Mak Lung-Yi, Chung Matthew Shing Hin, Li Xue, Lai Francisco Tsz Tsun, Wan Eric Yuk Fai, Chui Celine Sze Ling, Cheng Franco Wing Tak, Chan Esther Wai Yin, Cheung Ching Lung, Au Ivan Chi Ho, Xiong Xi, Seto Wai-Kay, Yuen Man-Fung, Wong Carlos King Ho, Wong Ian Chi Kei
Department of Medicine, The University of Hong Kong, Hong Kong, China.
State Key Laboratory of Liver Research, The University of Hong Kong, Hong Kong, China.
World J Hepatol. 2024 Feb 27;16(2):211-228. doi: 10.4254/wjh.v16.i2.211.
Chronic liver disease (CLD) was associated with adverse clinical outcomes among people with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection.
To determine the effects of SARS-CoV-2 infection on the incidence and treatment strategy of hepatocellular carcinoma (HCC) among patients with CLD.
A retrospective, territory-wide cohort of CLD patients was identified from an electronic health database in Hong Kong. Patients with confirmed SARS-CoV-2 infection [coronavirus disease 2019 (COVID-19)+CLD] between January 1, 2020 and October 25, 2022 were identified and matched 1:1 by propensity-score with those without (COVID-19-CLD). Each patient was followed up until death, outcome event, or November 15, 2022. Primary outcome was incidence of HCC. Secondary outcomes included all-cause mortality, adverse hepatic outcomes, and different treatment strategies to HCC (curative, non-curative treatment, and palliative care). Analyses were further stratified by acute (within 20 d) and post-acute (21 d or beyond) phases of SARS-CoV-2 infection. Incidence rate ratios (IRRs) were estimated by Poisson regression models.
Of 193589 CLD patients (> 95% non-cirrhotic) in the cohort, 55163 patients with COVID-19+CLD and 55163 patients with COVID-19-CLD were included after 1:1 propensity-score matching. Upon 249-d median follow-up, COVID-19+CLD was not associated with increased risk of incident HCC (IRR: 1.19, 95%CI: 0.99-1.42, = 0.06), but higher risks of receiving palliative care for HCC (IRR: 1.60, 95%CI: 1.46-1.75, < 0.001), compared to COVID-19-CLD. In both acute and post-acute phases of infection, COVID-19+CLD were associated with increased risks of all-cause mortality (acute: IRR: 7.06, 95%CI: 5.78-8.63, < 0.001; post-acute: IRR: 1.24, 95%CI: 1.14-1.36, < 0.001) and adverse hepatic outcomes (acute: IRR: 1.98, 95%CI: 1.79-2.18, < 0.001; post-acute: IRR: 1.24, 95%CI: 1.13-1.35, < 0.001), compared to COVID-19-CLD.
Although CLD patients with SARS-CoV-2 infection were not associated with increased risk of HCC, they were more likely to receive palliative treatment than those without. The detrimental effects of SARS-CoV-2 infection persisted in post-acute phase.
慢性肝病(CLD)与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染患者的不良临床结局相关。
确定SARS-CoV-2感染对CLD患者肝细胞癌(HCC)发病率和治疗策略的影响。
从香港的一个电子健康数据库中确定了一项回顾性、全地区范围的CLD患者队列。识别出2020年1月1日至2022年10月25日期间确诊SARS-CoV-2感染的患者[2019冠状病毒病(COVID-19)+CLD],并通过倾向评分与未感染患者(COVID-19-CLD)进行1:1匹配。对每位患者进行随访,直至死亡、出现结局事件或2022年11月15日。主要结局是HCC的发病率。次要结局包括全因死亡率、不良肝脏结局以及针对HCC的不同治疗策略(根治性、非根治性治疗和姑息治疗)。分析进一步按SARS-CoV-2感染的急性期(20天内)和急性后期(21天及以后)进行分层。发病率比(IRR)通过泊松回归模型估计。
在该队列的193589例CLD患者(>95%为非肝硬化患者)中,经过1:1倾向评分匹配后,纳入了55163例COVID-19+CLD患者和55163例COVID-19-CLD患者。在249天的中位随访期内,与COVID-19-CLD相比,COVID-19+CLD与HCC发病风险增加无关(IRR:1.19,95%CI:0.99-1.42,P=0.06),但接受HCC姑息治疗的风险更高(IRR:1.60,95%CI:1.46-1.75,P<0.001)。在感染的急性期和急性后期,与COVID-19-CLD相比,COVID-19+CLD全因死亡率(急性期:IRR:7.06,95%CI:5.78-8.63,P<0.001;急性后期:IRR:1.24,95%CI:1.14-1.36,P<0.001)和不良肝脏结局(急性期:IRR:1.98,95%CI:1.79-2.18,P<0.001;急性后期:IRR:1.24,95%CI:1.13-1.35,P<0.001)的风险均增加。
虽然感染SARS-CoV-2的CLD患者HCC发病风险未增加,但与未感染患者相比,他们更有可能接受姑息治疗。SARS-CoV-2感染的有害影响在急性后期持续存在。