Evidence map›Paper›PMID 38732370›Full record

ArticleDiagnostics (Basel, Switzerland)2024

Integrating Routine Hematological and Extended Inflammatory Parameters as a Novel Approach for Timely Diagnosis and Prognosis in Sepsis Management.

Sianny Herawati, I Ketut Agus Somia, Sully Kosasih, I Nyoman Wande, Jethro Felim, I Made Dwi Payana

Abstract read
In one paragraph

Article in Diagnostics (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Observational
  2. Review
  3. Article
  4. Article
  5. Review
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

6 authors.

Sianny HerawatiDepartment of Clinical Pathology, Faculty of Medicine, Universitas Udayana, Bali 80114, Indonesia.ORCID 0000-0002-7399-4259
I Ketut Agus SomiaDepartment of Internal Medicine, Faculty of Medicine, Universitas Udayana, Bali 80114, Indonesia.
Sully KosasihPT Sysmex Indonesia, Jakarta 12950, Indonesia.
I Nyoman WandeDepartment of Clinical Pathology, Faculty of Medicine, Universitas Udayana, Bali 80114, Indonesia.
Jethro FelimClinical Pathology Residency Education Program, Faculty of Medicine, Universitas Udayana, Bali 80114, Indonesia.
I Made Dwi PayanaClinical Pathology Residency Education Program, Faculty of Medicine, Universitas Udayana, Bali 80114, Indonesia.

Funding

Sysmex Asia Pacific Private Limited Company PEA0006/MKT/SKS/VIII/2022
6 · The paper itself

Abstract

Sepsis is one of the major causes of morbidity and mortality in hospitals, especially in low- and middle-income countries, and represents a challenge to health care providers to carry out early detection, and accurate diagnosis and prognosis with cost-effective diagnostic tools. An observational prospective study was conducted from December 2021 to December 2022 to investigate the extended inflammatory parameters (EIPs) for sepsis management and analyze the survival of septic patients in the emergency unit, intensive care unit (ICU) and inpatient ward. Patients suspected of having sepsis underwent a sequential organ failure assessment (SOFA) evaluation and had blood drawn for complete blood counts (CBCs). Significant changes were observed in various CBC parameters and EIPs, and the sepsis group was followed up with for 30-day mortality. The study highlighted a significant difference yet strong discriminatory power to differentiate sepsis with an AUC of 0.924 against the non-sepsis group and an AUC of 0.991 against the healthy control group using combination of white blood cells and EIPs. Furthermore, the study showed good predictive ability for 30-day mortality with a hazard ratio of 2.311. In summary, this study provides evidence that the utilization of EIPs may be valuable in diagnosing and predicting patient outcomes, and thus will be beneficial for sepsis management in the hospital.

Indexed as

extended inflammatory parametersmortalitysepsis

Identifiers

PMID38732370
PMCPMC11083944

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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.