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- IRMS - Nicolae Testemitanu SUMPh
- 1. COLECȚIA INSTITUȚIONALĂ
- MedEspera: International Medical Congress for Students and Young Doctors
- MedEspera 2014
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/18045
Title: | Studay of contemporary literature on the topic of congenital bowel obstruction |
Authors: | Burda, Evghenii |
Issue Date: | 2014 |
Publisher: | Ministry of Health of the Republic of Moldova, State Medical and Pharmaceutical University Nicolae Testemitanu, Medical Students and Residents Association |
Citation: | BURDA, Evghenii. Studay of contemporary literature on the topic of congenital bowel obstruction. In: MedEspera: the 5th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2014, p. 191. |
Abstract: | Background: Neonatal intestinal obstruction (N10) is one of the most common emergency
conditions a paediatric surgeon is called upon to assess during the neonatal period.
Successful management of NIO depends on timely diagnosis and referral for therapy.
Material of study: Intestinal obstructions are either intrinsic or extrinsic. Intrinsic lesions result
from absent (atresia) or partial (stenosis) recanalization of the intestine. In cases of atresia, the two
segments of the gut may be either completely separated or connected by a fibrous cord. In cases of
stenosis, the lumen of the gut is narrowed or the two intestinal segments are separated by a septum with
a central diaphragm. Apple-peel atresia is characterized by absence of a vast segment of the small
bowel, which can include distal duodenum, the entire jejunum and proximal ileus. Extrinsic obstructions
are caused by malrotation of the colon with volvulus, peritoneal bands, meconium ileus, and agangliosis
(Hirschsprung’s disease). The most frequent site of small bowel obstruction is distal ileus (35%),
followed by proximal jejunum (30%), distal jejunum (20%), proximal ileus (15%).
Result: Although the condition is usually sporadic, in multiple intestinal atresia, familial
cases have been described. Associated abnormalities and chromosomal defects are rare. In contrast
with anorectal atresia, associated defects such as genitourinary, vertebral, cardiovascular and
gastrointestinal anomalies are found in about 80% of cases.
Conclusion: Infants with bowel obstruction typically present in the early neonatal period with
symptoms of vomiting and abdominal distention. The prognosis is related to the gestational age at
delivery, the presence of associated abnormalities and site of obstruction. In those bom after 32 weeks
with isolated obstruction requiring resection of only a short segment of bowel, survival is more than
95%. Loss of large segments of bowel can lead to short gut syndrome, which is a lethal condition. |
metadata.dc.relation.ispartof: | MedEspera: The 5th International Medical Congress for Students and Young Doctors, May 14-17, 2014, Chisinau, Republic of Moldova |
URI: | http://repository.usmf.md/handle/20.500.12710/18045 |
Appears in Collections: | MedEspera 2014
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