,以及对宿主免疫反应的关键生物信息捕获不足。因此,人工智能增强的多组学分析已经成为肺癌和肺结节管理的核心组成部分,可以解读复杂的肿瘤生物学景观,为精确诊断和治疗提供新的维度,从而建立其综合疾病管理的基础组成部分。这种跨维度的数据综合不仅超越了单模方法固有的信息局限性,而且实现了从解剖结构到分子机制的综合分析,从而极大地推动了肺癌和肺结节的精确诊断和治疗的进步。然而,包括数据标准化不足和模型可解释性有限在内的持续挑战仍有待解决。临床验证延迟和多组学数据整合的技术复杂性进一步阻碍了转化途径。未来的研究工作应优先考虑实施前瞻性试验和开发新的人工智能技术,以克服这些障碍,最终实现肺癌和肺结节的早期发现和个性化治疗干预。
{"title":"[AI-assisted transformation from single imaging to multi-omics data analysis enhances the precision diagnosis and treatment of lung cancer/lung nodules].","authors":"J J Xu, D Lyu, L P Shi, Q Tan, S F Wang, M Zhou, G H Yang, Y Jin","doi":"10.3760/cma.j.cn112137-20250602-01355","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250602-01355","url":null,"abstract":"<p><p>Conventional radiomics approaches are constrained by suboptimal diagnostic performance, limited capacity to characterize molecular heterogeneity within the tumor microenvironment, and insufficient capture of critical biological information regarding host immune responses. In response, AI-augmented multi-omics analytics have emerged as a core component throughout the management of lung cancer and pulmonary nodules, decoding intricate tumor biological landscapes to deliver novel dimensions for precision diagnosis and treatment, thereby establishing a foundational component of their comprehensive disease management. This cross-dimensional data synthesis not only transcends the informational limitations inherent in unimodal methodologies but also enables integrative profiling spanning anatomical architecture to molecular mechanisms, thereby substantially propelling the advancement of precision diagnosis and treatment of lung cancer and pulmonary nodules. Nevertheless, persistent challenges including inadequate data standardization and limited model interpretability remain to be addressed. The translational pathway is further impeded by delayed clinical validation and technical complexities in multi-omics data integration. Future research endeavors should prioritize the implementation of prospective trials and the development of novel AI technologies to overcome these obstacles, ultimately enabling early detection and personalized therapeutic interventions for lung cancer and pulmonary nodules.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 44","pages":"4013-4018"},"PeriodicalIF":0.0,"publicationDate":"2025-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145649385","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
[Expert consensus on disability assessment in community-dwelling older adults (2026 edition)]. [社区老年人残疾评估专家共识(2026年版)]。
Q3 Medicine Pub Date : 2025-11-28 DOI: 10.3760/cma.j.cn112137-20250812-02052

As the aging process accelerates in China, disability has become a critical issue affecting the health and quality of life of the elderly. The incidence of disability significantly increases with age, adding to the caregiving burden on families and society. Disability results from the interaction between impairments in body functions and structures and environmental factors, rather than a single cause. This consensus focuses on the functional dimensions of eight core areas: mobility, cognition, emotion, vision, hearing, speech and swallowing, elimination, daily activities, and social participation, along with corresponding assessment measures. It systematically reviews clinical evidence and the latest developments of relevant assessment protocols both domestically and internationally. By integrating expert opinions from multiple disciplines using the Delphi method, the consensus presents eight assessment protocols and recommendations suitable for elderly populations in the community, aiming to provide evidence-based guidance for the early screening of disability in community-dwelling older adults.

