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Exploring ChatGPT in clinical inquiry: a scoping review of characteristics, applications, challenges, and evaluation. 在临床调查中探索ChatGPT:特征、应用、挑战和评估的范围审查。
IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-08 eCollection Date: 2024-12-01 DOI: 10.1097/MS9.0000000000002716
Shahabeddin Abhari, Yasna Afshari, Farhad Fatehi, Hosna Salmani, Ali Garavand, Dmytro Chumachenko, Somayyeh Zakerabasali, Plinio P Morita

Introduction: Recent advancements in generative AI, exemplified by ChatGPT, hold promise for healthcare applications such as decision-making support, education, and patient engagement. However, rigorous evaluation is crucial to ensure reliability and safety in clinical contexts. This scoping review explores ChatGPT's role in clinical inquiry, focusing on its characteristics, applications, challenges, and evaluation.

Methods: This review, conducted in 2023, followed PRISMA-ScR guidelines (Supplemental Digital Content 1, http://links.lww.com/MS9/A636). Searches were performed across PubMed, Scopus, IEEE, Web of Science, Cochrane, and Google Scholar using relevant keywords. The review explored ChatGPT's effectiveness in various medical domains, evaluation methods, target users, and comparisons with other AI models. Data synthesis and analysis incorporated both quantitative and qualitative approaches.

Results: Analysis of 41 academic studies highlights ChatGPT's potential in medical education, patient care, and decision support, though performance varies by medical specialty and linguistic context. GPT-3.5, frequently referenced in 26 studies, demonstrated adaptability across diverse scenarios. Challenges include limited access to official answer keys and inconsistent performance, underscoring the need for ongoing refinement. Evaluation methods, including expert comparisons and statistical analyses, provided significant insights into ChatGPT's efficacy. The identification of target users, such as medical educators and nonexpert clinicians, illustrates its broad applicability.

Conclusion: ChatGPT shows significant potential in enhancing clinical practice and medical education. Nevertheless, continuous refinement is essential for its successful integration into healthcare, aiming to improve patient care outcomes, and address the evolving needs of the medical community.

简介:以ChatGPT为例,生成式人工智能的最新进展为医疗保健应用(如决策支持、教育和患者参与)带来了希望。然而,严格的评估对于确保临床环境中的可靠性和安全性至关重要。这篇综述探讨了ChatGPT在临床研究中的作用,重点是它的特点、应用、挑战和评估。方法:本综述于2023年进行,遵循PRISMA-ScR指南(补充数字内容1,http://links.lww.com/MS9/A636)。使用相关关键词在PubMed、Scopus、IEEE、Web of Science、Cochrane和b谷歌Scholar上进行搜索。该综述探讨了ChatGPT在各种医疗领域、评估方法、目标用户以及与其他人工智能模型的比较中的有效性。数据综合和分析结合了定量和定性方法。结果:对41项学术研究的分析强调了ChatGPT在医学教育、患者护理和决策支持方面的潜力,尽管其表现因医学专业和语言背景而异。GPT-3.5在26项研究中经常被引用,显示出在不同情况下的适应性。挑战包括访问官方答案密钥的受限和不一致的性能,强调需要不断改进。评估方法,包括专家比较和统计分析,为ChatGPT的疗效提供了重要的见解。确定目标用户,如医学教育工作者和非专家临床医生,说明了其广泛的适用性。结论:ChatGPT在加强临床实践和医学教育方面具有重要的应用潜力。然而,持续改进对于其成功整合到医疗保健中至关重要,旨在改善患者护理结果,并满足医学界不断变化的需求。
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引用次数: 0
Distal femur osteosarcoma in a seven-year-old: a case report on acute symptom presentation. 7岁儿童股骨远端骨肉瘤一例急性症状报告。
IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-08 eCollection Date: 2024-12-01 DOI: 10.1097/MS9.0000000000002726
Neveen Shalalfa, Saleh Wajeeh, Zaina Sheeb, Omama Nawaja, Fatima Abuarqoub, Jameel Abufara, Shatha Shalalfa

Introduction and importance: Osteosarcoma is an exceptionally serious, uncommon disease in children with morbidity, mortality, and psychological burdens.

