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Behind the counter, behind the discourse: The paradox of pharmacist influence in Arabic women's health online 柜台背后,话语背后:药剂师对阿拉伯妇女在线健康影响的悖论
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2026-03-01 Epub Date: 2025-12-11 DOI: 10.1016/j.rcsop.2025.100697
Samar J. Melhem , Hamzeh Almomani , Rimal Mousa , Qais Alefan , Nadia Al Mazrouei , Beisan A. Mohammed , Iman Amrani , Rula M. Darwish , Razan Tubeileh , Yazan AlRashadan , Nailya Bulatova , Ibrahim Alabbadi

Background

Social media is now a major arena for Arabic women's health discourse in the MENA region, yet it is unclear how pharmacists' expertise influences both the accuracy and visibility of information across platforms.

Objective

To compare pharmacists' visibility and accuracy with other author groups and to assess how platform, sentiment, and follower dynamics shape the gap between information quality and reach.

Methods

We conducted a cross-sectional content analysis of 682 public Arabic-language posts on women's self-medication and over-the-counter care from Instagram, YouTube, TikTok, Threads, Facebook, and X (January 2024–March 2025). Two independent coders rated accuracy on a four-point scale and classified sentiment (κ > 0.80). Engagement was summarized using the Virtual Presence Index (VPI), an equally weighted composite of standardized likes, comments, and shares/reposts. Proportional-odds ordinal logistic regression modeled predictors of higher accuracy; a non-circular binary logistic model examined determinants of high engagement (above-median VPI) with platform, author type, sentiment, topic, and linear plus quadratic log₁₀(follower count) as covariates.

Results

Pharmacists authored 49.6 % of posts; physicians and other health professionals contributed 37.1 %. Overall, 71.8 % of posts were rated accurate, rising to 94.1 % for pharmacist-authored content. Platform was the strongest predictor of accuracy: compared with Instagram, Facebook, YouTube, Threads, and X had higher odds of higher accuracy, with TikTok showing a smaller but significant advantage. Pharmacist authorship independently predicted higher accuracy, whereas follower count did not. For engagement, platform dominated. With X as the reference, all other platforms had lower adjusted odds of high VPI. Positive sentiment increased the likelihood of high VPI, and follower count showed a U-shaped association, with mid-sized accounts disadvantaged. After adjustment, author-type differences in visibility were modest: pharmacists' posts were more accurate but did not enjoy consistent visibility advantages, especially on highly visual, fast-scroll platforms.

Conclusion

In Arabic women's health discourse online, who speaks matters less for reach than where and how they speak. Pharmacists deliver the most accurate content but often remain “invisible experts” in environments that reward aesthetics and emotion over credentials. The VPI helps quantify this quality–reach gap and can guide platform-specific, culturally attuned strategies to make evidence-based voices more discoverable.
社交媒体现在是中东和北非地区阿拉伯妇女健康话语的主要舞台,但尚不清楚药剂师的专业知识如何影响跨平台信息的准确性和可见性。目的比较药师与其他作者群体的可见性和准确性,并评估平台、情绪和追随者动态如何影响信息质量和覆盖范围之间的差距。方法对Instagram、YouTube、TikTok、Threads、Facebook和X网站(2024年1月至2025年3月)上682篇关于女性自我用药和非处方护理的公开阿拉伯语帖子进行了横断面内容分析。两名独立编码员以四分制对准确率进行评分,并对情绪进行分类(κ > 0.80)。参与度是用虚拟存在指数(VPI)来总结的,VPI是标准化的点赞、评论和分享/转发的加权组合。比例-几率有序logistic回归模型预测精度较高;非循环二元逻辑模型以平台、作者类型、情感、主题和线性加二次对数1 0(追随者数)为协变量,检验了高参与度(高于中位数VPI)的决定因素。结果药师占发文总数的49.6%;医生和其他卫生专业人员贡献了37.1%。总体而言,71.8%的帖子被评为准确,药剂师撰写的内容上升到94.1%。平台是准确性的最强预测指标:与Instagram、Facebook、YouTube、Threads和X相比,它们的准确率更高,而TikTok的优势较小,但很明显。药剂师作者独立预测更高的准确性,而追随者数量则没有。在用户粘性方面,平台占主导地位。以X为参照,所有其他平台的高VPI调整几率都较低。积极的情绪增加了高VPI的可能性,关注者数量呈u型关系,中等规模的账户处于不利地位。调整后,作者类型的可见性差异不大:药剂师的帖子更准确,但不具有一致的可见性优势,特别是在高度视觉化、快速滚动的平台上。结论在阿拉伯妇女在线健康讨论中,谁发言比她们在哪里以及如何发言更重要。药剂师提供最准确的内容,但往往是“隐形专家”在环境中,奖励美学和情感的凭据。VPI有助于量化这种质量覆盖差距,并可以指导针对特定平台的、与文化相适应的策略,使基于证据的声音更容易被发现。
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引用次数: 0
Field survey on warnings to prevent drug abuse when selling over-the-counter drugs at drugstores 实地调查药店销售非处方药时防止滥用药物的警告
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2026-03-01 Epub Date: 2025-12-03 DOI: 10.1016/j.rcsop.2025.100690
Kazuki Nagashima, Hinata Nasu, Yuko Sekine

