Impact of prematurity and co-morbidities on feeding milestones in neonates: a retrospective study

S R Jadcherla, M Wang, A S Vijayapal, S R Leuthner, S R Jadcherla, M Wang, A S Vijayapal, S R Leuthner

Abstract

Objective: Feeding problems are an important area of neonatal morbidity that requires attention. We defined the feeding milestones related to transition to per oral feeding among premature infants based on gestational (GA) and postmenstrual ages (PMA), and elucidated the co-morbidity variables affecting with these skills.

Study design: Feeding progress was tracked during the first hospitalization in a retrospective study involving 186 infants. We measured the age at acquisition of first feedings, maximum gavage feedings and maximum oral feedings. Resource usage measures included the total length of hospital stay (LOS), duration of gavage tube and duration of respiratory support. Effects of perinatal and co-morbidity factors on the acquisition of feeding milestones were evaluated. ANOVA, t-test, Wilcoxon rank sum test, chi(2) test, univariate and multivariate analysis, stepwise linear regression analysis and logistic regression analysis were applied as appropriate. Data were presented as mean+/-s.d., or as stated. P<0.05 was considered significant.

Result: We stratified the data into three groups based on GA at birth: <28.0 weeks (group-1), 28.0 to 32.0 weeks (group-2) and 32.0 to 35.0 weeks (group-3). Compared with group-3, group-1 needed four-fold more ventilation and five-fold more continuous positive airway pressure (CPAP) duration (all P<0.001); whereas group-2 needed two-fold more CPAP duration. Age at first feed correlated with age at full gavage feedings and age at full oral feedings (r=0.53 and r=0.71, both P<0.0001). Age at full gavage feedings correlated with age at full oral feedings (r=0.81, P<0.0001). Univariate analysis was significant for GA age, hypotension, the effects of gastroesophageal reflux, and duration of ventilation and CPAP on the PMA at maximal oral feedings (all P<0.05); multivariate analysis for these variables was also significant (R (2)=0.58, P<0.0001). The success rate for oral feedings at discharge accelerated with GA maturation and caffeine use; on the other hand, the need for respiratory support and management of positive blood culture were associated with failure rates (P<0.05).

Conclusion: Infants < 28 weeks GA have significant feeding delays with respect to initiation and progression to maximal gavage and oral feedings, as well as prolonged LOS. Infants >28 weeks GA attained successful feeding milestones by similar PMA. Specific aero-digestive co-morbidities significantly affected maximal oral feeding milestone. Delays in achieving maximum gavage and maximum oral feeding milestones suggest delays with the development of control and regulation of foregut motility.

Figures

Figure 1
Figure 1
Feeding status at discharge based on GA. Discharge feeding milestones were oral feedings exclusively, gavage plus oral feedings and gastrostomy tube feedings.
Figure 2
Figure 2
Length of hospital stay based on GA is shown in (a) and duration of gavage feeding based on GA in (b). Data are depicted as box plots with mean (dashed line), median (solid line) and interquartile range.
Figure 3
Figure 3
Duration of ventilation based on GA is shown in (a) and duration of CPAP based on GA in (b). Data are depicted as box plots with mean (dashed line), median (solid line) and interquartile range.

