Matches in SemOpenAlex for { <https://semopenalex.org/work/W2089818937> ?p ?o ?g. }
- W2089818937 endingPage "77.e2" @default.
- W2089818937 startingPage "73" @default.
- W2089818937 abstract "Objectives To describe the presentation and progress over the first year of life of neonates with Hirschsprung disease, to describe their physical and developmental outcomes at 12 months of age, and to compare the outcomes of infants with short- vs long-segment Hirschsprung disease. Study design A retrospective study of neonates born with Hirschsprung disease in Western Australia between January 1, 2001, and December 31, 2010, to review their presentation, progress, growth, and development at 12 months of age. Results Fifty-four infants were identified (40 with short and 11 with long segment and 3 with total colonic aganglionosis); 9 infants had a recognized syndrome and 1 infant died, unrelated to Hirschsprung disease. A primary pull-through procedure was performed in 97% and 21% of neonates with short- and non–short-segment Hirschsprung disease, respectively; 17 (31%) infants developed anal stenosis requiring dilatations. Enterocolitis occurred in 14 (26%) infants. Griffiths Mental Development Scale scores (1 year) were available in 31 of 45 nonsyndromic survivors: mean general quotient (94.2, SD 8.89) was significantly less than the population mean (P = .007), but the number of infants with developmental delay was within the expected range. Physical growth, except length, appeared adequate in nonsyndromic infants. There were no significant differences in the outcomes of infants with short- vs non–short-segment Hirschsprung disease. Conclusions At 1 year of age, many infants with Hirschsprung disease have ongoing gastrointestinal problems. Their overall growth appears satisfactory, and most infants are developing normally; however, their mean general quotient appears shifted to the left. Longer-term studies will better define developmental outcomes. To describe the presentation and progress over the first year of life of neonates with Hirschsprung disease, to describe their physical and developmental outcomes at 12 months of age, and to compare the outcomes of infants with short- vs long-segment Hirschsprung disease. A retrospective study of neonates born with Hirschsprung disease in Western Australia between January 1, 2001, and December 31, 2010, to review their presentation, progress, growth, and development at 12 months of age. Fifty-four infants were identified (40 with short and 11 with long segment and 3 with total colonic aganglionosis); 9 infants had a recognized syndrome and 1 infant died, unrelated to Hirschsprung disease. A primary pull-through procedure was performed in 97% and 21% of neonates with short- and non–short-segment Hirschsprung disease, respectively; 17 (31%) infants developed anal stenosis requiring dilatations. Enterocolitis occurred in 14 (26%) infants. Griffiths Mental Development Scale scores (1 year) were available in 31 of 45 nonsyndromic survivors: mean general quotient (94.2, SD 8.89) was significantly less than the population mean (P = .007), but the number of infants with developmental delay was within the expected range. Physical growth, except length, appeared adequate in nonsyndromic infants. There were no significant differences in the outcomes of infants with short- vs non–short-segment Hirschsprung disease. At 1 year of age, many infants with Hirschsprung disease have ongoing gastrointestinal problems. Their overall growth appears satisfactory, and most infants are developing normally; however, their mean general quotient appears shifted to the left. Longer-term studies will better define developmental outcomes." @default.
- W2089818937 created "2016-06-24" @default.
- W2089818937 creator A5020842830 @default.
- W2089818937 creator A5053659404 @default.
- W2089818937 creator A5058613997 @default.
- W2089818937 creator A5067865628 @default.
- W2089818937 date "2014-07-01" @default.
- W2089818937 modified "2023-09-27" @default.
- W2089818937 title "Growth and Developmental Outcomes of Infants with Hirschsprung Disease Presenting in the Neonatal Period: A Retrospective Study" @default.
- W2089818937 cites W1502207187 @default.
- W2089818937 cites W1534420475 @default.
- W2089818937 cites W1924118315 @default.
- W2089818937 cites W1963486307 @default.
- W2089818937 cites W1965217491 @default.
- W2089818937 cites W1966649323 @default.
- W2089818937 cites W1968398662 @default.
- W2089818937 cites W1972493712 @default.
- W2089818937 cites W1996593258 @default.
- W2089818937 cites W2000253273 @default.
- W2089818937 cites W2003302681 @default.
- W2089818937 cites W2011059782 @default.
- W2089818937 cites W2013727372 @default.
