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  • 文章类型: Journal Article
    根据循证实践制定中国常见癌症诊断和治疗指南,诊断和治疗产品的可用性,而精准医学的最新进展是中国临床肿瘤学会乳腺癌(CSCOBC)委员会的基本任务之一。
    具有高证据水平和良好可用性的协议被用作I级建议;具有相对高证据水平但专家共识略低或可用性差的协议被用作II级建议;临床适用但证据水平低的协议被视为III级建议。根据国内外临床研究的结果和CSCOBC专家的意见,CSCOBC指南确定了临床应用的推荐水平.
    对于人类表皮生长因子受体2(HER2)阳性乳腺癌,曲妥珠单抗和帕妥珠单抗联合方案被推荐为新辅助和一线转移性乳腺癌的I级推荐方案.根据在中国进行的最新研究,在一线和二线治疗中,吡替尼也被推荐为I级推荐。抗体药物缀合物也被推荐用于曲妥珠单抗进展的患者。对于三阴性乳腺癌,早期和转移性乳腺癌的免疫治疗在本版指南中得到了强调,并被列为新章节.对于激素受体(HR)阳性乳腺癌,细胞周期蛋白依赖性激酶4/6(CDK4/6)在不同阶段被推荐,尤其是辅助治疗。通过HR状态分层的低HER2乳腺癌也有了新的一章。
    我们坚信,可用性方面,和基于共识的指南在中国和其他有类似情况的国家的临床实践中更可行。
    UNASSIGNED: Developing guidelines for the diagnosis and treatment of common cancers in China based on the evidence-based practice, the availability of diagnosis and treatment products, and the up-to-date advances in precision medicine is one of the basic tasks of the Chinese Society of Clinical Oncology Breast Cancer (CSCO BC) Committee.
    UNASSIGNED: Protocols with high evidence level and good availability are used as the Level I recommendations; protocols with relatively high evidence level but slightly lower expert consensus or with poor availability are used as the Level II recommendations; and protocols that are clinically applicable but with low evidence level are regarded as the Level III recommendations. Based on the findings of clinical research at home and abroad and the opinions of CSCO BC experts, the CSCO BC guidelines determine the levels of recommendations for clinical application.
    UNASSIGNED: For human epidermal growth factor receptor 2 (HER2)-positive breast cancer, a combination of trastuzumab and pertuzumab regimen were recommended as Level I recommendation for neoadjuvant and first line metastatic breast cancer. Pyrotinib is also recommended as Level I recommendation in first line and second line therapy according to the latest studies conducted in China. Antibody drug conjugates was also recommended for patients with trastuzumab progression. For triple negative breast cancer, immunotherapy in early and metastatic breast cancer was highlighted and listed as new chapters in this version of guideline. For hormone receptor (HR)-positive breast cancer, cyclin dependent kinase 4/6 (CDK4/6) was recommended in different stages, especially in adjuvant therapy. There was also a new chapter for HER2-low breast cancer stratified by HR status.
    UNASSIGNED: We firmly believe that evidence-based, availability-concerned, and consensus-based guidelines will be more feasible for clinical practice in China and in other countries with similar situations.
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  • 文章类型: Journal Article
    背景:肺炎支原体(M.肺炎)是儿童社区获得性肺炎的重要原因。自1968年以来,日本最初报道了对大环内酯类抗生素耐药的肺炎支原体菌株,大环内酯耐药肺炎支原体(MRMP)已在世界许多国家被证明,发病率不同。MRMP感染导致对大环内酯类抗生素的反应不佳,经常导致长时间的发烧,延长抗生素治疗,住院率增加,重症监护室入院,接受糖皮质激素或二线抗生素的患者比例明显更高。自2000年以来,MRMP的全球发病率逐渐上升,尤其是在东亚,对儿童肺炎支原体感染的治疗提出了严峻的挑战,引起了儿科医生的广泛关注。然而,关于儿童MRMP的诊断和治疗仍未达成全球共识.
