Patidar Kavish R, Ma Ann T, Juanola Adrià, Barone Anna, Incicco Simone, Kulkarni Anand V, Hernández José Luis Pérez, Wentworth Brian, Asrani Sumeet K, Alessandria Carlo, Abdelkader Nadia Abdelaaty, Wong Yu Jun, Xie Qing, Pyrsopoulos Nikolaos T, Kim Sung-Eun, Fouad Yasser, Torre Aldo, Cerda Eira, Ferrer Javier Diaz, Maiwall Rakhi, Simonetto Douglas A, Papp Maria, Orman Eric S, Perricone Giovanni, Solé Cristina, Lange Christian M, Farias Alberto Queiroz, Pereira Gustavo, Gadano Adrian, Caraceni Paolo, Thevenot Thierry, Verma Nipun, Kim Jeong Han, Vorobioff Julio D, Cordova-Gallardo Jacqueline, Ivashkin Vladimir, Roblero Juan Pablo, Maan Raoel, Toledo Claudio, Gioia Stefania, Fassio Eduardo, Marino Monica, Nabilou Puria, Vargas Victor, Merli Manuela, Goncalves Luciana Lofego, Rabinowich Liane, Krag Aleksander, Balcar Lorenz, Montes Pedro, Mattos Angelo Z, Bruns Tony, Mohammed Abdulsemed, Laleman Wim, Carrera Enrique, Cabrera María Cecilia, Girala Marcos, Samant Hrishikesh, Raevens Sarah, Madaleno Joao, Kim Ray W, Arab Juan Pablo, Presa José, Ferreira Carlos Noronha, Galante Antonio, Allegretti Andrew S, Takkenberg Bart, Marciano Sebastian, Sarin Shiv K, Durand François, Ginès Pere, Angeli Paolo, Solà Elsa, Piano Salvatore
Section of Gastroenterology and Hepatology, Department of Medicine, Baylor College of Medicine, Houston, TX, USA; Michael E DeBakey Veterans Affairs Medical Center, Houston, TX, USA.
Toronto Centre for Liver Disease, University Health Network, Toronto, ON, Canada.
Lancet Gastroenterol Hepatol. 2025 May;10(5):418-430. doi: 10.1016/S2468-1253(25)00006-8. Epub 2025 Mar 6.
Acute kidney injury (AKI) is a serious complication of cirrhosis. A systematic, global characterisation of AKI occurring in patients with cirrhosis is lacking. We therefore aimed to assess global differences in the characteristics, management, and outcomes of AKI in hospitalised patients with cirrhosis.
In this prospective, multicentre, cohort study, we enrolled adults (≥18 years) with decompensated cirrhosis who were hospitalised for a cirrhosis-related complication, with or without AKI, at 65 centres across five continents. We captured AKI prevalence, stage, phenotype, and details on AKI management and clinical course. Universal health coverage index and gross national income per capita were also collected. The primary outcome was 28-day mortality. Multivariable models including demographic and clinical variables, cirrhosis cause, cirrhosis severity, AKI severity, AKI management variables, universal health coverage, and gross national income were used to analyse independent associations with 28-day mortality. Secondary outcomes were AKI classification, progression, and resolution. This study is complete and registered with ClinicalTrials.gov (NCT05387811).
