Pregnancy in Cystic Fibrosis-Past, Present, and Future.

J Clin Med

Pediatric Pulmonary Institute and CF Center, Rappaport Children's Hospital, Rambam Health Care Campus, Haifa 3109601, Israel.

Published: February 2023

AI Article Synopsis

  • The introduction of mutation-specific therapies has transformed cystic fibrosis from a severe, life-limiting disease into a manageable condition with better quality of life and the possibility of adulthood.
  • New challenges have emerged regarding fertility, pregnancy care, and postpartum issues for CF patients, highlighting the need for comprehensive support during these stages.
  • While CFTR modulators show promise for improving lung function in CF, there is still limited data on their safety during pregnancy, prompting ongoing research for better outcomes for both mothers and babies.

Article Abstract

The introduction of mutation-specific therapy led to a revolution in cystic fibrosis (CF) care. These advances in CF therapies have changed the disease profile from a severe incurable disease with limited survival to a treatable disease with improved quality of life and survival into adulthood. CF patients are now able to plan their future, including marriage and parenthood. Side by side with the optimism, new issues and concerns are arising, including fertility and preparation for pregnancy, maternal and fetal care during pregnancy, and post-partum care. While cystic fibrosis transmembrane regulator (CFTR) modulators show promising results for improving CF lung disease, data on their safety in pregnancy are still limited. We performed a literature review on pregnancy in CF from the past, with the first described pregnancy in 1960, through the current fascinating changes in the era of CFTR modulators, to ongoing studies and future directions. Current advances in knowledge give hope for improved outcomes of pregnancy, towards the best possible prognosis for the mother and for the baby.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9963833PMC
http://dx.doi.org/10.3390/jcm12041468DOI Listing

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