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肺动脉高压药物治疗后动脉血氧饱和度降低患者的结局。

Outcomes of patients with decreased arterial oxyhaemoglobin saturation on pulmonary arterial hypertension drugs.

机构信息

Pôle des Spécialités Médicales/Département de Pneumologie, CHRU de Nancy, Vandœuvre-lès-Nancy, France.

Faculté de Médecine de Nancy, INSERM UMR_S 1116, Université de Lorraine, Vandœuvre-lès-Nancy, France.

出版信息

Eur Respir J. 2021 Nov 4;58(5). doi: 10.1183/13993003.04066-2020. Print 2021 Oct.

Abstract

BACKGROUND

Drugs approved for the treatment of pulmonary arterial hypertension (PAH) improve long-term outcomes. These drugs have pulmonary vasodilator properties which may potentially cause a decrease in arterial oxyhaemoglobin saturation ( ) in some patients. The present retrospective study of the French Pulmonary Hypertension Registry aimed to describe the clinical characteristics and outcomes of patients showing a ≥3% decrease in while treated with PAH drugs.

METHODS

We reviewed 719 PAH patients. The exclusion criteria were PAH associated with congenital heart disease and PAH with overt features of venous/capillaries involvement.

RESULTS

173 (24%) patients had a ≥3% decrease in . At diagnosis, they were older with a lower diffusing capacity of the lung for carbon monoxide and a shorter 6-min walk distance compared with those who did not display a ≥3% decrease in . The percentage of patients meeting the European Society of Cardiology/European Respiratory Society (ESC/ERS) low-risk criteria at re-evaluation was significantly lower in those with a ≥3% decrease in and more patients started long-term oxygen therapy in this group (16% 5%; p<0.001). A ≥3% decrease in was associated with a poorer survival (hazard ratio 1.81, 95% CI 1.43-2.34; p<0.0001). In a multivariate Cox analysis, a ≥3% decrease in was a prognostic factor independent of age at diagnosis and ESC/ERS risk stratification at follow-up.

CONCLUSIONS

When treated with PAH drugs, a large subset of patients experience a ≥3% decrease in , which is associated with worse long-term outcomes and reduced survival.

摘要

背景

已批准用于治疗肺动脉高压 (PAH) 的药物可改善长期预后。这些药物具有肺血管扩张特性,可能会导致部分患者动脉血氧饱和度( )下降。本研究回顾性分析了法国肺动脉高压登记处的数据,旨在描述接受 PAH 药物治疗时 下降≥3%的患者的临床特征和结局。

方法

我们回顾了 719 名 PAH 患者。排除标准为先天性心脏病相关 PAH 和静脉/毛细血管受累明显的 PAH。

结果

173 名(24%)患者 下降≥3%。在诊断时,与未出现 下降≥3%的患者相比,他们年龄更大,一氧化碳弥散量更低,6 分钟步行距离更短。在重新评估时,符合欧洲心脏病学会/欧洲呼吸学会(ESC/ERS)低危标准的患者比例在 下降≥3%的患者中显著降低,且该组患者更开始接受长期氧疗(16% 5%;p<0.001)。 下降≥3%与生存较差相关(风险比 1.81,95%CI 1.43-2.34;p<0.0001)。在多变量 Cox 分析中, 下降≥3%是独立于诊断时年龄和随访时 ESC/ERS 风险分层的预后因素。

结论

在接受 PAH 药物治疗时,相当一部分患者 下降≥3%,这与较差的长期结局和生存率降低有关。

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