Pediatric Nutrition in Practice

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86 Lentze

particularly in premature infants coping with ex-
ternal feeding. Here, the response of the intestine
to a bolus feed depends on the maturity of the
gut. In small infants before 31 weeks of postcon-
ceptional age, who usually receive low volumes of
continuous enteral feed, ordinary postprandial
activity does not occur [9]. Between 31 and 35
weeks of postconceptional age, postprandial ac-
tivity is induced in infants by giving them larger
volumes of feed. However, the activity remains in
a fasting pattern with superimposed, more ran-
dom postprandial activity. Finally, in infants over
35 weeks of postconceptional age who receive
large volumes of bolus feed, there is a disruption
in cyclical fasting activity and replacement by
continuous activity. Whether this motility pat-
tern can be advanced by pharmacological mea-
sures such as the administration of cortisol re-
mains to be seen [10 , 11].


Conclusions

Feeding of premature infants below 35 weeks of
gestation requires knowledge of physiological
functions at this time. Whereas digestive and ab-
sorptive functions are mostly developed from the
24th week of postconceptional age, gastrointestinal
motility is still not very active. Premature formulas
or fortified breast milk can be given to VLBW in-
fants or extremely LBW infants in small quantities.
From the 31st postconceptional week onward, the
quantity of enteral feeds becomes less of a problem.
As far as macronutrients are concerned, protein is
digested and absorbed well. Carbohydrates, in
form of lactose, are also digested and absorbed
well. Starch can only be digested in small quanti-
ties. The digestion of fat increases quickly from the
26th week of gestation and can be enhanced by ad-
ministration of milk lipase via breast milk.

8 Terada T, Nakanuma Y: Expression of
pancreatic enzymes (α-amylase, tryp-
sinogen, and lipase) during human liver
development and maturation. Gastro-
enterology 1995; 108: 1236–1245.
9 Bisset WM, Watt J, Rivers RP, Milla PJ:
Postprandial motor response of the
small intestine to enteral feeds in pre-
term infants. Arch Dis Child 1989; 64:
1356–1361.
10 Bisset WM, Watt JB, Rivers RP, Milla PJ:
Ontogeny of fasting small intestinal mo-
tor activity in the human infant. Gut
1988; 29: 483–488.
11 Bisset WM, Watt JB, Rivers RP, Milla PJ:
Measurement of small-intestinal motor
activity in the preterm infant. J Biomed
Eng 1988; 10: 155–158.

References

1 Moxey PC, Trier JS: Development of
villous absorptive cells in the human
fetal small intestine: a morphological
and morphometric study. Anat Rec
1979; 195: 463–482.
2 Owen WL, Jone AL: Epithelial cell spe-
cialisation within human Peyer’s patch-
es: an ultrastructural study of intestinal
lymphoid follicles. Gastroenterology
1974; 66: 189–203.
3 Lentze MJ: Die Ernährung von Frühge-
borenen unter 1,500 g: Enterale
Voraussetzungen. Monatsschr Kinder-
heilkd 1986; 134: 502–507.
4 Menard D: Development of human in-
testinal and gastric enzymes. Acta Pae-
diatr Suppl 1994; 405: 1–6.


5 Davidson NO, Hausman AM, Ifkovits
CA, Buse JB, Gould GW, Burant CF, Bell
GI: Human intestinal glucose transport-
er expression and localization of
GLUT5. Am J Physiol 1992; 262:C795–
C800.
6 Adibi SA: Regulation of expression of
the intestinal oligopeptide transporter
(Pept-1) in health and disease. Am J
Physiol Gastrointest Liver Physiol 2003;
285:G779–G788.
7 Boehm G, Bierbach U, Senger H, Jakobs-
son I, Minoli I, Moro G, Räihä NC: Ac-
tivities of lipase and trypsin in duodenal
juice of infants small for gestational age.
J Pediatr Gastroenterol Nutr 1991; 12:
324–327.

Koletzko B, et al. (eds): Pediatric Nutrition in Practice. World Rev Nutr Diet. Basel, Karger, 2015, vol 113, pp 83–86
DOI: 10.1159/000360320
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