Research on the combined impact of high-flux dialysis and levocarnitine on the functionality of arteriovenous fistulas in patients undergoing maintenance hemodialysis.
Lei Pang, Shanshan Sun, Ying Shi, Xiaoyan Yu, Na Luo, Shuangyu Li
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引用次数: 0
Abstract
To explore the influence of levocarnitine on arteriovenous fistula (AVF) function in patients undergoing high-flux dialysis and delve into its potential mechanisms. Complication Reduction: The treatment group had markedly lower incidences of vascular stenosis (4.69% vs. 20%), thrombosis (3.13% vs. 15%), poor venous return (6.25% vs. 18.33%), and pre-dialysis hypotension (7.81% vs. 23.33%) (all P < 0.05). Hematological Benefits: Significant improvements in hemoglobin (11.57 ± 1.63 vs. 10.38 ± 1.49g/dL) and red blood cell count (3.89 ± 0.51 vs. 3.53 ± 0.46 ×10¹²/L) were observed in the treatment group (P < 0.001), alongside reduced white blood cell counts (6.05 ± 1.49 vs. 6.23 ± 1.60 ×109/L, P = 0.006). Quality of Life: Karnofsky Performance Scale (KPS) scores were significantly higher in the treatment group at both 1-month (P < 0.01) and 3-month follow-ups (P < 0.01). In the context of high-flux hemodialysis, supplementing with levocarnitine can appreciably improve AVF function in ESRD patients, mitigate the occurrence of complications, and potentially enhance the quality of life by alleviating dialysis-related issues. Levocarnitine emerges as a promising adjunctive therapy for patients with compromised AVF function.
探讨左卡尼汀对高通量透析患者动静脉瘘(AVF)功能的影响,并探讨其可能的机制。并发症减少:治疗组血管狭窄发生率(4.69% vs. 20%)、血栓发生率(3.13% vs. 15%)、静脉回流不良发生率(6.25% vs. 18.33%)、透析前低血压发生率(7.81% vs. 23.33%)均显著降低(均P < 0.05)。血液学益处:治疗组血红蛋白(11.57±1.63 vs. 10.38±1.49g/dL)和红细胞计数(3.89±0.51 vs. 3.53±0.46 ×10¹²/L)显著改善(P < 0.001),白细胞计数降低(6.05±1.49 vs. 6.23±1.60 ×109/L, P = 0.006)。生活质量:治疗组在随访1个月(P < 0.01)和随访3个月(P < 0.01)时Karnofsky Performance Scale (KPS)评分均显著高于对照组。在高通量血液透析的情况下,补充左卡尼汀可以明显改善ESRD患者的AVF功能,减轻并发症的发生,并可能通过减轻透析相关问题来提高生活质量。左卡尼汀是AVF功能受损患者的一种很有前途的辅助治疗方法。
期刊介绍:
Pakistan Journal of Pharmaceutical Sciences (PJPS) is a peer reviewed multi-disciplinary pharmaceutical sciences journal. The PJPS had its origin in 1988 from the Faculty of Pharmacy, University of Karachi as a biannual journal, frequency converted as quarterly in 2005, and now PJPS is being published as bi-monthly from January 2013.
PJPS covers Biological, Pharmaceutical and Medicinal Research (Drug Delivery, Pharmacy Management, Molecular Biology, Biochemical, Pharmacology, Pharmacokinetics, Phytochemical, Bio-analytical, Therapeutics, Biotechnology and research on nano particles.