Evidence map›Paper›PMID 42129064›Full record

ArticleAlimentary pharmacology & therapeutics2026

Epidemiology, Predictors of Antimicrobial Resistance and Empiric Treatment Strategies for Spontaneous Bacterial Peritonitis in Cirrhosis: A Multicentre SBP-INDIA Study.

Nipun Verma, Rohit Mehtani, Arun Valsan, Pratibha Garg, Rohit Kumar Nadda, Shilpa Prasad, Anand Sharma, Rohit Gupta, Balram Ji Omar, Naga Srikanth Darla and 25 more

Abstract readMulticenter Study
In one paragraph

Article in Alimentary pharmacology & therapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

35 authors.

Nipun VermaDepartment of Hepatology, PGIMER, Chandigarh, India.ORCID https://orcid.org/0000-0003-4328-0914
Rohit MehtaniDepartment of Hepatology, Amrita School of Medicine, Amrita Vishvavidyapeetham, Faridabad, Haryana, India.ORCID https://orcid.org/0000-0002-0007-0063
Arun ValsanDepartment of Hepatology, Amrita Institute of Medical Sciences, Kochi, India.
Pratibha GargDepartment of Hepatology, PGIMER, Chandigarh, India.
Rohit Kumar NaddaDepartment of Hepatology, PGIMER, Chandigarh, India.
Shilpa PrasadDepartment of Hepatology, Amrita Institute of Medical Sciences, Kochi, India.
Anand SharmaDepartment of Gastroenterology, AIIMS, Rishikesh, India.ORCID https://orcid.org/0000-0002-9841-8768
Rohit GuptaDepartment of Gastroenterology, AIIMS, Rishikesh, India.ORCID https://orcid.org/0000-0002-6641-2505
Balram Ji OmarDepartment of Microbiology, AIIMS, Rishikesh, India.
Naga Srikanth DarlaDepartment of Gastroenterology, AIIMS, Rishikesh, India.
Roshan AgarwalaDepartment of Gastroenterology, Apollo Hospitals, Guwahati, India.ORCID https://orcid.org/0000-0001-5265-2586
Mrinal Deb BarmaDepartment of Gastroenterology, Apollo Hospitals, Guwahati, India.
Mandira SarmaDepartment of Microbiology, Apollo Hospitals, Guwahati, India.
Ameet MandotDepartment of Hepatology, Gleneagles Hospital, Mumbai, India.
Wasim KhotDepartment of Hepatology, Gleneagles Hospital, Mumbai, India.
ShalimarDepartment of Gastroenterology and Human Nutrition, AIIMS, Delhi, India.
Akash ShuklaDepartment of Gastroenterology, KEM Hospital, Mumbai, India.
Arun VaidyaDepartment of Gastroenterology, KEM Hospital, Mumbai, India.
Mithra PrasadDepartment of Gastroenterology and Hepatology, VGM Hospital, Coimbatore, India.
Dibyalochan PraharajDepartment of Hepatology, KIMS, Bhubaneshwar, India.
Anil C AnandDepartment of Hepatology, KIMS, Bhubaneshwar, India.
Radha Krishan DhimanDepartment of Hepatology, SGPGI, Lucknow, India.
Surender SinghDepartment of Hepatology, SGPGI, Lucknow, India.ORCID https://orcid.org/0000-0002-0402-5534
Narendra Singh ChoudharyDepartment of Hepatology and Regenerative Medicine, Medanta Hospital, Gurgaon, India.
Anand KulkarniDepartment of Hepatology, AIG, Hyderabad, India.
Sandeep SatsangiDepartment of Gastroenterology and Hepatology, Apollo Hospitals, Bangalore, India.
Sahaj RathiDepartment of Hepatology, PGIMER, Chandigarh, India.
Arka DeDepartment of Hepatology, PGIMER, Chandigarh, India.ORCID https://orcid.org/0000-0002-8567-1676
Madhumita PremkumarDepartment of Hepatology, PGIMER, Chandigarh, India.ORCID https://orcid.org/0000-0003-2961-4148
Sunil TanejaDepartment of Hepatology, PGIMER, Chandigarh, India.
Virendra SinghDepartment of Hepatology, PGIMER, Chandigarh, India.
Archana AngrupDepartment of Medical Microbiology, PGIMER, Chandigarh, India.
Neelam TanejaDepartment of Medical Microbiology, PGIMER, Chandigarh, India.
Nusrat ShafiqDepartment of Pharmacology, PGIMER, Chandigarh, India.
Ajay DusejaDepartment of Hepatology, PGIMER, Chandigarh, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsThe rising burden of multidrug-resistant (MDRO) and carbapenem-resistant organisms (CRO) among patients with cirrhosis and spontaneous bacterial peritonitis (SBP) is compromising the effectiveness of standard empiric therapy. This multicentre study evaluated resistance patterns, independent predictors of MDRO and CRO infection, and clinical outcomes to inform risk-based empiric therapy and antimicrobial stewardship in ascitic infections.

methodsWe analysed clinical characteristics and outcomes of hospitalized patients with cirrhosis and culture-positive ascitic fluid infections from 13 centres across India. SBP was defined as ascitic neutrophil count (ANC) ≥ 250/mm

resultsAmong 319 patients (median age 49 years; 79.9% male; 65.8% with acute-on-chronic liver failure), 74.6% of isolates were gram-negative. MDRO and CRO were identified in 53.6% and 24.1% of infections, respectively. Nosocomial/healthcare-associated acquisition, circulatory failure, elevated leukocyte count and SBP prophylaxis were independently associated with MDRO infection, while the nosocomial setting, leukocyte count and circulatory failure predicted CRO infection. MDRO infection was associated with poorer survival. Respiratory failure, liver failure, systemic inflammation, presence of MDRO and higher ACLF severity independently predicted mortality. Nearly one-third of culture-positive infections had ANC < 250/mm

conclusionsThere is a high burden of MDRO and CRO in ascitic infections among hospitalized patients with cirrhosis, with clinically relevant impact on outcomes. Empiric antibiotic selection should be guided by acquisition setting, illness severity and resistance risk factors, with stewardship oversight. Similar outcomes between NNBA and SBP suggest that microbiological evidence, rather than neutrophil count alone, should guide decisions.

Indexed as

Anti-Bacterial AgentsBacterial InfectionsDrug Resistance, Multiple, BacterialLiver CirrhosisPeritonitisAdultAgedCarbapenemsFemaleHumansIndiaMaleMiddle AgedRisk FactorsAnti-Bacterial AgentsCarbapenemsantimicrobial resistancecarbapenem‐resistant organismscirrhosisempiric antibiotic therapymultidrug‐resistant organismsspontaneous bacterial peritonitis

Identifiers

PMID42129064
PMCPMC13420993

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.