    方法:我们组织了29名中国儿科肺病学和流行病学专家,撰写了世界上第一个关于小儿MRMP肺炎诊断和治疗的共识,基于证据收集。使用电子数据库进行证据搜索和审查,包括PubMed,Embase,WebofScience,CNKI,Medline,还有Cochrane图书馆.我们在术语“大环内酯抗性”中使用了变体,“肺炎支原体”,\"MP\",\"M.肺炎\“,\"肺炎\",\"MRMP\",“下呼吸道感染”,“肺炎支原体感染”,\"children\",和“儿科”。
    结果:流行病学,发病机制,临床表现,早期识别,实验室检查,抗生素使用原则,糖皮质激素和静脉注射免疫球蛋白的应用,并强调支气管镜检查的注意事项。现在,通过呼吸道标本中的聚合酶链反应和荧光探针技术,可以早期快速鉴定与MRMP相关的基因突变。尽管对大环内酯的耐药率仍然很高,幸运的是,肺炎支原体仍然对四环素和喹诺酮类药物等二线抗生素保持良好的体外敏感性,使它们成为由大环内酯类抗生素引起的初始治疗失败的患者的有效治疗选择。
    结论:这一共识,基于国际和国家科学证据,为儿童MRMP的诊断和治疗提供科学指导。迫切需要对儿童四环素和喹诺酮类药物进行进一步研究,以评估其对生长发育的影响。此外,制定抗生素轮换治疗策略对于降低MRMP菌株的患病率是必要的.
    BACKGROUND: Mycoplasma pneumoniae (M. pneumoniae) is a significant contributor to community-acquired pneumonia among children. Since 1968, when a strain of M. pneumoniae resistant to macrolide antibiotics was initially reported in Japan, macrolide-resistant M. pneumoniae (MRMP) has been documented in many countries worldwide, with varying incidence rates. MRMP infections lead to a poor response to macrolide antibiotics, frequently resulting in prolonged fever, extended antibiotic treatment, increased hospitalization, intensive care unit admissions, and a significantly higher proportion of patients receiving glucocorticoids or second-line antibiotics. Since 2000, the global incidence of MRMP has gradually increased, especially in East Asia, which has posed a serious challenge to the treatment of M. pneumoniae infections in children and attracted widespread attention from pediatricians. However, there is still no global consensus on the diagnosis and treatment of MRMP in children.
    METHODS: We organized 29 Chinese experts majoring in pediatric pulmonology and epidemiology to write the world\'s first consensus on the diagnosis and treatment of pediatric MRMP pneumonia, based on evidence collection. The evidence searches and reviews were conducted using electronic databases, including PubMed, Embase, Web of Science, CNKI, Medline, and the Cochrane Library. We used variations in terms for \"macrolide-resistant\", \"Mycoplasma pneumoniae\", \"MP\", \"M. pneumoniae\", \"pneumonia\", \"MRMP\", \"lower respiratory tract infection\", \"Mycoplasma pneumoniae infection\", \"children\", and \"pediatric\".
    RESULTS: Epidemiology, pathogenesis, clinical manifestations, early identification, laboratory examination, principles of antibiotic use, application of glucocorticoids and intravenous immunoglobulin, and precautions for bronchoscopy are highlighted. Early and rapid identification of gene mutations associated with MRMP is now available by polymerase chain reaction and fluorescent probe techniques in respiratory specimens. Although the resistance rate to macrolide remains high, it is fortunate that M. pneumoniae still maintains good in vitro sensitivity to second-line antibiotics such as tetracyclines and quinolones, making them an effective treatment option for patients with initial treatment failure caused by macrolide antibiotics.
    CONCLUSIONS: This consensus, based on international and national scientific evidence, provides scientific guidance for the diagnosis and treatment of MRMP in children. Further studies on tetracycline and quinolone drugs in children are urgently needed to evaluate their effects on the growth and development. Additionally, developing an antibiotic rotation treatment strategy is necessary to reduce the prevalence of MRMP strains.
