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Diseño del plan de acogida al paciente (onboarding) en una unidad multidisciplinar de asma grave 在多学科重症哮喘病房设计患者入职。
IF 1.3 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 DOI: 10.1016/j.farma.2025.07.003
Hilario Martínez-Barros , María Muñoz-García , Darío Antolín-Amérigo , Silvia Sánchez-Cuéllar , Ana Morales-Tirado , Ana de-Andrés-Martín , Gonzalo de-los-Santos-Granados , Laura Yeguas-Ramírez , Enrique Blitz-Castro , Alfonso Santamaría-Gadea , Belén de-la-Hoz-Caballer , Sagrario Martín-Aragón , David González-de-Olano , Ana María Álvarez-Díaz

Objetives

To design the patient onboarding in a multidisciplinary severe asthma unit, according to the needs identified by patients and professionals in the unit.

Methods

Qualitative study using the human-centred design conducted between November 2022 and February 2023. Patients and professionals from the severe asthma unit and experts in the methodology participated. Three workshops were held. In the first, we elaborated the patient experience map, identifying positive aspects and needs. Possible solutions were devised. In the second, we selected the solutions described in a previous project applicable to onboarding and determined the key moments. In the third, we finalised the definition of the key moments, the professionals in charge in each step and the tools to be incorporated. Finally, in short sessions (sprints) we developed the necessary material and infographics.

Results

We identified the main needs of patients (better control of the disease and autonomy in care, two-way conversation with professionals and receiving coordinated and personalised care) and professionals (defining, structuring, unifying and adapting the information provided to patients and managing to maintain open conversations with them). We determined that onboarding should establish a controlled welcome to the severe asthma unit, which is identifiable by patients, promotes the patient-professional relationship and the learning, use and functioning of the severe asthma unit.
Previously devised solutions applicable to onboarding, such as the landing kit or the patient diary, were selected. We established the key moments of onboarding (identification consultation, initial consultation, onboarding consultation and complementary consultations), the professionals involved and the necessary information, material and infographics.
Finally, we developed the design, structure and final content of the necessary tools, such as the patient diary or the asthma infographic.

Conclusions

This work has allowed us to design, structure and standardise the onboarding, providing an environment that facilitates self-care and open, empathetic, two-way conversation between patients and professionals, according with the key needs expressed by both. These findings may be useful for other multidisciplinary care units.
目的:根据患者和科室专业人员的需求,设计多学科重症哮喘病房的患者入职流程。方法:采用以人为本的定性研究,于2022年11月至2023年2月进行。重症哮喘病房的患者和专业人员以及研究方法的专家参与了调查。举办了三次讲习班。首先,我们详细阐述了患者体验图,确定了积极的方面和需求。他们想出了可能的解决办法。在第二部分中,我们选择了之前项目中描述的适用于入职的解决方案,并确定了关键时刻。第三,我们确定了关键时刻的定义,每个步骤中负责的专业人员以及需要使用的工具。最后,在简短的会议(冲刺)中,我们开发了必要的材料和信息图表。结果:我们确定了患者的主要需求(更好地控制疾病和自主护理,与专业人员进行双向对话,并接受协调和个性化的护理)和专业人员(定义、构建、统一和调整提供给患者的信息,并设法与他们保持开放的对话)。我们决定,入职应该建立一个受控的欢迎重症哮喘病房,这是由患者识别,促进患者-专业关系和学习,使用和严重哮喘病房的功能。选择了先前设计的适用于登机的解决方案,例如着陆套件或患者日记。我们建立了入职的关键时刻(识别咨询、初始咨询、入职咨询和补充咨询)、涉及的专业人员和必要的信息、材料和信息图表。最后,我们开发了必要工具的设计、结构和最终内容,如患者日记或哮喘信息图。结论:这项工作使我们能够根据患者和专业人员表达的关键需求,设计、构建和标准化入职培训,提供一个促进自我护理和开放、共情、双向对话的环境。这些发现可能对其他多学科护理单位有用。
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引用次数: 0
[Translated article] Reduction of unnecessary repackaging as an environmental sustainability measure 减少不必要的再包装作为环境可持续性措施。
IF 1.3 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 DOI: 10.1016/j.farma.2025.10.012
David García-Martínez , Manuela Martínez-Camacho , Aida Rueda-Naharro , David García-Marco

