Prescribing

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  • 文章类型: Journal Article
    近几十年来,随着该领域的新兴研究,人们对Türkiye的临床药学实践产生了兴趣。尽管最近在蒂尔基耶出现了各种药学实践研究,迄今为止,尚未对研究的总体类型和影响进行全面评估。
    本系统综述旨在记录和评估过去5年在Türkiye发表的药物政策和实践文献。另一个目的是总结已发表的研究对政策和实践研究的预期影响。
    系统审查是根据PRISMA声明中描述的指南进行的。全面的搜索方法,采用医学主题词(MeSH)查询和自由文本术语来查找与Türkiye的药学实践和政策相关的相关文献。搜索范围为2019年1月1日至2024年1月1日,涉及包括PubMed在内的电子数据库,MedlineOvid,Scopus,ScienceDirect,SpringerLink,PlosOne,BMC。
    在最后的分组中,73篇文章符合纳入标准,入选本综述。在定量研究中,大多数研究是横断面调查研究.通过严格的主题内容分析,从选定的文献中开发了七个研究领域:药物利用和合理用药,药剂师的新角色,获得药品和仿制药,社区药学实践,药物警戒/药物不良反应,和药物经济学研究。
    药剂师的角色正在演变;然而,充分发挥药剂师的潜力仍然存在一些挑战。这些包括监管障碍,公众对药剂师扩大角色的认识有限,劳动力能力问题,以及需要持续的专业发展和培训。在仿制药领域需要进行研究,药物依从性,社区和医院药学实践中的干预研究,以及药物经济学和药物警戒。
    UNASSIGNED: In recent decades, there has been an interest in clinical pharmacy practice in Türkiye with emerging studies in this area. Despite the recent emergence of diverse pharmacy practice studies in Türkiye, a comprehensive assessment of overall typology of studies and impact has not been conducted thus far.
    UNASSIGNED: This systematic review aims to document and assess pharmaceutical policy and practice literature published within the last 5 years in Türkiye. The other aim is to summarise the expected impact of published studies on policy and practice research.
    UNASSIGNED: The systematic review was conducted according to the guidelines described in the PRISMA Statement. A comprehensive search approach, incorporating Medical Subject Headings (MeSH) queries and free-text terms was employed to locate pertinent literature related to pharmacy practice and policy in Türkiye. The search covered the period from January 1, 2019, to January 1, 2024, and involved electronic databases including PubMed, Medline Ovid, Scopus, ScienceDirect, Springer Link, PlosOne, and BMC.
    UNASSIGNED: In the final grouping, 73 articles met the inclusion criteria and were selected for this review. Among the quantitative studies, majority studies were cross-sectional survey studies. Through the rigorous thematic content analysis seven research domains were developed from the selected literature: drug utilisation and rational drug use, the emerging role of pharmacist, access to medicines and generic medicines, community pharmacy practice, pharmacovigilance/adverse drug reactions, and pharmacoeconomic studies.
    UNASSIGNED: The pharmacist role is evolving; however, several challenges remain in fully realising the potential of pharmacists. These include regulatory barriers, limited public awareness of pharmacists\' expanded roles, workforce capacity issues, and the need for ongoing professional development and training. Research studies are needed in the areas of generic prescribing, medicine adherence, intervention studies in community and hospital pharmacy practice, and on pharmacoeconomics and pharmacovigilance.
