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Effectiveness of Megestrol for the Treatment of Patients with Atypical Endometrial Hyperplasia or Endometrial Endometrioid Adenocarcinoma (Stage IA, Well Differentiated). 甲地孕酮治疗不典型子宫内膜增生或子宫内膜样腺癌(IA期,高分化)的疗效。
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2021-12-25 eCollection Date: 2021-07-01 DOI: 10.4103/jrpp.JRPP_20_128
Setareh Akhavan, Fahimeh Sabet, Azam-Sadat Mousavi, Mitra Modarres Gilani, Shahrzad Sheikh Hasani

Objective: We aimed to evaluate treatment responses and recurrence rate of atypical endometrial hyperplasia (AEH) and endometrial endometrioid adenocarcinoma (EA) with Stage IA Grade 1 to megestrol in Iranian patients who are candidates for medical treatments.

Methods: In a retrospective cohort study that was conducted on 50 patients with AEH and 22 patients with EA who were referred to the oncology clinic of Imam Khomeini Hospital, Tehran, Iran, during 2006-2016, we recruited all patients with AEH or EA of Stage IA Grade 1 and their disease was diagnosed during endometrial curettage with or without hysteroscopy. Patients were initially treated with 160 mg of megestrol daily, along with aspirin up to 3 months, and then after 3-4 weeks of discharge of the drugs, patients underwent curettage with hysteroscopy.

Findings: The patients with AEH had 31 complete responses and five progressive diseases, and the patients with EA had seven complete responses and seven progressive diseases. After treatment, 25 cases with AEH and 5 cases with EA had an intention to get pregnant, whereas eight patients with AEH and 1 case with endometrial cancer became pregnant. Recurrence occurred in the 2 cases with AEH and 2 cases with endometrial cancer which the time of recurrence in the patients with AEH was longer than in patients with endometrial cancer (P = 0.011).

Conclusion: Megestrol is an effective therapeutic agent in endometrial hyperplasia or low-grade endometrial cancer patients who are willing to conserve their childbearing.

目的:我们的目的是评估不典型子宫内膜增生(AEH)和子宫内膜异构体腺癌(EA)的治疗效果和复发率与子宫内膜异构体腺癌(IA期1级)的伊朗患者的候选药物治疗。方法:回顾性队列研究2006-2016年在伊朗德黑兰伊玛目霍梅尼医院肿瘤学门诊转诊的50例AEH和22例EA患者,我们招募了所有在子宫内膜刮除术中诊断为IA期1级的AEH或EA患者,有或没有宫腔镜检查。患者最初每日服用160毫克甲孕酮,同时服用阿司匹林长达3个月,然后在药物停用3-4周后,患者接受宫腔镜刮除。结果:AEH患者完全缓解31例,疾病进展5例;EA患者完全缓解7例,疾病进展7例。治疗后,AEH患者有25例,EA患者有5例,AEH患者有8例,子宫内膜癌患者有1例妊娠。2例AEH患者和2例子宫内膜癌患者均出现复发,且AEH患者的复发时间较子宫内膜癌患者长(P = 0.011)。结论:甲地孕酮是一种治疗子宫内膜增生或低度子宫内膜癌的有效药物。
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引用次数: 0
Homocysteine-Lowering Interventions in Chronic Kidney Disease. 降低同型半胱氨酸干预慢性肾脏疾病。
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2021-12-25 eCollection Date: 2021-07-01 DOI: 10.4103/jrpp.jrpp_75_21
Shirinsadat Badri, Sahar Vahdat, Shiva Seirafian, Morteza Pourfarzam, Tahereh Gholipur-Shahraki, Sara Ataei

The incidence of cardiovascular events and mortality is higher in patients with chronic kidney disease (CKD) compared to the general population. Homocysteine (Hcy) appears to be an independent risk factor for cardiovascular diseases in general populations and patients with CKD. Further, hyperhomocysteinemia can cause endothelial damage and increase the activity and production of coagulation factors, and its prevalence among patients with end-stage renal disease is approximately 85%-100%. Most treatments, which lower Hcy levels and have been considered in previous studies, include folic acid, B vitamins, omega-3 fatty acids, and N-acetylcysteine. However, the effect of therapies that can decrease Hcy levels and thus cardiovascular events in these patients is still unclear. The results are conflicting and require further investigation. To guide treatment decisions and improve patient outcomes, multiple databases were searched, including Web of Science, PubMed, and Medline to summarize the available evidence (i.e., clinical trial and meta-analyses) on Hcy-lowering interventions and cardiovascular events.

