Evidence map›Paper›PMID 35228290›Full record

ArticleBMJ open2022

Using cluster analysis to describe phenotypical heterogeneity in extremely preterm infants: a retrospective whole-population study.

Theodore Dassios, Emma E Williams, Christopher Harris, Anne Greenough

Open access · goldAbstract read
In one paragraph

Article in BMJ open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 38% 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.

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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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 1 institution in 1 country.

Theodore DassiosDepartment of Women and Children's Health, School of Life Sciences, Faculty of Life Science and Medicine, King's College London, London, UK theodore.dassios@kcl.ac.uk.ORCID 0000-0001-5258-5301
Emma E WilliamsDepartment of Women and Children's Health, School of Life Sciences, Faculty of Life Science and Medicine, King's College London, London, UK.
Christopher HarrisDepartment of Women and Children's Health, School of Life Sciences, Faculty of Life Science and Medicine, King's College London, London, UK.
Anne GreenoughDepartment of Women and Children's Health, School of Life Sciences, Faculty of Life Science and Medicine, King's College London, London, UK.ORCID 0000-0002-8672-5349
King's College London · GB

Funding

Medical Research Council G1000758
6 · The paper itself

Abstract

objectiveTo use cluster analysis to identify discrete phenotypic groups of extremely preterm infants.

designSecondary analysis of a retrospective whole population study.

settingAll neonatal units in England between 2014 and 2019.

participantsInfants live-born at less than 28 weeks of gestation and admitted to a neonatal unit.

interventionsK-means cluster analysis was performed with the gestational age, Apgar score at 5 min and duration of mechanical ventilation as input variables. PRIMARY AND SECONDARY OUTCOME MEASURES: Bronchopulmonary dysplasia, discharge on home oxygen, intraventricular haemorrhage, death before discharge from neonatal care.

resultsTen thousand one hundred and ninety-seven infants (53% male) were classified into four clusters: Cluster 1 contained infants with intermediate gestation and duration of ventilation and had an intermediate mortality and incidence of bronchopulmonary dysplasia. Cluster 2 contained infants with the highest gestation, a shorter duration of ventilation and the lowest mortality. Cluster 3 contained infants with the lowest Apgar score and highest mortality and incidence of intraventricular haemorrhage. Cluster 4 contained infants with the lowest gestation, longest duration of ventilation and highest incidence of bronchopulmonary dysplasia.

conclusionClinical parameters can classify extremely preterm infants into discrete phenotypic groups with differing subsequent neonatal outcomes.

Indexed as

Bronchopulmonary DysplasiaInfant, Extremely PrematureCluster AnalysisFemaleGestational AgeHemorrhageHumansInfantInfant, NewbornMaleRetrospective Studiesneonatal intensive & critical careneonatologyrespiratory physiology

Identifiers

PMID35228290
PMCPMC8886439
OpenAlexW4214486671

What OpenQuestion holds

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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.