Between July 1, 2022, and May 31, 2023, we enrolled 3821 patients who were hospitalised for decompensated cirrhosis. Mean age was 57·7 years (SD 13·1), 2467 (64·6%) were men, and 1354 (35·4%) were women. Most patients were White (2128 [55·7%]). 1456 (38·1%, 95% CI 36·6-39·6) of 3821 patients had AKI (943 [64·8%] men and 513 [35·2%] women). Globally, patients presented with similar AKI stages, but patients from North America and Asia had the highest MELD-Na scores at presentation and the highest rates of peak AKI stage 3. Overall, hypovolaemic AKI was the most common phenotype (858 [58·9%] of 1456), followed by HRS-AKI (253 [17·4%]) and acute tubular necrosis (216 [14·8%]). The prevalences of hypovolaemic AKI and HRS-AKI were similar across regions, but acute tubular necrosis was more frequent in Asia (p<0·0001 across regions). Additionally, regional differences in the management of AKI (use of albumin, vasopressors, and diuretics) were found. 335 (28·6%) of 1171 patients with initial AKI stages 1 or 2 had progression to higher stages during hospitalisation. AKI resolved in 862 (59·2%) cases during hospitalisation. 333 (22·9%) patients with AKI had died by 28 days. Multivariable analyses showed that increased age, female sex, presence of ascites, presence of hepatic encephalopathy, increased white blood cell count, increased MELD-Na, hospital-acquired AKI, a lower universal health coverage index (<80), and not being in a high-income country were independently associated with an increased risk of 28-day mortality. Increased serum albumin was associated with a decreased risk of 28-day mortality.
This study found important regional differences in AKI severity, phenotype, management, and outcomes in patients with decompensated cirrhosis. Health-care coverage remains an important driver of survival in patients with cirrhosis and AKI.
European Association Study for the Study of the Liver and the Italian Society of Internal Medicine.
急性肾损伤(AKI)是肝硬化的一种严重并发症。目前缺乏对肝硬化患者发生的AKI进行系统的、全面的特征描述。因此,我们旨在评估肝硬化住院患者AKI在特征、管理和结局方面的全球差异。
在这项前瞻性、多中心队列研究中,我们纳入了年龄≥18岁、因肝硬化相关并发症住院的失代偿期肝硬化成人患者,这些患者来自五大洲的65个中心,伴有或不伴有AKI。我们记录了AKI的患病率、分期、表型以及AKI管理和临床过程的详细信息。还收集了全民健康覆盖指数和人均国民总收入。主要结局是28天死亡率。使用包括人口统计学和临床变量、肝硬化病因、肝硬化严重程度、AKI严重程度、AKI管理变量、全民健康覆盖和国民总收入的多变量模型来分析与28天死亡率的独立关联。次要结局是AKI分类、进展和缓解。本研究已完成,并在ClinicalTrials.gov(NCT05387811)注册。
在2022年7月1日至2023年5月31日期间,我们纳入了3821例因失代偿期肝硬化住院的患者。平均年龄为57.7岁(标准差13.1),男性2467例(64.6%),女性1354例(35.4%)。大多数患者为白人(2128例[55.7%])。3821例患者中有1456例(38.1%,95%CI 36.6 - 39.6)发生AKI(男性943例[64.8%],女性513例[35.2%])。在全球范围内,患者的AKI分期相似,但北美和亚洲的患者在就诊时MELD-Na评分最高,AKI 3期峰值发生率也最高。总体而言,低血容量性AKI是最常见的表型(1456例中的858例[58.9%]),其次是肝肾综合征相关性AKI(253例[17.4%])和急性肾小管坏死(216例[14.8%])。各地区低血容量性AKI和肝肾综合征相关性AKI的患病率相似,但急性肾小管坏死在亚洲更为常见(各地区p<0.0001)。此外,还发现了AKI管理(白蛋白、血管加压药和利尿剂的使用)的地区差异。1171例初始AKI 1期或2期患者中有335例(28.6%)在住院期间进展为更高分期。住院期间862例(59.2%)患者的AKI得到缓解。333例(22.9%)AKI患者在28天内死亡。多变量分析显示,年龄增加、女性、存在腹水、存在肝性脑病、白细胞计数增加、MELD-Na升高、医院获得性AKI、全民健康覆盖指数较低(<80)以及不在高收入国家与28天死亡率风险增加独立相关。血清白蛋白升高与28天死亡率风险降低相关。
本研究发现失代偿期肝硬化患者的AKI在严重程度、表型、管理和结局方面存在重要的地区差异。医疗保健覆盖仍然是肝硬化和AKI患者生存的重要驱动因素。
欧洲肝脏研究协会和意大利内科医学会。