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      Pulmonary hypertension in bronchopulmonary dysplasia

      review-article
      1 , , 2 , 3 , 4 , 5 , 6 , 7 , for the European Pediatric Pulmonary Vascular Disease Network (EPPVDN)
      Pediatric Research
      Nature Publishing Group US

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          Abstract

          Abstract

          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.

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          Most cited references77

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          2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: The Joint Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS): Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Heart and Lung Transplantation (ISHLT).

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            Haemodynamic definitions and updated clinical classification of pulmonary hypertension

            Since the 1st World Symposium on Pulmonary Hypertension (WSPH) in 1973, pulmonary hypertension (PH) has been arbitrarily defined as mean pulmonary arterial pressure (mPAP) ≥25 mmHg at rest, measured by right heart catheterisation. Recent data from normal subjects has shown that normal mPAP was 14.0±3.3 mmHg. Two standard deviations above this mean value would suggest mPAP >20 mmHg as above the upper limit of normal (above the 97.5th percentile). This definition is no longer arbitrary, but based on a scientific approach. However, this abnormal elevation of mPAP is not sufficient to define pulmonary vascular disease as it can be due to an increase in cardiac output or pulmonary arterial wedge pressure. Thus, this 6th WSPH Task Force proposes to include pulmonary vascular resistance ≥3 Wood Units in the definition of all forms of pre-capillary PH associated with mPAP >20 mmHg. Prospective trials are required to determine whether this PH population might benefit from specific management. Regarding clinical classification, the main Task Force changes were the inclusion in group 1 of a subgroup “pulmonary arterial hypertension (PAH) long-term responders to calcium channel blockers”, due to the specific prognostic and management of these patients, and a subgroup “PAH with overt features of venous/capillaries (pulmonary veno-occlusive disease/pulmonary capillary haemangiomatosis) involvement”, due to evidence suggesting a continuum between arterial, capillary and vein involvement in PAH.
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              Bronchopulmonary dysplasia.

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                Author and article information

                Contributors
                georg.hansmann@gmail.com
                Journal
                Pediatr Res
                Pediatr Res
                Pediatric Research
                Nature Publishing Group US (New York )
                0031-3998
                1530-0447
                10 June 2020
                10 June 2020
                2021
                : 89
                : 3
                : 446-455
                Affiliations
                [1 ]GRID grid.10423.34, ISNI 0000 0000 9529 9877, Department of Pediatric Cardiology and Critical Care, , Hannover Medical School, ; Hannover, Germany
                [2 ]GRID grid.6363.0, ISNI 0000 0001 2218 4662, Department of Pediatric Cardiology, , Charité University Medical Center, ; Berlin, Germany
                [3 ]GRID grid.410556.3, ISNI 0000 0001 0440 1440, Newborn Services, John Radcliffe Hospital, , Oxford University Hospitals NHS Foundation Trust, ; Oxford, UK
                [4 ]GRID grid.4991.5, ISNI 0000 0004 1936 8948, National Perinatal Epidemiology Unit, Nuffield Department of Population Health, Medical Sciences Division, , University of Oxford, ; Oxford, UK
                [5 ]GRID grid.38142.3c, ISNI 000000041936754X, Division of Newborn Medicine, Boston Children’s Hospital, , Harvard Medical School, ; Boston, MA USA
                [6 ]GRID grid.152326.1, ISNI 0000 0001 2264 7217, Division of Pediatric Pulmonary Medicine, , Vanderbilt University, ; Nashville, TN USA
                [7 ]GRID grid.11598.34, ISNI 0000 0000 8988 2476, Division of Pediatric Cardiology, , Medical University of Graz, ; Graz, Austria
                Article
                993
                10.1038/s41390-020-0993-4
                7979539
                32521539
                5dc7bf42-88c0-4c80-a212-c2150328b16d
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 4 March 2020
                : 24 April 2020
                : 12 May 2020
                Categories
                Review Article
                Custom metadata
                © International Pediatric Research Foundation, Inc 2021

                Pediatrics
                Pediatrics

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