Evidence map›Paper›PMID 35265034›Full record

ArticleFrontiers in endocrinology2022

The Prognosis of ART Is Not Altered in Cystic Fibrosis Women: A Case-Report Study.

Inès Braham, Adeline Morisot, Samir Boukaïdi, Marie Perceval, Isabelle Durieu, Christine Rousset-Jablonski, Sylvie Hieronimus, Sylvie Leroy, Nicolas Chevalier

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 54% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

9 authors at 3 institutions in 1 country.

Inès BrahamUniversité Côte d'Azur, CHU de Nice, Département d'Endocrinologie-Diabétologie et Reproduction, Nice, France.
Adeline MorisotUniversité Côte d'Azur, CHU de Nice, Département de Santé Publique, Nice, France.
Samir BoukaïdiUniversité Côte d'Azur, CHU de Nice, Centre d'aide médicale à la procréation, Nice, France.
Marie PercevalHospices Civils de Lyon, CHU de Lyon, Centre de Ressources et de Compétences de la Mucoviscidose, Lyon, France.
Isabelle DurieuHospices Civils de Lyon, CHU de Lyon, Centre de Ressources et de Compétences de la Mucoviscidose, Lyon, France.
Christine Rousset-JablonskiHospices Civils de Lyon, CHU de Lyon, Service de gynécologie-obstétrique, Lyon, France.
Sylvie HieronimusUniversité Côte d'Azur, CHU de Nice, Département d'Endocrinologie-Diabétologie et Reproduction, Nice, France.
Sylvie LeroyUniversité Côte d'Azur, CHU de Nice, Centre de Ressources et de Compétences de la Mucoviscidose, Nice, France.
Nicolas ChevalierUniversité Côte d'Azur, CHU de Nice, Département d'Endocrinologie-Diabétologie et Reproduction, Nice, France.
Centre Hospitalier Universitaire de Nice · FRHospices Civils de Lyon · FRUniversité Côte d'Azur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Research Question: Unlike in men, a very limited number of studies were focused on the specificity of ART management of cystic fibrosis (CF) in women. The purpose of this study was to determine the causes of infertility in patients, the appropriate ART treatment, and their prognosis in terms of pregnancy. Design: We conducted a multicentre analytical case-control study including CF women who were age-matched to non-CF women. We reported the causes of infertility, the ART management type and pregnancy outcomes. Results: 17 cases were compared to 34 controls. There was no significant difference between the groups concerning cause infertility. There was a non-statistically significant trend with a lower antral follicle count in CF compared to controls (19.5 versus 26.8, p=0.08). IUI seemed to be as successful as IVF/ICSI in CF as opposed to controls where the IVF/ICSI was the most effective (in CF group for HCG >100 UI/L: 38.8% vs. 36.8%, p=0.4175). There were more embryos obtained in CF than in controls (3.1 versus 1.6, p=0.02). The number of oocytes and embryos obtained and pregnancy outcomes remained similar between DF508 homozygous group and others CFTR mutations group. The results of ART procedures and pregnancy evolution were not influenced by FEV1. Conclusion: In absence of any other pathology, IUI may be first option for CF women. If insemination fails, IVF with a low dose of gonadotropins may be more appropriate to prevent the risk of hyperstimulation syndrome. FEV1 and genetic do not seem to be contributing factors in the prognosis of ART.

Indexed as

Cystic FibrosisInfertilityCase-Control StudiesFemaleHumansOocytesPregnancyPregnancy Outcomeassisted reproductive techniquescystic fibrosisfemaleinfertilitypregnancypregnancy outcome

Identifiers

PMID35265034
PMCPMC8898889
OpenAlexW4213160584

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.