{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,23]],"date-time":"2026-09-23T20:06:01Z","timestamp":1790193961473,"version":"4.1.0"},"reference-count":29,"publisher":"SAGE Publications","issue":"2","license":[{"start":{"date-parts":[[2015,3,22]],"date-time":"2015-03-22T00:00:00Z","timestamp":1426982400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Obstet Med"],"published-print":{"date-parts":[[2015,6]]},"abstract":"<jats:sec><jats:title>Background<\/jats:title><jats:p> Cystic fibrosis manifests as a multisystem disease, despite this female fertility is relatively preserved with levels approaching that of the non-cystic fibrosis population. We reviewed pregnancies in cystic fibrosis patients over a 10-year period from a UK adult cystic fibrosis centre by considering maternal and fetal outcomes. <\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p> We conducted a retrospective case-note review of pregnancies during 2003\u20132013 using respiratory and obstetric records. <\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p> We observed moderate falls in lung function immediately after delivery, which persisted at 12 months postpartum. We found that a decline in lung function at delivery was a marker for further decline in function during the subsequent postpartum period. We found baseline lung function was predictive of gestational age at delivery. We observed a high incidence of haemoptysis. <\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p> Consistent with current guidance we found pregnancy is feasible and well tolerated in the majority of patients with cystic fibrosis. There was a high incidence of haemoptysis, which warrants further study. <\/jats:p><\/jats:sec>","DOI":"10.1177\/1753495x15575628","type":"journal-article","created":{"date-parts":[[2015,3,24]],"date-time":"2015-03-24T00:13:27Z","timestamp":1427156007000},"page":"99-101","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":19,"title":["Pregnancy outcomes in cystic fibrosis: a 10-year experience from a UK centre"],"prefix":"10.1177","volume":"8","author":[{"given":"M","family":"Renton","sequence":"first","affiliation":[{"name":"St John\u2019s College, University of Oxford, Oxford, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L","family":"Priestley","sequence":"additional","affiliation":[{"name":"Oxford University Hospitals NHS Trust, Oxford, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L","family":"Bennett","sequence":"additional","affiliation":[{"name":"Oxford University Hospitals NHS Trust, Oxford, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L","family":"Mackillop","sequence":"additional","affiliation":[{"name":"Oxford University Hospitals NHS Trust, Oxford, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"SJ","family":"Chapman","sequence":"additional","affiliation":[{"name":"Oxford University Hospitals NHS Trust, Oxford, UK"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2015,3,22]]},"reference":[{"key":"bibr1-1753495X15575628","doi-asserted-by":"publisher","DOI":"10.1136\/bmj.39391.713229.AD"},{"key":"bibr2-1753495X15575628","doi-asserted-by":"publisher","DOI":"10.1016\/S0140-6736(09)60327-5"},{"key":"bibr3-1753495X15575628","unstructured":"Cystic Fibrosis Trust. 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