STOPP/START criteria

STOPP / START 标准
  • 文章类型: Journal Article
    目的:使2015年老年人处方筛查工具(STOPP)/筛查工具适应预期寿命为1.5至2年的老年疗养院患者的正确治疗(START)标准。
    方法:改良的德尔菲共识研究。
    方法:该研究在荷兰建立并在线进行。国际小组由23名具有老年人医学经验的专家组成。
    方法:使用在线调查程序(调查猴子)向专家小组介绍了2015STOPP/START标准。小组成员被要求就STOPP和START标准的适当性发表意见,以及在4分Likert量表上,预期寿命有限的老年疗养院患者对这些标准的适应。共识被定义为≥70%的小组成员回答(非常)不适当或(非常)适当,并且(完全)不同意或(完全)同意。
    结果:21名小组成员完成了所有3轮Delphi。“预期寿命有限的疗养院居民的代表性(ReNeWAL)”标准的最终列表包括132个标准:98个标准停止(70个原始STOPP标准和28个适应)和34个标准开始(16个原始START标准和18个适应)用于预期寿命有限的老年疗养院患者。小组成员提到的适应标准的考虑主要是预防和治疗不适。
    结论:很明显,老年疗养院患者的治疗非常复杂,需要考虑各种因素。ReNeWAL标准可能有助于增强预期寿命有限的老年疗养院患者的治疗效果。
    OBJECTIVE: To adapt the 2015 Screening Tool of Older Persons\' Prescriptions (STOPP)/Screening Tool to Alert to Right Treatment (START) criteria to older nursing home patients with a limited life expectancy of 1.5 to 2 years.
    METHODS: A modified Delphi consensus study.
    METHODS: The study was established in The Netherlands and conducted online. The international panel consisted of 23 experts with experience in medicine for older people.
    METHODS: The expert panel was presented with the 2015 STOPP/START criteria using an online survey program (Survey Monkey). The panelists were asked for their opinion on the appropriateness of the STOPP and START criteria, and adaptations to these criteria for older nursing home patients with a limited life expectancy on 4-point Likert scales. Consensus was defined as ≥70% of the panelists answering (very) inappropriate or (very) appropriate, and (completely) disagree or (completely) agree.
    RESULTS: Twenty-one panelists completed all 3 Delphi rounds. The final list of \"Represcribing for Nursing home residents With A Limited life expectancy (ReNeWAL)\" criteria comprises 132 criteria: 98 criteria to stop (70 original STOPP criteria and 28 adapted) and 34 criteria to start (16 original START criteria and 18 adapted) for older nursing home patients with a limited life expectancy. Considerations that panelists mentioned for adapting criteria were mainly prevention and treatment of discomfort.
    CONCLUSIONS: It is clear that represcribing for older nursing home patients is highly complex and requires the consideration of various elements. The ReNeWAL criteria may be useful in enhancing represcribing for older nursing home patients with a limited life expectancy.
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  • 文章类型: Journal Article
    背景:潜在不适当的处方(PIP)通常与不良健康结果的高风险相关。因此,在老年人中识别PIP很重要。然而,没有明确的优先策略来选择需要处方审查的患者.
    目的:本研究的目的是评估老年人高危(ISAR)评分与PIP数量之间的关联。
    方法:进行为期12个月的回顾性医院研究。PIPs,包括潜在的不适当药物(PIMs)和潜在的处方遗漏(PPOs),使用STOPP/START工具检测到。进行多元线性回归以确定与PIP数量相关的因素。灵敏度,特异性,尤登指数,并计算ROC曲线以确定ISAR评分的预测能力。
    结果:本研究包括266条记录。分析导致检测到420个PIM和210个PPO,患病率分别为80.1%和54.9%,分别。多元线性回归显示ISAR评分(p=0.041),药物数量(p<0.001)是PIP的决定因素。药物的数量仍然是PIM数量的唯一决定因素(p<0.001),而生活在疗养院是PPO数量的唯一决定因素(p=0.036)。
    结论:研究表明,ISAR评分和用药数量与PIP数量独立相关。考虑使用ISAR评分和药物的数量可能是有用的策略,可以优先考虑应使用明确标准评估处方适当性的患者。
    BACKGROUND: Potentially inappropriate prescribing (PIP) is usually associated with a higher risk of adverse health outcomes. It is therefore important to identify PIP in older adults. However, there are no clear prioritisation strategies to select patients requiring prescription reviews.
