ABSTRACT
Integration of Traditional Chinese medicine, including Chinese materia medica (CMM), into the national healthcare delivery system, is now an essential national policy in China and is increasing rapidly. This case study summarizes the profile of integration of CMM in China, describing markets, industries, management mechanisms, education, research and development, human resources and international cooperation related to Traditional Chinese medicine, and CMM in particular. It provides a basis for policies for integrating TM into national healthcare systems to save costs and improve the general health of the population. By the end of 2014, the overall sale value of CMM exceeded $US120bn, representing 31% of the total pharmaceutical industry markets in China. More than 200 CMM formulated drugs and 1100 prepared CMM are now on the national 'Essential Drug List' and the financial budget for CMM from the Chinese government in 2014 was approximately $US4.66bn, almost double that of 2011, indicating an increasing and long-term commitment to integrated medicine in China.
Subject(s)
Drugs, Chinese Herbal , Integrative Medicine , Materia Medica , Medicine, Chinese Traditional , China , Drugs, Chinese Herbal/economics , Drugs, Chinese Herbal/standards , Humans , Materia Medica/economics , Materia Medica/standardsABSTRACT
As an important part of the market commodity circulation, the standard grade of Chinese traditional medicine commodity is very important to restrict the market order and guarantee the quality of the medicinal material. The State Council issuing the "protection and development of Chinese herbal medicine (2015-2020)" also make clear that the important task of improving the circulation of Chinese herbal medicine industry norms and the commodity specification standard of common traditional Chinese medicinal materials. However, as a large class of Chinese herbal medicines, the standard grade of the radix is more confused in the market circulation, and lack of a more reasonable study model in the development of the standard. Thus, this paper summarizes the research background, present situation and problems, and several key points of the commodity specification and grade standard in radix herbs. Then, the research model is introduced as an example of Pseudostellariae Radix, so as to provide technical support and reference for formulating commodity specifications and grades standard in other radix traditional Chinese medicinal materials.
Subject(s)
Drugs, Chinese Herbal/standards , Materia Medica/standards , Medicine, Chinese Traditional/standards , Drugs, Chinese Herbal/chemistry , Drugs, Chinese Herbal/economics , Humans , Materia Medica/chemistry , Materia Medica/economics , Medicine, Chinese Traditional/economics , Models, Theoretical , Quality ControlABSTRACT
As an important reference index to evaluate the quality of Chinese medicinal materials, the commodity specification and grade of traditional Chinese medicine has an effect on the medicinal material's price, can promote "high quality and high price" of the traditional Chinese medicine, prompt market transactions more convenient and standard, and has a great significance to the development of the whole traditional Chinese medicine industry. The formation of traditional Chinese medicine specifications and grades experienced a long historical development process. In order to provide the reference for modification of the product specifications and grades standards and management of traditional Chinese medicine products, the author consulted a large number of materia medica books and related references, sorted and analyzed the historical development process. The author divided the formation and development process into four stages, including germination stage before the Southern and Northern Dynasties, development stage of Tang and Song Dynasty, mature period of the Ming and Qing Dynasties and the inheritance development stage since the foundation of the People's Republic. The author believes that the clinical curative effect is the driving force to promote the development of commodity specifications and grades. In addition, the national pharmaceutical policy, international status, the level of science and technology also influence the development of commodity specifications and grades in some extents. Finally, the author provides three piece of suggestions for the modification of the product specifications and grades standards, according to the historical development rule.
Subject(s)
Drugs, Chinese Herbal/economics , Materia Medica/economics , Medicine, Chinese Traditional/economics , China , Commerce/history , Drugs, Chinese Herbal/analysis , Drugs, Chinese Herbal/history , Drugs, Chinese Herbal/standards , History, Ancient , Humans , Materia Medica/chemistry , Materia Medica/history , Materia Medica/standards , Medicine in Literature/history , Medicine, Chinese Traditional/history , Medicine, Chinese Traditional/standardsABSTRACT
The general situation of the approved and concluded projects of National Natural Science Foundation of China in the field of processing Chinese Materia Medica in recent five years has been reviewed. The progresses and achievements of some projects have been summarized in accordance with research area such as the processing principle, the processing technology, quality evaluation, toxicity and safety evaluation, etc. The researchers and project support units of the funded projects have been analyzed, and the problems of the applications have been also summarized.
