首页 > 最新文献

Exploratory research in clinical and social pharmacy最新文献

英文 中文
Pharmacist perceptions on the presentation of social isolation and loneliness (SIL) in community pharmacy settings in Ireland – A mixed methods study 在爱尔兰社区药房环境中,药剂师对社会隔离和孤独(SIL)表现的看法-一项混合方法研究
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-20 DOI: 10.1016/j.rcsop.2025.100686
Jung-Ah Hong, Hebah Al-Rashed, Laura Rice, Fabian F. Sweeney
Social isolation and Loneliness (SIL) represent a critical public health issue as they are strongly associated with adverse physical, mental and emotional health and wellbeing outcomes. Community pharmacies are accessible and frequently accessed healthcare locations and are potentially valuable settings for interventions designed to support patients experiencing SIL. However, a barrier to the development of community pharmacy based SIL interventions is a knowledge gap regarding nature of the presentation of SIL in this setting. This study adopts a mixed methods approach to explore this from the perspectives of practicing community pharmacists in Ireland.
Semi-structured interviews were conducted with community pharmacists practicing in Ireland (n = 9) followed by a national survey of practicing community pharmacists (n = 95 participants).
Four themes were identified from the interview data: recognition of SIL, SIL risk factors, enablers and Barriers to supporting patients experiencing SIL. Pharmacists described frequent encounters with SIL particularly among older and underrepresented patents. SIL was often recognised through the presence of pharmaceutical care issues and other indirect approaches. Pharmacists expressed a strong sense of responsibility to support patients. Barriers to supporting patients were reported such as lack of appropriate training, signposting knowledge and resource constraints. Survey findings corroborated these themes with respondents reporting frequent encounters with SIL, and needs for guidance and resourcing support.
This study highlights the potential for pharmacies to act as valuable locations for interventions supporting social connectivity. However, integration of pharmacy services into wider support and wellbeing services, appropriate resourcing, inclusion of SIL in pharmacy education, and appropriate patient informed service co-design are critical for this potential to be fully realised.
社会孤立和孤独(SIL)是一个重要的公共卫生问题,因为它们与不利的身体、精神和情感健康和福祉结果密切相关。社区药房是可访问且经常访问的医疗保健地点,对于旨在支持SIL患者的干预措施来说,可能是有价值的设置。然而,基于社区药房的SIL干预发展的障碍是关于在这种情况下SIL表现的性质的知识差距。本研究采用混合方法的方法,从实践社区药剂师在爱尔兰的角度来探讨这一点。对在爱尔兰执业的社区药剂师进行了半结构化访谈(n = 9),随后对执业社区药剂师进行了全国调查(n = 95参与者)。从访谈数据中确定了四个主题:SIL的识别,SIL的危险因素,支持患者经历SIL的因素和障碍。药剂师描述了SIL的频繁遭遇,特别是在年龄较大和代表性不足的专利中。SIL通常通过存在药物保健问题和其他间接方法来识别。药师对支持患者表现出强烈的责任感。据报道,支持患者的障碍包括缺乏适当的培训、指示知识和资源限制。调查结果证实了这些主题,受访者报告经常遇到SIL,需要指导和资源支持。这项研究强调了药房作为支持社会联系的干预措施的有价值场所的潜力。然而,将药学服务整合到更广泛的支持和福利服务中,适当的资源,将SIL纳入药学教育,以及适当的患者知情服务共同设计对于充分实现这一潜力至关重要。
{"title":"Pharmacist perceptions on the presentation of social isolation and loneliness (SIL) in community pharmacy settings in Ireland – A mixed methods study","authors":"Jung-Ah Hong,&nbsp;Hebah Al-Rashed,&nbsp;Laura Rice,&nbsp;Fabian F. Sweeney","doi":"10.1016/j.rcsop.2025.100686","DOIUrl":"10.1016/j.rcsop.2025.100686","url":null,"abstract":"<div><div>Social isolation and Loneliness (SIL) represent a critical public health issue as they are strongly associated with adverse physical, mental and emotional health and wellbeing outcomes. Community pharmacies are accessible and frequently accessed healthcare locations and are potentially valuable settings for interventions designed to support patients experiencing SIL. However, a barrier to the development of community pharmacy based SIL interventions is a knowledge gap regarding nature of the presentation of SIL in this setting. This study adopts a mixed methods approach to explore this from the perspectives of practicing community pharmacists in Ireland.</div><div>Semi-structured interviews were conducted with community pharmacists practicing in Ireland (<em>n</em> = 9) followed by a national survey of practicing community pharmacists (<em>n</em> = 95 participants).</div><div>Four themes were identified from the interview data: <strong>recognition of SIL, SIL risk factors, enablers</strong> and <strong>Barriers to supporting patients experiencing SIL</strong>. Pharmacists described frequent encounters with SIL particularly among older and underrepresented patents. SIL was often recognised through the presence of pharmaceutical care issues and other indirect approaches. Pharmacists expressed a strong sense of responsibility to support patients. Barriers to supporting patients were reported such as lack of appropriate training, signposting knowledge and resource constraints. Survey findings corroborated these themes with respondents reporting frequent encounters with SIL, and needs for guidance and resourcing support.</div><div>This study highlights the potential for pharmacies to act as valuable locations for interventions supporting social connectivity. However, integration of pharmacy services into wider support and wellbeing services, appropriate resourcing, inclusion of SIL in pharmacy education, and appropriate patient informed service co-design are critical for this potential to be fully realised.</div></div>","PeriodicalId":73003,"journal":{"name":"Exploratory research in clinical and social pharmacy","volume":"21 ","pages":"Article 100686"},"PeriodicalIF":1.8,"publicationDate":"2025-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145618580","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
Translation, cross-cultural adaptation and validation of the revised Patients’ Attitudes Towards Deprescribing (rPATD) questionnaire in Japanese 修订后的日语患者处方态度问卷的翻译、跨文化改编与验证
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-19 DOI: 10.1016/j.rcsop.2025.100685
Mitsuaki Ishii , Shoichi Masumoto , Kureha Ara , Keisuke Kiyomiya , Hitoshi Kawazoe , Sachiko Ozone , Hisakazu Ohtani

Background

Deprescribing, a structured process aimed at improving medication safety, requires an approach that aligns with the beliefs and attitudes of patients and caregivers. The revised Patients' Attitudes Towards Deprescribing (rPATD), widely used across countries and disease contexts, may be able to capture the attitudes of older adults and caregivers toward deprescribing in Japan.

Objectives

To translate rPATD into Japanese and assess its cultural adaptability, and to examine its applicability to older adults and caregivers in Japan.

Methods

rPATD was translated into Japanese using a forward-back translation process. Psychometric properties were evaluated among older adults aged 65 years or older who used community pharmacies and caregivers recruited from a web panel. Face and content validity were assessed during the translation process, construct validity was examined using exploratory factor analysis (EFA), and reliability was evaluated using Cronbach's alpha and test-retest analysis with the intra-class correlation coefficient (ICC).

Results

384 older adults and 219 caregivers were included in the analysis. EFA results showed that, the same as the original version, the four factors (burden, belief in appropriateness, concern about stopping, and involvement) were identified for both the older adults and caregivers. Internal consistency was confirmed for all factors related to older adults and caregivers (Cronbach's alpha >0.70). Test-retest reliability was good for all factors (ICC >0.75).

