Different serum sodium assay, different model for end stage liver disease - sodium scores in patients awaiting liver transplant: A cross-sectional study.

IF 2.1 4区 医学 Q3 MEDICAL LABORATORY TECHNOLOGY Annals of Clinical Biochemistry Pub Date : 2024-03-01 Epub Date: 2023-08-20 DOI:10.1177/00045632231196052
Fatima Rodriguez-Alvarez, Paulina Moctezuma-Velázquez, Blanca Zuleyma Mota-Ayala, Paul Alonso Pamila-Tecuautzin, Ignacio García-Juárez, Carlos Moctezuma-Velázquez
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Abstract

Introduction and aims: Sodium can be measured with direct or indirect methods; abnormal plasma total protein concentration can impact on sodium measured by indirect ion-selective electrodes (ISE). Serum sodium is an important item to determine the Model for End Stage Liver Disease Sodium (MELD-Na) score, commonly used for liver graft allocation. Patients with cirrhosis usually have hypoproteinemia. The aim of this study was to determine if there was a significant difference between the MELD-Na scores calculated based on the results of two different serum sodium ISE: indirect and direct.

Methods: This was a retrospective study; we included 166 patients that underwent liver transplant assessment, and that had paired (i.e. same date and time) direct and indirect sodium determinations. We calculated the MELD-Na scores with both sodium determinations, and we compared them.

Results: There was a significant difference between MELD-Na scores; the mean difference was 0.4±1.3. If MELD-Na score had been determined by the sodium measured by the direct ISE, 69 patients (42%) would have stayed in the same place on the waiting list, 67 patients (40%) would have moved up, and 30 patients (18%) would have moved down.

Conclusions: There was a statistically significant difference between the MELD-Na scores calculated based on the two different sodium concentrations, which would theoretically result in changes in the order of the waiting list. This finding should prompt studies to assess if MELD-Na calculated based on direct methods has a better performance to predict clinically relevant outcomes.

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不同的血清钠测定,不同的肝病晚期模型--等待肝移植患者的钠评分:一项横断面研究。
导言和目的:钠可通过直接或间接方法测量;血浆总蛋白浓度异常会影响间接离子选择电极(ISE)测量的钠。血清钠是确定终末期肝病钠模型(MELD-Na)评分的重要项目,常用于肝移植分配。肝硬化患者通常有低蛋白血症。本研究旨在确定根据间接和直接两种不同的血清钠ISE结果计算出的MELD-Na评分之间是否存在显著差异:这是一项回顾性研究;我们纳入了 166 例接受肝移植评估的患者,这些患者的直接和间接钠测定结果是成对的(即同一日期和时间)。我们计算了两种钠测定结果的 MELD-Na 评分,并进行了比较:结果:MELD-Na 评分之间存在明显差异;平均差异为 0.4±1.3。如果 MELD-Na 评分由直接 ISE 测得的血钠决定,69 名患者(42%)将留在候诊名单的同一位置,67 名患者(40%)将向上移动,30 名患者(18%)将向下移动:根据两种不同的钠浓度计算出的 MELD-Na 分数之间存在统计学意义上的显著差异,理论上这将导致候选名单顺序的改变。这一发现应促使相关研究评估基于直接方法计算的 MELD-Na 是否能更好地预测临床相关结果。
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来源期刊
Annals of Clinical Biochemistry
Annals of Clinical Biochemistry Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
5.20
自引率
4.50%
发文量
61
期刊介绍: Annals of Clinical Biochemistry is the fully peer reviewed international journal of the Association for Clinical Biochemistry and Laboratory Medicine. Annals of Clinical Biochemistry accepts papers that contribute to knowledge in all fields of laboratory medicine, especially those pertaining to the understanding, diagnosis and treatment of human disease. It publishes papers on clinical biochemistry, clinical audit, metabolic medicine, immunology, genetics, biotechnology, haematology, microbiology, computing and management where they have both biochemical and clinical relevance. Papers describing evaluation or implementation of commercial reagent kits or the performance of new analysers require substantial original information. Unless of exceptional interest and novelty, studies dealing with the redox status in various diseases are not generally considered within the journal''s scope. Studies documenting the association of single nucleotide polymorphisms (SNPs) with particular phenotypes will not normally be considered, given the greater strength of genome wide association studies (GWAS). Research undertaken in non-human animals will not be considered for publication in the Annals. Annals of Clinical Biochemistry is also the official journal of NVKC (de Nederlandse Vereniging voor Klinische Chemie) and JSCC (Japan Society of Clinical Chemistry).
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