Case presentation: In this report, the authors present the case of a previously healthy 7-year-old girl who exhibited continuous, painful limping. Plain imaging and a MRI scan revealed the presence of a lytic lesion in the femur on the left side. The diagnosis of osteosarcoma was confirmed. There was no significant familial history of cancer. The girl and her family underwent the operation and chemotherapy, received follow-up and support for a year, and both the patient and the medical team expressed a lot of satisfaction.

Clinical discussion: The survival and prognosis from osteosarcoma in the literature was 59% for all patients at a median follow-up up 54 months, current treatment of osteosarcoma involves chemotherapy and limb surgery, with (60-80)% of patients in remission after 5 years.

Conclusion: This case emphasizes the importance of promptly considering osteosarcoma in a child when the clinical presentation and medical imaging align with the diagnosis.

简介及重要性:骨肉瘤是儿童中一种发病率、死亡率和心理负担都非常严重的罕见疾病。病例介绍:在本报告中,作者介绍了一个以前健康的7岁女孩,她表现出持续的,痛苦的跛行。平片和MRI扫描显示左侧股骨存在溶解性病变。确诊为骨肉瘤。没有明显的癌症家族史。女孩和她的家人接受了手术和化疗,并接受了一年的随访和支持,患者和医疗团队都表示非常满意。临床讨论:在54个月的中位随访中,文献中所有骨肉瘤患者的生存率和预后为59%,目前骨肉瘤的治疗包括化疗和肢体手术,(60- 80%)%的患者在5年后缓解。结论:本病例强调了当临床表现和医学影像与诊断相符时,及时考虑儿童骨肉瘤的重要性。
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引用次数: 0
The clinico-epidemiological, diagnostic, and therapeutic aspects of methadone poisoning: a registry-based clinical study. 美沙酮中毒的临床流行病学、诊断和治疗方面:一项基于登记的临床研究。
IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-08 eCollection Date: 2024-12-01 DOI: 10.1097/MS9.0000000000002709
Seyed M Hosseininejad, Ali Sharifpour, Fatemeh Akbarnezhad, Hossein Veisi, Zakaria Zakariaei

Objectives: Methadone is a long-acting synthetic agonist of opioid receptors, which is used as an analgesic and as an alternative treatment in opioid-dependent patients. Clinical manifestations of methadone poisoning include miotic pupils, low levels of consciousness (LOC), respiratory depression or apnea, and coma and death. Considering the high consumption of methadone in society and the prevalent instances of overdose and poisoning, whether accidental or intentional, the authors decided to investigate the clinico-epidemiological, diagnostic, and therapeutic characteristics of methadone poisoning in the Mazandaran province, northern Iran, from 2020 to 2022.

Methods: This study was a retrospective and descriptive cross-sectional registry-based study, wherein data was collected from the Mazandaran Registry Center of Opioids Poisoning (MRCOP), on patients with methadone poisoning. Data based on various parameters such as individual characteristics, ingestion motivation, and clinical outcomes were collected in a checklist.

Results: Of the 385 patients, who entered the study, 264 were men and 121 were women. The mean age of the patients was 29.02 years. Two hundred forty-four patients had intentionally consumed methadone. The most common symptoms observed among individuals with methadone poisoning were decreased arterial blood oxygen (225 patients) and decreased LOC (173 patients). The length of hospitalization for most patients was less than 1 week. Except for seven of them who died, most of them were discharged in good general condition.

Conclusion: The study identified sex, age, marital and employment status, and suicidal intent as the most significant factors influencing methadone poisoning, which should be considered in the design and implementation of public education and prevention programs.