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  • 文章类型: Systematic Review
    目的:这篇综述旨在评估与基于数字模拟的药理学教育相关的文献的质量和性质。具体来说,我们试图了解模拟对知识的影响,满意,以及参与此类教育计划的预注册护士和其他医疗保健学生的信心。
    方法:使用系统评价和荟萃分析(PRISMA)声明的首选报告项目进行系统评价。本研究已在前瞻性系统评价登记册(PROSPERO,注册编号:CRD42023437570)。
    方法:PubMed,MEDLINE,APAPsycInfo,ProQuest,WebofScience,ScienceDirect,和CINHAL数据库进行了搜索。
    方法:评论的重点是2016年至2023年发表的研究的定量结果。只有评估基于数字模拟的药理学教育对注册前的医疗保健学生知识的影响的研究,满意,和信心被选中进行审查。使用叙述方法综合数据。采用混合方法评价工具(MMAT)对纳入文章的质量进行评价。随后是叙事综合,以巩固主题。
    结果:在1587篇文章中,16符合纳入标准。已经使用了各种各样的数字技术,例如虚拟仿真,计算机仿真(2D/3D),混合现实,和增强现实,大多数使用虚拟仿真。所有研究都实施了单用户模拟。叙事综合中出现的主题表明,基于数字模拟的药理学课程是提高学生知识的有效工具,信心,和学习药理学概念的满意度。此外,采用混合方法的基于模拟的教学被发现是有益的。然而,在这些研究中,多重药房概念与专业内和跨专业教学方法的整合并不明显。
    结论:本系统文献综述提供了基于数字模拟的教育在医疗保健预注册学生的药理学教学中的潜力的证据。在未来的研究中,建议将多药学内容与专业内和跨专业的教学方式相结合.
    This review aimed to assess the quality and nature of the literature related to digital simulation-based pharmacology education. Specifically, we sought to understand the influence of simulations on the knowledge, satisfaction, and confidence of pre-registration nurses and other healthcare students participating in such educational programs.
    Systematic review using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) Statement. This study was registered in the Prospective Register of Systematic Reviews (PROSPERO, reg no: CRD42023437570).
    PubMed, MEDLINE, APA PsycInfo, ProQuest, Web of Science, ScienceDirect, and CINHAL databases were searched.
    The review focused on the quantitative findings from the studies published from 2016 to 2023. Only the studies that assessed the impact of digital simulation-based pharmacology education on pre-registration healthcare students\' knowledge, satisfaction, and confidence were selected for review. Data were synthesized using a narrative approach. The Mixed Methods Appraisal Tool (MMAT) was used to assess the quality of the included articles. This was followed by a narrative synthesis to consolidate the themes.
    Out of 1587 articles,16 met the inclusion criteria. A wide variety of digital technologies have been utilised, such as virtual simulation, computer simulation (2D/3D), mixed reality, and augmented reality, with the majority using virtual simulation. All studies implemented single-user simulations. The themes emerging from the narrative synthesis suggest that a digital simulation-based pharmacology course is an effective tool for enhancing students\' knowledge, confidence, and satisfaction in learning pharmacological concepts. Furthermore, simulation-based teaching with a blended approach was found to be beneficial. However, the integration of the polypharmacy concept and the intra and interprofessional approach to teaching and learning was not evident in these studies.
    This systematic literature review provides evidence of the potential of digital simulation-based education in pharmacology teaching among healthcare pre-registration students. In future studies, the integration of polypharmacy content with an intra and interprofessional teaching-learning approach is recommended.
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  • 文章类型: Systematic Review
    目的:本研究旨在探索牙医的知识,态度,以及对抗生素使用的看法。
    方法:我们对牙医的知识进行了系统回顾,对抗生素使用的态度和看法,通过搜索MEDLINE,EMBASE和WebofScience于1990年1月至2023年7月发布的所有原始论文,符合系统评论和荟萃分析的首选报告项目(PRISMA2020)指南。
    结果:评论包括37篇论文,(定性研究7项,定量研究30项)。可修改的因素(知识,据报道,态度)与牙医的抗生素处方有关,在37个中的30个中被引用。牙医最常见的态度是:自满(22/29);缺乏信任(16/29);需要推迟牙科手术(17/29);和恐惧(8/29)。还发现了知识差距(15/29)。其中只有一篇文章量化了报告的可改变因素与抗生素处方之间的影响。
    结论:该综述强调牙医的抗生素处方主要受可改变因素的影响。这一见解表明,有针对性的干预措施可能会减少不适当的抗生素使用。为减少抗生素耐药性的全球努力做出贡献。这项系统审查的方案可以在PROSPERO中找到,注册号为。CRD42021253937。
    OBJECTIVE: This study aims to explore dentists\' knowledge, attitudes, and perceptions regarding antibiotic use.
