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1. |
The ACGME Mandate: The 24/80 Approach to Pediatric Gastroenterology Training |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 37,
Issue 4,
2003,
Page 405-406
B Li,
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ISSN:0277-2116
出版商:OVID
年代:2003
数据来源: OVID
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2. |
Treatment for Biliary Atresia in 2003 |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 37,
Issue 4,
2003,
Page 407-408
Christophe Chardot,
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ISSN:0277-2116
出版商:OVID
年代:2003
数据来源: OVID
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3. |
Celiac Disease: A Bone Perspective |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 37,
Issue 4,
2003,
Page 409-411
Stefano Mora,
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ISSN:0277-2116
出版商:OVID
年代:2003
数据来源: OVID
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4. |
Coeliac Disease: An Update on Facts and Questions Based on the 10th International Symposium on Coeliac Disease |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 37,
Issue 4,
2003,
Page 412-421
Nadine Cerf-Bensussan,
Christophe Cellier,
Martine Heyman,
Nicole Brousse,
Jacques Schmitz,
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ISSN:0277-2116
出版商:OVID
年代:2003
数据来源: OVID
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5. |
Copper Deficiency And Excess In Infancy: Developing A Research Agenda |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 37,
Issue 4,
2003,
Page 422-429
Magdalena Araya,
Berthold Koletzko,
Ricardo Uauy,
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摘要:
Copper deficiency and excess have been recognized as potential health problems for infants and children worldwide. Clinical manifestations of copper deficiency and excess are well characterized but the precise sequence by which high copper intake interacts with genetic control systems, leading to liver damage in infants, is unknown. The possibility that genetic mutations or epigenetic factors related to the functional development of copper homeostasis, could make otherwise normal infants on normal copper intake more susceptible to copper toxicity has been an issue of concern. In January 2001 a group of pediatricians and researchers interested in this area met at Tegernsee, Bavaria, Germany, to reviewing the state of knowledge on the topic. They addressed six main issues: 1) The relevance of copper deficit and excess as health problems. 2) The appropriate biomarkers to identify and characterize copper status 3) The genetic variability in copper metabolism 4) The mechanisms of whole body copper homeostasis in early life and their changes with age 5) The development of experimental and animal models to address research questions on copper homeostasis in infants. 6) The safe upper and lower limits of copper intake/exposure from water and food. We present here the highlights of the discussions and the main conclusions of the meeting.
ISSN:0277-2116
出版商:OVID
年代:2003
数据来源: OVID
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6. |
Long-term Survival Following Kasai Portoenterostomy: Is Chronic Liver Disease Inevitable? |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 37,
Issue 4,
2003,
Page 430-433
Nedim Hadžić,
Mark Davenport,
Sarah Tizzard,
Jeanette Singer,
Edward Howard,
Giorgina Mieli-Vergani,
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摘要:
ObjectivesExtrahepatic biliary atresia (EHBA) is the most common indication for liver transplantation in childhood. Most children who do not undergo transplant are reported to have chronic liver disease and its complications. The aim of this single-center study was to identify children with normal laboratory indices and no clinical evidence of chronic liver disease 10 or more years after Kasai portoenterostomy (KP).MethodsA retrospective analysis of the medical notes of all children surgically treated at the authors' center between 1979 and 1991 was undertaken. Criteria for inclusion were absence of surgical complications, unremarkable clinical examination, and normal bilirubin, aspartate aminotransferase, albumin, international normalized prothrombin ratio, and platelet count.ResultsOf 244 children surgically treated during the observation period, the authors identified 28 (11%) adolescents (14 male) who fulfilled the entry criteria. Their median age was 13.4 years (range, 10.2–22.2 years). Twenty-six with type 3 EHBA had conventional KP, whereas 2 underwent modified operations. The corrective surgery was performed at a median age of 58 days (range, 20–99 days). Median time of complete clearance of jaundice from the date of KP was 75 days (range, 21–339 days). Twelve (43%) patients had history of cholangitis at a median age of 3.4 years. The liver histologic findings were suggestive of mild to moderate fibrosis in 54.2% and cirrhosis in 40.7% of the patients who underwent biopsy. No child had gastrointestinal bleeding during follow-up. Thirteen (46%) patients had an elective esophagogastroduodenoscopy, which was normal in all. Twenty-six (93%) patients were in mainstream education, whereas the remaining two (7%) attended special school because of reasons unrelated to liver disease.ConclusionsA sizable proportion of children with EHBA avoid significant chronic liver disease and its complications 10 years or more after conventional surgical correction and have an excellent quality of life. Their good outcome is not hampered by isolated episodes of ascending cholangitis. Whether or not the residual histologic damage will become symptomatic during their lifetime remains to be established.
