首页 > 最新文献

Medical Science Monitor最新文献

英文 中文
Histological Evaluation of the Effects of Intra-Articular Injection of Caffeic Acid on Cartilage Repair in a Rat Knee Microfracture Model. 咖啡酸关节内注射对大鼠膝关节微骨折模型软骨修复作用的组织学评价。
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-12-06 DOI: 10.12659/MSM.946845
Mustafa Serpi, Müjdat Adaş, Alev Cumbul, Murat Çakar, İsmail Demirkale

BACKGROUND Cartilage injuries are challenging to treat due to limited self-healing. Standard treatments often lead to the formation of less durable fibrocartilage. Caffeic acid phenethyl ester (CAPE), a polyphenolic compound, can improve cartilage repair. This animal study aimed to evaluate the histological effects of intra-articular injection of CAPE on cartilage repair in a rat model of microfracture of the knee joint. MATERIAL AND METHODS Twenty-four male Sprague-Dawley rats were divided into 4 groups. A cartilage defect was created in all groups, but Group A received no further intervention. Group B underwent a microfracture. Group C received intra-articular CAPE in the presence of a defect, without microfracture. Group D underwent both microfracture and CAPE treatment. Also, each rat underwent bilateral surgery, with one knee receiving CAPE (150 µg/kg) and the other receiving a control solution. After 28 days, histological analysis was performed on the cartilage tissue samples obtained from the defect sites by using the International Cartilage Research Society (ICRS-I and -II) visual assessment scale. Statistical analysis was performed using appropriate tests to compare histological scores between groups, with significance set at P<0.05. RESULTS Intra-articular CAPE significantly improved histopathological outcomes across several parameters, including reduced inflammation (P<0.05), enhanced tissue morphology (P<0.05), and improved cartilage matrix staining (P<0.05). No significant difference was observed in chondrocyte clustering or surface architecture among the groups. CONCLUSIONS Intra-articular CAPE enhances cartilage healing by improving tissue morphology and cartilage matrix quality.

背景:由于软骨损伤的自我愈合能力有限,其治疗具有挑战性。标准治疗通常会导致纤维软骨的形成不那么持久。咖啡酸苯乙酯(CAPE)是一种多酚类化合物,可以促进软骨修复。本动物实验旨在评估关节内注射CAPE对大鼠膝关节微骨折模型软骨修复的组织学影响。材料与方法雄性sd大鼠24只,随机分为4组。所有组均出现软骨缺损,但A组未进行进一步干预。B组行微骨折。C组在没有微骨折的情况下接受关节内CAPE。D组同时进行微骨折和CAPE治疗。此外,每只大鼠进行双侧手术,一只膝盖接受CAPE(150µg/kg),另一只膝盖接受对照溶液。28天后,采用国际软骨研究学会(ICRS-I和-II)视觉评估量表对缺损部位软骨组织样本进行组织学分析。采用适当的检验进行统计学分析,比较组间组织学评分,显著性设为P
{"title":"Histological Evaluation of the Effects of Intra-Articular Injection of Caffeic Acid on Cartilage Repair in a Rat Knee Microfracture Model.","authors":"Mustafa Serpi, Müjdat Adaş, Alev Cumbul, Murat Çakar, İsmail Demirkale","doi":"10.12659/MSM.946845","DOIUrl":"10.12659/MSM.946845","url":null,"abstract":"<p><p>BACKGROUND Cartilage injuries are challenging to treat due to limited self-healing. Standard treatments often lead to the formation of less durable fibrocartilage. Caffeic acid phenethyl ester (CAPE), a polyphenolic compound, can improve cartilage repair. This animal study aimed to evaluate the histological effects of intra-articular injection of CAPE on cartilage repair in a rat model of microfracture of the knee joint. MATERIAL AND METHODS Twenty-four male Sprague-Dawley rats were divided into 4 groups. A cartilage defect was created in all groups, but Group A received no further intervention. Group B underwent a microfracture. Group C received intra-articular CAPE in the presence of a defect, without microfracture. Group D underwent both microfracture and CAPE treatment. Also, each rat underwent bilateral surgery, with one knee receiving CAPE (150 µg/kg) and the other receiving a control solution. After 28 days, histological analysis was performed on the cartilage tissue samples obtained from the defect sites by using the International Cartilage Research Society (ICRS-I and -II) visual assessment scale. Statistical analysis was performed using appropriate tests to compare histological scores between groups, with significance set at P<0.05. RESULTS Intra-articular CAPE significantly improved histopathological outcomes across several parameters, including reduced inflammation (P<0.05), enhanced tissue morphology (P<0.05), and improved cartilage matrix staining (P<0.05). No significant difference was observed in chondrocyte clustering or surface architecture among the groups. CONCLUSIONS Intra-articular CAPE enhances cartilage healing by improving tissue morphology and cartilage matrix quality.</p>","PeriodicalId":48888,"journal":{"name":"Medical Science Monitor","volume":"30 ","pages":"e946845"},"PeriodicalIF":3.1,"publicationDate":"2024-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11629585/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142786786","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}
引用次数: 0
Impact of Comprehensive Preoperative Assessments on Gynecological Ambulatory Surgery Outcomes in a Chinese Hospital. 综合术前评估对中国某医院妇科门诊手术效果的影响
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-12-05 DOI: 10.12659/MSM.945771
Lu Bai, Yan Huang, Chuanya Huang, Xin Tan

BACKGROUND We aimed to investigate the implementation of outpatient comprehensive preoperative assessments in gynecological ambulatory surgery management in a hospital in China. MATERIAL AND METHODS Patients undergoing gynecologic minimally invasive surgery who received outpatient comprehensive preoperative assessment and ambulatory surgical procedures during November 2021 to December 2021 were classified into the intervention group (n=330). Those who received routine medical procedures during the same period were classified into the control group (n=336). A retrospective analysis was conducted with the medical records of the 2 groups of patients. RESULTS The scores for information transmission and patient education and for level of mastery of preoperative health knowledge in the intervention group were higher than that of the control group (P<0.05). Patient experience was positively correlated with level of mastery of preoperative health knowledge (r=0.525; P<0.01). No statistically significant differences were identified in the incidences of surgical complications and anesthetic complications among the 2 groups (P>0.05). The number of delayed surgery cases in the intervention group was higher than that of the control group (P<0.05). A statistically significant difference of P<0.05 was identified in the average length of hospital stay between the 2 groups, but no statistically significant differences were identified in patient satisfaction during hospitalization between the 2 groups (P>0.05). CONCLUSIONS The establishment of an outpatient comprehensive preoperative assessment unit for gynecological ambulatory surgery can improve patient experience and level of mastery of preoperative health knowledge.

