A provider survey assessing fetal impact of CFTR modulator use in males with CF during assisted and unassisted reproduction and partner pregnancy
Jennifer L. Taylor-Cousar
1, 2
,
Rachel Janney
3
,
Peter Hugh Middleton
4
,
Raksha Jain
5
,
Julia Nightingale
6
,
Natalie E. West
7
,
Michal Shteinberg
8, 9
,
Danielle Velez
10
,
Traci M. Kazmerski
11, 12
6
University Hospital Southhampton NHS Trust
11
Center for Innovative Research on Gender Health Equity (CONVERGE)
Publication type: Journal Article
Publication date: 2024-05-01
scimago Q1
wos Q1
SJR: 1.772
CiteScore: 10.0
Impact factor: 6.0
ISSN: 15691993, 18735010
PubMed ID:
37953181
Pulmonary and Respiratory Medicine
Pediatrics, Perinatology and Child Health
Abstract
Most males with cystic fibrosis (mwCF) are infertile but with CF transmembrane conductance regulator (CFTR) modulator-conferred benefits, more are utilizing assisted reproductive technologies (ART). Administration of normal human doses of modulators in animal reproductive models caused no genotoxicity; no human data exists. Potential health decline following modulator discontinuation makes the decision to withhold therapy during reproduction challenging.From August-October 2021, international CF clinicians completed an anonymous questionnaire regarding mwCF who used modulators during reproduction.We received 42 surveys for mwCF with partner pregnancies. Forty of 42 mwCF utilized ART; 35 continued modulators during sperm retrieval and 40/42 during partner pregnancy. One of four males who discontinued modulators experienced clinical deterioration. First trimester miscarriages occurred in 11.9 % of partner pregnancies. No congenital anomalies were reported.Use of CFTR modulators during reproduction and partner pregnancy in mwCF did not result in a higher-than-expected miscarriage rate nor congenital anomalies.
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Metrics
8
Total citations:
8
Citations from 2024:
8
(100%)
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GOST
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Taylor-Cousar J. L. et al. A provider survey assessing fetal impact of CFTR modulator use in males with CF during assisted and unassisted reproduction and partner pregnancy // Journal of Cystic Fibrosis. 2024. Vol. 23. No. 3. pp. 412-416.
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Taylor-Cousar J. L., Janney R., Middleton P. H., Jain R., Nightingale J., West N. E., Shteinberg M., Velez D., Kazmerski T. M. A provider survey assessing fetal impact of CFTR modulator use in males with CF during assisted and unassisted reproduction and partner pregnancy // Journal of Cystic Fibrosis. 2024. Vol. 23. No. 3. pp. 412-416.
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RIS
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TY - JOUR
DO - 10.1016/j.jcf.2023.10.022
UR - https://linkinghub.elsevier.com/retrieve/pii/S1569199323016673
TI - A provider survey assessing fetal impact of CFTR modulator use in males with CF during assisted and unassisted reproduction and partner pregnancy
T2 - Journal of Cystic Fibrosis
AU - Taylor-Cousar, Jennifer L.
AU - Janney, Rachel
AU - Middleton, Peter Hugh
AU - Jain, Raksha
AU - Nightingale, Julia
AU - West, Natalie E.
AU - Shteinberg, Michal
AU - Velez, Danielle
AU - Kazmerski, Traci M.
PY - 2024
DA - 2024/05/01
PB - Elsevier
SP - 412-416
IS - 3
VL - 23
PMID - 37953181
SN - 1569-1993
SN - 1873-5010
ER -
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BibTex (up to 50 authors)
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@article{2024_Taylor-Cousar,
author = {Jennifer L. Taylor-Cousar and Rachel Janney and Peter Hugh Middleton and Raksha Jain and Julia Nightingale and Natalie E. West and Michal Shteinberg and Danielle Velez and Traci M. Kazmerski},
title = {A provider survey assessing fetal impact of CFTR modulator use in males with CF during assisted and unassisted reproduction and partner pregnancy},
journal = {Journal of Cystic Fibrosis},
year = {2024},
volume = {23},
publisher = {Elsevier},
month = {may},
url = {https://linkinghub.elsevier.com/retrieve/pii/S1569199323016673},
number = {3},
pages = {412--416},
doi = {10.1016/j.jcf.2023.10.022}
}
Cite this
MLA
Copy
Taylor-Cousar, Jennifer L., et al. “A provider survey assessing fetal impact of CFTR modulator use in males with CF during assisted and unassisted reproduction and partner pregnancy.” Journal of Cystic Fibrosis, vol. 23, no. 3, May. 2024, pp. 412-416. https://linkinghub.elsevier.com/retrieve/pii/S1569199323016673.