Objective

The abuse of over-the-counter (OTC) medications is increasing and has led to a rise in overdose cases. This study examined commonly misused OTC drugs, developed checklist items related to warnings provided during their sale, and conducted field surveys to compare practices based on whether products contained ingredients designated by the Ministry of Health, Labour and Welfare (MHLW), Japan.

Methods

An eight items checklist was developed using MHLW-specified survey items, with additional items added by the researchers. Using this checklist, a researcher evaluated OTC purchases for 25 different drugs by marking each item as positive (〇) or negative (×) from 17 drugstores.

Results

Across 25 products surveyed, the most common positive item was “explanation by a qualified person” (11 positives, 44 %), followed by “point-of-purchase (POP) warning displays” (9 positives, 36 %) and “display near the cash register” (8 positives, 32 %). For OTC drugs containing designated ingredients (n = 13), the item achievement rates were as follows: “explanation by a qualified person,” 10 positives, 77 %; “POP warning displays,” 9 positives, 69 %; “display of empty boxes,” 2 positives, 15 %; and “verbal verification of age,” 1 positive, 8 %. The aforementioned items were less likely in the case of OTC drugs without designated ingredients with potential for abuse, with the number of instances of “explanation by a qualified person” and “POP warning displays” being significantly lower (p < 0.05).

Conclusion

To intervene with targets to prevent abuse and issue warnings about OTC drugs during a sale, proactive warnings about misused OTC drugs that do not contain designated ingredients are necessary.
目的滥用非处方药物(OTC)的情况正在增加,并导致药物过量的病例增加。本研究审查了常被滥用的非处方药,制定了与销售期间提供的警告有关的清单项目,并进行了实地调查,以根据产品是否含有日本卫生、劳动和福利部指定的成分来比较做法。方法采用《卫生与社会保障法》规定的调查项目编制8项问卷,并由研究者自行补充。使用该清单,研究人员通过将17家药店的25种不同药物标记为阳性(〇)或阴性(x)来评估OTC购买情况。结果在调查的25种产品中,最常见的正面项目是“有资格的人解释”(11个阳性,44%),其次是“购买点(POP)警告显示”(9个阳性,36%)和“收银机附近显示”(8个阳性,32%)。对于指定成分的非处方药(n = 13),项目完成率如下:“有资质人员解释”,阳性10个,77%;“POP警告显示”,9个阳性,69%;“展示空盒子”,2个阳性,15%;而“口头年龄验证”,1%是肯定的,8%。在没有指定成分的非处方药中,出现上述问题的可能性较低,出现“有资质人员解释”和“POP警告显示”的次数明显较低(p < 0.05)。结论要有针对性地进行干预,防止滥用,并在销售过程中对非处方药发出警告,有必要对不含指定成分的非处方药被滥用进行主动警告。
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引用次数: 0
Patients' perspectives and experiences regarding medication reviews: A cross-sectional survey study 患者对药物评价的看法和经验:一项横断面调查研究
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2026-03-01 Epub Date: 2025-12-05 DOI: 10.1016/j.rcsop.2025.100692
Charlotte Falke , Fatma Karapinar-Çarkit , Wilma Knol , Marcel Bouvy , Toine Egberts , Thomas Kempen , Marcia Vervloet , Mette Heringa

Background

Medication reviews are conducted worldwide to reduce medication-related problems. However, real-world patient perspectives and experiences remain underexplored. This study aimed to explore patients' perspectives and experiences regarding medication reviews and to assess differences across levels of polypharmacy.

Methods

A cross-sectional online survey was conducted among a panel of Dutch pharmacy visitors. Topics included perspectives and experiences regarding medication reviews. Descriptive statistics were used, and Chi-square tests were used to assess differences between levels of polypharmacy (non-polypharmacy: 1–4 medications; polypharmacy: 5–9 medications; hyperpolypharmacy: ≥10 medications).

Results

Among 4395 respondents (median age: 71; 43 % female), 48 % were aware of the existence of medication reviews, and 85 % deemed these important. Patients valued discussing the appropriateness, efficacy, side-effects, and risks of medication more than practical medication-related issues. These perspectives were consistent across polypharmacy levels. Overall, 1176 patients (27 %) had experienced a review (non-polypharmacy: 22 %; polypharmacy: 29 %; hyperpolypharmacy: 39 %). Of these, 92 % felt able to ask questions, and 62 % felt treatment options were sufficiently discussed. Patients reported that their review resulted in better medication understanding (68 %), increased confidence in medication usage (65 %), and fewer health issues (40 %). Patients with non-polypharmacy reported improvements in follow-up agreements (9 %) and involvement of secondary healthcare providers (11 %) less frequently than those with polypharmacy (14 %/15 %) and hyperpolypharmacy (19 %/26 %).