与一般人群相比,慢性肾脏疾病(CKD)患者的心血管事件发生率和死亡率更高。同型半胱氨酸(Hcy)似乎是普通人群和CKD患者心血管疾病的独立危险因素。此外,高同型半胱氨酸血症可引起内皮损伤,增加凝血因子的活性和产生,其在终末期肾病患者中的患病率约为85%-100%。大多数降低Hcy水平的治疗方法包括叶酸、B族维生素、omega-3脂肪酸和n -乙酰半胱氨酸。然而,在这些患者中降低Hcy水平和心血管事件的治疗效果仍不清楚。结果是相互矛盾的,需要进一步调查。为了指导治疗决策和改善患者预后,我们检索了多个数据库,包括Web of Science、PubMed和Medline,以总结关于降低hcy干预和心血管事件的现有证据(即临床试验和荟萃分析)。
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引用次数: 6
A Safety Evaluation of Midazolam use for Nasogastric Tube Placement. 咪达唑仑用于鼻胃管置入的安全性评价。
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2021-12-25 eCollection Date: 2021-07-01 DOI: 10.4103/jrpp.jrpp_78_21
Jenna B Wells, David H Murman, Alison L Sullivan

Objective: Nasogastric tube (NGT) insertion is one of the most painful procedures in the emergency department (ED). A recent study determined that giving intravenous (IV) midazolam before NGT insertion decreased patients' pain; however, the sample size was insufficient to draw the conclusions on safety. We conducted a retrospective chart review of patients who received IV midazolam for NGT insertion to determine the frequency of adverse events.

Methods: All patients treated at a Level 1 trauma center ED from June 2016 to June 2019 who received IV midazolam for NGT insertion were included. The medical records were screened for the following serious adverse events: hypoxia, respiratory suppression, excessive somnolence/sedation, hemodynamic instability, epistaxis, vomiting, and choking. Adverse events, patient demographics, chief complaint, diagnosis, disposition, number of midazolam administrations, dose per administration, and total dose were recorded for the analysis.

Findings: Three out of 159 participants (2%) were identified as having an adverse event. In two cases, the adverse event was hypoxia, which was corrected with the administration of supplemental oxygen through nasal cannula. The third adverse event was somnolence noted in a patient who was also hypotensive and in atrial fibrillation around the time of midazolam administration.

Conclusion: It is safe to premedicate patients with midazolam before NGT insertions. Patients with borderline oxygen saturation and those receiving opioid analgesics may warrant dose titration with close vital sign monitoring.

目的:鼻胃管(NGT)插入是急诊科(ED)最痛苦的手术之一。最近的一项研究表明,在NGT植入前静脉注射咪达唑仑可以减轻患者的疼痛;然而,样本量不足以得出安全性结论。我们对接受静脉咪达唑仑植入NGT的患者进行了回顾性图表回顾,以确定不良事件的频率。方法:纳入2016年6月至2019年6月在一级创伤中心急诊科接受静脉咪达唑仑植入NGT治疗的所有患者。医疗记录筛选以下严重不良事件:缺氧、呼吸抑制、过度嗜睡/镇静、血流动力学不稳定、鼻出血、呕吐和窒息。记录不良事件、患者人口统计、主诉、诊断、处置、咪达唑仑用药次数、每次用药剂量和总剂量进行分析。结果:159名参与者中有3人(2%)被确定有不良事件。在两个病例中,不良事件是缺氧,通过鼻插管给予补充氧来纠正。第三个不良事件是在咪达唑仑给药期间出现低血压和心房颤动的患者嗜睡。结论:在NGT植入前给予咪达唑仑是安全的。临界氧饱和度患者和接受阿片类镇痛药的患者可能需要剂量滴定并密切监测生命体征。
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引用次数: 0
Medical Device-related Counseling Practice and Barriers among Sudanese Pharmacists: A Questionnaire-Based Study. 苏丹药剂师医疗器械相关咨询实践和障碍:一项基于问卷的研究。
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2021-12-25 eCollection Date: 2021-07-01 DOI: 10.4103/jrpp.JRPP_21_32
Ahmed Ibrahim Fathelrahman

Objective: The aim of the present study was to assess medical devices-related counseling practice and barriers among pharmacists.

