Evidence map›Paper›PMID 36409365›Full record

ArticlePediatric nephrology (Berlin, Germany)2023

Predictive factors for survival in patients with oligohydramnios secondary to antenatal kidney disease.

Mathilde Baudin, Claire Herbez, Isabelle Guellec, Ferdinand Dhombres, Lucie Guilbaud, Cyrielle Parmentier, Jean Daniel Delbet, Catherine Garel, Eleonore Bondiaux, Jean Marie Jouannic and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Development of a fetal renal ultrasound score for predicting neonatal renal dysfunction.European journal of obstetrics & gynecology and reproductive biology: X · 2026
    Article
  2. Article
  3. Article
  4. 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

11 authors at 1 institution in 1 country.

Mathilde Baudin *Pediatric Nephrology Unit, Trousseau Hospital- ORIGYNE- AP-HP.Sorbonne Université, Paris, France.
Claire Herbez *Pediatric Nephrology Unit, Trousseau Hospital- ORIGYNE- AP-HP.Sorbonne Université, Paris, France.
Isabelle GuellecPediatric Intensive Care Unit, Trousseau Hospital- ORIGYNE- AP-HP.Sorbonne Université, Paris, France.
Ferdinand DhombresFetal Medicine Department, Trousseau Hospital- ORIGYNE- AP-HP.Sorbonne Université, Paris, France.
Lucie GuilbaudFetal Medicine Department, Trousseau Hospital- ORIGYNE- AP-HP.Sorbonne Université, Paris, France.
Cyrielle ParmentierPediatric Nephrology Unit, Trousseau Hospital- ORIGYNE- AP-HP.Sorbonne Université, Paris, France.
Jean Daniel DelbetPediatric Nephrology Unit, Trousseau Hospital- ORIGYNE- AP-HP.Sorbonne Université, Paris, France.
Catherine GarelRadiology Department, Trousseau Hospital- AP-HP.Sorbonne Université, Paris, France.
Eleonore BondiauxRadiology Department, Trousseau Hospital- AP-HP.Sorbonne Université, Paris, France.
Jean Marie JouannicFetal Medicine Department, Trousseau Hospital- ORIGYNE- AP-HP.Sorbonne Université, Paris, France.
Tim UlinskiPediatric Nephrology Unit, Trousseau Hospital- ORIGYNE- AP-HP.Sorbonne Université, Paris, France. tim.ulinski@aphp.fr.ORCID http://orcid.org/0000-0002-5338-6352
Sorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRenal oligohydramnios (ROH) is caused by bilateral congenital abnormalities, either of renal parenchymal or obstructive origin. ROH is a poor prognostic factor of neonatal survival; lung hypoplasia is reported to be the main cause of mortality. We aimed to describe the fetal morbidity and pre- and postnatal mortality in case of ROH due to renal congenital pathologies and to find predictive risk factors for morbidity and mortality.

methodsAll data were collected in Trousseau Hospital in the obstetric, neonatology, and pediatric nephrology units, from 2008 to 2020.

resultsWe included 66 fetuses with renal parenchymal pathologies posterior urethral valves (PUV) (N = 25), bilateral kidney agenesis (N = 10), hypodysplasia (N = 16), and polycystic kidney disease (N = 10) causing oligohydramnios identified on antenatal ultrasound. Total pre- and postnatal mortality was 76% (50/66). Mortality, excepting termination of pregnancy (TOP), was 65%. The presence of pneumomediastinum and pneumothorax was not different in survivors and non-survivors. Fetuses with kidneys having features of hypodysplasia on ultrasound at T2 and those with oligohydramnios before 32 weeks GA had a higher risk of death. There was a significant difference in plasma creatinine of the surviving patients compared to the deceased patients, from day 3 onwards (183 µmol/L [88; 255] vs. 295 µmol/L [247; 326]; p = 0.038).

conclusionsThe main differences between survivors and non-survivors among patients with "renal oligohydramnios" were oligohydramnios detection before 32 weeks GA, dysplasia detection on the second trimester ultrasound, and increase of serum creatinine from day 3 onwards. A higher resolution version of the Graphical abstract is available as Supplementary information.

Indexed as

OligohydramniosPolycystic Kidney DiseasesUrinary TractChildFemaleHumansInfant, NewbornKidneyPregnancyPregnancy Trimester, SecondUltrasonography, PrenatalAntenatal counselingCAKUTOligohydramniosPosterior urethral valvesPrognostic factorsRenal dysplasiaSurvival

Identifiers

PMID36409365
OpenAlexW4309513184

What OpenQuestion holds

Textmetadata
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.