首页 > 最新文献

Farmakoekonomika最新文献

英文 中文
Epigenetic aspects in rehabilitation of female cancer patients 女性癌症患者康复的表观遗传学方面
Q3 Medicine Pub Date : 2022-07-28 DOI: 10.17749/2070-4909/farmakoekonomika.2022.141
A. Solopova, D. Blinov, S. V. Demyanov, G. V. Demyanov, E. Achkasov, A. Y. Vlasina, L. Sandzhieva, D. M. Ampilogova
The influence of epigenetic processes on the development of malignant diseases, including gynaecological cancers, is now beyond doubt. DNA methylation, histone modification and post-transcriptional regulation by microRNAs lead to changes in the activity of various genes, contributing to female genital cancers (cervix, endometrium, ovarian). It should be noted that disruptions in gene expression do not only occur in malignant cells, but also in the tumour microenvironment, resulting in disease progression and relapse. However, “epigenetic markers” of carcinogenesis can be useful in the treatment and rehabilitation of patients, making a personalized approach possible.
表观遗传过程对恶性疾病,包括妇科癌症的发展的影响现在是毋庸置疑的。DNA甲基化、组蛋白修饰和microrna的转录后调控导致各种基因活性的变化,从而导致女性生殖器癌症(宫颈癌、子宫内膜癌、卵巢癌)的发生。应该指出的是,基因表达的中断不仅发生在恶性细胞中,也发生在肿瘤微环境中,导致疾病进展和复发。然而,癌变的“表观遗传标记”在患者的治疗和康复中是有用的,使个性化的方法成为可能。
{"title":"Epigenetic aspects in rehabilitation of female cancer patients","authors":"A. Solopova, D. Blinov, S. V. Demyanov, G. V. Demyanov, E. Achkasov, A. Y. Vlasina, L. Sandzhieva, D. M. Ampilogova","doi":"10.17749/2070-4909/farmakoekonomika.2022.141","DOIUrl":"https://doi.org/10.17749/2070-4909/farmakoekonomika.2022.141","url":null,"abstract":"The influence of epigenetic processes on the development of malignant diseases, including gynaecological cancers, is now beyond doubt. DNA methylation, histone modification and post-transcriptional regulation by microRNAs lead to changes in the activity of various genes, contributing to female genital cancers (cervix, endometrium, ovarian). It should be noted that disruptions in gene expression do not only occur in malignant cells, but also in the tumour microenvironment, resulting in disease progression and relapse. However, “epigenetic markers” of carcinogenesis can be useful in the treatment and rehabilitation of patients, making a personalized approach possible.","PeriodicalId":36464,"journal":{"name":"Farmakoekonomika","volume":"16 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78538549","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Pharmacotherapy of insomnia in childhood 儿童失眠症的药物治疗
Q3 Medicine Pub Date : 2022-07-28 DOI: 10.17749/2070-4909/farmakoekonomika.2022.127
Z. G. Tadtaeva, A. Galustyan, V. Rusanovsky, O. Gromova, I. S. Sardaryan, M. Y. Krivdina, N. A. Kuritsyna
Insomnia is the most common form of sleep disturbance in childhood. Sleep disorders and a decrease in its duration and quality lead to the development of cognitive disorders, change emotional and behavioral functions of the developing organism, and negatively affect medical and psychological aspects that require medical correction. The article provides an overview of current literature data on pharmacological approaches to insomnia therapy in childhood. The general principles of treatment and the use of various pharmacological groups of drugs are discussed. It is shown that pharmacotherapy of childhood insomnia should be carried out based on knowledge about the age characteristics of patients, efficacy, safety, analysis of pharmacodynamic and pharmacokinetic parameters of the drugs used. Drug therapy should be combined with cognitive behavioral techniques, including adherence to sleep patterns and hygiene.
失眠是儿童时期最常见的睡眠障碍。睡眠障碍及其持续时间和质量的减少导致认知障碍的发展,改变发育生物体的情绪和行为功能,并对需要医疗纠正的医学和心理方面产生负面影响。本文概述了目前文献资料的药理学方法治疗失眠在儿童。讨论了治疗的一般原则和各种药理学组药物的使用。结论:儿童失眠症的药物治疗应在了解患者年龄特征、疗效、安全性、所用药物的药效学和药动学参数分析的基础上进行。药物治疗应与认知行为技术相结合,包括坚持睡眠模式和卫生。
{"title":"Pharmacotherapy of insomnia in childhood","authors":"Z. G. Tadtaeva, A. Galustyan, V. Rusanovsky, O. Gromova, I. S. Sardaryan, M. Y. Krivdina, N. A. Kuritsyna","doi":"10.17749/2070-4909/farmakoekonomika.2022.127","DOIUrl":"https://doi.org/10.17749/2070-4909/farmakoekonomika.2022.127","url":null,"abstract":"Insomnia is the most common form of sleep disturbance in childhood. Sleep disorders and a decrease in its duration and quality lead to the development of cognitive disorders, change emotional and behavioral functions of the developing organism, and negatively affect medical and psychological aspects that require medical correction. The article provides an overview of current literature data on pharmacological approaches to insomnia therapy in childhood. The general principles of treatment and the use of various pharmacological groups of drugs are discussed. It is shown that pharmacotherapy of childhood insomnia should be carried out based on knowledge about the age characteristics of patients, efficacy, safety, analysis of pharmacodynamic and pharmacokinetic parameters of the drugs used. Drug therapy should be combined with cognitive behavioral techniques, including adherence to sleep patterns and hygiene.","PeriodicalId":36464,"journal":{"name":"Farmakoekonomika","volume":"15 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81096137","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Strengthening medical rehabilitation services in health system: a situation analysis 加强卫生系统医疗康复服务:现状分析
Q3 Medicine Pub Date : 2022-07-28 DOI: 10.17749/2070-4909/farmakoekonomika.2022.140
D. Blinov, A. Solopova, L. Sandzhieva, E. E. Achkasov, D. Korabelnikov, D. M. Ampilogova, S. M. Khlopkova
Objective: to evaluate the effectiveness of changes in the legal framework that regulates medical rehabilitation (MR) in the Russian Federation.Material and methods. We analyzed the valid Order of the Ministry of Health of the Russian Federation of June 31, 2020 No. 788n “Organization of medical rehabilitation of adults”, which came into legal power on January 1, 2021. It was proposed for public discussion on the introduction of amendments (project of amendments). The changes proposed in the project were compared with the original text of the document. Besides, other legal documents on the organization of medical rehabilitation were analyzed.Results. Order No. 788n regulates the stages of MR, specifies the formation and realization of an individual plan for a multi-disciplinary rehabilitation team based on the evaluation by Rehabilitation Routing Scale. The document includes in-house protocols of profile inpatient and outpatient departments of medical institutions, standards for doctor’s offices equipment, organization of day-time inpatient department, and regulations for MR centers. The project of amendments contains a variant of involvement of the existing additional Groups 1 and 2 medical divisions for the organization of MR, and limitation for the Stage 2 of MR in inpatient settings, which is now possible only for patients who need 24-hour care.Conclusion. The proposed changes have evolutionary character. A lot of issues in the regulatory framework of MR remain unsolved. It is necessary to improve the state policy for MR and perform further clinical studies of its benefits.
