Clinical and Neurologic Outcomes in Acetaminophen-Induced Acute Liver Failure: A 21-Year Multicenter Cohort Study

Acetaminophen (APAP)-induced acute liver failure (ALF) is a rare disease associated with high mortality rates. This study aimed to evaluate changes in interventions, psychosocial profile, and clinical outcomes over a 21-year period using data from the ALF Study Group registry. A retrospective review...

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Veröffentlicht in:Clinical gastroenterology and hepatology 2021-12, Vol.19 (12), p.2615-2625.e3
Hauptverfasser: MacDonald, Andrew J., Speiser, Jaime L., Ganger, Daniel R., Nilles, Kathleen M., Orandi, Babak J., Larson, Anne M., Lee, William M., Karvellas, Constantine J., Liou, Iris, Fix, Oren, Schilsky, Michael, McCashland, Timothy, Eileen Hay, J., Murray, Natalie, Shaikh, A. Obaid S., Blei, Andres, Ganger, Daniel, Zaman, Atif, Han, Steven H.B., Robert Fontana, McGuire, Brendan, Chung, Raymond T., Smith, Alastair, Brown, Robert, Crippin, Jeffrey, Harrison, Edwin, Reuben, Adrian, Munoz, Santiago, Reddy, Rajender, Todd Stravitz, R., Rossaro, Lorenzo, Satyanarayana, Raj, Hassanein, Tarek, Olson, Jodi, Subramanian, Ram, Hanje, James, Hameed, Bilal
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Sprache:eng
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Zusammenfassung:Acetaminophen (APAP)-induced acute liver failure (ALF) is a rare disease associated with high mortality rates. This study aimed to evaluate changes in interventions, psychosocial profile, and clinical outcomes over a 21-year period using data from the ALF Study Group registry. A retrospective review of this prospective, multicenter cohort study of all APAP–ALF patients enrolled during the study period (1998–2018) was completed. Primary outcomes evaluated were the 21-day transplant-free survival (TFS) and neurologic complications. Covariates evaluated included enrollment cohort (early, 1998–2007; recent, 2008–2018), intentionality, psychiatric comorbidity, and use of organ support including continuous renal replacement therapy (CRRT). Of 1190 APAP–ALF patients, recent cohort patients (n = 608) had significantly improved TFS (recent, 69.8% vs early, 61.7%; P = .005). Recent cohort patients were more likely to receive CRRT (22.2% vs 7.6%; P < .001), and less likely to develop intracranial hypertension (29.9% vs 51.5%; P < .001) or die by day 21 from cerebral edema (4.5% vs 11.6%; P < .001). Grouped by TFS status (non-TFS, n = 365 vs TFS, n = 704), there were no differences in psychiatric comorbidity (51.5% vs 55.0%; P = .28) or intentionality (intentional, 39.7% vs 41.6%; P = .58). On multivariable logistic regression adjusting for vasopressor support, development of grade 3/4 hepatic encephalopathy, King’s College criteria, and MELD score, the use of CRRT (odds ratio, 1.62; P = .023) was associated with significantly increased TFS (c-statistic, 0.86). In a second model adjusting for the same covariates, recent enrollment was associated significantly with TFS (odds ratio, 1.42; P = .034; c-statistic, 0.86). TFS in APAP–ALF has improved in recent years and rates of intracranial hypertension/cerebral edema have decreased, possibly related to increased CRRT use.
ISSN:1542-3565
1542-7714
DOI:10.1016/j.cgh.2020.09.016