随着中国老龄化进程的加速,残疾已成为影响老年人健康和生活质量的关键问题。残疾的发生率随着年龄的增长而显著增加,增加了家庭和社会的照顾负担。残疾是机体功能和结构缺陷与环境因素相互作用的结果,不是单一原因造成的。这一共识侧重于八个核心领域的功能维度:行动能力、认知、情感、视觉、听觉、言语和吞咽、消除、日常活动和社会参与,以及相应的评估措施。它系统地审查临床证据和国内外相关评估方案的最新发展。采用德尔菲法整合多学科专家意见,提出了适合社区老年人的8项评估方案和建议,旨在为社区居住老年人残疾早期筛查提供循证指导。
{"title":"[Expert consensus on disability assessment in community-dwelling older adults (2026 edition)].","authors":"","doi":"10.3760/cma.j.cn112137-20250812-02052","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250812-02052","url":null,"abstract":"<p><p>As the aging process accelerates in China, disability has become a critical issue affecting the health and quality of life of the elderly. The incidence of disability significantly increases with age, adding to the caregiving burden on families and society. Disability results from the interaction between impairments in body functions and structures and environmental factors, rather than a single cause. This consensus focuses on the functional dimensions of eight core areas: mobility, cognition, emotion, vision, hearing, speech and swallowing, elimination, daily activities, and social participation, along with corresponding assessment measures. It systematically reviews clinical evidence and the latest developments of relevant assessment protocols both domestically and internationally. By integrating expert opinions from multiple disciplines using the Delphi method, the consensus presents eight assessment protocols and recommendations suitable for elderly populations in the community, aiming to provide evidence-based guidance for the early screening of disability in community-dwelling older adults.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"106 ","pages":"57-73"},"PeriodicalIF":0.0,"publicationDate":"2025-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145640641","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
[Efficacy of modified endoscopic holmium laser-yellow zebra guidewire loop combined lithotripsy for giant refractory gastric bezoars]. [改良内镜钬激光-黄斑马导丝环联合碎石治疗巨大难治性胃牛黄的疗效]。
Q3 Medicine Pub Date : 2025-11-26 DOI: 10.3760/cma.j.cn112137-20250703-01909
C B Pu, M Li, R H Shi, M Y Li

A retrospective analysis was conducted on the clinical data of patients with giant refractory gastric bezoars treated at Zhongda Hospital of Southeast University between January 2019 and May 2025. All patients underwent modified endoscopic holmium laser-yellow zebra guidewire loop combined lithotripsy. Follow-up gastroscopy was performed 4 weeks postoperatively to analyze the efficacy of this combined technique in treating giant refractory gastric bezoars. A total of 38 patients were included, including 14 males and 24 females, aged (66±12) years (44-88 years). Thirty-five patients successfully achieved bezoar removal after a single treatment session, with a single-session success rate of 92.1% (35/38). Postoperative complications, such as nausea, vomiting, gastric mucosal injury, or pain, occurred in 4 patients (10.5%). At the 4-week follow-up gastroscopy, the complete ulcer healing rate was 87% (20/23). The modified endoscopic holmium laser-yellow zebra guidewire loop combined lithotripsy is a safe and effective treatment for giant refractory gastric bezoars.

回顾性分析2019年1月至2025年5月在东南大学中大医院治疗的巨型难治性胃牛黄患者的临床资料。所有患者均行改良内镜钬激光-黄斑马导丝环联合碎石术。术后4周进行随访胃镜检查,分析该联合技术治疗巨大难治性胃牛黄的疗效。共纳入38例患者,其中男性14例,女性24例,年龄(66±12)岁(44 ~ 88岁)。35例患者在单次治疗后成功去除牛黄,单次成功率为92.1%(35/38)。术后出现恶心、呕吐、胃黏膜损伤或疼痛等并发症4例(10.5%)。随访4周胃镜检查,溃疡完全愈合率为87%(20/23)。改良内镜钬激光-黄斑马导丝环联合碎石是治疗巨大难治性胃牛黄的一种安全有效的方法。
{"title":"[Efficacy of modified endoscopic holmium laser-yellow zebra guidewire loop combined lithotripsy for giant refractory gastric bezoars].","authors":"C B Pu, M Li, R H Shi, M Y Li","doi":"10.3760/cma.j.cn112137-20250703-01909","DOIUrl":"https://doi.org/10.3760/cma.j.cn112137-20250703-01909","url":null,"abstract":"<p><p>A retrospective analysis was conducted on the clinical data of patients with giant refractory gastric bezoars treated at Zhongda Hospital of Southeast University between January 2019 and May 2025. All patients underwent modified endoscopic holmium laser-yellow zebra guidewire loop combined lithotripsy. Follow-up gastroscopy was performed 4 weeks postoperatively to analyze the efficacy of this combined technique in treating giant refractory gastric bezoars. A total of 38 patients were included, including 14 males and 24 females, aged (66±12) years (44-88 years). Thirty-five patients successfully achieved bezoar removal after a single treatment session, with a single-session success rate of 92.1% (35/38). Postoperative complications, such as nausea, vomiting, gastric mucosal injury, or pain, occurred in 4 patients (10.5%). At the 4-week follow-up gastroscopy, the complete ulcer healing rate was 87% (20/23). The modified endoscopic holmium laser-yellow zebra guidewire loop combined lithotripsy is a safe and effective treatment for giant refractory gastric bezoars.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 ","pages":"1-4"},"PeriodicalIF":0.0,"publicationDate":"2025-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145606577","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
[Clinical practice guidelines for the in vitro preservation and repair of severed limbs (2025 edition)]. 【断肢体外保存与修复临床实践指南(2025年版)】。
Q3 Medicine Pub Date : 2025-11-25 DOI: 10.3760/cma.j.cn112137-20250423-00998