Objective

The main objective is to describe the project and evaluate the impact of replacing repackaged medications with unit dose presentations in 15 public hospitals within a regional health system. Secondary objectives include identifying differences in the changes implemented across the 15 audited hospitals and conducting an exploratory analysis of the potential impact in other non-audited centers that requested participation in the project.

Method

A database containing over 2,000 medications available in unit dose format was developed and is updated monthly. In parallel, an automated system based on decision-making algorithms was implemented to identify improvement opportunities in medication procurement. The system was adopted either individually by hospitals or through centralized structures at the regional or private level. The analysis included data from 15 public hospitals, where the reduction in repackaging and its environmental, economic, and operational impact were assessed by measuring material, time, and cost savings. The results were subsequently extrapolated to the 172 hospitals that applied.

Results

In the 15 monitored hospitals, repackaging of approximately 1.27 million tablets per year was avoided, resulting in estimated savings of 17,016 km of packaging material, 866 kg in weight, and 113,693 min of labor. The avoided costs in materials and machinery amounted to 36,274€ annually. No statistically significant differences were observed in project adoption across the hospitals (p = 0.234). The extrapolation to 172 hospitals suggests a potential impact of 16.67 million tablets no longer requiring repackaging per year, with an estimated savings of 2220.13 km of material, 24,723 h of labor, and 451,768€ annually.

Conclusions

Replacing repackaged medications with commercially available unit dose formats significantly reduced material consumption, labor time, and repackaging-related costs in the evaluated hospitals. The implementation of the project was consistent across the 15 monitored hospitals. Furthermore, the model proved to be scalable. The main limitation identified was the limited availability of unit dose medications on the market; therefore, it is recommended to prioritize their inclusion in procurement processes and to promote their development by the pharmaceutical industry.
目的:主要目的是描述该项目,并评估在区域卫生系统内的15家公立医院以单位剂量介绍取代重新包装药物的影响。次要目标包括确定在15家受审计医院中实施的变化的差异,并对要求参与该项目的其他未受审计中心的潜在影响进行探索性分析。方法:建立一个包含2000多种单位剂量药物的数据库,每月更新一次。同时,实施了基于决策算法的自动化系统,以识别药品采购中的改进机会。这一制度要么由医院单独采用,要么通过地区或私人一级的中央机构采用。分析包括来自15家公立医院的数据,通过测量材料、时间和成本节约来评估重新包装的减少及其对环境、经济和运营的影响。结果随后被外推到申请的172家医院。结果:在监测的15家医院中,每年避免重新包装约127万片,估计节省包装材料17016 公里,重量866 公斤,节省人工113693 分钟。每年可避免的材料和机械成本达36274欧元。各医院项目采用率差异无统计学意义(p = 0.234)。对172家医院的外推表明,每年不再需要重新包装的1667万片药片的潜在影响,估计可节省2220.13 公里的材料,24,723 小时的劳动力,每年节省451,768欧元。结论:在接受评估的医院中,用市售单位剂量格式替代重新包装的药物显著降低了材料消耗、劳动时间和重新包装相关成本。该项目在受监测的15家医院的执行是一致的。此外,该模型被证明是可扩展的。确定的主要限制是市场上单位剂量药物的供应有限;因此,建议优先将其纳入采购过程,并促进制药业的发展。
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引用次数: 0
Diseño y validación del índice de fragilidad IF-CSS basado en la valoración geriátrica integral para su aplicación en centros sociosanitarios 基于老年综合评价的IF-CSS衰弱指数在养老院应用的设计与验证。
IF 1.3 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 DOI: 10.1016/j.farma.2025.06.002
Juan Francisco Peris-Martí , Elia M. Fernández-Villalba , Patricia Bravo-José , Carmen Isabel Sáez-Lleó , Minerva Espert-Roig , Pilar Martínez-Antequera

Objective

To validate the IF-CSS frailty index according to its predictive capacity for mortality and to define the intervals compatible with frailty states.

