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Fred J Boyd 2023 oration 弗雷德-博伊德 2023 年致辞
IF 2.1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-12-17 DOI: 10.1002/jppr.1899
M. K. Dunkley
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引用次数: 0
Estimation of kidney function for medication dosing in adult patients with chronic kidney disease: a practice update 估计成年慢性肾病患者的肾功能以确定用药剂量:实践更新
IF 2.1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-11-13 DOI: 10.1002/jppr.1884
Sanja Mirkov BPharm, PGDipPH, Carla Scuderi MClinPharm, BPharm, Jess Lloyd BPharm, GradDipClinPharm,, John Coutsouvelis PhD, MClinPharm, BPharm, FSHP, Shaun O'Connor BPharm, MSHP, Simon Potts BPharm, BSc (Hons), Suzanne Newman BPharm, GradDipHospPharm, Jason Roberts PhD, BPharm (Hons), BAppSc, FSHP, FISAC, FAHMS

Chronic kidney disease (CKD) is a major health concern with a growing disease burden and inequalities in access to treatments. Glomerular filtration rate (GFR) is accepted as the best overall measure of kidney function and is considered the most important measure for medications cleared by the kidneys. In clinical practice, equations that estimate GFR using validated prediction equations are routinely used. This practice update was developed by a Working Group comprising clinical pharmacists representing the Society of Hospital Pharmacists of Australia (SHPA) Specialty Practice streams of Nephrology, Oncology and haematology, Critical care and Infectious diseases. It is intended to provide practical recommendations for clinical pharmacists who use equations to estimate GFR for medication dosing decisions. The limitations of the various equations in use — such as the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI), the Cockcroft–Gault equation and Modification of Diet in Renal Disease — are summarised and compared to direct measures of kidney function using exogenous markers. The CKD-EPI equation is recommended to be used routinely as a primary measure of kidney function. Dose adjustments should also consider medication-specific, patient-related, and disease-related characteristics. Kidney function and the response to therapy should be continuously assessed by monitoring the signs, symptoms and disease outcomes, the emergence of adverse reactions or medication-induced disorders and use therapeutic drug monitoring (if available) to adjust doses accordingly.

慢性肾脏病(CKD)是一个重大的健康问题,其疾病负担日益加重,且治疗机会不平等。肾小球滤过率(GFR)被认为是衡量肾功能的最佳综合指标,也被认为是衡量肾脏清除药物的最重要指标。在临床实践中,使用有效的预测方程估算 GFR 是常规方法。本实践更新由代表澳大利亚医院药剂师协会(SHPA)肾脏病学、肿瘤学和血液学、重症监护和传染病专业实践流的临床药剂师组成的工作组制定。该工作小组旨在为使用方程估算 GFR 以决定用药量的临床药剂师提供实用建议。文中总结了各种常用方程(如慢性肾脏病流行病学协作组 (CKD-EPI)、Cockcroft-Gault 方程和肾病饮食调整)的局限性,并将其与使用外源性标记物直接测量肾功能的方法进行了比较。建议将 CKD-EPI 方程作为肾功能的主要常规测量方法。剂量调整还应考虑药物特异性、患者相关性和疾病相关特性。应通过监测体征、症状和疾病结果、不良反应或药物引起的紊乱的出现来持续评估肾功能和对治疗的反应,并使用治疗药物监测(如有)来相应地调整剂量。
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引用次数: 0
Medication error reporting attitudes and practices in a regional Australian hospital: a qualitative study 澳大利亚一家地区医院报告用药错误的态度和做法:一项定性研究
IF 2.1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-11-10 DOI: 10.1002/jppr.1887
Shady Abdelmaksoud BPharm, MClinPharm, Mohammed S. Salahudeen BPharm, PharmD, PhD, FHEA, Colin M. Curtain BPharm, GradDipComp, PhD

Background

Medication errors are events that may cause or lead to inappropriate medication use or patient harm. Australians living outside metropolitan areas have poorer health outcomes than those living in urban areas. Medication error reporting (MER) practices vary due to the attitude of healthcare professionals (HCPs). MER can improve patient safety in community and hospital settings.

Aim

To explore HCPs' attitudes, practices, and recommendations towards MER in a regional hospital setting in Australia.

