Evidence map›Paper›PMID 39928335›Full record

Observational studyJAMA network open2025

Response to Inhaled Nitric Oxide and Mortality Among Very Preterm Neonates With Pulmonary Hypertension.

Michelle Baczynski, Dany Weisz, Laura Thomas, Stephanie Fevrier, Michael Castaldo, Amuchou Soraisham, Abbas Hyderi, Rula Agarushi, Soume Bhattacharya, Renjini Lalitha and 15 more

Abstract readObservational Study
In one paragraph

Observational study in JAMA network open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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

  1. Pooled it
  2. Trial
  3. Review
  4. Does inhaled nitric oxide treatment of pulmonary hypertension in extremely premature infants improve patient outcomes?Journal of perinatology : official journal of the California Perinatal Association · 2026
    Article
  5. Oral Delivery Systems for Gasotransmitters in Therapeutic Applications.Polymer science & technology (Washington, D.C.) · 2026
    Review
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

25 authors.

Michelle BaczynskiDepartment of Paediatrics, Mount Sinai Hospital, Toronto, Ontario, Canada.
Dany WeiszDepartment of Newborn & Developmental Paediatrics, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Laura ThomasDepartment of Paediatrics, Mount Sinai Hospital, Toronto, Ontario, Canada.
Stephanie FevrierDepartment of Newborn & Developmental Paediatrics, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Michael CastaldoDivision of Neonatology, BC Children's & Women's Health Centre, Vancouver, British Columbia, Canada.
Amuchou SoraishamFoothills Medical Centre, University of Calgary, Calgary, Alberta, Canada.
Abbas HyderiDivision of Neonatology, Royal Alexandra Hospital, Edmonton, Alberta, Canada.
Rula AgarushiDivision of Neonatology, Royal Alexandra Hospital, Edmonton, Alberta, Canada.
Soume BhattacharyaDivision of Neonatology, London Health Sciences Centre, London, Ontario, Canada.
Renjini LalithaDivision of Neonatology, London Health Sciences Centre, London, Ontario, Canada.
Amneet SidhuDivision of Neonatology, Hamilton Health Sciences Centre, Hamilton, Ontario, Canada.
Muzafar Gani Abdul WahabDivision of Neonatology, Hamilton Health Sciences Centre, Hamilton, Ontario, Canada.
Gabriel AltitDivision of Neonatology, Montreal Children's Hospital, Montreal, Quebec, Canada.
Audrey HébertDivision of Neonatology, Centre Hospitalier Universitaire de Québec, Québec City, Québec, Canada.
Deepak LouisDivision of Neonatology, Health Sciences Centre Winnipeg, Winnipeg, Manitoba, Canada.
Yasser ElsayedDivision of Neonatology, Saint Boniface Hospital, Winnipeg, Manitoba, Canada.
Souvik MitraDivision of Neonatology, University of British Columbia, Vancouver, British Columbia, Canada.
Poorva DeshpandeDepartment of Paediatrics, Mount Sinai Hospital, Toronto, Ontario, Canada.
Ashraf KharratDepartment of Paediatrics, Mount Sinai Hospital, Toronto, Ontario, Canada.
Faith ZhuDepartment of Paediatrics, Mount Sinai Hospital, Toronto, Ontario, Canada.
Joseph TingDivision of Neonatology, Stollery Children's Hospital, Edmonton, Alberta, Canada.
Eugene YoonDepartment of Paediatrics, Mount Sinai Hospital, Toronto, Ontario, Canada.
Prakesh S ShahDepartment of Paediatrics, Mount Sinai Hospital, Toronto, Ontario, Canada.
Amish JainDepartment of Paediatrics, Mount Sinai Hospital, Toronto, Ontario, Canada.
Canadian Neonatal Network Investigators

Funding

CIHR
6 · The paper itself

Abstract

Importance: Clinical observations of immediate improvement in fraction of inspired oxygen (FiO2) in a proportion of cases is often cited as the rationale for using inhaled nitric oxide (iNO) in the management of acute pulmonary hypertension among very preterm neonates (gestational age, <32 weeks). However, the clinical effectiveness of such a response pattern remains underinvestigated. Objective: To identify factors associated with predischarge mortality among very preterm neonates receiving iNO for acute pulmonary hypertension, with specific a priori emphasis on iNO responsiveness. Design, Setting, and Participants: This prospective observational cohort study was conducted from January 1, 2018, to December 31, 2022, at 12 Canadian tertiary neonatal intensive care units. Consecutive very preterm neonates who received iNO for a diagnosis of acute pulmonary hypertension and pretreatment FiO2 of 0.50 or more were included. Neonates with congenital anomalies or those who were treated for chronic pulmonary hypertension with iNO were excluded. Early acute pulmonary hypertension (≤72 hours of age) and late acute pulmonary hypertension (>72 hours of age) cohorts were analyzed separately. Statistical analysis was performed from January 2023 to January 2024. Exposure: Treatment with iNO for acute pulmonary hypertension. Main Outcomes and Measures: The study cohorts were divided for comparison based on the primary outcome of predischarge mortality. Logistic regression analyses were used with predefined variables, including iNO responsiveness, to identify factors associated with mortality. A positive response to iNO was defined as a pre-iNO minus 4-hour post-iNO FiO2 of 0.20 or more. Results: The early acute pulmonary hypertension group (mean [SD] birth gestational age, 26.3 [2.4] weeks; median treatment age, 1 day [IQR, 1-2 days]; 147 boys [56%]) included 262 neonates; 179 (68%) had a pre-iNO FiO2 of 1.0. The late acute pulmonary hypertension group (mean [SD] birth gestational age, 24.9 [1.7] weeks; median treatment age, 13 days [IQR, 9-20 days]; 72 boys [66%]) included 109 neonates; 51 (47%) had a pre-iNO FiO2 of 1.0. Neonates with early acute pulmonary hypertension more frequently had a positive iNO response (71% [186 of 262] vs 41% [45 of 109]) and lower mortality (34% [90 of 262] vs 49% [53 of 109]) than those with late acute pulmonary hypertension. Accounting for pretreatment illness factors, greater reduction in FiO2 with iNO remained associated with lower mortality for neonates with early acute pulmonary hypertension (adjusted odds ratio per FiO2 reduction of 0.10, 0.74 [95% CI, 0.65-0.84]). For those with late acute pulmonary hypertension, however, only pretreatment illness severity (lower pre-iNO FiO2 and higher pre-iNO pH), and not positive response to iNO (adjusted odds ratio, 0.47 [95% CI, 0.17-1.30]), was associated with mortality. Conclusions and Relevance: In this cohort study of very preterm neonates with acute pulmonary hypertension treated with iNO, responsiveness to iNO was associated with improved outcomes during the first 72 hours of age. The prognostic role of iNO response in acute pulmonary hypertension presenting after 72 hours of age remains unclear. Future studies should investigate the distinct pathophysiological mechanisms associated with late acute pulmonary hypertension in this population.

Indexed as

Hypertension, PulmonaryInfant, Premature, DiseasesNitric OxideAdministration, InhalationCanadaFemaleHumansInfant, Extremely PrematureInfant, NewbornIntensive Care Units, NeonatalMaleProspective StudiesNitric Oxide

Identifiers

PMID39928335
PMCPMC11811801

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.