Methods

An observational, retrospective, multicenter study of a cohort of elderly patients from four nursing homes with a follow up between 12 and 38 months was conducted. The IF-CSS comprised 17 variables across four domains from the comprehensive geriatric assessment. Contrast of hypothesis log-rank for survival curves according to IF-CSS index was performed. The predictive model of survival time was performed using a parametric accelerated failure model.

Results

535 patients with a mean age of 83.62 years (DE± 7.84) were included. Mortality rate during the study period was 39.8%. Survival curves by frailty intervals showed significant differences (χ2 = 92; p < 0.001). The comparative analysis also showed significant differences for almost all the variables included in the construct. The parametric model of accelerated failure estimated a 29% reduction in survival time for each tenth of an increase in the IF-CSS.

Conclusions

The IF-CSS results in a tool with a frailty discriminative and mortality predictive capacity that allows its use in the care programs of nursing homes.
目的:验证IF-CSS衰弱指数对死亡率的预测能力,确定与衰弱状态相适应的区间。方法:一项观察性、回顾性、多中心研究,对来自四家养老院的老年患者进行随访,随访时间为12至38 个月。IF-CSS包括综合老年评估四个领域的17个变量。根据IF-CSS指数对生存曲线的假设log-rank进行比较。采用参数加速失效模型建立存活时间预测模型。结果:纳入535例患者,平均年龄83.62 岁(DE±7.84)。研究期间的死亡率为39.8%。不同脆弱期生存率差异有统计学意义(χ2 = 92;p 结论:IF-CSS产生了一个具有虚弱判别和死亡率预测能力的工具,可以在养老院的护理计划中使用。
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引用次数: 0
Contribución del metabolito N-óxido en la monitorización terapéutica de voriconazol en un paciente con aspergilosis invasiva n -氧化物代谢物在侵袭性曲霉病患者伏立康唑治疗药物监测中的作用。
IF 1.3 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 DOI: 10.1016/j.farma.2025.05.012
Irene Orozco Cifuentes, Adrián Domínguez García, María Jiménez Meseguer, Elena García Benayas, Benito García Díaz
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引用次数: 0
[Translated article] Evaluation of penicillin allergy labeling in the emergency department: Retrospective study on the impact of a hospital pharmacist-led intervention algorithm 急诊科青霉素过敏标签评价:医院药师主导干预算法影响的回顾性研究。
IF 1.3 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 DOI: 10.1016/j.farma.2025.10.002
Fernando Salazar González , Mireia Iglesias Rodrigo , Gemma Garreta Fontelles , Mireia Mensa Vendrell , Jordi Nicolás Picó

Objective

To evaluate the impact of an intervention algorithm on penicillin allergy label reassessment in emergency department patients, aiming to optimize antibiotic selection and improve patient safety.

Methods

A retrospective observational study was conducted in a 450-bed hospital, including adult patients with a penicillin allergy label admitted to the emergency department between November 2023 and August 2024. An algorithm developed by the pharmacy service in collaboration with the ASP team was applied, based on validated tools such as the Penicillin Allergy De-Labelling Toolkit, PEN-FAST, and Antibiotic Allergy Assessment Tool. Demographic data, allergy history, and clinical outcomes were collected. The acceptance of recommendations and the incidence of adverse reactions were analyzed.

Results

A total of 66 patients were evaluated. Delabeling was proposed in 35 (53.03%) patients, skin testing in 13 (19.69%), oral provocation testing in 9 (13.63%), and label maintenance in 9 (13.63%). A total of 89.39% of the recommendations were accepted, achieving effective delabeling in 42 patients. No adverse reactions were recorded. In 21 cases, antibiotic therapy was optimized following the intervention.

