“…This article is focused on describing the state of the art and future perspectives in paediatric PAH, as formulated by the recent Paediatric Task Force of the 6th World Symposium on Pulmonary Hypertension. They are quite similar to the report of the 5th World Symposium (Nice 2013), in which the unique features of paediatric PAH were highlighted for the first time, but decidedly different from the classification proposed by the Pulmonary Vascular Research Institute Taskforce (Panama 2011) [2,3].…”
supporting
confidence: 82%
“…Normal perinatal transition has been previously defined with regard to echocardiogram-derived pulmonary artery pressure over time in the first days of life. Recently, a study of serial changes in estimated levels of pulmonary hypertension describes several different patterns of the transition in preterm infants, demonstrating striking changes in delayed pulmonary vascular transition being associated with degree of prematurity [2]. Of note, those preterm infants with delayed pulmonary vascular transition had the highest risk for late deaths and the subsequent development of bronchopulmonary dysplasia.…”
We read with close attention the report recently published in the European Respiratory Journal by ROSENZWEIG et al. [1]. We would like to congratulate the authors for their commendable effort, aimed at discussing recent advances, ongoing challenges and specific approaches in the care of children suffering from pulmonary arterial hypertension (PAH), and offer a few comments.
“…This article is focused on describing the state of the art and future perspectives in paediatric PAH, as formulated by the recent Paediatric Task Force of the 6th World Symposium on Pulmonary Hypertension. They are quite similar to the report of the 5th World Symposium (Nice 2013), in which the unique features of paediatric PAH were highlighted for the first time, but decidedly different from the classification proposed by the Pulmonary Vascular Research Institute Taskforce (Panama 2011) [2,3].…”
supporting
confidence: 82%
“…Normal perinatal transition has been previously defined with regard to echocardiogram-derived pulmonary artery pressure over time in the first days of life. Recently, a study of serial changes in estimated levels of pulmonary hypertension describes several different patterns of the transition in preterm infants, demonstrating striking changes in delayed pulmonary vascular transition being associated with degree of prematurity [2]. Of note, those preterm infants with delayed pulmonary vascular transition had the highest risk for late deaths and the subsequent development of bronchopulmonary dysplasia.…”
We read with close attention the report recently published in the European Respiratory Journal by ROSENZWEIG et al. [1]. We would like to congratulate the authors for their commendable effort, aimed at discussing recent advances, ongoing challenges and specific approaches in the care of children suffering from pulmonary arterial hypertension (PAH), and offer a few comments.
“…In infants born extremely preterm, however, delayed vascular transition with persistent elevation of PVR is more common than in subjects born at term, especially in the setting of HRF. 7 Infants born preterm with evidence of sustained PH at 7-14 days of postnatal age were more likely to have greater mortality, to have a prolonged need for mechanical ventilation and NICU admission, or to subsequently develop the diagnosis of BPD or BPD with late PH at 36 weeks of PMA. 18,19 Kinsella et al evaluated the ontogeny of the pulmonary vascular response to iNO and oxygen in lambs.…”
Section: Preclinical Studiesmentioning
confidence: 96%
“…Clinical data have shown that PPHN occurs and can contribute to hypoxemia in a subgroup of infants born preterm with severe HRF, especially in the setting of oligohydramnios and preterm prolonged rupture of membranes (preterm, prelabor rupture of membranes [PPROM]s). 6,7 Multiple clinical series have shown acute improvements in oxygenation in this subgroup of infants born preterm with HRF and proven pulmonary hypertension (PH), [8][9][10][11][12] but randomized controlled trial (RCT) data are lacking. 9 Unfortunately, clinical evidence supporting the use of alternative drug therapies for severe PPHN management in infants born preterm is extremely limited, especially in comparison with the number of published clinical observations and experience with the use of iNO therapy in the NICU setting.…”
“…Left ventricular failure leads to an increase in pressure and volume in the left atrium of the heart and pulmonary veins. Secondary right ventricular failure develops and when the hydrostatic pressure exceeds the colloid osmotic pressure in the blood, fluid enters the pulmonary parenchyma, which results in pulmonary oedema and lung stretch, and susceptibility are reduced [5,39,40]. In order to prevent iatrogenic overhydration in premature newborns, it is currently recommended to supply liquids in a volume of 60-80 ml/kg b.w./day on the first day of life of the newborn, which should be increased by about 20 ml/kg b.w./day up to a maximum value of 150 ml/kg b.w./day [41].…”
Section: Risk Factors and Pathophysiological Mechanisms Of Bpdmentioning
Wątroba S. J, Bryda J. Pathophysiological mechanisms and pharmacological methods of prevention and treatment of bronchopulmonary dysplasia in preterm infants.
AbstractIntroduction. Bronchopulmonary dysplasia (BPD) is a respiratory disease that is characterized by long-term respiratory failure and mainly affects premature infants with low birth weight (LBW), undergoing mechanical ventilation (MV) or requiring long-term oxygen therapy. In Europe, among newborns with birth weight <1500g, the incidence of BPD is around 15%. Objective. The purpose of this review was to analyze the pathophysiological mechanisms involved in the development of BPD in premature newborns and to discuss the current possibilities of pharmacological prevention and treatment of BPD. Description of the state of knowledge. The BPD pathogenesis is multifactorial. Lung damage is the result of barotrauma and volutrauma due to high-performance MV, actions of reactive oxygen species (ROS) and infectious agents. Currently used methods of pharmacological treatment of severe forms of BPD are mainly based on systemic steroid therapy and can not be considered completely effective and free of side effects. Conclusion. Despite the widespread use of proper pharmacotherapy and dynamic development of new methods of respiratory therapy, mortality in BPD is estimated at around 10% -20%. Infants with BPD are much more exposed to respiratory infections caused by respiratory syncytial virus (RSV), which may result in the development of bronchial hyperresponsiveness and bronchial asthma. Among children with BPD there are significantly higher cognitive and behavioral deficits compared to healthy children, and cerebral palsy is also significantly more common.Abbreviations AA -arachidonic acid; AAP COFN -Committee on Foetus and Newborn of the American Academy of Pediatrics; ACTHadrenocorticotropin; ADH -vasopressin, antidiuretic hormone; ASMC -airway smooth muscle cells; BPD -bronchopulmonary dysplasia; BTN -betamethasone; CAT -catalase; CC10 -Clara cell 10 kDa protein; CLD -chronic lung disease; COXcyclooxygenase; CPAP -continuous positive airway pressure; CPS FNC -Fetus and Newborn Committee of the Canadian Pediatric Society; DEX -dexamethasone; ELBW -extremely low birth weight; ENA-78 -epithelial protein activating neutrophils; EURAIL -Europe Against Immature Lung; FC -fludrocortisone; FiO 2 -oxygen concentration in the breathing mixture; FTP -fluticasone propionate; GCSs -glucocorticosteroids; GM-CSF -granulocyte and macrophage colonystimulating factor; GPx -glutathione peroxidase; HC -hydrocortisone; HO . -hydroxyl radical; HO 2 . -hydroperoxide radical; IFN-γ -gamma interferon; ILs -interleukins; IRDS -respiratory distress syndrome; IUGR -intrauterine growth retardation; IVH -intraventricular haemorrhage; LBW -low birth weight; LTs -leukotrienes; MAS -meconium aspiration syndrome; MIP-1 -macrophage inflammatory protein-1; MMPs -metalloproteinases; MRI -magnetic resonance imaging; MV -mechanical ventilation; n-CPAP -continuous positive airway pressure -nasal metho...
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