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Montgomery T-tube tracheal stent implantation with high-flow nasal oxygen under conscious sedation: A case report. 清醒镇静下高流量鼻吸氧蒙哥马利t管气管支架植入术1例。
IF 1.5 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2026-02-01 Epub Date: 2026-02-04 DOI: 10.1177/03000605251411746
Danqian Su, Yan Chen, Zhenyu Yang, Xinyu Yuan, Daxiong Zeng, Jian Li, Junhong Jiang

Montgomery T-tube tracheal stent placement is a well-established treatment for severe subglottic stenosis. This procedure is typically performed using a rigid bronchoscope under general anesthesia. However, a major limitation of this approach is the requirement for neck hyperextension, which is not feasible in patients with cervical spine injuries. This report details a complex case of subglottic stenosis in a patient with a cervical spinal cord injury and incomplete paraplegia, in whom conventional Montgomery T-tube tracheal stent placement was difficult to achieve. We performed Montgomery T-tube tracheal stent implantation under conscious sedation with oxygen support provided by high-flow nasal cannula, minimizing the risks of general anesthesia and cervical manipulation. The successful outcome suggests that the combination of conscious sedation and high-flow nasal cannula may represent a safe and practical strategy for treating carefully selected complex airway cases. Although this case highlights a promising pathway, further studies are required to confirm the efficacy of this strategy and define its clinical indications in larger patient populations.

