Evidence map›Paper›PMID 42458996›Full record

ArticlePediatric pulmonology2026

The Clinical Respiratory Score: Diagnostic Performance for Acute Chest Syndrome in Sickle Cell Disease.

Shaniqua J Anum, Andy C Yu, Jonathan M Flanagan, Danielle Guffey, Nicholas A Ettinger, Saleh Bhar, Julie Katkin, Shruti Chaturvedi, Gladstone Airewele, Venée N Tubman

Abstract read
In one paragraph

Article in Pediatric pulmonology, 2026. 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. Article
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

10 authors.

Shaniqua J AnumDepartment of Pediatrics, Division of Pediatric Hematology-Oncology, University of Alabama at Birmingham, Birmingham, Alabama, USA.ORCID https://orcid.org/0000-0002-3402-9624
Andy C YuDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Jonathan M FlanaganDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.ORCID https://orcid.org/0000-0003-1330-6618
Danielle GuffeyInstitute for Clinical and Translational Research, Baylor College of Medicine, Houston, Texas, USA.ORCID https://orcid.org/0000-0003-3721-614X
Nicholas A EttingerDepartment of Pediatrics, Division of Pediatric Critical Care, Emory University School of Medicine, Children's Healthcare of Atlanta, Atlanta, Georgia, USA.ORCID https://orcid.org/0000-0002-0388-7693
Saleh BharDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.ORCID https://orcid.org/0000-0002-9266-9304
Julie KatkinDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.ORCID https://orcid.org/0009-0006-0868-252X
Shruti ChaturvediDivision of Hematology, Department of Medicine, Johns Hopkins Hospital, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0001-6832-2389
Gladstone AireweleDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Venée N TubmanDepartment of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.ORCID https://orcid.org/0000-0002-5973-8507

Funding

Characterization of B Lymphocyte Deficiency in Pediatric Sickle Cell DiseaseK23HL148548 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI TUBMAN, VENEE N · 2020 to 2024
$816k
National Hemophilia FoundationNHLBI NIH HHS K23 HL148548NIH HHS K23-HL148548
6 · The paper itself

Abstract

backgroundAcute chest syndrome (ACS) is a leading cause of morbidity in pediatric sickle cell disease (SCD). The Clinical Respiratory Score (CRS) is used prospectively at the bedside for ACS, whereas the NHLBI Clinical Severity Index (CSI) classifies ACS severity retrospectively. We evaluated the diagnostic performance of peak CRS to identify severe ACS.

methodsWe conducted a retrospective cohort study of patients with ACS (one admission each) aged 3-21 years at a tertiary children's hospital (2015-2021). Peak CRS was abstracted from bedside documentation; CSI (1 = mild, 2 = moderate, 3 = severe) was assigned from the chart. The primary analysis estimated sensitivity, specificity, positive/negative predictive values (PPV/NPV), and accuracy of peak CRS ≥ 4 for identifying CSI = 3, with exact 95% confidence intervals. We prespecified a CRS 0-1 subgroup to assess NPV and de-escalation outcomes [respiratory support, transfusion, length of stay (LOS)].

resultsAmong 213 patients, peak CRS ≥ 4 predicted CSI = 3 with sensitivity 1.00 (95% CI 0.863-1.000), specificity 0.888 (0.835-0.926), PPV 0.543 (0.402-0.678), NPV 1.000 (0.978-1.000), and accuracy 0.901 (0.854-0.935). No severe events occurred with CRS < 4 (95% upper bound ~1.8%). In CRS 0-1 (n = 74), none had severe ACS (95% upper bound ~4.1%) nor required significant respiratory support; 75.7% were not transfused; and median LOS was 2.3 days (IQR 1.4-3.1).

conclusionPeak CRS ≥ 4 identifies a high-risk cohort for severe ACS; CRS 0-1 identifies a low-risk cohort requiring minimal intervention. CRS offers a bidirectional bedside tool to guide escalation and de-escalation of care; prospective validation is warranted.

Indexed as

Acute Chest SyndromeAnemia, Sickle CellAdolescentChildChild, PreschoolFemaleHumansMalePredictive Value of TestsRetrospective StudiesSensitivity and SpecificitySeverity of Illness IndexYoung Adulthigh‐flow nasal cannulamechanical ventilationnegative predictive valuenoninvasive ventilationsensitivity and specificity

Identifiers

PMID42458996
PMCPMC13373489

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.