Evidence map›Paper›PMID 40722815›Full record

ReviewBiomedicines2025

Pulmonary Hemorrhage in Premature Infants: Pathophysiology, Risk Factors and Clinical Management.

Sariya Sahussarungsi, Anie Lapointe, Andréanne Villeneuve, Audrey Hebert, Nina Nouraeyan, Satyan Lakshminrusimha, Yogen Singh, Christine Sabapathy, Tiscar Cavallé-Garrido, Guilherme Sant'Anna and 1 more

Abstract readReview
In one paragraph

Review in Biomedicines, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–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

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Observational
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

11 authors.

Sariya SahussarungsiDivision of Neonatology, Department of Pediatrics, Montreal Children's Hospital, McGill University, Montreal, QC H4A 3J1, Canada.
Anie LapointeDivision of Neonatology, Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montreal, QC H3T 1C5, Canada.ORCID 0000-0003-1464-2904
Andréanne VilleneuveDivision of Neonatology, Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montreal, QC H3T 1C5, Canada.
Audrey HebertDivision of Neonatology, Department of Pediatrics, Centre Hospitalier de l'Université Laval, Université Laval, Québec, QC G1V 0E8, Canada.
Nina NouraeyanJewish General Hospital, McGill University, Montreal, QC H4A 3J1, Canada.
Satyan LakshminrusimhaDivision of Neonatology, Department of Pediatrics, University of California, Davis, Sacramento, CA 95817, USA.ORCID 0000-0001-6098-2155
Yogen SinghDivision of Neonatology, Department of Pediatrics, University of California, Davis, Sacramento, CA 95817, USA.ORCID 0000-0002-5207-9019
Christine SabapathyDivision of Hematology, Department of Pediatrics, Montreal Children's Hospital, McGill University, Montreal, QC H4A 3J1, Canada.
Tiscar Cavallé-GarridoDivision of Cardiology, Department of Pediatrics, Montreal Children's Hospital, McGill University, Montreal, QC H4A 3J1, Canada.
Guilherme Sant'AnnaDivision of Neonatology, Department of Pediatrics, Montreal Children's Hospital, McGill University, Montreal, QC H4A 3J1, Canada.ORCID 0000-0003-1633-3654
Gabriel AltitDivision of Neonatology, Department of Pediatrics, Montreal Children's Hospital, McGill University, Montreal, QC H4A 3J1, Canada.ORCID 0000-0001-5141-0964

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pulmonary hemorrhage (PH) is a life-threatening complication predominantly affecting preterm infants, particularly those with very low birth weight (VLBW) and fetal growth restriction (FGR). Typically occurring within the first 72 h of life, PH is characterized by acute respiratory deterioration and significant morbidity and mortality. This review synthesizes current evidence on the multifactorial pathogenesis of PH, highlighting the roles of immature pulmonary vasculature, surfactant-induced hemodynamic shifts, and left ventricular diastolic dysfunction. Key risk factors include respiratory distress syndrome (RDS), hemodynamically significant patent ductus arteriosus (hsPDA), sepsis, coagulopathies, and genetic predispositions. Diagnostic approaches incorporate clinical signs, chest imaging, lung ultrasound, and echocardiography. Management strategies are multifaceted and include ventilatory support-particularly high-frequency oscillatory ventilation (HFOV)-surfactant re-administration, blood product transfusion, and targeted hemostatic agents. Emerging therapies such as recombinant activated factor VII and antifibrinolytics show promise but require further investigation. Preventive measures like antenatal corticosteroids and early indomethacin prophylaxis may reduce incidence, particularly in high-risk populations. Despite advancements in neonatal care, PH remains a major contributor to neonatal mortality and long-term neurodevelopmental impairment. Future research should focus on individualized risk stratification, early diagnostic tools, and optimized treatment protocols to improve outcomes. Multidisciplinary collaboration and innovation are essential to advancing care for this vulnerable population.

Indexed as

coagulopathyechocardiographyfetal growth restriction (FGR)lung ultrasoundpatent ductus arteriosus (PDA)preterm infantspulmonary hemorrhagerespiratory distress syndrome (RDS)surfactant therapyvery low birth weight (VLBW)

Identifiers

PMID40722815
PMCPMC12292498

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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.