首页> 外文期刊>Hepatology: Official Journal of the American Association for the Study of Liver Diseases >Incidence, Risk Factors, and Outcomes of Transition of Acute Kidney Injury to Chronic Kidney Disease in Cirrhosis: A Prospective Cohort Study
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Incidence, Risk Factors, and Outcomes of Transition of Acute Kidney Injury to Chronic Kidney Disease in Cirrhosis: A Prospective Cohort Study

机译:肝硬化急性肾脏损伤转型对慢性肾病的发病率,危险因素和结果:一项预期队列研究

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Transition to chronic kidney disease (CKD) after an episode of acute kidney injury (AKI) is known in patients without cirrhosis. We studied the incidence and risk factors for development of CKD in patients with cirrhosis. Competing risk analysis was performed to identify risk factors for CKD development. Of 818 patients with cirrhosis (age, 50.4?±?11.8?years; 84% males; Model for End‐Stage Liver Disease [MELD], 19.9?±?9.9), 36% had AKI at enrollment, 27% had previous AKI, and 61% developed new episodes of AKI during the follow‐up period. CKD developed in 269 (33%) patients. Serum cystatin C (CysC; subdistribution hazard ratio [SHR], 1.58; 1.07‐2.33), episodes of previous AKI (SHR, 1.26; 1.02‐1.56), and AKI stage at enrollment (no AKI [SHR, 1] vs. stage 1 [SHR, 3.28; 1.30‐8.25] vs. stage 2 [SHR, 4.33; 1.76‐10.66] vs. stage 3 [SHR, 4.5; 1.59‐12.73]) were identified as baseline risk factors for CKD development. On time‐varying competing risk analysis, MELD (SHR, 1.01; 1.00‐1.03), number of AKI episodes (SHR, 1.25; 1.15‐1.37), and CysC (SHR, 1.38; 1.01‐1.89) predicted CKD development. Development of CKD was associated with higher risk of death. Reduction in glomerular filtration rate (GFR) not meeting CKD criteria was observed in 66% of patients with cirrhosis, more so in those with previous AKI episodes and a high CysC level and MELD score. Renal histology, available in 55 patients, showed tubulointerstitial injury in 86%, cholemic nephrosis in 29%, and glomerular changes in 38%. Conclusion: Almost two‐thirds of patients with cirrhosis develop episodes of AKI and reduction in GFR; one‐third progress to CKD, resulting in adverse outcomes. Higher MELD and CysC levels and number of AKI episodes predict development of CKD in patients with cirrhosis.
机译:在没有肝硬化的患者中已知在急性肾脏损伤(AKI)发作后向慢性肾病(CKD)过渡。我们研究了肝硬化患者CKD发育的发病率和危险因素。进行竞争风险分析以确定CKD发展的危险因素。 818例肝硬化患者(年龄,50.4°?±11.8岁; 84%的男性;终末期肝病模型[MELD],19.9?±9.9),36%的AKI在注册时,27%以前的AKI ,61%在随访期间开发了新的AKI发作。 CKD在269名(33%)患者中开发。血清胱抑素C(Cysc;分区危险比[SHR],1.58; 1.07-2.33),先前AKI的发作(SHR,1.26; 1.02-1.56)和入学期间的AKI阶段(没有AKI [SHR,1]与舞台1 [SHR,3.28; 1.30-8.25]与阶段2 [SHR,4.33; 1.76-10.66]与阶段3 [SHR,4.5; 1.59-12.73]被确定为CKD开发的基线风险因素。在时变竞争风险分析中,融合(SHR,1.01; 1.00-1.03),AKI剧集数(SHR,1.25; 1.15-1.37)和CYSC(SHR,1.38; 1.01-1.89)预测CKD开发。 CKD的发展与更高的死亡风险有关。在66%的肝硬化患者中观察到不符合CKD标准的肾小球过滤速率(GFR),其中患有先前的AKI发作和高CYSC水平和融合得分。肾组织学,可在55名患者中提供,表现出浓度的血管间损伤86%,血腥肾病29%,肾小球变化为38%。结论:近三分之二的肝硬化患者患有AKI的发作和GFR减少; CKD的三分之一进展,导致不利的结果。较高的融合和CYSC水平和AKI剧集的数量预测肝硬化患者CKD的发展。

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