Method

Semistructured interviews were employed to identify the attitudes, practices, and recommendations of HCPs for the best utilisation of medication error reports. The study recruited HCPs (nurses, pharmacists, and doctors) working in all clinical areas from November 2021–February 2022. Interviews were recorded and transcribed via thematic analysis. Ethics approval was obtained from the Goulburn Valley Health (GVH) Human Research Ethics Committee (Reference no: GVH 35/21). Informed consent was obtained from participants via an information sheet and completion of a written consent form.

Results

Interviews with twelve HCPs elucidated four themes: barriers and enablers to reporting, and perceived benefits and recommendations for medication error reports. There was good understanding among regional HCPs about the benefits of MER. Attitudes and practices varied, with nurses reporting more medication errors than doctors, and pharmacists being concerned about the impact of reporting on interprofessional relations. Their recommendations involved standardising medication error definition and improving electronic system education.

Conclusion

Despite HCPs' understanding of the role of MER, their practices varied. We recommend improved protected time for learning, training with the incident reporting software, education about medication errors, and formalisation of test feedback to clinicians. The implementation of workplace cultural practice changes to improve organisational systems and enhance error reporting without fear of repercussions, and the adoption of additional solutions such as electronic prescribing are also encouraged.

背景用药错误是指可能造成或导致用药不当或对患者造成伤害的事件。与居住在城市地区的人相比,居住在大都市以外地区的澳大利亚人的健康状况较差。由于医疗保健专业人员(HCPs)的态度不同,用药错误报告(MER)的做法也不尽相同。用药错误报告可以改善社区和医院环境中的患者安全。 目的 探讨澳大利亚地区医院的医护人员对用药错误报告的态度、做法和建议。 方法 采用半结构式访谈,以确定医疗保健人员对最佳利用用药错误报告的态度、做法和建议。研究招募了 2021 年 11 月至 2022 年 2 月期间在所有临床领域工作的 HCP(护士、药剂师和医生)。研究人员对访谈进行了录音,并通过专题分析对访谈内容进行了转录。古尔本谷医疗机构(GVH)人类研究伦理委员会(参考编号:GVH 35/21)已批准了伦理研究。通过信息表和填写书面同意书获得了参与者的知情同意。 结果 对 12 名保健医生进行的访谈阐明了四个主题:报告的障碍和促进因素、感知到的好处以及对用药错误报告的建议。各地区的高级保健人员对 MER 的益处都有很好的理解。他们的态度和做法各不相同,护士比医生报告更多的用药错误,药剂师则担心报告对专业间关系的影响。他们的建议包括统一用药错误的定义和改进电子系统教育。 结论 尽管医疗保健人员对 MER 的作用有所了解,但他们的做法各不相同。我们建议改善受保护的学习时间、事故报告软件培训、用药错误教育以及对临床医生的测试反馈正规化。此外,我们还鼓励实施工作场所文化实践变革,以改进组织系统并加强错误报告,而不必担心受到影响,同时鼓励采用电子处方等其他解决方案。
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引用次数: 0
A case of extrapyramidal side effects due to possible paliperidone: voriconazole interaction 帕潘立酮:伏立康唑可能相互作用导致的锥体外系副作用病例
IF 2.1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-11-10 DOI: 10.1002/jppr.1892
Louise Beilby BPharm, GradCertPharmPrac, Lucy Arno BPharm (Hons), MHA

Background

It is thought that paliperidone, an active metabolite of risperidone, has limited potential for pharmacokinetic drug–drug interactions (DDIs) due to minimal metabolism by cytochrome P450 3A4 (CYP3A4) and cytochrome P450 2D6 (CYP2D6). However, DDIs have been reported and include a theoretical interaction between paliperidone and voriconazole based on interactions between risperidone and strong CYP3A4 inhibitor azoles.

Aim

To describe the first recorded DDI between paliperidone and voriconazole leading to extrapyramidal side effects (EPSEs).

Clinical details

A 34-year-old male presented with febrile neutropenia presumed due to clozapine. Clozapine was ceased and paliperidone commenced with voriconazole added to the patient's empiric piperacillin/tazobactam therapy due to a suspected fungal infection. Two days after starting voriconazole, the patient developed hypertonia and hyperreflexia in all limbs, thought most likely to be antipsychotic induced EPSEs. Paliperidone was withheld and EPSEs resolved.

