Division of Pulmonary Medicine, Department of Medicine, PSMMC, Riyadh, Saudi Arabia.
Department of Pediatric Cardiology, Section of Congenital Heart Disease, PSCC, Riyadh, Saudi Arabia.
Ann Thorac Med. 2014 Oct;9(4):209-15. doi: 10.4103/1817-1737.140127.
The main objective of this study is to describe patients' clinical characteristics and physiological and hemodynamic parameters at the time of diagnosis in a pulmonary hypertension center in Saudi Arabia.
This study reports the results from a single pulmonary hypertension specialized center in Riyadh, Saudi Arabia, namely Prince Sultan Medical Military City/Cardiac Center (PSMMC & CC). Both newly diagnosed (incidence) and referred (prevalence) cases of pulmonary arterial hypertension are included. All characteristics, including clinical, physiological, and hemodynamic parameters at the time of diagnosis are described.
A total of 107 patients were identified as having pulmonary arterial hypertension as diagnosed by right heart catheterization. The mean age at diagnosis was 36 (± 9) years, and there was a female preponderance of 62.6%. The mean duration between symptom onset and diagnosis was 27.8 (± 9.0) months. At the time of enrollment, 56.1% of patients were in functional class III and 16.8% were in functional class IV. Fifty five patients (51.4%) were diagnosed as idiopathic pulmonary arterial hypertension, 29 patients (27.1%) as congenital heart disease associated with pulmonary arterial hypertension, 16 patients (15.0%) as connective tissue diseases associated with pulmonary arterial hypertension, 4 patients (3.7%) as heritable pulmonary arterial hypertension, and 3 patients (2.8%) as portopulmonary hypertension.
This data highlights the current situation of pulmonary arterial hypertension in Saudi Arabia. Our patients are much younger than patients described in other international registries but still detected as late in the course of the disease. A majority of patients displays severe functional and hemodynamic compromise.
本研究的主要目的是描述沙特阿拉伯一家肺动脉高压中心患者在诊断时的临床特征、生理和血液动力学参数。
本研究报告了沙特阿拉伯利雅得的一家肺动脉高压专科中心(即苏丹王子军事医疗城/心脏中心(PSMMC & CC))的研究结果。包括新诊断的(发病率)和转诊的(患病率)肺动脉高压病例。描述了所有特征,包括诊断时的临床、生理和血液动力学参数。
共确定 107 例经右心导管检查诊断为肺动脉高压的患者。诊断时的平均年龄为 36(±9)岁,女性占 62.6%。从症状出现到诊断的平均时间为 27.8(±9.0)个月。入组时,56.1%的患者处于功能分级 III 级,16.8%处于功能分级 IV 级。55 例(51.4%)患者被诊断为特发性肺动脉高压,29 例(27.1%)为先天性心脏病相关肺动脉高压,16 例(15.0%)为结缔组织病相关肺动脉高压,4 例(3.7%)为遗传性肺动脉高压,3 例(2.8%)为门脉高压性肺动脉高压。
这些数据突出了沙特阿拉伯目前肺动脉高压的情况。我们的患者比其他国际登记处描述的患者年轻得多,但仍在疾病过程中晚期被发现。大多数患者表现出严重的功能和血液动力学障碍。