    OBJECTIVE: The aim of this study was to assess the association between the identification of seniors at risk (ISAR) score and the number of PIPs.
    METHODS: A 12-month retrospective hospital-based study was conducted. PIPs, including potentially inappropriate medications (PIMs) and potential prescribing omissions (PPOs), were detected using the STOPP/START tool. Multivariate linear regressions were conducted to identify factors associated with the number of PIPs. Sensitivity, specificity, Youden index, and ROC curve were calculated to determine the predictive power of ISAR score.
    RESULTS: This study included 266 records. The analysis led to the detection of 420 PIMs and 210 PPOs, with a prevalence of 80.1% and 54.9%, respectively. Multivariate linear regression revealed that the ISAR score (p = 0.041), and the number of medications (p < 0.001) were determinants of PIP. The number of medications remained the sole determinant of the number of PIMs (p < 0.001), while living in a nursing home was the only determinant of the number of PPOs (p = 0.036).
    CONCLUSIONS: The study showed that the ISAR score and the number of medications were independently associated with the number of PIPs. Considering the use of the ISAR score and the number of medications may be useful strategies to prioritise patients for whom prescribing appropriateness should be assessed using explicit criteria.
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  • 文章类型: Journal Article
    潜在不适当药物的STOPP/START标准(PIMs,STOPP)和潜在的处方遗漏(PPO,START)自2008年首次出版以来,已经获得了相当大的兴趣和吸引力。这篇综述着重于它们在各种临床环境中的吸收和影响。
    STOPP/START标准,现在在他们的第三次迭代中,明确的标准旨在促进在任何临床环境中常规药物审查期间检测常见和临床重要的PIMs和PPOs。我们研究标准的影响,特别是在侧重于其对临床相关终点的影响的临床试验中.
    STOPP/START标准在欧洲及其他几个国家广泛用于药物审查和审核。作为谨慎的干预,这些标准已经在几个单中心临床试验和两个大规模多中心临床试验中进行了测试.单中心试验表明,STOPP/START标准降低了多重用药,不适当的处方,ADR(药物不良反应),药物成本和下降。相比之下,SENATOR和OPERAM多中心试验未显示ADR显著减少,全因死亡率,与药物相关的医院再入院,也没有任何生活质量的改善。需要进一步的临床试验来检查STOPP/START标准作为干预措施是否可以在各种临床环境中以可重复的方式提供显著的临床益处。
    UNASSIGNED: STOPP/START criteria for potentially inappropriate medications (PIMs, STOPP) and potential prescribing omissions (PPOs, START) have gained considerable interest and traction since they were first published in 2008. This review focuses on their uptake and impact in various clinical settings.
    UNASSIGNED: STOPP/START criteria, now in their third iteration, are explicit criteria designed to facilitate detection of common and clinically important PIMs and PPOs during routine medication review in any clinical setting. We examine the influence of the criteria, particularly in clinical trials that focused on their impact on clinically relevant endpoints.
    UNASSIGNED: STOPP/START criteria are widely used in several countries within Europe and beyond for medication review and audit. As a discreet intervention, the criteria have been tested in several single-center and two large-scale multi-center clinical trials. The single-center trials indicate that STOPP/START criteria reduce polypharmacy, inappropriate prescribing, ADRs (adverse drug reactions), medication cost and falls. In contrast, the SENATOR and OPERAM multicentre trials did not demonstrate significant reduction in ADRs, all-cause mortality, drug-related hospital readmissions, nor any improvement in quality-of-life. Further clinical trials are required to examine whether STOPP/START criteria as an intervention can deliver significant clinical benefit in a reproducible manner in various clinical settings.