Conclusions

The implementation of a structured algorithm for penicillin allergy reassessment in emergency settings is both effective and safe. Its application facilitates antibiotic optimization, improves patient safety, and reduces broad-spectrum antibiotic use. This study highlights the role of hospital pharmacists in drug allergy management and antimicrobial stewardship.
目的:评价一种干预算法对急诊科患者青霉素过敏标签重评的影响,优化抗生素选择,提高患者安全。方法:在一家拥有450个床位的医院进行回顾性观察研究,包括2023年11月至2024年8月期间急诊科收治的青霉素过敏成人患者。基于青霉素过敏去标签工具包、PEN-FAST和抗生素过敏评估工具等经过验证的工具,应用了药房服务与ASP团队合作开发的算法。收集了人口统计数据、过敏史和临床结果。分析建议的接受程度和不良反应的发生率。结果:共评估66例患者。35例(53.03%)患者建议去标签,13例(19.69%)患者建议皮肤试验,9例(13.63%)患者建议口服激发试验,9例(13.63%)患者建议标签维持。共有89.39%的建议被接受,42例患者实现了有效的去标签。无不良反应记录。在21例中,抗生素治疗在干预后得到优化。结论:在紧急情况下实施结构化的青霉素过敏再评估算法是有效和安全的。它的应用促进了抗生素的优化,提高了患者的安全性,并减少了广谱抗生素的使用。本研究强调医院药师在药物过敏管理和抗菌药物管理中的作用。
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引用次数: 0
[Translated article] Achievements and challenges ahead for the journal Farmacia Hospilataria [译文]《医院药学》杂志的成就与挑战。
IF 1.3 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 DOI: 10.1016/j.farma.2025.11.009
Teresa Bermejo Vicedo, Maria Queralt Gorgas, Luis Margusino Framiñan
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引用次数: 0
[Translated article] Designing a patient onboarding in a multidisciplinary severe asthma unit 在多学科重症哮喘病房设计患者入职。
IF 1.3 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 DOI: 10.1016/j.farma.2025.10.009
Hilario Martínez-Barros , María Muñoz-García , Darío Antolín-Amérigo , Silvia Sánchez-Cuéllar , Ana Morales-Tirado , Ana de-Andrés-Martín , Gonzalo de-los-Santos-Granados , Laura Yeguas-Ramírez , Enrique Blitz-Castro , Alfonso Santamaría-Gadea , Belén de-la-Hoz-Caballer , Sagrario Martín-Aragón , David González-de-Olano , Ana María Álvarez-Díaz

Objetives

To design the patient onboarding in a multidisciplinary severe asthma unit, according to the needs identified by patients and professionals in the unit.

Methods

Qualitative study using the human-centred design conducted between November 2022 and February 2023. Patients and professionals from the severe asthma unit and experts in the methodology participated. Three workshops were held. In the first, we elaborated the patient experience map, identifying positive aspects and needs. Possible solutions were devised. In the second, we selected the solutions described in a previous project applicable to onboarding and determined the key moments. In the third, we finalised the definition of the key moments, the professionals in charge in each step and the tools to be incorporated. Finally, in short sessions (sprints) we developed the necessary material and infographics.

Results

We identified the main needs of patients (better control of the disease and autonomy in care, two-way conversation with professionals and receiving coordinated and personalised care) and professionals (defining, structuring, unifying and adapting the information provided to patients and managing to maintain open conversations with them). We determined that onboarding should establish a controlled welcome to the severe asthma unit, which is identifiable by patients, promotes the patient-professional relationship and the learning, use and functioning of the severe asthma unit.
Previously devised solutions applicable to onboarding, such as the landing kit or the patient diary, were selected. We established the key moments of onboarding (identification consultation, initial consultation, onboarding consultation and complementary consultations), the professionals involved and the necessary information, material and infographics.
Finally, we developed the design, structure and final content of the necessary tools, such as the patient diary or the asthma infographic.