- W2089818937 cites W2015784553 @default.
- W2089818937 cites W2019235974 @default.
- W2089818937 cites W2022663354 @default.
- W2089818937 cites W2032201228 @default.
- W2089818937 cites W2032544809 @default.
- W2089818937 cites W2034817406 @default.
- W2089818937 cites W2035937818 @default.
- W2089818937 cites W2037557484 @default.
- W2089818937 cites W2044439353 @default.
- W2089818937 cites W2046524519 @default.
- W2089818937 cites W2052639401 @default.
- W2089818937 cites W2052994127 @default.
- W2089818937 cites W2057348722 @default.
- W2089818937 cites W2077793101 @default.
- W2089818937 cites W2088154210 @default.
- W2089818937 cites W2092461394 @default.
- W2089818937 cites W2100870243 @default.
- W2089818937 cites W2115440200 @default.
- W2089818937 cites W2115795995 @default.
- W2089818937 cites W2130583261 @default.
- W2089818937 cites W2134506601 @default.
- W2089818937 cites W2142425768 @default.
- W2089818937 cites W2164714013 @default.
- W2089818937 doi "https://doi.org/10.1016/j.jpeds.2014.02.062" @default.
- W2089818937 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24721468" @default.
- W2089818937 hasPublicationYear "2014" @default.
- W2089818937 type Work @default.
- W2089818937 sameAs 2089818937 @default.
- W2089818937 citedByCount "12" @default.
- W2089818937 countsByYear W20898189372015 @default.
- W2089818937 countsByYear W20898189372017 @default.
- W2089818937 countsByYear W20898189372018 @default.
- W2089818937 countsByYear W20898189372019 @default.
- W2089818937 countsByYear W20898189372020 @default.
- W2089818937 countsByYear W20898189372021 @default.
- W2089818937 countsByYear W20898189372022 @default.
- W2089818937 countsByYear W20898189372023 @default.
- W2089818937 crossrefType "journal-article" @default.
- W2089818937 hasAuthorship W2089818937A5020842830 @default.
- W2089818937 hasAuthorship W2089818937A5053659404 @default.
- W2089818937 hasAuthorship W2089818937A5058613997 @default.
- W2089818937 hasAuthorship W2089818937A5067865628 @default.
- W2089818937 hasConcept C126322002 @default.
- W2089818937 hasConcept C141071460 @default.
- W2089818937 hasConcept C167135981 @default.
- W2089818937 hasConcept C187212893 @default.
- W2089818937 hasConcept C2776258884 @default.
- W2089818937 hasConcept C2777601897 @default.
- W2089818937 hasConcept C2779089422 @default.
- W2089818937 hasConcept C2779134260 @default.
- W2089818937 hasConcept C2908647359 @default.
- W2089818937 hasConcept C71924100 @default.
- W2089818937 hasConcept C99454951 @default.
- W2089818937 hasConceptScore W2089818937C126322002 @default.
- W2089818937 hasConceptScore W2089818937C141071460 @default.
- W2089818937 hasConceptScore W2089818937C167135981 @default.
- W2089818937 hasConceptScore W2089818937C187212893 @default.
- W2089818937 hasConceptScore W2089818937C2776258884 @default.
- W2089818937 hasConceptScore W2089818937C2777601897 @default.
- W2089818937 hasConceptScore W2089818937C2779089422 @default.
- W2089818937 hasConceptScore W2089818937C2779134260 @default.
- W2089818937 hasConceptScore W2089818937C2908647359 @default.
- W2089818937 hasConceptScore W2089818937C71924100 @default.
- W2089818937 hasConceptScore W2089818937C99454951 @default.
- W2089818937 hasIssue "1" @default.
- W2089818937 hasLocation W20898189371 @default.
- W2089818937 hasLocation W20898189372 @default.
- W2089818937 hasOpenAccess W2089818937 @default.
- W2089818937 hasPrimaryLocation W20898189371 @default.
- W2089818937 hasRelatedWork W1484170136 @default.
- W2089818937 hasRelatedWork W1973247265 @default.
- W2089818937 hasRelatedWork W1978464520 @default.
- W2089818937 hasRelatedWork W2005969064 @default.
- W2089818937 hasRelatedWork W2006107229 @default.
- W2089818937 hasRelatedWork W2052433957 @default.
- W2089818937 hasRelatedWork W2071032595 @default.