Outcomes

The patient had previously tolerated long-term paliperidone at higher doses, prior to transitioning to clozapine. The development of EPSEs occurred two days post azole initiation, indicating a probable paliperidone adverse drug reaction (ADR) due to strong CYP3A4 inhibition by voriconazole. This case appears to be the first documented report of this previous theoretical DDI in practice. Further studies, including therapeutic drug monitoring, are required to confirm findings.

Conclusion

Paliperidone may be affected by pharmacokinetic drug–drug interactions and patients should be monitored for ADRs when CYP3A4 inhibitors are concomitantly administered.

背景 据认为,由于细胞色素 P450 3A4 (CYP3A4) 和细胞色素 P450 2D6 (CYP2D6) 的代谢作用极小,利培酮的活性代谢产物帕利哌酮发生药代动力学药物相互作用 (DDI) 的可能性有限。然而,DDIs 已有报道,其中包括根据利培酮与强 CYP3A4 抑制剂唑类之间的相互作用而得出的帕利哌酮与伏立康唑之间的理论相互作用。 目的 描述帕利哌酮与伏立康唑之间导致锥体外系副作用(EPSE)的首次DDI记录。 临床详情 一名34岁的男性因发热性中性粒细胞减少症就诊,推测是氯氮平所致。由于怀疑是真菌感染,患者停用了氯氮平,开始服用帕利哌酮,并在哌拉西林/他唑巴坦的经验性治疗基础上加用了伏立康唑。开始服用伏立康唑两天后,患者出现四肢肌张力亢进和反射亢进,被认为很可能是抗精神病药物诱发的EPSE。患者停用帕潘立酮后,EPSE症状消失。 结果 患者在转用氯氮平之前曾长期耐受较高剂量的帕潘立酮。EPSE发生在开始使用唑类药物两天后,这表明帕利哌酮可能是由于伏立康唑对CYP3A4的强烈抑制而引起的药物不良反应(ADR)。本病例似乎是以前理论上的 DDI 在实践中的首次有据可查的报告。需要进一步研究,包括治疗药物监测,以确认研究结果。 结论 帕潘立酮可能会受到药代动力学药物相互作用的影响,当同时服用 CYP3A4 抑制剂时,应监测患者的 ADR。
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引用次数: 0
Pharmacists in Australian general practice: Discussion of the findings of an evaluation from 2016 to 2021 澳大利亚全科医师药剂师:2016年至2021年评估结果的讨论
IF 2.1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-11-07 DOI: 10.1002/jppr.1878
Louise S. Deeks BSc (Hons), PGDip, PGCert, Mark Naunton BPharm (Hons), PhD, Gregory M. Peterson BPharm (Hons), MBA, PhD, Thilini Sudeshika BPharm (Hons), PGDipToxicology, MPhil, Christopher Freeman BPharm, GDipClinPharm, PhD, Ravi Sharma MPharm (Hons), MSc, PGCert, Stacy Leavens BA, MA, Sam Kosari BPharm (Hons), PhD

Pharmacists embedded in general practice can improve medicines optimisation and patient safety, but Australia has been slower to adopt and fund this model than other comparable countries. Over the last decade there have been various local programs integrating pharmacists in general practice across Australia. This article summarises the results of an evaluation in Canberra from 2016–2021. Pharmacists predominantly conducted clinical activities, including medication reviews and clinical audits. General practitioner (GP) acceptance and implementation of medication review recommendations was high (75%). General practice pharmacists were able to achieve positive clinical outcomes in asthma and smoking cessation. Surveys and interviews identified that the general practice pharmacist role was welcomed by patients, GPs, and other healthcare professionals. Patient satisfaction was very high, with patients supporting the expansion of this pharmacy service. Collaboration between the pharmacists and other healthcare professionals was high. Some pharmacists left employment in general practice after less than a year. Introducing a clear job description could be beneficial in retaining pharmacists, improving trust and working relationships, and enhancing collaboration. The majority of clinical activities conducted by the pharmacists had the potential to improve patient care and decrease healthcare costs. Apart from healthcare savings, benefit–cost ratios of income generated and costs reduced by pharmacists when compared to salaries suggested that pharmacists may be cost-beneficial in some scenarios. Absence of funding for this model of care remains a barrier to wider adoption in Australia and needs addressing. This study was approved by the University of Canberra Human Research Ethics Committee (Project number: 15–235) and funded under the Primary Health Network Program (Grant number: 25097479).

