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    <link>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/736</link>
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    <pubDate>Tue, 26 May 2026 01:24:13 GMT</pubDate>
    <dc:date>2026-05-26T01:24:13Z</dc:date>
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      <title>Degree of Portal and Systemic Hemodynamic Alterations Predict Recurrent AKI and Chronic Kidney Disease in Patients With Cirrhosis</title>
      <link>http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/737</link>
      <description>Title: Degree of Portal and Systemic Hemodynamic Alterations Predict Recurrent AKI and Chronic Kidney Disease in Patients With Cirrhosis
Authors: Pasupuleti, Samba Siva Rao
Abstract: The relevance of hemodynamic derangements on the incidence of recurrent acute kidney injury (AKI) and chronic&#xD;
kidney disease (CKD) in patients with cirrhosis is largely unknown. Consecutive patients with cirrhosis with a complete&#xD;
record of baseline hemodynamics were followed for identifying risk factors for the development of recurrent&#xD;
AKI and CKD by using negative binomial regression and competing risk analysis, respectively. Consecutive patients&#xD;
with cirrhosis (n = 2013, age 50.1 ± 11.8 years, 80% male, Child A:B:C percentage 13.7:52.9:33.4, and mean Child-&#xD;
Turcotte-Pugh score 8.6 ± 1.8) were enrolled, 893 (44.3%) of whom received beta-blockers, with 44.2% responders.&#xD;
Prior AKI was noted in 12.4% at enrollment. At a median follow-up of 379 (interquartile range: 68-869) days, AKI&#xD;
developed at a rate of 0.37 episodes per person-year, and 26% patients developed CKD. A lower mean number of AKI&#xD;
episodes (0.05 ± 0.25 vs. 0.42 ± 0.868; P &lt; 0.001), CKD (subdistribution hazard ratio 0.74 [0.54-1.02]), and mortality&#xD;
(hazard ratio 0.21 [0.06-0.73]) were observed in beta-blocker responders. Albuminuria was an independent risk factor&#xD;
for recurrent AKI, CKD, and mortality (P &lt; 0.05). Lower systemic vascular resistance index predicted hemodynamic&#xD;
response (odds ratio 2.04 [1.29-3.22]), cumulative AKI episodes (ratio of means 0.10 [0.08-0.14]), and development&#xD;
of CKD (subdistribution hazard ratio 0.70 [0.58-0.83]). Higher hepatic venous pressure gradient (≥17 mm Hg) predicted&#xD;
AKI episodes (ratio of means 1.76 [1.32-2.35]) but not CKD. Conclusion: High portal pressure and severe&#xD;
vasodilatation predispose patients with cirrhosis to repeated AKI episodes and development of CKD. Response to&#xD;
beta-blockers and therapies targeting the vasodilatory state could prevent frequent AKI and the risk of CKD development.&#xD;
Albuminuria could serve as an early marker of renal dysfunction in patients with cirrhosis. (Hepatology&#xD;
Communications 2021;5:293-308).</description>
      <pubDate>Fri, 01 Jan 2021 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/737</guid>
      <dc:date>2021-01-01T00:00:00Z</dc:date>
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