    METHODS: We conducted a systematic review of dentists\' knowledge, attitudes and perceptions regarding antibiotic use, by searching the MEDLINE, EMBASE and Web of Science for all original paper published from January 1990 to July 2023, in accordance with the Preferred Reporting Items for systematic Reviews and Meta-analyses (PRISMA 2020) guidelines.
    RESULTS: The review included 37 papers, (7 qualitative and 30 quantitative studies). Modifiable factors (knowledge, attitudes) were reported as being associated with antibiotic prescribing by dentists which were cited in 30 of the 37. These attitudes most frequently identified by dentists were: complacency (22/29); lack of trust (16/29); the need to postpone the dental procedure (17/29); and fear (8/29). Gaps in knowledge were also identified (15/29). Only one of the included articles quantified the influence between the reported modifiable factors and antibiotic prescribing.
    CONCLUSIONS: The review emphasizes that dentists\' antibiotic prescribing is predominantly influenced by modifiable factors. This insight informs the potential for targeted interventions to curtail inappropriate antibiotic use, contributing to global efforts in reducing antibiotic resistance. The protocol of this systematic review can be found in PROSPERO under registration no. CRD42021253937.
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  • 文章类型: Journal Article
    鉴于阿片类药物在许多国家普遍滥用和转移,急诊科的阿片类药物处方和配药是一个值得注意的问题。对人口造成身体和经济伤害。高患者人数和急诊部门(ED)的急性急诊报告的随机性给正在考虑阿片类药物管理原则的处方者带来了挑战。这项研究调查了在实施国家减少包装尺寸的建议后,电子处方软件的更改对澳大利亚三级急诊科自动填充量的羟考酮立即释放(IR)的处方的影响。在2019年至2021年的两个六个月期间,对羟考酮IR处方进行了回顾性审查,软件调整的任一侧,以将处方的片剂的默认数量从20减少到10。收集患者的人口统计细节,并计算出处方年的实践,以纳入线性混合效应回归模型。软件更改后,每个处方的处方片剂数量减少(13.5至10.0,p<0.001),患者或处方人群的基本特征几乎没有变化,以及处方片剂总数减少11.65%。处方者多年的实践,研究发现,患者年龄和患者性别会影响处方量的增加.通过改变处方软件预充参数,可以减少处方羟考酮片剂的数量。提供进一步的证据来支持基于系统的政策干预,以影响卫生保健提供者的行为,并作为处方者考虑阿片类药物管理原则的强制功能.
    Opioid prescribing and dispensing from emergency departments is a noteworthy issue given widespread opioid misuse and diversion in many countries, contributing both physical and economic harm to the population. High patient numbers and the stochastic nature of acute emergency presentations to emergency departments (EDs) introduce challenges for prescribers who are considering opioid stewardship principles. This study investigated the effect of changes to electronic prescribing software on prescriptions with an auto-populated quantity of oxycodone immediate release (IR) from an Australian tertiary emergency department following the implementation of national recommendations for reduced pack sizes. A retrospective review of oxycodone IR prescriptions over two six-month periods between 2019 and 2021 was undertaken, either side of a software adjustment to reduce the default quantities of tablets prescribed from 20 to 10. Patient demographic details were collected, and prescriber years of practice calculated for inclusion in linear mixed effects regression modelling. A reduction in the median number of tablets prescribed per prescription following the software changes (13.5 to 10.0, p < 0.001) with little change in the underlying characteristics of the patient or prescriber populations was observed, as well as an 11.65% reduction in the total number of tablets prescribed. The prescriber\'s years of practice, patient age and patient sex were found to influence increased prescription sizes. Reduced quantity of oxycodone tablets prescribed was achieved by alteration of prescribing software prefill parameters, providing further evidence to support systems-based policy interventions to influence health care providers behaviour and to act as a forcing function for prescribers to consider opioid stewardship principles.
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  • 文章类型: Journal Article
    OBJECTIVE: Since assessment of prescribing competence is a key promoter of student learning and achievement, we aim to summarize existing national-level approaches, provide a systematic review of current literature, indicate the frequency of various methodologies, and make recommendations to promote and extend existing practice.
