Respiratory muscle strength in healthy infants and those with surgically correctable anomalies. Issue 1 (20th February 2014)

• Record Type: Journal Article
• Authors: Kassim, Zainab; Moxham, John; Davenport, Mark; Nicolaides, Kypros; Greenough, Anne; Rafferty, Gerrard F.
• Is Part Of: Pediatric pulmonology. Volume 50:Issue 1(2015:Jan.)
• Page Start: 71
• Page End: 78
• Publication Date: 2014-02-20
• Subjects: Pediatric respiratory diseases -- Periodicals; Pediatrics -- Periodicals; 618.922
• DOI: 10.1002/ppul.23007
• Languages: English
• ISSNs: 8755-6863

Abstract

<abstract abstract-type="main" xml:lang="en"> <title>Summary</title> <sec id="ppul23007-sec-0001" sec-type="section"> <p>Assessment of respiratory muscle strength provides important diagnostic and prognostic information. Normative data in healthy, term infants is, however, limited. Surgically correctable birth defects, congenital diaphragmatic hernia (CDH) and abdominal wall defects (AWD), commonly have impaired diaphragm function. The study aims were to obtain normative data for respiratory muscle strength in healthy, term born infants at birth and at 6 weeks postnatal age (PNA) and to investigate the influence of growth and maturation on inspiratory muscle strength in CDH/AWD infants. Maximal inspiratory (cPimax) and expiratory (cPemax) pressures during crying were measured at birth in 67 healthy, term born infants (mean (SD) gestational age (GA) 39.4 (1.7) weeks) and reassessed in 27 at 6 weeks PNA. cPimax and functional residual capacity (FRC) (22.3 (4.2) ml/kg) were also measured in 23 infants with AWD/CDH (mean (SD) GA 36.9 (2.1) weeks) and reassessed in 16 at median (range) 6.5 (1.5–15) months PNA. In healthy infants, mean (SD) cPimax was 88.8 (19.33) cmH<sub>2</sub>O and cPemax 61.8 (13.5) cmH<sub>2</sub>O at birth, increasing significantly at followup to 100.9 (15.2) cmH<sub>2</sub>O (<italic>P</italic> < 0.05) and 82.6 (19.4) cmH<sub>2</sub>O (<italic>P</italic> < 0.001) respectively. Mean (SD) cPimax was significantly lower (47.5 (22.4) cmH<sub>2</sub>O, <italic>P</italic> < 0.0001) in AWD/CDH infants compared to healthy infants at birth but had increased significantly to 88.1 (27.6) cmH<sub>2</sub>O (<italic>P</italic> < 0.0001) at followup which correlated significantly with increases in FRC (r<sup>2</sup> = 0.33, <italic>P</italic> = 0.0263). Infants with AWD and CDH have significantly reduced inspiratory muscle strength compared to healthy term born infants but strength increases markedly in early life. <bold>Pediatr Pulmonol. 2015; 50:71–78.</bold> © 2014 Wiley Periodicals, Inc.</p> </sec> </abstract>