蒙哥马利t管气管支架置入术是治疗严重声门下狭窄的有效方法。该手术通常在全身麻醉下使用刚性支气管镜进行。然而,该入路的一个主要限制是需要颈部过伸,这在颈椎损伤患者中是不可行的。本报告详细介绍了一个复杂的病例声门下狭窄患者颈脊髓损伤和不完全性截瘫,在传统的蒙哥马利t管气管支架置入是困难的。我们在清醒镇静下实施蒙哥马利t管气管支架植入术,高流量鼻插管提供氧气支持,最大限度地降低了全麻和颈椎操作的风险。成功的结果表明,有意识镇静和高流量鼻插管的结合可能是治疗精心挑选的复杂气道病例的一种安全实用的策略。虽然这个病例强调了一个有希望的途径,但需要进一步的研究来确认该策略的有效性,并在更大的患者群体中确定其临床适应症。
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引用次数: 0
Efficacy of arthroscopic debridement combined with platelet-rich plasma injection for knee osteoarthritis: An updated systematic review and meta-analysis of randomized controlled trials. 关节镜清创联合富血小板血浆注射治疗膝骨关节炎的疗效:一项随机对照试验的最新系统评价和荟萃分析。
IF 1.5 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2026-02-01 Epub Date: 2026-02-08 DOI: 10.1177/03000605251404774
Li Fengzhen, Lu Jinyan, Zhou Honghai, Wu Fengbiao, Xu Zichun, Chen Yulong
<p><p>ObjectiveThis study aimed to provide an updated assessment of the clinical efficacy and safety of arthroscopic debridement combined with platelet-rich plasma injection for the treatment of knee osteoarthritis.MethodsOn 16 August 2025, we systematically searched multiple databases, including the Cochrane Library, Embase, Ovid Medline, PubMed, Web of Science, China Biology Medicine Disc, China National Knowledge Infrastructure, Wanfang, and VIP Chinese Science and Technology Journal Database (VIPC), for randomized controlled trials evaluating the efficacy of arthroscopic debridement combined with platelet-rich plasma injection in the management of knee osteoarthritis. Outcome measures included the following: (a) clinical response rate; (b) visual analog scale score; (c) Lysholm score; (d) Western Ontario and McMaster Universities Osteoarthritis Index score; and (e) adverse reactions. Data were recorded and analyzed using RevMan 5.4 software. The systematic review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, and the research protocol was registered on the International Prospective Register of Systematic Reviews (PROSPERO) platform (registration number: CRD420251127571).ResultsA total of 17 studies involving 1587 patients were included. Meta-analysis results showed that compared with the control group, the treatment group demonstrated a statistically significant difference in the overall clinical response rate: odds ratio = 5.38; 95% confidence interval: 3.45, 8.38; <i>p</i> < 0.00001. Subgroup analyses based on follow-up duration (3, 6, and 12 months) demonstrated a <i>p</i> value of 1.00 and I² value of 0%. Meta-analysis results for each subgroup were as follows: odds ratio = 5.66; 95% confidence interval: 2.14, 14.94; <i>p</i> = 0.0005 for 3 months; odds ratio = 5.68; 95% confidence interval: 2.87, 11.27; <i>p</i> < 0.00001 for 6 months; and odds ratio = 5.40; 95% confidence interval: 2.44, 11.96; <i>p</i> < 0.0001 for 12 months. The treatment group also exhibited a statistically significant reduction in visual analog scale scores: mean difference = -0.62; 95% confidence interval: -1.03, -0.20; <i>p</i> = 0.004. Lysholm scores increased significantly in the treatment group: mean difference = 5.07; 95% confidence interval: 2.99, 7.14; <i>p</i> < 0.00001. The Western Ontario and McMaster Universities Osteoarthritis Index score indicated statistically significant difference: mean difference = -8.65; 95% confidence interval: -11.13, -6.18; <i>p</i> < 0.00001. Adverse reaction rate demonstrated no statistically significant difference: odds ratio = 0.73; 95% confidence interval: 0.28, 1.89; <i>P</i> = 0.52.ConclusionThe overall clinical response rate of arthroscopic debridement combined with platelet-rich plasma injection for knee osteoarthritis was significantly higher than that of the control group. The visual analog scale scores were lower, indicating effective pain relief in patient
目的评价关节镜下清创联合富血小板血浆注射治疗膝关节骨性关节炎的临床疗效和安全性。方法于2025年8月16日,系统检索Cochrane Library、Embase、Ovid Medline、PubMed、Web of Science、中国生物医学数据库、中国国家知识基础设施、万方、VIP中国科技期刊数据库(VIPC)等多个数据库,纳入评估关节镜清创联合富血小板血浆注射治疗膝关节骨性关节炎疗效的随机对照试验。结局指标包括:(a)临床缓解率;(b)视觉模拟量表评分;(c) Lysholm乐谱;(d)西安大略和麦克马斯特大学骨关节炎指数评分;(e)不良反应。采用RevMan 5.4软件对数据进行记录和分析。系统评价按照系统评价和荟萃分析指南的首选报告项目进行,研究方案在国际前瞻性系统评价注册(PROSPERO)平台上注册(注册号:CRD420251127571)。结果共纳入17项研究,1587例患者。meta分析结果显示,治疗组与对照组比较,总临床有效率差异有统计学意义:优势比= 5.38;95%置信区间:3.45,8.38;p p值为1.00,I²值为0%。各亚组meta分析结果如下:优势比= 5.66;95%置信区间:2.14,14.94;3个月P = 0.0005;优势比= 5.68;95%置信区间:2.87,11.27;p p = 0.004。治疗组Lysholm评分显著升高:平均差异= 5.07;95%置信区间:2.99,7.14;p p = 0.52。结论关节镜下清创联合富血小板血浆注射治疗膝关节骨性关节炎的临床总有效率明显高于对照组。视觉模拟量表得分较低,表明膝关节骨关节炎患者疼痛得到有效缓解。Lysholm评分较高,表明与对照组相比,膝关节功能有显著改善。西安大略省和麦克马斯特大学骨关节炎指数评分明显低于对照组,反映了关节镜清创联合富血小板血浆注射治疗膝关节骨关节炎通过改善疼痛、僵硬和功能损害的显著疗效。关节镜清创联合富血小板血浆注射组不良反应发生率与对照组无明显差异,说明富血小板血浆注射不会增加不良事件发生的风险。
{"title":"Efficacy of arthroscopic debridement combined with platelet-rich plasma injection for knee osteoarthritis: An updated systematic review and meta-analysis of randomized controlled trials.","authors":"Li Fengzhen, Lu Jinyan, Zhou Honghai, Wu Fengbiao, Xu Zichun, Chen Yulong","doi":"10.1177/03000605251404774","DOIUrl":"https://doi.org/10.1177/03000605251404774","url":null,"abstract":"&lt;p&gt;&lt;p&gt;ObjectiveThis study aimed to provide an updated assessment of the clinical efficacy and safety of arthroscopic debridement combined with platelet-rich plasma injection for the treatment of knee osteoarthritis.MethodsOn 16 August 2025, we systematically searched multiple databases, including the Cochrane Library, Embase, Ovid Medline, PubMed, Web of Science, China Biology Medicine Disc, China National Knowledge Infrastructure, Wanfang, and VIP Chinese Science and Technology Journal Database (VIPC), for randomized controlled trials evaluating the efficacy of arthroscopic debridement combined with platelet-rich plasma injection in the management of knee osteoarthritis. Outcome measures included the following: (a) clinical response rate; (b) visual analog scale score; (c) Lysholm score; (d) Western Ontario and McMaster Universities Osteoarthritis Index score; and (e) adverse reactions. Data were recorded and analyzed using RevMan 5.4 software. The systematic review was conducted following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, and the research protocol was registered on the International Prospective Register of Systematic Reviews (PROSPERO) platform (registration number: CRD420251127571).ResultsA total of 17 studies involving 1587 patients were included. Meta-analysis results showed that compared with the control group, the treatment group demonstrated a statistically significant difference in the overall clinical response rate: odds ratio = 5.38; 95% confidence interval: 3.45, 8.38; &lt;i&gt;p&lt;/i&gt; &lt; 0.00001. Subgroup analyses based on follow-up duration (3, 6, and 12 months) demonstrated a &lt;i&gt;p&lt;/i&gt; value of 1.00 and I² value of 0%. Meta-analysis results for each subgroup were as follows: odds ratio = 5.66; 95% confidence interval: 2.14, 14.94; &lt;i&gt;p&lt;/i&gt; = 0.0005 for 3 months; odds ratio = 5.68; 95% confidence interval: 2.87, 11.27; &lt;i&gt;p&lt;/i&gt; &lt; 0.00001 for 6 months; and odds ratio = 5.40; 95% confidence interval: 2.44, 11.96; &lt;i&gt;p&lt;/i&gt; &lt; 0.0001 for 12 months. The treatment group also exhibited a statistically significant reduction in visual analog scale scores: mean difference = -0.62; 95% confidence interval: -1.03, -0.20; &lt;i&gt;p&lt;/i&gt; = 0.004. Lysholm scores increased significantly in the treatment group: mean difference = 5.07; 95% confidence interval: 2.99, 7.14; &lt;i&gt;p&lt;/i&gt; &lt; 0.00001. The Western Ontario and McMaster Universities Osteoarthritis Index score indicated statistically significant difference: mean difference = -8.65; 95% confidence interval: -11.13, -6.18; &lt;i&gt;p&lt;/i&gt; &lt; 0.00001. Adverse reaction rate demonstrated no statistically significant difference: odds ratio = 0.73; 95% confidence interval: 0.28, 1.89; &lt;i&gt;P&lt;/i&gt; = 0.52.ConclusionThe overall clinical response rate of arthroscopic debridement combined with platelet-rich plasma injection for knee osteoarthritis was significantly higher than that of the control group. The visual analog scale scores were lower, indicating effective pain relief in patient","PeriodicalId":16129,"journal":{"name":"Journal of International Medical Research","volume":"54 2","pages":"3000605251404774"},"PeriodicalIF":1.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146142610","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Severe acute respiratory distress syndrome following laparoscopic appendectomy in a previously healthy middle-aged man: A case report. 先前健康的中年男子腹腔镜阑尾切除术后出现严重急性呼吸窘迫综合征1例报告。
IF 1.5 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2026-02-01 Epub Date: 2026-02-08 DOI: 10.1177/03000605261418802
Hongqun Zhang, Zhuoyin Wang, Yi Jin