Conclusion

Most patients valued medication reviews, yet only half were aware of their existence. Generally, levels of polypharmacy hardly impacted patient perspectives. Based on patients' experiences, shared decision-making, follow-ups, and multidisciplinary approaches could be better implemented in medication reviews.
在世界范围内进行药物审查是为了减少与药物有关的问题。然而,现实世界患者的观点和经验仍未得到充分探索。本研究旨在探讨患者对药物评价的看法和经验,并评估不同层次的综合用药的差异。方法采用横断面在线调查方法,对荷兰药店的来访人员进行调查。主题包括关于药物审查的观点和经验。采用描述性统计,并采用卡方检验评估多药水平(非多药:1-4种药物;多药:5-9种药物;多药:≥10种药物)之间的差异。结果在4395名受访者中(中位年龄:71岁,43%为女性),48%的人知道药物评价的存在,85%的人认为药物评价很重要。患者更重视讨论药物的适当性、疗效、副作用和风险,而不是实际的药物相关问题。这些观点是一致的在多药水平。总体而言,1176名患者(27%)接受了复查(非多种药物:22%;多种药物:29%;过度多种药物:39%)。其中,92%的人认为能够提出问题,62%的人认为治疗方案得到了充分的讨论。患者报告说,他们的回顾使他们更好地了解药物(68%),增加了对药物使用的信心(65%),减少了健康问题(40%)。与综合用药(14% / 15%)和综合用药(19% / 26%)的患者相比,非综合用药的患者在随访协议(9%)和二级医疗保健提供者的参与(11%)方面有所改善。结论大多数患者重视药物评价,但仅有一半患者意识到药物评价的存在。一般来说,多药水平几乎不影响患者的观点。基于患者的经验,共同决策、随访和多学科方法可以更好地在药物评审中实施。
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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 : 2026-03-01 Epub 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":"2026-03-01","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
Analysis of Defined Daily Dose (DDD) and antibiotic problems in Intensive Care Unit (ICU) patients 重症监护病房(ICU)患者限定日剂量(DDD)及抗生素问题分析
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2026-03-01 Epub Date: 2025-12-07 DOI: 10.1016/j.rcsop.2025.100688
Yulistiani Yulistiani , Hargus Haraudi Barkah , Febriansyah Nur Utomo , Lucky Andrianto , Alena Putri Jathi , Nurrizky Grahitaning Putra Rohmaana Yudistira

