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Background: Formative assessment (FA) is part of the assessment process according to the new competency based medical education curriculum and is believed to improve learning. Feedback from students is an integral part of FA which, if incorporated, may help in optimizing content and application of future FAs. Hence, the current study was conducted to assess feedback from 2nd year medical students regarding FAs in Pharmacology. Aim and Objectives: The objectives of the study were to assess the emotional impact of FA on students and to analyze their suggestions regarding FA. Materials and Methods: A well-designed, structured, and pre-validated questionnaire was filled by consenting students who had written the FA. The responses were compiled in an excel sheet and statistically analyzed. Results: Out of 121 students, 115 took FA and of them 100 students filled the questionnaire (Response rate 86.95%). When it comes to emotional impact, 64% students did not find these assessments burdensome and 81% were motivated to study better. When it comes to future suggestions, 100% wanted to be pre-informed. About 88% wanted a written assessment. About 75% wanted only multiple choices questions (MCQs) and 70% wanted MCQs + Essay type questions. About 65% students wanted FAs in practicals but only 36% wanted it in the same paper as theory FA. Conclusion: FA is a good tool to enhance learning which is not a burden on students but a good motivator for better reading. Students prefer a pre-informed, written assessment with MCQs over essay type questions and want these FAs to be conducted in practical’s also but not in the same paper.
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Central Asia is an important hub connecting the Asian continent and European continent, and one of the key regions for China's foreign exchange and cooperation in Traditional Chinese Medicine (TCM). Central Asian countries have relatively backward medical conditions, and TCM has become an important part of local healthcare. Regulations on traditional/complementary and alternative medicine have been issued in Kyrgyzstan, Kazakhstan and Tajikistan; acupuncture and moxibustion has been covered by medical insurance in Kyrgyzstan; TCM has existed in other Central Asian countries in form of folk medicine. Central Asian countries are extremely rich in medicinal plant resources, but weak in foundation of pharmaceutical industry. Chinese government has signed cooperation agreements on TCM with many Central Asian countries, and the practical cooperation in the field of traditional medicine have continued to expand. At present, the development of TCM in Central Asian countries still faces problems such as weak foundation for the development and utilization of medicinal materials, shortage of professionals talents in TCM education and small scale of TCM clinics. In view of the above, in order to promote the dissemination and development of TCM in Central Asian countries, it is recommended that relevant units promote the establishment of joint laboratories or research centers of Chinese materia medica; give full play to local resource advantages and promote the development of medicinal plant industry; to strengthen the construction of overseas centers of TCM; actively carry out joint education or further education projects, and cultivate localized senior talents.
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@#Cell culture medium is one of the essential raw materials in the field of life and health.In recent years,the performance and quality of domestic cell culture media have been improving,and the market share of domestic vendors has steadily increased from 19.2% in 2017 to 33.7% in 2021.However,there are also some problems and shortcomings in industrial development,mainly including:technology and process accumulation need to be strengthened;product quality need to be improved;lack of industry standards and norms.Based on literature research,special topic discussion and expert interview,this paper reviews the development history of cell culture medium,deeply analyzes and systematically combs the opportunities and challenges faced by the industry development from the basic situation,current situation and trend of the development of cell culture medium industry in China,and puts forward relevant countermeasures and suggestions.
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In recent years, the issue of conflicts of interest in the transformation of scientific and technological achievements in medical institutions in China has become prominent, mainly manifested as personal and institutional conflicts of interest, with the characteristics of complexity and sustainability. At present, there were some problems in the conflict management of scientific and technological achievements transformation of medical institutions, such as insufficient support of relevant laws, regulations and policies, insufficient supervision of medical institutions, and the lack of industry management atmosphere. The author suggestted that government departments should strengthen the formulation of relevant policies and regulations, medical institutions should establish an interest conflict management system and an independent management department, and industry associations should give full play to their role in assisting, so as to provide reference for promoting medical institutions to effectively manage interest conflicts in the transformation of scientific and technological achievements.