目的:评估俄罗斯联邦医疗康复法律框架改革的成效。材料和方法。我们分析了俄罗斯联邦卫生部2020年6月31日第788n号“成人医疗康复组织”的有效命令,该命令于2021年1月1日生效。建议公众讨论引入修正案(修正案项目)。将项目中提出的变更与文件原文进行对比。此外,还对组织医疗康复的其他法律文书进行了分析。第788n号命令规定了MR的阶段,规定了基于康复路径量表评估的多学科康复团队个体计划的形成和实现。该文件包括医疗机构概要住院和门诊部门的内部协议、医生办公室设备标准、日间住院部门的组织以及MR中心的规定。修订项目包括现有的额外的第1组和第2组医疗部门参与组织磁共振,以及限制住院环境中磁共振的第2阶段,现在只有需要24小时护理的患者才有可能。所提出的变化具有演化特征。MR监管框架中的许多问题仍未得到解决。有必要完善MR的国家政策,并对其益处进行进一步的临床研究。
{"title":"Strengthening medical rehabilitation services in health system: a situation analysis","authors":"D. Blinov, A. Solopova, L. Sandzhieva, E. E. Achkasov, D. Korabelnikov, D. M. Ampilogova, S. M. Khlopkova","doi":"10.17749/2070-4909/farmakoekonomika.2022.140","DOIUrl":"https://doi.org/10.17749/2070-4909/farmakoekonomika.2022.140","url":null,"abstract":"Objective: to evaluate the effectiveness of changes in the legal framework that regulates medical rehabilitation (MR) in the Russian Federation.Material and methods. We analyzed the valid Order of the Ministry of Health of the Russian Federation of June 31, 2020 No. 788n “Organization of medical rehabilitation of adults”, which came into legal power on January 1, 2021. It was proposed for public discussion on the introduction of amendments (project of amendments). The changes proposed in the project were compared with the original text of the document. Besides, other legal documents on the organization of medical rehabilitation were analyzed.Results. Order No. 788n regulates the stages of MR, specifies the formation and realization of an individual plan for a multi-disciplinary rehabilitation team based on the evaluation by Rehabilitation Routing Scale. The document includes in-house protocols of profile inpatient and outpatient departments of medical institutions, standards for doctor’s offices equipment, organization of day-time inpatient department, and regulations for MR centers. The project of amendments contains a variant of involvement of the existing additional Groups 1 and 2 medical divisions for the organization of MR, and limitation for the Stage 2 of MR in inpatient settings, which is now possible only for patients who need 24-hour care.Conclusion. The proposed changes have evolutionary character. A lot of issues in the regulatory framework of MR remain unsolved. It is necessary to improve the state policy for MR and perform further clinical studies of its benefits.","PeriodicalId":36464,"journal":{"name":"Farmakoekonomika","volume":"6 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88728786","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Clinical study of real-time polymerase chain reaction test kit for SARS-CoV-2 ribonucleic acids detection 实时聚合酶链反应试剂盒检测SARS-CoV-2核糖核酸的临床研究
Q3 Medicine Pub Date : 2022-07-28 DOI: 10.17749/2070-4909/farmakoekonomika.2022.111
M. Dmitryukova, A. A. Golod, M. Senina, A. E. Gushchin
Objective: development and validation of a reverse transcription polymerase chain reaction (RT-PCR) test kit for SARS-CoV-2 ribonucleic acids (RNA) qualitative detection adapted for using with automated station for RNA extraction.Material and methods. Assessment of clinical performance was carried out on biological samples (nasal and oropharyngeal swabs and sputum) obtained during the diagnostic procedure. The presence of novel coronavirus RNA was established using a reference kit. Sensitivity was evaluated on standard SARS-CoV-2 sample (EDX SARS-CoV-2 Standard, Bio-Rad Laboratories, USA).Results. Presence of SARS-CoV-2 RNA is detected by two genome regions. Sensitivity determined by testing SARS-CoV-2 standard was 250 copies/ml. Coefficient of variation during the testing of samples with the concentration of 104 copies/ml did not exceed 5% in different conditions. Diagnostic sensitivity against reference test was 100% (95% confidence interval (CI) 95.6–100) for nasal and oropharyngeal swabs and 100% (95% CI 94.8–100) for sputum. Diagnostic specificity was 100% (95% CI 95.6–100) for nasal and oropharyngeal swabs and 100% (95% CI 94.8–100) for sputum. The turnaround time for test from RNA extraction till obtaining results was about 3 hours when testing 96 samples using automated stations for RNA extraction.Conclusion. Using the kit together with automated station for RNA extraction will increase laboratory testing capacity in pandemic conditions.