本研究旨在调查中国某医院妇科门诊手术管理中门诊综合术前评估的实施情况。材料与方法将2021年11月至2021年12月接受妇科微创手术的门诊术前综合评估及门诊手术的患者分为干预组(n=330)。在同一时期接受常规医疗程序的患者被分为对照组(n=336)。对两组患者的病历资料进行回顾性分析。结果干预组患者信息传递、患者教育、术前健康知识掌握水平得分均高于对照组(P0.05)。干预组延迟手术例数高于对照组(P0.05)。结论建立妇科门诊手术术前综合评估单元可提高患者的术前体验,提高患者对术前健康知识的掌握水平。
{"title":"Impact of Comprehensive Preoperative Assessments on Gynecological Ambulatory Surgery Outcomes in a Chinese Hospital.","authors":"Lu Bai, Yan Huang, Chuanya Huang, Xin Tan","doi":"10.12659/MSM.945771","DOIUrl":"10.12659/MSM.945771","url":null,"abstract":"<p><p>BACKGROUND We aimed to investigate the implementation of outpatient comprehensive preoperative assessments in gynecological ambulatory surgery management in a hospital in China. MATERIAL AND METHODS Patients undergoing gynecologic minimally invasive surgery who received outpatient comprehensive preoperative assessment and ambulatory surgical procedures during November 2021 to December 2021 were classified into the intervention group (n=330). Those who received routine medical procedures during the same period were classified into the control group (n=336). A retrospective analysis was conducted with the medical records of the 2 groups of patients. RESULTS The scores for information transmission and patient education and for level of mastery of preoperative health knowledge in the intervention group were higher than that of the control group (P<0.05). Patient experience was positively correlated with level of mastery of preoperative health knowledge (r=0.525; P<0.01). No statistically significant differences were identified in the incidences of surgical complications and anesthetic complications among the 2 groups (P>0.05). The number of delayed surgery cases in the intervention group was higher than that of the control group (P<0.05). A statistically significant difference of P<0.05 was identified in the average length of hospital stay between the 2 groups, but no statistically significant differences were identified in patient satisfaction during hospitalization between the 2 groups (P>0.05). CONCLUSIONS The establishment of an outpatient comprehensive preoperative assessment unit for gynecological ambulatory surgery can improve patient experience and level of mastery of preoperative health knowledge.</p>","PeriodicalId":48888,"journal":{"name":"Medical Science Monitor","volume":"30 ","pages":"e945771"},"PeriodicalIF":3.1,"publicationDate":"2024-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11629586/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142781650","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}
引用次数: 0
Cost Reduction in Blood Transfusions After Implementation of Decision Protocol Based on Hemoglobin and Anemia Symptoms: A Pre-Post Analysis. 基于血红蛋白和贫血症状的决策方案实施后输血成本降低:前后分析
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-12-04 DOI: 10.12659/MSM.945854
Piotr F Czempik, Jan Herzyk, Dawid Wilczek, Anna Rogalska

BACKGROUND Blood products are an expensive resource. The study aimed to assess the cost spent on red blood cell (RBC) transfusions before and after implementing a 2-factorial RBC transfusion decision protocol and the current cost of an RBC transfusion procedure in the local healthcare system. MATERIAL AND METHODS Six-month periods before and after the implementation of the decision protocol were compared. The cost components considered included RBCs, laboratory tests, labor of healthcare workers involved in the procedure, and management of transfusion reactions. RESULTS Following the implementation of the decision protocol, there was a decrease in transfusion costs by €51,411 (56.4%) in our low transfusion rate setting. Inappropriate RBC transfusions amounted to €25,0146 (62.9% of all transfusions costs). The cost of a leucodepleted RBC transfusion increased in the periods being compared, from approximately €109 to €126 in the local healthcare system. CONCLUSIONS Implementing an RBC transfusion decision protocol based on a 2-factorial approach can lead to a more than 2-fold reduction in cost spent on RBC transfusions in a low transfusion rate setting. Even after the implementation of the protocol, further education of clinicians is required, as there may still be potential to reduce costs associated with inappropriate transfusions. The non-RBC acquisition cost of an RBC transfusion procedure approximates the cost of a blood component itself in the local healthcare system.