Replantation of amputated limbs is the most effective treatment for severe limb injuries, and allogeneic limb transplantation is also one of the potentially most effective methods to address limb amputation injuries in the future. The preservation and repair of severed limbs outside the body is a key factor in improving the success rate of limb replantation and transplantation. Currently, the techniques for preserving and repairing severed limbs outside the body include static refrigeration preservation technology, immersion in cryoprotective solution technology, deep cryogenic freezing technology, mechanical perfusion technology, temporary vascular shunt technology, autologous ectopic grafting technology, and experimental-stage xenogeneic cross-circulation technology. By optimizing key parameters such as temperature, pressure, and preservation solution, these techniques can extend the preservation time of the limbs and increase the success rate of replantation. Traditional techniques have a short preservation time and cannot meet clinical needs. Emerging technologies are in the ascendant and are subject to different opinions. National Clinical Research Center for Orthopedics Sports Medicine & Rehabilitation, the Microsurgery Branch of Chinese Medical Association and the Microsurgery Branch of Beijing Orthopedic Association, based on current evidence-based medical evidence, have formulated the "Clinical practice guidelines for the in vitro preservation and repair of severed limbs (2025 edition)". This guideline systematically evaluates a series of literature and related evidence-based medical research evidence published domestically and internationally in the field of organ preservation in recent years, and adds evidence-based medical research data based on the Chinese population, with the aim of further standardizing the relevant techniques for ex vivo preservation of amputated limbs in China, for industry reference.

断肢再植是严重肢体损伤最有效的治疗方法,异体肢体移植也是未来解决肢体截肢损伤最有效的方法之一。断肢的体外保存和修复是提高肢体再植和移植成功率的关键因素。目前体外保存修复断肢的技术有静态冷藏保存技术、冷冻保护液浸泡技术、深度低温冷冻技术、机械灌注技术、临时血管分流技术、自体异位移植技术、实验阶段异种交叉循环技术等。通过优化温度、压力、保存液等关键参数,延长义肢保存时间,提高再植成功率。传统方法保存时间短,不能满足临床需要。新兴技术方兴未艾,并受到不同意见的影响。国家骨科运动医学与康复临床研究中心、中华医学会显微外科分会、北京市骨科学会显微外科分会根据现有循证医学证据,制定了《断肢体外保存与修复临床实践指南(2025年版)》。本指南系统评价了近年来国内外在器官保存领域发表的一系列文献及相关循证医学研究证据,并增加了基于中国人群的循证医学研究数据,旨在进一步规范中国断肢离体保存相关技术,供行业参考。
{"title":"[Clinical practice guidelines for the in vitro preservation and repair of severed limbs (2025 edition)].","authors":"","doi":"10.3760/cma.j.cn112137-20250423-00998","DOIUrl":"10.3760/cma.j.cn112137-20250423-00998","url":null,"abstract":"<p><p>Replantation of amputated limbs is the most effective treatment for severe limb injuries, and allogeneic limb transplantation is also one of the potentially most effective methods to address limb amputation injuries in the future. The preservation and repair of severed limbs outside the body is a key factor in improving the success rate of limb replantation and transplantation. Currently, the techniques for preserving and repairing severed limbs outside the body include static refrigeration preservation technology, immersion in cryoprotective solution technology, deep cryogenic freezing technology, mechanical perfusion technology, temporary vascular shunt technology, autologous ectopic grafting technology, and experimental-stage xenogeneic cross-circulation technology. By optimizing key parameters such as temperature, pressure, and preservation solution, these techniques can extend the preservation time of the limbs and increase the success rate of replantation. Traditional techniques have a short preservation time and cannot meet clinical needs. Emerging technologies are in the ascendant and are subject to different opinions. National Clinical Research Center for Orthopedics Sports Medicine & Rehabilitation, the Microsurgery Branch of Chinese Medical Association and the Microsurgery Branch of Beijing Orthopedic Association, based on current evidence-based medical evidence, have formulated the \"Clinical practice guidelines for the in vitro preservation and repair of severed limbs (2025 edition)\". This guideline systematically evaluates a series of literature and related evidence-based medical research evidence published domestically and internationally in the field of organ preservation in recent years, and adds evidence-based medical research data based on the Chinese population, with the aim of further standardizing the relevant techniques for ex vivo preservation of amputated limbs in China, for industry reference.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 43","pages":"3932-3946"},"PeriodicalIF":0.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145551305","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
[Expert consensus on the diagnosis and treatment of metastatic paraganglioma and pheochromocytoma]. 【转移性副神经节瘤、嗜铬细胞瘤诊治专家共识】。
Q3 Medicine Pub Date : 2025-11-25 DOI: 10.3760/cma.j.cn112137-20250812-02062