This case report describes an exceptionally rare occurrence of severe acute respiratory distress syndrome following laparoscopic appendectomy in a previously healthy 57-year-old male. The patient presented with acute appendicitis and underwent an uncomplicated surgical procedure. Approximately 4 h postoperatively, he developed rapid respiratory deterioration with severe hypoxemia, fulfilling the Berlin criteria for severe acute respiratory distress syndrome (partial pressure of arterial oxygen/fraction of inspired oxygen ratio, 99.2). Other causes, including aspiration, pulmonary embolism, and cardiac failure, were excluded. The patient was managed in the intensive care unit with lung-protective ventilation in accordance with the Acute Respiratory Distress Syndrome Network (ARDSNet) protocol along with antibiotics and corticosteroids. He demonstrated rapid clinical improvement, was extubated on postoperative day 7, and discharged on postoperative day 8. This case highlights that severe acute respiratory distress syndrome, although rare, can complicate routine surgical procedures and underscores the importance of early recognition and multidisciplinary management in achieving favorable outcomes.

本病例报告描述了一个异常罕见的发生严重急性呼吸窘迫综合征后,腹腔镜阑尾切除术,先前健康的57岁男性。患者表现为急性阑尾炎,并接受了简单的外科手术。术后约4小时,患者出现严重低氧血症的快速呼吸恶化,符合严重急性呼吸窘迫综合征的柏林标准(动脉氧分压/吸入氧分数比,99.2)。排除其他原因,包括误吸、肺栓塞和心力衰竭。根据急性呼吸窘迫综合征网络(ARDSNet)方案,患者在重症监护病房接受肺保护性通气治疗,同时使用抗生素和皮质类固醇。患者临床改善迅速,术后第7天拔管,术后第8天出院。本病例强调了严重急性呼吸窘迫综合征虽然罕见,但会使常规外科手术复杂化,并强调了早期识别和多学科管理对获得良好结果的重要性。
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引用次数: 0
Effects of coenzyme Q10 analogs on oxidative stress, muscle, and metabolism after exercise: A meta-analysis and systematic review. 辅酶Q10类似物对运动后氧化应激、肌肉和代谢的影响:荟萃分析和系统回顾。
IF 1.5 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2026-02-01 Epub Date: 2026-02-09 DOI: 10.1177/03000605251411151
Yangqi Zhang, Yilang He, Mingling Ma, Hui Dong, Zijian Ma