Conclusions

The Japanese version of the rPATD demonstrated good psychometric properties and might be used to assess attitudes towards deprescribing among older adults and caregivers living in Japan.
开处方是一个旨在提高用药安全性的结构化过程,需要一种与患者和护理人员的信念和态度相一致的方法。修订后的患者对处方减少的态度(rPATD)广泛用于各国和疾病背景,可能能够捕捉到日本老年人和护理人员对处方减少的态度。目的将rPATD翻译成日语,评估其文化适应性,并检验其在日本老年人和护理人员中的适用性。方法采用前后翻译法将srpatd翻译成日语。在使用社区药房的65岁或以上的老年人和从网络小组中招募的护理人员中评估了心理测量特性。在翻译过程中评估面孔效度和内容效度,采用探索性因子分析(EFA)检验构念效度,采用Cronbach's alpha和类内相关系数(ICC)重测分析评估信度。结果384名老年人和219名护理人员被纳入分析。EFA结果显示,与原始版本相同,老年人和照顾者都确定了四个因素(负担,对适当性的信念,对停止的关注和参与)。所有与老年人和照顾者相关的因素均证实了内部一致性(Cronbach's alpha >0.70)。所有因素的重测信度均良好(ICC >0.75)。结论日本版rPATD表现出良好的心理测量特性,可用于评估生活在日本的老年人和护理人员对处方的态度。
{"title":"Translation, cross-cultural adaptation and validation of the revised Patients’ Attitudes Towards Deprescribing (rPATD) questionnaire in Japanese","authors":"Mitsuaki Ishii ,&nbsp;Shoichi Masumoto ,&nbsp;Kureha Ara ,&nbsp;Keisuke Kiyomiya ,&nbsp;Hitoshi Kawazoe ,&nbsp;Sachiko Ozone ,&nbsp;Hisakazu Ohtani","doi":"10.1016/j.rcsop.2025.100685","DOIUrl":"10.1016/j.rcsop.2025.100685","url":null,"abstract":"<div><h3>Background</h3><div>Deprescribing, a structured process aimed at improving medication safety, requires an approach that aligns with the beliefs and attitudes of patients and caregivers. The revised Patients' Attitudes Towards Deprescribing (rPATD), widely used across countries and disease contexts, may be able to capture the attitudes of older adults and caregivers toward deprescribing in Japan.</div></div><div><h3>Objectives</h3><div>To translate rPATD into Japanese and assess its cultural adaptability, and to examine its applicability to older adults and caregivers in Japan.</div></div><div><h3>Methods</h3><div>rPATD was translated into Japanese using a forward-back translation process. Psychometric properties were evaluated among older adults aged 65 years or older who used community pharmacies and caregivers recruited from a web panel. Face and content validity were assessed during the translation process, construct validity was examined using exploratory factor analysis (EFA), and reliability was evaluated using Cronbach's alpha and test-retest analysis with the intra-class correlation coefficient (ICC).</div></div><div><h3>Results</h3><div>384 older adults and 219 caregivers were included in the analysis. EFA results showed that, the same as the original version, the four factors (burden, belief in appropriateness, concern about stopping, and involvement) were identified for both the older adults and caregivers. Internal consistency was confirmed for all factors related to older adults and caregivers (Cronbach's alpha &gt;0.70). Test-retest reliability was good for all factors (ICC &gt;0.75).</div></div><div><h3>Conclusions</h3><div>The Japanese version of the rPATD demonstrated good psychometric properties and might be used to assess attitudes towards deprescribing among older adults and caregivers living in Japan.</div></div>","PeriodicalId":73003,"journal":{"name":"Exploratory research in clinical and social pharmacy","volume":"21 ","pages":"Article 100685"},"PeriodicalIF":1.8,"publicationDate":"2025-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145685430","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
Implementation priorities in Australian community pharmacy: A semi-structured survey of Australian pharmacists 澳大利亚社区药房的实施重点:对澳大利亚药剂师的半结构化调查
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-15 DOI: 10.1016/j.rcsop.2025.100683
Veronika Seda, Stephen R. Carter, Rebekah J. Moles, Carl R. Schneider

Background

Australian community pharmacy is undergoing transformation, with pharmacists increasingly contributing to primary care and providing professional services. Implementation science offers structured approaches to support the scalable and sustainable delivery of healthcare. However, most Australian research to date has been exploratory in nature.

Objective

To identify key factors influencing the implementation of professional services in Australian community pharmacies and develop a community pharmacist implementation importance scale (CPIIS).

Methods

A semi-structured national survey was conducted among Australian community pharmacists, guided by the Consolidated Framework for Implementation Research (CFIR) and Cochrane's twelve key implementation dimensions. Descriptive statistics summarised demographics and workplace practices. Exploratory factor analysis (EFA) examined perceived importance of implementation elements, and correlation analyses explored associations with pharmacist and practice characteristics.

Results

Data from 108 eligible respondents were analysed. Pharmacists reported delivering over 9000 services in the previous 14 days, with dose administration aids (67 %) and absence from work certificates (55 %) being most common. EFA identified two key dimensions: “Inner” and “Outer” contexts, with internal factors, such as staffing, workflow, and resource availability, rated as more important. Pharmacist experience was associated with a decrease in the perceived importance of the outer context. The model demonstrated good fit and internal consistency.

Conclusions

Australian community pharmacists currently provide an extensive number and range of professional services. Internal operational factors are prioritised for service implementation. CPIIS offers a practical tool to evaluate the priorities of community pharmacists for implementation of professional services.
Ethics registration: Ethics approval from the University of Sydney Ethics and Human Research Committee was obtained [2021/170].
澳大利亚社区药房正在经历转型,药剂师越来越多地为初级保健做出贡献,并提供专业服务。实施科学提供了结构化的方法来支持可扩展和可持续的医疗保健交付。然而,迄今为止,大多数澳大利亚的研究都是探索性的。目的找出影响澳大利亚社区药房专业服务实施的关键因素,编制社区药师实施重要性量表(CPIIS)。方法在实施研究综合框架(CFIR)和Cochrane十二个关键实施维度的指导下,对澳大利亚社区药师进行半结构化的全国性调查。描述性统计总结了人口统计和工作场所的做法。探索性因素分析(EFA)检查了实施要素的感知重要性,相关分析探索了药剂师和实践特征之间的联系。结果对108名符合条件的调查对象进行了数据分析。药剂师报告在过去14天内提供了9000多项服务,其中最常见的是给药辅助(67%)和没有工作证明(55%)。全民教育确定了两个关键维度:“内部”和“外部”环境,内部因素,如人员配置、工作流程和资源可用性,被认为是更重要的。药剂师经验与感知外部环境重要性的降低有关。模型具有良好的拟合性和内部一致性。结论澳大利亚社区药师目前提供的专业服务范围广泛。内部操作因素优先考虑服务实现。CPIIS提供了一个实用的工具来评估社区药剂师实施专业服务的优先事项。伦理注册:获得悉尼大学伦理与人类研究委员会的伦理批准[2021/170]。
{"title":"Implementation priorities in Australian community pharmacy: A semi-structured survey of Australian pharmacists","authors":"Veronika Seda,&nbsp;Stephen R. Carter,&nbsp;Rebekah J. Moles,&nbsp;Carl R. Schneider","doi":"10.1016/j.rcsop.2025.100683","DOIUrl":"10.1016/j.rcsop.2025.100683","url":null,"abstract":"<div><h3>Background</h3><div>Australian community pharmacy is undergoing transformation, with pharmacists increasingly contributing to primary care and providing professional services. Implementation science offers structured approaches to support the scalable and sustainable delivery of healthcare. However, most Australian research to date has been exploratory in nature.</div></div><div><h3>Objective</h3><div>To identify key factors influencing the implementation of professional services in Australian community pharmacies and develop a community pharmacist implementation importance scale (CPIIS).</div></div><div><h3>Methods</h3><div>A semi-structured national survey was conducted among Australian community pharmacists, guided by the Consolidated Framework for Implementation Research (CFIR) and Cochrane's twelve key implementation dimensions. Descriptive statistics summarised demographics and workplace practices. Exploratory factor analysis (EFA) examined perceived importance of implementation elements, and correlation analyses explored associations with pharmacist and practice characteristics.</div></div><div><h3>Results</h3><div>Data from 108 eligible respondents were analysed. Pharmacists reported delivering over 9000 services in the previous 14 days, with dose administration aids (67 %) and absence from work certificates (55 %) being most common. EFA identified two key dimensions: “Inner” and “Outer” contexts, with internal factors, such as staffing, workflow, and resource availability, rated as more important. Pharmacist experience was associated with a decrease in the perceived importance of the outer context. The model demonstrated good fit and internal consistency.</div></div><div><h3>Conclusions</h3><div>Australian community pharmacists currently provide an extensive number and range of professional services. Internal operational factors are prioritised for service implementation. CPIIS offers a practical tool to evaluate the priorities of community pharmacists for implementation of professional services.</div><div><strong>Ethics registration:</strong> Ethics approval from the University of Sydney Ethics and Human Research Committee was obtained [2021/170].</div></div>","PeriodicalId":73003,"journal":{"name":"Exploratory research in clinical and social pharmacy","volume":"21 ","pages":"Article 100683"},"PeriodicalIF":1.8,"publicationDate":"2025-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145584377","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
Adherence to oral anticancer medications in metastatic versus nonmetastatic breast cancer patients: Insights from a low-middle-income country 转移性与非转移性乳腺癌患者口服抗癌药物的依从性:来自中低收入国家的见解
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-10 DOI: 10.1016/j.rcsop.2025.100682
Abdel-Hameed I.M. Ebid , Rana Elshewy , Mahmoud I. Mostafa , Reem Eid , Emad Shash , Mohamed A. Mobarez