Subject(s)
Biomedical Research/economics , Chemistry, Pharmaceutical/economics , Financing, Organized/economics , Financing, Organized/organization & administration , Materia Medica/economics , Medicine, Chinese Traditional/economics , Biomedical Research/organization & administration , Chemistry, Pharmaceutical/organization & administration , China , HumansABSTRACT
There is time-honored history and culture of medicinal plant cultivation in China. In the present review, the medicinal plant cultivation history in china was summarized, its current situation and question were analyzed, and the prospects of medicinal plant cultivation research were pointed out, with the purpose of accelerating the growth of medicinal plant cultivation research.
Subject(s)
Drugs, Chinese Herbal/chemistry , Materia Medica/chemistry , Materia Medica/economics , Plants, Medicinal/growth & development , China , Drugs, Chinese Herbal/history , History, 15th Century , History, 16th Century , History, 17th Century , History, 18th Century , History, 19th Century , History, 20th Century , History, 21st Century , History, Ancient , History, Medieval , Materia Medica/history , Medicine, Chinese Traditional/history , Medicine, Chinese Traditional/trends , Plants, Medicinal/chemistryABSTRACT
The objects of research on the resources chemistry of Chinese medicinal materials (RCCMM) are promotion of efficient production, rational utilization and improving quality of CMM and natural products. The development of TCM cause depends on the efficient utilization and sustainable development of CMM, hinges on the technologies and methods for using and discovering medicinal biological resources, stand or fall on the extension of industy chains, detailed utilizaion of resource chemical components by multi-way, multi-level. All of these may help to the recycling utilization and sound development of RCMM. In this article, five respects were discussed to the RCCMM researches and resources recycling utilization ways and goals and tasks. First, based on the principle of resource scarcity, discovering or replacing CMM resources, protecting the rare or endangered species or resources. Second, based on the multifunctionality of CMM, realizing the value-added and value compensation, and promoting the utilization efficiency through systermatic and detailed exploitation and utilization. Third, based on the resource conservation and environment-friendly, reducing raw material consumption, lowering cost, promoting recycling utilization and elevating utilization efficiency. Fourth, based on the stratege of turning harm into good, using the invasive alien biological resources by multi-ways and enriching the medicial resources. Fifth, based on the method of structure modification of chemical components, exploring and enhancing the utility value of resouces chemical substances. These data should provide references and attention for improving the utilization efficiency, promoting the development of recycling economy, and changing the mode of economic growth of agriculture and industry of CMM fundamentally.
Subject(s)
Drugs, Chinese Herbal/chemistry , Materia Medica/chemistry , Plants, Medicinal/chemistry , Agriculture/economics , Agriculture/trends , China , Conservation of Natural Resources/economics , Conservation of Natural Resources/trends , Drugs, Chinese Herbal/economics , Materia Medica/economics , Medicine, Chinese Traditional/economics , Medicine, Chinese Traditional/trends , Plants, Medicinal/growth & developmentABSTRACT
The complex production processes and long industrial chain in traditional Chinese medicine (TCM) market result in difficulty in Chinese market microstructure research. Based on the defining the logical relationships among different concepts. This paper divides TCM market into two stages as Chinese materia medica resource market and traditional Chinese Patent Medicines market. Under this foundation, we investigated the supply capacity, approaching rules and motivation system of suppliers in TCM market, analyzed the demand situation in the perspective of demand side, and evaluated the purchasing power in terms of population profile, income, and insurance. Furthermore we also analyzed the price formation mechanism in two stages of TCM market. We hope this study can make a positive and promotion effect on TCM market related research.