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Objective:To analyze general information, diagnosis and treatment of digestive endoscopy departments in county-level hospitals of Yunnan Province, thus to provide evidence for improving the endoscopic diagnosis and therapy in these hospitals.Methods:An online survey was performed to collect quality-related information of digestive endoscopy centers (departments) at county-level hospitals of Yunnan from January 2019 to January 2020, including endoscopic equipment, endoscopic techniques, staffing, number of operations, and quality control.Results:A total of 143 county-level hospitals were involved in this study. Each hospital owned only 1.74 endoscopy operation rooms on average, 1.42 regular endoscopy workstation, 4 endoscopes. There were only 10 endoscopic ultrasonography workstations and 2 enteroscopy workstations respectively installed in these hospitals. Endoscopic retrograde cholangiopancreatography was independently performed in only 4 hospitals. There were 392 professional endoscopists in all 143 hospitals, 18.62% (73/392) of whom were able to perform endoscopic therapy of grade 4, while only 6.12% (24/392) of whom could perform endoscopic submucosal dissection (ESD) independently. In 2019, the early diagnostic rate of gastrointestinal tract cancer in these hospitals was 19.48% (1 133/5 817). The early diagnostic rate was 21.04% (276/1 312) for esophageal cancer, 19.53% (397/2 033) for gastric cancer, and 18.61% (460/2 472) for colorectal cancer. The colorectal adenoma detection rate was 12.83% (12 207/95 148). The rate of reaching cecum during colonoscopy was 70.49% (67 067/95 148). The complete resection rate of ESD was 12.54% (221/1 763).Conclusion:The general situation of digestive endoscopy in county-level hospitals of Yunnan is far from being well-developed, which may be attributed to slow upgrading of equipments, inadequate training of endoscopic professionals and undemanding quality control. It is highly significant to improve medical service and quality of diagnosis and treatment of digestive endoscopy in these hospitals, on the basis of a complete endoscopy quality control system with a high standard.
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OBJECTIVE To provid e reference and sugge stions for improving the volume-based procurement of drugs and medical consumables （hereinafter referred to as “consumables”）in China. METHODS The relevant policy documents of centralized volume-based procurement of drugs and consumables published from November 2018 to November 2021 were retrieved ； the implementation status and problems of centralized volume-based procurement of drugs and consumables in China were analyzed by using the policy analysis method and referring to relevant research literatures. RESULTS & CONCLUSIONS National health department and healthcare security administration guaranted the rational use of selected products in medical institutions through incentive and supervision measures ；healthcare security administration should optimize the way of medical insurance payment ， promote the medical institutions to control the fees by themselves ，and conduct the credit evaluation of bidding and procurement ； medical products administration should evaluate the consistency of drugs and supervise the quality of selected products. With the normalization of centralized volume-based procurement of drugs and consumables organized by the state and trans-regional alliance ， the drug varieties and dosage forms included in centralized procurement were increasingly in line with the demand of Chinese pharmaceutical market. The price of most selected drugs decreased by more than 50％，and the decrease of consumables was significantly higher than that of drugs. The selected enterprises were mainly domestic generic drug enterprises ，and domestic consumables had gradually become the competitors and substitute of imported consumables. However ，there were still some problems such as repeated bidding and procurement in various alliances and provinces （autonomous regions and municipalities ）， unclear construction of compensation mechanism in medical institutions ，inconsistent bidding and procurement rules and quality evaluation standards for consumables ，low localization rate of some consumables ，low innovation level and profitability of pharmaceutical enterprises and consumables manufacturers. Local centralized volume-based procurement should be encouraged ，and the bidding and procurement rules and quality evaluation standards of “one product ，one policy ”should be gradually established. Great importance should be paid to the construction of compensation mechanism of medical institutions ，standardize zhangqiuyu739632@126.com the dynamic adjustment of medical serv ice prices ；pharma- ceutical enterprises and consumables manufacturers should increase research and development investment to transform into innovative and diversified enterprises ，so as to improve the competitiveness of domestic drugs and consumables.
