Kurzyna Marcin, Zyłkowska Joanna, Fijałkowska Anna, Florczyk Michał, Wieteska Maria, Kacprzak Aneta, Burakowski Janusz, Szturmowicz Monika, Wawrzyńska Liliana, Torbicki Adam
Department of Chest Medicine, Institute of Tuberculosis and Lung Diseases, Warsaw, Poland.
Kardiol Pol. 2008 Oct;66(10):1033-9; discussion 1040-1.
New therapies for pulmonary arterial hypertension have prolonged survival but simultaneously increased the number of hospital admissions because of decompensated right heart failure (DRHF). The optimal approach in DRHF has not been established yet.
Analysis of clinical course of DRHF in a group of patients with pulmonary hypertension treated in a single referral centre.
We retrospectively analysed 60 episodes of DRHF in 37 patients (29 females, mean age 44+/-17 years) with pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension admitted to our hospital between 2005 and 2007. We assessed the cause of decompensation, vital signs at admission, functional class and laboratory values. We classified all episodes into four haemodynamic profiles using the value of systolic blood pressure together with presence of peripheral perfusion abnormalities (profile cold vs. warm) and symptoms of venous congestion (profile wet vs. dry). Primary end-point was in-hospital mortality.
The most common causes of DRHF were infection (27%), drug noncompliance (20%), and pulmonary embolism (3%). In 48% no causative factor was indentified. There were 19 (32%) in-hospital deaths. The highest mortality was observed among patients with connective tissue disease (61%). The haemodynamic profile 'warm-wet' was the most common (48%) and the profile 'cold-dry' was the rarest but was associated with a 100% mortality. Patients who died had higher value of functional class (3.84+/-0.38 vs. 3.51+/-0.55, p=0.01) and higher activity of aspartate transaminase (61+/-61 vs. 42+/-78 U/l, p=0.02) compared with those who survived. In multivariate analysis higher dopamine dose (RR 2.0/1 microg/kg/min, 95% CI 1.00-5.00, p <0.001) was an independent factor of in-hospital death. In contrast 'rescue therapy' with iloprost or treprostinil decreased mortality (RR 0.09, 95% CI 0.01-0.99, p=0.04). Mortality in patients receiving dopamine was higher (60 vs. 18%, p=0.001) than in patients treated without dopamine.
Mortality in patients with pulmonary hypertension and DRHF remains very high and seems to be related to haemodynamic profile on admission. The newly introduced therapy with parenteral prostanoids may be more beneficial than dopamine infusion.
肺动脉高压的新疗法延长了患者生存期,但同时因右心衰竭失代偿(DRHF)导致的住院次数增加。目前尚未确定DRHF的最佳治疗方法。
分析在单一转诊中心接受治疗的一组肺动脉高压患者中DRHF的临床病程。
我们回顾性分析了2005年至2007年间我院收治的37例(29例女性,平均年龄44±17岁)肺动脉高压和慢性血栓栓塞性肺动脉高压患者的60次DRHF发作。我们评估了失代偿的原因、入院时的生命体征、功能分级和实验室检查值。我们根据收缩压值以及外周灌注异常情况(冷型与暖型)和静脉充血症状(湿型与干型)将所有发作分为四种血流动力学类型。主要终点是住院死亡率。
DRHF最常见的原因是感染(27%)、药物治疗依从性差(20%)和肺栓塞(3%)。48%的病例未发现致病因素。有19例(32%)住院死亡。结缔组织病患者的死亡率最高(61%)。“暖-湿”血流动力学类型最常见(48%),“冷-干”类型最罕见,但死亡率为100%。死亡患者的功能分级值较高(3.84±0.38对3.51±0.55,p=0.01),天冬氨酸转氨酶活性较高(61±61对42±78 U/l,p=0.02),与存活患者相比。多因素分析显示,较高的多巴胺剂量(RR 2.0/1微克/千克/分钟,95%可信区间1.00-5.00,p<0.001)是住院死亡的独立因素。相比之下,用伊洛前列素或曲前列尼尔进行“挽救治疗”可降低死亡率(RR 0.09,95%可信区间0.01-0.99,p=0.04)。接受多巴胺治疗的患者死亡率较高(60%对18%,p=0.001),高于未接受多巴胺治疗的患者。
肺动脉高压合并DRHF患者的死亡率仍然很高,似乎与入院时的血流动力学类型有关。新引入的胃肠外前列腺素类药物治疗可能比多巴胺输注更有益。