Duffels Mariëlle, van Loon Laura, Berger Rolf, Boonstra Anco, Vonk-Noordegraaf Anton, Mulder Barbara
Academic Medical Center-Department of Cardiology, Amsterdam, The Netherlands.
Congenit Heart Dis. 2007 Jul-Aug;2(4):242-9. doi: 10.1111/j.1747-0803.2007.00104.x.
Pulmonary arterial hypertension (PAH) associated with congenital heart defect (CHD), and especially Eisenmenger syndrome, is associated with impaired exercise tolerance and reduced quality of life. In this study, we describe medium-term follow-up of adult patients with PAH associated with CHD, treated in a single center with different types of advanced medication.
The treatment and clinical course of 15 patients (11 female, median age 53, range 28-74 years) with PAH associated with CHD is retrospectively described. Data on patient characteristics, exercise test, right-heart catheterization, and type of advanced therapy were collected from medical files. Advanced medical therapy consisted of either intravenous prostacyclin, or endothelin receptor antagonists, or phosphodiesterase-5-inhibitors. Additional therapy was started in case of persistent clinical deterioration or insufficient improvement with monotherapy.
All patients (10 patients with Eisenmenger syndrome, 5 patients with a closed defect and PAH) were exposed to different durations of advanced medication. Median period of treatment was 2.5 (range 0.7-6.3) years. Atrial septal defect, type secundum, was the most frequent underlying diagnosis (n = 10). Most patients (n = 9) received a combination of advanced medical therapy. Six-minute walk distance (6-MWD) remained unchanged with an increase of 44 +/- 78 m (P = 0.2) and 41 +/- 80 m (P = 0.3) compared with baseline after respectively 1 and 2 years of treatment. Younger age was associated with better performance (beta = -7 m per year, P < 0.05), patients younger than 45 years showed a greater improvement in 6-MWD after 2 years of treatment (P < 0.05). During a mean follow-up of 23 (range 4-58) months, mean pulmonary arterial pressure (53 +/- 24-49 +/- 17 mmHg, P = 0.3) and pulmonary vascular resistance (770 +/- 1090-650 +/- 444 dynes s/cm5, P = 0.7) showed no deterioration.
Advanced treatment strategies in patients with PAH associated with CHD are useful. The treatment effect seems to be one of disease stabilization and decreasing the rate of deterioration. Younger age was associated with a greater improvement of 6-MWD.
与先天性心脏病(CHD)相关的肺动脉高压(PAH),尤其是艾森曼格综合征,与运动耐量受损和生活质量下降有关。在本研究中,我们描述了在单一中心接受不同类型先进药物治疗的CHD相关PAH成年患者的中期随访情况。
回顾性描述了15例(11例女性,中位年龄53岁,范围28 - 74岁)CHD相关PAH患者的治疗及临床病程。从病历中收集了患者特征、运动试验、右心导管检查及先进治疗类型的数据。先进药物治疗包括静脉注射前列环素、内皮素受体拮抗剂或磷酸二酯酶 - 5抑制剂。若临床持续恶化或单一疗法改善不足,则开始额外治疗。
所有患者(10例艾森曼格综合征患者,5例闭合性缺损合并PAH患者)均接受了不同时长的先进药物治疗。中位治疗期为2.5(范围0.7 - 6.3)年。继发孔型房间隔缺损是最常见的潜在诊断(n = 10)。大多数患者(n = 9)接受了联合先进药物治疗。治疗1年和2年后,六分钟步行距离(6 - MWD)与基线相比分别增加了44±78米(P = 0.2)和41±80米(P = 0.3),但仍无变化。年龄较小与更好的表现相关(β = -7米/年,P < 0.05),45岁以下患者在治疗2年后6 - MWD改善更大(P < 0.05)。在平均23(范围4 - 58)个月的随访期间,平均肺动脉压(53±24 - 49±17 mmHg,P = 0.3)和肺血管阻力(770±1090 - 650±444达因·秒/厘米⁵,P = 0.7)未显示恶化。
CHD相关PAH患者的先进治疗策略是有效的。治疗效果似乎是疾病稳定并降低恶化率。年龄较小与6 - MWD的更大改善相关。