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Cognitive behavior therapy(CBT) is one of the most widely used psychotherapy methods in the world.However, its origin in Western culture makes many researchers doubt whether it can be effectively applied to other cultural groups.The discussion on this issue is conducive to further adjusting CBT from an international perspective to better serve different cultural groups.This review focuses on the research progress of acculturation in CBT at home and abroad.Firstly, it discusses the necessity of acculturation and introduces the relevant major researchers in this field abroad, so as to explain how to carry out the work of acculturation.Then the effectiveness of current acculturation work is demonstrated, and the research progress of acculturation related to Chinese culture is introduced emphatically.In previous studies, most scholars supported the development of acculturation, and preliminary evidence has shown that CBT after acculturation has equal or even better effectiveness.Based on this, different researchers have put forward their own acculturation framework or adaptation suggestions.However, there are still many shortcomings in current research, which are mainly reflected in six aspects: few comparative studies, lack of unified framework, blank fields in some areas, shallow level of acculturation, unknown mechanism and lack of bottom-up research.Thus, this review is aimed to point out the urgency and necessity of CBT cultural adaptation in China, and put forward some suggestions and preliminary ideas for the further development of more culturally adaptable CBT in China, in order to better promote the application of CBT in China.
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Objective: To explore the occupational hazards caused by three kinds of welding operations, and to provide data support for individual protection. Methods: In October 2020, the welding fumes, metal elements and welding arc generated by three welding operations of argon gas shielded welding (JS80 welding wire) , manual welding (ZS60A welding rod) and carbon dioxide shielded welding (907A flux cored wire) were collected and measured in the welding laboratory. The samples were analyze and compare in the laboratory, and the differences of the occupational hazard factors of the three welding operations were judged. Results: The concentration of welding fume produced by carbon dioxide shielded welding, manual welding (ZS60A electrode) , and argon gas shielded welding (JS80 welding wires) were 6.80 mg/m(3), 6.17 mg/m(3), and 3.13 mg/m(3), respectively. The effective irradiance of the welding arc outside the welding mask from high to low is manual welding (ZS60A electrode) , carbon dioxide shielded welding (907A flux-cored welding wire) , and argon shielded welding (JS80 welding wire) , respectively 1 010.7, 740.9, 589.5 μW/cm(2). The long-wave ultraviolet UVA intensity generated by argon shielded welding (JS80 welding wire) is the largest, which is 1 500 μW/cm(2). The content of Mn in the three welding operations is the highest, and JS80 welding wire has the highest Mn content of 128493.2 mg/kg. 907A flux cored wire has the highest Ti content, which is 24355.5mg/kg. The electrode ZS60A has the highest Cu content, which is 24422.12 mg/kg. Conclusion: The intensity of occupational hazards is different in the three kinds of welding operations, so the methods of personal protective equipment, field exposure assessment and health monitoring should be more targeted.
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Air Pollutants, Occupational/analysis , Argon/analysis , Carbon Dioxide/analysis , Gases/analysis , Occupational Exposure/analysis , Welding/methodsABSTRACT
Traditional Chinese Medicine (TCM) has become an important part in the healthcare system of Latin American countries, especially the TCM therapy represented by acupuncture and moxibustion. Acupuncture and moxibustion has been included in the medical insurance system of Brazil and Ecuador, and many universities in Brazil, Cuba, Mexico and other countries offer courses related to traditional medicine, including acupuncture and moxibustion courses. Latin American counties are rich in medicinal plant resources. Argentina, Chile, Colombia and other countries have publicized regulations related to the use of herbs.China has signed cooperation agreements on TCM with many Latin American countries and, they have showed desire to strengthen cooperation with China. At present, the development of TCM in Latin American countries faces some problems, such as the scale of TCM clinics is small, the quality of TCM training are unbalanced, and there are many restrictions on TCM products entering the Latin American market. In order to promote cooperation with Latin American countries in TCM and expand its scale and development, it is suggested that China should carry out in-depth cooperation on global public health governance at the national level, plan the layout of overseas centers of TCM in Latin America and promote the construction, while scientific research institutions of TCM should carry out joint research on TCM with Latin American countries, and strengthen cooperation in running schools to standardize TCM education.
