伊朗COVID-19治疗与当地治疗建议的比较评估:一项关于处方药使用和成本的人口水平研究。

IF 0.8 Q4 PHARMACOLOGY & PHARMACY Journal of Research in Pharmacy Practice Pub Date : 2022-08-18 eCollection Date: 2022-01-01 DOI:10.4103/jrpp.jrpp_6_22
Amir Hashemi-Meshkini, Reza Koochak, Shekoufeh Nikfar, Ehsan Rezaei-Darzi, Saeed Yaghoubifard
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引用次数: 0

摘要

目的:在本研究中,我们将伊朗COVID-19治疗的人口水平数据与卫生部(MOH)公布的指南进行比较,以更好地了解这种疾病的护理质量。方法:采用2020年3月21日至2021年3月21日或伊朗年1399年期间全国各推荐和非推荐COVID-19药物的销售数据进行代理使用。根据新冠肺炎前的平均增长率、推荐剂量和治疗时间调整销售数据,估算新冠肺炎相关销售额和患者人数。接下来,将它们与卫生部门诊和住院指导方针进行比较。提取市场前10大分子和价值前10大COVID-19指示分子清单,评估COVID-19处方药的经济负担及其份额。结果:门诊接受羟氯喹等推荐药物治疗的患者估计超过220万。法匹拉韦和瑞德西韦两种住院药物共26万;然而,这两种药物都没有在卫生部指南中推荐。在地塞米松、强的松龙、阿奇霉素、萘普生等特异性较弱的药物中,估计的新冠肺炎患者数与研究年度官方公布的确诊病例数无法比较,这可能与未确诊病例、不合理使用或处方有关,也可能与我们的数据和研究的局限性有关。covid -19相关候选药物的总市场超过15万亿里亚尔(几乎占总市场的4.3%)。Remdesivir占COVID-19总市场的60%以上,其次是favipiravir,是价值最高的药物之一。结论:尽管伊朗卫生部发布了COVID-19指南,但执行决定的不一致是一个严重的弱点(favipiravir和remdesivir的案例)。这一弱点给卫生保健系统带来了一些经济负担,并引发了伦理问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Evaluation of COVID-19 Treatments in Iran in Comparison with Local Therapeutic Recommendations: A Population-Level Study on Utilization and Costs of Prescription Drugs.

Objective: In this study, we assess population-level data of COVID-19 treatments in Iran compared to Ministry of Health (MOH)-published guidelines to gain a better insight into the quality of care for this disease.

Methods: National sales data of each recommended and nonrecommended COVID-19 medicine were used to proxy utilization between March 21, 2020, and March 21, 2021, or Iranian year 1399. COVID-19-attributed sales volume and number of patients were estimated by adjusting sales data with pre-COVID-19 average growth rate, recommended dose, and duration of treatment. Next, they were compared with the MOH guidelines in outpatient and inpatient settings. Furthermore, the list of top 10 molecules of the market and top 10 COVID-19-indicated molecules in terms of values were extracted to assess the economic burden of COVID-19 prescription drugs and their share.

Findings: The estimated number of patients receiving COVID-19 treatments in some outpatient medicines such as recommended hydroxychloroquine was over 2.2 million. Favipiravir and remdesivir were collectively about two inpatient medicines 260,000; however, neither of these two medicines was recommended in the MOH guidelines. In some fewer specific medicines such as dexamethasone, prednisolone, azithromycin, and naproxen, the estimated number of COVID-19-attributed patients were incomparable with the officially announced number of confirmed cases in the year of study, which could be related to nonconfirmed diagnosed cases, irrational use, or prescribing, or limitations of our data and study. The total COVID-19-attributed market of candidate medicines was over 15 trillion IR Rials (almost 4.3% of the total market). Remdesivir, with over 60% of the total COVID-19 attributed market, followed by favipiravir, was among the highest value medicines.

Conclusion: Despite the release of the COVID-19 guideline by Iran MOH, misalignment in the enforcement of decisions was a serious weakness (cases of favipiravir and remdesivir). This weakness led to some economic burden on the health-care system and raised ethical concerns.

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来源期刊
Journal of Research in Pharmacy Practice
Journal of Research in Pharmacy Practice PHARMACOLOGY & PHARMACY-
自引率
0.00%
发文量
8
审稿时长
21 weeks
期刊介绍: The main focus of the journal will be on evidence-based drug-related medical researches (with clinical pharmacists’ intervention or documentation), particularly in the Eastern Mediterranean region. However, a wide range of closely related issues will be also covered. These will include clinical studies in the field of pharmaceutical care, reporting adverse drug reactions and human medical toxicology, pharmaco-epidemiology and toxico-epidemiology (poisoning epidemiology), social aspects of pharmacy practice, pharmacy education and economic evaluations of treatment protocols (e.g. cost-effectiveness studies). Local reports of medication utilization studies at hospital or pharmacy levels will only be considered for peer-review process only if they have a new and useful message for the international pharmacy practice professionals and readers.
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