Background

The increasing prevalence of antimicrobial resistance (AMR) in Intensive Care Unit (ICU) is posing a significant challenge to effective infection management. This shows the need for quantitative evaluation of antibiotic use through the Defined Daily Dose (DDD) method, combined with Drug Related Problems (DRPs) analysis to support Antimicrobial Stewardship (AMS) programs. Therefore, this study aimed to analyze the quantitative use of antibiotic using DDD method and identify DRP in ICU patients at Airlangga University Hospital. A retrospective cross-sectional study was conducted using medical records of ICU patients from July to December 2022. Antibiotic consumption was calculated in DDD per 100 patient-days following WHO standards, while DRPs were identified using the Cipolle and Pharmaceutical Care Network Europe (PCNE) v9.1 classifications. A total of 125 ICU patients met the inclusion criteria, with a predominance of pneumonia (40 %) and sepsis (25 %). The results showed that the total antibiotic consumption was 91.54 DDD/100 patient-days, with ceftriaxone having the highest (31.57 DDD/100 patient-days). The most frequent DRPs were unnecessary drug therapy (20 %) and suboptimal therapeutic effects (23 %), mainly due to inappropriate indications and deviations from treatment guidelines. Antibiotic use in ICU was dominated by ceftriaxone, and the high rate of DRPs showed the need for improved AMS. This study showed that strengthening interdisciplinary collaboration, regular audits, and adherence to clinical guidelines were essential steps to optimize antibiotic use and minimize the risk of resistance.
重症监护病房(ICU)抗菌素耐药性(AMR)的日益流行对有效的感染管理提出了重大挑战。这表明需要通过限定日剂量(DDD)方法对抗生素使用进行定量评估,并结合药物相关问题(DRPs)分析,以支持抗菌药物管理(AMS)计划。因此,本研究旨在利用DDD法分析艾朗加大学医院ICU患者抗生素的定量使用情况,并对DRP进行鉴定。对2022年7月至12月ICU患者病历进行回顾性横断面研究。按照世卫组织标准,以每100患者日的DDD计算抗生素消费量,而使用Cipolle和欧洲药物保健网络(PCNE) v9.1分类确定抗菌素。共有125例ICU患者符合纳入标准,以肺炎(40%)和败血症(25%)为主。结果显示,该院抗菌药物总用量为91.54 DDD/100患者-d,其中头孢曲松用量最高,为31.57 DDD/100患者-d。最常见的drp是不必要的药物治疗(20%)和治疗效果不理想(23%),主要是由于适应症不适当和偏离治疗指南。ICU的抗生素使用以头孢曲松为主,高DRPs率表明需要改进AMS。这项研究表明,加强跨学科合作、定期审核和遵守临床指南是优化抗生素使用和最大限度地减少耐药风险的必要步骤。
{"title":"Analysis of Defined Daily Dose (DDD) and antibiotic problems in Intensive Care Unit (ICU) patients","authors":"Yulistiani Yulistiani ,&nbsp;Hargus Haraudi Barkah ,&nbsp;Febriansyah Nur Utomo ,&nbsp;Lucky Andrianto ,&nbsp;Alena Putri Jathi ,&nbsp;Nurrizky Grahitaning Putra Rohmaana Yudistira","doi":"10.1016/j.rcsop.2025.100688","DOIUrl":"10.1016/j.rcsop.2025.100688","url":null,"abstract":"<div><h3>Background</h3><div>The increasing prevalence of antimicrobial resistance (AMR) in Intensive Care Unit (ICU) is posing a significant challenge to effective infection management. This shows the need for quantitative evaluation of antibiotic use through the Defined Daily Dose (DDD) method, combined with Drug Related Problems (DRPs) analysis to support Antimicrobial Stewardship (AMS) programs. Therefore, this study aimed to analyze the quantitative use of antibiotic using DDD method and identify DRP in ICU patients at Airlangga University Hospital. A retrospective cross-sectional study was conducted using medical records of ICU patients from July to December 2022. Antibiotic consumption was calculated in DDD per 100 patient-days following WHO standards, while DRPs were identified using the Cipolle and Pharmaceutical Care Network Europe (PCNE) v9.1 classifications. A total of 125 ICU patients met the inclusion criteria, with a predominance of pneumonia (40 %) and sepsis (25 %). The results showed that the total antibiotic consumption was 91.54 DDD/100 patient-days, with ceftriaxone having the highest (31.57 DDD/100 patient-days). The most frequent DRPs were unnecessary drug therapy (20 %) and suboptimal therapeutic effects (23 %), mainly due to inappropriate indications and deviations from treatment guidelines. Antibiotic use in ICU was dominated by ceftriaxone, and the high rate of DRPs showed the need for improved AMS. This study showed that strengthening interdisciplinary collaboration, regular audits, and adherence to clinical guidelines were essential steps to optimize antibiotic use and minimize the risk of resistance.</div></div>","PeriodicalId":73003,"journal":{"name":"Exploratory research in clinical and social pharmacy","volume":"21 ","pages":"Article 100688"},"PeriodicalIF":1.8,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145736978","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
Optimizing inpatient access to oral contraceptives: A quality improvement approach in behavioral health 优化住院患者获得口服避孕药:行为健康的质量改进方法
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2026-03-01 Epub Date: 2026-01-06 DOI: 10.1016/j.rcsop.2026.100703
Rachel S. Pierce , Devon N. Crews , Benjamin J. Pierce , Courtney K. Wulffson

Background

Continuity of oral contraceptive use during hospitalization is critical for reproductive health, yet behavioral health settings often deprioritize this need. At a Midwestern community hospital, pre-admission oral contraceptives were frequently withheld due to absent workflows, inventory limitations, and provider uncertainty.

Objective

The purpose of this quality improvement initiative was to design, implement, and evaluate a structured oral contraceptive procurement workflow to improve continuity of care and support reproductive autonomy for hospitalized behavioral health patients.

Methods

A quality improvement initiative introduced a structured oral contraceptive procurement workflow in an adult inpatient behavioral health unit. Using Plan-Do-Study-Act cycles, the multidisciplinary team addressed medication reconciliation, pharmacy coordination, and provider education. Data were collected retrospectively (2022−2023) and prospectively (January–April 2025) for females aged 18–49 prescribed oral contraceptives prior to admission.

Results

Oral contraceptive administration improved from 33 % (17/51) pre-intervention to 78 % (7/9) post-intervention (p = .023). Patients were seven times more likely to receive oral contraceptives after implementation, with a 95 % confidence interval ranging from 1.31 to 37.40. Missed doses persisted due to provider unawareness of workflow and outpatient pharmacy stock constraints.

