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Ten‐year‐old children with a history of bronchopulmonary dysplasia have regional abnormalities in ventilation perfusion matching
Author(s) -
Kjellberg Malin,
SanchezCrespo Alejandro,
Jonsson Baldvin
Publication year - 2019
Publication title -
pediatric pulmonology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.866
H-Index - 106
eISSN - 1099-0496
pISSN - 8755-6863
DOI - 10.1002/ppul.24273
Subject(s) - medicine , bronchopulmonary dysplasia , perfusion , ventilation (architecture) , hypoxemia , pediatrics , perfusion scanning , cardiology , gestational age , pregnancy , mechanical engineering , genetics , engineering , biology
Aim The ratio of ventilation to blood flow is an important determinant for regional gas exchange in the lung and hypoxemia is one of the clinical hallmarks in infants with bronchopulmonary dysplasia (BPD). We have previously demonstrated ventilation/perfusion ratio (V/Q) abnormalities in infants with BPD at 36 weekś postconceptional age. The status of V/Q matching in older children with a history of BPD in infancy is unknown. In this study, we examined if 10‐year‐old children with a history of BPD had V/Q impairments. Methods Three‐dimensional V/Q‐scintigraphy (SPECT) was performed in 26 children. Results In the BPD group, lung volume with mismatch, (V>Q) was larger compared to areas with reverse mismatch (Q>V), 26.2% and 11.8%, respectively, implying that perfusion defects contribute more than ventilation defects in the V/Q mismatch. Also, the mean fractional distribution of V and Q to V/Q in children with BPD was reduced compared to healthy children, 31% and 51% compared to 64% and 89%, respectively ( P < 0.01). Conclusion At 10 years of age children with a history of BPD had ventilation/perfusion abnormalities, with prominent perfusion defects. These V/Q abnormalities suggest the presence of residual alveolar‐capillary impairment.