Approximately 15%-25% paragangliomas and pheochromocytomas (PPGL) can metastasize. Untreated metastatic PPGL (MPP) patients have a 5-year survival rate below 50%, while standardized diagnosis and treatment can significantly improve prognosis. Currently, there has been no established national guidelines for MPP management in China. To address this gap, the Adrenal Group of Chinese Society of Endocrinology convened a multidisciplinary panel of experts from endocrinology, oncology, surgery, nuclear medicine, radiation oncology, pathology, laboratory medicine, and interventional therapy. Based on evidence-based medicine, the latest global research, and clinical data from China, the panel has developed a consensus statement. This consensus encompasses various aspects of MPP, including its epidemiology, pathogenesis, risk factors and prediction for dissemination, clinical manifestations, diagnosis, treatment, and prognosis. A total of 16 recommendation statements have been formulated, with the aim of assisting clinicians in developing standardized strategies for the diagnosis and treatment of MPP.

大约15%-25%的副神经节瘤和嗜铬细胞瘤(PPGL)可以转移。未经治疗的转移性PPGL (MPP)患者5年生存率低于50%,而标准化的诊断和治疗可显著改善预后。目前,中国还没有建立MPP管理的国家指导方针。为了弥补这一差距,中国内分泌学会肾上腺组召集了来自内分泌学、肿瘤学、外科、核医学、放射肿瘤学、病理学、检验医学和介入治疗的多学科专家小组。基于循证医学、最新的全球研究和来自中国的临床数据,该小组制定了一份共识声明。这一共识涵盖了MPP的各个方面,包括其流行病学、发病机制、危险因素和传播预测、临床表现、诊断、治疗和预后。共制定了16项建议声明,目的是协助临床医生制定诊断和治疗MPP的标准化战略。
{"title":"[Expert consensus on the diagnosis and treatment of metastatic paraganglioma and pheochromocytoma].","authors":"","doi":"10.3760/cma.j.cn112137-20250812-02062","DOIUrl":"10.3760/cma.j.cn112137-20250812-02062","url":null,"abstract":"<p><p>Approximately 15%-25% paragangliomas and pheochromocytomas (PPGL) can metastasize. Untreated metastatic PPGL (MPP) patients have a 5-year survival rate below 50%, while standardized diagnosis and treatment can significantly improve prognosis. Currently, there has been no established national guidelines for MPP management in China. To address this gap, the Adrenal Group of Chinese Society of Endocrinology convened a multidisciplinary panel of experts from endocrinology, oncology, surgery, nuclear medicine, radiation oncology, pathology, laboratory medicine, and interventional therapy. Based on evidence-based medicine, the latest global research, and clinical data from China, the panel has developed a consensus statement. This consensus encompasses various aspects of MPP, including its epidemiology, pathogenesis, risk factors and prediction for dissemination, clinical manifestations, diagnosis, treatment, and prognosis. A total of 16 recommendation statements have been formulated, with the aim of assisting clinicians in developing standardized strategies for the diagnosis and treatment of MPP.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 43","pages":"3917-3931"},"PeriodicalIF":0.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145551270","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
[Expert consensus on the construction of stroke centers at high altitude (2025 edition)]. 【高原卒中中心建设专家共识(2025年版)】。
Q3 Medicine Pub Date : 2025-11-25 DOI: 10.3760/cma.j.cn112137-20250608-01398