目的:美沙酮是一种阿片受体的长效合成激动剂,被用作镇痛剂和阿片类药物依赖患者的替代治疗药物。美沙酮中毒的临床表现包括瞳孔缩小、低意识水平(LOC)、呼吸抑制或呼吸暂停、昏迷和死亡。考虑到美沙酮在社会上的高消费量以及过量和中毒(无论是意外还是故意)的普遍情况,作者决定调查 2020 年至 2022 年伊朗北部马赞达兰省美沙酮中毒的临床流行病学、诊断和治疗特征:本研究是一项以登记为基础的回顾性和描述性横断面研究,从马赞达兰阿片类药物中毒登记中心(MRCOP)收集美沙酮中毒患者的数据。通过核对表收集了基于个人特征、摄入动机和临床结果等各种参数的数据:在参与研究的 385 名患者中,264 人为男性,121 人为女性。患者的平均年龄为 29.02 岁。244 名患者曾故意服用美沙酮。美沙酮中毒患者最常见的症状是动脉血氧减少(225 名患者)和 LOC 减少(173 名患者)。大多数患者的住院时间不超过一周。除 7 名患者死亡外,大多数患者出院时一般状况良好:研究发现,性别、年龄、婚姻和就业状况以及自杀意向是影响美沙酮中毒的最主要因素,在设计和实施公共教育和预防计划时应考虑这些因素。
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引用次数: 0
Sinus mucocele leads to unilateral proptosis in an infant patient with cystic fibrosis: a literature review and a case report study. 婴儿囊性纤维化患者的鼻窦粘液囊肿导致单侧突出:文献回顾和病例报告研究。
IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-07 eCollection Date: 2024-12-01 DOI: 10.1097/MS9.0000000000002700
Narges Lashkarbolouk, Mahdi Mazandarani, Parastou Biazar, Lobat Shahkar

Introduction and importance: Cystic fibrosis (CF) is a widespread life-shortening recessive genetic disease and can present with sinus mucocele. Sinus mucocele is a rare condition, with limited prevalence data on unilateral proptosis.

Case presentation: The authors present a case of a 19-month-old boy with CF who experienced worsening proptosis and exotropia in his right eye. A brain and orbit MRI revealed diffuse polypoid mucosal thickening, possible dense fungal deposit, deformity of the mid face, especially on the right side, with more prominent bulging of medical and inferior walls of the right lobe, a right ethmoidal mucocele causing ocular globe displacement, medial rectus compression, and optic nerve. An examination of the eye fundus showed disc edema and vascular congestion. Endoscopic sinus surgery successfully drained the mucocele, and treatment with antibiotics and corticosteroids led to symptom improvement and resolution of proptosis within 3 weeks.

Clinical discussion: Mucoceles represent an uncommon complication associated with CF in pediatric patients. Consequently, any child presenting with this issue should undergo evaluation for CF. Investigating this infrequent condition's underlying mechanisms and consequences may improve treatment approaches and outcomes for those impacted.

Conclusion: Sinus mucocele with unilateral proptosis in CF patients is uncommon, and endoscopic sinus surgery appears to be an effective cure for this complication, even in the pediatric population at high risk, like CF patients.

导言和重要性:囊性纤维化(CF)是一种广泛存在的缩短寿命的隐性遗传病,可表现为鼻窦粘液囊肿。鼻窦粘液囊是一种罕见病,单侧突眼的发病率数据有限:作者介绍了一例 19 个月大的 CF 男孩的病例,他的右眼突眼和外斜视不断加重。脑部和眼眶核磁共振成像检查显示:弥漫性息肉状粘膜增厚,可能有致密的真菌沉积,中面部畸形,尤其是右侧,右叶内侧和下壁隆起更明显,右侧乙状粘液瘤导致眼球移位,内侧直肌受压,视神经受压。眼底检查显示眼盘水肿和血管充血。内窥镜鼻窦手术成功引流了粘液瘤,并使用抗生素和皮质类固醇治疗,症状在三周内得到改善,突眼症状也得到缓解:粘液囊是儿童患者中与 CF 相关的一种不常见的并发症。因此,任何出现此问题的儿童都应接受 CF 评估。研究这种罕见病症的潜在机制和后果可能会改善治疗方法和受影响患者的治疗效果:结论:CF 患者鼻窦粘液囊伴有单侧突眼的情况并不常见,内窥镜鼻窦手术似乎是治疗这种并发症的有效方法,即使在 CF 患者等高风险儿科人群中也是如此。
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引用次数: 0
Dandy-Walker syndrome: a bibliometric analysis of the most 100 cited articles. Dandy-Walker综合征:引用次数最多的100篇文章的文献计量学分析。
IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-07 eCollection Date: 2024-12-01 DOI: 10.1097/MS9.0000000000002725
Khadeja Alrefaie, Noyan Jawed, Aalaa Saleh, Farah Shibli, Yasser F Almealawy, Sura N Alrubaye, Wireko Andrew Awuah, Toufik Abdul-Rahman, Bipin Chaurasia, Oday Atallah

Introduction: Dandy-Walker syndrome (DWS), a complex neurodevelopmental disorder, has intrigued clinicians and researchers since its description by physicians Walter Dandy and Arthur Walker. Despite its recognition for nearly a century, understanding its etiology, pathogenesis, and clinical manifestations remains elusive. This bibliometric analysis aims to elucidate influential academic works on DWS.