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  • 文章类型: Journal Article
    为了贯彻提供临床和经济有效护理的原则,必须评估当前的医疗保健状况,必须应对挑战。作为医生在这种情况下的角色的一部分,一个工具包括确定药物相关问题(MRP),并相应地实施最佳实践和创新策略,以改善患者的医疗保健结果.预计老年人群将经历自然衰老过程,并经历了影响其身体和生活的一些生理和生物学变化。在存在老年综合征和消耗的药物数量增加的情况下,MRP的风险,如多重用药,潜在不当药物(PIM),不良事件,药物-药物相互作用,和不坚持的风险增加。研究了侧重于实践和感知障碍的不同干预措施,和不同的工具来定义与PIM相关的临床重要处方问题已经建立。Beers标准和STOPP(老年人处方筛查工具)/START(提醒正确治疗的筛查工具)标准是最广泛使用的一套明确的PIM标准;然而,他们在沙特阿拉伯仍然有限。这些工具应在临床环境中考虑,以改善老年人群的医疗保健结果,从患者和保健医生的角度,也应该探讨增强药物的临床相关性。
    In order to implement the principles of providing clinically and economically effective care, the current state of healthcare must be evaluated, and challenges must be addressed. As part of a physician\'s role in such a context, one tool consists of identifying medication-related problems (MRPs) and accordingly implementing best practices and innovative strategies to improve patient healthcare outcomes. The geriatric population is expected to have passed through the natural ageing process and experienced several physiological and biological changes that impact their bodies and lives. In the presence of geriatric syndromes and the increased number of medications consumed, the risk of MRPs such as polypharmacy, potentially inappropriate medication (PIM), adverse events, drug-drug interactions, and risk of non-adherence increases. Different interventions that focus on practical and perceptual barriers have been studied, and different tools to define clinically important prescribing problems relating to PIM have been established. The Beers Criteria and STOPP (Screening Tool of Older Persons\' Prescriptions)/START (Screening Tool to Alert to Right Treatment) criteria are the most widely used sets of explicit PIM criteria; however, they are still limited in Saudi Arabia. These tools should be considered in clinical settings to improve healthcare outcomes in the geriatric population, and the clinical relevance of enhancing medication should also be explored from the point of view of both the patient and healthcare practitioners.
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  • 文章类型: Systematic Review
    STOPP/START标准是基于生理系统的明确标准,总结了与使用潜在不适当药物(STOPP标准)和潜在处方遗漏(START标准)相关的临床相关处方问题的证据。STOPP/START标准的前两个版本分别于2008年和2015年发布,西班牙语版本分别于2009年和2015年发布。这些标准的版本3刚刚在2023年发布。本文的目的是提供西班牙语翻译版本,并回顾2015年版本2在我们的语言中的使用和影响。由专业专家进行了从英语到西班牙语的翻译,具有STOPP/START标准第3版的高水平英语,其中包含2014年4月至2022年3月发布的证据。此外,对使用STOPP/START标准前一版本(2015年第2版)西班牙语翻译的出版物进行了系统评价.新版本,在这篇文章中,有190个STOPP/START标准(133个STOPP标准和57个START标准),与以前的版本相比,标准数量增加了40%。该综述发现了37项研究(21项观察性研究,11介入和5其他)使用西班牙语版本而不是国际版本。STOPP/START标准的西班牙语版本3是最新的明确列表,列出了潜在的不适当药物和处方中可能的遗漏,旨在优化药物治疗并最大程度地减少老年人药物审查期间的药物不良反应。特别是那些具有多发病率和多药房的人。有了这个新版本,原始标准旨在在讲西班牙语的医疗保健社区中更广泛地传播.STOPP/START的西班牙语版本2已被广泛使用,因此,我们认为,在我们的语言环境中,西班牙语的翻译有助于改善老年患者的药物治疗。
    The STOPP/START criteria are explicit physiologic systems-based criteria that summarize evidence on clinically relevant prescribing problems related to the use of potentially inappropriate medications (STOPP criteria) and potential prescribing omissions (START criteria). The two previous versions of the STOPP/START criteria were published in 2008 and 2015, and their Spanish versions in 2009 and 2015. Version3 of these criteria has just been published in 2023. The aim of this article is to present the Spanish