Keywords
Presepsin, infectious disease, bronchiolitis
This article is included in the Pathogens gateway.
Presepsin, infectious disease, bronchiolitis
Presepsin is a new marker of inflammation formed by cleavage of N-terminal of soluble CD14, a member of the Toll-like receptors group; this protein is present in macrophage and other granulocyte cells on their cell membranes, and it is responsible for intracellular transduction of endotoxin signals.1 In the last years, presepsin has been increasingly used in clinical practice as an indicator of presence and severity of serious infections like sepsis, as it is released by immune system cells involved in the response to pathogenic bacteria, although its utility in patients’ prognosis is not yet fully understood, particularly in children.2
In pediatrics, it has been particularly studied for the early diagnosis of neonatal sepsis, in combination with other classic inflammation markers such as procalcitonin,3 while the role of presepsin in discriminating bacterial from viral infections in other clinical scenarios is less studied. For example, respiratory diseases still represent a major cause of mortality, morbidity and antibiotic use, and in this context presepsin could be used as a useful discriminator of bacterial pneumonia or severity,4 and it could be also related to the mortality risk of critical patients.
Although its use in neonates is well characterized,3 the evidence for the use of this marker in children aged > 6 months is not clear because it is not a test routinely used in clinical practice and it has been studied mainly in critically ill patients or with important comorbidities such as neutropenia,5,6 with excellent results.
This scoping review aims to analyze the use of presepsin and procalcitonin in pediatric respiratory infectious diseases, analyzing the ability to distinguish the severity and type of respiratory pathology. In addition, we will also focus on comparing presepsin with procalcitonin, a better studied marker of severe bacterial infections in children.
The main review question will be “What is known about the diagnostic role of presepsin and/or procalcitonin in the differential diagnosis of respiratory tract infection’s severity and etiology?”
This review will also assess the following sub-questions:
1. Does the adjunction of presepsin to the use of procalcitonin improves the accuracy in identifying bacterial infectious diseases?
2. What is the role of presepsin and procalcitonin in the subgroup of children with bronchiolitis?
3. What is the role of presepsin and procalcitonin in the subgroup of children with respiratory syncytial virus bronchiolitis?
This review will include studies performed on children and adolescents (younger than 18 years) with a confirmed diagnosis of upper and/or lower respiratory infectious disease (clinical, microbiological or radiological diagnosis). We will include children diagnosed with pneumonia, bronchiolitis, bronchitis, croup, and other types of infectious respiratory diseases.
The main concept of this review will be the use of presepsin and procalcitonin in pediatric respiratory infectious diseases.
We started our research in February 2023 in the following bibliographic databases: PubMed, EMBASE, Cochrane and SCOPUS.
There were no date restrictions. Only articles written in English will be included.
Patients younger than 18 years of age were considered as children or pediatric patients. The search strategy for Pubmed is available as supplementary material of this protocol (Appendix 1 available at https://doi.org/10.6084/m9.figshare.22155131.v1); the terms used for this search were adapted for use with other bibliographic databases.
After the search, the studies have been exported to Rayyan. A first screen to exclude duplicates was performed by one author.
Titles and/or abstracts of studies retrieved using the search strategy will be screened independently by two reviewers to identify studies that could be inserted in the review. Full texts of potentially eligible studies will be retrieved and independently assessed for eligibility by two reviewers. Each researcher will be blinded to the decision of the other researcher. Any disagreement between them over the eligibility of studies will be resolved through discussion and, in case of further disagreement, by discussion with a third reviewer.
All the studies that will not meet the inclusion criteria will be excluded and a table with the reason why those studies were excluded will be inserted in the final manuscript.
The results of the search will be reported in the PRISMA flow diagram.
Two review authors will extract data independently, everyone on a different Excel spreadsheet. Each researcher will be blinded to the decision of the other researcher. When the process will be completed, in case of discordance, any disagreement will be identified and resolved through discussion (with a third author if necessary).
An Excel file will be used to store data. When available, extracted information will include:
1. study general features: title, author, year of publication, type of study, number of patients included in the study, geographical area where the study has been performed
2. participant general features: sample size of each group, nationality, age, socio-economic status, comorbidities
3. clinical manifestations of children included in our review
4. main imaging findings: type of lung involvement at chest X-Ray and/or CT scan
5. microbiological results
6. results of the inflammation indices performed (procalcitonin and presepsin)
7. antibiotic use
8. hospitalization, including pediatric intensive care
9. outcomes (death, survival; survival with or without sequelae; type of sequelae)
To report our findings, we will follow Preferred Reporting Items for Systematic reviews and Meta-Analyses extension for Scoping Reviews (PRISMA-ScR) Checklist.
We will produce a narrative synthesis of the findings from the studies included in the review describing the results we have obtained and providing our opinion on their interpretation. For the narrative synthesis we will prefer articles in which etiological diagnosis was specified.
We will also use tables and charts to summarize both study characteristics and the most important clinical, diagnostics, treatments and outcomes data.
More specifically, we will summarize our findings using tables. The first one will include the characteristics of included studies (number of studies, study design, year of publication, characteristics of the study populations, and countries where studies were conducted) and the second one will include participant general features. Then we will provide different tables or figures summarizing main data about clinical presentation, type of respiratory disease analyzed, imaging characteristics, hematochemical results with procalcitonin and presepsin levels, treatments performed, outcomes and possible predictors of outcome.
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Is the rationale for, and objectives of, the study clearly described?
Yes
Is the study design appropriate for the research question?
Partly
Are sufficient details of the methods provided to allow replication by others?
No
Are the datasets clearly presented in a useable and accessible format?
Partly
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: ID
Alongside their report, reviewers assign a status to the article:
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Version 1 09 Mar 23 |
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