目的:研制并验证一种适用于RNA自动提取工作站的SARS-CoV-2核糖核酸(RNA)定性检测的逆转录聚合酶链反应(RT-PCR)检测试剂盒。材料和方法。对诊断过程中获得的生物样本(鼻咽拭子和痰液)进行临床表现评估。使用参比试剂盒确定存在新型冠状病毒RNA。对标准SARS-CoV-2样品(EDX SARS-CoV-2 standard, Bio-Rad Laboratories, USA)进行敏感性评价。通过两个基因组区域检测SARS-CoV-2 RNA的存在。检测SARS-CoV-2标准品的灵敏度为250拷贝/ml。对于浓度为104拷贝/ml的样品,不同条件下的变异系数均不超过5%。鼻和口咽拭子对参考试验的诊断敏感性为100%(95%可信区间(CI) 95.6-100),痰液对参考试验的诊断敏感性为100% (95% CI 94.8-100)。鼻咽拭子的诊断特异性为100% (95% CI 95.6-100),痰液的诊断特异性为100% (95% CI 94.8-100)。采用RNA自动提取站对96份样品进行检测,从提取到得到结果所需时间约为3小时。将该试剂盒与自动RNA提取站一起使用将提高实验室在大流行条件下的检测能力。
{"title":"Clinical study of real-time polymerase chain reaction test kit for SARS-CoV-2 ribonucleic acids detection","authors":"M. Dmitryukova, A. A. Golod, M. Senina, A. E. Gushchin","doi":"10.17749/2070-4909/farmakoekonomika.2022.111","DOIUrl":"https://doi.org/10.17749/2070-4909/farmakoekonomika.2022.111","url":null,"abstract":"Objective: development and validation of a reverse transcription polymerase chain reaction (RT-PCR) test kit for SARS-CoV-2 ribonucleic acids (RNA) qualitative detection adapted for using with automated station for RNA extraction.Material and methods. Assessment of clinical performance was carried out on biological samples (nasal and oropharyngeal swabs and sputum) obtained during the diagnostic procedure. The presence of novel coronavirus RNA was established using a reference kit. Sensitivity was evaluated on standard SARS-CoV-2 sample (EDX SARS-CoV-2 Standard, Bio-Rad Laboratories, USA).Results. Presence of SARS-CoV-2 RNA is detected by two genome regions. Sensitivity determined by testing SARS-CoV-2 standard was 250 copies/ml. Coefficient of variation during the testing of samples with the concentration of 104 copies/ml did not exceed 5% in different conditions. Diagnostic sensitivity against reference test was 100% (95% confidence interval (CI) 95.6–100) for nasal and oropharyngeal swabs and 100% (95% CI 94.8–100) for sputum. Diagnostic specificity was 100% (95% CI 95.6–100) for nasal and oropharyngeal swabs and 100% (95% CI 94.8–100) for sputum. The turnaround time for test from RNA extraction till obtaining results was about 3 hours when testing 96 samples using automated stations for RNA extraction.Conclusion. Using the kit together with automated station for RNA extraction will increase laboratory testing capacity in pandemic conditions.","PeriodicalId":36464,"journal":{"name":"Farmakoekonomika","volume":"3 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83731227","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Current opportunities for the export of medical services in Russia 目前俄罗斯医疗服务出口的机会
Q3 Medicine Pub Date : 2022-07-28 DOI: 10.17749/2070-4909/farmakoekonomika.2022.119
S. Russkikh, E. Tarasenko, S. Grin, M. Yugay, K. K. Kryukova, L. Moskvicheva
Objective: to identify factors and barriers for the development of medical services export (MSE) in the Russian Federation (RF), to establish recommendations for its stimulation, and to promote Russia as an exporter of medical services in the international arena.Material and methods. An analysis of the practice of MSE organizing and regulatory documents of 2018–2021 was carried out, as well as the quantitative sociological survey of 184 doctors, healthcare managers and experts and the in-depth semi-structured interviews with 8 high-level healthcare experts conducted in 2020. The survey was performed using the “snowball” method. To increase the level of representativeness of the survey results, doctors, organizers and healthcare experts with current work experience in organizations and government bodies in the healthcare sector (Ministry of Health of the RF, Roszdravnadzor, Central Research Institute of Organization and Informatization of Public Health, etc.) were involved as respondents including practicing physicians and heads of medical organizations.Results. The aim of MSE state regulation and stimulation is to choose the optimal model for supporting inbound medical tourism (IMT) in the RF. At the moment, three models of supporting foreign citizens in the medical services market are developing: 1) creating expert medical consortia of leading medical clinics; 2) forming an infrastructure for agency support in the Russian IMT market, including the development of infrastructure in regional IMT markets with high, medium and low export potential; 3) paid medical services in all types of medical care are successfully provided in public and private clinics to foreign citizens who live, work or study in the RF on a permanent or temporary basis. The third model is а self-organizing patient flow of foreign citizens, uncontrolled by Russian medical organizations.Conclusion. The main strategic directions of MSE development for the growth of an organized and controlled patient flow in the RF are medical care services in the field of neurosciences, high-tech surgery and rehabilitation, reproductive medicine, immunotherapy of oncological diseases, and cross-border diagnostic services. It is necessary to take certain measures to stimulate MSE, including the introduction of international standards for the safety and quality of medical care, increasing the service component of the provision of medical services, building channels of marketing communications with foreign patients and the promotion of Russia as an exporter of medical services in the international arena.
