Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 Feb 11;5(5):100698.
doi: 10.1016/j.jhepr.2023.100698. eCollection 2023 May.

Low haemoglobin level predicts early hospital readmission in patients with cirrhosis and acute decompensation

Affiliations

Low haemoglobin level predicts early hospital readmission in patients with cirrhosis and acute decompensation

Enrico Pompili et al. JHEP Rep. .

Abstract

Background & aims: Patients with decompensated cirrhosis present frequent hospitalisations with a relevant clinical and socio-economic impact. This study aims to characterise unscheduled readmissions up to 1-year follow-up and identify predictors of 30-day readmission after an index hospitalisation for acute decompensation (AD).

Methods: We performed a secondary analysis of a prospectively collected cohort of patients admitted for AD. Laboratory and clinical data at admission and at discharge were collected. Timing and causes of unscheduled readmissions and mortality were recorded up to 1 year.

Results: A total of 329 patients with AD were included in the analysis. Acute-on-chronic liver failure was diagnosed in 19% of patients at admission or developed in an additional 9% of patients during the index hospitalisation. During the 1-year follow-up, 182 patients (55%) were rehospitalised and 98 (30%) more than once. The most frequent causes of readmission were hepatic encephalopathy (36%), ascites (22%), and infection (21%). Cumulative incidence of readmission was 20% at 30 days, 39% at 90 days, and 63% at 1 year. Fifty-four patients were readmitted for emergent liver-related causes within 30 days. Early readmission was associated with a higher 1-year mortality (47 vs. 32%, p = 0.037). Multivariable Cox regression analysis showed that haemoglobin (Hb) ≤8.7 g/dl (hazard ratio 2.63 [95% CI 1.38-5.02], p = 0.003) and model for end-stage liver disease-sodium score (MELD-Na) >16 at discharge (hazard ratio 2.23 [95% CI 1.27-3.93], p = 0.005), were independent predictors of early readmission. In patients with MELD-Na >16 at discharge, the presence of Hb ≤8.7 g/dl doubles the risk of early rehospitalisation (44% vs. 22%, p = 0.02).

Conclusion: Besides MELD-Na, a low Hb level (Hb ≤8.7 g/dl) at discharge emerged as a new risk factor for early readmission, contributing to identification of patients who require closer surveillance after discharge.

Impact and implications: Patients with decompensated cirrhosis face frequent hospitalisations. In the present study, type and causes of readmissions were analysed during 1-year follow-up in patients discharged after the index hospitalisation for an acute decompensation of the disease. Early (30-day) liver-related readmission was associated with higher 1-year mortality. The model for end-stage liver disease-sodium score and low haemoglobin at discharge were identified as independent risk factors for early readmissions. Haemoglobin emerged as a new easy-to-use parameter associated with early readmission warranting further investigation.

Keywords: Anaemia; Early readmission; Haemoglobin; Hospitalisation; Liver cirrhosis; MELD score; Systemic inflammation.

PubMed Disclaimer

Conflict of interest statement

All authors declare no conflicts of interest that are relevant to the content of this article. Please refer to the accompanying ICMJE disclosure forms for further details.

Figures

None
Graphical abstract
Fig. 1
Fig. 1
Flow chart of the study.
Fig. 2
Fig. 2
Number of readmissions and cumulative incidence of readmissions during the follow-up period. (A) Number of patients with one, two, three, or four or more readmissions during the follow-up period. (B) Kaplan-Meier estimate of the cumulative incidence of all cause readmissions during follow-up (purple line, death and transplant considered as censoring events) and cumulative incidence of all cause readmission or death (green line, transplant considered as censoring event).
Fig. 3
Fig. 3
Cumulative incidence of liver-related early readmissions and cumulative incidence of death during the follow-up period. (A) Thirty-day cumulative incidence of liver-related early readmissions. (B) Cumulative incidence function of mortality considering liver transplantation as a competing event in patients readmitted within 30 days (early readmission) for liver-related causes as compared with those not early readmitted. The cumulative incidence was compared using Gray's test.
Fig. 4
Fig. 4
Cumulative incidence of liver-related early readmissions according to the presence of the risk factors identified in the analyses. (A) Thirty-day cumulative incidence of liver-related early readmissions in patients presenting none, one, or two of the following independent risk factors: Hb ≤8.7 g/dl and MELD-Na >16 at discharge of the index hospitalisation. (B) Thirty-day cumulative incidence of liver-related early readmissions in patients with MELD-Na >16 presenting a Hb level of at least or lower than 8.7 g/dl at discharge. Comparisons were made using the log-rank test. Hb, haemoglobin; MELD-Na, model for end-stage liver disease-sodium.

Similar articles

Cited by

References

    1. Sepanlou S.G., Safiri S., Bisignano C., Ikuta K.S., Merat S., Saberifiroozi M., et al. The global, regional, and national burden of cirrhosis by cause in 195 countries and territories, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet Gastroenterol Hepatol. 2020;5:245–266. - PMC - PubMed
    1. Berman K., Tandra S., Forssell K., Vuppalanchi R., Vuppalanch R., Burton J.R., et al. Incidence and predictors of 30-day readmission among patients hospitalized for advanced liver disease. Clin Gastroenterol Hepatol Off Clin Pract J Am Gastroenterol Assoc. 2011;9:254–259. - PMC - PubMed
    1. Volk M.L., Tocco R.S., Bazick J., Rakoski M.O., Lok A.S. Hospital readmissions among patients with decompensated cirrhosis. Am J Gastroenterol. 2012;107:247–252. - PMC - PubMed
    1. Bajaj J.S., Reddy K.R., Tandon P., Wong F., Kamath P.S., Garcia-Tsao G., et al. The 3-month readmission rate remains unacceptably high in a large North American cohort of patients with cirrhosis. Hepatology. 2016;64:200–208. - PMC - PubMed
    1. Mumtaz K., Issak A., Porter K., Kelly S., Hanje J., Michaels A.J., et al. Validation of risk score in predicting early readmissions in decompensated cirrhotic patients: a model based on the administrative database. Hepatology. 2019;70:630–639. - PubMed

LinkOut - more resources