Background

Optimal treatment outcomes in breast cancer rely heavily on patient adherence to oral anticancer medications (OAMs).

Aim

This study aimed to assess adherence to OAMs and identify factors associated with nonadherence in metastatic and nonmetastatic breast cancer patients.

Methods

In this cross-sectional study at the National Cancer Institute, Cairo University, 500 breast cancer patients were categorised into metastatic (45.6 %) and nonmetastatic (54.4 %) groups. Adherence was measured using the Morisky Medication Adherence Scale (MMAS-8) and the Medication Possession Ratio (MPR), with nonadherence defined as an MMAS-8 score < 8 or an MPR < 80 %. Data collection was augmented by patient interviews and examinations of outpatient pharmacy dispensing records.

Results

Adherence rates were 46.4 % as per MMAS-8 and 71 % according to MPR. Specifically, in the nonmetastatic group, MMAS-8 revealed a 28.3 % adherence rate, MPR showed 75.4 % adherence rate. Metastatic patients displayed significantly higher adherence (MASS-8, 68 %) (p < 0.001). There was a notable inverse correlation between adherence and the severity of side effects like musculoskeletal pain, neurological symptoms, fatigue, and hot flushes (p < 0.001). Additionally, adherence varied with treatment duration, with shorter periods associated with better adherence.

Conclusion

This study confirms that adherence to OAMs is significantly affected by both the metastatic status and the severity of side effects. This highlights the urgent need for enhanced educational and management strategies tailored to the specific challenges faced by breast cancer patients, especially those dealing with severe side effects. Ongoing research should focus on developing and testing targeted interventions to improve adherence in these patient groups.
背景:乳腺癌的最佳治疗结果在很大程度上取决于患者对口服抗癌药物(OAMs)的依从性。目的本研究旨在评估转移性和非转移性乳腺癌患者对OAMs的依从性,并确定与不依从性相关的因素。方法在开罗大学国家癌症研究所的横断面研究中,500名乳腺癌患者被分为转移(45.6%)和非转移(54.4%)组。依从性采用莫里斯基药物依从性量表(MMAS-8)和药物持有率(MPR)进行测量,不依从性定义为MMAS-8评分为8分或MPR为80%。通过患者访谈和门诊药房调剂记录的检查,增加了数据收集。结果MMAS-8的依从率为46.4%,MPR的依从率为71%。具体来说,在非转移性组中,MMAS-8的依从率为28.3%,MPR的依从率为75.4%。转移性患者表现出更高的依从性(mass - 8,68 %) (p < 0.001)。依从性与肌肉骨骼疼痛、神经系统症状、疲劳和潮热等副作用的严重程度呈显著的负相关(p < 0.001)。此外,依从性随治疗时间的长短而变化,治疗时间越短依从性越好。结论本研究证实OAMs的依从性受转移状态和副作用严重程度的显著影响。这突出表明迫切需要加强针对乳腺癌患者所面临的具体挑战的教育和管理战略,特别是那些处理严重副作用的患者。正在进行的研究应侧重于开发和测试有针对性的干预措施,以提高这些患者群体的依从性。
{"title":"Adherence to oral anticancer medications in metastatic versus nonmetastatic breast cancer patients: Insights from a low-middle-income country","authors":"Abdel-Hameed I.M. Ebid ,&nbsp;Rana Elshewy ,&nbsp;Mahmoud I. Mostafa ,&nbsp;Reem Eid ,&nbsp;Emad Shash ,&nbsp;Mohamed A. Mobarez","doi":"10.1016/j.rcsop.2025.100682","DOIUrl":"10.1016/j.rcsop.2025.100682","url":null,"abstract":"<div><h3>Background</h3><div>Optimal treatment outcomes in breast cancer rely heavily on patient adherence to oral anticancer medications (OAMs).</div></div><div><h3>Aim</h3><div>This study aimed to assess adherence to OAMs and identify factors associated with nonadherence in metastatic and nonmetastatic breast cancer patients.</div></div><div><h3>Methods</h3><div>In this cross-sectional study at the National Cancer Institute, Cairo University, 500 breast cancer patients were categorised into metastatic (45.6 %) and nonmetastatic (54.4 %) groups. Adherence was measured using the Morisky Medication Adherence Scale (MMAS-8) and the Medication Possession Ratio (MPR), with nonadherence defined as an MMAS-8 score &lt; 8 or an MPR &lt; 80 %. Data collection was augmented by patient interviews and examinations of outpatient pharmacy dispensing records.</div></div><div><h3>Results</h3><div>Adherence rates were 46.4 % as per MMAS-8 and 71 % according to MPR. Specifically, in the nonmetastatic group, MMAS-8 revealed a 28.3 % adherence rate, MPR showed 75.4 % adherence rate. Metastatic patients displayed significantly higher adherence (MASS-8, 68 %) (<em>p</em> &lt; 0.001). There was a notable inverse correlation between adherence and the severity of side effects like musculoskeletal pain, neurological symptoms, fatigue, and hot flushes (<em>p</em> &lt; 0.001). Additionally, adherence varied with treatment duration, with shorter periods associated with better adherence.</div></div><div><h3>Conclusion</h3><div>This study confirms that adherence to OAMs is significantly affected by both the metastatic status and the severity of side effects. This highlights the urgent need for enhanced educational and management strategies tailored to the specific challenges faced by breast cancer patients, especially those dealing with severe side effects. Ongoing research should focus on developing and testing targeted interventions to improve adherence in these patient groups.</div></div>","PeriodicalId":73003,"journal":{"name":"Exploratory research in clinical and social pharmacy","volume":"20 ","pages":"Article 100682"},"PeriodicalIF":1.8,"publicationDate":"2025-11-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145519450","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
Longitudinal study on the seasonal variation in methylphenidate consumption in the South African private healthcare sector 南非私营医疗保健部门哌甲酯消费季节性变化的纵向研究
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-03 DOI: 10.1016/j.rcsop.2025.100680
Ilse Truter, Ashmitha Munasur-Naidoo

Background

A steady growth in the consumption of medicine for Attention-Deficit/Hyperactivity Disorder (ADHD) has been evident over the past two decades. The Coronavirus disease 2019 (COVID-19) pandemic is reported to have had an effect on stimulant consumption. Methylphenidate is the main active ingredient used in the treatment of ADHD, both in children and adults.