Methods: This was a cross-sectional study conducted using a convenient sample of Sudanese pharmacists. An online-version survey was used to collect data.

Findings: One hundred and thirty pharmacists responded to the online survey. Most pharmacists in this sample were master or Ph.D. degree holders (62.3% and 12.3%, respectively), having a clinical training experience (70%) and substantial proportion are board-certified (30%). Medical devices reported to be commonly inquired by patients were blood glucose monitors, nebulizers, blood pressure monitors, dry powder inhalers, and insulin pens. Devices most frequently requiring counselling were blood glucose monitors, blood pressure monitors, syringes, thermometers, nebulizers, dry powder inhalers, insulin, and weighing scales. The most frequently supplied devices reported were syringes, blood glucose monitors, insulin pens, blood pressure monitors, thermometers, nebulizers, and dry powder inhalers. Devices least frequently requiring counselling were implanted devices, respirometers, and stethoscopes. The least frequently supplied devices were respirometers, implanted devices, and heart rate monitors.

Conclusion: Medical devices reported to be commonly inquired by patients were most frequently requiring counseling, and most frequently supplied. Findings reflect the availability of devices in the market and pharmacists' response to the needs of their patients. Pharmacists should maintain adequate knowledge about the proper use of medical devices because this is a common patient inquiry.

目的:本研究的目的是评估药师的医疗器械相关咨询实践和障碍。方法:采用苏丹药剂师方便取样的横断面研究。一项在线调查被用来收集数据。结果:130名药剂师回应了在线调查。样本中大部分药师具有硕士或博士学位(分别为62.3%和12.3%),具有临床培训经验(70%),相当比例的药师具有委员会认证(30%)。据报告,患者常询问的医疗设备有血糖监测仪、雾化器、血压监测仪、干粉吸入器和胰岛素笔。最常需要咨询的设备是血糖监测仪、血压监测仪、注射器、体温计、雾化器、干粉吸入器、胰岛素和称重秤。报告中最常供应的设备是注射器、血糖监测器、胰岛素笔、血压监测器、体温计、雾化器和干粉吸入器。最不需要咨询的设备是植入式设备、呼吸计和听诊器。最不常用的设备是呼吸计、植入式设备和心率监测器。结论:患者最常询问的医疗器械是最常需要咨询的,也是最常提供的。调查结果反映了市场上设备的可获得性和药剂师对患者需求的反应。药剂师应该对医疗器械的正确使用保持足够的了解,因为这是一个常见的患者询问。
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引用次数: 0
Cost-Effectiveness and Cost-Utility Analysis of the Use of Clopidogrel and Pantoprazole in Comparison with Clopidogrel and Omeprazole for the Secondary Prevention of Myocardial Infarction in Iran. 氯吡格雷和泮托拉唑与氯吡格雷和奥美拉唑在伊朗心肌梗死二级预防中的成本-效果和成本-效用分析
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2021-08-03 eCollection Date: 2021-04-01 DOI: 10.4103/jrpp.JRPP_21_22
Mohammadreza Amirsadri, Valiollah Hajhashemi, Amir Shahriar Asemi

Objective: Gastrointestinal bleeding, a side effect of clopidogrel, is usually prevented by proton-pump inhibitors (PPIs). Due to omeprazole's inhibitory effects on the liver enzyme CYP2C19, its concomitant use with clopidogrel is argued to increase the risk of myocardial infarction (MI) recurrence, as CYP2C19 activates clopidogrel. Pantoprazole as an alternative PPI has shown no inhibitory effect on CYP2C19. This study investigates the cost-effectiveness of concomitant use of clopidogrel and pantoprazole in MI patients compared to the simultaneous use of clopidogrel and omeprazole.

Methods: We used the Markov-modeling technique with a hypothetical cohort of 1000 acute MI patients aged 55 years using Microsoft Excel 2013 software. The study was done from the payer perspective, and a lifetime horizon with 1-year cycles was considered in the model. Life-years gained (LYG) and quality-adjusted life-years (QALYs) were used to quantify the health effects of these interventions. Two separate scenarios of public tariffs and private tariffs with various discount rates (0%, 3%, and 7.2% discounts (only for costs)) were evaluated, and an incremental cost-effectiveness ratio (ICER) was used to report the results. One-way and probabilistic sensitivity analyses were used to deal with uncertainty. Data were sourced from published literature and tariff book of the Iranian ministry of health.