血液制品是一种昂贵的资源。该研究旨在评估在实施2因子红细胞输血决策方案之前和之后红细胞(RBC)输血的成本以及当地医疗系统中红细胞输血程序的当前成本。材料与方法比较决策方案实施前后6个月的情况。考虑的成本组成部分包括红细胞、实验室检测、参与手术的医护人员的劳动力以及输血反应的管理。结果执行决策方案后,在我们的低输血率设置中,输血成本降低了51,411欧元(56.4%)。不适当的红细胞输血达25,0146欧元(占所有输血费用的62.9%)。在比较期间,在当地医疗保健系统中,低白细胞红细胞输血的费用从大约109欧元增加到126欧元。结论:在低输血率环境下,实施基于2因子方法的红细胞输血决策方案可使红细胞输血成本降低2倍以上。即使在实施该方案之后,仍需要对临床医生进行进一步教育,因为仍有可能降低与不适当输血相关的费用。在当地的医疗保健系统中,红细胞输血过程的非红细胞获取成本近似于血液成分本身的成本。
{"title":"Cost Reduction in Blood Transfusions After Implementation of Decision Protocol Based on Hemoglobin and Anemia Symptoms: A Pre-Post Analysis.","authors":"Piotr F Czempik, Jan Herzyk, Dawid Wilczek, Anna Rogalska","doi":"10.12659/MSM.945854","DOIUrl":"10.12659/MSM.945854","url":null,"abstract":"<p><p>BACKGROUND Blood products are an expensive resource. The study aimed to assess the cost spent on red blood cell (RBC) transfusions before and after implementing a 2-factorial RBC transfusion decision protocol and the current cost of an RBC transfusion procedure in the local healthcare system. MATERIAL AND METHODS Six-month periods before and after the implementation of the decision protocol were compared. The cost components considered included RBCs, laboratory tests, labor of healthcare workers involved in the procedure, and management of transfusion reactions. RESULTS Following the implementation of the decision protocol, there was a decrease in transfusion costs by €51,411 (56.4%) in our low transfusion rate setting. Inappropriate RBC transfusions amounted to €25,0146 (62.9% of all transfusions costs). The cost of a leucodepleted RBC transfusion increased in the periods being compared, from approximately €109 to €126 in the local healthcare system. CONCLUSIONS Implementing an RBC transfusion decision protocol based on a 2-factorial approach can lead to a more than 2-fold reduction in cost spent on RBC transfusions in a low transfusion rate setting. Even after the implementation of the protocol, further education of clinicians is required, as there may still be potential to reduce costs associated with inappropriate transfusions. The non-RBC acquisition cost of an RBC transfusion procedure approximates the cost of a blood component itself in the local healthcare system.</p>","PeriodicalId":48888,"journal":{"name":"Medical Science Monitor","volume":"30 ","pages":"e945854"},"PeriodicalIF":3.1,"publicationDate":"2024-12-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11626835/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142773792","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}
引用次数: 0
Machine Learning Models for Predicting 24-Hour Intraocular Pressure Changes: A Comparative Study. 预测24小时眼压变化的机器学习模型:比较研究。
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-12-03 DOI: 10.12659/MSM.945483
Chen Ranran, Lei Jinming, Liao Yujie, Jin Yiping, Wang Xue, Li Hong, Bi Yanlong, Zhu Haohao

BACKGROUND Predicting 24-hour intraocular pressure (IOP) fluctuations is crucial for enhancing glaucoma management. Traditional methods of measuring 24-hour IOP fluctuations are complex and present certain limitations. The present study leverages machine learning techniques to forecast 24-hour IOP fluctuations based on daytime IOP measurements. MATERIAL AND METHODS A binary method was used to classify 24-hour IOP fluctuations as either >8 mmHg or £8 mmHg. Data were collected from 24-hour IOP monitoring, including 22 different features. Feature selection involved the chi-square test and point-biserial correlation, leading to the establishment of 4 subsets with significance levels of P<1, P<0.1, P<0.05, and P<0.025. Five binary classification machine learning algorithms were used to construct the model. Model performance was assessed by comparing accuracy, specificity, 10-fold cross-validation, precision, sensitivity, F1 score, area under the curve (AUC), and Area Under the Precision-Recall Curve (AUCPR). The model with the highest performance was selected, and feature importance was assessed using Shapley additive explanations.   RESULTS In the subset of features where P<0.05, all models performed better than those in the other subsets, with XGBoost standing out the most. The XGBoost algorithm achieved an accuracy of 0.886, a specificity of 0.972, a 10-fold cross-validation of 0.872, a precision of 0.857, a sensitivity of 0.585, and an F1 score of 0.696. Additionally, it obtained an AUC of 0.890 and an AUCPR of 0.794. CONCLUSIONS Our study illustrates the predictive capabilities of machine learning algorithms in forecasting 24-hour IOP fluctuations. The exceptional performance of the XGBoost algorithm in predicting IOP fluctuations underscores its significance for future research and clinical applications.

背景:预测24小时眼内压(IOP)波动对加强青光眼治疗至关重要。测量24小时眼压波动的传统方法很复杂,存在一定的局限性。目前的研究利用机器学习技术来预测基于白天IOP测量的24小时IOP波动。材料和方法采用二元方法将24小时眼压波动分为bbb8mmhg或£8mmhg。24小时IOP监测数据,包括22个不同特征。特征选择涉及卡方检验和点双列相关,从而建立了4个显著性水平为P的子集
{"title":"Machine Learning Models for Predicting 24-Hour Intraocular Pressure Changes: A Comparative Study.","authors":"Chen Ranran, Lei Jinming, Liao Yujie, Jin Yiping, Wang Xue, Li Hong, Bi Yanlong, Zhu Haohao","doi":"10.12659/MSM.945483","DOIUrl":"10.12659/MSM.945483","url":null,"abstract":"<p><p>BACKGROUND Predicting 24-hour intraocular pressure (IOP) fluctuations is crucial for enhancing glaucoma management. Traditional methods of measuring 24-hour IOP fluctuations are complex and present certain limitations. The present study leverages machine learning techniques to forecast 24-hour IOP fluctuations based on daytime IOP measurements. MATERIAL AND METHODS A binary method was used to classify 24-hour IOP fluctuations as either >8 mmHg or £8 mmHg. Data were collected from 24-hour IOP monitoring, including 22 different features. Feature selection involved the chi-square test and point-biserial correlation, leading to the establishment of 4 subsets with significance levels of P<1, P<0.1, P<0.05, and P<0.025. Five binary classification machine learning algorithms were used to construct the model. Model performance was assessed by comparing accuracy, specificity, 10-fold cross-validation, precision, sensitivity, F1 score, area under the curve (AUC), and Area Under the Precision-Recall Curve (AUCPR). The model with the highest performance was selected, and feature importance was assessed using Shapley additive explanations.   RESULTS In the subset of features where P<0.05, all models performed better than those in the other subsets, with XGBoost standing out the most. The XGBoost algorithm achieved an accuracy of 0.886, a specificity of 0.972, a 10-fold cross-validation of 0.872, a precision of 0.857, a sensitivity of 0.585, and an F1 score of 0.696. Additionally, it obtained an AUC of 0.890 and an AUCPR of 0.794. CONCLUSIONS Our study illustrates the predictive capabilities of machine learning algorithms in forecasting 24-hour IOP fluctuations. The exceptional performance of the XGBoost algorithm in predicting IOP fluctuations underscores its significance for future research and clinical applications.</p>","PeriodicalId":48888,"journal":{"name":"Medical Science Monitor","volume":"30 ","pages":"e945483"},"PeriodicalIF":3.1,"publicationDate":"2024-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11624606/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142773841","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}
引用次数: 0
A Review of Muscle Relaxants in Anesthesia in Patients with Neuromuscular Disorders Including Guillain-Barré Syndrome, Myasthenia Gravis, Duchenne Muscular Dystrophy, Charcot-Marie-Tooth Disease, and Inflammatory Myopathies. 肌肉松弛剂在神经肌肉疾病(包括格林-巴勒综合征、重症肌无力、杜氏肌营养不良、腓骨肌病和炎性肌病)患者麻醉中的应用综述
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-12-02 DOI: 10.12659/MSM.945675
Paweł Radkowski, Hubert Oniszczuk, Justyna Opolska, Iwona Podlińska, Mateusz Pawluczuk, Dariusz Onichimowski