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  • 文章类型: Journal Article
    背景:大型语言模型显示出改善放射学工作流程的希望,但是它们在结构化放射任务(例如报告和数据系统(RADS)分类)上的表现仍未得到探索。
    目的:本研究旨在评估3个大型语言模型聊天机器人-Claude-2、GPT-3.5和GPT-4-在放射学报告中分配RADS类别并评估不同提示策略的影响。
    方法:这项横断面研究使用30个放射学报告(每个RADS标准10个)比较了3个聊天机器人,使用3级提示策略:零射,几枪,和指南PDF信息提示。这些病例的基础是2018年肝脏影像学报告和数据系统(LI-RADS),2022年肺部CT(计算机断层扫描)筛查报告和数据系统(Lung-RADS)和卵巢附件报告和数据系统(O-RADS)磁共振成像,由董事会认证的放射科医生精心准备。每份报告都进行了6次评估。两名失明的评论者评估了聊天机器人在患者级RADS分类和总体评级方面的反应。使用Fleissκ评估了跨重复的协议。
    结果:克劳德-2在总体评分中获得了最高的准确性,其中少量提示和指南PDF(提示-2),在6次运行中获得57%(17/30)的平均准确率,在k-pass投票中获得50%(15/30)的准确率。没有及时的工程,所有聊天机器人都表现不佳。结构化示例提示(prompt-1)的引入提高了所有聊天机器人整体评分的准确性。提供prompt-2进一步改进了Claude-2的性能,GPT-4未复制的增强。TheinterrunagreementwassubstantialforClaude-2(k=0.66foroverallratingandk=0.69forRADScategorization),对于GPT-4来说是公平的(两者的k=0.39),对于GPT-3.5来说是公平的(总体评分k=0.21,RADS分类k=0.39)。与Lung-RADS版本2022和O-RADS相比,2018年的所有聊天机器人均显示出更高的准确性(P<0.05);在2018年LI-RADS版本中,使用prompt-2,Claude-2实现了75%(45/60)的最高总体评分准确性。
    结论:当配备结构化提示和指导PDF时,Claude-2显示了根据既定标准(如LI-RADS版本2018)将RADS类别分配给放射学病例的潜力。然而,当前一代的聊天机器人滞后于根据最新的RADS标准对案件进行准确分类。
    BACKGROUND: Large language models show promise for improving radiology workflows, but their performance on structured radiological tasks such as Reporting and Data Systems (RADS) categorization remains unexplored.
    OBJECTIVE: This study aims to evaluate 3 large language model chatbots-Claude-2, GPT-3.5, and GPT-4-on assigning RADS categories to radiology reports and assess the impact of different prompting strategies.
    METHODS: This cross-sectional study compared 3 chatbots using 30 radiology reports (10 per RADS criteria), using a 3-level prompting strategy: zero-shot, few-shot, and guideline PDF-informed prompts. The cases were grounded in Liver Imaging Reporting & Data System (LI-RADS) version 2018, Lung CT (computed tomography) Screening Reporting & Data System (Lung-RADS) version 2022, and Ovarian-Adnexal Reporting & Data System (O-RADS) magnetic resonance imaging, meticulously prepared by board-certified radiologists. Each report underwent 6 assessments. Two blinded reviewers assessed the chatbots\' response at patient-level RADS categorization and overall ratings. The agreement across repetitions was assessed using Fleiss κ.
    RESULTS: Claude-2 achieved the highest accuracy in overall ratings with few-shot prompts and guideline PDFs (prompt-2), attaining 57% (17/30) average accuracy over 6 runs and 50% (15/30) accuracy with k-pass voting. Without prompt engineering, all chatbots performed poorly. The introduction of a structured exemplar prompt (prompt-1) increased the accuracy of overall ratings for all chatbots. Providing prompt-2 further improved Claude-2\'s performance, an enhancement not replicated by GPT-4. The interrun agreement was substantial for Claude-2 (k=0.66 for overall rating and k=0.69 for RADS categorization), fair for GPT-4 (k=0.39 for both), and fair for GPT-3.5 (k=0.21 for overall rating and k=0.39 for RADS categorization). All chatbots showed significantly higher accuracy with LI-RADS version 2018 than with Lung-RADS version 2022 and O-RADS (P<.05); with prompt-2, Claude-2 achieved the highest overall rating accuracy of 75% (45/60) in LI-RADS version 2018.