translated version, and to review the use and impact that version2 of 2015 has had in our language. A translation from English to Spanish was performed by expert professionals with a high level of English of version3 of the STOPP/START criteria, which incorporates the evidence published from April 2014 to March 2022. In addition, a systematic review of publications that have used the Spanish translation of the previous version (version2 of 2015) of the STOPP/START criteria was performed. The new version, presented in this article, has 190 STOPP/START criteria (133 STOPP criteria and 57 START criteria), which is a 40% increase in the number of criteria compared to the previous version. The review found 37 studies (21 observational, 11 interventional and 5 other) that used the Spanish version instead of the international version. The Spanish version 3 of the STOPP/START criteria is an updated explicit list of potentially inappropriate medications and possible omissions in prescribing that aims to optimize medication and minimize adverse drug reactions during medication review in the elderly, particularly those with multimorbidity and polypharmacy. With this new version, the original criteria are intended to be more widely disseminated within the Spanish-speaking healthcare community. The Spanish version2 of the STOPP/START has been widely used, so we consider that the translation into Spanish has helped to improve pharmacotherapy in older patients with polypharmacy and multimorbidity in our linguistic environment.
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  • 文章类型: Journal Article
    目的:STOPP/START是一套基于生理系统的明确标准,试图定义与潜在不适当药物(PIMs-STOPP标准)和潜在处方遗漏(PPOs-START标准)相关的临床重要处方问题。STOPP/START标准的前两个版本分别于2008年和2015年发布。本研究描述了标准的修订和更新的第三版。
    方法:对2014年4月至2022年3月发表的文献进行了详细的系统审查,目的是纳入临床重要的新的明确PIM和PPO标准,并删除任何被认为不再正确或过时的标准。由来自8个欧洲国家的11名在老年药物治疗方面具有公认专业知识的学术医师组成的小组参加了Delphi小组,其任务是验证标准草案。使用SurveyMonkey®在线平台向小组提交了新标准草案,在该平台中,小组成员被要求以五点李克特量表表示他们的协议水平。
    结果:基于证据的标准草案(145个STOPP标准,59个START标准)提交给小组成员,使用德尔菲验证方法进行评估。在四轮Delphi验证过程中,小组就133项STOPP标准和57项START标准达成共识,即,总共190个STOPP/START标准,与2015年发布的STOPP/START第2版相比,标准数量增加了66.7%。
    结论:欧洲专家小组使用Delphi共识程序验证了STOPP/START标准的完全修订和更新版本。
    STOPP/START is a physiological systems-based explicit set of criteria that attempts to define the clinically important prescribing problems relating to potentially inappropriate medications (PIMs-STOPP criteria) and potential prescribing omissions (PPOs-START criteria). The previous two versions of STOPP/START criteria were published in 2008 and 2015. The present study describes the revised and updated third version of the criteria.
    A detailed system-by-system review of the published literature from April 2014 to March 2022 was undertaken with the aim of including clinically important new explicit PIM and PPO criteria and removing any criteria considered to be no longer correct or outdated. A panel of 11 academic physicians with recognized expertise in geriatric pharmacotherapy from 8 European countries participated in a Delphi panel with the task of validating the draft criteria. The panel was presented with the draft new criteria using the SurveyMonkey® on-line platform in which panelists were asked to indicate their level of agreement on a five-point Likert scale.