Findings: The estimated ICERs were 342 USD/QALY and 236 USD/LYG per patient for the base-case scenario.

Conclusion: Abiding by the WHO threshold for cost-effectiveness, the concomitant use of pantoprazole and clopidogrel can be considered cost-effective compared to the use of omeprazole and clopidogrel.

目的:胃肠道出血是氯吡格雷的一个副作用,通常通过质子泵抑制剂(PPIs)来预防。由于奥美拉唑对肝酶CYP2C19有抑制作用,因此与氯吡格雷合用会增加心肌梗死(MI)复发的风险,因为CYP2C19会激活氯吡格雷。泮托拉唑作为替代PPI对CYP2C19无抑制作用。本研究探讨了与同时使用氯吡格雷和奥美拉唑相比,在心肌梗死患者中同时使用氯吡格雷和泮托拉唑的成本-效果。方法:采用markov建模技术,采用Microsoft Excel 2013软件对1000名55岁急性心肌梗死患者进行假设队列分析。本研究是从付款人的角度进行的,模型中考虑了1年周期的生命周期。使用获得生命年(LYG)和质量调整生命年(QALYs)来量化这些干预措施对健康的影响。评估了具有不同贴现率(0%、3%和7.2%折扣(仅针对成本))的公共关税和私人关税两种不同情景,并使用增量成本效益比(ICER)来报告结果。采用单向和概率敏感性分析来处理不确定性。数据来自已出版的文献和伊朗卫生部的关税手册。结果:在基本情况下,每位患者的ICERs估计为342美元/QALY和236美元/LYG。结论:在符合WHO成本-效果阈值的情况下,泮托拉唑和氯吡格雷合用比奥美拉唑和氯吡格雷合用更具成本效益。
{"title":"Cost-Effectiveness and Cost-Utility Analysis of the Use of Clopidogrel and Pantoprazole in Comparison with Clopidogrel and Omeprazole for the Secondary Prevention of Myocardial Infarction in Iran.","authors":"Mohammadreza Amirsadri,&nbsp;Valiollah Hajhashemi,&nbsp;Amir Shahriar Asemi","doi":"10.4103/jrpp.JRPP_21_22","DOIUrl":"https://doi.org/10.4103/jrpp.JRPP_21_22","url":null,"abstract":"<p><strong>Objective: </strong>Gastrointestinal bleeding, a side effect of clopidogrel, is usually prevented by proton-pump inhibitors (PPIs). Due to omeprazole's inhibitory effects on the liver enzyme CYP2C19, its concomitant use with clopidogrel is argued to increase the risk of myocardial infarction (MI) recurrence, as CYP2C19 activates clopidogrel. Pantoprazole as an alternative PPI has shown no inhibitory effect on CYP2C19. This study investigates the cost-effectiveness of concomitant use of clopidogrel and pantoprazole in MI patients compared to the simultaneous use of clopidogrel and omeprazole.</p><p><strong>Methods: </strong>We used the Markov-modeling technique with a hypothetical cohort of 1000 acute MI patients aged 55 years using Microsoft Excel 2013 software. The study was done from the payer perspective, and a lifetime horizon with 1-year cycles was considered in the model. Life-years gained (LYG) and quality-adjusted life-years (QALYs) were used to quantify the health effects of these interventions. Two separate scenarios of public tariffs and private tariffs with various discount rates (0%, 3%, and 7.2% discounts (only for costs)) were evaluated, and an incremental cost-effectiveness ratio (ICER) was used to report the results. One-way and probabilistic sensitivity analyses were used to deal with uncertainty. Data were sourced from published literature and tariff book of the Iranian ministry of health.</p><p><strong>Findings: </strong>The estimated ICERs were 342 USD/QALY and 236 USD/LYG per patient for the base-case scenario.</p><p><strong>Conclusion: </strong>Abiding by the WHO threshold for cost-effectiveness, the concomitant use of pantoprazole and clopidogrel can be considered cost-effective compared to the use of omeprazole and clopidogrel.</p>","PeriodicalId":17158,"journal":{"name":"Journal of Research in Pharmacy Practice","volume":"10 2","pages":"90-95"},"PeriodicalIF":1.0,"publicationDate":"2021-08-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/a0/19/JRPP-10-90.PMC8420933.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39420379","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Consumer's Satisfaction with Community Pharmacies in Sindh, Pakistan. 巴基斯坦信德省消费者对社区药房的满意度。
IF 0.8 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2021-08-03 eCollection Date: 2021-04-01 DOI: 10.4103/jrpp.JRPP_20_108
Yun Jin Kim, Muhammad Shahzad Aslam, Syed Muhammad Fahim, Waris Ali Khan, Linchao Qian

Objective: The present research is the first comprehensive cross-sectional study of consumer satisfaction with community pharmacies in Sindh, Pakistan. Moreover, the study has also designed a nonorder theoretical model for consumer satisfaction with community pharmacies.