    CONCLUSIONS: When equipped with structured prompts and guideline PDFs, Claude-2 demonstrated potential in assigning RADS categories to radiology cases according to established criteria such as LI-RADS version 2018. However, the current generation of chatbots lags in accurately categorizing cases based on more recent RADS criteria.
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  • 文章类型: Journal Article
    为了完善制定中西医结合(ICWM)临床实践指南(CPG)的方法,促进诚信的形成,整合中西医优势的可实施建议。
    使用标称分组技术(NGT)方法,成立了一个多学科专家小组。小组通过文献回顾和反复讨论,确定了ICWM-CPG开发中的关键方法问题,并制定了解决这些问题的方法建议。最后一组提案是通过小组成员之间的共识达成的。
    合作努力导致确定了五个关键的方法论问题,并随后建立了22个具体建议。这些包括严格遵守著名的标准,例如医学研究所(IOM)和国际准则网络(G-I-N)提出的建议,采用诸如等级方法和正确陈述之类的方法,平衡发展集团的战略构成,以ICWM为重点的临床调查的熟练识别,不同证据来源的细微差别整合,以及透明的细节,可实施的建议。
    本研究集中于ICWM-CPG开发中最关键和最普遍的方法学问题,提出一系列建议。这些建议来自多学科专家共识,旨在为ICWM-CPG开发人员提供方法学指导,建立在当前的基础方法上。
    UNASSIGNED: To refine the methods of developing clinical practice guidelines (CPGs) for integrative Chinese-Western medicine (ICWM), promoting the formation of trustworthy, implementable recommendations that integrate the strengths of Chinese and Western medicine.
    UNASSIGNED: Using a nominal group technique (NGT) approach, a multidisciplinary expert panel was established. The panel identified key methodological issues in ICWM-CPG development through literature review and iterative discussions, and formulated methodological proposals to address these issues. The final set of proposals was achieved through consensus among the panel members.
    UNASSIGNED: The collaborative effort resulted in the identification of five pivotal methodological issues and the subsequent establishment of 22 specific recommendations. These encompass strict adherence to renowned standards, such as those proposed by the Institute of Medicine (IOM) and Guidelines International Network (G-I-N), the employment of methodologies like the GRADE approach and RIGHT statement, the strategic constitution of a balanced development group, the adept identification of ICWM-focused clinical inquiries, the nuanced integration of diverse evidence sources, and the detailed crafting of transparent, implementable recommendations.
    UNASSIGNED: This study concentrates on the most crucial and prevalent methodological issues in ICWM-CPG development, proposing a series of recommendations. These suggestions result from a multidisciplinary expert consensus, aiming to provide methodological guidance for ICWM-CPG developers, building upon the current foundational methodologies.
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  • 文章类型: Journal Article
    基于循证实践,制定中国常见癌症诊断和治疗指南,诊断和治疗产品的可用性,精准医学的最新进展是中国临床肿瘤学会(CSCO)的基本任务之一。近年来,医疗资源的可用性已成为临床指南中的主要关注点,这对发展中国家或社会经济多样化的国家和地区尤为重要。中国是世界上最大的发展中国家,幅员辽阔,经济和学术发展不平衡。CSCO准则必须考虑到地区发展的差异,药物和诊断方法的可用性,以及癌症治疗的社会价值。因此,对于CSCO指南中的每个临床问题和干预,证据等级应根据现有证据和专家共识进行分级,建议的等级应基于产品的可用性和成本效益。具有高证据水平和良好可用性的协议被用作I级建议;具有相对较高的证据水平但略低的专家共识或具有较差可用性的协议被用作II级建议;临床适用但证据水平低的协议被视为III级建议。根据国内外临床研究的结果和CSCO专家的意见,CSCO指南确定了临床应用的推荐水平.CSCO指导工作组坚信,以证据为基础,可用性方面,以共识为基础的指南将更适合临床实践。再一次,我们的读者的任何意见都非常感谢,并将在这些指南的更新中考虑,为了保持准确性,公平,以及CSCO指南的及时性。
    Developing guidelines for the diagnosis and treatment of common cancers in China based on the evidence-based practice, the availability of diagnosis and treatment products, and the up-to-date advances in precision medicine is one of the basic tasks of the Chinese Society of Clinical Oncology (CSCO). In recent years, the availability of medical resources has become a major concern in clinical guidelines, which is particularly important for developing countries or socioeconomically diverse countries and territories. China is the world\'s largest developing country, with a large territory and uneven economic and academic developments. The CSCO guidelines must take into account the differences in regional development, the availability of medicines and diagnostic methods, and the social value of cancer treatment. Therefore, for each clinical problem and intervention in the CSCO guidelines, the levels of evidence should be graded according to the currently available evidences and expert consensuses, and the grades of recommendations should be based on the availability and cost-effectiveness of the products. Protocols with high evidence level and good availability are used as the Level I recommendations; protocols with relatively high evidence level but slightly lower expert consensus or with poor availability are used as the Level II recommendations; and protocols that are clinically applicable but with low evidence level are regarded as the Level III recommendations. Based on the findings of clinical research at home and abroad and the opinions of CSCO experts, the CSCO guidelines determine the levels of recommendations for clinical application. The CSCO Guidance Working Group firmly believes that evidence-based, availability-concerned, and consensus-based guidelines will be more feasible for clinical practice. Again, any comments from our readers are greatly appreciated and will be considered in updates of these guidelines, so as to maintain the accuracy, fairness, and timeliness of the CSCO guidelines.