    METHODS: Regulatory body websites were accessed for details of national examinations. PubMed, Embase, the Allied and Complementary Medicine, and CINAHL databases were systematically searched in August 2023 for studies in English from Europe, North America, Australia and New Zealand reporting assessment of prescribing competencies among students/practitioners. Additional articles were identified through citation tracking.
    RESULTS: National approaches are described for several jurisdictions. A total of 20 514 articles were retrieved, of which 54 met the inclusion criteria. Most articles came from the UK, with medical students and qualified doctors most frequently featured. Multiple choice formats were most common, with short answer questions, calculations and scenario-based skills tests also featured. Direct observations of skills through Objective Structured Clinical Examinations and similar methods were less commonly described. Test reliability generally employed Classical Test Theory. Costs of developing and delivering assessments, differential attainment by demographics, and predictive validity were not indicated.
    CONCLUSIONS: We recommend measurement of the predictive validity of prescribing competence assessments, the routine inclusion of performance by demographic characteristics, extension of competence assessments to professions other than medicine, and structured reporting of methods and findings, including costs and cost-effectiveness. Situational judgement tests would be a valuable addition to assessment practices.
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  • 文章类型: Journal Article
    背景:历史上,急性肾损伤(AKI)期间的静脉和肠内液体在引入连续性肾脏替代疗法(CRRT)之前受到限制,因为更多的液体可以改善危重症患者的营养。然而,当在净超滤(NUF)体积目标的流体平衡处方和每日审查中未考虑每天较高的体积时,可能会发生流体积聚。
    结论:每天进行CRRT的时间对于实现体液平衡至关重要,而休假治疗使任务更具挑战性。缺乏CRRT经验的临床医生使AKI管理的这一方面成为高级监督四舍五入的重点,清晰的沟通,和“精确”一个临床目标。与脓毒症相关的AKI可能是一个复杂的患者,其中复苏和入院日具有积极的液体负荷和更换心态。随后在ICU的几天需要调节液体,移除,在规定每日流体平衡目标和实现此目标所需的每小时净血浆水去除率(NUF率)之前,进行全面的多层评估。预测和预测是必要的。
    结论:未来的机器可能包括高级软件,新警报-显示指标,消息和与机器学习和“AKI模型”的关联,用于设置,监测,并保证流体去除。这也可以链接到当前的硬件,例如具有连续血细胞比容测量的在线血容量评估。
    BACKGROUND: Historically IV and enteral fluids given during acute kidney injury (AKI) were restricted before the introduction of continuous renal replacement therapies (CRRTs) when more liberal fluids improved nutrition for the critically ill. However, fluid accumulation can occur when higher volumes each day are not considered in the fluid balance prescribing and the NET ultrafiltration (NUF) volume target.
    CONCLUSIONS: The delivered hours of CRRT each day are vital for achievement of fluid balance and time off therapy makes the task more challenging. Clinicians inexperienced with CRRT make this aspect of AKI management a focus of rounding with senior oversight, clear communication, and \"precision\" a clinical target. Sepsis-associated AKI can be a complex patient where resuscitation and admission days are with a positive fluid load and replacement mind set. Subsequent days in ICU requires fluid regulation, removal, with a comprehensive multilayered assessment before prescribing the daily fluid balance target and the required hourly NET plasma water removal rate (NUF rate). Future machines may include advanced software, new alarms - display metrics, messages and association with machine learning and \"AKI models\" for setting, monitoring, and guaranteeing fluid removal. This could also link to current hardware such as on-line blood volume assessment with continuous haematocrit measurement.
    CONCLUSIONS: Fluid balance in the acutely ill is a challenge where forecasting and prediction are necessary. NUF rate and volume each hour should be tracked and adjusted to achieve the daily target. This requires human and machine connections.
