Evidence map›Paper›PMID 39272020›Full record

ArticleBMC infectious diseases2024

Significant drop in serum C-reactive protein in patients with solid neoplasia and bacterial infection is associated with a better prognosis and identifies candidates for short-course antibiotic therapy.

Guilherme Monteiro de Barros, Isabela Nascimento Borges, Cecilia Gómez Ravetti, Paulo Henrique Diniz, Samuel Rosa Ferreira, Lara Hemerly De Mori, Rafael Castro, Getúlio H Okamura, Felipe Gatto, Vandack Nobre and 1 more

Abstract read
In one paragraph

Article in BMC infectious diseases, 2024. 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. 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

11 authors.

Guilherme Monteiro de BarrosGraduate Program in Infectious Diseases and Tropical Medicine, School of Medicine, Universidade Federal de Minas Gerais, Av. Prof. Alfredo Balena, 190, Santa Efigênia, Belo Horizonte MG, CEP: 30130-100, Brazil. guimbarros@hotmail.com.
Isabela Nascimento BorgesHospital das Clínicas, Universidade Federal de Minas Gerais, Av. Prof. Alfredo Balena, Santa Efigênia, Belo Horizonte MG, 190CEP: 30130-100, Brazil.
Cecilia Gómez RavettiHospital das Clínicas, Universidade Federal de Minas Gerais, Av. Prof. Alfredo Balena, Santa Efigênia, Belo Horizonte MG, 190CEP: 30130-100, Brazil.
Paulo Henrique DinizHospital das Clínicas, Universidade Federal de Minas Gerais, Av. Prof. Alfredo Balena, Santa Efigênia, Belo Horizonte MG, 190CEP: 30130-100, Brazil.
Samuel Rosa FerreiraHospital das Clínicas, Universidade Federal de Minas Gerais, Av. Prof. Alfredo Balena, Santa Efigênia, Belo Horizonte MG, 190CEP: 30130-100, Brazil.
Lara Hemerly De MoriHospital das Clínicas, Universidade Federal de Minas Gerais, Av. Prof. Alfredo Balena, Santa Efigênia, Belo Horizonte MG, 190CEP: 30130-100, Brazil.
Rafael CastroHospital das Clínicas, Universidade Federal de Minas Gerais, Av. Prof. Alfredo Balena, Santa Efigênia, Belo Horizonte MG, 190CEP: 30130-100, Brazil.
Getúlio H OkamuraHospital das Clínicas, Universidade Federal de Minas Gerais, Av. Prof. Alfredo Balena, Santa Efigênia, Belo Horizonte MG, 190CEP: 30130-100, Brazil.
Felipe GattoHospital das Clínicas, Universidade Federal de Minas Gerais, Av. Prof. Alfredo Balena, Santa Efigênia, Belo Horizonte MG, 190CEP: 30130-100, Brazil.
Vandack NobreGraduate Program in Infectious Diseases and Tropical Medicine, School of Medicine, Universidade Federal de Minas Gerais, Av. Prof. Alfredo Balena, 190, Santa Efigênia, Belo Horizonte MG, CEP: 30130-100, Brazil.
“Núcleo Interdisciplinar de Investigação em Medicina Intensiva” (NIIMI)

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe greater predisposition to infections, as well as the possibility of a worse response to treatment, can lead to the excessive use of antimicrobials among cancer patients. C-reactive protein (CRP) has gained prominence as a tool for monitoring therapeutic responses and reducing the duration of antibiotic therapy; however, few studies have analyzed this protein in cancer patient populations. We hypothesize that cancer patients with a good response to antibiotic therapy show a faster decline in serum CRP levels, which would allow us to identify candidates for short-course treatments.

objectiveTo evaluate the behavior of serum CRP levels among adult cancer patients using antibiotic therapy, and its association with the duration of this treatment, therapeutic response, and clinical recurrence.

methodsThis work consisted of a retrospective study with cancer patients admitted to a university hospital between September 2018 and December 2019. Adults (age ≥ 18 years) who underwent at least one course of antibiotic therapy were included. CRP behavior over the first 7 days of treatment was classified as: i) good response: when the CRP value on the fifth day of therapy reached 50% or less of the peak value detected in the first 48 h of treatment, and ii) poor response: Maintenance, within the same interval, of a CRP value > 50% of the peak value in the first 48 h. The duration of antibiotic therapy was categorized as up to seven full days or more. Outcomes were assessed by events that occurred during the 30 days of hospitalization or until hospital discharge. PRIMARY OUTCOME: Clinical recurrence of the index infection. SECONDARY OUTCOMES: i) Death from any cause; ii) microbiological recurrence; iii) therapeutic response; iv) colitis associated with Clostridioides difficile; and v) isolation of multi-resistant bacteria, whether in clinical or surveillance samples.

resultsThe final analysis consisted of 212 patients, with a median age (IQ) of 59.2 (48 - 67) years old and a predominance of females (65%), who were hypertensive (35%), smokers (21%), and diabetics (17.8%). There was no difference in clinical recurrence between the two groups (8.1% vs. 12.2%; p = 0.364), with a lower 30-day mortality in the good CRP response group (32.2% vs. 14.5%; p = 0.002). Despite the tendency towards a lower occurrence of other secondary outcomes in the good response group, these differences were not statistically significant. In the poor CRP response group, outcomes like clinical recurrence, mortality, and therapeutic response were significantly worse, regardless of the duration of antibiotic treatment.

conclusionIn this study, cancer patients with a good CRP response during antibiotic therapy presented lower mortality and a higher proportion of satisfactory therapeutic responses. CRP can be a useful tool when combined with other clinical information in optimizing the duration of antimicrobial treatment in a hospitalized cancer population.

Indexed as

Anti-Bacterial AgentsBacterial InfectionsC-Reactive ProteinNeoplasmsAdultAgedFemaleHumansMaleMiddle AgedPrognosisRetrospective StudiesTreatment OutcomeAnti-Bacterial AgentsC-Reactive ProteinAcute bacterial infectionsAntibiotic therapyC-reactive proteinOncology

Identifiers

PMID39272020
PMCPMC11401243

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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.