目标:确定影响俄罗斯联邦医疗服务出口发展的因素和障碍,提出促进出口的建议,并在国际舞台上推广俄罗斯作为医疗服务出口国的地位。材料和方法。对2018-2021年MSE组织实践和规范性文件进行分析,并在2020年对184名医生、医疗管理人员和专家进行定量社会学调查,对8名高水平医疗专家进行深度半结构化访谈。该调查采用“滚雪球”法进行。为了提高调查结果的代表性,调查对象包括执业医师和医疗机构负责人,包括目前在医疗保健部门的组织和政府机构(联邦卫生部、罗斯德拉夫纳佐尔、中央公共卫生组织和信息化研究所等)工作的医生、组织者和医疗专家。MSE状态调控和激励的目的是选择最优的模式来支持RF的入境医疗旅游。目前,在医疗服务市场支持外籍公民的三种模式正在发展:1)建立领先医疗诊所的专家医疗联盟;2)在俄罗斯IMT市场形成机构支持的基础设施,包括在具有高、中、低出口潜力的区域IMT市场发展基础设施;3)公立和私立诊所成功地向在俄罗斯联邦永久或临时生活、工作或学习的外国公民提供各种医疗保健的有偿医疗服务。第三种模式是外国公民的自组织病人流动,不受俄罗斯医疗机构的控制。MSE发展的主要战略方向是在神经科学、高科技外科和康复、生殖医学、肿瘤疾病的免疫治疗和跨界诊断服务领域提供医疗保健服务,以促进RF有组织和有控制的患者流动。有必要采取某些措施来刺激MSE,包括引入医疗安全和质量的国际标准,增加提供医疗服务的服务部分,建立与外国患者的营销沟通渠道,并在国际舞台上推广俄罗斯作为医疗服务出口国的地位。
{"title":"Current opportunities for the export of medical services in Russia","authors":"S. Russkikh, E. Tarasenko, S. Grin, M. Yugay, K. K. Kryukova, L. Moskvicheva","doi":"10.17749/2070-4909/farmakoekonomika.2022.119","DOIUrl":"https://doi.org/10.17749/2070-4909/farmakoekonomika.2022.119","url":null,"abstract":"Objective: to identify factors and barriers for the development of medical services export (MSE) in the Russian Federation (RF), to establish recommendations for its stimulation, and to promote Russia as an exporter of medical services in the international arena.Material and methods. An analysis of the practice of MSE organizing and regulatory documents of 2018–2021 was carried out, as well as the quantitative sociological survey of 184 doctors, healthcare managers and experts and the in-depth semi-structured interviews with 8 high-level healthcare experts conducted in 2020. The survey was performed using the “snowball” method. To increase the level of representativeness of the survey results, doctors, organizers and healthcare experts with current work experience in organizations and government bodies in the healthcare sector (Ministry of Health of the RF, Roszdravnadzor, Central Research Institute of Organization and Informatization of Public Health, etc.) were involved as respondents including practicing physicians and heads of medical organizations.Results. The aim of MSE state regulation and stimulation is to choose the optimal model for supporting inbound medical tourism (IMT) in the RF. At the moment, three models of supporting foreign citizens in the medical services market are developing: 1) creating expert medical consortia of leading medical clinics; 2) forming an infrastructure for agency support in the Russian IMT market, including the development of infrastructure in regional IMT markets with high, medium and low export potential; 3) paid medical services in all types of medical care are successfully provided in public and private clinics to foreign citizens who live, work or study in the RF on a permanent or temporary basis. The third model is а self-organizing patient flow of foreign citizens, uncontrolled by Russian medical organizations.Conclusion. The main strategic directions of MSE development for the growth of an organized and controlled patient flow in the RF are medical care services in the field of neurosciences, high-tech surgery and rehabilitation, reproductive medicine, immunotherapy of oncological diseases, and cross-border diagnostic services. It is necessary to take certain measures to stimulate MSE, including the introduction of international standards for the safety and quality of medical care, increasing the service component of the provision of medical services, building channels of marketing communications with foreign patients and the promotion of Russia as an exporter of medical services in the international arena.","PeriodicalId":36464,"journal":{"name":"Farmakoekonomika","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"83898008","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Pharmacoeconomic analysis of using benralizumab for treatment of severe asthma in inpatient and outpatient settings benralizumab用于治疗住院和门诊重症哮喘的药物经济学分析
Q3 Medicine Pub Date : 2022-07-27 DOI: 10.17749/2070-4909/farmakoekonomika.2022.143
M. Zhuravleva, S. Avdeev, Yu. V. Gagarina, T. V. Marin
Objective: evaluation of the pharmacoeconomic feasibility of using benralizumab in the form of autoinjector (pen-injector device) in outpatient facilities compared with its use in the form of a syringe in hospital settings for the treatment of severe asthma (SA).Material and methods. The cost minimization and budget impact analysis methods were used. The current practice of treating patients with SA with benralizumab in hospital settings at the expense of compulsory medical insurance funds was compared with the simulated practice. The simulated price was calculated as half patients receiving benralizumab in the hospital transferred to outpatient facilities at the expense of regional funds for 3 years. Direct medical costs included drug cost and outpatient patient monitoring services cost.Results. The direct medical costs associated with benralizumab therapy in outpatient facilities were lower than the costs required for benralizumab therapy in the hospital settings and amounted to 0.99 million rubles versus 1.17 million rubles per one patient per year, respectively. Thus, the use of benralizumab in outpatient facilities leads to savings of 185 thousand rubles (16%). In 2021, 93 patients were prescribed benralizumab in hospital settings. The expansion of the application of benralizumab use in outpatient facilities will lead to a reduction in medical costs in the first year of therapy (when switching 16.7% of patients) by 5.9 million rubles (4,9%). The consistent expansion of the practice of benralizumab use in outpatient facilities over a 3-year horizon (when switching 50% of patients) will lead to a reduction in medical costs by 46.6 million rubles (12.1%).Conclusion. Expansion of benralizumab use in outpatient facilities with a new form of autoinjector (pen-injector device) will lead to savings in medical costs and reduce the burden on the health care system, thus it is economically feasible.