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This paper systematically combs and analyzes the existing research related to the textual research of famous classical formulas， summarizes the problems and deficiencies of the current research， and puts forward the key points and suggestions of the textual research of famous classical formulas， so as to provide reference for the research related to the textual research of famous classical formulas. This paper discusses from the perspectives of paying attention to the similarities and differences of ancient and modern drug textual research connotation， paying attention to the comprehensive utilization of multi-dimensional information， paying attention to the combing and textual research of different key links of drug historical evolution， paying attention to the combing of the evolution of modern scientific name textual research， paying attention to the textual research principle of respecting the ancient but not sticking to it， and paying attention to the basic knowledge of philology， and puts forward the current situation， problems and countermeasures of formula textual research to herbal textual research based on the in-depth summary and analysis of the results， absorbs the advantages of previous scholars， supplements the shortcomings of previous research， and forms a unique research system according to the characteristics of famous classical formulas. That is， pay attention to the context of historical changes and cross-sectional analysis. On the basis of a comprehensive analysis of the historical changes of different key links such as the origin， authentic production areas， medicinal parts and processing， the reasonable key information of famous classical formula drugs in different periods was given by fully absorbing the research results of modern times and combining the current productivity and cognitive level， laying a foundation for the development of famous classical formulas.
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In recent years, China has issued many laws and regulations on enhancing hospital security order management, and the related system has been gradually improved. However, the management requirements of hospitals are hard to implement. In this way, hospitals have burdened intensive internal pressure to implement the policies, with the dilemma of insufficient external support. Based on the perspective of social co-governance, this study discussed the development of policies related to hospital security order management in China. Also, it summarized the best practices about how to ensure hospitals security order from the aspects of the government, hospitals as well as social organizations. Additionally, it analysed current existing problems, such as the lack of sufficient cooperation of the police-doctor linkage mechanism, the inadequate implementation of technical prevention measures, the delayed mediation and disposal of doctor-patient contradiction, the imperfect of supporting policies and etc.Finally, this paper provided relevant suggestions on long-term mechanism to ensure the security order of hospitals.
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Objective To describe the development status of the prevention and control of chronic non-communicable diseases (hereinafter referred to as "chronic diseases") at home and abroad, and to explore coping strategies suitable for the prevention and control of chronic diseases in China. Methods Through literature review relevant data on chronic diseases as well as the prevention and control strategies and measures were collected. A comprehensive analysis on the data was conducted. Results The epidemic trend of chronic diseases is relatively serious both in China and in the world. To cope with the rapid development and epidemic of chronic diseases, China and many other countries have implemented relevant policies to curb the growth and development of chronic diseases and have achieved different results to a certain extent. Conclusion Chronic diseases have become the main cause of death and health threats in human society. The implementation and practice of chronic disease prevention and control strategies should be strengthened, in combination with successful experience at home and abroad, to rapidly develop the strategies for the prevention and control of chronic diseases in line with national conditions in China.
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Objective:Proposed suggestions to improve the quality of investigator-initiated trials follow-up management under the normalization of COVID-19.Methods:Analyzed current status and challenges of follow-up management in China investigator initiated trial through a combination of literature review and previous work reflection, in the context of normalization of COVID-19.Results:Follow-up management of investigator initiated trial had shown variations in follow-up contents, methods, personnel and auxiliary tools. The insufficient research funding and lacking of professional clinical research team support have led to the challenges of low follow-up visits, insufficient follow-up personnel, lack of electronic follow-up platforms, and unknown follow-up time windows for investigator-initiated trials, which became more prominent in the context of COVID-19.Conclusions:In order to improve the quality of follow-up management during the normalization of COVID-19, appropriate amendment of the investigator-initiated trials follow up should be carefully considered. For instance, taking into account of the characteristics of the research disease, the main research endpoints, the content of the key indicators of the research key follow-up, follow-up methods, follow-up frequency, and follow-up tools to make sure the scientific validity and feasibility, as well as the mandate of clinical research related laws, regulations and ethical requirement. The possible amendments may include follow content, method, mode, frequency, time window. At the same time, re-consent or sufficient disclosure of information should be carried out with compliance of the updated protocols to assure the quality of clinical research follow up.
