基于VOSviewer和CiteSpace的消防针的临床随机对照试验的视觉分析
Yuqiang Song1, Linbo Shen2, Yuanbo Fu3,4
1Department of Acupuncture and Moxibustion, Beijing Hospital of TCM Affiliated to Capital Medical University, Beijing Key Laboratory of Acupuncture Neuromodulation, Beijing 100010, China. alfred0106@163.com.
Zhongguo zhen jiu = Chinese acupuncture & moxibustion
|February 19, 2024
概括
本文献分析揭示了消防针临床随机对照试验 (RCT) 的研究趋势. 未来的研究应该扩大应用,完善设计,并加强高水平证据的合作.
科学领域:
- 传统中国医药 传统中国医药
- 临床研究 临床研究
- 图书统计学 图书统计学
背景情况:
- 火针治疗是中国传统医学 (TCM) 的重要组成部分.
- 了解火针临床随机对照试验 (RCT) 的研究环境对于指导未来调查至关重要.
研究的目的:
- 分析过去十年来火针临床RCT文献的研究热点,边界和趋势.
- 提供关于火针研究的演变和未来方向的见解,使用文献计量和知识映射技术.
主要方法:
- 对六个中英数据库 (CNKI,万芳,VIP,SinoMed,PubMed,Web of Science) 进行了全面的搜索,以寻找火针RCT.
- 用CiteSpace V6.1.R6和VOSviewer V1.6.18软件进行了图书统计分析和知识映射.
- 分析包括合作网络,关键词的同时出现,聚类,时间表和新兴趋势.
主要成果:
- 总共有1973篇中文和3篇英语文章被纳入分析.
- 消防针研究的领先机构被确定为广州大学CM,黑龙江大学CM和北京医院TCM.
- 用火针治疗的常见研究条件包括,白风,腰椎间盘,疹,中风后果,面部和膝关节关节炎,通常与针,和放血相结合.
结论:
- 消防针治疗的当前研究前沿涉及其与其他治疗方法的联合应用,临床机制的探索和疗效评估指数的改进.
- 未来的研究应该专注于扩大治疗疾病的范围,优化研究设计,促进机构间合作,并进行高质量的临床试验.
相关概念视频
Clinical Trials
6.7K
Clinical trials are prospective experimental studies conducted on humans to determine the safety and efficacy of treatments, drugs, diet methods, and medical devices. Using statistics in clinical trials enables researchers to derive reasonable and accurate conclusions from the collected data, allowing them to make wise decisions in uncertain situations. In medical research, statistical methods are crucial for preventing errors and bias.
There are four phases in a clinical trial. A phase one...
There are four phases in a clinical trial. A phase one...
6.7K
Hazard Ratio
122
The hazard ratio (HR) is a widely used measure in clinical trials to compare the risk of events, such as death or disease recurrence, between two groups over time. It reflects the ratio of hazard rates—the instantaneous risk of the event occurring—between a treatment group and a control group. This measure provides valuable insights into the relative effectiveness of a treatment by assessing how the risk of an event differs between the two groups.
For example, in a clinical trial...
For example, in a clinical trial...
122
Blinding
2.4K
Blinding is a commonly used method of not telling participants which treatment a subject is receiving. Blinding is a critical part of a randomized control trial or RCT. It reduces the bias that affects the results. In an RCT, blinding is used in the form of a placebo. A placebo effect occurs when untreated subjects falsely believe they have received the treatment and report improved symptoms. A placebo or a dummy treatment is administered to subjects to negate the bias caused by such an effect.
2.4K
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches
126
Biopharmaceutical studies constitute a vital field aiming to enhance drug delivery methods and refine therapeutic approaches, drawing upon diverse interdisciplinary knowledge. In research methodologies, the choice between controlled and non-controlled studies significantly influences the study's reliability and accuracy.
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast,...
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast,...
126
Comparing the Survival Analysis of Two or More Groups
186
Survival analysis is a cornerstone of medical research, used to evaluate the time until an event of interest occurs, such as death, disease recurrence, or recovery. Unlike standard statistical methods, survival analysis is particularly adept at handling censored data—instances where the event has not occurred for some participants by the end of the study or remains unobserved. To address these unique challenges, specialized techniques like the Kaplan-Meier estimator, log-rank test, and...
186