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  • 文章类型: Journal Article
    目标:尽管认可的助产士开出了10年的预定药物,对处方实践知之甚少。
    背景:认可的助产士可以开预定的药物,并可以获得Medicare回扣以支持服务提供。认可的助产士有可能改善妇女获得药物的机会,然而,遇到障碍,包括州和国家立法的不一致。
    目的:为了搜索澳大利亚关于认可助产士处方预定药物的发布内容,关于文献的报告,综合研究结果并讨论结果。
    方法:使用JoannaBrigg研究所方法的范围审查。搜索CINAHL,PubMed,进行了ScienceDirect和Medline数据库。确定了七篇同行评审的文章;三篇讨论论文,一篇文献综述和三篇研究论文,在2016年至2023年之间以英文出版。定性内容分析用于确定主题领域。
    结果:确定了四个主题领域:1)认可的助产士增加了妇女获得处方药的机会;2)药物福利计划具有限制性并减少了助产处方;3)药物处方取决于内部和外部结构;4)专业关系支持处方。
    结论:处方授权助产士的实践,改善及时获得药物并提高角色满意度。药物福利计划等障碍阻碍了助产处方的有效使用,不适当的药物配方,和设计不当的卫生服务政策。
    结论:为了在所有产妇护理环境中充分利用认可的助产士处方,发展教育需要进一步的工作,消除障碍,并证明助产处方的安全性和有效性。
    OBJECTIVE: Despite 10 years of prescribing scheduled medicines by Endorsed Midwives, little is known about prescribing practices.
    BACKGROUND: Endorsed Midwives can prescribe scheduled medicines and have access to Medicare rebates to support service provision. Endorsed Midwives have the potential to improve access to medications for women, however, are met with barriers, including inconsistencies in state and national legislation.
    OBJECTIVE: To search for what is published regarding Endorsed Midwife prescribing of scheduled medicines in Australia, report on the literature, synthesise the findings and discuss the results.
    METHODS: A scoping review utilising the Joanna Brigg\'s Institute methodology. A search of CINAHL, PubMed, Science Direct and Medline databases was conducted. Seven peer-reviewed articles were identified; three discussion papers, one literature review and three research papers, published between 2016 and 2023 in English. Qualitative content analysis was used to identify topic areas.
    RESULTS: Four topic areas were identified: 1) Endorsed Midwives increase women\'s access to prescribed medications; 2) the Pharmaceutical Benefits Scheme is restrictive and diminishes midwifery prescribing; 3) medication prescribing depends on internal and external structures; 4) professional relationships support prescribing.
    CONCLUSIONS: The authority to prescribe augments Endorsed Midwives\' practice, improves timely access to medications and enhances role satisfaction. The effective use of midwifery prescribing is hampered by barriers such as the Pharmaceutical Benefits Scheme, inappropriate medication formularies, and poorly designed health service policy.
    CONCLUSIONS: To fully utilise Endorsed Midwife prescribing in all settings of maternity care, further work is required to develop education, remove barriers, and demonstrate the safety and effectiveness of midwifery prescribing.
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  • 文章类型: Journal Article
    目标:已经做出了相当大的努力,通过取消实施来提高医疗保健指南的依从性,例如减少不适当药物的处方。然而,我们对有效性的了解有限,障碍,在二级保健环境中针对不适当药物处方的取消实施策略的促进因素和后果。进行这篇综述是为了了解这些因素,以有助于更好地复制和优化未来的去实施工作,以减少低价值护理。
    方法:对随机对照试验进行系统评价。论文通过CINAHL进行鉴定,EMBASE,截至2021年2月,MEDLINE和Cochrane进行了对照试验登记。符合条件的研究是随机对照试验,评估行为策略,以取消二级医疗保健中不适当的处方。使用Cochrane偏差风险工具评估偏差风险。干预特点,有效性,障碍,研究文本中确定了促进因素和结果,并将其制成表格.