Subject(s)
Materia Medica/economics , Materia Medica/supply & distribution , Medicine, Chinese Traditional/economics , Statistics as TopicABSTRACT
This paper aims to summarize the achievements during the implementation process of good agricultural practice (GAP) in Chinese Materia Medica (CMM), and on basis of analyzing the existing problems of GAP, to propose further implementation of GAP in TCM growing. Since the launch of GAP in CMM growing ten years ago, it has acquired great achievements, including: (1) The promulgation of a series of measures for the administration of the GAP approval in the CMM growing; (2) The expanded planting area of CMM; (3) The increased awareness of standardized CMM growing among farmers and enterprises; (4) The establishment of GAP implementation bases for CMM growing; (5) The improvement of theory and methodology for CMM growing; (6) The development of a large group of experts and scholars in GAP approval for CMM production. The problems existing in the production include: (1) A deep understanding of GAP and its certification is still needed; (2) The distribution of the certification base is not reasonable; (3) The geo-economics effect and the backward farming practices are thought to be the bottlenecks in the standardization of CMM growing and the scale production of CMM; (4) Low comparative effectiveness limits the development of the GAP; (5) The base of breeding improved variety is blank; (6) The immature of the cultivation technique lead to the risk of production process; (7) The degradation of soil microbial and the continuous cropping obstacle restrict the sustainable development of the GAP base. To further promote the health and orderly GAP in the CMM growing, the authors propose: (1) To change the mode of production; (2) To establish a sound standard system so as to ensure quality products for fair prices; (3) To fully consider the geo-economic culture and vigorously promote the definite cultivating of traditional Chinese medicinal materials; (4) To strengthen the transformation and generalization of basic researches and achievements, in order to provide technical support for the CMM production; (5) To deepen the understanding of GAP, to vigorously promote ecological planting and precision agriculture, in order to overcome the continuous cropping obstacle. The authors think that despite the fact that we are still facing with a huge array of management and technological problems, the GAP in the CMM growing has already enjoyed widespread support and showed great potential. In the future, with people's deeper understanding of GAP and the great progress of the science and technology, the GAP will constantly be fused with the theory, methodology and technology in the modern agriculture like precision agriculture, eco-agriculture and etc.
Subject(s)
Agriculture/standards , Drugs, Chinese Herbal/standards , Materia Medica/standards , Plants, Medicinal/growth & development , Agriculture/economics , Agriculture/methods , Agriculture/trends , China , Drugs, Chinese Herbal/analysis , Drugs, Chinese Herbal/economics , Humans , Materia Medica/chemistry , Materia Medica/economics , Plants, Medicinal/chemistryABSTRACT
Pharmaceutical market is a typical market with information asymmetry, and which can lead to "lemons" problem. In all developed countries, firms must receive regulatory approval to market a pharmaceutical product. Such administrative department including SFDA, EMA, FDA and so on. Chinese materia medica is a special part of pharmaceutical market in China. The management of Chinese materia medica is a special challenge in China.
Subject(s)
Materia Medica/economics , Medicine, Chinese Traditional/economics , Accreditation , Materia Medica/standards , Medicine, Chinese Traditional/standards , Reference Standards , Social Control, FormalSubject(s)
Commerce , Complementary Therapies/ethics , Complementary Therapies/legislation & jurisprudence , Homeopathy , Informed Consent , Policy , Commerce/ethics , Commerce/legislation & jurisprudence , Homeopathy/ethics , Homeopathy/legislation & jurisprudence , Hospitals, Special/ethics , Hospitals, Special/legislation & jurisprudence , Humans , Informed Consent/ethics , Informed Consent/legislation & jurisprudence , Manipulation, Chiropractic/ethics , Materia Medica/economics , Placebo Effect , Treatment Outcome , United Kingdom , United StatesABSTRACT
OBJECTIVE: To test the feasibility of a pragmatic trial design with economic evaluation and nested qualitative study, comparing usual care (UC) with UC plus individualised homeopathy, in children requiring secondary care for asthma. This included recruitment and retention, acceptability of outcome measures patients' and health professionals' views and experiences and a power calculation for a definitive trial. METHODS: In a pragmatic parallel group randomised controlled trial (RCT) design, children on step 2 or above of the British Thoracic Society Asthma Guidelines (BTG) were randomly allocated to UC or UC plus a five visit package of homeopathic care (HC). Outcome measures included the Juniper Asthma Control Questionnaire, Quality of Life Questionnaire and a resource use questionnaire. Qualitative interviews were used to gain families' and health professionals' views and experiences. RESULTS: 226 children were identified from hospital clinics and related patient databases. 67 showed an interest in participating, 39 children were randomised, 18 to HC and 21 to UC. Evidence in favour of adjunctive homeopathic treatment was lacking. Economic evaluation suggests that the cost of additional consultations was not offset by the reduced cost of homeopathic remedies and the lower use of primary care by children in the homeopathic group. Qualitative data gave insights into the differing perspectives of families and health care professionals within the research process. CONCLUSIONS: A future study using this design is not feasible, further investigation of a potential role for homeopathy in asthma management might be better conducted in primary care with children with less severe asthma.