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  • 文章类型: Journal Article
    快速审查(RR)可以通过使用各种快捷方式简化或省略步骤来加速传统的系统审查(SR)过程。随着RR的日益普及,出现了许多捷径,但是在如何选择最合适的问题上没有达成共识。本研究从开始到2023年12月21日,在PubMed进行了文献检索,使用诸如“快速审查”“快速评估”“快速系统审查”和“快速评估”等术语。我们还扫描了参考列表,并对纳入影响研究进行了引文跟踪,以获得更多纳入研究。我们对所有RR方法进行了叙述性综合,快捷方式和研究评估它们在每个阶段的效果。根据目前的证据,我们提供了在RR中使用某些快捷方式的建议。最终,我们确定了185项研究,重点是总结RR方法和捷径,或评估其影响。有相对充分的证据支持在RR中使用以下快捷方式:将研究限制为以英语发表的研究;进行缩写的数据库搜索(例如,仅搜索PubMed/MEDLINE,Embase,和CENTRAL);省略灰色文献的检索;将搜索时间限制在最近20年的医疗干预时间和最近15年的诊断测试准确性审查时间;由经验丰富的筛选员进行一次筛选。在某种程度上,上述捷径也适用于SRs。本研究为未来RR研究人员选择捷径提供了参考。它也为方法学家提出了一个潜在的研究课题。
    Rapid review (RR) could accelerate the traditional systematic review (SR) process by simplifying or omitting steps using various shortcuts. With the increasing popularity of RR, numerous shortcuts had emerged, but there was no consensus on how to choose the most appropriate ones. This study conducted a literature search in PubMed from inception to December 21, 2023, using terms such as \"rapid review\" \"rapid assessment\" \"rapid systematic review\" and \"rapid evaluation\". We also scanned the reference lists and performed citation tracking of included impact studies to obtain more included studies. We conducted a narrative synthesis of all RR approaches, shortcuts and studies assessing their effectiveness at each stage of RRs. Based on the current evidence, we provided recommendations on utilizing certain shortcuts in RRs. Ultimately, we identified 185 studies focusing on summarizing RR approaches and shortcuts, or evaluating their impact. There was relatively sufficient evidence to support the use of the following shortcuts in RRs: limiting studies to those published in English-language; conducting abbreviated database searches (e.g., only searching PubMed/MEDLINE, Embase, and CENTRAL); omitting retrieval of grey literature; restricting the search timeframe to the recent 20 years for medical intervention and the recent 15 years for reviewing diagnostic test accuracy; conducting a single screening by an experienced screener. To some extent, the above shortcuts were also applicable to SRs. This study provided a reference for future RR researchers in selecting shortcuts, and it also presented a potential research topic for methodologists.