Objective

The primary aim was to analyze the consumption patterns of methylphenidate in the private healthcare sector in South Africa by means of a drug utilization study using the Defined Daily Dose (DDD) methodology to establish trends, detect seasonal variations and to compare the results with international studies.

Methods

A retrospective descriptive drug utilization study was conducted. IQVIA sales data from the South African private healthcare sector from 2013 to 2023 were analyzed. Consumption patterns were expressed as the number of Defined Daily Doses (DDDs)/1000 inhabitants/day and DDDs/1000 inhabitants/month. Ethical approval for the study was granted.

Results

Methylphenidate consumption showed a steady increase in the years around the pandemic period, from 9.07 (in 2018) to 9.88 DDDs/1000 inhabitants/day (in 2023), with a notable lower consumption in 2020 when the COVID-19 pandemic started. Consumption in 2013 was only 6.01 DDD/1000 inhabitants/day, which indicates an increase of 64.39 % over the 11-year period. Seasonal peaks in consumption were observed in February, May, August and November, coinciding with times before assessment periods in schools and universities.

Conclusions

There was a clear visible upward trend in the consumption of methylphenidate, with a decrease during 2020, as was also observed in other countries. Similar studies are recommended for other central nervous system drug classes.
背景:在过去的二十年中,治疗注意力缺陷/多动障碍(ADHD)的药物消费量稳步增长。据报道,2019年冠状病毒病(COVID-19)大流行对兴奋剂消费产生了影响。哌甲酯是治疗儿童和成人多动症的主要有效成分。目的:主要目的是通过使用限定日剂量(DDD)方法进行药物利用研究,分析南非私营医疗保健部门哌甲酯的消费模式,以确定趋势,检测季节性变化,并将结果与国际研究进行比较。方法采用回顾性描述性药物使用研究。分析了2013年至2023年南非私人医疗保健部门的IQVIA销售数据。消费模式表示为限定日剂量(DDDs)/1000居民/天和DDDs/1000居民/月。该研究获得了伦理批准。结果在大流行期间,哌甲酯消费量呈稳步增长趋势,从2018年的9.07 DDDs/1000人/天增加到2023年的9.88 DDDs/1000人/天,而在2019冠状病毒病大流行开始的2020年,哌甲酯消费量明显下降。2013年的消费量仅为6.01 DDD/1000居民/天,11年间增长了64.39%。在2月、5月、8月和11月观察到季节性消费高峰,与学校和大学评估期之前的时间相吻合。结论与其他国家一样,2020年哌醋甲酯消费量呈明显上升趋势,呈下降趋势。其他中枢神经系统药物也建议进行类似的研究。
{"title":"Longitudinal study on the seasonal variation in methylphenidate consumption in the South African private healthcare sector","authors":"Ilse Truter,&nbsp;Ashmitha Munasur-Naidoo","doi":"10.1016/j.rcsop.2025.100680","DOIUrl":"10.1016/j.rcsop.2025.100680","url":null,"abstract":"<div><h3>Background</h3><div>A steady growth in the consumption of medicine for Attention-Deficit/Hyperactivity Disorder (ADHD) has been evident over the past two decades. The Coronavirus disease 2019 (COVID-19) pandemic is reported to have had an effect on stimulant consumption. Methylphenidate is the main active ingredient used in the treatment of ADHD, both in children and adults.</div></div><div><h3>Objective</h3><div>The primary aim was to analyze the consumption patterns of methylphenidate in the private healthcare sector in South Africa by means of a drug utilization study using the Defined Daily Dose (DDD) methodology to establish trends, detect seasonal variations and to compare the results with international studies.</div></div><div><h3>Methods</h3><div>A retrospective descriptive drug utilization study was conducted. IQVIA sales data from the South African private healthcare sector from 2013 to 2023 were analyzed. Consumption patterns were expressed as the number of Defined Daily Doses (DDDs)/1000 inhabitants/day and DDDs/1000 inhabitants/month. Ethical approval for the study was granted.</div></div><div><h3>Results</h3><div>Methylphenidate consumption showed a steady increase in the years around the pandemic period, from 9.07 (in 2018) to 9.88 DDDs/1000 inhabitants/day (in 2023), with a notable lower consumption in 2020 when the COVID-19 pandemic started. Consumption in 2013 was only 6.01 DDD/1000 inhabitants/day, which indicates an increase of 64.39 % over the 11-year period. Seasonal peaks in consumption were observed in February, May, August and November, coinciding with times before assessment periods in schools and universities.</div></div><div><h3>Conclusions</h3><div>There was a clear visible upward trend in the consumption of methylphenidate, with a decrease during 2020, as was also observed in other countries. Similar studies are recommended for other central nervous system drug classes.</div></div>","PeriodicalId":73003,"journal":{"name":"Exploratory research in clinical and social pharmacy","volume":"20 ","pages":"Article 100680"},"PeriodicalIF":1.8,"publicationDate":"2025-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145465618","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 impact of comprehensive pharmaceutical care on medication safety in gynecologic oncology chemotherapy patients 综合药学服务对妇科肿瘤化疗患者用药安全的影响
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-03 DOI: 10.1016/j.rcsop.2025.100681
Zhiqi Zhang , Zhuo Zhang , Qianxin Liu , Yan Zhang , Peng Jia , Lan Mi , Rui Lian , Fei Chen , Xiaocong Pang , Ying Zhou

Objectives

To evaluate the impact of our hospital's full-course pharmacy service on the safety and rationality of medication in patients with gynecologic malignancies undergoing chemotherapy.

Methods

A retrospective cohort analysis was conducted on patients who underwent chemotherapy in the Gynecologic Oncology Ward at Peking University First Hospital between September 2022 and September 2024. Patients were divided into a control group, who received routine pharmaceutical care based on clinical medication prescription review, and the intervention group, who received comprehensive pharmaceutical care throughout their treatment. This included prescription review, medication education, drug consultation, and adverse reaction management. The incidence of severe adverse reactions, the appropriateness of leukopoietic treatment and monitoring, and the rate of unplanned hospital admissions were compared between the two groups.

Results

The intervention group demonstrated a significantly lower incidence of severe nausea (6.1 % vs 11.4 %, P = 0.034), anorexia (3.3 % vs 9.3 %, P = 0.003), and leukopenia (9.4 % vs 15.7 %, P = 0.034) compared to the control group. Additionally, the appropriateness of leukopoietic treatment (93.5 % vs 85.0 %, P = 0.001) and monitoring (89.2 % vs 65.0 %, P < 0.001), as well as the rate of unexpected hospital admissions (2.2 % vs 6.4 %, P = 0.013), have shown significant improvement in the intervention group.