ObjectiveThis study aimed to investigate whether coenzyme Q10 is effective in preventing exercise-induced oxidative stress and muscle damage.MethodsFourteen randomized controlled studies examining the effects of supplementation with coenzyme Q10 analogs on postexercise oxidative stress and muscle damage were identified through searches in literature databases, including PubMed, the Cochrane Library, Embase, and Web of Science, and then the quality of the included studies was assessed. Quantitative and qualitative analyses were performed.ResultsThe study screened 14 randomized controlled trials that included a total of 433 subjects. The results demonstrated that oral coenzyme Q10 elevated blood coenzyme Q10 concentration (standardized mean difference: 2.710, 95% confidence interval: 1.57-3.85, p < 0.00001) and reduced blood malondialdehyde concentration (standardized mean difference: -0.289, 95% confidence interval: -0.541 to -0.038, p = 0.024). Additionally, oral coenzyme Q10 was found to reduce blood creatine kinase values (standardized mean difference: -1.532, 95% confidence interval: -2.856 to -0.209, p = 0.023), suggesting a potential protective effect on skeletal muscle. The metabolism-related blood lactate and maximal oxygen uptake levels were not affected by coenzyme Q10 (standardized mean difference: -0.68, 95% confidence interval: -1.89 to 0.53, p = 0.271; standardized mean difference: -0.156, 95% confidence interval: -0.79 to 0.478, p = 0.630).ConclusionsCoenzyme Q10 may reduce exercise-induced oxidative stress on blood malondialdehyde and exert a protective effect on muscle; however, no effect was observed from the anaerobic and aerobic metabolism of the organism.

目的探讨辅酶Q10是否能有效预防运动引起的氧化应激和肌肉损伤。方法通过检索PubMed、Cochrane图书馆、Embase和Web of Science等文献数据库,确定了14项研究补充辅酶Q10类似物对运动后氧化应激和肌肉损伤影响的随机对照研究,并对纳入研究的质量进行评估。进行了定量和定性分析。结果本研究筛选了14项随机对照试验,共纳入433名受试者。结果表明,口服辅酶Q10可提高血中辅酶Q10浓度(标准化平均差值:2.710,95%可信区间:1.57-3.85,p
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引用次数: 0
Safety profile of progesterone: Insights from an FDA Adverse Event Reporting System (FAERS)-based pharmacovigilance study. 黄体酮的安全性:来自FDA不良事件报告系统(FAERS)的药物警戒研究的见解。
IF 1.5 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2026-02-01 Epub Date: 2026-02-08 DOI: 10.1177/03000605261417447
Ren Xu, Xiaona Wang, Junqin Zhang, Yanan Ren, Luyang Su, Lu Sang, Jianzhi Su

ObjectiveThis study aimed to evaluate the safety profile of progesterone by analyzing adverse event data from the Food and Drug Administration Adverse Event Reporting System (FAERS) between 2004 and 2024.Materials and methodsThis retrospective, observational pharmacovigilance study was based on data from the FAERS database. A total of 1827 adverse event reports associated with progesterone were retrieved. Disproportionality analysis methods, including the reporting odds ratio, proportional reporting ratio, Bayesian confidence propagation neural network, and multi-item gamma Poisson shrinker, were used to evaluate the frequency, signal strength, and time-to-onset of adverse events.ResultsAmong 24,589,239 adverse event reports in the reporting system, 1827 were associated with progesterone, covering 22 system organ classes and 152 preferred terms. The most frequently reported preferred terms were maternal exposure during pregnancy (151 cases), spontaneous abortion (144 cases), and abnormal product odor (114 cases). The top three preferred terms showing the strongest signals were decidual cast (reporting odds ratio: 2825.23), chondrodermatitis nodularis chronica helicis (reporting odds ratio: 3897.61), and autoimmune dermatitis (reporting odds ratio: 1519.29). Most adverse events occurred within 30 to 180 days after exposure. Newly identified preferred terms associated with progesterone included acute eosinophilic pneumonia, meningioma, and autoimmune dermatitis.ConclusionsThis study identified notable safety concerns associated with progesterone use and detected several rare adverse events. These findings underscore the need for continued monitoring, updated prescribing guidelines, and further investigation into progesterone formulations and adverse event mechanisms.