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BACKGROUND: Urban barrier-free facilities are imperfect in China, but visually impaired people need barrier-free facilities urgently. OBJECTIVE: To understand the public’s cognition and problems about urban barrier-free facilities, and put forward improvement suggestions by researching the application status of barrier-free facilities in Shijiazhuang (taking tactile ground surface indicator as an example). METHODS: One hundred and eighteen citizens and 51 ordinary sanitation workers at Shijiazhuang were randomly selected, and underwent cognitive survey by questionnaire. Meanwhile, 60 visually impaired persons were tactile ground surface indicator using survey by questionnaire. RESULTS AND CONCLUSION: Most citizens, sanitation workers and visually impaired person have a certain understanding of tactile ground surface indicator, but the awareness rate is still low. Totally 7% citizens and 18% sanitation workers did not know the tactile ground surface indicator, and the travel rate of visually impaired people was extremely low, only 38% visually impaired person were able to travel frequently. More than 50% people thought that the tactile ground surface indicator had not actually effect. Only 19% citizens were more satisfied with the supervision, maintenance and maintenance of the tactile ground surface indicator. 56% visually impaired people believed that it had no practical effect, and 42% visually impaired people said that their travel range was less than 1 km. It means that the public cognition rate and the tactile ground surface indicator utilization rate are low. We also put forward improvement suggestions from three aspects: Strengthening publicity education and training, rehabilitation training for the visually impaired persons, strengthen construction and maintenance, so as to protect the rights and interests for disabled people, promote them return to society and improve their quality of life.
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Based on systematic review of the role of clinical treatment, disease control and scientific research, and combining with the problems exposed by the COVID-19 epidemic, suggestions were proposed to reform and improve the prevention and treatment system for major epidemics diseases in China. In clinical treatment, it is necessary to enhance clinical staff's awareness of law-based reporting, capabilities of syndromic surveillance, the use of infectious diseases reporting systems, and to improve national or local monitoring platforms for emerging infectious diseases detection. In terms of disease control, it is important to provide authorities to disease control departments through laws and regulations, improve the quantity and quality of related human resources, and strengthen the applied research and technical readiness targeted infections disease prevention, control and emergency preparedness. As for scientific research in major epidemic response, it is essential to strengthen research projects guided by national requests, build research institutions that can 'make a final decision', establish national and regional key laboratories, and strengthen strategic technical reserve for emergency disease control and treatment.
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Telemedicine service can effectively improve the diagnosis and treatment, rationally allocate medical resources, and fully reduce medical expenditure, so as to meet people′s health care needs. As introduced by the authors, Beijing Geriatric Hospital provides telemedicine services for chronic diseases guidance, medical consultation and home care services through mobile App, realizing hierarchical medical services, resource sharing and service collaboration in the region, and making up for the shortcomings of time and space in conventional model of face-to-face services. However, in the process of promotion and application, a series of ethical issues have also been found, such as the change of doctor-patient relationship, the protection of patient privacy, the safety of data and information, and the management of medical quality. By discussing the ethical risks in the telemedicine environment and thinking about the relevant countermeasures, we can promote the establishment of a corresponding medical ethics system and promote the sustainable development of telemedicine.