Subject(s)
Asthma/therapy , Homeopathy/methods , Materia Medica/therapeutic use , Precision Medicine/methods , Severity of Illness Index , Asthma/economics , Child , Child Health Services/organization & administration , Feasibility Studies , Female , Homeopathy/economics , Humans , Male , Materia Medica/economics , Outcome Assessment, Health Care , Precision Medicine/economics , Quality Assurance, Health Care/methods , Treatment Outcome , United KingdomABSTRACT
According to the survey on 7 medicinal material markets, 15 factories of Chinese materia medica slices, 27 medicine shops and 110 samples collected, this report anglyzed and summarized, the sources, provenances, characters of crude drugs, characters of decocting slices and merchandise circulation of Epimedium material drugs and decoction pieces.
Subject(s)
Drugs, Chinese Herbal/economics , Epimedium/chemistry , Materia Medica/economics , Drugs, Chinese Herbal/analysis , Drugs, Chinese Herbal/standards , Marketing , Materia Medica/analysis , Materia Medica/standards , Product Surveillance, Postmarketing , Quality ControlABSTRACT
The Chinese government has recently established a national project to improve the standards of Chinese Materia Medica (CMM) products, particularly regarding their quality control and safety evaluation, in order to promote modernization and increase international trade. In 2006, the global sales value of Chinese medicinal products increased to 20 billion US$, and the export value of CMM was up to more than 1 billion US$. However, the standard of these products still needs to be improved to meet the more stringent requirements of the international markets. Over the past decade we have witnessed the increasing growth in popularity of health foods and herbal medicinal products, especially Chinese Materia Medica products (CMM).
Subject(s)
Drug-Related Side Effects and Adverse Reactions/prevention & control , Drugs, Chinese Herbal/standards , Materia Medica/standards , China , Drug-Related Side Effects and Adverse Reactions/economics , Drugs, Chinese Herbal/economics , Humans , Materia Medica/economics , Quality ControlABSTRACT
In this paper, the production and marketing of medicinal materials of plant origin are sorted and analyzed. The total annual yield and total output value are presented. The resources sustainable development is discussed by three aspects, i.e., the yield Top 60 items, rare and endangered species and several wild drugs should be deeply concerned. Relevant measures and implementation are recommended respectively.
Subject(s)
Conservation of Natural Resources , Marketing , Materia Medica/economics , Conservation of Natural Resources/economics , Endangered Species , Plants, Medicinal/growth & developmentSubject(s)
Materia Medica , Patients/psychology , Physician-Patient Relations/ethics , Placebo Effect , Placebos , Clinical Trials as Topic/ethics , Deception , Europe , Evidence-Based Medicine , France , Humans , Informed Consent , Materia Medica/administration & dosage , Materia Medica/economics , Personal Autonomy , Placebos/administration & dosage , Placebos/economics , Practice Patterns, Physicians'/ethics , Safety , Suggestion , Treatment Outcome , United Kingdom , United StatesABSTRACT
CONTEXT: Allergies are the most common immunologic diseases among the general population. Increasing evidence suggests that the incidence of allergic disorders is rising dramatically. Conventional medicine provides only limited relief and does not offer a complete cure to this health problem. Consequently, patients seek additional approaches and therapies to integrate into their healthcare. Homeopathy is one of the leading complementary modalities used to treat this health problem. OBJECTIVE: This preliminary study assessed the effect of integrating homeopathic treatment in allergic diseases on conventional medication consumption in a health maintenance organization. DESIGN: Retrospective outcome study designed as a before-after trial. SETTING: Patients were studied in a complementary medicine clinic affiliated with an Israeli health maintenance organization. PARTICIPANTS: Forty-eight patients were treated for allergic diseases with homeopathic remedies and conventional medications. MAIN OUTCOME MEASURES: A computerized medication chart for each patient was evaluated for conventional medication consumption 3 months before and 3 months after the homeopathic intervention. Each patient served as his or her own control. RESULTS: Fifty-six percent of patients in this study reduced their use of conventional medication following the homeopathic intervention. Patients who used conventional medications for their allergic disorders reduced their medication expense by an average of 60%, with an average savings of $24 per patient in the 3-month period following the homeopathic intervention. CONCLUSIONS: This retrospective outcome study demonstrates cost savings for an Israeli health maintenance organization. The homeopathic intervention led to a modest but significant reduction in the use of medications commonly used to treat allergic conditions and their complications. Larger controlled studies are needed to verify these findings.
