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izvor podataka: crosbi

Infection as a predictor of mortality in decompensated liver cirrhosis: exploring the relationship to severity of liver failure (CROSBI ID 301509)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Grgurević, Ivica ; Trkulja, Vladimir ; Božin, Tonči ; Madir, Anita ; Miletić, Maja ; Marušić, Srećko ; Škrlin, Jasenka ; Šestan Crnek, Sandra ; Dobrović, Karolina Infection as a predictor of mortality in decompensated liver cirrhosis: exploring the relationship to severity of liver failure // European journal of gastroenterology & hepatology, 32 (2020), 11; 1458-1465. doi: 10.1097/MEG.0000000000001667

Podaci o odgovornosti

Grgurević, Ivica ; Trkulja, Vladimir ; Božin, Tonči ; Madir, Anita ; Miletić, Maja ; Marušić, Srećko ; Škrlin, Jasenka ; Šestan Crnek, Sandra ; Dobrović, Karolina

engleski

Infection as a predictor of mortality in decompensated liver cirrhosis: exploring the relationship to severity of liver failure

Background Infections are common in patients with liver cirrhosis and increase mortality. We explored the relationship between infection and liver dysfunction in their effects on mortality. Methods Single-center data on decompensated liver cirrhosis patients hospitalized between March 2014 and December 2017 (index period) were reviewed until death, liver transplantation or 31 December 2018. Infections were classified as community- acquired infection (CAi) or hospital/healthcare associated infection (HCAi). Child-Pugh, model for the end-stage liver disease (MELD) and chronic liver failure-organ failure (CLiF-OF) scores indicated liver (dys)function. Results We enrolled 155 patients (85% alcoholic liver disease), 65 without infection at first hospitalization, 48 with CAi and 42 with HCAi. Multidrug resistant agents were confirmed in 2/48 (4.2%) CAi and 10/42 (23.8%) HCAi patients. At first hospitalization, infection was independently associated with worse liver dysfunction and vice versa, and with higher 30-day mortality [odds ratio (OR) = 2.73, 95% confidence interval (CI) 1.07–6.94]. The association was reduced with adjustment for MELD/CLiF-OF scores, but mediation analysis detected an indirect (via liver dysfunction) association. Twenty-eight patients were repeatedly hospitalized, 11 with new HCAi. HCAi was independently associated with twice higher risk of medium-term mortality and added an additional risk to any level of liver dysfunction, considering all or patients who survived the first 30 days. In those repeatedly hospitalized, HCAi appeared independently associated with a higher probability of infection and higher MELD scores at subsequent hospitalizations. Conclusion Infection (particularly HCAi) adds mortality risk to any level of liver dysfunction in decompensated liver cirrhosis patients. Mechanisms of long(er)-term effects (in acute episode survivors) seemingly include enhanced deterioration of liver function.

infection ; liver cirrhosis ; liver function ; mortality

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Podaci o izdanju

32 (11)

2020.

1458-1465

objavljeno

0954-691X

1473-5687

10.1097/MEG.0000000000001667

Povezanost rada

Kliničke medicinske znanosti

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