    Two hundred and four evidence-based draft criteria (one hundred and forty-five STOPP criteria, fifty-nine START criteria) were presented to panelists for assessment using the Delphi validation method. Over the course of four rounds of Delphi validation, the panel achieved consensus on 133 STOPP criteria and 57 START criteria, i.e., 190 STOPP/START criteria in total representing a 66.7% increase in the number of criteria compared to STOPP/START version 2 published in 2015.
    A fully revised and updated version of STOPP/START criteria has been validated by a European expert panel using the Delphi consensus process.
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  • 文章类型: Journal Article
    背景:心房颤动(AF)在老年人中很常见。房颤管理的一个关键组成部分是口服抗凝治疗(OAT),由维生素K拮抗剂(VKAs)或直接口服抗凝剂(DOAC)组成。本研究的目的是检查,使用STOPP(老年人处方筛查工具)/START(提醒正确治疗的筛查工具)标准,如果此类药物在患有房颤的老年人群中可能被不当处方/遗漏,并确定它们对死亡率的影响。
    方法:本研究纳入了2013年至2019年在老年门诊连续评估的非瓣膜性房颤患者(n=427)。蒙塞拉托大学医院,卡利亚里,意大利,并随访了36个月。OAT组包括330名患者;其他97名患者构成非OAT组。评估样品的STOPP/START标准。
    结果:我们发现合并症负担没有差异(p>0.1),脆弱,两组的心脑血管疾病患病率,36个月死亡率也没有差异(p=0.97)。OAT总体上是适当的,62.4%的OAT组提出了服用抗血小板的START标准,但也提出了不服用抗血小板的STOPP标准,因为同时摄入抗凝剂。在非OAT组中,69.1%的人提出了服用抗凝剂的START标准,和21.6%的START标准服用抗血小板。
    结论:房颤患者往往容易出现处方不足或处方过多,特别是抗血栓药物。STOPP/START标准是评估和纠正错误治疗选择的有效工具。在虚弱和合并症的科目中,生存率与OAT的假设无关。
    Atrial Fibrillation (AF) is common in the elderly. A key component of AF management is Oral Anticoagulant Therapy (OAT), consisting of Vitamin K Antagonists (VKAs) or Direct Oral Anticoagulants (DOACs). The aim of the present study is to check, using STOPP (Screening Tool of Older Persons\' Prescriptions)/START (Screening Tool to Alert to Right Treatment) Criteria, if such drugs are potentially inappropriately prescribed/omitted in an elderly population with AF, and to determine their impact on mortality.
    This study included patients (n = 427) with nonvalvular AF consecutively evaluated between 2013 and 2019 at the Geriatric Outpatient Service, University Hospital of Monserrato, Cagliari, Italy, and followed up for 36 months. The OAT group included 330 patients; the other 97 patients constituted the non-OAT group. The sample was assessed for STOPP/START criteria.
    We found no difference (p > 0.1) in comorbidity burden, frailty, and cardio-cerebro-vascular disease prevalence in the two groups, which also did not present a difference in 36-month mortality (p = 0.97). OAT was overall appropriately taken, and 62.4% of OAT-group presented the START criterion to take antiplatelets but also the STOPP criterion not to take them, because of the simultaneous anticoagulant intake. In the non-OAT group, 69.1% presented the START criterion to take anticoagulants, and 21.6% the START criterion to take antiplatelets.
    Patients with AF are often prone to under or over-prescription, particularly of antithrombotic drugs. The STOPP/START criteria are a valid tool to assess and correct wrong therapeutic choices. In frail and comorbid subjects, survival is not correlated with the assumption of OAT.