Methods: In January 2024, the authors conducted a Scopus search for articles on DWS and identified the top 100 referenced publications. The Harzing Publish or Perish search engine was utilized with relevant terms, including 'Dandy-Walker', 'Dandy-Walker Syndrome', and 'Dandy-Walker Malformation'. Data from Scopus, including publication details and citation counts, were compiled and organized using Microsoft Excel. Statistical analysis and data visualization were performed using Python, with Pandas, Matplotlib, Seaborn, and NetworkX libraries employed for this purpose.

Results: The bibliometric analysis of DWS research revealed key insights. Significant research output was noted in the 2000-2009 and 1990-1999 decades. The cumulative citations totaled 6059, with an average of 2.60 citations per year per article. Leading authors included W B Dobyns, Kathleen J Millen, and G Pilu. Institutions such as the University of California and Harvard Medical School were prominent, with the United States being the predominant contributor. Major journals like the American Journal of Medical Genetics played significant roles.

Conclusion: This bibliometric study summarizes the most-cited articles on DWS, providing light on the field and its seminal works that have shaped both present-day clinical treatment and the trajectory of future research.

简介:ddy -Walker综合征(DWS)是一种复杂的神经发育障碍,自Walter Dandy和Arthur Walker医生描述以来,一直引起临床医生和研究人员的兴趣。尽管它的认识近一个世纪,了解其病因,发病机制和临床表现仍然难以捉摸。本文的文献计量分析旨在阐明有影响的DWS学术著作。方法:作者于2024年1月对DWS上的文章进行Scopus检索,筛选出被引用文献前100名。Harzing发布或灭亡搜索引擎使用了相关术语,包括“Dandy-Walker”,“Dandy-Walker综合征”和“Dandy-Walker畸形”。来自Scopus的数据,包括发表细节和引用计数,使用Microsoft Excel进行编译和组织。统计分析和数据可视化使用Python, Pandas、Matplotlib、Seaborn和NetworkX库用于此目的。结果:DWS研究的文献计量学分析揭示了关键的见解。2000-2009年和1990-1999年的研究成果显著。累计被引6059次,平均每年被引2.60次。主要作者包括W·B·多宾斯、凯瑟琳·J·米伦和G·皮卢。加州大学和哈佛医学院等机构表现突出,其中美国是主要贡献者。《美国医学遗传学杂志》等主要期刊发挥了重要作用。结论:这项文献计量学研究总结了被引用最多的关于DWS的文章,为该领域及其影响当今临床治疗和未来研究轨迹的开创性工作提供了光明。
{"title":"Dandy-Walker syndrome: a bibliometric analysis of the most 100 cited articles.","authors":"Khadeja Alrefaie, Noyan Jawed, Aalaa Saleh, Farah Shibli, Yasser F Almealawy, Sura N Alrubaye, Wireko Andrew Awuah, Toufik Abdul-Rahman, Bipin Chaurasia, Oday Atallah","doi":"10.1097/MS9.0000000000002725","DOIUrl":"10.1097/MS9.0000000000002725","url":null,"abstract":"<p><strong>Introduction: </strong>Dandy-Walker syndrome (DWS), a complex neurodevelopmental disorder, has intrigued clinicians and researchers since its description by physicians Walter Dandy and Arthur Walker. Despite its recognition for nearly a century, understanding its etiology, pathogenesis, and clinical manifestations remains elusive. This bibliometric analysis aims to elucidate influential academic works on DWS.</p><p><strong>Methods: </strong>In January 2024, the authors conducted a Scopus search for articles on DWS and identified the top 100 referenced publications. The Harzing Publish or Perish search engine was utilized with relevant terms, including 'Dandy-Walker', 'Dandy-Walker Syndrome', and 'Dandy-Walker Malformation'. Data from Scopus, including publication details and citation counts, were compiled and organized using Microsoft Excel. Statistical analysis and data visualization were performed using Python, with Pandas, Matplotlib, Seaborn, and NetworkX libraries employed for this purpose.</p><p><strong>Results: </strong>The bibliometric analysis of DWS research revealed key insights. Significant research output was noted in the 2000-2009 and 1990-1999 decades. The cumulative citations totaled 6059, with an average of 2.60 citations per year per article. Leading authors included W B Dobyns, Kathleen J Millen, and G Pilu. Institutions such as the University of California and Harvard Medical School were prominent, with the United States being the predominant contributor. Major journals like the American Journal of Medical Genetics played significant roles.</p><p><strong>Conclusion: </strong>This bibliometric study summarizes the most-cited articles on DWS, providing light on the field and its seminal works that have shaped both present-day clinical treatment and the trajectory of future research.</p>","PeriodicalId":8025,"journal":{"name":"Annals of Medicine and Surgery","volume":"86 12","pages":"7278-7289"},"PeriodicalIF":1.7,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11623816/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142799156","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Hereditary multiple exostoses with cervical spine involvement: a case report: Retraction. 受累于颈椎的遗传性多发性骨质增生:病例报告:撤回。
IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-06 eCollection Date: 2024-11-01 DOI: 10.1097/MS9.0000000000002651