Conclusions

Implementing a standardized workflow significantly enhanced oral contraceptive continuity for behavioral health inpatients. This systems-based approach demonstrates the value of interdisciplinary collaboration and pharmacy integration in closing reproductive care gaps. Future priorities include sustainability, electronic medical record integration, and broader adoption to advance reproductive health equity.
背景:住院期间持续使用口服避孕药对生殖健康至关重要,但行为健康机构往往不重视这一需求。在中西部的一家社区医院,由于缺乏工作流程、库存限制和提供者不确定,入院前口服避孕药经常被拒绝使用。目的:设计、实施和评估结构化的口服避孕药采购工作流程,以提高住院行为健康患者的护理连续性和生殖自主性。方法一项质量改进倡议在一家成人住院行为健康部门引入了结构化的口服避孕药采购工作流程。采用计划-执行-研究-行动周期,多学科团队解决了药物协调、药房协调和提供者教育问题。回顾性(2022 - 2023)和前瞻性(2025年1月- 4月)收集入院前处方口服避孕药的18-49岁女性的数据。结果口服避孕药给药率由干预前的33%(17/51)提高至干预后的78% (7/9)(p = 0.023)。实施后,患者接受口服避孕药的可能性增加了7倍,95%置信区间为1.31至37.40。由于供应商不了解工作流程和门诊药房库存限制,错过的剂量持续存在。结论实施标准化工作流程可显著提高行为健康住院患者口服避孕药的连续性。这种基于系统的方法证明了跨学科合作和药房整合在缩小生殖保健差距方面的价值。未来的优先事项包括可持续性、电子病历整合和更广泛的采用,以促进生殖健康公平。
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引用次数: 0
Coping strategies for managing medication side effects among patients with chronic diseases in Northwest Ethiopia: An interpretive phenomenological study. 埃塞俄比亚西北部慢性病患者药物副作用处理策略:一项解释性现象学研究。
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2026-03-01 Epub Date: 2026-02-01 DOI: 10.1016/j.rcsop.2026.100712
Desalegn Addis Mussie , Samuel Berihun Dagnew , Tigabu Eskeziya Zerihun , Abel Temeche kassaw , Woretaw Sisay Zewdu , Abaynesh Fentahun Bekalu , Tilaye Arega Moges , Fasil Bayafers Tamene , Samuel Agegnew Wondm , Getachew Yitayew Tarekegn

Background

Chronic diseases such as diabetes, cardiovascular conditions, and arthritis often require lifelong pharmacotherapy. Medication side effects can negatively affect patients' quality of life and adherence. Understanding how patients cope with these side effects is essential for improving patient-centered care.

Objective

This study aimed to explore the coping strategies used by patients with chronic diseases to manage medication-related side effects in Northwest Ethiopia.

Methods

An interpretive phenomenological study was conducted in five hospitals in the Amhara region between May and August 2025. Forty-seven adults experiencing medication side effects were purposively selected. Data were collected through in-depth interviews, transcribed verbatim, and analyzed thematically using Open Code version 4.03.

Results

Four major themes and nine subthemes emerged. Patients coped with side effects by modifying medication use (stopping, reducing, or changing timing), relying on faith and positive thinking, seeking alternative treatments (e.g., herbal remedies or traditional healers), and obtaining support from healthcare providers, family, and friends. While self-modification of medication sometimes provided temporary relief, it posed potential risks. In contrast, support from healthcare providers and social networks enhanced adherence and psychological resilience.

Conclusion

Patients in Ethiopia use diverse, culturally rooted strategies to cope with medication side effects. Some practices may compromise treatment effectiveness, highlighting the need for proactive, culturally sensitive interventions that combine patient education, spiritual support, and improved patient–provider communication to promote safe medication use, adherence, and overall well-being.
背景:慢性疾病如糖尿病、心血管疾病和关节炎往往需要终身药物治疗。药物副作用会对患者的生活质量和依从性产生负面影响。了解患者如何应对这些副作用对于改善以患者为中心的护理至关重要。目的:本研究旨在探讨埃塞俄比亚西北部慢性病患者处理药物相关副作用的应对策略。方法:于2025年5月至8月在阿姆哈拉地区5家医院进行解释性现象学研究。有目的地选择了47名经历药物副作用的成年人。通过深入访谈收集数据,逐字记录,并使用Open Code version 4.03进行主题分析。结果:出现了4个主要主题和9个次要主题。患者通过改变药物使用(停止、减少或改变时间)、依靠信念和积极思考、寻求替代治疗(例如草药或传统治疗师)以及获得医疗保健提供者、家人和朋友的支持来应对副作用。虽然药物的自我调整有时能暂时缓解症状,但也会带来潜在风险。相比之下,来自医疗保健提供者和社会网络的支持增强了依从性和心理弹性。结论:埃塞俄比亚的患者使用不同的、根植于文化的策略来应对药物副作用。一些做法可能会损害治疗效果,强调需要积极主动、文化敏感的干预措施,将患者教育、精神支持和改进的患者与提供者沟通结合起来,以促进安全用药、依从性和整体健康。
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引用次数: 0
Transition to electronic prescriptions in pharmacies: Workflows, services, and access to medication – A mixed methods approach 药店向电子处方的过渡:工作流程、服务和药物获取——混合方法方法。
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2026-03-01 Epub Date: 2026-01-25 DOI: 10.1016/j.rcsop.2026.100706
Alexander Graf, Maike Henningsen, Maximillian Zinner

Background

Germany's declining number of pharmacies raised concerns about patients' access to medication. To address this, pharmacies have started offering (digital) services, including analog and digital options such as phone consultation or medication delivery. According to existing literature, these services could improve access to medication. However, before the introduction of electronic prescriptions (ePs) in 2022, using these services in Germany was cumbersome.

