de Jesus Rosangela Passos, de Carvalho Jozélio Freire, de Oliveira Lucivalda Pereira Magalhães, Cunha Carla de Magalhães, Alves Thaisy Cristina Honorato Santos, Vieira Sandra Tavares Brito, Figueiredo Virginia Maria, Bueno Allain Amador
Postgraduate Program in Food, Nutrition and Health at the School of Nutrition of the Federal University of Bahia, Salvador 40.110-150, Bahia, Brazil.
Institute of Health Sciences, Federal University of Bahia, Salvador 40231-300, Bahia, Brazil.
World J Hepatol. 2022 Jan 27;14(1):80-97. doi: 10.4254/wjh.v14.i1.80.
Obesity, diabetes, cardiovascular and respiratory diseases, cancer and smoking are risk factors for negative outcomes in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which can quickly induce severe respiratory failure in 5% of cases. Coronavirus disease-associated liver injury may occur during progression of SARS-CoV-2 in patients with or without pre-existing liver disease, and damage to the liver parenchyma can be caused by infection of hepatocytes. Cirrhosis patients may be particularly vulnerable to SARS-CoV-2 if suffering with cirrhosis-associated immune dysfunction. Furthermore, pharmacotherapies including macrolide or quinolone antibiotics and steroids can also induce liver damage. In this review we addressed nutritional status and nutritional interventions in severe SARS-CoV-2 liver patients. As guidelines for SARS-CoV-2 in intensive care (IC) specifically are not yet available, strategies for management of sepsis and SARS are suggested in SARS-CoV-2. Early enteral nutrition (EN) should be started soon after IC admission, preferably employing iso-osmolar polymeric formula with initial protein content at 0.8 g/kg per day progressively increasing up to 1.3 g/kg per day and enriched with fish oil at 0.1 g/kg per day to 0.2 g/kg per day. Monitoring is necessary to identify signs of intolerance, hemodynamic instability and metabolic disorders, and transition to parenteral nutrition should not be delayed when energy and protein targets cannot be met EN. Nutrients including vitamins A, C, D, E, B6, B12, folic acid, zinc, selenium and ω-3 fatty acids have in isolation or in combination shown beneficial effects upon immune function and inflammation modulation. Cautious and monitored supplementation up to upper limits may be beneficial in management strategies for SARS-CoV-2 liver patients.
肥胖、糖尿病、心血管和呼吸系统疾病、癌症以及吸烟都是严重急性呼吸综合征冠状病毒2(SARS-CoV-2)导致不良后果的风险因素,SARS-CoV-2可在5%的病例中迅速引发严重呼吸衰竭。冠状病毒病相关肝损伤可能在SARS-CoV-2感染过程中发生,无论患者有无基础肝病,肝细胞感染都可能导致肝实质损伤。肝硬化患者若伴有肝硬化相关免疫功能障碍,可能对SARS-CoV-2尤为易感。此外,包括大环内酯类或喹诺酮类抗生素以及类固醇在内的药物治疗也可导致肝损伤。在本综述中,我们探讨了重症SARS-CoV-2感染肝病患者的营养状况及营养干预措施。由于尚无专门针对重症监护(IC)中SARS-CoV-2的指南,故建议采用治疗脓毒症和SARS的策略来管理SARS-CoV-2感染患者。应在入住IC后尽早开始早期肠内营养(EN),最好采用等渗聚合物配方,初始蛋白质含量为每天0.8 g/kg,逐渐增加至每天1.3 g/kg,并添加每天0.1 g/kg至0.2 g/kg的鱼油。有必要进行监测以识别不耐受、血流动力学不稳定和代谢紊乱的迹象,当无法达到能量和蛋白质目标时,不应延迟过渡到肠外营养。包括维生素A、C、D、E、B6、B12、叶酸、锌、硒和ω-3脂肪酸在内的营养素单独或联合使用已显示出对免疫功能和炎症调节有益。谨慎并在监测下补充至上限可能对SARS-CoV-2感染肝病患者的管理策略有益。