Analysis of factors affecting enoxaparin effectiveness on coagulation, inflammation, and clinical outcomes in patients with COVID-19

IF 1.2 Q4 PHARMACOLOGY & PHARMACY
Budi Suprapti, Liana Debora, Rifdah Atikah Safitri, Dewi Kusumawati, Arina Dery Puspitasari
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引用次数: 0

Abstract

Context: Hypercoagulopathy is a COVID-19 extra-pulmonary manifestation has drawn the attention of the scientists due to its risk of thromboembolism. Enoxaparin is an anticoagulant used to prevent hypercoagulopathy. Many factors have been associated with enoxaparin effectiveness. Aims: To analyze factors affecting enoxaparin effectiveness on coagulation, inflammation, and clinical outcomes. Methods: This retrospective cohort study involved hospitalized adult patients with COVID-19 from November 2020 to April 2021. Patients’ age, gender, body mass index (BMI), comorbidity, and laboratory results were extracted from medical records. Factors influencing enoxaparin efficacy on coagulation, inflammation, and clinical outcomes were analyzed using path analysis with SmartPLS 3.0 software. D-dimer and platelet values was determined as coagulation outcomes and C-reactive protein (CRP) value as an inflammation outcome. Clinical outcomes comprised of mortality, ventilator usage, and length of stay. Results: A total of 269 patients fulfilled the inclusion criteria. Most of the subjects were male (58%), 66% had comorbidities, 48.3% were aged ≥60 years old, and 65.8% had a BMI ≥ 25 kg/m2. Path analysis showed that age, BMI, and comorbidity affected disease severity (p<0.05). Disease severity strongly influenced enoxaparin dosage (p=0.000). Dosage affected platelet value, ventilator usage, and mortality (p<0.05). Gender did not influence disease severity, and dosage displayed no significant effect on length of stay, CRP, and D-dimer (p>0.05). Conclusions: Dosage is the main factor influencing enoxaparin efficacy on coagulation, inflammation, and clinical outcomes. The dosage is strongly affected by disease severity, in which is predominantly influenced by age, BMI, and comorbidity.
影响依诺肝素对COVID-19患者凝血、炎症及临床结局疗效的因素分析
背景:高凝血病是新冠肺炎的肺外表现,由于其血栓栓塞的风险引起了科学家的注意。依诺肝素是一种用于预防高凝病的抗凝剂。许多因素与依诺肝素的有效性有关。目的:分析影响依诺肝素治疗凝血、炎症及临床预后的因素。方法:本回顾性队列研究纳入2020年11月至2021年4月住院的成年COVID-19患者。从医疗记录中提取患者的年龄、性别、体重指数(BMI)、合并症和实验室结果。采用SmartPLS 3.0软件进行通径分析,分析影响依诺肝素凝血、炎症及临床结局的因素。d -二聚体和血小板值作为凝血结果,c反应蛋白(CRP)值作为炎症结果。临床结果包括死亡率、呼吸机使用和住院时间。结果:269例患者符合纳入标准。大多数受试者为男性(58%),66%有合并症,48.3%年龄≥60岁,65.8% BMI≥25 kg/m2。通径分析显示,年龄、BMI和合并症影响疾病严重程度(p < 0.05)。疾病严重程度强烈影响依诺肝素剂量(p=0.000)。剂量影响血小板值、呼吸机使用和死亡率(p < 0.05)。性别对疾病严重程度无影响,剂量对住院时间、CRP和d -二聚体无显著影响(p < 0.05)。结论:剂量是影响依诺肝素凝血、消炎及临床疗效的主要因素。剂量受疾病严重程度的强烈影响,其中主要受年龄、BMI和合并症的影响。
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来源期刊
CiteScore
3.00
自引率
20.00%
发文量
0
审稿时长
8 weeks
期刊介绍: The Journal of Pharmacy & Pharmacognosy Research (JPPRes) is an international, specialized and peer-reviewed open access journal, under the auspices of AVAGAX – Diseño, Publicidad y Servicios Informáticos, which publishes studies in the pharmaceutical and herbal fields concerned with the physical, botanical, chemical, biological, toxicological properties and clinical applications of molecular entities, active pharmaceutical ingredients, devices and delivery systems for drugs, vaccines and biologicals, including their design, manufacture, evaluation and marketing. This journal publishes research papers, reviews, commentaries and letters to the editor as well as special issues and review of pre-and post-graduate thesis from pharmacists or professionals involved in Pharmaceutical Sciences or Pharmacognosy.
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