Conclusion

Comprehensive pharmaceutical care has a positive impact on medication safety for gynecologic oncology patients, significantly reducing the incidence of severe adverse reactions and the rate of unplanned hospital admissions.
目的评价我院全程药学服务对妇科恶性肿瘤化疗患者用药安全性和合理性的影响。方法对2022年9月至2024年9月北京大学第一医院妇科肿瘤病房化疗患者进行回顾性队列分析。将患者分为对照组和干预组,对照组在临床用药处方回顾的基础上接受常规药学服务,干预组在整个治疗过程中接受综合药学服务。这包括处方审查、药物教育、药物咨询和不良反应管理。比较两组患者的严重不良反应发生率、白细胞治疗和监测的适宜性以及意外住院率。结果干预组患者的严重恶心发生率(6.1% vs 11.4%, P = 0.034)、厌食发生率(3.3% vs 9.3%, P = 0.003)、白细胞减少发生率(9.4% vs 15.7%, P = 0.034)明显低于对照组。此外,干预组的造血治疗适宜性(93.5% vs 85.0%, P = 0.001)和监测适宜性(89.2% vs 65.0%, P = 0.001)以及意外住院率(2.2% vs 6.4%, P = 0.013)均有显著改善。结论综合药学服务对妇科肿瘤患者用药安全有积极影响,可显著降低严重不良反应发生率和意外住院率。
{"title":"The impact of comprehensive pharmaceutical care on medication safety in gynecologic oncology chemotherapy patients","authors":"Zhiqi Zhang ,&nbsp;Zhuo Zhang ,&nbsp;Qianxin Liu ,&nbsp;Yan Zhang ,&nbsp;Peng Jia ,&nbsp;Lan Mi ,&nbsp;Rui Lian ,&nbsp;Fei Chen ,&nbsp;Xiaocong Pang ,&nbsp;Ying Zhou","doi":"10.1016/j.rcsop.2025.100681","DOIUrl":"10.1016/j.rcsop.2025.100681","url":null,"abstract":"<div><h3>Objectives</h3><div>To evaluate the impact of our hospital's full-course pharmacy service on the safety and rationality of medication in patients with gynecologic malignancies undergoing chemotherapy.</div></div><div><h3>Methods</h3><div>A retrospective cohort analysis was conducted on patients who underwent chemotherapy in the Gynecologic Oncology Ward at Peking University First Hospital between September 2022 and September 2024. Patients were divided into a control group, who received routine pharmaceutical care based on clinical medication prescription review, and the intervention group, who received comprehensive pharmaceutical care throughout their treatment. This included prescription review, medication education, drug consultation, and adverse reaction management. The incidence of severe adverse reactions, the appropriateness of leukopoietic treatment and monitoring, and the rate of unplanned hospital admissions were compared between the two groups.</div></div><div><h3>Results</h3><div>The intervention group demonstrated a significantly lower incidence of severe nausea (6.1 % vs 11.4 %, <em>P</em> = 0.034), anorexia (3.3 % vs 9.3 %, <em>P</em> = 0.003), and leukopenia (9.4 % vs 15.7 %, P = 0.034) compared to the control group. Additionally, the appropriateness of leukopoietic treatment (93.5 % vs 85.0 %, <em>P</em> = 0.001) and monitoring (89.2 % vs 65.0 %, <em>P</em> &lt; 0.001), as well as the rate of unexpected hospital admissions (2.2 % vs 6.4 %, <em>P</em> = 0.013), have shown significant improvement in the intervention group.</div></div><div><h3>Conclusion</h3><div>Comprehensive pharmaceutical care has a positive impact on medication safety for gynecologic oncology patients, significantly reducing the incidence of severe adverse reactions and the rate of unplanned hospital admissions.</div></div>","PeriodicalId":73003,"journal":{"name":"Exploratory research in clinical and social pharmacy","volume":"20 ","pages":"Article 100681"},"PeriodicalIF":1.8,"publicationDate":"2025-11-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145519449","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
Off-label prescribing of tamsulosin: A nationwide retrospective study combining prescription and regulatory data 坦索罗辛说明书外处方:一项结合处方和监管数据的全国性回顾性研究
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-02 DOI: 10.1016/j.rcsop.2025.100679
Anna Artner , Ákos Niedermüller , Máté Attila Csapó , Nikoletta Ngo Hanh , Emília Fekete , Romána Zelkó , Szilvia Sebők

Background

Off-label use of medicines raises important safety and regulatory concerns. Tamsulosin, an alpha-1 adrenergic receptor blocker originally approved for benign prostatic hyperplasia (BPH) in men, is also prescribed beyond licensed indications.

Aim

This study aimed to describe national on-label and off-label prescribing patterns of tamsulosin in Hungary using insurance and regulatory data.

Methods

We conducted a retrospective, cross-sectional descriptive analysis of two national datasets: the National Health Insurance Fund (NEAK) database of reimbursed prescriptions (2019–2023) and the National Institute of Pharmacy and Nutrition (NNGYK) records of off-label authorisations (2009–2023). Prescriptions were analyzed by sex and International Classification of Diseases 10th Revision (ICD-10) codes.

Results

A total of 906,011 prescriptions were linked to 214 ICD-10 codes; 805 entries lacked identifiable codes. Of these, 888,830 (98.1 %) were for men and 17,181 (1.9 %) for women. Female prescriptions most frequently carried codes for ureteral stones (2805; 16.3 %), dysuria (1872; 10.9 %), urinary retention (1722; 10.0 %), and kidney stones (1498; 8.7 %). Notably, 2845 prescriptions (16.6 %) in women were linked to prostate-related codes, suggesting coding errors. NNGYK approved eight individual off-label requests, mainly for urological indications.