Anesthesia management in neuromuscular diseases (NMDs) is a complex challenge, requiring careful preoperative evaluation, tailored treatment strategies, and vigilant perioperative monitoring. This review examines the nuances of anesthesia in patients with NMD, addressing potential complications such as intubation difficulties, respiratory failure, and adverse effects of anesthetics and neuromuscular conduction blocking agents (NMBAs). Nondepolarizing NMBAs, including steroidal agents and benzylisoquinolines, are analyzed for their role, risks, and optimal use based on procedural requirements and patient characteristics. Challenges with depolarizing agents such as succinylcholine are highlighted, emphasizing the need for careful evaluation and monitoring to reduce the risk of adverse events such as malignant hyperthermia and hyperkalemia. The review highlights the role of reversal agents, particularly sugammadex, as a safer and more effective alternative to traditional acetylcholinesterase inhibitors such as neostigmine. Sugammadex reduces the risk of complications such as prolonged paralysis and respiratory failure in patients with NMD. In addition, anesthesia considerations tailored to specific NMDs, including Guillain-Barre syndrome, myasthenia gravis, Duchenne muscular dystrophy, Charcot-Marie-Tooth disease, and inflammatory myopathies are presented, including monitoring techniques and individualized approaches. Based on the available literature and the authors' clinical experience, this review aims to discuss the role of muscle relaxants in anesthesia in patients with the aforementioned neuromuscular disorders. This document uses the latest possible articles, covering items from 1992 to 2024.

神经肌肉疾病(nmd)的麻醉管理是一项复杂的挑战,需要仔细的术前评估、量身定制的治疗策略和警惕的围手术期监测。这篇综述探讨了NMD患者麻醉的细微差别,解决了潜在的并发症,如插管困难、呼吸衰竭、麻醉剂和神经肌肉传导阻滞剂(nmba)的不良反应。非去极化NMBAs,包括甾体类药物和苯基异喹啉类药物,分析了它们的作用、风险和基于程序要求和患者特征的最佳使用。报告强调了琥珀胆碱等去极化药物的挑战,强调需要仔细评估和监测,以减少恶性高热和高钾血症等不良事件的风险。该综述强调了逆转药物的作用,特别是sugammadex,作为传统乙酰胆碱酯酶抑制剂(如新斯的明)更安全、更有效的替代品。Sugammadex可降低NMD患者的并发症风险,如长时间瘫痪和呼吸衰竭。此外,还介绍了针对特定nmd(包括格林-巴利综合征、重症肌无力、杜氏肌营养不良症、腓骨肌萎缩症和炎性肌病)的麻醉考虑,包括监测技术和个体化方法。根据现有文献和作者的临床经验,本文旨在讨论肌肉松弛剂在上述神经肌肉疾病患者麻醉中的作用。本文档使用了最新的文章,涵盖了1992年至2024年的项目。
{"title":"A Review of Muscle Relaxants in Anesthesia in Patients with Neuromuscular Disorders Including Guillain-Barré Syndrome, Myasthenia Gravis, Duchenne Muscular Dystrophy, Charcot-Marie-Tooth Disease, and Inflammatory Myopathies.","authors":"Paweł Radkowski, Hubert Oniszczuk, Justyna Opolska, Iwona Podlińska, Mateusz Pawluczuk, Dariusz Onichimowski","doi":"10.12659/MSM.945675","DOIUrl":"10.12659/MSM.945675","url":null,"abstract":"<p><p>Anesthesia management in neuromuscular diseases (NMDs) is a complex challenge, requiring careful preoperative evaluation, tailored treatment strategies, and vigilant perioperative monitoring. This review examines the nuances of anesthesia in patients with NMD, addressing potential complications such as intubation difficulties, respiratory failure, and adverse effects of anesthetics and neuromuscular conduction blocking agents (NMBAs). Nondepolarizing NMBAs, including steroidal agents and benzylisoquinolines, are analyzed for their role, risks, and optimal use based on procedural requirements and patient characteristics. Challenges with depolarizing agents such as succinylcholine are highlighted, emphasizing the need for careful evaluation and monitoring to reduce the risk of adverse events such as malignant hyperthermia and hyperkalemia. The review highlights the role of reversal agents, particularly sugammadex, as a safer and more effective alternative to traditional acetylcholinesterase inhibitors such as neostigmine. Sugammadex reduces the risk of complications such as prolonged paralysis and respiratory failure in patients with NMD. In addition, anesthesia considerations tailored to specific NMDs, including Guillain-Barre syndrome, myasthenia gravis, Duchenne muscular dystrophy, Charcot-Marie-Tooth disease, and inflammatory myopathies are presented, including monitoring techniques and individualized approaches. Based on the available literature and the authors' clinical experience, this review aims to discuss the role of muscle relaxants in anesthesia in patients with the aforementioned neuromuscular disorders. This document uses the latest possible articles, covering items from 1992 to 2024.</p>","PeriodicalId":48888,"journal":{"name":"Medical Science Monitor","volume":"30 ","pages":"e945675"},"PeriodicalIF":3.1,"publicationDate":"2024-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11623016/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142773659","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}
引用次数: 0
Rituximab use in Rheumatoid Arthritis: A Seven-Year Retrospective Study of 52 Patients at a Saudi Arabian Hospital. 利妥昔单抗在类风湿关节炎中的应用:沙特阿拉伯一家医院52例患者的7年回顾性研究
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-12-01 DOI: 10.12659/MSM.946178
Sumayah Sulaiman Bafana, Fahidah Alenzi, Ibrahim Almaghlouth, Eman Alqurtas, Mohammed K Bedaiwi, Haya M M Almalag, Mohammed A Omair

