Saumya Sharma1, Kabir M Abubakar1, Martin Keszler2. 1. Division of Neonatology, Department of Pediatrics, Georgetown University Hospital, Washington, District of Columbia. 2. Department of Pediatrics, Brown University, Providence, Rhode Island.
Abstract
OBJECTIVE: This study aims to test the hypothesis that the tidal volume (VT) required for maintaining eucapnia in infants with congenital diaphragmatic hernia (CDH) is not reduced to the same degree as their lung mass. STUDY DESIGN: Records of infants with CDH admitted to our hospital from 1997 to 2009 managed with conventional ventilation were reviewed. Demographics, ventilator settings, observed VT, respiratory rate (RR), and blood gas values pre- and postsurgery were recorded. Minute ventilation (MV) was calculated as a product of RR × VT. Only VT values with corresponding Paco 2 between 35 and 60 mm Hg were included. Mean VT/kg and MV/kg were calculated for each patient. Forty term/late preterm infants ventilated for lung disease other than CDH or pulmonary hypoplasia served as controls. RESULTS: Birth weights of the 19 patients with CDH and 40 control infants were similar (3,360 ± 480 g and 3,300 ± 640 g). Mean gestational age was 38.5 ± 2 and 37.4 ± 1.5 week, p = 0.02. Infants with CDH required similar VT and MV as controls to maintain equal Paco 2. CONCLUSIONS: Infants with CDH require similar VT to clear their CO2 production compared with infants of similar size without pulmonary hypoplasia. These are the first reference values to guide selection of VT in infants with CDH. Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.
OBJECTIVE: This study aims to test the hypothesis that the tidal volume (VT) required for maintaining eucapnia in infants with congenital diaphragmatic hernia (CDH) is not reduced to the same degree as their lung mass. STUDY DESIGN: Records of infants with CDH admitted to our hospital from 1997 to 2009 managed with conventional ventilation were reviewed. Demographics, ventilator settings, observed VT, respiratory rate (RR), and blood gas values pre- and postsurgery were recorded. Minute ventilation (MV) was calculated as a product of RR × VT. Only VT values with corresponding Paco 2 between 35 and 60 mm Hg were included. Mean VT/kg and MV/kg were calculated for each patient. Forty term/late preterm infants ventilated for lung disease other than CDH or pulmonary hypoplasia served as controls. RESULTS: Birth weights of the 19 patients with CDH and 40 control infants were similar (3,360 ± 480 g and 3,300 ± 640 g). Mean gestational age was 38.5 ± 2 and 37.4 ± 1.5 week, p = 0.02. Infants with CDH required similar VT and MV as controls to maintain equal Paco 2. CONCLUSIONS:Infants with CDH require similar VT to clear their CO2 production compared with infants of similar size without pulmonary hypoplasia. These are the first reference values to guide selection of VT in infants with CDH. Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.
Authors: Arin L Madenci; Joseph T Church; Robert J Gajarski; Kathryn Marchetti; Edwin J Klein; Megan A Coughlin; Jeannie Kreutzmann; Marjorie Treadwell; Maria Ladino-Torres; George B Mychaliska Journal: Eur J Pediatr Surg Date: 2017-10-16 Impact factor: 2.191