目的:评估在门诊设施中使用自动注射器形式(笔式注射器装置)与在医院环境中使用注射器形式用于治疗严重哮喘(SA)的药物经济学可行性。材料和方法。采用了成本最小化和预算影响分析方法。目前在医院使用benralizumab治疗SA患者的做法是以强制性医疗保险基金为代价的,并与模拟实践进行了比较。模拟价格的计算方法是,在医院接受benralizumab治疗的患者中,有一半在3年内以地区资金为代价转到门诊设施。直接医疗费用包括药品费用和门诊病人监护服务费用。门诊设施中与贝纳利珠单抗治疗相关的直接医疗费用低于医院环境中贝纳利珠单抗治疗所需的费用,分别为99万卢布/年和117万卢布/年。因此,在门诊设施使用贝纳利珠单抗可节省18.5万卢布(16%)。2021年,93名患者在医院接受了贝纳利珠单抗处方。扩大benralizumab在门诊设施的应用范围,将使治疗第一年(16.7%的患者转用)的医疗费用减少590万卢布(4.9%)。在3年的时间里(当转换50%的患者时),在门诊设施中持续扩大使用benralizumab的做法将导致医疗费用减少4660万卢布(12.1%)。使用新型自动注射器(笔式注射器装置)扩大benralizumab在门诊设施的使用将节省医疗费用并减轻卫生保健系统的负担,因此在经济上是可行的。
{"title":"Pharmacoeconomic analysis of using benralizumab for treatment of severe asthma in inpatient and outpatient settings","authors":"M. Zhuravleva, S. Avdeev, Yu. V. Gagarina, T. V. Marin","doi":"10.17749/2070-4909/farmakoekonomika.2022.143","DOIUrl":"https://doi.org/10.17749/2070-4909/farmakoekonomika.2022.143","url":null,"abstract":"Objective: evaluation of the pharmacoeconomic feasibility of using benralizumab in the form of autoinjector (pen-injector device) in outpatient facilities compared with its use in the form of a syringe in hospital settings for the treatment of severe asthma (SA).Material and methods. The cost minimization and budget impact analysis methods were used. The current practice of treating patients with SA with benralizumab in hospital settings at the expense of compulsory medical insurance funds was compared with the simulated practice. The simulated price was calculated as half patients receiving benralizumab in the hospital transferred to outpatient facilities at the expense of regional funds for 3 years. Direct medical costs included drug cost and outpatient patient monitoring services cost.Results. The direct medical costs associated with benralizumab therapy in outpatient facilities were lower than the costs required for benralizumab therapy in the hospital settings and amounted to 0.99 million rubles versus 1.17 million rubles per one patient per year, respectively. Thus, the use of benralizumab in outpatient facilities leads to savings of 185 thousand rubles (16%). In 2021, 93 patients were prescribed benralizumab in hospital settings. The expansion of the application of benralizumab use in outpatient facilities will lead to a reduction in medical costs in the first year of therapy (when switching 16.7% of patients) by 5.9 million rubles (4,9%). The consistent expansion of the practice of benralizumab use in outpatient facilities over a 3-year horizon (when switching 50% of patients) will lead to a reduction in medical costs by 46.6 million rubles (12.1%).Conclusion. Expansion of benralizumab use in outpatient facilities with a new form of autoinjector (pen-injector device) will lead to savings in medical costs and reduce the burden on the health care system, thus it is economically feasible.","PeriodicalId":36464,"journal":{"name":"Farmakoekonomika","volume":"5 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-07-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85343517","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Improving the efficiency of the medicine provision system for patients with malignant neoplasms 提高恶性肿瘤患者用药制度的效率
Q3 Medicine Pub Date : 2022-07-27 DOI: 10.17749/2070-4909/farmakoekonomika.2022.137
Y. Agafonova, D. Fedyaev, A. Snegovoy, V. Omelyanovskiy
Background. One of the priorities of health care is the balance between the financial resources and the availability of effective medical care. The current approach of access to cancer medicines limits the timeliness and availability of treatment. At the same time, financial support from the government provides great costs on cancer drugs. However, these great costs are not rational.Objective: to assess the financing needs of the complete transfer of financial support of medical care in the field of oncology to the Compulsory Health Insurance (CHI) system by means of optimizing the functions of the day hospital.Material and methods. The achievement of the goal is planned to be reached by eliminating the unusual functions of oncological day hospital. We analyzed the regulatory legal documents regulating drug care and drug provision in the Russian Federation, data from depersonalized (anonymized) registers of the structure of hospitalizations in a day hospital for 2021. The methods of expert assessments, mathematical modeling, as well as literature data analysis were used. The study developed a model for assessing the need to finance the full transfer of medicine provision to the CHI system, including taking into account the hidden deficit.Results. The total amount of funds released from the reduction of irrational hospitalizations in day hospital conditions amounted to 2.08% of the funding level of the analyzed schemes. Taking into account the data of hospitalizations in oncological day hospital for 2021, the number of irrational hospitalizations in case of transfer of selected schemes to the outpatient stage will decrease by 16.1%. The transfer of all the medicine therapy to financing from the CHI funds will require significant additional budget expenditures in the amount of 62.5 billion rubles or 2.65% of the total costs of the State Guarantees Program for Provision of Free Medical Care to Citizens.Conclusion. Despite the rationality of the proposed changes in the field of improving access to medicine provision concerning cancer drugs and the identified justifications for changing the distribution of financial resources within the State Guarantees Program, there are difficulties. In order to solve this problem, a coordinated consideration of potential strategies to address the access to cancer medicines is needed.
背景。卫生保健的优先事项之一是在财政资源和提供有效医疗保健之间取得平衡。目前获得癌症药物的方法限制了治疗的及时性和可获得性。与此同时,政府的财政支持为抗癌药物提供了巨大的成本。然而,这些巨大的代价是不合理的。目的:通过优化日间医院的功能,评估肿瘤领域医疗财政支持完全转移到强制医疗保险(CHI)系统的资金需求。材料和方法。该目标的实现计划通过消除肿瘤日间医院的异常功能来实现。我们分析了俄罗斯联邦关于药物护理和药物供应的规范性法律文件,以及2021年日间医院住院结构的非个性化(匿名)登记册数据。采用专家评价、数学建模、文献资料分析等方法。该研究开发了一个模型,用于评估将药品供应完全转移到CHI系统所需的资金,包括考虑隐藏的赤字。减少日间住院条件下的不合理住院所释放的资金总额占所分析方案供资水平的2.08%。考虑到2021年肿瘤日间医院的住院数据,在将选定方案转移到门诊阶段的情况下,不合理住院人数将减少16.1%。将所有药物治疗转移到卫生保健基金资助将需要大量额外预算支出,总额为625亿卢布,占向公民提供免费医疗国家保障方案总费用的2.65%。尽管在改善癌症药物提供的可及性方面提出的改革建议是合理的,并且确定了在国家保障方案内改变财政资源分配的理由,但仍存在困难。为了解决这一问题,需要协调考虑解决获得癌症药物问题的潜在战略。