BACKGROUND Rituximab (RTX) is a chimeric therapeutic monoclonal antibody that targets the CD20 molecule on B lymphocytes. RTX is approved for the treatment of rheumatoid arthritis (RA) in patients who do not respond to disease-modifying anti-rheumatic drugs (DMARDs) or other biologics. The purpose of this retrospective study was to report our experience with RTX treatment at a single center in Saudi Arabia between 2015 and 2022 in 52 patients with RA. MATERIAL AND METHODS This retrospective cohort study at King Khalid University Hospital in Riyadh examined 52 patients with RA who received RTX from April 2015 to October 2022. Data were collected from electronic health records, including patient demographics, disease activity, and treatment details. The primary outcome was prednisolone tapering, with secondary outcomes including adverse reactions and disease activity. Statistical analysis was conducted using SPSS. RESULTS Out of 678 screened patients, 52 (7.7%) were recruited. Of these, 44 (84.6%) were female, with a mean disease duration of 28±7 years and a mean age of 57.1±11 years. Prednisolone was used by 22 patients (42.31%) at RTX initiation, with a mean dose of 10.45±10.25 mg. After RTX, the dose significantly dropped to 3.41±5.54 mg (P<0.001). Older patients, those from outside Riyadh, and those with fewer prior DMARDs were more likely to taper off without full dose reinstatement. CONCLUSIONS This retrospective study supports the findings from other studies and current clinical guidelines that recommend rituximab in patients with rheumatoid arthritis, highlighting the importance of patient monitoring during treatment. Multicenter studies are required to determine the economic impact of tapering biological drugs.

Rituximab (RTX)是一种靶向B淋巴细胞CD20分子的嵌合治疗性单克隆抗体。RTX被批准用于治疗对改善疾病的抗风湿药物(DMARDs)或其他生物制剂无反应的类风湿性关节炎(RA)患者。本回顾性研究的目的是报告我们在2015年至2022年期间在沙特阿拉伯单一中心对52名RA患者进行RTX治疗的经验。材料和方法这项在利雅得哈立德国王大学医院进行的回顾性队列研究检查了2015年4月至2022年10月期间接受RTX治疗的52例RA患者。从电子健康记录中收集数据,包括患者人口统计、疾病活动和治疗细节。主要结局是强的松龙逐渐减少,次要结局包括不良反应和疾病活动性。采用SPSS进行统计分析。结果:在678名筛查患者中,52名(7.7%)被招募。其中女性44例(84.6%),平均病程28±7年,平均年龄57.1±11岁。22例(42.31%)患者在RTX开始时使用强的松龙,平均剂量为10.45±10.25 mg。RTX后剂量显著下降至3.41±5.54 mg (P
{"title":"Rituximab use in Rheumatoid Arthritis: A Seven-Year Retrospective Study of 52 Patients at a Saudi Arabian Hospital.","authors":"Sumayah Sulaiman Bafana, Fahidah Alenzi, Ibrahim Almaghlouth, Eman Alqurtas, Mohammed K Bedaiwi, Haya M M Almalag, Mohammed A Omair","doi":"10.12659/MSM.946178","DOIUrl":"10.12659/MSM.946178","url":null,"abstract":"<p><p>BACKGROUND Rituximab (RTX) is a chimeric therapeutic monoclonal antibody that targets the CD20 molecule on B lymphocytes. RTX is approved for the treatment of rheumatoid arthritis (RA) in patients who do not respond to disease-modifying anti-rheumatic drugs (DMARDs) or other biologics. The purpose of this retrospective study was to report our experience with RTX treatment at a single center in Saudi Arabia between 2015 and 2022 in 52 patients with RA. MATERIAL AND METHODS This retrospective cohort study at King Khalid University Hospital in Riyadh examined 52 patients with RA who received RTX from April 2015 to October 2022. Data were collected from electronic health records, including patient demographics, disease activity, and treatment details. The primary outcome was prednisolone tapering, with secondary outcomes including adverse reactions and disease activity. Statistical analysis was conducted using SPSS. RESULTS Out of 678 screened patients, 52 (7.7%) were recruited. Of these, 44 (84.6%) were female, with a mean disease duration of 28±7 years and a mean age of 57.1±11 years. Prednisolone was used by 22 patients (42.31%) at RTX initiation, with a mean dose of 10.45±10.25 mg. After RTX, the dose significantly dropped to 3.41±5.54 mg (P<0.001). Older patients, those from outside Riyadh, and those with fewer prior DMARDs were more likely to taper off without full dose reinstatement. CONCLUSIONS This retrospective study supports the findings from other studies and current clinical guidelines that recommend rituximab in patients with rheumatoid arthritis, highlighting the importance of patient monitoring during treatment. Multicenter studies are required to determine the economic impact of tapering biological drugs.</p>","PeriodicalId":48888,"journal":{"name":"Medical Science Monitor","volume":"30 ","pages":"e946178"},"PeriodicalIF":3.1,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11619177/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142773859","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}
引用次数: 0
Editorial: The 2024 Revision of the Declaration of Helsinki and its Continued Role as a Code of Ethics to Guide Medical Research. 社论:2024年赫尔辛基宣言的修订及其继续作为指导医学研究的道德准则的作用。
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-12-01 DOI: 10.12659/MSM.947428
Dinah V Parums

This year, 2024, marks the 60th anniversary of the Declaration of Helsinki, with the latest revision adopted by the World Medical Association (WMA) in October 2024. The 2024 Declaration of Helsinki is a statement document of ethical principles for research involving humans, human data, and human cells and tissues. Revising the 2013 Declaration of Helsinki document was undertaken over more than two years with international collaboration to enhance the inclusivity of medical research, protect the rights of research study participants, and address contemporary research challenges such as global health emergencies and data privacy. The revised Declaration document does not replace the roles of the Institutional Review Board and the local Ethics Committee in reviewing and approving all research study protocols but continues to provide ethical guidance for the individuals who support, review, and conduct medical research. This editorial highlights the timely revisions in the 2024 Declaration of Helsinki and the importance of updating and maintaining an international consensus for a code of ethics that guides medical research.

