Evidence map›Paper›PMID 27753120›Full record

ArticleThe Laryngoscope2017

Longitudinal analysis of inflammatory biomarkers during acute rhinosinusitis.

Timo J Autio, Timo Koskenkorva, Tuomo K Leino, Petri Koivunen, Olli-Pekka Alho

Open access · bronzeAbstract read
In one paragraph

Article in The Laryngoscope, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
1.9field-weighted citation impact, top 14% 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

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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 19 citations in OpenAlex.

  1. Procalcitonin as a Biomarker in Rhinosinusitis: A Systematic Review.American journal of rhinology & allergy · 2019
    Pooled it
  2. Pooled it
  3. Review
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  5. Review
  6. Article
  7. Review
  8. Article
  9. Inflammatory Biomarkers During Bacterial Acute Rhinosinusitis.Current allergy and asthma reports · 2018
    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

5 authors at 3 institutions in 1 country.

Timo J AutioDepartment of Otorhinolaryngology and Head and Neck Surgery, Oulu University Hospital, Oulu, Finland.
Timo KoskenkorvaDepartment of Otorhinolaryngology and Head and Neck Surgery, Oulu University Hospital, Oulu, Finland.
Tuomo K LeinoAir Force Command Finland, Finnish Defense Forces, Tikkakoski, Finland.
Petri KoivunenDepartment of Otorhinolaryngology and Head and Neck Surgery, Oulu University Hospital, Oulu, Finland.
Olli-Pekka AlhoDepartment of Otorhinolaryngology and Head and Neck Surgery, Oulu University Hospital, Oulu, Finland.
Oulu University of Applied Sciences · FIFinnish Defence Forces · FIOulu University Hospital · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo illuminate the pathophysiology of acute rhinosinusitis (ARS) with sequential monitoring of inflammatory biomarkers during an ARS episode and to clarify their diagnostic usability in bacterial ARS. STUDY

designInception cohort study with 50 conscripts with ARS.

methodsWe collected peripheral blood high-sensitive C-reactive protein (hs-CRP), white blood cell (WBC), procalcitonin, and nasal nitric oxide (nNO) counts at 2 to 3 and 9 to 10 days of symptoms during an ARS episode. We simultaneously gathered various clinical parameters and microbiological samples. Bacterial ARS was confirmed with a positive culture of sinus aspirate.

resultsReciprocal correlations and a significant change in biomarker levels between the two visits suggest that ARS involves a local and systemic inflammatory response that was strongest at 2 to 3 days. High-sensitive CRP and nNO reflected responses best (52% had increased CRP levels at 2-3 days; 66% had decreased nNO levels). White blood cell and procalcitonin counts rarely exceeded the reference range. Increased local and systemic inflammatory response were linked to multiple, adenoviral, or influenza A viral etiology or the detection of bacterial ARS. Local response correlated with imaging findings of wide paranasal sinus involvement and ostiomeatal complex occlusion. At 9 to 10 days, elevated (≥ 11 mg/L) and moderately elevated (≥ 49 mg/L) hs-CRP predicted bacterial ARS well (likelihood ratio [LR]+ 3.3 and LR+ 15.8, respectively), but the sensitivity for both findings remained low.

conclusionAcute rhinosinusitis (particularly bacterial ARS) involves a local and systemic inflammatory response that is strongest at the beginning of symptoms. Elevated hs-CRP supports the diagnosis of bacterial ARS. LEVEL OF EVIDENCE: 4. Laryngoscope, 2016 127:E55-E61, 2017.

Indexed as

Acute DiseaseAdolescentBiomarkersCohort StudiesC-Reactive ProteinFemaleHumansInflammation MediatorsLongitudinal StudiesMaleRhinitisSensitivity and SpecificitySinusitisStatistics as TopicVirus DiseasesYoung AdultBiomarkersC-Reactive ProteinInflammation MediatorsAcute rhinosinusitisbacterialC-reactive proteinCRPhigh-sensitive CRPnasal nitric oxideNOprocalcitonin

Identifiers

PMID27753120
PMCPMC7165676
OpenAlexW2537808153

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.