Methods: This is a cross-sectional descriptive study from a general population of Sindh, Pakistan, with a total of four hundred and fifteen (n = 415) participants. A confirmatory factor analysis was used to verify the factor structure between Pharmaceutical services (PS), the Skill of Pharmacists, Non-pharmaceutical services (NPS), and pricing (P). Pearson correlation analysis, Kendall's tau correlation analysis, and Spearman's rho correlation analysis were used to identify the correlation between different factors, such as PS, SKP, NPS, and P.

Findings: The 23-item scale that consisted of four elements have shown an acceptable root mean squared error of approximation (0.076), Cronbach's alpha (0.787), and Chi-square value (3.381) (P < 0.001). Of the respondents, 56.4% rated their satisfaction on pharmacist attitude, whereas 67.2%, 41.4%, and 51.8% were satisfied with other services, such as receipt provided on medication they take, prescription drug service and availability of pharmacies on the weekend and public holidays, respectively.

Conclusion: This cross-sectional study confirms that there are relationships among PS, SPK, NPS, and P. Moreover, there is a lack of facilities in community pharmacies in Sindh, such as the unavailability of a consultation room, immunization services, information on routine health matters, and medication record.

研究目的本研究是首次对巴基斯坦信德省消费者对社区药房的满意度进行全面的横断面研究。此外,本研究还设计了一个消费者对社区药房满意度的无序理论模型:这是一项横断面描述性研究,研究对象是巴基斯坦信德省的普通人群,共有四百一十五名参与者(n = 415)。研究采用了确认性因子分析来验证制药服务(PS)、药剂师技能、非制药服务(NPS)和定价(P)之间的因子结构。使用了皮尔逊相关分析、肯德尔头相关分析和斯皮尔曼 rho 相关分析来确定不同因子(如 PS、SKP、NPS 和 P)之间的相关性:由四个要素组成的 23 个项目量表的均方根近似误差(0.076)、克朗巴赫α值(0.787)和奇偶校验值(3.381)(P < 0.001)均可接受。在受访者中,56.4% 的人对药剂师的态度表示满意,而 67.2%、41.4% 和 51.8% 的人对其他服务表示满意,如提供服用药物的收据、处方药服务以及周末和公共节假日药房的供应情况等:这项横断面研究证实了 PS、SPK、NPS 和 P 之间的关系。此外,信德省的社区药房还存在设施不足的问题,如没有咨询室、免疫接种服务、常规健康信息和用药记录。
{"title":"Consumer's Satisfaction with Community Pharmacies in Sindh, Pakistan.","authors":"Yun Jin Kim, Muhammad Shahzad Aslam, Syed Muhammad Fahim, Waris Ali Khan, Linchao Qian","doi":"10.4103/jrpp.JRPP_20_108","DOIUrl":"10.4103/jrpp.JRPP_20_108","url":null,"abstract":"<p><strong>Objective: </strong>The present research is the first comprehensive cross-sectional study of consumer satisfaction with community pharmacies in Sindh, Pakistan. Moreover, the study has also designed a nonorder theoretical model for consumer satisfaction with community pharmacies.</p><p><strong>Methods: </strong>This is a cross-sectional descriptive study from a general population of Sindh, Pakistan, with a total of four hundred and fifteen (<i>n</i> = 415) participants. A confirmatory factor analysis was used to verify the factor structure between Pharmaceutical services (PS), the Skill of Pharmacists, Non-pharmaceutical services (NPS), and pricing (P). Pearson correlation analysis, Kendall's tau correlation analysis, and Spearman's rho correlation analysis were used to identify the correlation between different factors, such as PS, SKP, NPS, and P.</p><p><strong>Findings: </strong>The 23-item scale that consisted of four elements have shown an acceptable root mean squared error of approximation (0.076), Cronbach's alpha (0.787), and Chi-square value (3.381) (<i>P</i> < 0.001). Of the respondents, 56.4% rated their satisfaction on pharmacist attitude, whereas 67.2%, 41.4%, and 51.8% were satisfied with other services, such as receipt provided on medication they take, prescription drug service and availability of pharmacies on the weekend and public holidays, respectively.</p><p><strong>Conclusion: </strong>This cross-sectional study confirms that there are relationships among PS, SPK, NPS, and P. Moreover, there is a lack of facilities in community pharmacies in Sindh, such as the unavailability of a consultation room, immunization services, information on routine health matters, and medication record.</p>","PeriodicalId":17158,"journal":{"name":"Journal of Research in Pharmacy Practice","volume":"10 2","pages":"78-82"},"PeriodicalIF":0.8,"publicationDate":"2021-08-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/9b/99/JRPP-10-78.PMC8420935.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39420454","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effect of 2 mg Versus 4 mg of Intravenous Zoledronic Acid on Bone Mineral Density at the Lumbar Spine in Indian Postmenopausal Women with Osteoporosis: A Double-blind Parallel-arm Randomized Controlled Trial. 静脉注射2mg与4mg唑来膦酸对印度绝经后骨质疏松症妇女腰椎骨密度的影响:一项双盲平行随机对照试验
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2021-08-03 eCollection Date: 2021-04-01 DOI: 10.4103/jrpp.JRPP_20_130
Harsh Durgia, Sadishkumar Kamalanathan, Govindarajalou Ramkumar, Sonali Sarkar, Sagili Vihaya Bhaskar Reddy, Jayaprakash Sahoo, Rajan Palui, Henith Raj