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  • 文章类型: Journal Article
    目的:本研究的目的是使用指南研究与评估(AGREEII)工具系统地评估与按摩相关的临床实践指南(CPGs)/共识的方法学质量,并总结CPGs中建议的现状。
    方法:中国国家知识基础设施(CNKI),万方数据,中国科技期刊数据库(VIP),中国生物医学光盘(CBM),PubMed,Embase,和指南网站(如中国医学王牌基地,中国中医药协会,世界卫生组织,国际网络准则,国家健康与护理卓越研究所,苏格兰校际指南网络)从开始到2022年10月31日进行了搜索。此外,回顾了相关研究的参考清单,以确定国内外按摩CPG/共识。搜索词采用了主题词和自由词的组合,主要包括中药,补充疗法,推拿,按摩,操纵,整脊/整骨疗法,脊柱,穴位按摩,指导方针,和共识。两名研究人员独立完成了符合条件的记录并提取了数据。在正式研究之前,在AGREEII上进行了两次校准,所有评审人员三次完成试点测试,直到他们理解并就评估项目达成一致。三名研究人员使用AGREEII仪器评估了纳入指南的方法学质量,并计算了协议的总体组内相关系数(ICC)。
    结果:评估结果显示,在49个合格的CPG/共识中,4个(8.2%)CPG/共识被认为是“推荐”,15(30.6%)CPG/共识被认为是“建议修改”,30个(61.2%)CPG/共识被认为“不推荐”,而共识被认为是“不建议”。一般来说,指南的六个领域的得分均高于共识。对36个CPGs的总体质量评估结果表明,有4个(11%)为“良好质量”,15人(42%)“质量足够”,17人(47%)“质量较低”。领域的AGREEII质量评分范围为0.30至0.75([ICC=0.993,95%CI(0.992,0.995)])。范围和目的域(域1),中位数为0.75(0.52~0.91),在AGREEII指南中表现最好,利益相关者参与(领域2)[中位数0.39(0.31〜0.56)]和应用(领域5)[中位数0.30(0.17〜0.47)获得了较低的分数。域1的一致得分为26.0(21.6~44.8),其次是严格的发展(领域3),得分18.0(10.0〜28.9)。从49条指引/共识中,共抽取119条按摩相关建议,包括“赞成”(102,85.7%),“反对”(9.7.6%),和“没有提出建议”(8,6.7%)。
    结论:纳入指南的总体质量较低,大多数指南都不是“推荐”。在未来的指南更新中,应该利用现有的证据,丰富专家组成员的专业组成,应充分考虑患者的价值观和偏好。有必要提出可识别的建议,并加强指南制定的严谨性和标准化。因此,可制定明确的标准指南,更好地指导临床实践。
    OBJECTIVE: The purpose of this study was to systematically evaluate the methodological quality of massage-related clinical practice guidelines (CPGs)/consensus on massage using the Appraisal of Guidelines Research and Evaluation (AGREE II) instrument and to summarize the current status of recommendations in the CPGs.
    METHODS: The Chinese National Knowledge Infrastructure (CNKI), WanFang Data, China Science and Technology Journal Database (VIP), China Biology Medicine disc (CBM), PubMed, Embase, and guideline websites (such as the Chinese Medical Ace Base, the China Association of Chinese Medicine, the World Health Organization, Guideline International Network, National Institute for Health and Care Excellence, Scottish Intercollegiate Guidelines Network) were searched from inception to October 31, 2022. In addition, the reference lists of relevant studies were reviewed to identify domestic and overseas massage CPGs/consensus. The search terms adopted a combination of subject words and free words, mainly including traditional Chinese medicine, complementary therapies, Tuina, massage, manipulation, chiropractic/osteopathic, spinal, acupressure, guideline, and consensus. Two researchers independently completed the eligible records and extracted the data. Before the formal research, calibrations were performed twice on AGREE II, and all reviewers completed the pilot test three times until they understood and reached an agreement on the assessment items. Three researchers appraised the methodological quality of the included guidelines using the AGREE II instrument and calculated the overall intraclass correlation coefficient (ICC) of agreement.
