Implementation of a Pharmacist-Driven Protocol to Improve Screening and Treatment of Iron Deficiency in Hospitalized Patients with Chronic Kidney Disease.

IF 0.8 Q4 PHARMACOLOGY & PHARMACY Hospital Pharmacy Pub Date : 2024-08-07 DOI:10.1177/00185787241267730
Karissa Chow, Brandon Trollinger, Matthew Blum, Sami Alasfar, Jose Manuel Monroy-Trujillo, Dannielle Brown
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Abstract

Purpose: While intravenous (IV) iron repletion is an effective tool to treat anemia and improve outcomes in chronic kidney disease (CKD), guideline laboratory definitions of iron deficiency differ, resulting in variability in screening and repletion strategies. This study sought to describe current practices surrounding identification and treatment of iron deficiency in CKD and then implement a pharmacist-led protocol to optimize care at a tertiary medical center. Methods: This single center, retrospective, pre- and post-protocol implementation study of adults with CKD admitted to the inpatient setting first analyzed historic practices for iron deficiency screening and treatment, followed by deployment of a pharmacist-driven protocol for iron deficiency screening and treatment. Iron deficiency was defined as transferrin saturation of ≤30% and ferritin of ≤500 ng/mL. Improvement in screening and repletion rates was analyzed. Results: Historic pre-protocol practices were reviewed in 7155 admissions of which 2559 (35.8%) included screening for iron deficiency. Over the 2 months intervention (post-protocol) period, 315 admissions were included. The average age of patients in the post-protocol cohort was 64.1 years, 53.7% were female, and 26.4% were dialysis dependent. Compared to pre-protocol, patients were 2.33 (95% CI 2.20-2.47) times more likely to be screened and deficient patients were 2.05 (95% CI 1.46-2.86) times more likely to be treated, with most receiving IV iron therapy (85.4%), in the post-protocol cohort. Patients were 3.58 times (95% CI 1.97-6.48) more likely to receive IV iron versus oral alone in the post-protocol cohort compared to pre-protocol. Conclusion: The frequency of patients with CKD screened and treated with iron increased after implementation of a pharmacist-driven protocol. This study underscores the need for a systematic approach to identification/treatment of iron deficiency in this population.

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实施以药剂师为主导的方案,改善慢性肾病住院患者铁缺乏症的筛查和治疗。
目的:虽然静脉注射补铁是治疗慢性肾脏病(CKD)患者贫血和改善预后的有效手段,但实验室对缺铁的指导性定义各不相同,导致筛查和补铁策略存在差异。本研究旨在描述目前识别和治疗 CKD 缺铁症的方法,然后在一家三级医疗中心实施以药剂师为主导的方案,以优化护理。方法:这项针对住院成人 CKD 患者的单中心、回顾性、方案实施前后研究首先分析了缺铁筛查和治疗的历史做法,然后部署了药剂师主导的缺铁筛查和治疗方案。铁缺乏的定义是转铁蛋白饱和度≤30%,铁蛋白≤500 ng/mL。分析了筛查和补铁率的提高情况。结果:对 7155 例入院患者进行了协议前的历史回顾,其中 2559 例(35.8%)包括缺铁筛查。在为期 2 个月的干预(协议后)期间,共纳入 315 例入院患者。协议后组群中患者的平均年龄为 64.1 岁,53.7% 为女性,26.4% 依赖透析治疗。与方案实施前相比,方案实施后队列中患者接受筛查的几率是方案实施前的 2.33 倍(95% CI 2.20-2.47),缺乏铁质的患者接受治疗的几率是方案实施前的 2.05 倍(95% CI 1.46-2.86),其中大多数患者接受了静脉注射铁剂治疗(85.4%)。与方案实施前相比,方案实施后队列中患者接受静脉注射铁剂治疗的几率是方案实施前的 3.58 倍(95% CI 1.97-6.48)。结论在实施药剂师驱动的方案后,接受铁剂筛查和治疗的慢性肾脏病患者人数有所增加。这项研究强调,需要采用系统的方法来识别/治疗这类人群的铁缺乏症。
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来源期刊
Hospital Pharmacy
Hospital Pharmacy PHARMACOLOGY & PHARMACY-
CiteScore
1.70
自引率
0.00%
发文量
63
期刊介绍: Hospital Pharmacy is a monthly peer-reviewed journal that is read by pharmacists and other providers practicing in the inpatient and outpatient setting within hospitals, long-term care facilities, home care, and other health-system settings The Hospital Pharmacy Assistant Editor, Michael R. Cohen, RPh, MS, DSc, FASHP, is author of a Medication Error Report Analysis and founder of The Institute for Safe Medication Practices (ISMP), a nonprofit organization that provides education about adverse drug events and their prevention.
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