Objectives

Given this context, the aim of the study was to examine the challenges and potentials of electronic prescriptions in German pharmacies.

Methods

A two-stage sequential mixed methods approach was used, combining semi-structured interviews with an online survey among 1215 pharmacists.

Results

Nearly half of surveyed pharmacists (49.3%) supported the transition to electronic prescriptions, while 37.0% opposed it. Technical errors were widespread (mentioned by 90.5%) and disrupted both dispensing and service workflows. Over half (53.3%) believed ePs worsened in-pharmacy pick-up for patients, while 59.3% saw no major effect on (digital) services. More than one in four (28.5%) observed improvements in medication delivery through digital transfer, but many noted increased competition from large online pharmacies, increased workflow complexity, limited perceived patient demand and low profitability.

Conclusion

Electronic prescriptions were associated with many challenges for pharmacists. Although they might have the potential to improve patient access to medications, this remains limited by technical instability, low patient digital literacy, and pharmacists' perceptions of limited usefulness. Enhancing pharmacist and patient experiences by reducing technical errors, ensuring profitability of (digital) services, and improving patients' readiness is essential to realize the potential of ePs.
背景:德国药房数量的减少引起了人们对患者获得药物的担忧。为了解决这个问题,药店已经开始提供(数字)服务,包括模拟和数字选项,如电话咨询或药物递送。根据现有文献,这些服务可以改善获得药物的途径。然而,在2022年引入电子处方(ePs)之前,在德国使用这些服务很麻烦。目的:在这种背景下,研究的目的是检查德国药房电子处方的挑战和潜力。方法:采用两阶段顺序混合方法,对1215名药师进行半结构化访谈与在线调查相结合。结果:近半数受访药师(49.3%)支持向电子处方过渡,37.0%反对。技术错误普遍存在(90.5%的人提到),并扰乱了分配和服务工作流程。超过一半(53.3%)的人认为ePs恶化了患者在药房取药的情况,而59.3%的人认为对(数字)服务没有重大影响。超过四分之一(28.5%)的受访者表示,通过数字传输改善了药物交付,但许多人指出,来自大型在线药店的竞争加剧,工作流程复杂性增加,患者需求有限,盈利能力低下。结论:电子处方给药师带来了诸多挑战。尽管它们可能有潜力改善患者获得药物的机会,但这仍然受到技术不稳定、患者数字素养低以及药剂师认为有用性有限的限制。通过减少技术错误、确保(数字)服务的盈利能力和提高患者的准备程度来改善药剂师和患者的体验,对于实现ePs的潜力至关重要。
{"title":"Transition to electronic prescriptions in pharmacies: Workflows, services, and access to medication – A mixed methods approach","authors":"Alexander Graf,&nbsp;Maike Henningsen,&nbsp;Maximillian Zinner","doi":"10.1016/j.rcsop.2026.100706","DOIUrl":"10.1016/j.rcsop.2026.100706","url":null,"abstract":"<div><h3>Background</h3><div>Germany's declining number of pharmacies raised concerns about patients' access to medication. To address this, pharmacies have started offering (digital) services, including analog and digital options such as phone consultation or medication delivery. According to existing literature, these services could improve access to medication. However, before the introduction of electronic prescriptions (ePs) in 2022, using these services in Germany was cumbersome.</div></div><div><h3>Objectives</h3><div>Given this context, the aim of the study was to examine the challenges and potentials of electronic prescriptions in German pharmacies.</div></div><div><h3>Methods</h3><div>A two-stage sequential mixed methods approach was used, combining semi-structured interviews with an online survey among 1215 pharmacists.</div></div><div><h3>Results</h3><div>Nearly half of surveyed pharmacists (49.3%) supported the transition to electronic prescriptions, while 37.0% opposed it. Technical errors were widespread (mentioned by 90.5%) and disrupted both dispensing and service workflows. Over half (53.3%) believed ePs worsened in-pharmacy pick-up for patients, while 59.3% saw no major effect on (digital) services. More than one in four (28.5%) observed improvements in medication delivery through digital transfer, but many noted increased competition from large online pharmacies, increased workflow complexity, limited perceived patient demand and low profitability.</div></div><div><h3>Conclusion</h3><div>Electronic prescriptions were associated with many challenges for pharmacists. Although they might have the potential to improve patient access to medications, this remains limited by technical instability, low patient digital literacy, and pharmacists' perceptions of limited usefulness. Enhancing pharmacist and patient experiences by reducing technical errors, ensuring profitability of (digital) services, and improving patients' readiness is essential to realize the potential of ePs.</div></div>","PeriodicalId":73003,"journal":{"name":"Exploratory research in clinical and social pharmacy","volume":"21 ","pages":"Article 100706"},"PeriodicalIF":1.8,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146168193","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
Self-medication with psychedelics: a scoping review and narrative synthesis of review-level evidence 自我用药与致幻剂:一个范围审查和叙述性综合审查水平的证据。
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2026-03-01 Epub Date: 2026-01-26 DOI: 10.1016/j.rcsop.2026.100709
Shreya Shiju , Rohan Tirumala , Elliot Marseille

