求助 原发性肺动脉高压# WaterWorld - 未名水世界
l*3
1 楼
同学的儿子在国内检查出的毛病，原发性肺动脉高压或者叫做 特发性肺动脉高压，国
内很难治疗，同学一家伤心，崩溃，接受事实。现在孩子高一，同学已经办好EB5，准
备落户东湾，请教大家哪里医院可以治疗这病啊？
内很难治疗，同学一家伤心，崩溃，接受事实。现在孩子高一，同学已经办好EB5，准
备落户东湾，请教大家哪里医院可以治疗这病啊？
a*r
2 楼
再生一个吧。
IPAH has no cure. Untreated IPAH leads to right-sided heart failure and
death. Prior to the 1990s, therapeutic options were limited. The emergence
of prostacyclin analogues, endothelin receptor antagonists,
phosphodiesterase-5 inhibitors, and other novel drug therapies has greatly
improved the outlook for patients with IPAH and IPAH-like diseases.
For untreated IPAH, the estimated 3-year survival rate is approximately 41%.
In one study of long-term continuous intravenous prostacyclin therapy, 3-
year survival increased to approximately 63%.[15] With newer therapies,
perhaps in combination, these figures are expected to improve further.
IPAH has no cure. Untreated IPAH leads to right-sided heart failure and
death. Prior to the 1990s, therapeutic options were limited. The emergence
of prostacyclin analogues, endothelin receptor antagonists,
phosphodiesterase-5 inhibitors, and other novel drug therapies has greatly
improved the outlook for patients with IPAH and IPAH-like diseases.
For untreated IPAH, the estimated 3-year survival rate is approximately 41%.
In one study of long-term continuous intravenous prostacyclin therapy, 3-
year survival increased to approximately 63%.[15] With newer therapies,
perhaps in combination, these figures are expected to improve further.
l*3
3 楼
谢谢auger回复！
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