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  • 文章类型: Journal Article
    UNASSIGNED:本研究旨在评估STOPP/START标准在确定保加利亚老年心血管疾病患者可能不适当的药物和潜在处方遗漏方面的应用。发病率和死亡率过高与毒品相关问题和医疗保健服务的使用增加有关,这对保加利亚来说是一个未被研究的问题。
    未经批准:预期,在保加利亚25家药店的543名老年患者中进行了问卷调查。社会人口统计学特征,疾病概况,症状,并收集用药数据。该问卷是为EUROAGEISM项目开发的。在所有543名患者中,仅抽取有心血管疾病记录的患者,并使用STOPP/START标准第2版对每位患者的用药情况进行潜在不适当用药(PIMs)和潜在处方遗漏(PPOs)评估.此外,潜在不适当处方(PIPs)的几种风险,PPO和PIM的计算重点是制定PIP的可能性和风险。
    UNASSIGNED:531名已知心血管疾病(CVDs)治疗的患者中的四百二十八名被纳入PIP分析(40.52%年龄在65-69岁之间,61.88%女性,64%的人有多达6种合并症,和21.72%的人出现多重用药)。在应用STOPP标准的过程中,在64例多重用药患者中总共发现了71例PIMs。56%的患者每天服用以上五种药物有PIMs。大多数PIMs(31%)与心血管疾病治疗有关,其次是PIMs治疗内分泌疾病(22.54%),重复药物(8.46%)和长期使用苯二氮卓类药物(8.46%)。按照START标准确定了44个PPO。22.72%与胃食管疾病中缺乏质子泵抑制剂(PPI)有关,和相同的百分比是缺乏钙-维生素D补充骨质疏松症。应用风险计算方法,PPO的样本风险为2.1%,PIM为3.4%。在样本水平上,PPO的相对风险是PIM风险的62%,在人群水平上在42.8和89.8%之间变化,具有统计学意义。事件发生所需的治疗数量为77.5,这意味着每78个处方都有机会出现PIP。
    UNASSIGNED:在保加利亚,应用检测潜在不适当处方的方法学不是常规临床实践的一部分。我们的研究表明,在患有多种药物的老年患者中,潜在的不适当药物的比例很高。随着保加利亚人口老龄化,多重用药的经济负担和心血管疾病的患病率,尤其重要的是解决心血管患者可能不适当的药物使用问题.作为老年患者的去处方策略的一部分,有必要实施早期发现潜在不适当药物和潜在处方遗漏的措施。
    This study aims to evaluate the use of STOPP/START criteria in the identification of Potentially inappropriate medication and potential prescribing omissions in older patients with cardiovascular diseases in Bulgaria. Excessive morbidity and mortality has been linked to drug-related problems and increased use of healthcare services and is an understudied problem for Bulgaria.
    A prospective, questionnaire-based study was conducted among 543 older patients across 25 pharmacies in Bulgaria. Socio-demographic characteristic, disease profile, symptoms, and medication data were collected. The questionnaire was developed for the purposes of the EUROAGEISM project. Out of all 543 patients, only those with documented cardio-vascular diseases were extracted and the medication profile per patient was evaluated for Potentially inappropriate medication (PIMs) and potentially prescribing omissions (PPOs) using STOPP/START criteria version 2. In addition, several risks for potentially inappropriate prescribing (PIPs), PPOs and PIMs were calculated with the focus being on the Odds and Risks to develop a PIP.
    Four hundred and twenty eight from 531 patients with known therapy for cardiovascular diseases (CVDs) were included in the analysis of PIP (40.52% aged 65-69 years, 61.88% female, 64% had up to 6 comorbidities, and 21.72% presenting with polypharmacy). A total of 71 PIMs in 64 patients with polypharmacy were identified during applying STOPP criteria. 56% of patients taking above five medicines daily had PIMs. The majority of PIMs (31%) were related to CVDs treatment, followed by PIMs in the treatment of endocrine diseases (22.54%), duplication of medicines (8.46%) and prolonged treatment with benzodiazepines (8.46%). Forty four PPOs were identified with START criteria. 22.72% were related to lack of proton pump inhibitors (PPI) in the presence of gastroesophageal disorders, and the same percentage was for lack of Calcium-vitamin D supplementation in osteoporosis. Applying the methodology of risks calculation the sample risk for PPO was 2.1% and for PIM 3.4%. At sample level the relative risk for PPO was 62% out of the risk for PIM and at population level varied between 42.8 and 89.8% and it is statistically significant. The number needed to treat for the event to happen is 77.5, meaning that at every 78 prescriptions there is a chance to appear PIP.