    结果:纳入了11项研究,其中7项被报告为有效取消低价值处方。纳入的研究被认为主要处于选择偏差的低至中等风险,以及通常表现和报告偏差的高风险。这些策略中的大多数是在“护理点”的临床决策支持。临床决策支持工具是最常见和最有效的。他们被发现是一种低成本和简单的策略。然而,障碍,如临床医生不愿接受建议,或临床环境是他们成功的潜在障碍。教育策略是第二大报告的干预类型,但是教育策略用于取消实施的效用仍然各不相同。与环境背景有关的多重障碍和促进者,在研究中,资源和知识被确定为可能影响取消实施的因素。确定了各种后果;然而,很少有人衡量取消实施对通常适当做法的影响。
    结论:这篇综述提供了对干预策略的见解,潜在的障碍,可能影响二级保健中低价值处方的取消实施的促进因素和后果。识别这些关键特征有助于理解这些策略如何以及为什么是有效的以及取消实施的更广泛的(期望的或不期望的)影响。这些发现有助于成功复制或优化未来用于取消低价值处方实践的策略。
    背景:审查方案已在PROSPERO注册(ID:CRD42021243944)。
    OBJECTIVE: Considerable efforts have been made to improve guideline adherence in healthcare through de-implementation, such as decreasing the prescription of inappropriate medicines. However, we have limited knowledge about the effectiveness, barriers, facilitators and consequences of de-implementation strategies targeting inappropriate medication prescribing in secondary care settings. This review was conducted to understand these factors to contribute to better replication and optimisation of future de-implementation efforts to reduce low-value care.
    METHODS: A systematic review of randomised control trials was conducted. Papers were identified through CINAHL, EMBASE, MEDLINE and Cochrane register of controlled trials to February 2021. Eligible studies were randomised control trials evaluating behavioural strategies to de-implement inappropriate prescribing in secondary healthcare. Risk of bias was assessed using the Cochrane Risk of Bias tool. Intervention characteristics, effectiveness, barriers, facilitators and consequences were identified in the study text and tabulated.
    RESULTS: Eleven studies were included, of which seven were reported as effectively de-implementing low-value prescribing. Included studies were judged to be mainly at low to moderate risk for selection biases and generally high risk for performance and reporting biases. The majority of these strategies were clinical decision support at the \'point of care\'. Clinical decision support tools were the most common and effective. They were found to be a low-cost and simple strategy. However, barriers such as clinician\'s reluctance to accept recommendations, or the clinical setting were potential barriers to their success. Educational strategies were the second most reported intervention type however the utility of educational strategies for de-implementation remains varied. Multiple barriers and facilitators relating to the environmental context, resources and knowledge were identified across studies as potentially influencing de-implementation. Various consequences were identified; however, few measured the impact of de-implementation on usual appropriate practice.
    CONCLUSIONS: This review offers insight into the intervention strategies, potential barriers, facilitators and consequences that may affect the de-implementation of low-value prescribing in secondary care. Identification of these key features helps understand how and why these strategies are effective and the wider (desirable or undesirable) impact of de-implementation. These findings can contribute to the successful replication or optimisation of strategies used to de-implement low-value prescribing practices in future.
    BACKGROUND: The review protocol was registered at PROSPERO (ID: CRD42021243944).
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  • 文章类型: Journal Article
    目的:本综述的目的是确定工具和指南,以帮助潜在不适当药物(PIM)的开药过程,评估开发和验证方法,并描述药物纳入的证据水平。
    方法:在MEDLINE(Ovid)上进行了搜索,Embase.com,CochraneCDSR,CINAHL(EBSCO),WebofScience核心合集,和指南数据库从开始之日起至2022年7月7日,并于2023年7月17日检查更新的工具。我们分析了工具和指南的内容。
    结果:来自23项系统评价和指南,我们确定了95个工具(72个明确的,12混合,11条隐含)和9条准则。大多数工具(83.2%)是为老年人开发的,包括14个寿命有限的人。七种工具适用于18岁以下的儿童(7.37%)。最明确/混合的工具(78.57%)和所有指南都得到了验证。我们发现484个PIM和202个药物具有不同的适当性,独立于疾病的老年人与正常和有限的预期寿命,分别。只有两个工具和八个指南报告了证据水平,四分之一的药物有高质量的证据.