Conclusions

This work has allowed us to design, structure and standardise the onboarding, providing an environment that facilitates self-care and open, empathetic, two-way conversation between patients and professionals, according with the key needs expressed by both. These findings may be useful for other multidisciplinary care units.
目的:根据患者和科室专业人员的需求,设计多学科重症哮喘病房的患者入职流程。方法:采用以人为本的定性研究,于2022年11月至2023年2月进行。重症哮喘病房的患者和专业人员以及研究方法的专家参与了调查。举办了三次讲习班。首先,我们详细阐述了患者体验图,确定了积极的方面和需求。他们想出了可能的解决办法。在第二部分中,我们选择了之前项目中描述的适用于入职的解决方案,并确定了关键时刻。第三,我们确定了关键时刻的定义,每个步骤中负责的专业人员以及需要使用的工具。最后,在简短的会议(冲刺)中,我们开发了必要的材料和信息图表。结果:我们确定了患者的主要需求(更好地控制疾病和自主护理,与专业人员进行双向对话,并接受协调和个性化的护理)和专业人员(定义、构建、统一和调整提供给患者的信息,并设法与他们保持开放的对话)。我们决定,入职应该建立一个受控的欢迎重症哮喘病房,这是由患者识别,促进患者-专业关系和学习,使用和严重哮喘病房的功能。选择了先前设计的适用于登机的解决方案,例如着陆套件或患者日记。我们建立了入职的关键时刻(识别咨询、初始咨询、入职咨询和补充咨询)、涉及的专业人员和必要的信息、材料和信息图表。最后,我们开发了必要工具的设计、结构和最终内容,如患者日记或哮喘信息图。结论:这项工作使我们能够根据患者和专业人员表达的关键需求,设计、构建和标准化入职培训,提供一个促进自我护理和开放、共情、双向对话的环境。这些发现可能对其他多学科护理单位有用。
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引用次数: 0
[Translated article] Contribution of N-oxide metabolite in the therapeutic drug monitoring of voriconazole in a patient with invasive aspergillosis n -氧化物代谢物在侵袭性曲霉病患者伏立康唑治疗药物监测中的作用。
IF 1.3 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 DOI: 10.1016/j.farma.2025.05.019
Irene Orozco Cifuentes, Adrián Domínguez García, María Jiménez Meseguer, Elena García Benayas, Benito García Díaz
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引用次数: 0
Evaluación de etiquetas de alergia a penicilinas en urgencias: estudio retrospectivo del impacto de un algoritmo de intervención liderado por farmacéuticos hospitalarios 急诊科青霉素过敏标签评价:医院药师主导干预算法影响的回顾性研究。
IF 1.3 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 DOI: 10.1016/j.farma.2025.05.013
Fernando Salazar González , Mireia Iglesias Rodrigo , Gemma Garreta Fontelles , Mireia Mensa Vendrell , Jordi Nicolás Picó

Objective

To evaluate the impact of an intervention algorithm on penicillin allergy label reassessment in emergency department patients, aiming to optimize antibiotic selection and improve patient safety.

Methods

A retrospective observational study was conducted in a 450-bed hospital, including adult patients with a penicillin allergy label admitted to the emergency department between November 2023 and August 2024. An algorithm developed by the pharmacy service in collaboration with the ASP team was applied, based on validated tools such as the Penicillin Allergy De-Labelling Toolkit, PEN-FAST, and Antibiotic Allergy Assessment Tool. Demographic data, allergy history, and clinical outcomes were collected. The acceptance of recommendations and the incidence of adverse reactions were analyzed.

Results

A total of 66 patients were evaluated. Delabeling was proposed in 35 (53.03%) patients, skin testing in 13 (19.69%), oral provocation testing in 9 (13.63%), and label maintenance in 9 (13.63%). A total of 89.39% of the recommendations were accepted, achieving effective delabeling in 42 patients. No adverse reactions were recorded. In 21 cases, antibiotic therapy was optimized following the intervention.