    Application of methodologies for detection of potentially inappropriate prescribing is not part of routine clinical practice in Bulgaria. Our study demonstrates a high percentage of potentially inappropriate medication among older patients with polypharmacy. Along with the aging population in Bulgaria, economic burden of polypharmacy and the prevalence of cardiovascular diseases, it is especially important to address potentially inappropriate medication use in cardiovascular patients. There is a considerable necessity for implementation of measures for early detection of potentially inappropriate medication and potentially prescribing omission as a part of de-prescribing strategies in older patients.
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  • 文章类型: Journal Article
    UNASSIGNED:老年患者患有慢性疾病,并且容易进行多重用药和潜在的不适当处方(PIP)。这项研究旨在确定三级护理医院环境中老年患者中潜在的不适当药物(PIMs)和潜在的处方遗漏(PPOs),并估计多种药物的患病率。
    UNASSIGNED:这项多中心回顾性观察性研究回顾了来自两家主要巴勒斯坦医院的患者数据。收集的数据包括患者的人口统计,合并症,以及住院和出院期间服用的药物。该研究包括2019年1月至2019年12月期间住院的247名年龄≥65岁的患者。STOPP/START标准第2版用于确定PIMs和PPOs的患病率。临床药师验证了数据,采用SPSS进行数据分析。描述性统计,单尾双变量相关性,和Pearson检验应用于感兴趣的变量,以检查它们与STOPP/START标准的关联。
    UNASSIGNED:总共247名患者被纳入研究,女性占50.2%。因此,165名(66.8%)参与者被确定为PIP,包括30名PPOs患者,91与PIMs,44和两者。此外,住院和出院期间PIP的患病率分别为56.29%和64.39%,分别。在住院和出院期间,多药(5-9种药物)分别为44.5%和52.1%,分别,住院和出院期间,多药过量(十种药物或更多)分别为33.6%和16.4%,分别。此外,47.3%的患者的合并症指数≥5。
    UNASSIGNED:这项研究发现,老年患者在入院和出院期间PIP的患病率很高。此外,在这项研究中,超过一半的老年患者患有PIP,且多重用药的患病率较高.因此,这项研究强调了适应循证工具的重要性,如STOPP/START标准,优化患者药物治疗,并指导处方者识别和解决PIM和PPO。
    UNASSIGNED: Elderly patients suffer from chronic diseases and are prone to polypharmacy and potentially inappropriate prescribing (PIP). This study aimed to identify potentially inappropriate medications (PIMs) and potential prescribing omissions (PPOs) among elderly patients in a tertiary care hospital setting and to estimate the prevalence of polypharmacy.
    UNASSIGNED: This multicenter retrospective observational study reviewed patient data from two major Palestinian hospitals. The collected data included patient demographics, comorbidities, and medications administered during hospitalization and discharge. The study included 247 patients aged ≥ 65 years hospitalized between January 2019 and December 2019. The STOPP/START criteria version 2 was used to identify the prevalence of PIMs and PPOs. Clinical pharmacists verified the data, and SPSS was used for data analysis. Descriptive statistics, one-tailed bivariate correlations, and Pearson\'s test were applied to the variables of interest to examine their association with the STOPP/START criteria.
    UNASSIGNED: A total of 247 patients were included in the study, and 50.2% were females. As a result, 165 (66.8%) participants were identified with PIPs, including 30 patients with PPOs, 91 with PIMs, and 44 with both. Furthermore, the prevalence of PIP during hospitalization and discharge was 56.29% and 64.39%, respectively. Polypharmacy (5-9 medications) was 44.5% and 52.1% during hospitalization and discharge, respectively, and excessive polypharmacy (ten medications or more) was 33.6% and 16.4% during hospitalization and discharge, respectively. Moreover, 47.3% of the patients had a comorbidity index of ≥ 5.
