Pulmonary arterial hypertension and pregnancy

被引:0
作者
Terek, Demet [1 ]
Kayikcioglu, Meral [2 ]
Kultursay, Hakan [2 ]
Ergenoglu, Mete [3 ]
Yalaz, Mehmet [1 ]
Musayev, Oktay [2 ]
Mogulkoc, Nesrin [4 ]
Gunusen, Ilkben [5 ]
Akisu, Mete [1 ]
Kultursay, Nilgun [1 ]
机构
[1] Ege Univ, Fac Med, Dept Pediat, Div Neonatol, TR-35100 Izmir, Turkey
[2] Ege Univ, Fac Med, Dept Cardiol, TR-35100 Izmir, Turkey
[3] Ege Univ, Fac Med, Dept Obstet & Gynecol, TR-35100 Izmir, Turkey
[4] Ege Univ, Fac Med, Dept Chest Med, TR-35100 Izmir, Turkey
[5] Ege Univ, Fac Med, Dept Anesthesiol, TR-35100 Izmir, Turkey
来源
JOURNAL OF RESEARCH IN MEDICAL SCIENCES | 2013年 / 18卷 / 01期
关键词
Iloprost; newborn; pregnancy; pulmonary hypertension; sildenafil; survival; therapy; THERAPY; DISEASE;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This is the case report of a pregnant woman who refused pregnancy termination when diagnosed with pulmonary arterial hypertension (PAH) functional class 2-3 at the 24th week of gestation and of her newborn. A pregnant woman with PAH functional class 2-3 was treated with inhaled prostacyclin analog ( iloprost), oral sildenafil, oxygen, and low molecular weight heparin. She delivered at 32nd week by Cesarean section. The infant required oxygen up to 36th week postconceptional age and had a short steroid treatment. The mother needed close cardiovascular monitorization, intensive oxygen and pulmonary vasodilator therapy for 2 months and was discharged with oxygen and oral iloprost treatment. A multidisciplinary approach together with pulmonary vasodilator therapy may be succesful in such a high-risk pregnant woman.
引用
收藏
页码:73 / 76
页数:4
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