融入全科实践的药剂师可以改善药物优化和患者安全,但与其他可比国家相比,澳大利亚采用和资助这种模式的速度较慢。在过去的十年里,有各种各样的地方项目将药剂师整合到澳大利亚的一般实践中。本文总结了2016-2021年在堪培拉进行的评估结果。药剂师主要进行临床活动,包括药物审查和临床审计。全科医生(GP)接受和执行药物审查建议的比例很高(75%)。全科执业药师能够在哮喘和戒烟方面取得积极的临床结果。调查和访谈表明,普通执业药师的角色受到患者、全科医生和其他医疗保健专业人员的欢迎。患者满意度非常高,患者支持扩大药房服务。药剂师和其他医疗专业人员之间的合作程度很高。一些药剂师在不到一年的时间里就离开了全科诊所。引入明确的工作描述可能有利于留住药剂师,改善信任和工作关系,并加强合作。药剂师进行的大多数临床活动都有可能改善患者护理并降低医疗保健费用。除了节省医疗费用外,与工资相比,药剂师产生的收入和减少的费用的效益成本比表明,药剂师在某些情况下可能具有成本效益。这种护理模式缺乏资金仍然是澳大利亚广泛采用这种模式的障碍,需要加以解决。这项研究由堪培拉大学人类研究伦理委员会批准(项目编号:15-235),并由初级卫生网络计划(资助编号:25097479)资助。
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引用次数: 0
Evaluation of local guideline introduction on surgical antimicrobial prophylaxis prescribing for open reduction internal fixations at an Australian tertiary hospital 对澳大利亚一家三级医院引入开刀复位内固定手术抗菌药预防处方地方指南的评估
IF 2.1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-10-03 DOI: 10.1002/jppr.1886
Sarah Hassan BPharm (Hons), PhD, Vincent Chan BSc (Hons), BPharm, MPH, PhD, GradCertAcadPrac, AACPA, Julie E. Stevens BSc, BPharm (Hons), PhD, Ieva Stupans BPharm (Hons), PhD, Juliette Gentle MBBS, FRACS (Orth)

Background

Guidelines advocate for the use of single-dose prophylaxis in open reduction internal fixation (ORIF) procedures. The presence of local (institutional) guidelines may assist in the uptake of evidence-based recommendations.

Aim

To determine the impact of local guideline introduction on prescribing practice for ORIF procedures at a metropolitan hospital in relation to our previous audit investigating adherence to national guidelines, which found that only 20.4% of ORIF patients received single-dose prophylaxis.

Method

Antibiotic prescribing was audited for patients undergoing ORIF of closed fractures from July–December 2021 at a metropolitan, tertiary hospital following guideline introduction in April 2021. Data on perioperative prescribing regimens were collected, with results compared to recommendations in local guidelines. Descriptive statistics, chi-squared test, and Fisher's exact test were used to report categorical variables. Ethics approval was granted by Northern Health Office of Research, Ethics, and Governance (Reference no: NLR 72459) and registered with the RMIT University College Human Ethics Advisory Network (Reference no: RM 24642).

Results

Data were collected for 165 patients. Almost all patients (93.5%) received cefazolin preoperatively as per guidelines. Only 22.6% of patients received single-dose prophylaxis as per local guideline recommendations, with overall adherence to guidelines only 16.4%.

Conclusion

Little change was observed in the proportion of patients who received single-dose prophylaxis as compared to our previous audit. There is a need to understand why guidelines are not adhered to despite the availability of national and local guidelines. An evaluation of local barriers may assist with informing future implementation strategies.

