Evidence map›Paper›PMID 42447407›Full record

Observational studyRevista medica del Instituto Mexicano del Seguro Social2026

[Twelve-month clinical follow-up of patients diagnosed with bronchopulmonary dysplasia].

Ana Karen Constantino-Solano, Mariana Paulina García-Bermúdez, Jorge Antonio Quirarte-Gómez, Arturo García-Galicia, Álvaro José Montiel-Jarquín, Nancy Rosalía Bertado-Ramírez, Carlos Alberto López-Bernal, Josué Cruz-Meza

Abstract readEnglish AbstractObservational Study
In one paragraph

Observational study in Revista medica del Instituto Mexicano del Seguro Social, 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

8 authors.

Ana Karen Constantino-SolanoInstituto Mexicano del Seguro Social, Hospital General de Zona No. 20 La Margarita, Servicio de Pediatría. Puebla, Puebla, México.ORCID 0000-0002-6890-3826
Mariana Paulina García-BermúdezInstituto Mexicano del Seguro Social, Hospital General Regional No. 36, Servicio de Neonatología. Puebla, Puebla, México.ORCID 0009-0008-4205-2710
Jorge Antonio Quirarte-GómezInstituto Mexicano del Seguro Social, Hospital General de Zona No. 20 La Margarita, Servicio de Pediatría. Puebla, Puebla, México.ORCID 0000-0002-9141-6639
Arturo García-GaliciaInstituto Mexicano del Seguro Social, Centro Médico Nacional "Gral. de Div. Manuel Ávila Camacho", Hospital de Especialidades de Puebla, Dirección de Educación e Investigación en Salud. Puebla, Puebla, México.ORCID 0000-0003-2535-4967
Álvaro José Montiel-JarquínInstituto Mexicano del Seguro Social, Centro Médico Nacional "Gral. de Div. Manuel Ávila Camacho", Hospital de Especialidades de Puebla, Dirección de Educación e Investigación en Salud. Puebla, Puebla, México.ORCID 0000-0003-0531-9611
Nancy Rosalía Bertado-RamírezInstituto Mexicano del Seguro Social, Centro Médico Nacional "Gral. de Div. Manuel Ávila Camacho", Hospital de Especialidades de Puebla, Dirección de Educación e Investigación en Salud. Puebla, Puebla, México.ORCID 0000-0003-1879-3152
Carlos Alberto López-BernalInstituto Mexicano del Seguro Social, Centro Médico Nacional "Gral. de Div. Manuel Ávila Camacho", Hospital de Especialidades de Puebla, Servicio de Cirugía General. Puebla, Puebla, México.ORCID 0000-0002-3187-0899
Josué Cruz-MezaInstituto Mexicano del Seguro Social, Centro Médico Nacional "Gral. de Div. Manuel Ávila Camacho", Hospital de Especialidades de Puebla, Servicio de Cirugía General. Puebla, Puebla, México.ORCID 0009-0000-8849-1630

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Bronchopulmonary dysplasia (BPD) is a chronic disease with a high prevalence in premature infants. Its development is related to multiple risk factors, including prolonged oxygen use, mechanical ventilation, and the presence of infections. Objective: To analyze the clinical characteristics and factors associated with readmission in patients with bronchopulmonary dysplasia after 12 months of follow-up. Materials and methods: This was an observational, analytical, and longitudinal study. Patients born before 36 weeks of gestation with BPD, seen in the Pediatric Pulmonology outpatient clinic between September 2023 and August 2024, were included. Results: Eighty-one patients were analyzed. The median gestational age was 30 weeks (IQR 5; 25th percentile: 28 weeks; 75th percentile: 33 weeks); 53% were female, and 64.2% presented with moderate BPD. All patients had at least one hospital readmission. 61.7% presented with retinopathy of prematurity. 30% required oxygen for more than one year. A significant association was found between low birth weight at one year and a higher number of readmissions (OR: 9.08; 95% CI: 2.10-39.2; p = 0.002). Conclusions: The clinical course of patients with bronchopulmonary dysplasia (BPD) remains unfavorable. Low birth weight at one year was the main factor associated with readmissions. Nutritional monitoring and infection prevention strategies are needed to improve long-term prognosis.

Indexed as

Bronchopulmonary DysplasiaPatient ReadmissionFemaleFollow-Up StudiesGestational AgeHumansInfantInfant, NewbornInfant, PrematureLongitudinal StudiesMaleRisk FactorsTime FactorsBronchopulmonary DysplasiaDisplasia BroncopulmonarDistrés Respiratorio NeonatalInfant, PrematureInfant, Very Low Birth WeightNeonatal Respiratory Distress SyndromeRecién Nacido de muy Bajo PesoRecién Nacido Prematuro

Identifiers

PMID42447407
PMCPMC13375252

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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.