目的通过分析2004年至2024年美国食品药品监督管理局不良事件报告系统(FAERS)的不良事件数据,评价黄体酮的安全性。材料和方法本回顾性观察性药物警戒研究基于FAERS数据库的数据。共检索到1827例与黄体酮相关的不良事件报告。歧化分析方法,包括报告优势比、比例报告比、贝叶斯置信传播神经网络和多项目伽玛泊松收缩器,用于评估不良事件的频率、信号强度和发病时间。结果报告系统中24589239例不良事件报告中,与黄体酮相关的不良事件1827例,涉及22个系统器官类别和152个首选术语。最常报道的首选术语是怀孕期间母亲暴露(151例),自然流产(144例)和异常产品气味(114例)。显示最强信号的前三个首选术语是蜕膜性皮炎(报告优势比:2825.23)、慢性螺旋结节性软骨性皮炎(报告优势比:3897.61)和自身免疫性皮炎(报告优势比:1519.29)。大多数不良事件发生在接触后30至180天内。新发现的与黄体酮相关的首选术语包括急性嗜酸性肺炎、脑膜瘤和自身免疫性皮炎。结论:本研究发现了与黄体酮使用相关的显著安全性问题,并发现了一些罕见的不良事件。这些发现强调需要继续监测,更新处方指南,并进一步调查黄体酮配方和不良事件机制。
{"title":"Safety profile of progesterone: Insights from an FDA Adverse Event Reporting System (FAERS)-based pharmacovigilance study.","authors":"Ren Xu, Xiaona Wang, Junqin Zhang, Yanan Ren, Luyang Su, Lu Sang, Jianzhi Su","doi":"10.1177/03000605261417447","DOIUrl":"https://doi.org/10.1177/03000605261417447","url":null,"abstract":"<p><p>ObjectiveThis study aimed to evaluate the safety profile of progesterone by analyzing adverse event data from the Food and Drug Administration Adverse Event Reporting System (FAERS) between 2004 and 2024.Materials and methodsThis retrospective, observational pharmacovigilance study was based on data from the FAERS database. A total of 1827 adverse event reports associated with progesterone were retrieved. Disproportionality analysis methods, including the reporting odds ratio, proportional reporting ratio, Bayesian confidence propagation neural network, and multi-item gamma Poisson shrinker, were used to evaluate the frequency, signal strength, and time-to-onset of adverse events.ResultsAmong 24,589,239 adverse event reports in the reporting system, 1827 were associated with progesterone, covering 22 system organ classes and 152 preferred terms. The most frequently reported preferred terms were maternal exposure during pregnancy (151 cases), spontaneous abortion (144 cases), and abnormal product odor (114 cases). The top three preferred terms showing the strongest signals were decidual cast (reporting odds ratio: 2825.23), chondrodermatitis nodularis chronica helicis (reporting odds ratio: 3897.61), and autoimmune dermatitis (reporting odds ratio: 1519.29). Most adverse events occurred within 30 to 180 days after exposure. Newly identified preferred terms associated with progesterone included acute eosinophilic pneumonia, meningioma, and autoimmune dermatitis.ConclusionsThis study identified notable safety concerns associated with progesterone use and detected several rare adverse events. These findings underscore the need for continued monitoring, updated prescribing guidelines, and further investigation into progesterone formulations and adverse event mechanisms.</p>","PeriodicalId":16129,"journal":{"name":"Journal of International Medical Research","volume":"54 2","pages":"3000605261417447"},"PeriodicalIF":1.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146142648","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Retrospective observational assessment of the safety, performance, and utility of an antimicrobial/antithrombogenic peripherally inserted central catheter in pediatric patients. 在儿科患者中使用抗菌/抗血栓形成外周中心导管的安全性、性能和效用的回顾性观察性评估。
IF 1.5 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2026-02-01 Epub Date: 2026-02-04 DOI: 10.1177/03000605261418861
Thomas E Philbeck, Caroline Ryan, Amy Bardin

BackgroundTo determine the safety and performance of an antimicrobial/antithrombogenic peripherally inserted central catheter, a retrospective cohort study was conducted.MethodsData were collected using chart audits by clinicians in the US, UK, and EU in 2021 and 2022 for patients requiring an antimicrobial/antithrombogenic peripherally inserted central catheter. The primary outcome endpoint was successful completion of treatment without elective device removal due to adverse events. The secondary outcome endpoint was the incidence of device-related adverse events. Following the initial analysis of the index study, which included adult and pediatric patients, data from additional pediatric cases were collected. Charts lacking primary endpoint data were excluded. Standard descriptive statistics and analyses of categorical variables were performed without adjustment and with minimal stratification.ResultsA total of 38 healthcare providers collected data for 175 evaluable cases, of which 54.3% were male. The duration of use ranged from less than 1 day to 253 days. Treatment was successfully completed without elective device removal due to adverse events in 90.3% of cases. In 18 cases (10.3%), the patients experienced adverse events, with a total of 21 device-related adverse events reported, corresponding to 5 events per 1000 catheter days. None of the reported events were deemed serious or unexpected.ConclusionsThese findings suggest the potential for safe use of the antimicrobial/antithrombogenic peripherally inserted central catheter in the pediatric patient population, with no elective device removal due to adverse events in 90% of cases. No cases of central line-associated bloodstream infection, thrombosis, or anaphylaxis were reported; however, these findings should be interpreted with caution given the moderate sample size and the rarity of such events in general practice. Owing to the limitations of this study, including the risk of bias inherent to retrospective studies, prospective controlled trials with rigorous outcome assessments are needed to confirm these observations.