Conclusions

Off-label tamsulosin prescribing in Hungary is relatively infrequent but concentrated in women. These findings highlight the importance of pharmacovigilance, clinician awareness, and further research to clarify its therapeutic role in non-BPH indications.
未经标签使用药物引起了重要的安全和监管问题。坦索罗辛是一种α -1肾上腺素能受体阻滞剂,最初被批准用于男性良性前列腺增生(BPH),也被用于超出许可适应症的处方。目的本研究旨在利用保险和监管数据描述匈牙利坦索罗辛在标签上和标签外的处方模式。方法对两个国家数据集进行回顾性、横断面描述性分析:国家健康保险基金(NEAK)报销处方数据库(2019-2023)和国家药学与营养研究所(NNGYK)超说明书授权记录(2009-2023)。处方按性别及国际疾病分类第十版(ICD-10)编码进行分析。结果214个ICD-10代码共链接处方906011张;805个条目缺乏可识别的代码。其中,男性为888,830人(98.1%),女性为17,181人(1.9%)。女性处方中最常见的编码是输尿管结石(2805例,16.3%)、排尿困难(1872例,10.9%)、尿潴留(1722例,10.0%)和肾结石(1498例,8.7%)。值得注意的是,2845张女性处方(16.6%)与前列腺相关代码相关,提示编码错误。NNGYK批准了8个单独的超说明书申请,主要用于泌尿外科适应症。结论匈牙利非标坦索罗辛处方相对较少,但主要集中在妇女中。这些发现强调了药物警戒、临床医生意识和进一步研究阐明其在非前列腺增生症中的治疗作用的重要性。
{"title":"Off-label prescribing of tamsulosin: A nationwide retrospective study combining prescription and regulatory data","authors":"Anna Artner ,&nbsp;Ákos Niedermüller ,&nbsp;Máté Attila Csapó ,&nbsp;Nikoletta Ngo Hanh ,&nbsp;Emília Fekete ,&nbsp;Romána Zelkó ,&nbsp;Szilvia Sebők","doi":"10.1016/j.rcsop.2025.100679","DOIUrl":"10.1016/j.rcsop.2025.100679","url":null,"abstract":"<div><h3>Background</h3><div>Off-label use of medicines raises important safety and regulatory concerns. Tamsulosin, an alpha-1 adrenergic receptor blocker originally approved for benign prostatic hyperplasia (BPH) in men, is also prescribed beyond licensed indications.</div></div><div><h3>Aim</h3><div>This study aimed to describe national on-label and off-label prescribing patterns of tamsulosin in Hungary using insurance and regulatory data.</div></div><div><h3>Methods</h3><div>We conducted a retrospective, cross-sectional descriptive analysis of two national datasets: the National Health Insurance Fund (NEAK) database of reimbursed prescriptions (2019–2023) and the National Institute of Pharmacy and Nutrition (NNGYK) records of off-label authorisations (2009–2023). Prescriptions were analyzed by sex and International Classification of Diseases 10th Revision (ICD-10) codes.</div></div><div><h3>Results</h3><div>A total of 906,011 prescriptions were linked to 214 ICD-10 codes; 805 entries lacked identifiable codes. Of these, 888,830 (98.1 %) were for men and 17,181 (1.9 %) for women. Female prescriptions most frequently carried codes for ureteral stones (2805; 16.3 %), dysuria (1872; 10.9 %), urinary retention (1722; 10.0 %), and kidney stones (1498; 8.7 %). Notably, 2845 prescriptions (16.6 %) in women were linked to prostate-related codes, suggesting coding errors. NNGYK approved eight individual off-label requests, mainly for urological indications.</div></div><div><h3>Conclusions</h3><div>Off-label tamsulosin prescribing in Hungary is relatively infrequent but concentrated in women. These findings highlight the importance of pharmacovigilance, clinician awareness, and further research to clarify its therapeutic role in non-BPH indications.</div></div>","PeriodicalId":73003,"journal":{"name":"Exploratory research in clinical and social pharmacy","volume":"20 ","pages":"Article 100679"},"PeriodicalIF":1.8,"publicationDate":"2025-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145465657","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 triple burden: A systematic review and meta-analysis of essential medicine availability, price, and affordability across Ethiopian health facilities 三重负担:对埃塞俄比亚卫生机构基本药物可得性、价格和可负担性的系统回顾和荟萃分析
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-10-27 DOI: 10.1016/j.rcsop.2025.100674
Tsegaye Melaku, Dula Dessalegn, Mestawet Getachew

Background

Access to essential medicines is a fundamental component of achieving universal health coverage, as outlined by the World Health Organization's(WHO) framework. Despite various efforts to improve access to essential medicines, there remains a gap in comprehensive data regarding their availability, price, and affordability at health facilities in Ethiopia. This systematic review and meta-analysis aimed to assess the pooled estimates of availability, price, and affordability of generic essential medicines at health facilities in Ethiopia.

Methods

We conducted a complete search of electronic databases (PubMed/MEDLINE, EMBASE, Science Direct, Web of Science, Scopus, African Index Medicus, AJOL, Google Scholar, and Organization repositories such as the Ministry of Health, Ethiopian Pharmaceuticals Supply Service) to find relevant articles on the topic from inception to August 2025. Data was analyzed using STATA version 18.0. Random-effect model meta-analysis and descriptive statistics were performed to determine the pooled availability and affordability, respectively. Statistical significance was considered at a p-value less than 0.05.

Results

A total of 46 studies, encompassing data from 2302 health facilities, were included in the final analysis. The overall mean availability of essential medicines was 63.89 % (± 19.48 SD). In public health facilities, the pooled availability was 64 % (95 % CI: 58 %–70 %), while in private facilities it was lower at 54 % (95 % CI: 42 %–66 %). The pooled proportion of unaffordable medicines was 62 % (95 % CI: 45 %–79 %). Analysis of the Median Price Ratios (MPRs) revealed that, in public health facilities, MPRs ranged from 0.55 to 5.21, with an overall median (IQR) of 1.45 (1.26–2.31). In private health facilities, MPRs ranged from 0.88 to 11.17, with a higher overall median (IQR) of 3.66 (2.12–4.10), reflecting greater price variability and reduced affordability in the private sector.

Conclusion

The availability of generic essential medicines in Ethiopia was below the WHO target of 80 % in both public and private health facilities. Prices of these medicines were higher than international reference prices, with significant variations across sectors. About two-thirds of the evaluated medicines were unaffordable. Addressing these challenges will require coordinated efforts, including policy refinement, supply chain improvements, and context-specific interventions, to progressively enhance equitable access to essential medicines across all sectors.
Systematic review registration number: PROSPERO CRD420251137000.
根据世界卫生组织(世卫组织)框架的概述,获得基本药物是实现全民健康覆盖的一个基本组成部分。尽管为改善基本药物的可及性作出了各种努力,但在埃塞俄比亚的卫生设施中,关于这些药物的可得性、价格和可负担性的综合数据仍然存在差距。本系统综述和荟萃分析旨在评估埃塞俄比亚卫生机构对非专利基本药物的可得性、价格和可负担性的综合估计。方法全面检索PubMed/MEDLINE、EMBASE、Science Direct、Web of Science、Scopus、African Index Medicus、AJOL、谷歌Scholar和组织库(Ministry of Health, Ethiopian medicines Supply Service)自成立至2025年8月的相关文章。数据分析采用STATA 18.0版本。随机效应模型荟萃分析和描述性统计分别确定了合用性和可负担性。p值小于0.05时认为具有统计学意义。结果最终分析共纳入46项研究,包括来自2302家卫生机构的数据。总体平均基本药物可获得性为63.89%(±19.48 SD)。在公共卫生设施中,综合可用性为64%(95%置信区间:58% - 70%),而在私营设施中,这一比例较低,为54%(95%置信区间:42% - 66%)。负担不起药品的总比例为62%(95%可信区间:45% - 79%)。对中位数价格比(mpr)的分析显示,在公共卫生设施中,mpr的范围为0.55至5.21,总体中位数(IQR)为1.45(1.26-2.31)。在私营保健设施中,mpr从0.88到11.17不等,总体中位数(IQR)较高,为3.66(2.12-4.10),反映出价格波动较大,私营部门的负担能力降低。结论埃塞俄比亚公立和私立卫生机构的仿制药基本药物可得性均低于世卫组织80%的目标。这些药品的价格高于国际参考价格,各部门之间差异很大。大约三分之二的评估药物是负担不起的。应对这些挑战需要协调努力,包括完善政策、改善供应链和针对具体情况的干预措施,以逐步加强所有部门公平获得基本药物的机会。系统评价注册号:PROSPERO CRD420251137000。
{"title":"The triple burden: A systematic review and meta-analysis of essential medicine availability, price, and affordability across Ethiopian health facilities","authors":"Tsegaye Melaku,&nbsp;Dula Dessalegn,&nbsp;Mestawet Getachew","doi":"10.1016/j.rcsop.2025.100674","DOIUrl":"10.1016/j.rcsop.2025.100674","url":null,"abstract":"<div><h3>Background</h3><div>Access to essential medicines is a fundamental component of achieving universal health coverage, as outlined by the World Health Organization's(WHO) framework. Despite various efforts to improve access to essential medicines, there remains a gap in comprehensive data regarding their availability, price, and affordability at health facilities in Ethiopia. This systematic review and meta-analysis aimed to assess the pooled estimates of availability, price, and affordability of generic essential medicines at health facilities in Ethiopia.</div></div><div><h3>Methods</h3><div>We conducted a complete search of electronic databases (PubMed/MEDLINE, EMBASE, Science Direct, Web of Science, Scopus, African Index Medicus, AJOL, Google Scholar, and Organization repositories such as the Ministry of Health, Ethiopian Pharmaceuticals Supply Service) to find relevant articles on the topic from inception to August 2025. Data was analyzed using STATA version 18.0. Random-effect model meta-analysis and descriptive statistics were performed to determine the pooled availability and affordability, respectively. Statistical significance was considered at a <em>p</em>-value less than 0.05.</div></div><div><h3>Results</h3><div>A total of 46 studies, encompassing data from 2302 health facilities, were included in the final analysis. The overall mean availability of essential medicines was 63.89 % (± 19.48 SD). In public health facilities, the pooled availability was 64 % (95 % CI: 58 %–70 %), while in private facilities it was lower at 54 % (95 % CI: 42 %–66 %). The pooled proportion of unaffordable medicines was 62 % (95 % CI: 45 %–79 %). Analysis of the Median Price Ratios (MPRs) revealed that, in public health facilities, MPRs ranged from 0.55 to 5.21, with an overall median (IQR) of 1.45 (1.26–2.31). In private health facilities, MPRs ranged from 0.88 to 11.17, with a higher overall median (IQR) of 3.66 (2.12–4.10), reflecting greater price variability and reduced affordability in the private sector.</div></div><div><h3>Conclusion</h3><div>The availability of generic essential medicines in Ethiopia was below the WHO target of 80 % in both public and private health facilities. Prices of these medicines were higher than international reference prices, with significant variations across sectors. About two-thirds of the evaluated medicines were unaffordable. Addressing these challenges will require coordinated efforts, including policy refinement, supply chain improvements, and context-specific interventions, to progressively enhance equitable access to essential medicines across all sectors.</div><div><strong>Systematic review registration number:</strong> PROSPERO CRD420251137000.</div></div>","PeriodicalId":73003,"journal":{"name":"Exploratory research in clinical and social pharmacy","volume":"20 ","pages":"Article 100674"},"PeriodicalIF":1.8,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145415759","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
Design and evaluation of a comprehensive training program for hospital-based clinical pharmacists - various, active, and work-integrated learning 设计和评估医院临床药师的综合培训计划-各种,积极的,与工作结合的学习
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-10-27 DOI: 10.1016/j.rcsop.2025.100677
Marianne Lea , Elin Trapnes , Hanne Steen , Nina Bjerketveit Ødegaard

