Evidence map›Paper›PMID 41892019›Full record

ArticleInternational journal of neonatal screening2026

Exposure to CFTR Modulators During Pregnancy in Cystic Fibrosis: Four Cases to Highlight Neonatal Diagnostic Challenges and Outcomes.

Louis Domenach, Adrien Pagin, Camille Cisterne, Marie-Pierre Audrezet, Laure Couderc, Laetitia Monteil, Léa Roditis, Marlène Murris, Julie Macey, Michael Fayon and 2 more

Abstract readCase Reports
In one paragraph

Article in International journal of neonatal screening, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Louis DomenachLaboratoire de Génétique Moléculaire, CHU de Bordeaux, 33076 Bordeaux Cedex, France.ORCID 0009-0004-5885-0179
Adrien PaginService de Toxicologie et Génopathies, CHU de Lille, 59037 Lille, France.ORCID 0000-0001-5350-9263
Camille CisterneService de Pneumologie-Allergologie Pédiatrique, CHU de Lille, 59037 Lille, France.ORCID 0009-0002-9342-2124
Marie-Pierre AudrezetLaboratoire de Génétique Moléculaire, CHU de Brest, 29609 Brest, France.ORCID 0000-0003-0161-9473
Laure CoudercCRCM Pédiatrique, Département de Pédiatrie Médicale, CHU de Rouen, 76031 Rouen, France.
Laetitia MonteilService de Génétique Médicale, CHU de Toulouse, 31300 Toulouse, France.
Léa RoditisCRCM Pédiatrique, Service de Pneumo-Allergologie Pédiatrique, CHU de Toulouse, 31059 Toulouse, France.
Marlène MurrisCRCM Adulte, Service de Pneumologie-Allergologie, CHU de Toulouse, 31059 Toulouse, France.
Julie MaceyCRCM Adulte, Service de Pneumologie, CHU de Bordeaux, 33600 Pessac, France.
Michael FayonDépartement de Pédiatrie, CIC-P INSERM 1401, Centre de Recherche Cardio-Thoracique de Bordeaux, INSERM U1045, CHU Bordeaux & Université de Bordeaux, 33000 Bordeaux, France.ORCID 0000-0002-1238-2128
Stéphanie BuiDépartement de Pédiatrie, CIC-P INSERM 1401, Centre de Recherche Cardio-Thoracique de Bordeaux, INSERM U1045, CHU Bordeaux & Université de Bordeaux, 33000 Bordeaux, France.ORCID 0000-0003-3576-2518
Marie-Pierre ReboulLaboratoire de Génétique Moléculaire, CHU de Bordeaux, 33076 Bordeaux Cedex, France.ORCID 0009-0002-1779-4882

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CFTR modulators have transformed the clinical evolution of patients with CF. The number of pregnancies is increasing in women with CF, most of whom are now treated with CFTR modulators such as elexacaftor/tezacaftor/ivacaftor (ETI) or Tezacaftor/Ivacaftor. This raises some questions as we still lack data on foetal and maternal safety. The preliminary data seem to support the continuation of modulators. Some of these mothers may also give birth to newborns with CF and this raises more questions. We report here four cases of CF newborns whose mothers were treated with CFTR modulators throughout pregnancy to help refine potential foetal outcomes of in utero administration of CF modulators. No maternal or foetal complications could be attributed to CFTR modulators. Three CF newborns were exposed to ETI and were false negative of the newborn screening. Two of them were pancreatic sufficient at birth. The remaining patient, exposed to Tezacaftor/Ivacaftor (TI) alone, showed elevated immunoreactive trypsin (IRT) and severe pancreatic insufficiency at birth. These cases highlight that in utero administration of ETI could potentially improve neonatal outcomes of CF newborns and cause newborn screening false negative.

Indexed as

case reportsCFTRCFTR modulatorscystic fibrosisnewborn screeningpregnancies

Identifiers

PMID41892019
PMCPMC13026445

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.