    结论:工具可用于多种种群。相同的药物在某些工具中被归类为不适当,而在其他工具中被归类为适当的,存在差异。可能是由于证据质量低。特别是,基于非常有限的证据开发了针对预期寿命有限的患者的工具,非常需要研究来产生这种证据。我们的药物清单,随着证据的水平,可以促进加强证据的努力。
    The aim of this umbrella review was to identify tools and guidelines to aid the deprescribing process of potentially inappropriate medications (PIMs), evaluate development and validation methods, and describe evidence levels for medication inclusion.
    Searches were conducted on MEDLINE (Ovid), Embase.com, Cochrane CDSR, CINAHL (EBSCO), Web of Science Core Collection and guideline databases from the date of inception to 7 July 2022. Following the initial search, an additional search was conducted to identify an updated versions of tools on 17 July 2023. We analysed the contents of tools and guidelines.
    From 23 systematic reviews and guidelines, we identified 95 tools (72 explicit, 12 mixed and 11 implicit) and nine guidelines. Most tools (83.2%) were developed to use for older persons, including 14 for those with limited life expectancy. Seven tools were for children <18 years (7.37%). Most explicit/mixed tools (78.57%) and all guidelines were validated. We found 484 PIMs and 202 medications with different appropriateness independent of disease for older persons with normal and limited life expectancy, respectively. Only two tools and eight guidelines reported the evidence level, and a quarter of medications had high-quality evidence.
    Tools are available for a diversity of populations. There were discrepancies, with the same medication being classified as inappropriate in some tools and appropriate in others, possibly due to low-quality evidence. In particular, tools for patients with limited life expectancy were developed based on very limited evidence, and research to generate this evidence is urgently needed. Our medication lists, along with the level of evidence, could facilitate efforts to strengthen the evidence.
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  • 文章类型: Journal Article
    背景:护士处方师的角色正在迅速发展,以满足全球日益增长的医疗保健需求。然而,开处方是一个复杂的过程,需要护士接受适当的教育。
    目的:确定在护士处方教育研究领域中已知的知识。
    方法:Arksey和O\'Malley的五阶段方法框架被用来指导这一范围审查。
    方法:PubMed,WebofScience,CINAHL,Embase,还有Cochrane图书馆.
    方法:从开始到2022年12月31日检索数据库。使用数据图表从符合纳入标准的论文中提取数据,并使用叙述方法进行综合。
    结果:71项研究纳入范围审查。确定了五个教育内容主题和四个教育模式。此外,还发现了护士处方教育的积极作用和护士的学习需求。
    结论:护士处方教育内容和模式存在相当的异质性。这项范围审查强调了实施教育计划以使护士为处方做好准备的好处。然而,护士在处方教育方面仍然有一些未满足的需求。需要更多的纵向研究和评估工具来确定长期效果。未来的护士处方教育计划可以考虑双重指导制度,互动教育活动,和专业课程,以提高护士的积极性和教育质量。
    BACKGROUND: The role of nurse prescribers is developing rapidly to meet rising health care demands worldwide. However, prescribing is a complex process that requires nurses to receive the proper education.
    OBJECTIVE: To identify what is known in the research field on nurse prescribing education.
    METHODS: Arksey and O\'Malley\'s five-stage methodological framework was used to guide this scoping review.
    METHODS: PubMed, Web of Science, CINAHL, Embase, and the Cochrane Library.
    METHODS: Databases were searched from inception to December 31, 2022. Data were extracted from papers meeting the inclusion criteria using the data chart and synthesized using a narrative method.
    RESULTS: Seventy-one studies were included in the scoping review. Five education content themes and four education modes were identified. In addition, positive effects of nurse prescribing education and the learning needs of nurses were also found.
    CONCLUSIONS: There is considerable heterogeneity in nurse prescribing education content and mode. This scoping review highlights the benefits of implementing education programs to prepare nurses for prescribing. However, nurses still have some unmet needs for prescribing education. More longitudinal studies and evaluation tools are needed to determine long-term effects. Future nurse prescribing education programs could consider the dual mentorship system, interactive educational activities, and specialized courses to improve the motivation of nurses and the quality of education.
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