今年,即2024年,是《赫尔辛基宣言》发表60周年,世界医学协会(WMA)于2024年10月通过了最新修订版。2024年赫尔辛基宣言是一份关于涉及人类、人类数据、人类细胞和组织的研究的伦理原则的声明文件。在两年多的时间里,通过国际合作对2013年《赫尔辛基宣言》文件进行了修订,以加强医学研究的包容性,保护研究参与者的权利,并应对全球突发卫生事件和数据隐私等当代研究挑战。修订后的《声明》文件并不取代机构审查委员会和当地伦理委员会在审查和批准所有研究方案方面的作用,而是继续为支持、审查和开展医学研究的个人提供伦理指导。这篇社论强调了对2024年《赫尔辛基宣言》的及时修订,以及更新和维护指导医学研究的道德准则国际共识的重要性。
{"title":"Editorial: The 2024 Revision of the Declaration of Helsinki and its Continued Role as a Code of Ethics to Guide Medical Research.","authors":"Dinah V Parums","doi":"10.12659/MSM.947428","DOIUrl":"10.12659/MSM.947428","url":null,"abstract":"<p><p>This year, 2024, marks the 60th anniversary of the Declaration of Helsinki, with the latest revision adopted by the World Medical Association (WMA) in October 2024. The 2024 Declaration of Helsinki is a statement document of ethical principles for research involving humans, human data, and human cells and tissues. Revising the 2013 Declaration of Helsinki document was undertaken over more than two years with international collaboration to enhance the inclusivity of medical research, protect the rights of research study participants, and address contemporary research challenges such as global health emergencies and data privacy. The revised Declaration document does not replace the roles of the Institutional Review Board and the local Ethics Committee in reviewing and approving all research study protocols but continues to provide ethical guidance for the individuals who support, review, and conduct medical research. This editorial highlights the timely revisions in the 2024 Declaration of Helsinki and the importance of updating and maintaining an international consensus for a code of ethics that guides medical research.</p>","PeriodicalId":48888,"journal":{"name":"Medical Science Monitor","volume":"30 ","pages":"e947428"},"PeriodicalIF":3.1,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11619173/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142773708","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}
引用次数: 0
Role of Sleep in Depressive Disorders and the Potential Therapeutic Role of Short-Term Sleep Deprivation and Light Therapy: A Review. 睡眠在抑郁症中的作用以及短期睡眠剥夺和光疗法的潜在治疗作用:综述。
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-11-30 DOI: 10.12659/MSM.945319
Wiktoria Bojarska, Karolina Bury, Radosław Januszczak, Bartosz Burda, Justyna Pawęzka

Depression affects about 280 million people globally and is marked by persistent sadness and impaired daily functioning. Sleep disturbances are prevalent in major depressive disorder, affecting roughly 90% of patients, and are linked to the severity and progression of depression. This review emphasizes the critical role of sleep in depressive disorders and evaluates the alternative treatments bright light therapy and sleep deprivation. Sleep disturbances are not only symptoms but also mediators in the relationship between depression and other conditions, such as anxiety, chronic inflammation, emotional dysregulation, and cognitive decline. Effective management of depressive disorders must address these sleep issues. Bright light therapy, which uses artificial light to mimic natural sunlight, is effective for treating seasonal affective disorder and non-seasonal major depressive disorder. It is well tolerated, can be used alone or with antidepressants, and often improves both mood and sleep quality. In contrast, sleep deprivation, which involves enforced wakefulness, can provide rapid symptom relief. However, its effects are generally short-lived, and there is a risk of inducing mania in patients with bipolar disorder. In conclusion, sleep significantly impacts the severity and progression of depressive disorders. Bright light therapy and sleep deprivation offer promising alternatives to conventional treatments. The aim of this review is to underscore the importance of sleep in depression and advocate for the consideration of these alternative treatment methods to improve patient outcomes.