背景指南提倡在开放复位内固定术(ORIF)中使用单剂量预防疗法。地方(机构)指南的存在可能有助于采纳循证建议。 目的 针对我们之前对国家指南遵守情况的审计发现,仅有 20.4% 的 ORIF 患者接受了单剂量预防治疗,从而确定地方指南的引入对一家都市医院 ORIF 手术处方实践的影响。 方法 在 2021 年 4 月引入指南后,我们于 2021 年 7 月至 12 月对一家大都市三级医院接受闭合性骨折 ORIF 手术的患者的抗生素处方进行了审核。收集了围手术期处方方案的数据,并将结果与当地指南的建议进行了比较。描述性统计、卡方检验和费雪精确检验用于报告分类变量。该研究获得了北部卫生部研究、伦理和管理办公室的伦理批准(编号:NLR 72459),并在皇家墨尔本理工大学学院人类伦理咨询网络注册(编号:RM 24642)。 结果 收集了 165 名患者的数据。几乎所有患者(93.5%)都按照指南在术前接受了头孢唑啉治疗。只有 22.6% 的患者按照当地指南的建议接受了单剂量预防治疗,而遵守指南的总体比例仅为 16.4%。 结论 与我们之前的审计相比,接受单剂量预防的患者比例变化不大。我们有必要了解,尽管有国家和地方指南,但为何仍有人不遵守指南。对当地存在的障碍进行评估有助于为未来的实施策略提供依据。
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引用次数: 0
Management of thyroid disorders in older people 老年人甲状腺疾病的管理
IF 2.1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-10-03 DOI: 10.1002/jppr.1883
Gauri Godbole BPharm, MClinPharm, BCGP, AdvPP(II), AcSHP, CDP, FSHP, Tripti Joshi MBBS, MD, MPH, FRACP, MPhil, Monica Majumder BMed, BSc(Med)Hons

Thyroid disorders are common in older people and cause significant morbidity. There may be fewer symptoms at presentation and increased susceptibility to adverse events, making diagnosis and management more challenging. The approach to management of thyroid disorders in older people differs from that for younger individuals. Factors that need to be considered include frailty, concurrent illness, polypharmacy, drug–drug interactions, and target organ sensitivity to treatment. This review discusses the clinical presentation, pathophysiology, and management of thyroid disorders and the effects of medications on thyroid function in older people.

