- Meeting abstract
- Open Access
Feeding difficulties during the neonatal period
© Corvaglia and Martini 2015
- Published: 30 September 2015
- Excessive Weight Loss
- Cleft Palate
- Central Nervous System Disease
- Nervous System Disease
Feeding difficulties (FD) are a major issue in neonatology, as they could hamper the assessment of an adequate enteral nutrition, delay hospital discharge and lead to breastfeeding failure.
Functional and anatomical maturation of the gastrointestinal tract is strictly related to gestational age (GA); hence, premature infants are more prone to develop FD. Feeding intolerance (FI) is very common among preterm infants; clinical symptoms of FI (e.g. abdominal distension, vomiting, bilious gastric residuals, occult or gross bloody stools) are observed in nearly 29% of such neonates . FI could represent an early sign of necrotizing enterocolitis (NEC), which is the most feared gastrointestinal complication of prematurity. Hence, FI often brings clinicians to withhold, decrease or discontinue enteral feeds, thus hampering the establishment of an adequate enteral nutrition and leading to a prolonged duration of both parenteral nutrition (PN) and central lines, with increased risks of such complications as liver cholestasis or sepsis.
The coordination between sucking, swallowing and breathing is usually achieved at 34-36 weeks GA; hence, preterm infants are usually fed via an intragastric tube, through intermittent boluses or continuously. Poor sucking and sucking-swallowing incoordination are the major causes of FD and breastfeeding failure among late preterm infants (GA 34-366/7 weeks), with an increased risk of hypoglycemia, excessive weight loss, hyperbilirubinemia, dehydration. Due to FD, up to 27% of all late preterm infants need to be initially supplemented with intravenous fluids; moreover, tube feeding is frequently required for feeding administration in the first days of life.
The abovementioned problems are infrequent in healthy term newborns. Term neonates developing FD such as poor sucking and/or vomiting need to be evaluated for pathological causes. Physical examination could aid to identify anatomical malformations possibly responsible for FD (e.g. cleft palate). FD and sleepiness can be due to hyperbilirubinemia, hypoglycemia or electrolyte disturbances, but could also subtend an underlying metabolic disease, such as hypothyroidism. FD, lethargy and/or other clinical neurological signs (e.g. seizures, focal neurological signs, hypo- or hypertonia, bulging fontanel, central apnoea) could address for central nervous system diseases (i.e. subarachnoid haemorrhage, ischaemic stroke, metabolic encephalopathy etc.). FD and lethargy could also represent a warning sign for invasive infections, especially if associated with respiratory distress, apnoea and bradycardia, temperature instability and increased capillary refill time. Blood tests (including blood cells count, C-reactive protein, glucose, bilirubin, electrolytes, blood gas analysis) and cerebral ultrasound scan are useful tools to aid neonatologists in the differential diagnosis.
- Moore TA, Wilson ME, Schmid KK, Anderson-Berry A, French JA, Berger AM: Relations between feeding intolerance and stress biomarkers in preterm infants. J Pediatr Gastroenterol Nutr. 2013, 57: 356-62. 10.1097/MPG.0b013e3182953093.PubMedView ArticleGoogle Scholar
- Embleton ND, Simmer K: Practice of parenteral nutrition in VLBW and ELBW infants. World Rev Nutr Diet. 2014, 110: 177-89.PubMedView ArticleGoogle Scholar
- Adamkin DH: Feeding Problems in the Late Preterm Infant. Clin Perinatol. 2006, 33: 831-7. 10.1016/j.clp.2006.09.003.PubMedView ArticleGoogle Scholar
- Wang ML, Dorer DJ, Fleming MP, Catlin EA: Clinical outcomes of near-term infants. Pediatrics. 2004, 114: 372-6. 10.1542/peds.114.2.372.PubMedView ArticleGoogle Scholar
- Webb T, Nugent M, Simpson P, Melzer-Lange M: Diagnostic findings in infants presenting to a pediatric emergency department for lethargy or feeding complaints. Pediatr Emerg Care. 2014, 30: 151-6. 10.1097/PEC.0000000000000083.PubMedView ArticleGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.