Evidence map›Paper›PMID 40457440›Full record

ArticleReproductive biology and endocrinology : RB&E2025

Fertility and family-building experiences and perspectives of males with cystic fibrosis.

Ishaan Jathal, Olivia M Stransky, Catherine E Wright, Asher Prangley, Vin Tangpricha, Raksha Jain, Jennifer L Taylor-Cousar, Kara S Hughan, Sigrid Ladores-Barrett, Natalie E West and 2 more

Abstract read
In one paragraph

Article in Reproductive biology and endocrinology : RB&E, 2025. 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
–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

1 citing paper in PubMed.

  1. Review
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.

Ishaan JathalDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Olivia M StranskyDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Catherine E WrightUniversity of Washington School of Public Health, Seattle, WA, USA.
Asher PrangleyDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Vin TangprichaDivision of Endocrinology, Metabolism, and Lipids, Department of Medicine, Emory University School of Medicine, Atlanta, GA, USA.
Raksha JainInternal Medicine, Pulmonary and Critical Care, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Jennifer L Taylor-CousarNational Jewish Health, Internal Medicine and Pediatrics, Pulmonary, Denver, CO, USA.
Kara S HughanDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Sigrid Ladores-BarrettUniversity of Nevada Las Vegas School of Nursing, Las Vegas, NV, USA.
Natalie E WestDepartment of Medicine, Johns Hopkins University, Baltimore, MD, USA.
Gregory S SawickiBoston Children's Hospital, Boston, MA, USA.
Traci M KazmerskiDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA. traci.kazmerski@chp.edu.

Funding

Cystic Fibrosis Foundation KAZMER21A0
6 · The paper itself

Abstract

backgroundNearly all males with cystic fibrosis (MwCF) are infertile and, thus, require the use of assisted reproductive technology (ART) to have biologic children. This study aims to describe the fertility and family-building knowledge, experiences, and care utilization of this population and to compare these findings to the general United States (US) population.

methodsWe conducted an anonymous cross-sectional study of self-reported survey data compared to data from the 2017-2019 US National Survey for Family Growth (NSFG). We recruited MwCF age 15 years and older at seven US cystic fibrosis (CF) centers.

resultsA total of 532 MwCF (mean age 35.3 ± 11.6 years) completed the survey. 83% knew that almost all MwCF are infertile and 84% were aware that MwCF can have biological children. 71% correctly identified the most common cause of male CF infertility. One third of MwCF stated they had never been told by anyone they were infertile due to their CF (mean age of discussion 19.3 ± 8.8 years). 31% reported being a parent. Among parents, 66% were a parent to a biological child born of a partner's pregnancy, 20% via step-parenthood, 15% adoption, 4.3% surrogacy, and 0.6% foster parenthood. Compared to 44% of NSFG males, 18% of MwCF age 15-49 years reported being a parent to a biological child born of their partner's pregnancy (p < 0.001). Among all MwCF, 82% with a biological child reported that they required medical assistance. Among those age 15-49 years, 87% of MwCF with a biological child required medical assistance compared to 9.4% of NSFG males (p < 0.001). Nearly three-quarters (73%) of MwCF who were biological parents underwent sperm retrieval via a variety of extraction techniques. 91% of those utilizing ART underwent in vitro fertilization and 9% intrauterine insemination of their partner.

conclusionsMwCF face significant disease-related fertility and family-building implications with suboptimal counseling. Most MwCF who are parents pursue biological parenthood via a variety of ART services, but one-third chose alternative paths to parenthood. Further research is needed to best understand and support the family-building of MwCF. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Cystic FibrosisFertilityHealth Knowledge, Attitudes, PracticeInfertility, MaleReproductive Techniques, AssistedAdolescentAdultCross-Sectional StudiesFemaleHumansMaleMiddle AgedPregnancySurveys and QuestionnairesUnited StatesYoung AdultAssisted reproductive technologyCystic fibrosisMale infertilityParenthood

Identifiers

PMID40457440
PMCPMC12128490

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.