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dc.contributor.authorTokgöz, Hacer Ceren
dc.contributor.authorAkbal, Özgür Yaşar
dc.contributor.authorKaragöz, Ali
dc.contributor.authorKültürsay, Barkın
dc.contributor.authorTanyeri, Seda
dc.contributor.authorKeskin, Berhan
dc.contributor.authorHakgör, Aykun
dc.contributor.authorKülahçıoğlu, Şeyhmus
dc.contributor.authorBayram, Zübeyde
dc.contributor.authorEfe, Süleyman Çağan
dc.contributor.authorDoğan, Cem
dc.contributor.authorTanboğa, İbrahim Halil
dc.date.accessioned2022-12-09T10:38:13Z
dc.date.available2022-12-09T10:38:13Z
dc.date.issued2022en_US
dc.identifier.citationTokgöz, H. C., Akbal, Ö. Y., Karagöz, A., Kültürsay, B., Tanyeri, S., Keskin, B. ... Tanboğa, İ. H. (2022). Maternal and fetal outcomes in pregnant women with pulmonary arterial hypertension: A single-center experience and review of current literature. Anatolian Journal of Cardiology, 26(12), 902-913. https://doi.org/10.5152/AnatolJCardiol.2022.1762en_US
dc.identifier.issn2149-2271
dc.identifier.issn2149-2263
dc.identifier.urihttps://doi.org/10.5152/AnatolJCardiol.2022.1762
dc.identifier.urihttps://hdl.handle.net/20.500.12511/10103
dc.description.abstractBACKGROUND: Although pregnancy in women with pulmonary arterial hypertension has been considered a high-risk condition, current data regarding pregnancy with pulmonary arterial hypertension are scarce. In this study, we aimed to evaluate our single-center data on maternal and fetal outcomes in pregnant women with PAH and review currently available risk-based management strategies. METHODS: Our single-center study group comprised 35 women who became pregnant after the diagnosis of pulmonary arterial hypertension or in whom pulmonary arterial hypertension was diagnosed within early post-partum period. Clinical, laboratory, echocardiographic, and hemodynamic characteristics of pregnant and non-pregnant productive women with pulmonary arterial hypertension were compared, and similar comparison was also repeated for survivors and non-survivors in pregnant patient group. RESULTS: Pregnancy was noted in 15% of the 228 females with pulmonary arterial hypertension who were of hormonally productive ages, generally well-tolerated until delivery. Elective abortion and pre-term delivery were documented in 1 (2.8%) and 12 (35.3%) pregnant women, respectively. Switching to sildenafil was the standard medication during pregnancy. Cesarian section was the preferred method of delivery in all pregnant women with pulmonary arterial hypertension and was performed without any complication. Clinic deteoriation within the first week of delivery was observed in 5 (41.6%) patients. Maternal mortality was noted in 13 (37.1%) patients and was documented to cumulate within the first month of delivery. However, any sign predicting post-partum clinical deterioration was not found. No fetal mortality was observed. CONCLUSION: Despite the development of advanced therapies, pregnancy in pulmonary arterial hypertension still carries a high mortality risk and requires multi-disciplinary expert center care with more proactive management strategies.en_US
dc.language.isoengen_US
dc.publisherNLM (Medline)en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.rightsAttribution-NonCommercial 4.0 International*
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/*
dc.subjectPulmonary Arterial Hypertensionen_US
dc.subjectMortalityen_US
dc.subjectPregnancyen_US
dc.titleMaternal and fetal outcomes in pregnant women with pulmonary arterial hypertension: A single-center experience and review of current literatureen_US
dc.typearticleen_US
dc.relation.ispartofAnatolian Journal of Cardiologyen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Kardiyoloji Ana Bilim Dalıen_US
dc.authorid0000-0001-6560-6503en_US
dc.identifier.volume26en_US
dc.identifier.issue12en_US
dc.identifier.startpage902en_US
dc.identifier.endpage913en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.5152/AnatolJCardiol.2022.1762en_US
dc.institutionauthorHakgör, Aykun
dc.identifier.wosqualityQ4en_US
dc.identifier.wos000910895300008en_US
dc.identifier.scopus2-s2.0-85142941116en_US
dc.identifier.trdizinid1168782en_US
dc.identifier.pmid35983602en_US
dc.identifier.scopusqualityQ3en_US


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