Background

Medication reconciliation and -reviews are not emphasized in the pharmacy curriculums in Norway and graduated pharmacists are at novice level. Therefore, a postgraduate training program for hospital-based clinical pharmacists was developed. The aim of this paper is to describe the program design and evaluation of the last four years (2021–2024).

Method

The training program, established in 2012, used Southern Sweden's training in Integrated Medicines Management as inspiration. Experienced clinical pharmacists in Norway have further developed and improved the program. The training program comprises i) a three-day in-class and skill training course in a simulation lab ii) eight days in a hospital ward performing medication reconciliations and - reviews under individual supervision from a clinical supervisor, i.e. an experienced clinical pharmacist, and iii) independently conducted medication reconciliations and –reviews presented to the supervisor for feedback and reflection.

Results

Of 46 participants in the last four years, 39 (85 %) completed a questionnaire. Participants scored their overall satisfaction with a median of 6 (range 4–6) on a scale from 1 to 6. Participants highlighted the way the course is organized and facilitated by skilled lecturers, active learning with feedback, peer learning, and work relevance as positive factors.

Conclusion

A comprehensive work-integrated training program with various and active learning methods that can be used as a template in settings where pharmacists graduate at novice level in medication reconciliation and -reviews has been developed. The program is appreciated by participants, seems to improve their professional confidence, and could ensure standardised high quality clinical pharmacy services.
挪威的药学课程不强调药物调和和回顾,毕业的药剂师处于初级水平。为此,制定了以医院为基础的临床药师研究生培养计划。本文的目的是描述过去四年(2021-2024)的计划设计和评估。方法2012年建立的培训项目以瑞典南部的综合药物管理培训为灵感。挪威经验丰富的临床药师进一步发展和改进了该计划。培训计划包括:(1)在模拟实验室进行为期三天的课堂和技能培训课程;(2)在医院病房进行为期八天的药物调解和审查,由临床主管(即经验丰富的临床药剂师)进行个人监督;(3)独立进行药物调解和审查,并向主管提交反馈和反思。结果在过去四年的46名参与者中,39名(85%)完成了问卷调查。在1到6的范围内,参与者对整体满意度的中位数为6(范围为4-6)。参与者强调了课程的组织方式和由熟练的讲师提供的便利,积极的反馈学习,同侪学习和工作相关性作为积极因素。结论建立了一套以多种主动学习方法为基础的综合性工作结合培训方案,可作为初级毕业药师用药和解与评价培训的模板。该项目得到了参试人员的认可,提高了参试人员的专业信心,保证了规范化的高质量临床药学服务。
{"title":"Design and evaluation of a comprehensive training program for hospital-based clinical pharmacists - various, active, and work-integrated learning","authors":"Marianne Lea ,&nbsp;Elin Trapnes ,&nbsp;Hanne Steen ,&nbsp;Nina Bjerketveit Ødegaard","doi":"10.1016/j.rcsop.2025.100677","DOIUrl":"10.1016/j.rcsop.2025.100677","url":null,"abstract":"<div><h3>Background</h3><div>Medication reconciliation and -reviews are not emphasized in the pharmacy curriculums in Norway and graduated pharmacists are at novice level. Therefore, a postgraduate training program for hospital-based clinical pharmacists was developed. The aim of this paper is to describe the program design and evaluation of the last four years (2021–2024).</div></div><div><h3>Method</h3><div>The training program, established in 2012, used Southern Sweden's training in Integrated Medicines Management as inspiration. Experienced clinical pharmacists in Norway have further developed and improved the program. The training program comprises i) a three-day in-class and skill training course in a simulation lab ii) eight days in a hospital ward performing medication reconciliations and - reviews under individual supervision from a clinical supervisor, i.e. an experienced clinical pharmacist, and iii) independently conducted medication reconciliations and –reviews presented to the supervisor for feedback and reflection.</div></div><div><h3>Results</h3><div>Of 46 participants in the last four years, 39 (85 %) completed a questionnaire. Participants scored their overall satisfaction with a median of 6 (range 4–6) on a scale from 1 to 6. Participants highlighted the way the course is organized and facilitated by skilled lecturers, active learning with feedback, peer learning, and work relevance as positive factors.</div></div><div><h3>Conclusion</h3><div>A comprehensive work-integrated training program with various and active learning methods that can be used as a template in settings where pharmacists graduate at novice level in medication reconciliation and -reviews has been developed. The program is appreciated by participants, seems to improve their professional confidence, and could ensure standardised high quality clinical pharmacy services.</div></div>","PeriodicalId":73003,"journal":{"name":"Exploratory research in clinical and social pharmacy","volume":"20 ","pages":"Article 100677"},"PeriodicalIF":1.8,"publicationDate":"2025-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145571225","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 short medication adherence scale (SMAS-7): Development and psychometric validation in a general population sample 短药物依从性量表(SMAS-7):在一般人群样本中的发展和心理测量验证
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2025-10-25 DOI: 10.1016/j.rcsop.2025.100676
Fouad Sakr , Mariam Dabbous , Jihan Safwan , Mohamad Rahal , Pascale Salameh

Background

Medication adherence is essential for treatment success across both chronic and acute conditions. However, concise, multidimensional, and broadly applicable validated tools to measure medication adherence remain scarce.

