Evidence map›Paper›PMID 40971056›Full record

Observational studyMetabolic brain disease2025

Prospective observational study on systemic inflammation and prognostic significance of hepatic encephalopathy.

Venkatesh Vaithiyam, Sarang Mahanaik, Barjesh Chander Sharma, Sanjeev Sachdeva, Siddharth Srivastava, Ajay Kumar, Ashok Dalal, Ujjwal Sonika, Bhawna Mahajan

Abstract readObservational Study
PubMed Publisher
In one paragraph

Observational study in Metabolic brain disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Venkatesh VaithiyamDepartment of Gastroenterology, GB Pant Institute of Postgraduate Medical Education and Research (GIPMER), New Delhi, 110002, India.ORCID 0000-0002-0713-5501
Sarang MahanaikDepartment of Gastroenterology, GB Pant Institute of Postgraduate Medical Education and Research (GIPMER), New Delhi, 110002, India.
Barjesh Chander SharmaDepartment of Gastroenterology, GB Pant Institute of Postgraduate Medical Education and Research (GIPMER), New Delhi, 110002, India. dr.bcsharma@delhi.gov.in.ORCID 0000-0002-5878-2661
Sanjeev SachdevaDepartment of Gastroenterology, GB Pant Institute of Postgraduate Medical Education and Research (GIPMER), New Delhi, 110002, India.ORCID 0000-0002-5588-1111
Siddharth SrivastavaDepartment of Gastroenterology, GB Pant Institute of Postgraduate Medical Education and Research (GIPMER), New Delhi, 110002, India.ORCID 0000-0001-7550-0358
Ajay KumarDepartment of Gastroenterology, GB Pant Institute of Postgraduate Medical Education and Research (GIPMER), New Delhi, 110002, India.
Ashok DalalDepartment of Gastroenterology, GB Pant Institute of Postgraduate Medical Education and Research (GIPMER), New Delhi, 110002, India.ORCID 0000-0001-7590-2226
Ujjwal SonikaDepartment of Gastroenterology, GB Pant Institute of Postgraduate Medical Education and Research (GIPMER), New Delhi, 110002, India.ORCID 0000-0003-0949-2382
Bhawna MahajanDepartment of Biochemistry, GB Pant Institute of Postgraduate Medical Education and Research (GIPMER), New Delhi, 110002, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatic encephalopathy (HE) is a common decompensating event in liver cirrhosis, with a prevalence of 10-14% in newly diagnosed cirrhotic and 30-40% during the course of the disease. The study aimed to evaluate the clinical spectrum, systemic inflammation, treatment outcomes, prognostic significance, and survival probability of HE in patients with liver cirrhosis. Over five years, consecutive patients hospitalized with HE were evaluated for symptoms, signs, etiology, inflammatory markers, prognostic index, and response to treatment. Primary outcomes included reversal of HE up to 10 days of admission and mortality at 28 days. Secondary outcomes included length of hospital stay, time taken for resolution of HE, adverse events, and recurrence of HE over 28 days. 539 patients were included. The median (range) age was 46 (18-82) years, with 84.4% males. Hyponatremia (65.4%) was the most common precipitating factor. Complete reversal of HE occurred in 62.8%. Median (range) Mean hospital stay was 7(27) days, and 28-day mortality during the study period was 26.1%. The survival probability was higher in grade 2 HE than in grade 3 and grade 4 (79.79 vs. 74.31 vs. 60.22%, p = 0.0020). Patients with resolution of HE had better survival {HR 0.271 [95% C. I (0.187-0.394)], p < 0.005}. Arterial ammonia, serum IL-6, and albumin were independent prognostic factors. Patients were classified into two groups according to a prognostic index calculated from these three variables. Survival probability at 28 days was 80.67% vs. 67% (p = 0.0001), respectively, in patients with low prognostic and high prognostic indexes. Approximately one-third of patients with liver cirrhosis with acute episodes of HE have non-reversal of HE and poor survival. The development of HE and its resolution is a crucial prognostic event in liver cirrhosis patients. The prognostic significance of hepatic encephalopathy has been previously studied in unison or combination with other decompensating events. However, data on the prognostic role of systemic inflammatory markers in patients with hepatic encephalopathy have not been well evaluated. This prospective observational study assessed the systemic inflammation, short-term prognostic significance, and survival probability of patients with hepatic encephalopathy (HE) with liver cirrhosis over 5 years. This study identified a prognostic index that could stratify patients with hepatic encephalopathy into those with a high or low survival risk. The development of HE and its resolution is a crucial prognostic event in liver cirrhosis patients. These early stratifications can help in identifying patients with a high risk of death, and advanced treatment or early transplantation can be advised.

Indexed as

Hepatic EncephalopathyInflammationLiver CirrhosisAdolescentAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedPrognosisProspective StudiesYoung AdultAmmoniaInterleukinsLactuloseLOLAPrognostic indexRifaximin

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.