Analysis of Enoxaparin Effectiveness Based on COVID-19 Severity: A Study in a Secondary Hospital in Bandung, Indonesia

IF 0.7 Q4 PHARMACOLOGY & PHARMACY INDONESIAN JOURNAL OF PHARMACY Pub Date : 2022-07-05 DOI:10.22146/ijp.4133
Budi Suprapti, Liana Debora, Dewi Kusumawati, Arina Dery PS, Gabriella Nathasya T, Mustika Novi Arini, Lusiana Dwi Aryanti
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引用次数: 1

Abstract

Li Coagulopathy is a common predictor of mortality in COVID-19. Meanwhile, enoxaparin is an anticoagulant with anti-inflammatory, endothelial protection, and viral antagonist properties. Therefore, thromboprophylaxis with enoxaparin in COVID-19 is common in clinical settings. This study aims to assess enoxaparin's efficacy across different severity levels by examining its effect on primary outcomes comprising Length of stay (LOS), invasive mechanical ventilation, and mortality as well as secondary in the form of D-dimer, platelets, C-reactive protein (CRP), Neutrophil Lymphocyte Ratio (NLR), and Absolute Lymphocyte Count (ALC). During hospitalization, 269 patients received enoxaparin across varying severity levels comprising mild, moderate, and severe, while the Wilcoxon test was used to analyze the efficacy in each group. Additionally, the differences in patient characteristic profiles across the severity levels were determined using the Kruskal-Wallis test. The increase in mortality rate and the need for mechanical ventilation were directly proportional to the level of severity. D-dimer decreased from 1308.87 ng/ml to 979.83 ng/ml (p=<0,001) as well as from 1758.41 ng/ml to 1510.68 ng/ml (p=<0,001) in the mild and moderate levels respectively. The platelet increased from 225.65 to 369.39 x103/µl (p=<0,001) in mild and 256.77 to 398.97 x103/µl (p=<0,001) in moderate. Moreover, CRP improved in both mild 52.62 to 49.58 mg/l (p=0.031) and moderate 92.99 to 42.66 mg/l, (p=<0,001). Based on the results, enoxaparin effectively improves D-dimer, platelet, and CRP levels in mild and moderate but not in severe conditions, however, no effect was found on LOS, NLR, and ALC.
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基于COVID-19严重程度的依诺肝素疗效分析:印度尼西亚万隆一家二级医院的研究
凝血功能障碍是COVID-19死亡率的常见预测指标。同时,依诺肝素是一种抗凝血剂,具有抗炎、内皮保护和病毒拮抗剂的特性。因此,依诺肝素在COVID-19患者的血栓预防在临床环境中很常见。本研究旨在通过检查依诺肝素对主要结局(包括住院时间(LOS)、有创机械通气和死亡率)以及次要结局(d -二聚体、血小板、c反应蛋白(CRP)、中性粒细胞淋巴细胞比率(NLR)和绝对淋巴细胞计数(ALC))的影响,评估依诺肝素在不同严重程度的疗效。在住院期间,269名患者接受了依诺肝素治疗,其严重程度不同,包括轻度、中度和重度,同时使用Wilcoxon检验分析每组患者的疗效。此外,使用Kruskal-Wallis测试确定不同严重程度患者特征谱的差异。死亡率的增加和机械通气的需要与严重程度成正比。d -二聚体在轻度和中度水平分别从1308.87 ng/ml降至979.83 ng/ml (p=< 0.001)和从1758.41 ng/ml降至1510.68 ng/ml (p=< 0.001)。轻度组血小板从225.65增加到369.39 x103/µl (p=< 0.001),中度组血小板从256.77增加到398.97 x103/µl (p=< 0.001)。此外,CRP在轻度52.62 ~ 49.58 mg/l (p=0.031)和中度92.99 ~ 42.66 mg/l (p=< 0.001)均有改善。结果表明,依诺肝素可有效改善轻度和中度患者的d -二聚体、血小板和CRP水平,但对重度患者无影响,但对LOS、NLR和ALC无影响。
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来源期刊
INDONESIAN JOURNAL OF PHARMACY
INDONESIAN JOURNAL OF PHARMACY PHARMACOLOGY & PHARMACY-
CiteScore
1.20
自引率
0.00%
发文量
38
审稿时长
12 weeks
期刊介绍: The journal had been established in 1972, and online publication was begun in 2008. Since 2012, the journal has been published in English by Faculty of Pharmacy Universitas Gadjah Mada (UGM) Yogyakarta Indonesia in collaboration with IAI (Ikatan Apoteker Indonesia or Indonesian Pharmacist Association) and only receives manuscripts in English. Indonesian Journal of Pharmacy is Accredited by Directorate General of Higher Education. The journal includes various fields of pharmaceuticals sciences such as: -Pharmacology and Toxicology -Pharmacokinetics -Community and Clinical Pharmacy -Pharmaceutical Chemistry -Pharmaceutical Biology -Pharmaceutics -Pharmaceutical Technology -Biopharmaceutics -Pharmaceutical Microbiology and Biotechnology -Alternative medicines.
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