Department of Pediatric Cardiology and Critical Care, Hannover Medical School, Hannover, Germany.
Department of Pediatric Cardiology, Charité University Medical Center, Berlin, Germany.
Pediatr Res. 2021 Feb;89(3):446-455. doi: 10.1038/s41390-020-0993-4. Epub 2020 Jun 10.
Bronchopulmonary dysplasia (BPD) is a major complication in prematurely born infants. Pulmonary hypertension (PH) associated with BPD (BPD-PH) is characterized by alveolar diffusion impairment, abnormal vascular remodeling, and rarefication of pulmonary vessels (vascular growth arrest), which lead to increased pulmonary vascular resistance and right heart failure. About 25% of infants with moderate to severe BPD develop BPD-PH that is associated with high morbidity and mortality. The recent evolution of broader PH-targeted pharmacotherapy in adults has opened up new treatment options for infants with BPD-PH. Sildenafil became the mainstay of contemporary BPD-PH therapy. Additional medications, such as endothelin receptor antagonists and prostacyclin analogs/mimetics, are increasingly being investigated in infants with PH. However, pediatric data from prospective or randomized controlled trials are still sparse. We discuss comprehensive diagnostic and therapeutic strategies for BPD-PH and briefly review the relevant differential diagnoses of parenchymal and interstitial developmental lung diseases. In addition, we provide a practical framework for the management of children with BPD-PH, incorporating the modified definition and classification of pediatric PH from the 2018 World Symposium on Pulmonary Hypertension, and the 2019 EPPVDN consensus recommendations on established and newly developed therapeutic strategies. Finally, current gaps of knowledge and future research directions are discussed. IMPACT: PH in BPD substantially increases mortality. Treatment of BPD-PH should be conducted by an interdisciplinary team and follow our new treatment algorithm while still kept tailored to the individual patient. We discuss recent developments in BPD-PH, make recommendations on diagnosis, monitoring and treatment of PH in BPD, and address current gaps of knowledge and potential research directions. We provide a practical framework, including a new treatment algorithm, for the management of children with BPD-PH, incorporating the modified definition and classification of pediatric PH (2018 WSPH) and the 2019 EPPVDN consensus recommendations on established and newly developed therapeutic strategies for BPD-PH.
支气管肺发育不良(BPD)是早产儿的主要并发症。与 BPD 相关的肺动脉高压(PH)(BPD-PH)的特征是肺泡扩散受损、血管异常重塑和肺血管稀疏(血管生长停滞),这导致肺血管阻力增加和右心衰竭。大约 25%的中重度 BPD 婴儿会发展为 BPD-PH,其发病率和死亡率都很高。近年来,成人广泛的 PH 靶向药物治疗的发展为 BPD-PH 婴儿开辟了新的治疗选择。西地那非已成为当代 BPD-PH 治疗的基础。其他药物,如内皮素受体拮抗剂和前列环素类似物/模拟物,在 PH 婴儿中的应用也越来越多。然而,前瞻性或随机对照试验的儿科数据仍然很少。我们讨论了 BPD-PH 的综合诊断和治疗策略,并简要回顾了实质和间质发育性肺疾病的相关鉴别诊断。此外,我们为患有 BPD-PH 的儿童提供了一种实用的管理框架,纳入了 2018 年世界肺动脉高压研讨会的小儿 PH 修订定义和分类,以及 2019 年 EPPVDN 关于已建立和新开发的治疗策略的共识建议。最后,讨论了当前的知识差距和未来的研究方向。影响:BPD 中的 PH 大大增加了死亡率。BPD-PH 的治疗应由多学科团队进行,并遵循我们的新治疗算法,同时仍然针对个体患者进行调整。我们讨论了 BPD-PH 的最新进展,就 BPD 中 PH 的诊断、监测和治疗提出建议,并讨论当前的知识差距和潜在的研究方向。我们为 BPD-PH 儿童的管理提供了一个实用的框架,包括小儿 PH 的新治疗算法(2018 年 WSPH)和 2019 年 EPPVDN 关于已建立和新开发的 BPD-PH 治疗策略的共识建议。