Background

As public and scientific interest in psychedelics grows, unsupervised use for health purposes is increasing. In the U.S., past-year hallucinogen use nearly doubled from 2015 to 2023. Many individuals report self-treating physical or psychological symptoms without medical supervision using psychedelics—a practice termed self-medication. Despite this trend, review-level syntheses remain scarce.

Aim

This scoping review aimed to map and synthesize review-level evidence on the self-medication of psychedelics, including which substances are used, for what health-related purposes, and what benefits and harms have been reported.

Methods

We conducted a scoping review of review-level evidence on self-medication with psychedelics, following the PRISMA PRISMA-ScR (2018) checklist. Searches in PubMed, PsycINFO, and Google Scholar (October–November 2024) used the terms (“self-medication” OR “self-treatment”) AND “psychedelics.” Eligible reviews examined unsupervised use of classical or non-classical psychedelics for physical, mental, or behavioral conditions. Four reviewers independently screened all records. Data extraction was conducted using Elicit AI and was manually verified by reviewers. Methodological quality was assessed using AMSTAR criteria.

Results

Three reviews met inclusion criteria (systematic, scoping, narrative). Psilocybin and LSD were most frequently reported, primarily for cluster headache and chronic pain. Outcomes included abortive relief, prophylactic relief, and prolonged remission, often from microdosed regimens. Approximately 40% achieved full remission; 70% reported preventive benefit. Adverse effects were rare and brief. Motivations for self-use centered on coping, desperation, and dissatisfaction with conventional care.

Conclusions

Preliminary review-level evidence suggests that individuals self-medicating with psychedelics—particularly psilocybin and LSD—report symptom relief for conditions such as cluster headache, though findings remain limited by scarce and heterogeneous data. More rigorous research is needed to clarify effectiveness, safety, and real-world patterns of use.
背景:随着公众和科学界对致幻剂兴趣的增长,出于健康目的的无监督使用正在增加。在美国,过去一年的致幻剂使用量从2015年到2023年几乎翻了一番。许多人报告在没有医疗监督的情况下使用迷幻药自我治疗身体或心理症状——这种做法被称为自我用药。尽管有这种趋势,审查级别的综合仍然很少。目的:本范围审查的目的是绘制和综合关于致幻剂自我用药的审查级证据,包括使用哪些物质、出于何种健康相关目的以及已报告的益处和危害。方法:我们根据PRISMA PRISMA- scr(2018)清单,对自我使用迷幻药的评价级证据进行了范围审查。在PubMed, PsycINFO和谷歌Scholar(2024年10月至11月)的搜索中使用了术语(“自我用药”或“自我治疗”)和“迷幻药”。符合条件的综述检查了无监督使用经典或非经典迷幻药对身体、精神或行为的影响。四名审稿人独立筛选所有记录。数据提取使用Elicit AI进行,并由审稿人手动验证。采用AMSTAR标准评估方法学质量。结果:3篇综述符合纳入标准(系统性、范围性、叙述性)。裸盖菇素和LSD最常被报道,主要用于丛集性头痛和慢性疼痛。结果包括流产缓解、预防性缓解和延长缓解,通常来自微剂量方案。约40%达到完全缓解;70%报告了预防效果。不良反应罕见且短暂。自残的动机主要集中在应对、绝望和对传统护理的不满。结论:初步评价水平的证据表明,自我服用迷幻药的个体——尤其是裸盖菇素和lsd——报告了集束性头痛等症状的缓解,尽管研究结果仍然受到稀缺和异质性数据的限制。需要更严格的研究来澄清有效性、安全性和实际使用模式。
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引用次数: 0
Integrated pharmaceutical care model by unit-based clinical pharmacists: Implementation and clinical impact 以单位为单位的临床药师整合药学服务模式:实施及临床影响
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2026-03-01 Epub Date: 2025-12-18 DOI: 10.1016/j.rcsop.2025.100700
Kezhen Feng , Xinyan Han , Nan Lv , Chaogang Xiong , Yajing Li , Bo Yang , Jingjing Yi , Tao Zhang

Background

In response to China's National Health Commission mandates promoting unit-based clinical pharmacists, healthcare institutions face severe workforce shortages, creating a critical policy-resource disparity.