    UNASSIGNED: This study identified a high prevalence of PIPs among elderly patients during hospital admission and discharge. In addition, more than half of the geriatric patients in this study had PIP and a high prevalence of polypharmacy. Therefore, this study emphasizes the importance of adapting evidence-based tools, such as the STOPP/START criteria, to optimize patient medication therapy and guide prescribers in identifying and resolving PIMs and PPOs.
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  • 文章类型: Journal Article
    评估医院医生和老年患者与药物治疗团队个性化基于STOPP/START的药物优化建议的一致性。
    这项研究嵌入了一个大型的欧洲,多中心,整群随机对照试验,研究结构化药物审查对多种药物(≥3种慢性疾病)老年人(≥70岁)与多种药物(≥5种慢性药物)相关的住院患者的影响,叫做OPERAM。来自该试验的荷兰干预组的数据用于该研究。由具有综合STOPP/START标准的临床决策支持系统支持的医师和药剂师(即药物治疗团队)联合进行药物审查。与患者和主治医生讨论了基于STOPP/START的个性化药物优化建议。
    139名患者被纳入,平均(SD)年龄78.3(5.1)岁,47%的男性和中位(IQR)入院时的药物数量11(9-14)。总的来说,与患者和医生讨论了371项建议,STOPP的总体同意率为61.6%,START建议为60.7%.发现开始使用骨质疏松症药物和停用质子泵抑制剂的一致性最高(均为74%)。多变量分析中与较高一致性相关的因素是:女性(+17.1%[3.7;30.4]),过去一年≥1下降(+15.0%[1.5;28.5])和肾损害,即eGFR30-50ml/min/1.73m2;(+18.0%[2.0;34.0])。分歧的主要原因(40%)是患者不愿停止或开始用药。
    关于药物治疗的益处/风险平衡的更好的患者和医生教育,除了更精确和最新的医疗记录,以避免不相关的建议,可能会导致对未来药物治疗优化建议的更高依从性。
    试验注册号NCT02986425。
    To evaluate the agreement of hospital physicians and older patients with individualised STOPP/START-based medication optimisation recommendations from a pharmacotherapy team.
    This study was embedded within a large European, multicentre, cluster randomised controlled trial examining the effect of a structured medication review on drug-related hospital admissions in multimorbid (≥ 3 chronic conditions) older people (≥ 70 years) with polypharmacy (≥ 5 chronic medications), called OPERAM. Data from the Dutch intervention arm of this trial were used for this study. Medication review was performed jointly by a physician and pharmacist (i.e. pharmacotherapy team) supported by a Clinical Decision Support System with integrated STOPP/START criteria. Individualised STOPP/START-based medication optimisation recommendations were discussed with patients and attending hospital physicians.
    139 patients were included, mean (SD) age 78.3 (5.1) years, 47% male and median (IQR) number of medications at admission 11 (9-14). In total, 371 recommendations were discussed with patients and physicians, overall agreement was 61.6% for STOPP and 60.7% for START recommendations. Highest agreement was found for initiation of osteoporosis agents and discontinuation of proton pump inhibitors (both 74%). Factors associated with higher agreement in multivariate analysis were: female gender (+ 17.1% [3.7; 30.4]), ≥ 1 falls in the past year (+ 15.0% [1.5; 28.5]) and renal impairment i.e. eGFR 30-50 ml/min/1.73 m2; (+ 18.0% [2.0; 34.0]). The main reason for disagreement (40%) was patients\' reluctance to discontinue or initiate medication.
    Better patient and physician education regarding the benefit/risk balance of pharmacotherapy, in addition to more precise and up-to-date medical records to avoid irrelevant recommendations, will likely result in higher adherence with future pharmacotherapy optimisation recommendations.
    Trial Registration Number NCT02986425.
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