Clinical implications of haemoptysis in patients with pulmonary arterial hypertension.

Clinical implications of haemoptysis in patients with pulmonary arterial hypertension.
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DOI:
10.1111/ijcp.12004
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发表时间:
2012-10
期刊:
International journal of clinical practice. Supplement
影响因子:
--
通讯作者:
Safdar Z
Safdar Z
中科院分区:
其他
文献类型:
--
作者:
Cantu J;Wang D;Safdar Z

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肺动脉高压(PAH)是一种致残疾病,可导致咯血。与以咯血为表现的其他类型PAH患者相比,先天性心脏病相关PAH患者(CHD-APAH)可能具有生存优势。PAH患者咯血的病因和后续治疗选择的影响尚不明确。我们对到卫理公会医院就诊的伴有咯血的冠心病- apah与所有其他亚型PAH患者进行了结果分析。21例患者,冠心病- apah组13例,非冠心病组8例。我们评估了该队列中与治疗相关的结果(支气管动脉栓塞与保守治疗)、住院时间、死亡率和生存率。CHD-APAH组和非chd组具有相似的基线人口统计学、血流动力学和实验室值,只是非chd组的BMI更高,CHD-APAH组的红细胞压积更高。与非冠心病组相比,冠心病- apah患者28天死亡率(0%对31%)和1年死亡率(0%对54%)较低。冠心病- apah组总随访期生存率差异有统计学意义(p = 0.02)。虽然无统计学意义,但BAE患者的住院时间较短(4.0天±4.0比13.7天±22.5;p = 0.26)。在接受BAE治疗的患者中,有43%的患者再次咯血。PAH患者咯血是一种严重的疾病,死亡率很高。冠心病- apah似乎具有生存优势,与所采用的治疗方法无关。除频繁的再出血发作外,BAE咳血终止迅速,并发症相对较少。需要进一步的研究来确定可能使PAH患者因咯血而死亡率过高的危险因素,并确定最佳的治疗方式。
Pulmonary arterial hypertension (PAH) is a disabling disease that may result in haemoptysis. Patients with congenital heart disease associated PAH (CHD-APAH) may have a survival advantage when compared with patients with other types of PAH presenting with haemoptysis. The effects of aetiology and sub-sequent management choice of haemoptysis in PAH patients is not well-defined. We conducted outcome analysis in CHD-APAH vs. all other subtypes of PAH patients presenting with haemoptysis to The Methodist Hospital. Twenty-one patients were identified, thirteen patients in the CHD-APAH group and eight patients in the non-CHD group. We evaluated outcomes related to treatment (bronchial artery embolization vs. conservative management), hospital length of stay, mortality rates and survival in this cohort. The CHD-APAH and non-CHD groups had similar baseline demographic, haemodynamic and laboratory values except BMI was higher in the non-CHD group and haematocrit was higher in the CHD-APAH group. Twenty-eight-day mortality (0% vs. 31%) and 1-year mortality (0% vs. 54%) was lower in the CHD-APAH patients as compared with non-CHD group. A statistically significant difference was found in the survival rate in favour of CHD-APAH group for the total follow-up period (p = 0.02). Although not statistically significant, patients treated with BAE had shorter length of stay (4.0 days ± 4.0 vs. 13.7 days ± 22.5; p = 0.26). There was recurrent haemoptysis in 43% of patients treated with BAE. Haemoptysis in PAH patients is a serious event with a high mortality rate. CHD-APAH seems to confer a survival advantage, independent of therapy utilised. Termination of haemoptysis with BAE is rapid with relatively few complications except for frequent re-bleeding episodes. Further studies are needed to determine the risk factors that may predispose PAH patients to excessive mortality from haemoptysis and to identify an optimal therapeutic modality.
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