Evidence map›Paper›PMID 39322920›Full record

ArticleInfectious diseases and therapy2024

Combination Versus Monotherapy for Carbapenem-Resistant Acinetobacter Species Serious Infections: A Prospective IPTW Adjusted Cohort Study.

Abi Manesh, Mithun Mohan George, Prasannakumar Palanikumar, V Nagaraj, Kundakarla Bhanuprasad, Ramya Krishnan, G Nivetha, Binesh Lal, K Rajitha Triveni, Priyanka Gautam and 17 more

Abstract read
In one paragraph

Article in Infectious diseases and therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Changes in Susceptibility Profiles ofJournal of clinical medicine · 2026
    Article
  4. Review
  5. Article
  6. Review
  7. 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

27 authors.

Abi ManeshDepartment of Infectious Diseases, Christian Medical College, Tamil Nadu, Vellore, 632004, India. abimanesh@gmail.com.
Mithun Mohan GeorgeDepartment of Infectious Diseases, Christian Medical College, Tamil Nadu, Vellore, 632004, India.
Prasannakumar PalanikumarDepartment of Infectious Diseases, Christian Medical College, Tamil Nadu, Vellore, 632004, India.
V NagarajDepartment of Infectious Diseases, Christian Medical College, Tamil Nadu, Vellore, 632004, India.
Kundakarla BhanuprasadDepartment of Infectious Diseases, Christian Medical College, Tamil Nadu, Vellore, 632004, India.
Ramya KrishnanDepartment of Infectious Diseases, Christian Medical College, Tamil Nadu, Vellore, 632004, India.
G NivethaDepartment of Infectious Diseases, Christian Medical College, Tamil Nadu, Vellore, 632004, India.
Binesh LalDepartment of Clinical Microbiology, Christian Medical College, Vellore, Tamil Nadu, India.
K Rajitha TriveniDepartment of Biostatistics, Christian Medical College, Vellore, Tamil Nadu, India.
Priyanka GautamDepartment of Infectious Diseases, Christian Medical College, Tamil Nadu, Vellore, 632004, India.
Biju GeorgeDepartment of Heamatology, Christian Medical College, Vellore, Tamil Nadu, India.
Uday KulkarniDepartment of Heamatology, Christian Medical College, Vellore, Tamil Nadu, India.
Vikram MathewsDepartment of Heamatology, Christian Medical College, Vellore, Tamil Nadu, India.
K SubramaniDepartment of Critical Care, Christian Medical College, Vellore, Tamil Nadu, India.
Shoma RaoDepartment of Critical Care, Christian Medical College, Vellore, Tamil Nadu, India.
Binila ChackoDepartment of Critical Care, Christian Medical College, Vellore, Tamil Nadu, India.
Anand ZachariahDepartment of Medicine, Christian Medical College, Vellore, Tamil Nadu, India.
Sowmya SathyendraDepartment of Medicine, Christian Medical College, Vellore, Tamil Nadu, India.
Samuel George HansdakDepartment of Medicine, Christian Medical College, Vellore, Tamil Nadu, India.
Ooriapadickal Cherian AbrahamDepartment of Medicine, Christian Medical College, Vellore, Tamil Nadu, India.
Ramya IyaduraiDepartment of Medicine, Christian Medical College, Vellore, Tamil Nadu, India.
Rajiv KarthikDepartment of Infectious Diseases, Christian Medical College, Tamil Nadu, Vellore, 632004, India.
John Victor PeterDepartment of Critical Care, Christian Medical College, Vellore, Tamil Nadu, India.
Yin MoCentre for Tropical Medicine and Global Health, Nuffield Department of Medicine, University of Oxford, Oxford, UK.
Balaji VeeraraghavanDepartment of Clinical Microbiology, Christian Medical College, Vellore, Tamil Nadu, India.
George M VargheseDepartment of Infectious Diseases, Christian Medical College, Tamil Nadu, Vellore, 632004, India.
David Leslie PatersonSaw Swee Hock School of Public Health, National University of Singapore, Singapore, Singapore.

Funding

The Wellcome Trust DBT India Alliance IA/CPHE/21/1/505972
6 · The paper itself

Abstract

introductionInternational guidelines recommend definitive combination antibiotic therapy for the management of serious infections involving carbapenem-resistant Acinetobacter (CRAB) species. The commonly available combination options include high-dose sulbactam, polymyxins, tetracyclines, and cefiderocol. Scanty prospective data exist to support this approach.

methodsPatients with CRAB bacteraemia, ventilator-associated pneumonia (VAP), or both were categorized based on whether they received combination therapy or monotherapy. The 30-day mortality was compared between the two groups. Inverse probability treatment weighting (IPTW) was done using propensity score (PS) for a balanced comparison between groups.

resultsBetween January 2021 and May 2023, of the 161 patients with CRAB bacteraemia (n = 55, 34.2%), VAP (n = 46, 28.6%), or both (n = 60, 37.3%) who received appropriate intravenous antibiotic therapy, 70% (112/161) received monotherapy, and the rest received combination therapy. The overall 30-day mortality was 62% (99/161) and not different (p = 0.76) between the combination therapy (31/49, 63.3%) and monotherapy (68/112, 60.7%) groups. The propensity score matching using IPTW did not show a statistical difference (p = 0.47) in 30-day mortality for receiving combination therapy with an adjusted odds ratio (OR) P of 1.29 (0.64, 2.58).

conclusionCombination therapy for CRAB infections needs further study in a randomised controlled trial, as this observational study showed no difference in 30-day mortality between monotherapy and combination therapy.

Indexed as

AcinetobacterCombination therapyCRAB infectionsPolymyxins

Identifiers

PMID39322920
PMCPMC11499560

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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.