In response to the urgent needs and existing challenges of stroke prevention and treatment in high-altitude areas, the Expert Committee of the Million Disability Reduction Project of the National Health Commission took the lead and jointly developed "Expert consensus on the construction of stroke centers at high altitude (2025 edition)" with multidisciplinary experts, on the bsais of the guidelines and standards for the construction of secondary and tertiary stroke centers in high-altitude areas. The consensus clarifies the purpose, the coverage, the initiating and supporting units, the expert group and the process of formulation. It elaborates the construction goals of stroke centers in high-altitude areas and the functional roles of secondary and tertiary stroke centers. It also specifies the organizational management structures for these centers, the construction standards for secondary and tertiary stroke centers, and the quality management systems for stroke prevention and treatment, etc. By providing a framework for the allocation of medical resources and quality oversight in plateau regions, this consensus aims to standardize the stroke diagnosis and treatment processes, enhance the efficiency and quality of stroke care, improve patient prognosis, and elevate the overall level of stroke medical service system construction in China. It is recommended to promote and apply it in relevant medical institutions in high-altitude areas.

针对高海拔地区脑卒中防治的迫切需求和存在的挑战,国家卫健委百万降残工程专家委员会牵头与多学科专家共同制定了《高海拔地区脑卒中中心建设专家共识(2025年版)》。根据高海拔地区二、三级卒中中心建设的指导意见和标准。共识明确了目的、范围、发起单位和支持单位、专家组和制定过程。阐述了高海拔地区脑卒中中心的建设目标和二级、三级脑卒中中心的功能作用。规定了脑卒中中心的组织管理机构、二、三级脑卒中中心的建设标准、脑卒中防治质量管理体系等。该共识为高原地区医疗资源配置和质量监督提供框架,旨在规范卒中诊疗流程,提高卒中诊疗效率和质量,改善患者预后,提升中国卒中医疗服务体系建设整体水平。建议在高海拔地区相关医疗机构推广应用。
{"title":"[Expert consensus on the construction of stroke centers at high altitude (2025 edition)].","authors":"","doi":"10.3760/cma.j.cn112137-20250608-01398","DOIUrl":"10.3760/cma.j.cn112137-20250608-01398","url":null,"abstract":"<p><p>In response to the urgent needs and existing challenges of stroke prevention and treatment in high-altitude areas, the Expert Committee of the Million Disability Reduction Project of the National Health Commission took the lead and jointly developed \"Expert consensus on the construction of stroke centers at high altitude (2025 edition)\" with multidisciplinary experts, on the bsais of the guidelines and standards for the construction of secondary and tertiary stroke centers in high-altitude areas. The consensus clarifies the purpose, the coverage, the initiating and supporting units, the expert group and the process of formulation. It elaborates the construction goals of stroke centers in high-altitude areas and the functional roles of secondary and tertiary stroke centers. It also specifies the organizational management structures for these centers, the construction standards for secondary and tertiary stroke centers, and the quality management systems for stroke prevention and treatment, etc. By providing a framework for the allocation of medical resources and quality oversight in plateau regions, this consensus aims to standardize the stroke diagnosis and treatment processes, enhance the efficiency and quality of stroke care, improve patient prognosis, and elevate the overall level of stroke medical service system construction in China. It is recommended to promote and apply it in relevant medical institutions in high-altitude areas.</p>","PeriodicalId":24023,"journal":{"name":"Zhonghua yi xue za zhi","volume":"105 43","pages":"3947-3954"},"PeriodicalIF":0.0,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145551317","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
期刊
Zhonghua yi xue za zhi
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1