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牛磺酸和肝素作为血液透析中心静脉导管的封管液。

Taurolidine and Heparin as Catheter Lock Solution for Central Venous Catheters in Hemodialysis.

机构信息

Arnold & Marie Schwartz College of Pharmacy and Health Sciences, Long Island University, Brooklyn, NY.

Division of Infectious Diseases, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY; and.

出版信息

Am J Ther. 2024;31(4):e398-e409. doi: 10.1097/MJT.0000000000001736. Epub 2024 May 7.

Abstract

BACKGROUND

Chronic kidney disease can lead to end-stage renal disease, and the prevalence is increasing. Many patients starting hemodialysis require central venous catheters (CVCs). Catheter-related bloodstream infections (CRBSIs) are a common complication and lead to significant morbidity and mortality. Interventions to prevent CRBSI include antimicrobial lock therapy but concern for the development of antimicrobial resistance and adverse effects. Nonantimicrobial antiseptics as catheter lock solutions have also been used. Taurolidine and heparin catheter lock solution is first approved by the Food and Drug Administration for the prevention of CRBSI in patients on hemodialysis. Taurolidine has a unique mechanism of action and favorable safety profile.

MECHANISM OF ACTION, PHARMACODYNAMICS, AND PHARMACOKINETICS: Taurolidine and heparin catheter lock solution have both antimicrobial and anticoagulant properties. Taurolidine is derivative of the amino acid taurine, and heparin is derived from porcine intestinal mucosa. Taurolidine not only damages microbial cell walls but also prevents the adherence of microorganisms to biological surfaces, preventing biofilm formation. Taurolidine and heparin catheter lock solution is intended to be used intraluminally within the catheter and should be aspirated. Because it is used locally, limited pharmacokinetic and pharmacodynamic data are available.

CLINICAL TRIALS

The LOCK-IT-100 trial is a randomized, double-blind, phase 3 study, which included 795 end-stage renal disease patients on hemodialysis with CVC. Taurolidine and heparin was compared with the control heparin alone. The results of the study showed a 71% risk reduction in CRBSI for taurolidine and heparin arm (95% confident interval, 38%-86%, P = 0.0006). Other studies have also shown that taurolidine lock solution leads to decreased CRBSI episodes. Several systematic reviews and meta-analysis consisted of taurolidine in adult, and pediatric populations also showed reduction in the incidence of CRBSIs.

THERAPEUTIC ADVANCE

Taurolidine and heparin lock solution represents a novel preventive strategy for those undergoing hemodialysis through a CVC by reducing the risk of CRBSI. This is significant progress because there are no other similar options available for patients for whom catheters are the only options for their life-saving treatment.

摘要

背景

慢性肾脏病可导致终末期肾病,其发病率正在上升。许多开始血液透析的患者需要中央静脉导管(CVC)。导管相关血流感染(CRBSI)是一种常见的并发症,可导致显著的发病率和死亡率。预防 CRBSI 的干预措施包括抗菌锁治疗,但人们担心会产生抗菌耐药性和不良反应。非抗菌防腐剂作为导管锁溶液也已被使用。牛磺罗定和肝素导管锁溶液首先获得美国食品和药物管理局批准,用于预防血液透析患者的 CRBSI。牛磺罗定具有独特的作用机制和良好的安全性。

作用机制、药效学和药代动力学:牛磺罗定和肝素导管锁溶液都具有抗菌和抗凝特性。牛磺罗定是氨基酸牛磺酸的衍生物,肝素是从猪肠黏膜中提取的。牛磺罗定不仅破坏微生物细胞壁,还防止微生物附着在生物表面,防止生物膜形成。牛磺罗定和肝素导管锁溶液旨在在导管内腔内使用,并应被抽吸。由于它是局部使用的,因此可用的药代动力学和药效学数据有限。

临床试验

LOCK-IT-100 试验是一项随机、双盲、3 期研究,共纳入 795 例接受血液透析的终末期肾病患者,他们使用 CVC。牛磺罗定和肝素与单独使用肝素的对照组进行比较。该研究的结果显示,牛磺罗定和肝素组的 CRBSI 风险降低了 71%(95%置信区间,38%-86%,P=0.0006)。其他研究也表明,牛磺罗定锁溶液可降低 CRBSI 发作次数。几项包括成人和儿科人群的牛磺罗定的系统评价和荟萃分析也显示 CRBSI 发生率降低。

治疗进展

牛磺罗定和肝素锁溶液通过降低 CRBSI 的风险,为通过 CVC 接受血液透析的患者提供了一种新的预防策略。这是一项重大进展,因为对于那些导管是救命治疗唯一选择的患者来说,没有其他类似的选择。

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