甲状腺疾病在老年人中很常见,并引起显著的发病率。出现时症状可能较少,对不良事件的易感性增加,使诊断和管理更具挑战性。老年人甲状腺疾病的治疗方法不同于年轻人。需要考虑的因素包括虚弱、并发疾病、多种药物、药物相互作用和靶器官对治疗的敏感性。本文综述了老年人甲状腺疾病的临床表现、病理生理、治疗以及药物对甲状腺功能的影响。
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引用次数: 0
Safety and efficacy comparisons of intravenous trastuzumab biosimilars to the reference product medicine in treatment-naïve and switch-over patients with breast cancer: a systematic and meta-analysis 静脉注射曲妥珠单抗生物仿制药与参比产品药物在乳腺癌新患者和转归患者中的安全性和疗效比较:系统和荟萃分析
IF 2.1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-09-27 DOI: 10.1002/jppr.1882
Nina K. Song BPharm (Hons), Hala Musa BSc (Hons), MSc, MPharm, Michael Soriano BS Pharmacy (PH), Mellissa Batger BSc, MPharm, Bryson Hawkins BPharm (Hons), Iqbal Ramzan Dip Pharmacy (NZ), MSc, PhD, David E. Hibbs BSc (Hons), PhD, Grad Cert Ed (Higher Ed), Jennifer Ong BPharm (Hons), PhD, Grad Cert Ed Studies (Higher Ed)
<div> <section> <h3> Aim</h3> <p>To compare the efficacy and safety of trastuzumab biosimilars to reference trastuzumab in patients with breast cancer. Trastuzumab, a biologic pharmaceutical product, has improved survival in hormone-oestrogen receptor 2 positive breast cancer. However, due to its high economic burden, ‘highly similar’ products known as biosimilars have been developed. Yet, concerns remain around the equivalency of efficacy and safety between biosimilars and their reference biologic.</p> </section> <section> <h3> Data Sources</h3> <p>A systematic review with meta-analysis was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. MEDLINE, EMBASE, and Cochrane Central databases were searched from inception to 26 April 2021 to obtain all randomised control trial data reporting on safety and efficacy outcomes of patients with breast cancer treated with trastuzumab biosimilars.</p> </section> <section> <h3> Study Selection</h3> <p>Studies were required to investigate and report on the safety and/or efficacy of trastuzumab. No restrictions were placed on study setting or intervention type and any study which reported at least one efficacy or safety outcome was included. A head-to-head comparison between the biosimilar and its reference biologic was not required for inclusion in the results. Only studies using randomised control trials were included. There was no restriction on the language the study was published in, and all abstracts, raw clinical trial data, and full-text studies were eligible.</p> </section> <section> <h3> Results</h3> <p>Forty-one studies were identified to report on patients treated with trastuzumab. The odds of achieving an overall response rate in patients treated with a trastuzumab biosimilar compared to the reference over at least 24 weeks of treatment was 1.10 (95% confidence interval [CI] 0.94–1.29). The proportion of patients experiencing any treatment emergent adverse events were comparable between the two study arms, 1.07 (95% CI 0.87–1.32). The switching group contained one study with 342 patients in the meta-analysis.</p> </section> <section> <h3> Conclusion</h3> <p>Trastuzumab biosimilars have comparable efficacy and safety to reference trastuzumab in treatment-naïve patients. However, evidence is lacking for switching patients from reference trastuzumab to biosimilars, so further work is required in the switch-over population.</p>
目的 比较曲妥珠单抗生物仿制药与参考曲妥珠单抗对乳腺癌患者的疗效和安全性。曲妥珠单抗是一种生物制药产品,可提高激素-雌激素受体2阳性乳腺癌患者的生存率。然而,由于其经济负担较重,被称为生物仿制药的 "高度相似 "产品已被开发出来。然而,人们对生物仿制药与其参照生物制剂之间的疗效和安全性的等效性仍存在担忧。 数据来源 根据《系统综述和元分析首选报告项目》(Preferred Reporting Items for Systematic Reviews and Meta-Analyses,PRISMA)指南进行了系统综述和元分析。检索了 MEDLINE、EMBASE 和 Cochrane Central 数据库,检索时间从开始到 2021 年 4 月 26 日,以获得所有报告使用曲妥珠单抗生物仿制药治疗乳腺癌患者的安全性和疗效结果的随机对照试验数据。 研究选择 要求对曲妥珠单抗的安全性和/或疗效进行调查和报告。研究环境或干预类型不受限制,任何报告了至少一项疗效或安全性结果的研究均可纳入。生物仿制药与其参照生物制剂之间的正面比较无需纳入结果。只有采用随机对照试验的研究才被纳入。研究发表的语言没有限制,所有摘要、原始临床试验数据和全文研究均符合条件。 结果 41 项研究报告了接受曲妥珠单抗治疗的患者的情况。接受曲妥珠单抗生物类似物治疗的患者在至少24周的治疗中获得总体应答率的几率为1.10(95% 置信区间[CI] 0.94-1.29)。两组研究中出现治疗突发不良事件的患者比例相当,均为1.07(95% 置信区间为0.87-1.32)。在荟萃分析中,转换组包含一项有 342 名患者的研究。 结论 曲妥珠单抗生物仿制药在治疗新药患者方面的疗效和安全性与参考曲妥珠单抗相当。然而,目前还缺乏将患者从参考曲妥珠单抗转为生物仿制药的证据,因此还需要在转换人群中开展进一步的工作。
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引用次数: 0
A retrospective study investigating the management, risk factors, and outcomes of patients diagnosed with Clostridioides difficile infection 一项回顾性研究调查诊断为艰难梭菌感染的患者的管理、危险因素和结局
IF 2.1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-09-12 DOI: 10.1002/jppr.1881
Mitt M. Vongphakdi BPharm(Hons), Nicholas Ah Yui BPharm, GCClinPharm, Kevin OCallaghan MB BCh BAO, MPHTM, FRACP

Background

The rate of clostridioides difficile infection (CDI) in Australia has increased by more than 8% between 2016–2018. This can be attributed to multiple factors including an ageing population, widespread antibiotic and proton-pump-inhibitor usage.

Aim

The aim of this study was to investigate the management, risk factors and outcomes for CDI to identify strategies to reduce its incidence.

Method

A single-centre retrospective audit was completed using medical records for patients admitted to a 250-bed regional Queensland hospital with CDI in 2020–2021. Data surrounding CDI management for each patient was analysed against the Therapeutic Guidelines. This study was approved by The Prince Charles Hospital Human Research Ethics Committee (Reference No: LNR/HREC/QPCH/81287).