    RESULTS: The evaluation results showed that among the 49 eligible CPGs/consensus, 4 (8.2%) CPGs/consensus were considered \"recommended\", 15 (30.6%) CPGs/consensus were considered \"recommended with modifications\", and 30 (61.2%) CPGs/consensus were considered \"not recommended\", while the consensus was considered \"not recommended\". Generally, the scores in the six domains of the guidelines were all higher than the consensus. Evaluation results for the overall quality of 36 CPGs showed that 4 (11%) were \"good quality\", 15 (42%) were \"sufficient quality\" and 17 (47%) were \"lower quality\". The AGREE II quality scores of domains ranged from 0.30 to 0.75 ([ICC = 0.993, 95% CI (0.992, 0.995)]). The domain of scope and purpose (domain 1), with a median score of 0.75 (0.52~0.91), performed best in the guidelines with AGREE II, and stakeholder involvement (domain 2) [median 0.39 (0.31~0.56)] and application (domain 5) [median 0.30 (0.17~0.47] obtained lower scores. The consensus score of domain 1 was better at 26.0 (21.6~44.8), followed by rigor of development (domain 3) with a score of 18.0 (10.0~28.9). A total of 119 massage-related recommendations were extracted from 49 guidelines/consensuses, including \"in favor\" (102, 85.7%), \"against\" (9, 7.6%), and \"did not make recommendations\" (8, 6.7%).
    CONCLUSIONS: The overall quality of the included guidelines was low, and most of the guidelines were not \"recommended\". In future guideline updates, the existing evidence should be used, the professional composition of members of the expert group should be enriched, and patients\' values and preferences should be fully considered. It is necessary to clearly propose recognizable recommendations and strengthen the rigor and standardization of guideline formulation. Thus, clear standard guidelines can be formulated to better guide clinical practice.
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  • 文章类型: Journal Article
    在这个信息爆炸的时代,推荐系统在帮助用户在海量信息中发现感兴趣的内容方面发挥着关键作用。在保持准确性的同时追求广泛的召回是当前推荐系统的核心挑战。在本文中,提出了一种新的推荐算法模型,交互式高阶双塔(IHDT),它通过在双塔神经网络之间添加交互性和高阶特征学习来改进当前模型。构造一个包含不同类型节点的异构图,如用户,items,和属性,通过元路径提取更丰富的特征表示。要实现功能交互,引入了交互式学习机制,以在用户和项目塔之间注入相关功能。此外,该方法利用图卷积网络进行高阶特征学习,合并双塔的节点嵌入,以获得增强的最终用户和项目表示。在MovieLens数据集上评估IHDT,优于多种基线方法。消融实验验证了交互式学习和高阶GCN组件的贡献。
    In this era of information explosion, recommendation systems play a key role in helping users to uncover content of interest among massive amounts of information. Pursuing a breadth of recall while maintaining accuracy is a core challenge for current recommendation systems. In this paper, we propose a new recommendation algorithm model, the interactive higher-order dual tower (IHDT), which improves current models by adding interactivity and higher-order feature learning between the dual tower neural networks. A heterogeneous graph is constructed containing different types of nodes, such as users, items, and attributes, extracting richer feature representations through meta-paths. To achieve feature interaction, an interactive learning mechanism is introduced to inject relevant features between the user and project towers. Additionally, this method utilizes graph convolutional networks for higher-order feature learning, pooling the node embeddings of the twin towers to obtain enhanced end-user and item representations. IHDT was evaluated on the MovieLens dataset and outperformed multiple baseline methods. Ablation experiments verified the contribution of interactive learning and high-order GCN components.
