Mathai Stephen C, Suber Tomeka, Khair Rubina M, Kolb Todd M, Damico Rachel L, Hassoun Paul M
1 Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland; and.
2 Division of Pulmonary, Allergy, and Critical Care Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Ann Am Thorac Soc. 2016 Jan;13(1):31-9. doi: 10.1513/AnnalsATS.201412-572OC.
Pulmonary arterial hypertension is a progressive disease with high morbidity and mortality despite advances in medical therapy. The relationship between patient-related outcomes, such as health-related quality of life (HRQOL), and survival is not well described.
To assess the relationship between HRQOL and outcomes in patients with pulmonary arterial hypertension.
Consecutive patients with right heart catheterization-proven pulmonary arterial hypertension who completed the Medical Outcomes Survey Short Form-36 survey (SF-36) were included. Demographic, clinical, physiological, and hemodynamic data were collected at baseline. Survival was assessed from the time of diagnosis of pulmonary arterial hypertension. Cox proportional hazard models were constructed to assess the relationship between HRQOL and transplant-free survival.
Eighty-seven patients with pulmonary arterial hypertension were enrolled and followed prospectively for a median of 3.8 years. At baseline, HRQOL was significantly worse than U.S. normal values for six of eight domains of the SF-36. Several domains demonstrated moderate correlation (r value ≥ 0.40) with 6-minute-walk distance and World Health Organization functional class; there were no significant associations with hemodynamics. In univariable Cox proportional hazard models, six of eight domains and both summary scores were significantly associated with survival. In multivariable models, adjusted for age, disease type, and cardiac function, these relationships largely persisted.
In this cohort of patients with pulmonary arterial hypertension, HRQOL, as assessed by the SF-36, was strongly associated with transplant-free survival. These relationships persisted when controlling for potential confounders such as disease type and disease severity. These findings suggest that HRQOL may be an important predictor of outcomes in pulmonary arterial hypertension and therefore a target for future therapeutic interventions.
尽管药物治疗取得了进展,但肺动脉高压是一种发病率和死亡率都很高的进行性疾病。患者相关结局,如健康相关生活质量(HRQOL)与生存率之间的关系尚未得到充分描述。
评估肺动脉高压患者的HRQOL与结局之间的关系。
纳入经右心导管检查证实为肺动脉高压且完成医学结局研究简表36(SF-36)调查的连续患者。在基线时收集人口统计学、临床、生理和血流动力学数据。从肺动脉高压诊断之时开始评估生存率。构建Cox比例风险模型以评估HRQOL与无移植生存之间的关系。
87例肺动脉高压患者入组并进行前瞻性随访,中位随访时间为3.8年。在基线时,SF-36八个领域中的六个领域,HRQOL显著低于美国正常值。几个领域与6分钟步行距离和世界卫生组织功能分级呈中度相关(r值≥0.40);与血流动力学无显著关联。在单变量Cox比例风险模型中,八个领域中的六个领域以及两个综合评分均与生存率显著相关。在多变量模型中,在调整年龄、疾病类型和心功能后,这些关系基本持续存在。
在这个肺动脉高压患者队列中,通过SF-36评估的HRQOL与无移植生存密切相关。在控制疾病类型和疾病严重程度等潜在混杂因素后,这些关系依然存在。这些发现表明,HRQOL可能是肺动脉高压结局的一个重要预测指标,因此是未来治疗干预的一个靶点。