Evidence map›Paper›PMID 28056845›Full record

ArticleBMC infectious diseases2017

Plasma presepsin level is an early diagnostic marker of severe febrile neutropenia in hematologic malignancy patients.

Yusuke Koizumi, Kaoru Shimizu, Masayo Shigeta, Takafumi Okuno, Hitoshi Minamiguchi, Katsuyuki Kito, Keiko Hodohara, Yuka Yamagishi, Akira Andoh, Yoshihide Fujiyama and 1 more

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 17% of its field
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

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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

16 citing papers in PubMed, 24 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Yusuke KoizumiDepartment of Clinical Infectious Diseases, Aichi Medical University, 1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan. ykoizumi@aichi-med-u.ac.jp.
Kaoru ShimizuDepartment of Laboratory Medicine, Shiga University of Medical Science, Otsu, 520-2192, Japan.
Masayo ShigetaDepartment of Laboratory Medicine, Shiga University of Medical Science, Otsu, 520-2192, Japan.
Takafumi OkunoDepartment of Gastroenterology and Hematology, Shiga University of Medical Science, Otsu, 520-2192, Japan.
Hitoshi MinamiguchiDepartment of Gastroenterology and Hematology, Shiga University of Medical Science, Otsu, 520-2192, Japan.
Katsuyuki KitoDepartment of Gastroenterology and Hematology, Shiga University of Medical Science, Otsu, 520-2192, Japan.
Keiko HodoharaDepartment of Gastroenterology and Hematology, Shiga University of Medical Science, Otsu, 520-2192, Japan.
Yuka YamagishiDepartment of Clinical Infectious Diseases, Aichi Medical University, 1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan.
Akira AndohDepartment of Gastroenterology and Hematology, Shiga University of Medical Science, Otsu, 520-2192, Japan.
Yoshihide FujiyamaDepartment of Gastroenterology and Hematology, Shiga University of Medical Science, Otsu, 520-2192, Japan.
Hiroshige MikamoDepartment of Clinical Infectious Diseases, Aichi Medical University, 1-1 Yazakokarimata, Nagakute, Aichi, 480-1195, Japan.
Shiga University of Medical Science · JPAichi Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFebrile neutropenia (FN) is a common infectious complication in chemotherapy. The mortality of FN is higher in hematologic malignancy patients, and early diagnostic marker is needed. Presepsin is a prompt and specific marker for bacterial sepsis, but its efficacy in severe febrile neutropenia (FN) is not well confirmed. We tried to clarify whether it is a useful maker for early diagnosis of FN in patients during massive chemotherapy.

methodsWe measured plasma presepsin levels every 2-3 day in FN cases and evaluated its change during the course of massive chemotherapy. The patients had hematologic malignancy or bone marrow failure, and in all cases, neutropenia was severe during the episode. The baseline levels, onset levels, increase rate at FN onset, and onset / baseline ratio were evaluated for their efficacy of early FN diagnosis.

resultsEleven episodes of bacteremia (six gram negatives and five gram positives) in severe neutropenia were analyzed in detail. While plasma presepsin level was strongly associated to the CRP level (r = 0.61, p < 0.01), it was not associated with the absolute WBC count (r = -0.19, p = 0.19), absolute neutrophil count (r = -0.11, p = 0.41) or absolute monocyte count (r = -0.12, p = 0.40). The average of onset presepsin level was 638 ± 437 pg/mL and the cutoff value (314 pg/mL) has detected FN onset in 9 of 11 cases. The two cases undetected by presepsin were both Bacillus species bacteremia.

conclusionsPlasma presepsin level is a reliable marker of FN even in massive chemotherapy with very low white blood cell counts. Closer monitoring of this molecule could be a help for early diagnosis in FN. But bacteremia caused by Bacillus species was an exception in our study.

Indexed as

BacteremiaBiomarkersEarly DiagnosisFebrile NeutropeniaHematologic NeoplasmsHumansLeukocyte CountLipopolysaccharide ReceptorsNeutropeniaPeptide FragmentsBiomarkersLipopolysaccharide ReceptorsPeptide Fragmentspresepsin protein, humanBacteremiaCD14ChemotherapyFebrile neutropeniaPresepsin(soluble CD14-ST)

Identifiers

PMID28056845
PMCPMC5217328
OpenAlexW2570771899

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Registered trials

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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.