Evidence map›Paper›PMID 42724323›Full record

ArticleTranslational pediatrics2026

Development and validation of an early warning score for refractory

Dani Qin, Mengke Cheng, Xujiao Pu, Lingyun Xia, Xueping Zhu

Abstract read
In one paragraph

Article in Translational pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Dani Qin *Department of Neonatology, Children's Hospital of Soochow University, Suzhou, China.ORCID https://orcid.org/0000-0002-1857-2387
Mengke Cheng *Department of Pediatrics, The Affiliated Yixing Hospital of Jiangsu University, Wuxi, China.ORCID https://orcid.org/0009-0000-1448-4323
Xujiao PuDepartment of Neonatology, Children's Hospital of Soochow University, Suzhou, China.
Lingyun XiaDepartment of Pediatrics, The Affiliated Yixing Hospital of Jiangsu University, Wuxi, China.ORCID https://orcid.org/0009-0002-0906-3967
Xueping ZhuDepartment of Neonatology, Children's Hospital of Soochow University, Suzhou, China.ORCID https://orcid.org/0000-0002-3502-7655

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Methods: A retrospective study was performed using clinical data of children with MPP admitted during the period of January 2023 to December 2024. The patients were categorized into the general MPP (GMPP) group (56 cases) and RMPP group (34 cases) depending on the occurrence of progression to RMPP. The two groups were compared with regard to clinical features, laboratory findings, radiographic appearances, and features of the pathogen. Multivariate logistic regression analysis was performed to identify independent risk factors, and an RMPP early warning scoring system (RMPP-EWS) was developed. The receiver operating characteristic (ROC) curve analysis was used to assess model performance. To mitigate overfitting and quantify the optimism in predictive performance, an internal bootstrap validation with 1,000 resamples was conducted. Furthermore, a sensitivity analysis was performed to assess the impact of excluding fever duration from the prediction model, and a comparative evaluation was carried out between an equal-weighted scoring system and a coefficient-based weighted scoring system. Results: The RMPP group had a significantly increased pre-admission fever duration, C-reactive protein (CRP), lactate dehydrogenase (LDH), D-dimer level, and more atelectasis and A2063G mutation than the GMPP group (P<0.05). Multivariate analysis showed that duration of fever ≥7 days [odds ratio (OR) =6.40, 95% confidence interval (CI): 2.30-17.82], CRP ≥20 mg/L (OR =3.43), LDH ≥400 U/L (OR =4.29), D-dimer ≥500 µg/L (OR =3.07), atelectasis (OR =5.35), and A2063G mutation (OR =3.84) were predictors of RMPP. The RMPP-EWS (0-12 points) was developed based on these indicators. The analysis of the ROC curve showed an area under the curve (AUC) value of 0.892 (95% CI: 0.823-0.961), and the optimal cutoff value was ≥6 points, with a sensitivity of 85.3% and a specificity of 82.1%. The optimism-corrected AUC from bootstrap validation was 0.871 (95% CI: 0.802-0.940), with a shrinkage factor of 0.92. The five-variable model (excluding fever duration) demonstrated an AUC of 0.854 (95% CI: 0.771-0.937), and the coefficient-based weighted score showed an AUC of 0.896 (95% CI: 0.828-0.964), which was not significantly different from the equal-weighted score (DeLong test, P=0.68). The risk stratification included the following: low risk (0-4 points, RMPP incidence 10.7%), moderate risk (5-8 points, 36.8%), and high risk (9-12 points, 70.8%). Conclusions: The RMPP-EWS shows a predictive value and has the capacity to help in the early detection of high-risk RMPP patients to inform individual treatment decisions. This score may assist clinicians in early risk stratification. External validation in a larger multicenter cohort is warranted before clinical implementation.

Indexed as

childrenearly warningMycoplasma pneumoniae pneumonia (MPP)refractoryscoring system

Identifiers

PMID42724323
PMCPMC13559103

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.