Objective: The primary purpose was to compare the effect of 2 mg and 4 mg of intravenous zoledronic acid (ZA) on change in the lumbar spine (LS) bone mineral density (BMD) at the end of 1 year in postmenopausal women with osteoporosis. The secondary objectives were changes in BMD at the total hip and femoral neck, change in bone turnover markers (BTMs), and the incidence of new fractures.

Methods: This was a double-blind, parallel-arm, randomized control trial with an allocation ratio of 1:1 done in 70 postmenopausal women with osteoporosis.

Findings: The mean (±standard deviation) percentage increase in LS BMD at the end of 1 year was 4.86% ± 3.05% and 5.35% ± 3.73% in the 2 mg and 4 mg group, respectively. The dose of 2 mg ZA proved to be inferior to 4 mg with a noninferiority margin of 0.5%. There was no difference in BMD change at hip and BTMs between the two groups at the end of 1 year. Only one patient in 4 mg group developed two new vertebral fractures during a 12-month follow-up. Acute-phase reactions were the most common (43%) side-effects noted without any difference between the two groups (P = 0.63).

Conclusion: This study failed to show the noninferiority of 2 mg ZA compared to 4 mg ZA for change in LS BMD at the end of 1 year.

目的:主要目的是比较静脉注射2 mg和4 mg唑来膦酸(ZA)对绝经后骨质疏松症妇女1年后腰椎(LS)骨密度(BMD)变化的影响。次要目标是全髋关节和股骨颈的骨密度变化,骨转换标志物(BTMs)的变化以及新骨折的发生率。方法:这是一项双盲、平行组、随机对照试验,分配比例为1:1,在70名绝经后骨质疏松症妇女中进行。结果:2 mg和4 mg组1年后LS骨密度的平均(±标准差)百分比分别为4.86%±3.05%和5.35%±3.73%。2mg ZA的剂量低于4mg,非劣效边际为0.5%。1年后,两组患者髋部骨密度变化及btm无差异。在12个月的随访中,4mg组只有1例患者出现了两次新的椎体骨折。急性期反应是最常见的副作用(43%),两组间无差异(P = 0.63)。结论:本研究未能显示2 mg ZA与4 mg ZA在1年后对LS BMD变化的非劣效性。
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引用次数: 1
Efficacy of the Combination of Indomethacin and Methocarbamol versus Indomethacin Alone in Patients with Acute Low Back Pain: A Double-Blind, Randomized Placebo-Controlled Clinical Trial. 吲哚美辛联合甲氨基氨基酚与单用吲哚美辛治疗急性腰痛的疗效比较:一项双盲、随机安慰剂对照临床试验
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2021-08-03 eCollection Date: 2021-04-01 DOI: 10.4103/jrpp.JRPP_21_31
Shiva Samsamshariat, Mehdi Sharifi-Sade, Shafeajafar Zoofaghari, Asieh Maghami Mehr, Ali Mohammad Sabzghabaee

Objective: Acute low back pain is a common ailment and causes pain and disability. Physicians often prescribe nonsteroidal anti-inflammatory drugs (NSAIDs) to treat acute low back pain; however, due attention has recently been drawn to muscle relaxants to reduce the severity of patients' daily physical dysfunction. Therefore, this study aimed to evaluate the therapeutic effect of the administration of indomethacin alone compared with methocarbamolas a muscle relaxant and indomethacin as an NSAID on the treatment of acute low back pain.