Conclusions

The implementation of a structured algorithm for penicillin allergy reassessment in emergency settings is effective and safe. Its application facilitates antibiotic optimization, improves patient safety, and reduces broad-spectrum antibiotic use. This study highlights the role of hospital pharmacists in drug allergy management and antimicrobial stewardship.
目的:评价一种干预算法对急诊科患者青霉素过敏标签重评的影响,优化抗生素选择,提高患者安全。方法:在一家拥有450个床位的医院进行回顾性观察研究,包括2023年11月至2024年8月期间急诊科收治的青霉素过敏成人患者。基于青霉素过敏去标签工具包、PEN-FAST和抗生素过敏评估工具等经过验证的工具,应用了药房服务与ASP团队合作开发的算法。收集了人口统计数据、过敏史和临床结果。分析建议的接受程度和不良反应的发生率。结果:共评估66例患者。35例(53.03%)患者建议去标签,13例(19.69%)患者建议皮肤试验,9例(13.63%)患者建议口服激发试验,9例(13.63%)患者建议标签维持。共有89.39%的建议被接受,42例患者实现了有效的去标签。无不良反应记录。在21例中,抗生素治疗在干预后得到优化。结论:在紧急情况下实施结构化的青霉素过敏再评估算法是有效和安全的。它的应用促进了抗生素的优化,提高了患者的安全性,并减少了广谱抗生素的使用。本研究强调医院药师在药物过敏管理和抗菌药物管理中的作用。
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引用次数: 0
Autorización de medicamentos de uso off-label en un hospital de tercer nivel: perspectiva de 5 años 三级医院超说明书用药的授权:5年展望
IF 1.3 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2026-01-01 DOI: 10.1016/j.farma.2025.05.018
Lupe Rodríguez-de Francisco, Ángela María Villalba-Moreno, Eva Rocío Alfaro-Lara

Introduction

The off-label use of drugs requires scientific support to balance risk/benefit, being limited to exceptional cases in which there are no therapeutic alternatives.

Methods

Retrospective descriptive study of the reports of the Pharmacy and Therapeutics Committee between 2018 and 2022 in a third level hospital; analyzing the requests, drugs, final opinion, reasons, level of evidence and economic impact.

Results

A total of 124 reports were analyzed, highlighting oncohematological (41.9%) and autoimmune (27.4%) diseases as main indications. Oncology (37.1%) and Pediatrics (18.5%) were the main applicants, with 87.9% for antineoplastic and immunomodulatory drugs. A total of 74.2% of the applications were approved due to lack of alternatives and solid evidence (phase II-III trials), while 25.8% were denied due to the availability of therapeutic options or insufficient evidence. In terms of cost, 53% of oncohematological drugs cost between €10,000–50,000/treatment and 62.1% of non-oncohematological drugs cost between €1,000–10,000/year. Approval of the rejected treatments would have generated an additional expenditure of €2,272,603.

Conclusion

An increase of up to four times in the evaluation of off-label use drugs was evidenced, with a high approval rate.
药物的超说明书使用需要科学支持来平衡风险/收益,仅限于没有治疗替代方案的特殊情况。方法:对某三级医院2018 - 2022年药学与治疗学委员会报告进行回顾性描述性研究;分析请求、药品、最终意见、原因、证据水平和经济影响。结果:共分析124例报告,以血液病(41.9%)和自身免疫性疾病(27.4%)为主要适应症。肿瘤(37.1%)和儿科(18.5%)是主要的申请人,抗肿瘤和免疫调节药物占87.9%。共有74.2%的申请由于缺乏替代方案和可靠的证据(II-III期试验)而被批准,而25.8%的申请由于治疗方案的可用性或证据不足而被拒绝。在费用方面,53%的血液肿瘤药物费用在1万-5万欧元/次治疗之间,62.1%的非血液肿瘤药物费用在1000 -1万欧元/年之间。批准被拒绝的治疗将产生2,272,603欧元的额外支出。结论:超说明书用药的审评增加了4倍以上,审评合格率较高。
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引用次数: 0
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FARMACIA HOSPITALARIA
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