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Telemedicine service can effectively improve the diagnosis and treatment,rationally allocate medical resources,and fully reduce medical expenditure,so as to meet people's health care needs.As introduced by the authors,Beijing Geriatric Hospital provides telemedicine services for chronic diseases guidance,medical consultation and home care services through mobile App,realizing hierarchical medical services,resource sharing and service collaboration in the region,and making up for the shortcomings of time and space in conventional model of face-to-face services.However,in the process of promotion and application,a series of ethical issues have also been found,such as the change of doctor-patient relationship,the protection of patient privacy,the safety of data and information,and the management of medical quality.By discussing the ethical risks in the telemedicine environment and thinking about the relevant countermeasures,we can promote the establishment of a corresponding medical ethics system and promote the sustainable development of telemedicine.
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OBJECTIVE： To provide reference for ensuring clinical drug safety and promoting the development of characteristic chemical preparations in medical institutions. METHODS： From three aspects such as registration declaration of new preparations， supplementary application declaration and re-registration declaration， the problems found during the technical review of registration of chemical preparation in medical institutions of Guangdong province have been summed up， the causes of above problems also have been analyzed， and the relevant suggestions have been given at the same time. RESULTS & CONCLUSIONS： There were deficiencies in the registration declaration of new preparations， such as insufficient basis for the title， the lack of key process parameters in the study of preparation process and the failure of stability test conditions to meet the requirements of the Pharmacopoeia， etc. There were deficiencies in the supplementary application declaration， such as the unreasonable formulation of drug， the interaction between the drugs packing material and the drug， and unreasonable setting of storage conditions. There were deficiencies in the re-registration declaration， such as the supply of existing drugs on the market， the lack of production conditions for the formulation unit， the inability to purchase the original excipient materials， and the incomplete attention items. The main reasons were that the lack of technical guidelines for the research of chemical preparations， imperfection of the Standards for the Quality Management of Pharmaceutical Preparation in Medical Institutions and authorized preparation of chemical agents not allowed in Measures for the Registration and Administration of Pharmaceutical Preparation in Medical Institutions， and some kinds of chemical preparations could not adapt to the development of the new situation. The solutions are to improve the regulations of medicinal preparation in medical institutions and develop chemical preparations selectively based on safety and efficiency. In the future， the problems can be solved by formulating the technical guidelines for the research of chemical preparations in medical institutions， refining the rules for the retention of samples in finished products， increasing the requirements for continuous stability inspections， allowing authorized chemical preparations to be commissioned and prepared， phasing out the chemical preparations that do not adapt to the new situation， and developing valuable chemical preparations， to provide safe and effective chemical preparations for clinical use.
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OBJECTIVE： To provide reference for perfecting the quality standard revision of TCM preparations in medical institutions， and improving the quality standard of TCM preparations in medical institutions. METHODS： By sorting out the quality standards of TCM preparations in Guangdong provincial medical institution preparation specification， this paper summarized the main problems and put forward suggestions for improvement. RESULTS & CONCLUSIONS： There are 897 kinds of TCM preparations included in the Guangdong provincial medical institution preparation specification. The recent quality standards （2017 edition） have been greatly improved compared with those of the first edition （1985 edition）； however， there are still some problems in the overall quality control of preparations， quantitative control of indicative components， project specificity， source control of medicinal materials， control of medicinal materials not included in the Chinese Pharmacopoeia and quality standards of the same series of varieties. It is suggested that on the premise of considering both advancement and applicability， the quality control of the whole， local and toxic preparations of TCM hospitals should be strengthened， the detection methods with good specificity and reproducibility should be properly updated， the control of key parameters of production process should be strengthened， the quality standard of TCM preparations in medical institutions should be fully improved， so as to provide the products with safe， effective and controllable in quality products in medical institutions.
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Custom ocular prosthesis as a kind of product to make up the eye defects. It can not only improve patient's comfort adaptation and restore the normal structures but also let the patient regain confidence. However, it is in infant stage in our country for custom ocular prosthesis that the professional engineer is not enough, standards for the products are shortage. These factors together result in poor understanding of product management control and impede the development of ocular prostheses. This article gives the suggestions for quality management mainly focus on human resources, raw material, production and so on.