[This retracts the article DOI: 10.1097/MS9.0000000000002452.].

[本文撤回了文章 DOI:10.1097/MS9.0000000000002452]。
{"title":"Hereditary multiple exostoses with cervical spine involvement: a case report: Retraction.","authors":"","doi":"10.1097/MS9.0000000000002651","DOIUrl":"https://doi.org/10.1097/MS9.0000000000002651","url":null,"abstract":"<p><p>[This retracts the article DOI: 10.1097/MS9.0000000000002452.].</p>","PeriodicalId":8025,"journal":{"name":"Annals of Medicine and Surgery","volume":"86 11","pages":"6903"},"PeriodicalIF":1.7,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11543168/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142613526","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Acalvaria, rare congenital malformation in Palestine: case report and literature review: Retraction. 巴勒斯坦罕见的先天性畸形 Acalvaria:病例报告和文献综述:撤回。
IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-06 eCollection Date: 2024-11-01 DOI: 10.1097/MS9.0000000000002729

[This retracts the article DOI: 10.1097/MS9.0000000000002643.].

[本文撤消了文章 DOI:10.1097/MS9.0000000000002643]。
{"title":"Acalvaria, rare congenital malformation in Palestine: case report and literature review: Retraction.","authors":"","doi":"10.1097/MS9.0000000000002729","DOIUrl":"https://doi.org/10.1097/MS9.0000000000002729","url":null,"abstract":"<p><p>[This retracts the article DOI: 10.1097/MS9.0000000000002643.].</p>","PeriodicalId":8025,"journal":{"name":"Annals of Medicine and Surgery","volume":"86 11","pages":"6904"},"PeriodicalIF":1.7,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11543137/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142613549","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Repotrectinib: a promising new therapy for advanced nonsmall cell lung cancer. Repotrectinib:一种治疗晚期非小细胞肺癌的新疗法。
IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-05 eCollection Date: 2024-12-01 DOI: 10.1097/MS9.0000000000002717
Taruba Rais, Amna Shakeel, Laiba Naseem, Nathalie Nasser, Minahil Aamir

Nonsmall cell lung cancer (NSCLC) is the major cause of cancer-related mortality worldwide, accounting for 84% of lung cancer cases. The newly FDA-approved kinase inhibitor, repotrectinib (AUGTYRO), offers a promising option for treating advanced or metastatic NTRK/ROS1-positive Nonsmall cell lung cancer. Repotrectinib has demonstrated significant efficacy in clinical trials. Notably, the phase 1/2 TRIDENT-1 study showed impressive progression-free survival and intracranial activity in both TKI-naïve and pretreated patients. With its high response rates and manageable side effects, repotrectinib is set to play a significant role in treating ROS1+ and NTRK+advanced solid tumors, highlighting the ongoing need for research and clinical application.

