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实施由药剂师主导的方案以改善慢性肾脏病住院患者缺铁的筛查与治疗。

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

作者信息

Chow Karissa, Trollinger Brandon, Blum Matthew, Alasfar Sami, Monroy-Trujillo Jose Manuel, Brown Dannielle

机构信息

The Johns Hopkins Hospital Deparment of Pharmacy, Baltimore, MD, USA.

Johns Hopkins University School of Medicine, Department of Nephrology, Baltimore, MD, USA.

出版信息

Hosp Pharm. 2024 Aug 7:00185787241267730. doi: 10.1177/00185787241267730.

Abstract

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. 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. 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. 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.

摘要

虽然静脉补铁是治疗慢性肾脏病(CKD)贫血及改善预后的有效手段,但缺铁的指南实验室定义存在差异,导致筛查和补铁策略存在差异。本研究旨在描述CKD中铁缺乏的识别和治疗的当前实践,然后在一家三级医疗中心实施由药剂师主导的方案以优化护理。这项针对入住住院病房的成年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既往实践,随后部署了由药剂师推动的缺铁筛查和治疗方案。缺铁定义为转铁蛋白饱和度≤30%且铁蛋白≤500 ng/mL。分析了筛查率和补铁率的改善情况。在7155例入院病例中回顾了既往方案实施前的实践,其中2559例(35.8%)包括缺铁筛查。在2个月的干预(方案实施后)期内,纳入了315例入院病例。方案实施后队列中的患者平均年龄为64.1岁,53.7%为女性,26.4%依赖透析。与方案实施前相比,方案实施后队列中的患者接受筛查的可能性高2.33倍(95%CI 2.20 - 2.47),缺铁患者接受治疗的可能性高2.05倍(95%CI 1.46 - 2.86),大多数接受静脉铁剂治疗(85.4%)。与方案实施前相比,方案实施后队列中的患者接受静脉铁剂而非仅口服铁剂的可能性高3.58倍(95%CI 1.97 - 6.48)。实施由药剂师推动的方案后,CKD患者接受铁筛查和治疗的频率增加。本研究强调了对该人群缺铁进行识别/治疗采取系统方法的必要性。

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Intravenous Iron in Patients Undergoing Maintenance Hemodialysis.维持性血液透析患者的静脉铁剂治疗。
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