# Key Predictors of Neonatal Respiratory Compromise in Placenta Accreta Spectrum: An 11-Year Retrospective Cohort Study

**Authors:** Praew Chareesri, Supaporn Dissaneevate, Anucha Thatrimontrichai, Gunlawadee Maneenil, Manapat Praditaukrit, Pattima Pakhathirathien, Savitree Pranpanus, Chanon Kongkamol

PMC · DOI: 10.3390/jcm15041542 · 2026-02-15

## TL;DR

This study identifies key factors that predict respiratory issues in newborns of mothers with placenta accreta spectrum, helping clinicians identify high-risk infants.

## Contribution

A novel weighted scoring model is developed to predict neonatal respiratory compromise in placenta accreta spectrum pregnancies.

## Key findings

- 112 out of 237 neonates (47.3%) experienced respiratory compromise.
- A predictive score > 7 showed fair discrimination with 67.6% sensitivity and 72.9% specificity.
- Six independent predictors were identified and assigned weighted points for the model.

## Abstract

Background/Objectives: Placenta accreta spectrum (PAS) is associated with substantial maternal and perinatal morbidity and may lead to respiratory distress in newborns. However, limited evidence exists regarding predictors of respiratory compromise (RC) in neonates born to pregnancies complicated by PAS. Methods: This retrospective cohort study included neonates born to pregnancies complicated by PAS between 1 January 2014 and 31 December 2024. Independent predictors of RC were identified using logistic regression, and a weighted scoring model was developed. Model performance and internal validity were assessed using area under the receiver operating characteristic curve, calibration plots, and bootstrap re-sampling. Results: Among 237 neonates born to PAS-complicated pregnancies, 112 (47.3%) experienced RC. Six independent predictors were identified and assigned weighted points: maternal vaginal bleeding within 24 h before delivery (2 points); placenta type—accreta (reference), increta (1 point), and percreta (2 points); absence of antenatal corticosteroid use (1 point); gestational age—29–31 weeks (5 points) and 32–36 weeks (3 points); birth weight < 2500 g (2 points); and male sex (2 points). At a score threshold of 7, the model demonstrated good discrimination, with an area under the receiver operating characteristic curve of 0.75, sensitivity of 67.6%, and specificity of 72.9%. Conclusions: A predictive score > 7 provides fair discrimination for identifying RC in neonates born to pregnancies complicated by PAS and may assist clinicians in identifying high-risk infants who require closer monitoring and early respiratory support.

## Full-text entities

- **Genes:** AVP (arginine vasopressin) [NCBI Gene 551] {aka ADH, ARVP, AVP-NPII, AVRP, VP}
- **Diseases:** maternal (MESH:D000079262), respiratory distress (MESH:D012128), Neonatal hypotension (MESH:D007022), hypoxemia (MESH:D000860), Pulmonary hypertension (MESH:D006976), PAS (MESH:D010921), bleeding (MESH:D006470), Gestational diabetes (MESH:D016640), RC (MESH:D012131), prematurity (MESH:C536271), trisomy 13 (MESH:D000073839), Neonatal anemia (MESH:D000751), chromosomal abnormalities (MESH:D002869), cyanosis (MESH:D003490), Diabetes mellitus (MESH:D003920), trisomy 18 (MESH:D000073842), placentation (MESH:D010922), Hypoglycemia (MESH:D007003), gestational hypertension (MESH:D046110), preterm birth (MESH:D047928), hemorrhagic shock (MESH:D012771), blood loss (MESH:D016063), tachypnea (MESH:D059246), preeclampsia (MESH:D011225), Vaginal bleeding (MESH:D014592), fetal growth restriction (MESH:D005317), congenital anomalies (MESH:D000013), Hypovolemic shock (MESH:D012769), anemia (MESH:D000740), injury to (MESH:D014947), respiratory complications (MESH:D012140), placenta previa (MESH:D010923), Hypertensive disorders (MESH:D006973), cardiovascular and hematologic compromise (MESH:D006402)
- **Chemicals:** milrinone (MESH:D020105), dopamine (MESH:D004298), norepinephrine (MESH:D009638), glucose (MESH:D005947), dexamethasone (MESH:D003907), epinephrine (MESH:D004837), oxygen (MESH:D010100), dobutamine (MESH:D004280)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12942072/full.md

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Source: https://tomesphere.com/paper/PMC12942072