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  • 文章类型: Journal Article
    图神经网络在排名推荐方面显示出强大的潜力。现有的基于二分图的排序推荐方法主要集中在同构图,通常将用户和项目节点视为同一种节点,然而,用户-项目二部图总是异构的。此外,各种类型的节点对建议有不同的影响,并且可以通过成功区分相同类型的节点来学习良好的节点表示。在本文中,我们开发了一个节点个性化多图卷积网络(NP-MGCN)用于排名推荐。它由节点重要性感知块组成,图构造模块,和节点信息传播和聚合框架。具体来说,提出了一种节点重要性感知块,利用节点度信息对节点进行编码,以突出节点之间的差异。随后,设计了Jaccard相似度和共生矩阵融合图构造模块,以获取用户-用户和项目-项目图,丰富用户之间和项目之间的关联信息。最后,一种复合跳节点信息传播和聚合框架,包括单跳和双跳分支,是设计的。高阶连通性用于聚合单跳分支的异构信息,而多跳依赖性用于聚合双跳分支的同构信息。它使用户和项目节点嵌入更具区别性,并将不同节点的异构性集成到模型中。在多个数据集上的实验表明,NP-MGCN比现有方法具有出色的推荐性能。
    Graph neural networks have revealed powerful potential in ranking recommendation. Existing methods based on bipartite graphs for ranking recommendation mainly focus on homogeneous graphs and usually treat user and item nodes as the same kind of nodes, however, the user-item bipartite graph is always heterogeneous. Additionally, various types of nodes have varying effects on recommendations, and a good node representation can be learned by successfully differentiating the same type of nodes. In this paper, we develop a node-personalized multi-graph convolutional network (NP-MGCN) for ranking recommendation. It consists of a node importance awareness block, a graph construction module, and a node information propagation and aggregation framework. Specifically, a node importance awareness block is proposed to encode nodes using node degree information to highlight the differences between nodes. Subsequently, the Jaccard similarity and co-occurrence matrix fusion graph construction module is devised to acquire user-user and item-item graphs, enriching correlation information between users and between items. Finally, a composite hop node information propagation and aggregation framework, including single-hop and double-hop branches, is designed. The high-order connectivity is used to aggregate heterogeneous information for the single-hop branch, while the multi-hop dependency is utilized to aggregate homogeneous information for the double-hop branch. It makes user and item node embedding more discriminative and integrates the different nodes\' heterogeneity into the model. Experiments on several datasets manifest that NP-MGCN achieves outstanding recommendation performance than existing methods.
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  • 文章类型: Journal Article
    创建SPIRIT-TCM扩展2018是为了指导中药(TCM)临床试验方案的设计和报告。本研究旨在调查癌症护理研究相关领域与该指南的一致性程度。
    对2019年1月以来以中英文发表的中医癌症试验方案进行范围审查。五大学术数据库(MEDLINE,EMBASE,CINAHL,中部,和中国国家知识基础设施)进行了搜索。通过描述性分析评估与2018年SPIRIT-TCM扩展的一致性。
    确定了53项中医癌症治疗试验方案,包括23个针灸,26中草药(CHM),和4个太极拳/气功(TCQ)干预措施。大多数清单项目的一致性较低,特别是在质量控制和安全报告方面,剂量,中医诊断模式,西医和中医干预之间可能的相互作用,和中医相关的结果评估。
    尽管SPIRIT-TCMExtension2018指南是通过广泛的Delphi咨询制定的,已发表的中医癌症治疗临床试验方案与指南的一致性较低.进一步的研究是必要的,以了解低的协调率和如何科学的报告可以提高在中医癌症护理研究。
    UNASSIGNED: The SPIRIT-TCM Extension 2018 was created to guide the design and reporting of Traditional Chinese Medicine (TCM) clinical trial protocols. This study aims to investigate the extent of concordance with this guideline in the relevant field of cancer care research.
    UNASSIGNED: A scoping review of TCM cancer trial protocols published in English and Chinese since January 2019 was conducted. Five major academic databases (MEDLINE, EMBASE, CINAHL, CENTRAL, and China National Knowledge Infrastructure) were searched. Concordance with the SPIRIT-TCM Extension 2018 was assessed by descriptive analysis.
    UNASSIGNED: Fifty-three TCM cancer care trial protocols were identified, comprising 23 acupuncture, 26 Chinese herbal medicine (CHM), and 4 Tai Chi/Qigong (TCQ) interventions. The majority of the checklist items had a low rate of concordance, especially in the reporting of quality control and safety, dosage, TCM diagnostic patterns, possible interactions between Western Medicine and TCM interventions, and TCM-related outcome assessments.
    UNASSIGNED: Although the SPIRIT-TCM Extension 2018 guideline was established through extensive Delphi consultation, there are low rates of concordance between published TCM cancer care clinical trial protocols with the guideline. Further research is necessary to understand the low rate of concordance and how scientific rigors of reporting can be improved in TCM cancer care research.
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