Subject(s)
Hypersensitivity/therapy , Materia Medica/therapeutic use , Adolescent , Adult , Chi-Square Distribution , Child , Child, Preschool , Cost of Illness , Cost-Benefit Analysis , Drug Utilization/statistics & numerical data , Female , Humans , Hypersensitivity/drug therapy , Hypersensitivity/economics , Hypersensitivity, Immediate/therapy , Israel , Male , Materia Medica/economics , Middle Aged , Retrospective Studies , Statistics, NonparametricSubject(s)
Colon , Complementary Therapies/economics , Electromagnetic Phenomena , Expert Testimony/legislation & jurisprudence , Hydrotherapy/economics , Insurance Coverage/legislation & jurisprudence , Materia Medica/economics , National Health Programs/legislation & jurisprudence , Organotherapy/economics , Costs and Cost Analysis , Female , Germany , Humans , Insurance Claim Review/legislation & jurisprudence , Middle AgedABSTRACT
INTRODUCTION: In order to address the limitations of the standard pragmatic RCT design, the innovative 'cohort multiple RCT' design was developed. The design was first piloted by addressing a clinical question " What is the clinical and cost effectiveness of treatment by a homeopath for women with menopausal hot flushes?". METHODS: A cohort with the condition of interest (hot flushes) was recruited through an observational study of women's midlife health and consented to provide observational data and have their data used comparatively. The 'Hot Flush' Cohort were then screened in order to identify patients eligible for a trial of the offer of treatment by a homeopath (Eligible Trial Group). A proportion of the Eligible Trial Group was then randomly selected to the Offer Group and offered treatment. A "patient centred" approach to information and consent was adopted. Patients were not (i) told about treatments that they would not be offered, and trial intervention information was only given to the Offer Group after random selection. Patients were not (ii) given prior information that their treatment would be decided by chance. RESULTS: The 'cohort multiple RCT' design was acceptable to the NHS Research Ethics Committee. The majority of patients completed multiple questionnaires. Acceptance of the offer was high (17/24). DISCUSSION: This pilot identified the feasibility of an innovative design in practice. Further research is required to test the concept of undertaking multiple trials within a cohort of patients and to assess the acceptability of the "patient centred" approach to information and consent.
Subject(s)
Hot Flashes/drug therapy , Materia Medica/economics , Materia Medica/therapeutic use , Research Design , Aged , Cost-Benefit Analysis , Female , Humans , Materia Medica/administration & dosage , Medication Adherence , Middle Aged , Pilot Projects , Quality of Life , Surveys and Questionnaires , Women's HealthABSTRACT
Though homeopathy has been in successful and continuous use for well over 200 years, in the United Kingdom it is under growing pressure, from scientific detractors and sections of the media. As such, homeopathy's free National Health Service provision is threatened because it is derided as 'unproven', 'unscientific', and even 'deadly'. While refuting these and other detractions, this paper considers possible reasons for the current plight of homeopathy UK. Thus, the current attacks against homeopathy should be viewed more in the context of the globalised pharmaceutical industry which is itself in crisis, and a succession of UK governments seemingly supine in the face of legislation originating from the European Union.