Evidence map›Paper›PMID 16774297›Full record

ReviewPaediatric drugs2006

Persistent pulmonary hypertension of the newborn: pathogenesis, etiology, and management.

Enrique M Ostrea, Esterlita T Villanueva-Uy, Girija Natarajan, Herbert G Uy

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Paediatric drugs, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02875860 (TOTAL TRIAL), which is not on this map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
4.9field-weighted citation impact, top 5% of its field
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.

NCT02875860 phase2completednot on this mapstarted 2017, after this paper: background citation

TOTAL TRIAL: Randomized Trial of Fetoscopic Endoluminal Tracheal Occlusion (FETO) Versus Expectant Management During Pregnancy in Fetuses With Left-Sided and Isolated Congenital Diaphragmatic Hernia and Moderate Pulmonary Hypoplasia

TypeinterventionalSponsorMichael A BelfortRan2017 to 2019Enrolled5ConditionsHernia, Hernia, Diaphragmatic, Hernia, DIaphragmatic, Congenital, Pathological Conditions, AnatomicalArmsGoldBal2 detachable balloon, Baltaccidbpe100 Delivery Catheter, Standardized postnatal care
3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 100 citations in OpenAlex.

  1. Hydralazine in infants with persistent hypoxemic respiratory failure.The Cochrane database of systematic reviews · 2013
    Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Review
  6. Article
  7. Article
  8. Pentraxin 3: A Potential Novel Predictor for Neonatal Pulmonary Hypertension.Open access Macedonian journal of medical sciences · 2019
    Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
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

4 authors at 2 institutions in 2 countries.

Enrique M OstreaWayne State University, Detroit, Michigan, USA. eostrea@med.wayne.edu
Esterlita T Villanueva-Uy
Girija Natarajan
Herbert G Uy
Philippine General Hospital · PHWayne State University · US

Funding

NICHD NIH HHS 1R01HD039428001A1
6 · The paper itself

Abstract

Persistent pulmonary hypertension of the newborn (PPHN) is characterized by severe hypoxemia shortly after birth, absence of cyanotic congenital heart disease, marked pulmonary hypertension, and vasoreactivity with extrapulmonary right-to-left shunting of blood across the ductus arteriosus and/or foramen ovale. In utero, a number of factors determine the normally high vascular resistance in the fetal pulmonary circulation, which results in a higher pulmonary compared with systemic vascular pressure. However, abnormal conditions may arise antenatally, during, or soon after birth resulting in the failure of the pulmonary vascular resistance to normally decrease as the circulation evolves from a fetal to a postnatal state. This results in cyanosis due to right-to-left shunting of blood across normally existing cardiovascular channels (foramen ovale or ductus arteriosus) secondary to high pulmonary versus systemic pressure. The diagnosis is made by characteristic lability in oxygenation of the infant, echocardiographic evidence of increased pulmonary pressure, with demonstrable shunts across the ductus arteriosus or foramen ovale, and the absence of cyanotic heart disease lesions. Management of the disease includes treatment of underlying causes, sedation and analgesia, maintenance of adequate systemic blood pressure, and ventilator and pharmacologic measures to increase pulmonary vasodilatation, decrease pulmonary vascular resistance, increase blood and tissue oxygenation, and normalize blood pH. Inhaled nitric oxide has been one of the latest measures to successfully treat PPHN and significantly reduce the need for extracorporeal membrane oxygenation.

Indexed as

Extracorporeal Membrane OxygenationHumansInfant, NewbornPersistent Fetal Circulation SyndromeRandomized Controlled Trials as TopicRespiratory Distress Syndrome, NewbornTolazolineVasodilator AgentsTolazolineVasodilator Agents

Identifiers

PMID16774297
OpenAlexW37342125

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.