Objective

This study aimed to implement and evaluate a hybrid unit-based clinical pharmacist model in respiratory wards to address this gap.

Methods

A structured workflow was implemented, integrating morning clinical activities (joint physician-pharmacist rounds, medication reconciliation, and real-time interventions) with afternoon analytical tasks (medication order surveillance). The model was evaluated quantitatively from 2021 to 2024.

Results

Post-implementation, antimicrobial use density dropped from 114.43 to 103.82 DDDs/100 patient-days (a 9.3 % reduction), dual antimicrobial therapy fell from 29.89 % to 11.34 % (a 62.1 % reduction), and pharmacist-patient interactions rose 3.3-fold. Medication safety was enhanced, with adverse drug reaction reports growing from 34 to 61 (a 79.4 % increase). Seven representative cases illustrated the resolution of critical drug therapy issues, demonstrating the framework's capacity to augment stewardship and safety despite staffing constraints.

Conclusions

The hybrid model provides a scalable framework for hospitals addressing the clinical pharmacy staffing gap in China. By strategically allocating limited pharmacist resources, it enhances antimicrobial stewardship and medication safety while complying with national reforms.
为了响应中国国家卫生健康委员会推动以单位为基础的临床药师的要求,医疗机构面临着严重的劳动力短缺,造成了严重的政策-资源差距。目的在呼吸内科病房实施和评估混合单位临床药师模式,以解决这一问题。方法采用结构化的工作流程,将上午的临床活动(医药师联合查房、药物调解和实时干预)与下午的分析任务(医嘱监督)相结合。从2021年到2024年对该模型进行了定量评估。结果实施后,抗菌药物使用密度从114.43 DDDs/100患者-d下降到103.82 DDDs/100患者-d(下降9.3%),双重抗菌药物治疗从29.89%下降到11.34%(下降62.1%),药师与患者的相互作用增加了3.3倍。用药安全得到加强,药品不良反应报告从34例增加到61例(增加79.4%)。七个有代表性的案例说明了关键药物治疗问题的解决,证明了该框架在人员配备有限的情况下加强管理和安全的能力。结论混合模式为解决中国医院临床药学人员缺口提供了一个可扩展的框架。通过战略性地分配有限的药剂师资源,它加强了抗微生物药物管理和用药安全,同时符合国家改革。
{"title":"Integrated pharmaceutical care model by unit-based clinical pharmacists: Implementation and clinical impact","authors":"Kezhen Feng ,&nbsp;Xinyan Han ,&nbsp;Nan Lv ,&nbsp;Chaogang Xiong ,&nbsp;Yajing Li ,&nbsp;Bo Yang ,&nbsp;Jingjing Yi ,&nbsp;Tao Zhang","doi":"10.1016/j.rcsop.2025.100700","DOIUrl":"10.1016/j.rcsop.2025.100700","url":null,"abstract":"<div><h3>Background</h3><div>In response to China's National Health Commission mandates promoting unit-based clinical pharmacists, healthcare institutions face severe workforce shortages, creating a critical policy-resource disparity.</div></div><div><h3>Objective</h3><div>This study aimed to implement and evaluate a hybrid unit-based clinical pharmacist model in respiratory wards to address this gap.</div></div><div><h3>Methods</h3><div>A structured workflow was implemented, integrating morning clinical activities (joint physician-pharmacist rounds, medication reconciliation, and real-time interventions) with afternoon analytical tasks (medication order surveillance). The model was evaluated quantitatively from 2021 to 2024.</div></div><div><h3>Results</h3><div>Post-implementation, antimicrobial use density dropped from 114.43 to 103.82 DDDs/100 patient-days (a 9.3 % reduction), dual antimicrobial therapy fell from 29.89 % to 11.34 % (a 62.1 % reduction), and pharmacist-patient interactions rose 3.3-fold. Medication safety was enhanced, with adverse drug reaction reports growing from 34 to 61 (a 79.4 % increase). Seven representative cases illustrated the resolution of critical drug therapy issues, demonstrating the framework's capacity to augment stewardship and safety despite staffing constraints.</div></div><div><h3>Conclusions</h3><div>The hybrid model provides a scalable framework for hospitals addressing the clinical pharmacy staffing gap in China. By strategically allocating limited pharmacist resources, it enhances antimicrobial stewardship and medication safety while complying with national reforms.</div></div>","PeriodicalId":73003,"journal":{"name":"Exploratory research in clinical and social pharmacy","volume":"21 ","pages":"Article 100700"},"PeriodicalIF":1.8,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145924739","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
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