{"title":"Improving the efficiency of the medicine provision system for patients with malignant neoplasms","authors":"Y. Agafonova, D. Fedyaev, A. Snegovoy, V. Omelyanovskiy","doi":"10.17749/2070-4909/farmakoekonomika.2022.137","DOIUrl":"https://doi.org/10.17749/2070-4909/farmakoekonomika.2022.137","url":null,"abstract":"Background. One of the priorities of health care is the balance between the financial resources and the availability of effective medical care. The current approach of access to cancer medicines limits the timeliness and availability of treatment. At the same time, financial support from the government provides great costs on cancer drugs. However, these great costs are not rational.Objective: to assess the financing needs of the complete transfer of financial support of medical care in the field of oncology to the Compulsory Health Insurance (CHI) system by means of optimizing the functions of the day hospital.Material and methods. The achievement of the goal is planned to be reached by eliminating the unusual functions of oncological day hospital. We analyzed the regulatory legal documents regulating drug care and drug provision in the Russian Federation, data from depersonalized (anonymized) registers of the structure of hospitalizations in a day hospital for 2021. The methods of expert assessments, mathematical modeling, as well as literature data analysis were used. The study developed a model for assessing the need to finance the full transfer of medicine provision to the CHI system, including taking into account the hidden deficit.Results. The total amount of funds released from the reduction of irrational hospitalizations in day hospital conditions amounted to 2.08% of the funding level of the analyzed schemes. Taking into account the data of hospitalizations in oncological day hospital for 2021, the number of irrational hospitalizations in case of transfer of selected schemes to the outpatient stage will decrease by 16.1%. The transfer of all the medicine therapy to financing from the CHI funds will require significant additional budget expenditures in the amount of 62.5 billion rubles or 2.65% of the total costs of the State Guarantees Program for Provision of Free Medical Care to Citizens.Conclusion. Despite the rationality of the proposed changes in the field of improving access to medicine provision concerning cancer drugs and the identified justifications for changing the distribution of financial resources within the State Guarantees Program, there are difficulties. In order to solve this problem, a coordinated consideration of potential strategies to address the access to cancer medicines is needed.","PeriodicalId":36464,"journal":{"name":"Farmakoekonomika","volume":"24 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-07-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75036032","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pharmacoeconomic study of the treatment of arterial hypertension in children and adolescents using cost-of-illness analysis 使用疾病成本分析对儿童和青少年动脉高血压治疗进行药物经济学研究
Q3 Medicine Pub Date : 2022-07-27 DOI: 10.17749/2070-4909/farmakoekonomika.2022.123
O. S. Mikhaylova, A. V. Krikova
Background. The cost-of-illness (COI) analysis allows to estimate and plan costs for calculations between the subjects of the health care system and medical insurance organizations. The primary morbidity of the population with diseases of the circulatory system increased from 4,784 thousand people in 2018 to 5,136 thousand in 2019. A growth in the number of cases resulted in an increase in the demand for drugs for the treatment of cardiovascular diseases.Objective: to perform a pharmacoeconomic study of the treatment of arterial hypertension in children and adolescents by COI-analysis.Material and methods. The source of information for COI-analysis was the real clinical practice – medical records of sick children and adolescents. A pharmacoeconomic study using COI-analysis was carried out at the inpatient and outpatient stages of care and included the calculation of direct medical costs (the costs of laboratory, instrumental medical services, non-drug and drug antihypertensive therapy). The study included 102 children diagnosed with arterial hypertension. The average stay of patients in the hospital was 10 (10.4±0.35) bed-days and treatment on an outpatient basis varied from 3 months to 1 year.Results. The leading place in the structure of costs for antihypertensive therapy is occupied by the beta-blockers pharmacological group (35%). The total cost of arterial hypertension in children and adolescents in inpatient and outpatient settings was 4,459.00 and 29,638.90 rubles, respectively.Conclusion. The COI-analysis of arterial hypertension confirms the need for timely diagnosis and treatment and preventive measures for high blood pressure in children and adolescents to reduce the development of risk factors for such serious cardiovascular complications as stroke and myocardial infarction in adulthood, the treatment of which requires large cash costs.
背景。疾病成本(COI)分析允许估算和计划医疗保健系统和医疗保险组织主体之间的计算成本。循环系统疾病患者的原发性发病率从2018年的478.4万人增加到2019年的513.6万人。病例数量的增加导致对治疗心血管疾病的药物的需求增加。目的:应用coi分析对儿童和青少年高血压的治疗进行药物经济学研究。材料和方法。coi分析的信息来源是真实的临床实践-患病儿童和青少年的医疗记录。在住院和门诊阶段进行了一项使用coi分析的药物经济学研究,包括直接医疗费用的计算(实验室、仪器医疗服务、非药物和药物降压治疗的费用)。该研究包括102名被诊断为动脉高血压的儿童。患者平均住院时间为10(10.4±0.35)个床日,门诊治疗时间从3个月到1年不等。在降压治疗的费用结构中占主导地位的是受体阻滞剂药理学组(35%)。儿童和青少年动脉高血压在住院和门诊的总费用分别为4,459.00卢布和29,638.90卢布。动脉高血压的coi分析证实,儿童和青少年的高血压需要及时诊断和治疗,并采取预防措施,以减少成年后中风和心肌梗死等严重心血管并发症的危险因素的发展,这些疾病的治疗需要大量的现金成本。
{"title":"Pharmacoeconomic study of the treatment of arterial hypertension in children and adolescents using cost-of-illness analysis","authors":"O. S. Mikhaylova, A. V. Krikova","doi":"10.17749/2070-4909/farmakoekonomika.2022.123","DOIUrl":"https://doi.org/10.17749/2070-4909/farmakoekonomika.2022.123","url":null,"abstract":"Background. The cost-of-illness (COI) analysis allows to estimate and plan costs for calculations between the subjects of the health care system and medical insurance organizations. The primary morbidity of the population with diseases of the circulatory system increased from 4,784 thousand people in 2018 to 5,136 thousand in 2019. A growth in the number of cases resulted in an increase in the demand for drugs for the treatment of cardiovascular diseases.Objective: to perform a pharmacoeconomic study of the treatment of arterial hypertension in children and adolescents by COI-analysis.Material and methods. The source of information for COI-analysis was the real clinical practice – medical records of sick children and adolescents. A pharmacoeconomic study using COI-analysis was carried out at the inpatient and outpatient stages of care and included the calculation of direct medical costs (the costs of laboratory, instrumental medical services, non-drug and drug antihypertensive therapy). The study included 102 children diagnosed with arterial hypertension. The average stay of patients in the hospital was 10 (10.4±0.35) bed-days and treatment on an outpatient basis varied from 3 months to 1 year.Results. The leading place in the structure of costs for