非小细胞肺癌(NSCLC)是全球癌症相关死亡的主要原因,占肺癌病例的84%。新获fda批准的激酶抑制剂repotrectinib (AUGTYRO)为治疗晚期或转移性NTRK/ ros1阳性非小细胞肺癌提供了一个有希望的选择。Repotrectinib在临床试验中显示出显著的疗效。值得注意的是,1/2期TRIDENT-1研究显示TKI-naïve和预处理患者的无进展生存期和颅内活动令人印象深刻。repotrectinib反应率高,副作用可控,有望在ROS1+和NTRK+晚期实体瘤的治疗中发挥重要作用,研究和临床应用的需求仍在继续。
{"title":"Repotrectinib: a promising new therapy for advanced nonsmall cell lung cancer.","authors":"Taruba Rais, Amna Shakeel, Laiba Naseem, Nathalie Nasser, Minahil Aamir","doi":"10.1097/MS9.0000000000002717","DOIUrl":"10.1097/MS9.0000000000002717","url":null,"abstract":"<p><p>Nonsmall cell lung cancer (NSCLC) is the major cause of cancer-related mortality worldwide, accounting for 84% of lung cancer cases. The newly FDA-approved kinase inhibitor, repotrectinib (AUGTYRO), offers a promising option for treating advanced or metastatic NTRK/ROS1-positive Nonsmall cell lung cancer. Repotrectinib has demonstrated significant efficacy in clinical trials. Notably, the phase 1/2 TRIDENT-1 study showed impressive progression-free survival and intracranial activity in both TKI-naïve and pretreated patients. With its high response rates and manageable side effects, repotrectinib is set to play a significant role in treating ROS1+ and NTRK+advanced solid tumors, highlighting the ongoing need for research and clinical application.</p>","PeriodicalId":8025,"journal":{"name":"Annals of Medicine and Surgery","volume":"86 12","pages":"7265-7269"},"PeriodicalIF":1.7,"publicationDate":"2024-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11623886/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142799081","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The prevalence and associated factors of intraoperative hypotension following thoracic surgery in resources limited area, 2023: multicentre approach. 2023年资源有限地区胸外科手术后术中低血压的患病率及相关因素:多中心入路
IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-05 eCollection Date: 2024-12-01 DOI: 10.1097/MS9.0000000000002665
Yisehak Wolde, Adugna Argawi, Yabtsega Alemayehu, Mitiku Desalegn, Sintayehu Samuel

Background: Hypotension is an independent predictor of long-term patient morbidity and duration of hospital stay. Multiple factors contribute to the development of intraoperative hypotension. Prevention and treatment of these factors may reduce patients' hypotension and its associated morbidity and mortality. This study aimed to assess the prevalence and associated factors of intraoperative hypotension in patients undergoing elective thoracic surgery.

Methods: This institution-based cross-sectional study was conducted among 174 adult patients who underwent elective thoracic surgery. A systematic random sampling technique was used, and quantitative data were collected through interviews and data retrieval from charts via a pretested questionnaire. Both bivariable and multivariable logistic regression analyses were performed to evaluate the associations between independent and dependent variables. The level of statistical significance was defined as a P-value less than 0.05. The data were entered into Info 7.2.1 and analyzed via SPSS version 26 software, which was used to calculate descriptive statistics, and bivariate and multivariate logistic regression were performed.

Results: In general, information was collected from 174 patients during the study period. The results of the present study revealed that 65 (41%) patients developed intraoperative hypotension (95% CI: 36.43-48%). Intraoperative blood loss was significantly associated with intraoperative hypotension [AOR=9.58, 95% CI (2.57-35.8)] (P=0.001).

Conclusion and recommendation: The findings of this study revealed high rates of intraoperative hypotension episodes, which were 41%, in patients who underwent elective thoracic surgery. Age, ASA class, type of intraoperative blood loss, type of procedure pre-existence comorbidity, and duration of surgery were predictors of intraoperative hypotension in patients who underwent elective thoracic surgery. The anaesthetist's, surgeon, and PACU staff's understanding of these factors is very crucial for close follow-up of this group of patients.