抑郁症影响着全球约2.8亿人,其特征是持续的悲伤和日常功能受损。睡眠障碍在重度抑郁症中很普遍,影响了大约90%的患者,并且与抑郁症的严重程度和进展有关。本文综述了睡眠在抑郁症中的重要作用,并对强光疗法和睡眠剥夺的替代疗法进行了评价。睡眠障碍不仅是抑郁症的症状,而且是抑郁症与其他疾病(如焦虑、慢性炎症、情绪失调和认知衰退)之间关系的媒介。抑郁症的有效管理必须解决这些睡眠问题。强光疗法是一种利用人造光模拟自然阳光的疗法,对治疗季节性情感障碍和非季节性重度抑郁症有效。它耐受性良好,可以单独使用或与抗抑郁药一起使用,通常可以改善情绪和睡眠质量。相反,剥夺睡眠,包括强制清醒,可以快速缓解症状。然而,它的效果通常是短暂的,并且在双相情感障碍患者中有诱发躁狂症的风险。总之,睡眠显著影响抑郁症的严重程度和进展。强光疗法和剥夺睡眠为传统疗法提供了有希望的替代方案。本综述的目的是强调睡眠在抑郁症中的重要性,并提倡考虑这些替代治疗方法来改善患者的预后。
{"title":"Role of Sleep in Depressive Disorders and the Potential Therapeutic Role of Short-Term Sleep Deprivation and Light Therapy: A Review.","authors":"Wiktoria Bojarska, Karolina Bury, Radosław Januszczak, Bartosz Burda, Justyna Pawęzka","doi":"10.12659/MSM.945319","DOIUrl":"10.12659/MSM.945319","url":null,"abstract":"<p><p>Depression affects about 280 million people globally and is marked by persistent sadness and impaired daily functioning. Sleep disturbances are prevalent in major depressive disorder, affecting roughly 90% of patients, and are linked to the severity and progression of depression. This review emphasizes the critical role of sleep in depressive disorders and evaluates the alternative treatments bright light therapy and sleep deprivation. Sleep disturbances are not only symptoms but also mediators in the relationship between depression and other conditions, such as anxiety, chronic inflammation, emotional dysregulation, and cognitive decline. Effective management of depressive disorders must address these sleep issues. Bright light therapy, which uses artificial light to mimic natural sunlight, is effective for treating seasonal affective disorder and non-seasonal major depressive disorder. It is well tolerated, can be used alone or with antidepressants, and often improves both mood and sleep quality. In contrast, sleep deprivation, which involves enforced wakefulness, can provide rapid symptom relief. However, its effects are generally short-lived, and there is a risk of inducing mania in patients with bipolar disorder. In conclusion, sleep significantly impacts the severity and progression of depressive disorders. Bright light therapy and sleep deprivation offer promising alternatives to conventional treatments. The aim of this review is to underscore the importance of sleep in depression and advocate for the consideration of these alternative treatment methods to improve patient outcomes.</p>","PeriodicalId":48888,"journal":{"name":"Medical Science Monitor","volume":"30 ","pages":"e945319"},"PeriodicalIF":3.1,"publicationDate":"2024-11-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11616206/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142755634","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}
引用次数: 0
Effects of Nutritional Protocol Changes on Hemodialysis Adequacy and Patient Health During the COVID-19 Pandemic. COVID-19大流行期间营养方案改变对血液透析充分性和患者健康的影响
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-11-29 DOI: 10.12659/MSM.946471
Cebrail Karaca, Safak Mirioglu, Aydan Mutis Alan, Saadet Usakli, Beyza Nur Aydin Keskin, Mehmet Erdem, Ahmet Murt, Mevlut Tamer Dincer, Nurhan Seyahi, Sinan Trabulus

BACKGROUND During the COVID-19 pandemic, strict feeding restrictions were implemented in many dialysis centers to minimize transmission between patients. This study aims to evaluate the effects of these feeding restrictions on dry weight, intradialytic hypotension (IDH), and dialysis adequacy in hemodialysis patients. MATERIAL AND METHODS In this retrospective single-center study involving 76 hemodialysis patients, data from 2 consecutive 6-month periods were analyzed: the first before the COVID-19 pandemic when intradialytic nutrition was supported, and the second during the pandemic when intradialytic nutrition was restricted. Data from the patients' monthly visits during both periods were evaluated, averages were recorded, and a comparison was made between the 2 periods. RESULTS The frequency of IDH was significantly higher during the feeding period compared with the no-feeding period (1.4±1.2/month vs 0.81±0.86/month, P=0.01). Conversely, the urea reduction ratio was greater in the no-feeding period [72.5% (69-76) vs 71% (68-75), P=0.01], as were the single-pool Kt/V values (1.59±0.23 vs 1.52±0.26, P=0.004) and ultrafiltration rates (mL/h/kg) (11.4±3.0 vs 10.4±3.2, P=0.01). However, the dry weight of the patients was similar in the 2 periods (65.4±13.7 kg vs 65.7±14.2 kg, P=0.62). CONCLUSIONS During the COVID-19 pandemic, mandatory feeding restrictions for hemodialysis patients, aimed at reducing transmission, were linked to a decrease in IDH frequency and improved dialysis adequacy. However, no significant reduction in patients' dry weights was observed.

背景:在COVID-19大流行期间,许多透析中心实施了严格的喂养限制,以尽量减少患者之间的传播。本研究旨在评估这些喂养限制对血液透析患者干重、分析性低血压(IDH)和透析充分性的影响。材料与方法本回顾性单中心研究纳入76例血液透析患者,对连续2个6个月的数据进行分析:第一组在COVID-19大流行前支持透析营养,第二组在大流行期间限制透析营养。对两期患者每月就诊的数据进行评估,记录平均值,并对两期进行比较。结果采食期IDH发生率显著高于非采食期(1.4±1.2/月vs 0.81±0.86/月,P=0.01)。相反,尿素还原率在不进料期更高[72.5% (69-76)vs 71% (68-75), P=0.01],单池Kt/V值(1.59±0.23 vs 1.52±0.26,P=0.004)和超滤速率(mL/h/kg)(11.4±3.0 vs 10.4±3.2,P=0.01)。但两期患者的干重基本相同(65.4±13.7 kg vs 65.7±14.2 kg, P=0.62)。结论:在2019冠状病毒病大流行期间,针对血液透析患者的强制性喂养限制旨在减少传播,与IDH频率的降低和透析充分性的改善有关。然而,没有观察到患者干重的显著减少。
{"title":"Effects of Nutritional Protocol Changes on Hemodialysis Adequacy and Patient Health During the COVID-19 Pandemic.","authors":"Cebrail Karaca, Safak Mirioglu, Aydan Mutis Alan, Saadet Usakli, Beyza Nur Aydin Keskin, Mehmet Erdem, Ahmet Murt, Mevlut Tamer Dincer, Nurhan Seyahi, Sinan Trabulus","doi":"10.12659/MSM.946471","DOIUrl":"10.12659/MSM.946471","url":null,"abstract":"<p><p>BACKGROUND During the COVID-19 pandemic, strict feeding restrictions were implemented in many dialysis centers to minimize transmission between patients. This study aims to evaluate the effects of these feeding restrictions on dry weight, intradialytic hypotension (IDH), and dialysis adequacy in hemodialysis patients. MATERIAL AND METHODS In this retrospective single-center study involving 76 hemodialysis patients, data from 2 consecutive 6-month periods were analyzed: the first before the COVID-19 pandemic when intradialytic nutrition was supported, and the second during the pandemic when intradialytic nutrition was restricted. Data from the patients' monthly visits during both periods were evaluated, averages were recorded, and a comparison was made between the 2 periods. RESULTS The frequency of IDH was significantly higher during the feeding period compared with the no-feeding period (1.4±1.2/month vs 0.81±0.86/month, P=0.01). Conversely, the urea reduction ratio was greater in the no-feeding period [72.5% (69-76) vs 71% (68-75), P=0.01], as were the single-pool Kt/V values (1.59±0.23 vs 1.52±0.26, P=0.004) and ultrafiltration rates (mL/h/kg) (11.4±3.0 vs 10.4±3.2, P=0.01). However, the dry weight of the patients was similar in the 2 periods (65.4±13.7 kg vs 65.7±14.2 kg, P=0.62). CONCLUSIONS During the COVID-19 pandemic, mandatory feeding restrictions for hemodialysis patients, aimed at reducing transmission, were linked to a decrease in IDH frequency and improved dialysis adequacy. However, no significant reduction in patients' dry weights was observed.</p>","PeriodicalId":48888,"journal":{"name":"Medical Science Monitor","volume":"30 ","pages":"e946471"},"PeriodicalIF":3.1,"publicationDate":"2024-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11613781/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142752097","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}
引用次数: 0
Enhanced Diagnostic Imaging: Arrival-Time Parametric Imaging in Contrast-Enhanced Ultrasound for Multi-Organ Assessment. 增强诊断成像:用于多器官评估的对比增强超声中的到达时间参数成像。
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-11-28 DOI: 10.12659/MSM.945281
Nan Jiang, Jun-Ying Cao, Zhuang Jin, Tian-Qi Yu, Shu-Ting Chen, Yun Zhang