antihypertensive therapy is occupied by the beta-blockers pharmacological group (35%). The total cost of arterial hypertension in children and adolescents in inpatient and outpatient settings was 4,459.00 and 29,638.90 rubles, respectively.Conclusion. The COI-analysis of arterial hypertension confirms the need for timely diagnosis and treatment and preventive measures for high blood pressure in children and adolescents to reduce the development of risk factors for such serious cardiovascular complications as stroke and myocardial infarction in adulthood, the treatment of which requires large cash costs.","PeriodicalId":36464,"journal":{"name":"Farmakoekonomika","volume":"141 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-07-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80084655","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Pharmacoeconomic analysis of the use of a fixed combination of tiotropium bromide and olodaterol as maintenance therapy in patients with chronic obstructive pulmonary disease in the Russian Federation 俄罗斯联邦慢性阻塞性肺病患者使用噻托溴铵和奥替特罗固定组合维持治疗的药物经济学分析
Q3 Medicine Pub Date : 2022-07-13 DOI: 10.17749/2070-4909/farmakoekonomika.2022.144
S. Zyryanov, I. Dyakov
Objective: to evaluate the pharmacoeconomic effectiveness of the use of a fixed double combination of tiotropium bromide + olodаterol in order to treat chronic obstructive pulmonary disease (COPD) in comparison with less expensive monotherapy with long-acting beta-2agonists (LABA) or long-acting anticholinergics (LAAC) with its insufficient effectiveness.Material and methods. The analysis of the impact on the health care system budget of the use of a fixed double chemical combination was carried out. The combination used was the one of tiotropium bromide + olodаterol in patients suffering from COPD who do not achieve effective disease control during LABA or LAAC monotherapy. We used published data on the distribution of patients into groups according to the classification of the Global Initiative for Chronic Obstructive Lung Disease (GOLD), also according to the therapy used and the frequency of exacerbations with hospitalization, obtained in a Russian epidemiological study. Direct and indirect costs associated with basic therapy and treatment of exacerbations requiring hospitalization were estimated as well.Results. Previously, it was shown that about 21.8% of patients with GOLD D severity of COPD receive therapy of insufficient efficacy (LABA monotherapy or long-acting M-cholinolytics). The use of a fixed combination of tiotropium bromide + olodaterol in such patients instead of monotherapy will reduce the direct costs of hospitalization by 21.1%, and the total costs (direct and indirect) – by 4.6%. On the scale of the Russian Federation, this will save 17.2 billion rubles a year.Conclusion. The results obtained showed that, despite the reasonably high cost of a fixed double combination in comparison with monopreparations, the use of double bronchodilating therapy allows to achieve more effective treatment and reduces both direct medical costs associated with hospitalization of patients with exacerbations of COPD, and direct non-medical and indirect costs associated with absenteeism of patients to work due to temporary disability as a result of hospitalization.
目的:评价噻托溴铵+榄叶甾醇固定双联用治疗慢性阻塞性肺疾病(COPD)的药物经济学效果,并与长效β -2激动剂(LABA)或长效抗胆碱能药(LAAC)单药治疗效果不足的情况进行比较。材料和方法。分析了使用固定双化学组合物对卫生保健系统预算的影响。对于在LABA或LAAC单药治疗期间未获得有效疾病控制的COPD患者,所使用的组合是噻托溴铵+ olodterol。我们根据俄罗斯流行病学研究中获得的全球慢性阻塞性肺疾病倡议(GOLD)的分类,以及所使用的治疗方法和住院时病情加重的频率,使用了关于患者分组分布的已发表数据。与基础治疗和需要住院治疗的恶化相关的直接和间接费用也进行了估计。先前的研究表明,约21.8%的GOLD D严重程度的COPD患者接受的治疗效果不足(LABA单药治疗或长效m -胆碱解药)。在这类患者中使用噻托溴铵+奥替特罗的固定组合代替单一治疗将使住院的直接费用降低21.1%,总费用(直接和间接)降低4.6%。以俄罗斯联邦的规模来看,这将每年节省172亿卢布。所获得的结果表明,尽管与单一手术相比,固定双重联合手术的成本相当高,但使用双重支气管扩张治疗可以实现更有效的治疗,并降低与COPD加重患者住院相关的直接医疗成本,以及与患者因住院而暂时残疾而缺勤相关的直接非医疗和间接成本。
{"title":"Pharmacoeconomic analysis of the use of a fixed combination of tiotropium bromide and olodaterol as maintenance therapy in patients with chronic obstructive pulmonary disease in the Russian Federation","authors":"S. Zyryanov, I. Dyakov","doi":"10.17749/2070-4909/farmakoekonomika.2022.144","DOIUrl":"https://doi.org/10.17749/2070-4909/farmakoekonomika.2022.144","url":null,"abstract":"Objective: to evaluate the pharmacoeconomic effectiveness of the use of a fixed double combination of tiotropium bromide + olodаterol in order to treat chronic obstructive pulmonary disease (COPD) in comparison with less expensive monotherapy with long-acting beta-2agonists (LABA) or long-acting anticholinergics (LAAC) with its insufficient effectiveness.Material and methods. The analysis of the impact on the health care system budget of the use of a fixed double chemical combination was carried out. The combination used was the one of tiotropium bromide + olodаterol in patients suffering from COPD who do not achieve effective disease control during LABA or LAAC monotherapy. We used published data on the distribution of patients into groups according to the classification of the Global Initiative for Chronic Obstructive Lung Disease (GOLD), also according to the therapy used and the frequency of exacerbations with hospitalization, obtained in a Russian epidemiological study. Direct and indirect costs associated with basic therapy and treatment of exacerbations requiring hospitalization were estimated as well.Results. Previously, it was shown that about 21.8% of patients with GOLD D severity of COPD receive therapy of insufficient efficacy (LABA monotherapy or long-acting M-cholinolytics). The use of a fixed combination of tiotropium bromide + olodaterol in such patients instead of monotherapy will reduce the direct costs of hospitalization by 21.1%, and the total costs (direct and indirect) – by 4.6%. On the scale of the Russian Federation, this will save 17.2 billion rubles a year.Conclusion. The results obtained showed that, despite the reasonably high cost of a fixed double combination in comparison with monopreparations, the use of double bronchodilating therapy allows to achieve more effective treatment and reduces both direct medical costs associated with hospitalization of patients with exacerbations of COPD, and direct non-medical and indirect costs associated with absenteeism of patients to work due to temporary disability as a result of hospitalization.","PeriodicalId":36464,"journal":{"name":"Farmakoekonomika","volume":"19 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-07-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"72515530","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The current state of the veterinary drugs market in Tyumen Region 秋明地区兽药市场现状