背景:低血压是患者长期发病率和住院时间的独立预测因子。术中低血压的发生与多种因素有关。预防和治疗这些因素可以降低患者的低血压及其相关的发病率和死亡率。本研究旨在评估择期胸外科患者术中低血压的患病率及相关因素。方法:本研究以医院为基础,对174例接受择期胸外科手术的成年患者进行了横断面研究。本研究采用系统随机抽样技术,通过访谈和预测问卷从图表中提取数据,收集定量数据。采用双变量和多变量logistic回归分析来评估自变量和因变量之间的相关性。以p值小于0.05定义统计学显著性水平。数据输入Info 7.2.1,通过SPSS version 26软件进行统计分析,计算描述性统计,并进行双变量和多变量logistic回归。结果:总体而言,在研究期间收集了174例患者的信息。本研究结果显示,65例(41%)患者出现术中低血压(95% CI: 36.43-48%)。术中出血量与术中低血压显著相关[AOR=9.58, 95% CI (2.57 ~ 35.8)] (P=0.001)。结论和建议:本研究结果显示,接受择期胸外科手术的患者术中低血压发作的发生率很高,为41%。年龄、ASA等级、术中出血量类型、手术前存在的合并症类型和手术时间是择期胸外科患者术中低血压的预测因素。麻醉师、外科医生和PACU工作人员对这些因素的理解对于这组患者的密切随访至关重要。
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引用次数: 0
K wire migration into spinal canal: an infrequent cause of neurological morbidity - a case report. K线向椎管内移位:一种少见的神经系统疾病的病因-一例报告。
IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL Pub Date : 2024-11-05 eCollection Date: 2024-12-01 DOI: 10.1097/MS9.0000000000002707
Ashbin Bhattarai, Bijaya Gurung, Binod Sherchan, Badri Rijal, Prasanna D Karki

Introduction: K wire is one of the most common implants used for fixation of acromioclavicular joint dislocation. The migration of K wire from the AC joint to the spinal canal is a rare occurrence. In this report, the authors present a case of a young adult who presented with weakness of the left upper limb secondary to migration of the K wire from the AC joint to the spinal canal.

Case presentation: A 46-year-old male farmer presented with complaints of pain in the neck, tingling sensation in the left upper limb, and a tender palpable swelling on the left side of his neck with weakness of finger flexors and abductors. He had had an open reduction and fixation with K wire for Acromioclavicular dislocation three months back. CT confirmed the K wire is passing through the neural foramen between C5 and C6 vertebra and extending across the entire diameter of the spinal canal. Under intravenous anesthesia, a transverse skin incision was made over the prominent swelling on the neck, and the wire was gently removed. Minimal seepage of spinal fluid was observed, which stopped on its own after a few days.

Discussion: Although AC joint stabilization by K wire fixation provides a safe and easy fixation with low morbidity, complications such as a loss of fixation or loosening can occur. Migration of K wire into a spinal canal is a well-known but infrequent complication. Resorption of bone, muscle action, and negative intrathoracic pressures associated with respiration and heat necrosis causes progressive loosening and dislodgement. Spinal migration is very dangerous because it can cause serious damage to the dura mater, spinal cord, and vertebral artery.

Conclusion: Early identification and removal of the K wire, once it has migrated from the site of use, is mandatory to prevent its grievous complications.

简介:K线是固定肩锁关节脱位最常用的植入物之一。K针从交流关节向椎管的移位是罕见的。在本报告中,作者报告了一例年轻成人,其表现为左上肢无力,继发于K线从AC关节向椎管迁移。病例介绍:46岁男性农民,主诉颈部疼痛,左上肢麻刺感,颈部左侧可触及的柔软肿胀,手指屈肌和外展肌无力。三个月前,他因肩锁关节脱位接受了切开复位和K针固定。CT证实K针穿过C5和C6椎体之间的神经孔,并穿过椎管的整个直径。在静脉麻醉下,在颈部突出的肿胀处做一个横向皮肤切口,轻轻地取出金属丝。观察到极少的脊髓液渗漏,几天后自行停止。讨论:虽然用K线固定交流关节是一种安全、简单且发病率低的固定方法,但仍可能发生固定物丢失或松动等并发症。钢丝向椎管内移位是一种众所周知但并不常见的并发症。骨的吸收、肌肉的活动以及与呼吸和热坏死相关的胸内负压导致进行性松动和脱位。脊髓移位是非常危险的,因为它会对硬脑膜、脊髓和椎动脉造成严重的损伤。结论:一旦K针从使用部位迁移,早期识别和移除K针是必须的,以防止其严重并发症。
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引用次数: 0
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