Contrast-enhanced ultrasonography (CEUS) is a novel technology in ultrasound medicine that has gained widespread application in clinical practice. While CEUS offers various quantitative and qualitative parameters, it is limited by factors such as the single-color transient coverage of the contrast agent and its dependence on the operator, rendering it less suitable for detecting blood in organ lesions. Additionally, fluid dynamic perfusion remains unsatisfactory. Recently, arrival-time parametric imaging (At-PI) has emerged as a promising alternative; this technology not only uses color overlay to statically represent the dynamic perfusion of blood flow within lesions but also enhances visualization, minimizes operator variability, and provides insights into the vascular patterns of both benign and malignant lesions. At-PI has demonstrated numerous advantages and has been successfully applied to the liver, adrenal gland, breast, lymph nodes, prostate, and gastrointestinal tract, yielding encouraging preliminary results. This review synthesizes existing research findings, highlights significant parameters, examines the current global research landscape regarding this technology, and outlines the research directions pursued by scholars in the field. Furthermore, we offer a critical analysis and discussion of the limitations of these findings. The ultimate aim is to elucidate the role of At-PI in clinical diagnosis and treatment.

对比增强超声造影(CEUS)是超声医学领域的一项新技术,已在临床上得到广泛应用。虽然 CEUS 可提供各种定量和定性参数,但受造影剂单色瞬时覆盖和对操作者的依赖性等因素的限制,使其不太适合检测器官病变中的血液。此外,液体动态灌注的效果仍不理想。最近,到达时间参数成像(At-PI)成为一种有前途的替代方法;该技术不仅使用颜色叠加来静态呈现病变内的动态血流灌注,还能增强可视化,最大限度地减少操作者的可变性,并提供对良性和恶性病变血管模式的深入了解。At-PI 已显示出诸多优势,并已成功应用于肝脏、肾上腺、乳腺、淋巴结、前列腺和胃肠道,取得了令人鼓舞的初步成果。本综述综合了现有的研究成果,强调了重要的参数,考察了当前全球有关该技术的研究情况,并概述了该领域学者的研究方向。此外,我们还对这些研究成果的局限性进行了批判性分析和讨论。最终目的是阐明 At-PI 在临床诊断和治疗中的作用。
{"title":"Enhanced Diagnostic Imaging: Arrival-Time Parametric Imaging in Contrast-Enhanced Ultrasound for Multi-Organ Assessment.","authors":"Nan Jiang, Jun-Ying Cao, Zhuang Jin, Tian-Qi Yu, Shu-Ting Chen, Yun Zhang","doi":"10.12659/MSM.945281","DOIUrl":"10.12659/MSM.945281","url":null,"abstract":"<p><p>Contrast-enhanced ultrasonography (CEUS) is a novel technology in ultrasound medicine that has gained widespread application in clinical practice. While CEUS offers various quantitative and qualitative parameters, it is limited by factors such as the single-color transient coverage of the contrast agent and its dependence on the operator, rendering it less suitable for detecting blood in organ lesions. Additionally, fluid dynamic perfusion remains unsatisfactory. Recently, arrival-time parametric imaging (At-PI) has emerged as a promising alternative; this technology not only uses color overlay to statically represent the dynamic perfusion of blood flow within lesions but also enhances visualization, minimizes operator variability, and provides insights into the vascular patterns of both benign and malignant lesions. At-PI has demonstrated numerous advantages and has been successfully applied to the liver, adrenal gland, breast, lymph nodes, prostate, and gastrointestinal tract, yielding encouraging preliminary results. This review synthesizes existing research findings, highlights significant parameters, examines the current global research landscape regarding this technology, and outlines the research directions pursued by scholars in the field. Furthermore, we offer a critical analysis and discussion of the limitations of these findings. The ultimate aim is to elucidate the role of At-PI in clinical diagnosis and treatment.</p>","PeriodicalId":48888,"journal":{"name":"Medical Science Monitor","volume":"30 ","pages":"e945281"},"PeriodicalIF":3.1,"publicationDate":"2024-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11613779/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142741067","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}
引用次数: 0
期刊
Medical Science Monitor
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:481959085
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