背景:为了确定抗菌/抗血栓形成外周中心导管的安全性和性能,进行了一项回顾性队列研究。方法由美国、英国和欧盟的临床医生在2021年和2022年对需要抗菌/抗血栓形成的外周插入中心导管的患者进行图表审计,收集数据。主要结局终点是成功完成治疗,没有因不良事件而选择性移除装置。次要终点是器械相关不良事件的发生率。在对包括成人和儿科患者的指数研究进行初步分析后,收集了其他儿科病例的数据。排除了缺乏主要终点数据的图表。标准的描述性统计和分类变量分析在没有调整和最小分层的情况下进行。结果38家医疗服务提供者共收集175例可评估病例资料,其中男性54.3%。用药时间从不到1天到253天不等。在90.3%的病例中,治疗成功完成,没有因不良事件而选择性移除器械。18例(10.3%)患者出现不良事件,共报告了21例器械相关不良事件,相当于每1000个导管天发生5次不良事件。报告的事件都不被认为是严重或意外的。结论:这些发现提示在儿科患者中安全使用抗菌/抗血栓形成的外周插入中心导管的潜力,90%的病例不会因不良事件而选择性取出导管。没有中心静脉相关血流感染、血栓形成或过敏反应的病例报告;然而,这些发现应该谨慎地解释,因为样本大小适中,这类事件在一般实践中很少见。由于本研究的局限性,包括回顾性研究固有的偏倚风险,需要有严格结果评估的前瞻性对照试验来证实这些观察结果。
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引用次数: 0
Application of modified pre-set double-wire intraocular lens suture fixation technique in aphakic eyes: A retrospective study. 改良预置双丝人工晶状体缝合固定技术在无晶状体眼中的应用回顾性研究。
IF 1.5 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2026-02-01 Epub Date: 2026-02-04 DOI: 10.1177/03000605261417475
Zhao Li, Wen Gao, Xiao Wang, Yongli Yang

ObjectiveSurgery for aphakic eyes without capsular bag support is challenging and remains a key area of research for ophthalmologists. This retrospective study introduces a novel surgical method for suture fixation of intraocular lenses in such eyes.MethodsThe modified surgery was performed on eight eyes without a natural lens. The two haptic tabs of the three-piece intraocular lens were secured with two crystal sutures using a wireless junction-defined as a connection point where the loop or haptic is anchored to the eye wall without knots through techniques such as intrascleral pocket embedding, flanged end creation, or sutureless tuck-without creating a scleral flap.ResultsAll eight patients demonstrated improved postoperative visual acuity. The intraocular lenses were reliably fixed, properly centered, and well positioned. No serious complications occurred after the surgery.ConclusionsThis modified technique appears to offer procedural simplification and a favorable trend in postoperative visual acuity improvement. However, its long-term safety and efficacy require confirmation through larger, controlled studies.

目的无囊袋支持的无晶状体眼的手术治疗具有挑战性,是眼科医生研究的重点领域。本回顾性研究介绍了一种新的手术方法缝合固定人工晶状体在这种眼睛。方法对8只无自然晶状体的眼进行改良手术。三片式人工晶状体的两个触觉片使用无线连接的两个晶体缝合线固定,该缝合线被定义为连接点,通过诸如巩膜内袋嵌入、法兰末端创建或无缝合线缝合等技术将环路或触觉片固定在眼壁上而不打结,而无需创建巩膜瓣。结果8例患者术后视力均有明显改善。人工晶状体固定可靠,居中正确,定位良好。术后未发生严重并发症。结论该方法简化了手术程序,对提高术后视力有良好的应用前景。然而,它的长期安全性和有效性需要通过更大规模的对照研究来证实。
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引用次数: 0
Early postoperative pain and opioid use after liver surgery: A systematic review and meta-analysis. 肝术后早期疼痛和阿片类药物使用:系统回顾和荟萃分析。
IF 1.5 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2026-02-01 Epub Date: 2026-02-08 DOI: 10.1177/03000605261416668
Yatao Liu, Zhaohui Gao, Xiaodong Su, Chengying Ji, Qian Fu

