Nawaytou Hythem, Fineman Jeffrey R, Moledina Shahin, Ivy Dunbar, Abman Steven H, Cerro Maria J Del
Department of Pediatrics, University of California, San Francisco, CA, USA.
Department of Pediatrics, University College London, London, UK.
Pulm Circ. 2021 Feb 9;11(1):2045894021991446. doi: 10.1177/2045894021991446. eCollection 2021 Jan-Mar.
Development of pulmonary hypertension (PH) in patients with left side heart disease (LHD) is a predictor of poor prognosis. The use of pulmonary vasodilators in PH associated with LHD (PH-LHD) is controversial. In this study, we describe the practice patterns regarding the use of pulmonary vasodilators in PH-LHD among a group of international pediatric PH specialists. A survey was distributed to the members of three pediatric PH networks: PPHNet, PVRI, and REHIPED. The survey queried participants on the rationale, indications, and contraindications of the use of pulmonary vasodilators in children with PH-LHD. Forty-seven PH specialists from 39 PH centers completed the survey. Participants included PH specialists from North America (57%), South America (15%), and Europe (19%). The majority of participants (74%) recommended the use of pulmonary vasodilators only in patients with combined pre-capillary and post-capillary pulmonary hypertension. Participants required the presence of clinical symptoms or signs of heart failure (68%) or right ventricular dysfunction by echocardiography (51%) in order to recommend pulmonary vasodilator therapy. There was no agreement regarding hemodynamic criteria used to recommend pulmonary vasodilators or the etiologies of LHD considered contraindications for using pulmonary vasodilators to manage PH-LHD. Of the available PH-targeted drugs, most participants preferred the use of phosphodiesterase-5-inhibitors for this indication. In conclusion, the practice of recommending pulmonary vasodilators in PH-LHD is highly variable among international pediatric PH specialists. Most specialists of those surveyed (57% in North America) would consider the use of pulmonary vasodilators in PH-LHD only if pre-capillary pulmonary hypertension and right ventricular dysfunction are present.
左心疾病(LHD)患者发生肺动脉高压(PH)是预后不良的一个预测指标。在与LHD相关的PH(PH-LHD)中使用肺血管扩张剂存在争议。在本研究中,我们描述了一组国际儿科PH专家在PH-LHD中使用肺血管扩张剂的实践模式。向三个儿科PH网络(PPHNet、PVRI和REHIPED)的成员发放了一份调查问卷。该问卷询问了参与者在PH-LHD儿童中使用肺血管扩张剂的基本原理、适应症和禁忌症。来自39个PH中心的47名PH专家完成了该调查。参与者包括来自北美洲(57%)、南美洲(15%)和欧洲(19%)的PH专家。大多数参与者(74%)建议仅在合并毛细血管前和毛细血管后肺动脉高压的患者中使用肺血管扩张剂。参与者要求存在心力衰竭的临床症状或体征(68%)或超声心动图显示右心室功能障碍(51%),才会推荐肺血管扩张剂治疗。对于用于推荐肺血管扩张剂的血流动力学标准或被视为使用肺血管扩张剂治疗PH-LHD的禁忌症的LHD病因,没有达成共识。在现有的针对PH的药物中,大多数参与者在此适应症上更倾向于使用磷酸二酯酶-5抑制剂。总之,国际儿科PH专家在PH-LHD中推荐使用肺血管扩张剂的实践差异很大。大多数接受调查的专家(北美洲为57%)仅在存在毛细血管前肺动脉高压和右心室功能障碍时才会考虑在PH-LHD中使用肺血管扩张剂。