Pub Date : 2026-02-01Epub Date: 2026-02-04DOI: 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.
{"title":"Montgomery T-tube tracheal stent implantation with high-flow nasal oxygen under conscious sedation: A case report.","authors":"Danqian Su, Yan Chen, Zhenyu Yang, Xinyu Yuan, Daxiong Zeng, Jian Li, Junhong Jiang","doi":"10.1177/03000605251411746","DOIUrl":"10.1177/03000605251411746","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":16129,"journal":{"name":"Journal of International Medical Research","volume":"54 2","pages":"3000605251411746"},"PeriodicalIF":1.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12876648/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146119320","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-02-08DOI: 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":"<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","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}
Pub Date : 2026-02-01Epub Date: 2026-02-08DOI: 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.
{"title":"Severe acute respiratory distress syndrome following laparoscopic appendectomy in a previously healthy middle-aged man: A case report.","authors":"Hongqun Zhang, Zhuoyin Wang, Yi Jin","doi":"10.1177/03000605261418802","DOIUrl":"https://doi.org/10.1177/03000605261418802","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":16129,"journal":{"name":"Journal of International Medical Research","volume":"54 2","pages":"3000605261418802"},"PeriodicalIF":1.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146142612","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}
Pub Date : 2026-02-01Epub Date: 2026-02-09DOI: 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
{"title":"Effects of coenzyme Q10 analogs on oxidative stress, muscle, and metabolism after exercise: A meta-analysis and systematic review.","authors":"Yangqi Zhang, Yilang He, Mingling Ma, Hui Dong, Zijian Ma","doi":"10.1177/03000605251411151","DOIUrl":"https://doi.org/10.1177/03000605251411151","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":16129,"journal":{"name":"Journal of International Medical Research","volume":"54 2","pages":"3000605251411151"},"PeriodicalIF":1.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146142622","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}
Pub Date : 2026-02-01Epub Date: 2026-02-08DOI: 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.
{"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}
Pub Date : 2026-02-01Epub Date: 2026-02-04DOI: 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.
{"title":"Retrospective observational assessment of the safety, performance, and utility of an antimicrobial/antithrombogenic peripherally inserted central catheter in pediatric patients.","authors":"Thomas E Philbeck, Caroline Ryan, Amy Bardin","doi":"10.1177/03000605261418861","DOIUrl":"10.1177/03000605261418861","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":16129,"journal":{"name":"Journal of International Medical Research","volume":"54 2","pages":"3000605261418861"},"PeriodicalIF":1.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12876637/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146119281","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-02-04DOI: 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.
{"title":"Application of modified pre-set double-wire intraocular lens suture fixation technique in aphakic eyes: A retrospective study.","authors":"Zhao Li, Wen Gao, Xiao Wang, Yongli Yang","doi":"10.1177/03000605261417475","DOIUrl":"10.1177/03000605261417475","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":16129,"journal":{"name":"Journal of International Medical Research","volume":"54 2","pages":"3000605261417475"},"PeriodicalIF":1.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12876651/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146119185","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2026-02-08DOI: 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。
{"title":"Early postoperative pain and opioid use after liver surgery: A systematic review and meta-analysis.","authors":"Yatao Liu, Zhaohui Gao, Xiaodong Su, Chengying Ji, Qian Fu","doi":"10.1177/03000605261416668","DOIUrl":"https://doi.org/10.1177/03000605261416668","url":null,"abstract":"<p><p>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; <i>p</i> < 0.001; I<sup>2</sup> = 55%) and decreased 24-h opioid consumption by 11.6 mg morphine equivalents (95% confidence interval: -19.3 to -3.9 mg; <i>p</i> = 0.003; I<sup>2</sup> = 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.</p>","PeriodicalId":16129,"journal":{"name":"Journal of International Medical Research","volume":"54 2","pages":"3000605261416668"},"PeriodicalIF":1.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146142478","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}
Pub Date : 2026-02-01Epub Date: 2026-02-08DOI: 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.
{"title":"Associations between neutrophil-to-high-density lipoprotein cholesterol ratio and albuminuria: A cross-sectional study.","authors":"Pai Pang, Jiaqi Wang, Jianing Wu, Kai Lin","doi":"10.1177/03000605261416749","DOIUrl":"https://doi.org/10.1177/03000605261416749","url":null,"abstract":"<p><p>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 <i>p</i> = 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.</p>","PeriodicalId":16129,"journal":{"name":"Journal of International Medical Research","volume":"54 2","pages":"3000605261416749"},"PeriodicalIF":1.5,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146142551","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}
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.
{"title":"Multimodal prediction models integrating radiomics and three-dimensional deep learning for acute respiratory distress syndrome in acute pancreatitis patients.","authors":"Jielu Zhou, Yuying Wu, Wen Liang, Lin Liu, Chenyang Zhang, Yiping Shen, Meiyu Chen, Yu Wang, Chen Chao, Minyue Yin, Jinzhou Zhu, Hailong Ge","doi":"10.1177/03000605251410432","DOIUrl":"10.1177/03000605251410432","url":null,"abstract":"<p><p>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.</p>","PeriodicalId":16129,"journal":{"name":"Journal of International Medical Research","volume":"54 1","pages":"3000605251410432"},"PeriodicalIF":1.5,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12799975/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145966167","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}