Results

There were 72 cases with CDI during the study timeframe. Recent antibiotic prescription, proton-pump-inhibitor (PPI) use and antibiotic allergy labels were common. Thirty-five per cent of cases were treated appropriately. Eight per cent died, and nine per cent had relapsed CDI within 12 weeks of diagnosis. Common gaps found in the results included inappropriate selection of antibiotics based on the severity of disease and lack of documentation surrounding CDI cases left untreated.

Conclusion

There are multiple opportunities for pharmacists to improve the care of patients with CDI which range from promoting guideline adherence, influencing prescriber antibiotic selection based on disease severity, prompting review of PPIs upon CDI diagnosis and prompting provider follow-up of CDI laboratory results pending at the point of patient discharge. The results of this study have prompted antimicrobial stewardship service review of all CDI admissions at the study site and indicates the need for a larger multiple-site study to raise awareness of CDI risk factors and severity criteria.

2016-2018年间,澳大利亚艰难梭菌感染率(CDI)增加了8%以上。这可归因于多种因素,包括人口老龄化,抗生素和质子泵抑制剂的广泛使用。目的本研究的目的是探讨CDI的管理、危险因素和结果,以确定降低其发病率的策略。方法采用单中心回顾性审计方法,对昆士兰州一家拥有250个床位的地区医院2020-2021年收治的CDI患者的医疗记录进行审计。根据治疗指南对每位患者的CDI管理数据进行分析。本研究已获查尔斯王子医院人类研究伦理委员会批准(参考编号:LNR/HREC/QPCH/81287)。结果研究期间共发生72例CDI。最近的抗生素处方、质子泵抑制剂(PPI)使用和抗生素过敏标签是常见的。35%的病例得到了适当的治疗。8%的患者死亡,9%的患者在确诊后的12周内复发。在结果中发现的常见差距包括根据疾病严重程度不适当地选择抗生素,以及缺乏关于未经治疗的CDI病例的记录。结论药师有多种机会改善CDI患者的护理,包括促进指南的遵守,根据疾病严重程度影响处方抗生素的选择,在CDI诊断时提示PPIs的审查,以及在患者出院时提示提供者对CDI实验室结果的随访。这项研究的结果促使对研究地点所有CDI入院的抗菌药物管理服务进行审查,并表明需要进行更大规模的多地点研究,以提高对CDI风险因素和严重程度标准的认识。
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引用次数: 0
Selecting performance indicators for hospital pharmacy practice: A Canadian initiative 选择医院药学实践的绩效指标:加拿大的一项举措
IF 2.1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-08-31 DOI: 10.1002/jppr.1880
France Boucher BPharm, MSc, Benoît Lemire BPharm, MSc, Sylvie Schryve BArch, DEA, Linda Vaillant BPharm, MSc, MBA, FCSHP

Activity-based funding is a method of funding hospitals according to the type and volume of services provided and adjusted to their patient population. Currently, pharmacy practice is mainly evaluated with costs and volumes, which are insufficient to properly measure the contribution of pharmacists. Facing the province of Quebec statewide implementation of activity-based funding, expert committees were set up to develop a set of indicators using a predefined framework to assess pharmacy performance throughout all hospital activities and patient care. Through consultations, partners and stakeholders showed strong support for the initiative, putting more emphasis on the assessment of appropriateness as well as quality and safety. Among the different roles of pharmacists, respondents favoured the assessment of the pharmaceutical care and education of trainees and colleagues. Of the 150 candidate indicators initially identified, 24 were selected, of which 13 were prioritised for experimentation.

基于活动的资助是一种根据医院提供的服务类型和数量并根据患者群体进行调整的资助方法。目前,对药学实践的评价以成本和数量为主,不足以恰当衡量药师的贡献。面对魁北克省在全州范围内实施的基于活动的资金,设立了专家委员会,利用预定义的框架制定一套指标,以评估所有医院活动和患者护理中的药房绩效。通过磋商,合作伙伴和持份者对这一倡议表示大力支持,更加重视评估适当性以及质量和安全。在不同角色的药师中,受访者更倾向于对学员和同事的药学服务和药学教育的评价。在最初确定的150个候选指标中,选择了24个,其中13个优先用于实验。
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引用次数: 0
期刊
Journal of Pharmacy Practice and Research
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