Methods: The present double-blind clinical trial was performed on 64 patients with acute low back pain. The patients were categorized into two groups and received the treatments as follows. Indomethacin capsules of 25 mg every 8 h and placebo tablets every 8 h were administered in the first group (Group I). Indomethacin capsules of 25 mg every 8 h and methocarbamol tablets of 500 mg every 8 h were administered in the second group (Group I + M). Patient pain intensity and physical function based on Back Pain Function Scale (BPFS) were recorded before and 1 week after the intervention.

Findings: The present study results revealed that the mean pain reduction of patients in Group I + M was significantly higher than that of Group I (3.66 ± 3.17 vs. 1.84 ± 1.53; P < 0.001). Moreover, the mean BPFS increase in Group I + M was significantly higher than that of Group I (19.44 ± 8.66 vs. 4.75 ± 4.35; P < 0.001).

Conclusion: According to the results of the present study, concomitant administration of indomethacin and methocarbamol can be more effective in reducing pain intensity and improving the patient's physical function (or performance).

目的:急性腰痛是一种常见的疾病,可引起疼痛和残疾。医生经常开非甾体抗炎药(NSAIDs)来治疗急性腰痛;然而,肌肉松弛剂最近引起了人们的注意,以减轻患者日常身体功能障碍的严重程度。因此,本研究旨在评价单独应用吲哚美辛与肌松剂甲氧甲氨酰胺及吲哚美辛作为非甾体抗炎药治疗急性腰痛的疗效。方法:对64例急性腰痛患者进行双盲临床试验。将患者分为两组,采用如下治疗方法。第一组(I组)给予吲哚美辛胶囊25 mg / 8 h,安慰剂片每8 h,第二组(I + M组)给予吲哚美辛胶囊25 mg / 8 h,甲氨氨基酚片500 mg / 8 h,分别于干预前和干预后1周记录患者疼痛强度和背部疼痛功能量表(BPFS)生理功能。结果:本研究结果显示,I + M组患者的平均疼痛减轻程度显著高于I组(3.66±3.17∶1.84±1.53;P < 0.001)。此外,I + M组BPFS的平均增幅显著高于I组(19.44±8.66∶4.75±4.35;P < 0.001)。结论:根据本研究结果,吲哚美辛与甲氨基酚合用能更有效地减轻疼痛强度,改善患者的身体机能(或工作表现)。
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引用次数: 0
Assessment Methods and Competency Mapping in Pharmacy Education: Understanding of Components and Quality Parameters. 药学教育的评估方法和能力映射:对成分和质量参数的理解。
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2021-08-03 eCollection Date: 2021-04-01 DOI: 10.4103/jrpp.JRPP_21_29
Syed Wasif Gillani, Kishore Gnana Sam, Fithawit Bahran Gebreigziabher, Jumana Al-Salloum, Rizah Anwar Assadi, Shabaz Mohiuddin Gulam

Centre of advanced pharmaceutical education have developed 15 subsets of competencies required to be competent pharmacist and able to provide optimum care. These competencies were further categorized; Level 1 intermediate, Level 2 efficient, and Level 3 professional. These competencies are cross-mapped to achieve desirable outcomes. Where personal and professional development skills incorporate knowledge, for being a holistic pharmacist. In healthcare education curriculums, active learning tools such as simulation-based patient cases and other innovative learning activities are used to teach clinical skills, patient assessments, and pharmacotherapy concepts. The advance team-based learning technique for the development of stepwise understanding of disease management (simple-complex cases) and students can communicate and collaborate for the critical thinking and decision-making process. Many studies showed the positive impact of the peer teaching on the students; enhanced their academic performance, increase the cognitive congruence, and allows the students to share their own learning struggles to come up with solutions to overcome these challenges. Pharmacy is a healthcare professional required intensive training and professional skills to provide optimum care to patients. The emerging clinical role of pharmacy focused on the patient-centered model, comprehensive assessment, and teaching methods are required to fulfill the professional competencies.