References

    1. Kliegman RM. Neonatal technology, perinatal survival, social consequences, and the perinatal paradox. Am J Public Health. 1995;85:909–913.
    1. American Academy of Pediatrics, Committee on Children with Disabilities Managed care and children with special health care needs. Pediatrics. 2004;114:1693–1698.
    1. American Academy of Pediatrics, Committee on Fetus and Newborn Hospital discharge of the high risk neonate: proposed guidelines. Pediatrics. 2008;122:1119–1126.
    1. Hack M, Cartar L.Growth outcomes of preterm and very low birth weight infantsIn: Thureen PJ, Hay WW (eds). Neonatal Nutrition and Metabolism2nd ednCambridge University Press: Cambridge, UK; 2006640–653.
    1. Sadler TW.Special embryology: respiratory system and digestive systemIn: Sadler TW (ed). Langman's Medical Embryology7th ednWilliams and Wilkins: Baltimore, MD; 1995232–271.
    1. Bu'Lock F, Woolridge MW, Bairn JD. Development of coordination of sucking, swallowing, and breathing: ultrasound study of term and preterm infants. Dev Med Child Neurol. 1990;32:669–678.
    1. AAP Guidelines Hospital discharge of the high-risk neonate. Pediatrics. 1998;102:411–417.
    1. Örtenstrand A, Waldenström U, Winbladh B. Early discharge of preterm infants needing limited special care, followed by domiciliary nursing care. Acta Paediatr. 1999;88:1024–1030.
    1. Collins CT, Makrides M, McPhee AJ. Early discharge with home support of gavage feeding for stable preterm infants who have not established full oral feeds. Cochrane Database Syst Rev. 2003;9 4:CD003743.
    1. Ballard JL, Khoury JC, Wedig K, Wang L, Eilers-Walsman BL, Lipp R. New Ballard Score, expanded to include extremely premature infants. J Pediatr. 1991;119 3:417–423.
    1. Dubowitz LM, Dubowitz V, Goldberg C. Clinical assessment of gestational age in the newborn infant. J Pediatr. 1970;77 1:1–10.
    1. al Tawil Y, Berseth CL. Gestational and postnatal maturation of duodenal motor responses to intragastric feeding. J Pediatr. 1996;129 3:374–381.
    1. Ittmann PI, Amarnath R, Berseth CL. Maturation of antroduodenal motor activity in preterm and term infants. Dig Dis Sci. 1992;37 1:14–19.
    1. Berseth CL. Neonatal small intestinal motility: motor responses to feeding in term and preterm infants. J Pediatr. 1990;117 5:777–782.
    1. Jadcherla SR, Klee G, Berseth CL. Regulation of migrating motor complexes by motilin and pancreatic polypeptide in human infants. Pediatr Res. 1997;42:365–369.
    1. Jadcherla SR, Berseth CL. Effect of erythromycin on gastroduodenal contractile activity in developing neonates. J Pediatr Gastroenterol Nutr. 2002;34:16–22.
    1. Jadcherla SR, Duong HQ, Hofmann C, Hoffmann RG, Shaker R. Characteristics of upper oesophageal sphincter and oesophageal body during maturation in healthy human neonates compared with adults. Neurogastroenterol Motil. 2005;17:663–670.
    1. Jadcherla SR, Vijayapal AS, Leuthner S. Feeding abilities in neonates with congenital heart disease: a retrospective study. J Perinatol. 2009;29 2:112–118.
    1. Armitage P, Berry G. Statistical Methods in Medical Research. Blackwell Scientific Publications: Oxford; 1987.
    1. Snedecor GW, Cochrann WG.Statistical Methods7th edn, The Iowa State University Press: Iowa City, IA; 1980
    1. Berseth CL, McCoy HH. Birth asphyxia alters neonatal intestinal motility in term neonates. Pediatrics. 1992;90 5:669–673.
    1. Jadcherla SR, Berseth CL. Antroduodenal motility and feeding outcomes among neonatal extra corporeal membrane oxygenation survivors. J Pediatr Gastroenterol Nutr. 2005;41:347–350.
    1. Estep M, Barlow SM, Vantipalli R, Lee J, Finan D. Non-nutritive suck burst parametrics in preterm infants with RDS and oral feeding complications. J Neonatal Nurs. 2008;14 1:28–34.
    1. Barlow SM, Finan DS, Chu S, Lee J. Patterns for the premature brain: synthetic orocutaneous stimulation entrains preterm infants with feeding difficulties to suck. J Perinatol. 2008;28:541–548.
    1. Barlow SM. Oral and respiratory control for preterm feeding. Curr Opin Otolaryngol Head Neck Surg. 2009;17:179–186.
    1. Poore M, Zimmerman E, Barlow SM, Wang J, Gu F. NTrainer therapy increases suck spatiotemporal stability in preterm infants. Acta Paediatr. 2008;97:920–927.
    1. Hawdon JM, Beauregard N, Kennedy G. Identification of Neonates at Risk of Developing Feeding Problems in Infancy. Dev Med Child Neurol. 2000;42:235–239.
    1. Jadcherla SR, Stoner E, Gupta A, Bates DG, Di Lorenzo C, Linscheid T. Evaluation and management of neonatal dysphagia: impact of pharyngo-esophageal motility studies and multidisciplinary feeding strategy. J Pediatr Gastroenterol Nutr. 2009;48:186–192.
    1. Jadcherla SR, Berseth CL. Acute and chronic intestinal motor activity responses to two infant formulas. Pediatrics. 1995;96:331–335.
    1. Dodrill P, Donovan T, Cleghorn G, Mcmahon S, Davie PSW. Attainment of early feeding milestones in preterm neonates. J Perinatol. 2008;28:549–555.
    1. Amaizu N, Shulman RJ, Schanler RJ, Lau C. Maturation of oral feeding skills in preterm infants. Acta Paediatr. 2008;97:61–67.
    1. Simpson C, Schanler RJ, Lau C. Early introduction of oral feeding in preterm infants. Pediatrics. 2002;110:517–522.
    1. Howe TH, Sheu CF, Hinojosa J, Lin J, Holzman IR. Multiple factors related to bottle-feeding performance in preterm infants. Nurs Res. 2007;56 5:307–311.
    1. Jadcherla SR, Gupta A, Coley BD, Fernandez S, Shaker R. Esophago-glottal closure reflex in human infants: a novel reflex elicited with concurrent manometry and ultrasonography. Am J Gastroenterol. 2007;102:2286–2293.
    1. Jadcherla SR, Gupta A, Stoner E, Fernandez S, Shaker R. Pharyngeal swallowing: defining pharyngeal and upper esophageal sphincter relationships in human neonates. J Pediatr. 2007;151:597–603.
    1. Jadcherla SR, Duong HQ, Hoffman R, Shaker R. Esophageal body and UES motor responses due to abrupt esophageal provocation in premature infants. J Pediatr. 2003;143:31–38.
    1. Jadcherla SR, Hoffmann RG, Shaker R. Effect of maturation on the magnitude of mechanosensitive and chemosensitive reflexes in the premature human esophagus. J Pediatr. 2006;141 1:77–82.

Source: PubMed

3
Suscribir