Objectives

This study primarily aimed to develop and validate the Short Medication Adherence Scale (SMAS-7) and, secondarily, to assess adherence levels and related factors in a general adult population.

Methods

A cross-sectional study was conducted among Lebanese adults aged ≥18 years from the general population. Individuals who declined follow-up contact for the test-retest phase were excluded. The 7-item SMAS-7, developed from the LMAS-14, was administered electronically in Arabic using an online questionnaire. Exploratory and confirmatory factor analyses (EFA and CFA) were performed on two random subsamples to assess factorial structure and model fit. Internal consistency (Cronbach's α, McDonald's ω), test-retest reliability (ICC), and construct and criterion validity were evaluated. Multivariable logistic regression identified predictors of adherence using a ROC curve-derived SMAS-7 cut-off score.

Results

A total of 501 participants were included in the study. EFA revealed a 3-factor structure, psychological, economic, and behavioral domains, supported by KMO = 0.830 and significant Bartlett's test (P < 0.001). CFA confirmed the structure with excellent fit (χ2/df = 1.757, CFI = 0.992, TLI = 0.985, RMSEA = 0.055, SRMR = 0.020). The SMAS-7 demonstrated high internal consistency (α = 0.889, ω = 0.945) and test-retest reliability (ICC = 0.779). Criterion validity was excellent (AUC = 0.985; sensitivity = 91.2 %; specificity = 96.0 %). Suboptimal adherence was observed in 52.3 % of participants. Significant predictors of adherence included gender (P = 0.030), region (P = 0.014), financial well-being (P = 0.002), chronic illness (P = 0.009), communication barriers (P = 0.013), and patient perception (P = 0.029).

Conclusion

The SMAS-7 demonstrated strong preliminary psychometric properties in this initial validation study. It offers a valuable resource for researchers, clinicians, and policymakers seeking to monitor and enhance adherence behaviors. While these findings are encouraging, further studies in diverse populations and clinical settings are required to confirm its external validity and generalizability. The findings revealed suboptimal adherence and underscored the multifaceted nature of its predictors, highlighting the need for targeted, multidimensional interventions.
药物依从性对于慢性和急性疾病的治疗成功至关重要。然而,衡量药物依从性的简洁、多维、广泛适用的有效工具仍然很少。本研究的主要目的是开发和验证短药物依从性量表(SMAS-7),其次是评估一般成年人的依从性水平和相关因素。方法对黎巴嫩普通人群中年龄≥18岁的成年人进行横断面研究。拒绝在测试-重新测试阶段进行后续接触的个体被排除在外。从LMAS-14发展而来的7个项目的SMAS-7使用在线问卷以阿拉伯语进行电子管理。对两个随机子样本进行探索性和验证性因子分析(EFA和CFA)以评估因子结构和模型拟合。评估内部一致性(Cronbach’s α, McDonald’s ω)、重测信度(ICC)、结构效度和标准效度。多变量逻辑回归使用ROC曲线衍生的SMAS-7截止评分确定依从性的预测因子。结果本研究共纳入501名受试者。EFA揭示了心理、经济和行为领域的三因素结构,KMO = 0.830, Bartlett检验显著(P < 0.001)。CFA证实结构拟合良好(χ2/df = 1.757, CFI = 0.992, TLI = 0.985, RMSEA = 0.055, SRMR = 0.020)。SMAS-7具有较高的内部一致性(α = 0.889, ω = 0.945)和重测信度(ICC = 0.779)。标准效度极好(AUC = 0.985;灵敏度= 91.2%;特异性= 96.0%)。52.3%的参与者未达到最佳依从性。依从性的显著预测因子包括性别(P = 0.030)、地区(P = 0.014)、经济状况(P = 0.002)、慢性疾病(P = 0.009)、沟通障碍(P = 0.013)和患者感知(P = 0.029)。结论在初步验证研究中,SMAS-7具有较强的初步心理测量特性。它为寻求监测和加强依从性行为的研究人员、临床医生和政策制定者提供了宝贵的资源。虽然这些发现令人鼓舞,但需要在不同人群和临床环境中进行进一步的研究,以确认其外部有效性和普遍性。研究结果揭示了非最佳依从性,并强调了其预测因素的多面性,强调了有针对性的多维干预措施的必要性。
{"title":"The short medication adherence scale (SMAS-7): Development and psychometric validation in a general population sample","authors":"Fouad Sakr ,&nbsp;Mariam Dabbous ,&nbsp;Jihan Safwan ,&nbsp;Mohamad Rahal ,&nbsp;Pascale Salameh","doi":"10.1016/j.rcsop.2025.100676","DOIUrl":"10.1016/j.rcsop.2025.100676","url":null,"abstract":"<div><h3>Background</h3><div>Medication adherence is essential for treatment success across both chronic and acute conditions. However, concise, multidimensional, and broadly applicable validated tools to measure medication adherence remain scarce.</div></div><div><h3>Objectives</h3><div>This study primarily aimed to develop and validate the Short Medication Adherence Scale (SMAS-7) and, secondarily, to assess adherence levels and related factors in a general adult population.</div></div><div><h3>Methods</h3><div>A cross-sectional study was conducted among Lebanese adults aged ≥18 years from the general population. Individuals who declined follow-up contact for the test-retest phase were excluded. The 7-item SMAS-7, developed from the LMAS-14, was administered electronically in Arabic using an online questionnaire. Exploratory and confirmatory factor analyses (EFA and CFA) were performed on two random subsamples to assess factorial structure and model fit. Internal consistency (Cronbach's α, McDonald's ω), test-retest reliability (ICC), and construct and criterion validity were evaluated. Multivariable logistic regression identified predictors of adherence using a ROC curve-derived SMAS-7 cut-off score.</div></div><div><h3>Results</h3><div>A total of 501 participants were included in the study. EFA revealed a 3-factor structure, psychological, economic, and behavioral domains, supported by KMO = 0.830 and significant Bartlett's test (<em>P</em> &lt; 0.001). CFA confirmed the structure with excellent fit (χ<sup>2</sup>/df = 1.757, CFI = 0.992, TLI = 0.985, RMSEA = 0.055, SRMR = 0.020). The SMAS-7 demonstrated high internal consistency (α = 0.889, ω = 0.945) and test-retest reliability (ICC = 0.779). Criterion validity was excellent (AUC = 0.985; sensitivity = 91.2 %; specificity = 96.0 %). Suboptimal adherence was observed in 52.3 % of participants. Significant predictors of adherence included gender (<em>P</em> = 0.030), region (<em>P</em> = 0.014), financial well-being (<em>P</em> = 0.002), chronic illness (<em>P</em> = 0.009), communication barriers (<em>P</em> = 0.013), and patient perception (<em>P</em> = 0.029).</div></div><div><h3>Conclusion</h3><div>The SMAS-7 demonstrated strong preliminary psychometric properties in this initial validation study. It offers a valuable resource for researchers, clinicians, and policymakers seeking to monitor and enhance adherence behaviors. While these findings are encouraging, further studies in diverse populations and clinical settings are required to confirm its external validity and generalizability. The findings revealed suboptimal adherence and underscored the multifaceted nature of its predictors, highlighting the need for targeted, multidimensional interventions.</div></div>","PeriodicalId":73003,"journal":{"name":"Exploratory research in clinical and social pharmacy","volume":"20 ","pages":"Article 100676"},"PeriodicalIF":1.8,"publicationDate":"2025-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145415761","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
Exploratory research in clinical and social pharmacy
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:604180095
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