BackgroundPostoperative pain following liver resection remains a clinical challenge, and the optimal analgesic strategy is still debated.ObjectiveTo determine whether a single intrathecal morphine injection provides superior analgesia and opioid-sparing effects compared with conventional systemic or regional techniques in adult patients undergoing liver surgery.MethodsPubMed, Embase, Web of Science citation index, and the Cochrane Library were searched from inception to August 2025 for randomized controlled trials comparing intrathecal morphine with alternative analgesic regimens in liver resection. The primary outcome was pain intensity at rest 24 h after surgery (standardized mean difference). Secondary outcomes included pain intensity at 48 and 72 h and cumulative opioid consumption within 24 h postoperatively. Random-effects meta-analyses and I² statistics were used to assess pooled effects and heterogeneity.ResultsEleven randomized controlled trials (n = 535) met the inclusion criteria. Intrathecal morphine reduced 24-h postoperative pain scores with a moderate effect (standardized mean difference = -0.64; 95% confidence interval: -0.84 to -0.44; p < 0.001; I2 = 55%) and decreased 24-h opioid consumption by 11.6 mg morphine equivalents (95% confidence interval: -19.3 to -3.9 mg; p = 0.003; I2 = 96%). Differences in pain intensity at 48 and 72 h were not statistically significant. Adverse-event profiles were comparable between groups.ConclusionA single dose of intrathecal morphine provides clinically meaningful early analgesia and opioid-sparing benefits after liver resection without increasing adverse events. Incorporating intrathecal morphine into multimodal analgesic protocols may accelerate recovery; however, further high-quality trials are warranted to refine dosing and identify optimal patient selection.

背景肝切除术后的术后疼痛仍然是一个临床挑战,最佳的镇痛策略仍在争论中。目的探讨单次鞘内注射吗啡对成人肝脏手术患者的镇痛和阿片类药物节约效果是否优于常规全身或局部注射。方法检索spubmed、Embase、Web of Science引文索引和Cochrane图书馆自成立至2025年8月的随机对照试验,比较鞘内吗啡与替代镇痛方案在肝切除术中的应用。主要终点是术后24小时休息时疼痛强度(标准化平均差)。次要结局包括48和72小时的疼痛强度以及术后24小时内阿片类药物的累积消耗。随机效应荟萃分析和I²统计用于评估合并效应和异质性。结果6项随机对照试验(n = 535)符合纳入标准。鞘内吗啡降低术后24小时疼痛评分,效果中等(标准化平均差= -0.64;95%可信区间:-0.84至-0.44;p 2 = 55%), 24小时阿片类药物消耗减少11.6 mg吗啡当量(95%可信区间:-19.3至-3.9 mg; p = 0.003; I2 = 96%)。48和72 h疼痛强度差异无统计学意义。组间不良事件概况具有可比性。结论单剂量鞘内吗啡在肝切除术后早期镇痛和节省阿片类药物方面具有临床意义,且不增加不良事件。将鞘内吗啡纳入多模式镇痛方案可能会加速恢复;然而,需要进一步的高质量试验来完善剂量和确定最佳患者选择。
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引用次数: 0
Associations between neutrophil-to-high-density lipoprotein cholesterol ratio and albuminuria: A cross-sectional study. 中性粒细胞与高密度脂蛋白胆固醇比值与蛋白尿之间的关系:一项横断面研究。
IF 1.5 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2026-02-01 Epub Date: 2026-02-08 DOI: 10.1177/03000605261416749
Pai Pang, Jiaqi Wang, Jianing Wu, Kai Lin

Background and objectiveAlbuminuria is a critical early warning marker for the development of chronic kidney disease. The neutrophil-to-high-density lipoprotein cholesterol ratio (NHR) has been identified as a novel biomarker for the assessment of both inflammatory status and lipid metabolism. The present study was designed to explore the association between NHR and albuminuria.MethodsWe conducted a cross-sectional study using data from the National Health and Nutrition Examination Survey between 2017 and 2020. In total, 7772 eligible adult participants were included. Multivariate logistic regression models, threshold effect analysis, and sensitivity and subgroup analyses were performed to analyze the association between NHR and albuminuria.ResultsWe found a notable positive association between the NHR and the likelihood of albuminuria. In fully adjusted models, each unit rise in the NHR was associated with a 1.13-fold higher likelihood of albuminuria (1.13 (1.09-1.18)). When classified according to quartiles, participants in the highest NHR quartile had a markedly elevated likelihood of albuminuria compared with those in the lowest quartile (2.01 (1.59-2.53)). The smooth curve analysis suggested a nonlinear relationship, with a threshold at 4.58. In subgroup analyses, the positive association between NHR and albuminuria differed significantly across race categories (interaction test p = 0.0166).ConclusionAn increased level of NHR was significantly associated with an elevated odds ratio for the occurrence of albuminuria in our study. NHR may be an efficacious biomarker for the assessment of albuminuria risk, and future studies should further investigate its predictive value.