高级药学教育中心开发了15个能力子集,需要成为合格的药剂师,能够提供最佳的护理。这些能力被进一步分类;1级中级,2级高效,3级专业。这些能力是交叉映射的,以实现理想的结果。个人和专业发展技能结合知识,成为一名整体药剂师。在医疗保健教育课程中,主动学习工具(如基于模拟的患者病例和其他创新学习活动)用于教授临床技能、患者评估和药物治疗概念。先进的以团队为基础的学习技术,有助于逐步理解疾病管理(简单到复杂的病例),学生可以在批判性思维和决策过程中进行沟通和协作。许多研究表明同伴教学对学生产生了积极的影响;提高了他们的学习成绩,增加了认知一致性,并允许学生分享自己的学习困难,想出解决这些挑战的办法。药剂学是一种医疗保健专业,需要密集的培训和专业技能来为患者提供最佳的护理。以患者为中心的模式、综合评估和教学方法是满足专业能力的必要条件。
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引用次数: 1
The Pattern of Medication Usage in the Southern Region of Iran: A population-based Pharmacoepidemiological Study. 伊朗南部地区药物使用模式:基于人群的药物流行病学研究。
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2021-08-03 eCollection Date: 2021-04-01 DOI: 10.4103/jrpp.JRPP_21_5
Marziyeh Zare, Saba Afifi, Amir Hossein Alizadeh Bahmani, Iman Karimzadeh, Mohammad Salehi-Marzijarani, Leila Zarei, Behnam Honarvar, Sulmaz Ghahremani, Kamran B Lankarani, Ali Mohammad Sabzghabaee, Payam Peymani

Objective: The purpose of this study was to document the demographic data, to assess the proportion of consumed medicines and the amounts and types of drugs available to households, and to to estimate the probable prevalence of certain diseases in the southern region of Iran.

Methods: In this cross-sectional population-based study carried out in Shiraz (the central city in the Southern part of Iran), we documented and evaluated the drug usage details in a random sample of 1000 households during 2018-2020. We analyzed the usage of drug categories based on the anatomical therapeutic chemical classification, which the World Health Organization recommends.

Findings: In the studied population, the average age (± standard deviation) was 45.54 ± 15.82, ranged 18-91 years. More than 90% had medical insurance coverage. About 81.8% of the participants had individual family medicine practitioners, and most of them (93.8%) received medications with a physician's prescription. The most frequently used medications were cough and cold preparations (12.9%), nervous system drugs (12.6%), and cardiovascular system drugs (11.6%).

Conclusion: Despite the easy access to medications for most participants, few individuals (about 6%) received their medications without a prescription. The most frequently prescribed medicines were the common cold, acetaminophen, and metformin. Common cold, gastrointestinal (GI) disorder, and diabetes were the most commonly used medication classes. Furthermore, we have found a probably higher than average prevalence of cardiovascular, GI, and endocrine disorders. This information could be used by the local policymakers as a basis for the estimation and allotment of health-care resources.

目的:本研究的目的是记录人口数据,评估所消耗药物的比例以及家庭可获得药物的数量和种类,并估计伊朗南部地区某些疾病的可能流行情况。方法:在设拉子(伊朗南部中心城市)进行的这项基于人口的横断面研究中,我们记录并评估了2018-2020年期间1000个家庭的随机样本中的药物使用细节。我们根据世界卫生组织推荐的解剖治疗化学分类分析了药物类别的使用情况。结果:研究人群平均年龄(±标准差)为45.54±15.82岁,年龄范围为18-91岁。90%以上的人有医疗保险。约81.8%的受访者曾个别聘用家庭医生,其中大部份(93.8%)是凭医生处方服药。最常用的药物是咳嗽和感冒药(12.9%)、神经系统药物(12.6%)和心血管系统药物(11.6%)。结论:尽管大多数参与者很容易获得药物,但很少有人(约6%)在没有处方的情况下接受药物治疗。最常见的处方药是普通感冒药、对乙酰氨基酚和二甲双胍。普通感冒、胃肠道(GI)紊乱和糖尿病是最常用的药物类别。此外,我们还发现心血管、胃肠道和内分泌疾病的患病率可能高于平均水平。这些信息可被地方决策者用作估计和分配保健资源的基础。
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引用次数: 1
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Journal of Research in Pharmacy Practice
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