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The relationship between uric acid concentration and cardiovascular risk: Retrospective analysis of patients on hemodialysis 尿酸浓度与心血管风险的关系:血液透析患者的回顾性分析
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2019-01-01 DOI: 10.5937/arhfarm1905323r
A. Radovic, N. Milinković, M. Stosovic, V. Dopsaj, S. Ignjatović
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引用次数: 2
Water for pharmaceutical use: Importance, types and quality requirements 制药用水:重要性、类型和质量要求
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2019-01-01 DOI: 10.5937/arhfarm1902090q
B. Čalija, D. Krajišnik, J. Milić
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引用次数: 0
Challenges of in vitro characterization of nonbiological complex drugs: Example of parenteral preparations with liposomal drug carriers 非生物复合药物体外表征的挑战:以脂质体药物载体的肠外制剂为例
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2019-01-01 DOI: 10.5937/arhfarm1903176k
D. Krajišnik, J. Milić, S. Savić
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引用次数: 0
Childhood vaccination in the twenty-first century: Parental concerns and challenges for physicians 21世纪的儿童疫苗接种:父母对医生的关注和挑战
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2019-01-01 DOI: 10.5937/arhfarm1906452j
S. Janković
Vaccination is one of the most important methods of prevention of infectious disease, saving millions of lives worldwide and protecting people from potentially debilitating complications. It is therefore hailed as one of the greatest advances of science-based medicine of all times. Although repeatedly proven safe and effective, vaccination has been questioned and resented throughout its long history. Vaccine hesitancy and refusal are once again on the rise in this century, due to a complex interplay of numerous factors and circumstances. A decline in childhood vaccination rates has already resulted in resurgence of hitherto eliminated vaccinepreventable diseases in many countries, and is now perceived as a major public health threat. This decline is closely related to increasing spread of misinformation regarding vaccine safety and effectiveness, coupled with a growing anti-vaccine activism. This, among other issues, underscores the need to improve communication between healthcare workers and parents, as well as devise a more comprehensive approach to boosting vaccine confidence, where scientists, physicians, media and the general public all have important roles to play. In this paper, we discuss the phenomenology and causal structure of vaccine hesitancy and refusal, and briefly review some widespread vaccine-related questions of everyday practical importance.
疫苗接种是预防传染病的最重要方法之一,在全世界挽救了数百万人的生命,并保护人们免受可能使人衰弱的并发症的侵害。因此,它被誉为有史以来以科学为基础的医学最伟大的进步之一。尽管一再证明疫苗接种是安全有效的,但在其漫长的历史中,疫苗接种一直受到质疑和憎恨。由于众多因素和情况的复杂相互作用,本世纪对疫苗的犹豫和拒绝再次上升。儿童疫苗接种率的下降已经导致迄今已被消灭的疫苗可预防疾病在许多国家死灰复燃,现在被视为一个重大的公共卫生威胁。这一下降与关于疫苗安全性和有效性的错误信息日益传播以及反疫苗活动日益增加密切相关。除其他问题外,这突出表明需要改善卫生保健工作者和家长之间的沟通,并设计一种更全面的方法来增强疫苗信心,在这方面,科学家、医生、媒体和公众都可以发挥重要作用。在本文中,我们讨论了疫苗犹豫和拒绝的现象学和因果结构,并简要回顾了一些在日常实践中具有重要意义的广泛的疫苗相关问题。
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引用次数: 0
Antifungal activity of the esssential oil of Seseli rigidum Waldst. & Kit. (Apiaceae) on the growth of isolates of Candida albicans 山参精油的抗真菌活性研究。和装备。(蜂科)白色念珠菌分离株生长的研究
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2019-01-01 DOI: 10.5937/arhfarm1902067x
M. Marčetić, D. Božić, M. Milenković, Mirjana Kovačević, N. Kovačević
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引用次数: 0
Novel pharmaceutical dosage forms of analgesics 镇痛药的新剂型
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2019-01-01 DOI: 10.5937/ARHFARM1806054D
Ljiljana Đekić, M. Primorac
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引用次数: 0
The role of pharmacists in the management of certain common acute pain states 药师在某些常见急性疼痛状态管理中的作用
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2019-01-01 DOI: 10.5937/arhfarm1901015m
A. Micov, M. Tomić
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引用次数: 0
Opioids and adjuvant analgesics in current treating of pain 阿片类药物和辅助镇痛药在当前疼痛治疗中的应用
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2019-01-01 DOI: 10.5937/ARHFARM1806009S
R. Stepanović-Petrović, M. Tomić
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引用次数: 0
Providing clinical evidence under the MDR 2017/745: New challenges for manufacturers in medical device industry 根据MDR 2017/745提供临床证据:医疗器械行业制造商面临的新挑战
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2019-01-01 DOI: 10.5937/arhfarm1901039i
Elena Ivanovska, Jasmina Tonic-Ribarska, Jelena Lazova, Nada Popstefanova, Marija Davcheva-Jovanoska, S. Trajković-Jolevska
Summary Providing necessary clinical evidence throughout the systems for Clinical Evaluation and Post-Market Surveillance in accordance with new MDR 2017/745 requirements imposes new challenges for manufacturers in medical device industry. Manufacturers should make clinical evaluation a continuous process that summarizes findings and results from several mutually connected processes: PMS, vigilance, CIs. Gathered clinical evidence should also be used as input for SSCP, PSUR, CEAR. CIs should be designed, authorised, conducted, recorded and reported in accordance with provisions of Articles 62-81 and Annex XV. PMS and PMCF activities should provide appropriate evidence of planning, implementation of protocol and reporting; target residual risks and confirm safety and performance over device’s lifetime; include activities that address specific questions/residual risks. All activities are aimed towards several goals: improving quality, safety and reliability of devices and strengthening transparency of information for consumers.
根据新的MDR 2017/745要求,在整个系统中为临床评估和上市后监测提供必要的临床证据,给医疗器械行业的制造商带来了新的挑战。制造商应使临床评价成为一个持续的过程,总结几个相互关联的过程的发现和结果:经前症候群、警惕性、CIs。收集到的临床证据也应作为SSCP、PSUR、ear的输入。ci应按照第62-81条和附件十五的规定设计、批准、实施、记录和报告。PMS和PMCF活动应提供适当的规划、实施方案和报告的证据;确定剩余风险并确认设备使用寿命内的安全性和性能;包括处理特定问题/剩余风险的活动。所有活动都旨在实现几个目标:提高设备的质量、安全性和可靠性,加强消费者信息的透明度。
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引用次数: 3
Significance of glycosylated haemoglobin determination for the assessment of lower-extremity amputation risk in patients with diabetic foot 糖化血红蛋白测定对糖尿病足患者下肢截肢风险评估的意义
Q4 Pharmacology, Toxicology and Pharmaceutics Pub Date : 2019-01-01 DOI: 10.5937/arhfarm1902051x
T. Stefanović, S. Bosić, J. Vekić, V. Spasojević-Kalimanovska, V. Todorovic, Marina Pijanović, A. Zeljković, A. Stefanović, Z. Jelić-Ivanović
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引用次数: 0
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Arhiv za Farmaciju
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