Evidence map›Paper›PMID 40274678›Full record

ArticleDigestive diseases and sciences2025

Predictive Factors of Post-ERCP Hepatic Decompensation in Patients with Cirrhosis: A Retrospective Case-Control Study.

Mohammed Abusuliman, Sanad Dawod, Faisal Nimri, Taher Jamali, Gordon Jacobsen, Muhammad Zarrar Khan, Remy Arwani, Omar Shamaa, Suhaib Alhaj Ali, Spandana Alluri and 11 more

Abstract read
PubMed Publisher
In one paragraph

Article in Digestive diseases and sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

21 authors.

Mohammed Abusuliman *Department of Internal Medicine, Henry Ford Hospital, 2799 W. Grand Blvd, Detroit, MI, 48072, USA. Mabusul1@hfhs.org.
Sanad Dawod *Department of Internal Medicine, Henry Ford Hospital, 2799 W. Grand Blvd, Detroit, MI, 48072, USA.
Faisal NimriDivision of Gastroenterology and Hepatology, Henry Ford Hospital, Detroit, MI, USA.
Taher JamaliDivision of Gastroenterology and Hepatology, Henry Ford Hospital, Detroit, MI, USA.
Gordon JacobsenDivision of Behavioral Health Sciences, Henry Ford Hospital, Detroit, MI, USA.
Muhammad Zarrar KhanDivision of Gastroenterology and Hepatology, Henry Ford Hospital, Detroit, MI, USA.
Remy ArwaniDivision of Gastroenterology and Hepatology, Henry Ford Hospital, Detroit, MI, USA.
Omar ShamaaDivision of Gastroenterology and Hepatology, Henry Ford Hospital, Detroit, MI, USA.
Suhaib Alhaj AliDepartment of Internal Medicine, Henry Ford Hospital, 2799 W. Grand Blvd, Detroit, MI, 48072, USA.
Spandana AlluriDepartment of Internal Medicine, Henry Ford Hospital, 2799 W. Grand Blvd, Detroit, MI, 48072, USA.
Rami YoussefDepartment of Internal Medicine, Henry Ford Hospital, 2799 W. Grand Blvd, Detroit, MI, 48072, USA.
Abdulmalik SaleemDepartment of Internal Medicine, Henry Ford Hospital, 2799 W. Grand Blvd, Detroit, MI, 48072, USA.
Ahmad AlomariDepartment of Internal Medicine, Henry Ford Hospital, 2799 W. Grand Blvd, Detroit, MI, 48072, USA.
Muhammad Saad FaisalDepartment of Internal Medicine, Henry Ford Hospital, 2799 W. Grand Blvd, Detroit, MI, 48072, USA.
Haya OmeishDepartment of Internal Medicine, Henry Ford Hospital, 2799 W. Grand Blvd, Detroit, MI, 48072, USA.
Muhammad Salman FaisalDepartment of Internal Medicine, Henry Ford Hospital, 2799 W. Grand Blvd, Detroit, MI, 48072, USA.
Amr AbusulimanFaculty of Medicine, Tanta University, Tanta, Gharbia Governorate, Egypt.
Sumit SinglaDivision of Gastroenterology and Hepatology, Henry Ford Hospital, Detroit, MI, USA.
Cyrus PirakaDivision of Gastroenterology and Hepatology, Henry Ford Hospital, Detroit, MI, USA.
Mazen ElatracheDivision of Gastroenterology and Hepatology, Henry Ford Hospital, Detroit, MI, USA.
Tobias ZuchelliDivision of Gastroenterology and Hepatology, Henry Ford Hospital, Detroit, MI, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimEndoscopic retrograde cholangiopancreatography (ERCP) is a crucial diagnostic and therapeutic procedure in patients with cirrhosis; however, it carries the risk of post-procedural hepatic decompensation. This study aims to identify predictive factors associated with post-ERCP hepatic decompensation in patients with cirrhosis to better inform clinical decision-making and minimize adverse outcomes.

methodsA retrospective analysis was conducted on patients with cirrhosis undergoing ERCP. Clinical, biochemical, and procedural variables were evaluated to determine their association with hepatic decompensation. Multivariate analysis was performed to identify independent predictors.

resultsA total of 277 patients with cirrhosis who underwent an ERCP were included. The cohort had a mean age of 63.4 years, with a male predominance (65.3%) and various etiologies of cirrhosis, including alcohol-related (39.3%) and hepatitis C (11.4%). Post-ERCP complications occurred in 26.7% of patients. The most common complications were hepatic decompensation events (18.4%), sepsis (10.8%), and cholangitis (6.1%). Patients with complications had significantly higher baseline MELD scores, INR, chronic kidney disease (CKD) and history of ascites, hepatic encephalopathy, and hepatorenal syndrome (HRS). A Multivariate analysis revealed that factors such as higher MELD score, ascites, hepatic encephalopathy, and stent placement were associated with post-ERCP complications. Subgroup analyses indicated that patients who developed hepatic decompensation events (ascites, SBP, or HRS) had a more severe liver dysfunction at baseline, as reflected by a higher MELD score and INR, and prior episodes of ascites and hepatic encephalopathy.

conclusionPre-procedural liver function parameters and procedural factors are crucial predictors of post-ERCP hepatic decompensation in patients with cirrhosis. Key risk factors include higher MELD score, CKD, history of ascites, and hepatic encephalopathy. Careful pre-procedural evaluation and management are essential to reduce these risks.

Indexed as

Cholangiopancreatography, Endoscopic RetrogradeLiver CirrhosisLiver FailurePostoperative ComplicationsAgedCase-Control StudiesFemaleHumansLiver Function TestsMaleMiddle AgedMultivariate AnalysisRetrospective StudiesRisk AssessmentRisk FactorsSeverity of Illness IndexCirrhosisEndoscopic retrograde cholangiopancreatographyERCPHepatic decompensationPost-ERCP complications

Identifiers

What OpenQuestion 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 OpenQuestion graph.