背景与目的蛋白尿是慢性肾脏疾病发展的重要预警指标。中性粒细胞与高密度脂蛋白胆固醇比率(NHR)已被确定为评估炎症状态和脂质代谢的一种新的生物标志物。本研究旨在探讨NHR与蛋白尿之间的关系。方法采用2017 - 2020年全国健康与营养调查数据进行横断面研究。总共包括7772名符合条件的成年参与者。采用多变量logistic回归模型、阈值效应分析、敏感性和亚组分析来分析NHR与蛋白尿之间的关系。结果我们发现NHR与蛋白尿的可能性有显著正相关。在完全调整的模型中,NHR每增加一个单位,蛋白尿的可能性增加1.13倍(1.13(1.09-1.18))。当按照四分位数进行分类时,与最低四分位数的参与者相比,NHR最高四分位数的参与者患蛋白尿的可能性显着升高(2.01(1.59-2.53))。平滑曲线分析表明两者之间存在非线性关系,阈值为4.58。在亚组分析中,NHR和蛋白尿之间的正相关在不同种族之间差异显著(相互作用检验p = 0.0166)。结论在我们的研究中,NHR水平的升高与蛋白尿发生率升高的优势比显著相关。NHR可能是评估蛋白尿风险的有效生物标志物,未来的研究应进一步探讨其预测价值。
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引用次数: 0
Multimodal prediction models integrating radiomics and three-dimensional deep learning for acute respiratory distress syndrome in acute pancreatitis patients. 结合放射组学和三维深度学习的急性胰腺炎患者急性呼吸窘迫综合征多模态预测模型。
IF 1.5 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2026-01-01 Epub Date: 2026-01-13 DOI: 10.1177/03000605251410432
Jielu Zhou, Yuying Wu, Wen Liang, Lin Liu, Chenyang Zhang, Yiping Shen, Meiyu Chen, Yu Wang, Chen Chao, Minyue Yin, Jinzhou Zhu, Hailong Ge

ObjectivesThis study aimed to develop a multimodal predictive model that integrates clinical data, radiomics, and three-dimensional deep learning to forecast acute respiratory distress syndrome in patients with acute pancreatitis.MethodsThis retrospective study analyzed data from 759 patients with acute pancreatitis treated at three hospitals. Radiomics features were extracted from three-dimensional computed tomography images, and a three-dimensional deep learning model was developed using convolutional networks. These components were combined with clinical data using the XGBoost algorithm to construct a multimodal model. The performance of the model was compared with that of single-modal models and traditional scoring systems (Modified Computed Tomography Severity Index, Ranson score, and Bedside Index for Severity in Acute Pancreatitis), using area under the curve as the primary metric. Model interpretability was enhanced using variable importance analysis, SHapley Additive exPlanations, local interpretable model-agnostic explanations, calibration plots, and decision curve analysis.ResultsThe multimodal model achieved area under the curve values of 0.872 (training set) and 0.876 (test set), outperforming traditional scores (Modified Computed Tomography Severity Index: 0.747 and 0.759; Ranson score: 0.575 and 0.568; and Bedside Index for Severity in Acute Pancreatitis: 0.748 and 0.757, respectively) and single-modal models (radiomics: 0.638 and 0.727 and deep learning: 0.756 and 0.727, respectively).ConclusionBy integrating clinical tabular data, radiomics, and deep learning features, the multimodal model can predict the risk of acute respiratory distress syndrome in patients with acute pancreatitis at an early stage.

本研究旨在建立一种综合临床数据、放射组学和三维深度学习的多模式预测模型,以预测急性胰腺炎患者的急性呼吸窘迫综合征。方法回顾性分析3家医院759例急性胰腺炎患者的资料。从三维计算机断层扫描图像中提取放射组学特征,并利用卷积网络建立三维深度学习模型。将这些成分与临床数据结合使用XGBoost算法构建多模态模型。将该模型的性能与单模态模型和传统评分系统(改进的计算机断层扫描严重程度指数、Ranson评分和急性胰腺炎严重程度床边指数)进行比较,并将曲线下面积作为主要指标。通过变量重要性分析、SHapley加性解释、局部可解释的模型不可知解释、校准图和决策曲线分析,增强了模型的可解释性。结果多模态模型曲线下面积分别为0.872(训练集)和0.876(测试集),优于传统模型(改进计算机断层扫描严重程度指数分别为0.747和0.759,Ranson评分分别为0.575和0.568,急性胰腺炎床边严重程度指数分别为0.748和0.757)和单模态模型(放射组学:0.638和0.727,深度学习:0.756和0.727)。结论多模态模型通过整合临床表格数据、放射组学和深度学习等特征,可以早期预测急性胰腺炎患者发生急性呼吸窘迫综合征的风险。
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Journal of International Medical Research
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