Q3 Medicine Pub Date : 2022-06-02 DOI: 10.17749/2070-4909/farmakoekonomika.2022.133
V. V. Byshenko, О. I. Knysh, L. N. Zadirachenko, А. О. Egorova, Yu. S. Rodina
Objective: to assess the current state of the veterinary medical product market in the Tyumen Region.Material and methods. The objects of the study included data from the State Register of Medicinal Products for Veterinary Use for 2019–2022; veterinary pharmacy organizations and veterinary clinics in the Tyumen Region (33); price lists of veterinary pharmaceutical organizations; questionnaires of veterinary specialists (69) and consumers of medicinal products for veterinary use (93).Results. An analysis of the Register of Medicinal Products for Veterinary Use registered in the Russian Federation revealed a positive trend in the registration of new positions: with 2190 registered drugs about 300 more positions are registered annually. It was determined that the ratio of veterinary drugs of various pharmacotherapeutic groups is critically uneven (31.05% – antibacterial agents; 28% – immunobiological drugs; 0.46% – cardiovascular drugs; 0.14% – antitumor drugs). The study of the wholesale segment of the veterinary drugs market on the territory of the Tyumen Region showed that the range of wholesale trade organizations in veterinary drugs mainly consists of products for animals (at the largest one veterinary drugs account for only 16%). As a result, low indicators of the assortment are observed (breadth and completeness coefficients for pharmacotherapeutic groups), and there are problems with the availability of veterinary drugs. The analysis of the assortment of veterinary pharmaceutical organizations and clinics (retail segment of the market) revealed low breadth coefficients for medicinal products for veterinary use (median 0.09). A sociological survey showed a low level of awareness of all veterinary drugs consumer groups about the scope of their circulation.Conclusion. The study of the current state of the veterinary medicinal product market in the Tyumen Region identified the problems of their availability both in the wholesale and retail segments, which need to be addressed with the help of state regulation (including the introduction of a minimum range of drugs for veterinary use) and normalization of the assortment policy at the level of veterinary pharmacies and clinics. Because of the lack of registration for some drugs necessary for the treatment of animals, veterinarians are forced to put into practice drugs for medical use, deliberately violating the law. Given the experience of many foreign countries, we consider it expedient to allow the use (in special cases) of medical drugs in veterinary medicine. This will solve the problem of pharmacotherapy availability and allow veterinarians to provide better care to animals.
目的:了解秋明地区兽药市场现状。材料和方法。该研究的对象包括2019-2022年国家兽医用药品登记处的数据;秋明地区兽药组织和兽医诊所(33个);兽药机构价目表;兽医专家(69人)和兽药消费者(93人)的问卷调查。对在俄罗斯联邦注册的兽医用医药产品登记册进行的分析显示,在新职位的注册方面出现了积极的趋势:有2190种注册药物,每年约有300多个职位注册。结果表明,各药物治疗组兽药占比极不均匀(31.05% -抗菌药物;28% -免疫生物药物;心血管药物0.46%;0.14% -抗肿瘤药物)。对秋明地区兽药批发市场的研究表明,兽药批发贸易组织的范围主要由动物产品组成(兽药最大仅占16%)。因此,观察到分类的低指标(药物治疗组的宽度和完整性系数),并且兽药的可获得性存在问题。兽药组织和诊所(市场零售部分)分类的分析显示,兽药产品的宽度系数较低(中位数为0.09)。一项社会学调查显示,所有兽药消费群体对其流通范围的认识水平较低。对秋明地区兽药产品市场现状的研究确定了批发和零售领域的兽药供应问题,这些问题需要通过国家监管(包括引入兽药的最低范围)和兽药药房和诊所分类政策的正常化来解决。由于一些治疗动物所必需的药物没有注册,兽医被迫行医,故意违反法律。鉴于许多国外的经验,我们认为允许(在特殊情况下)在兽药中使用药物是权宜之计。这将解决药物治疗可用性的问题,并允许兽医为动物提供更好的护理。
{"title":"The current state of the veterinary drugs market in Tyumen Region","authors":"V. V. Byshenko, О. I. Knysh, L. N. Zadirachenko, А. О. Egorova, Yu. S. Rodina","doi":"10.17749/2070-4909/farmakoekonomika.2022.133","DOIUrl":"https://doi.org/10.17749/2070-4909/farmakoekonomika.2022.133","url":null,"abstract":"Objective: to assess the current state of the veterinary medical product market in the Tyumen Region.Material and methods. The objects of the study included data from the State Register of Medicinal Products for Veterinary Use for 2019–2022; veterinary pharmacy organizations and veterinary clinics in the Tyumen Region (33); price lists of veterinary pharmaceutical organizations; questionnaires of veterinary specialists (69) and consumers of medicinal products for veterinary use (93).Results. An analysis of the Register of Medicinal Products for Veterinary Use registered in the Russian Federation revealed a positive trend in the registration of new positions: with 2190 registered drugs about 300 more positions are registered annually. It was determined that the ratio of veterinary drugs of various pharmacotherapeutic groups is critically uneven (31.05% – antibacterial agents; 28% – immunobiological drugs; 0.46% – cardiovascular drugs; 0.14% – antitumor drugs). The study of the wholesale segment of the veterinary drugs market on the territory of the Tyumen Region showed that the range of wholesale trade organizations in veterinary drugs mainly consists of products for animals (at the largest one veterinary drugs account for only 16%). As a result, low indicators of the assortment are observed (breadth and completeness coefficients for pharmacotherapeutic groups), and there are problems with the availability of veterinary drugs. The analysis of the assortment of veterinary pharmaceutical organizations and clinics (retail segment of the market) revealed low breadth coefficients for medicinal products for veterinary use (median 0.09). A sociological survey showed a low level of awareness of all veterinary drugs consumer groups about the scope of their circulation.Conclusion. The study of the current state of the veterinary medicinal product market in the Tyumen Region identified the problems of their availability both in the wholesale and retail segments, which need to be addressed with the help of state regulation (including the introduction of a minimum range of drugs for veterinary use) and normalization of the assortment policy at the level of veterinary pharmacies and clinics. Because of the lack of registration for some drugs necessary for the treatment of animals, veterinarians are forced to put into practice drugs for medical use, deliberately violating the law. Given the experience of many foreign countries, we consider it expedient to allow the use (in special cases) of medical drugs in veterinary medicine. This will solve the problem of pharmacotherapy availability and allow veterinarians to provide better care to animals.","PeriodicalId":36464,"journal":{"name":"Farmakoekonomika","volume":"24 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-06-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"74296244","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Farmakoekonomika
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1