ISSN:0277-2116
出版商:OVID
年代:2003
数据来源: OVID
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7. |
Bone Mineral Density in Children With Untreated and Treated Celiac Disease |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 37,
Issue 4,
2003,
Page 434-436
Umut Kavak,
Aysel Yüce,
Nurten Koçak,
Hülya Demir,
İnci Saltik,
Figen Gürakan,
Hasan Özen,
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摘要:
ObjectivesOsteopenia is a common complication in adults with celiac disease. The effect of a gluten-free diet on bone mineral density is a matter of controversy. The aim of this study was to investigate bone mineral density in children with celiac disease at diagnosis and in patients treated for 1 year.MethodsBone mineral density and bone mineral content were measured in 34 children with untreated celiac disease at diagnosis and in 28 patients on a gluten-free diet for 1 year. The results were compared with those of 64 gender- and age-matched healthy control subjects. Serum calcium, phosphate, alkaline phosphatase, 25 -hydroxy vitamin D, and intact parathormone levels were determined in treated and untreated patients.ResultsThe mean values of bone mineral density and bone mineral content of untreated patients with celiac were significantly lower than the control group (P= 0.006 andP= 0.005, respectively) and treated patients (P= 0.015 andP= 0.011 respectively). Treated patients had mean bone mineral density and bone mineral content values not significantly different from those of healthy control subjects. Minor hypocalcemia was detected in 17.6% of the patients with new diagnoses and 3.6% of the treated patients. Of the untreated patients, 29.4% had high intact parathormone concentrations; in untreated patients, the total was 14.3%. Untreated patients had significantly lower serum calcium and significantly higher intact parathormone levels than did treated patients. The other bone metabolism parameters were similar in the two celiac groups.ConclusionChildren with celiac disease are at risk for reduced bone mineral density. A strict gluten-free diet improves bone mineralization, even in 1 year. Early diagnosis and treatment of celiac disease during childhood will protect the patient from osteoporosis.
ISSN:0277-2116
出版商:OVID
年代:2003
数据来源: OVID
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8. |
Growth and Development of Premature Infants Fed Predominantly Human Milk, Predominantly Premature Infant Formula, or a Combination of Human Milk and Premature Formula |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 37,
Issue 4,
2003,
Page 437-446
Deborah O'Connor,
Joan Jacobs,
Robert Hall,
David Adamkin,
Nancy Auestad,
Marcella Castillo,
William Connor,
Sonja Connor,
Kathleen Fitzgerald,
Sharon Groh-Wargo,
E. Hartmann,
Jeri Janowsky,
Alan Lucas,
Dean Margeson,
Patricia Mena,
Martha Neuringer,
Gail Ross,
Lynn Singer,
Terence Stephenson,
Joanne Szabo,
Vance Zemon,
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摘要:
BackgroundIn a recent meta-analysis, human milk feeding of low birth-weight (LBW) infants was associated with a 5.2 point improvement in IQ tests. However, in the studies in this meta-analysis, feeding regimens were used (unfortified human milk, term formula) that no longer represent recommended practice.ObjectiveTo compare the growth, in-hospital feeding tolerance, morbidity, and development (cognitive, motor, visual, and language) of LBW infants fed different amounts of human milk until term chronologic age (CA) with those of LBW infants fed nutrient-enriched formulas from first enteral feeding.MethodsThe data in this study were collected in a previous randomized controlled trial assessing the benefit of supplementing nutrient-enriched formulas for LBW infants with arachidonic acid and docosahexaenoic acid. Infants (n = 463, birth weight, 750–1,800 g) were enrolled from nurseries located in Chile, the United Kingdom, and the United States. If human milk was fed before hospital discharge, it was fortified (3,050–3,300 kJ/L, 22–24 kcal/oz). As infants were weaned from human milk, they were fed nutrient-enriched formula with or without arachidonic and docosahexaenoic acids (3,300 kJ/L before term, 3,050 kJ/L thereafter) until 12 months CA. Formula fed infants were given nutrient-enriched formula with or without added arachidonic and docosahexaenoic acids (3,300 kJ/L to term, 3,050 kJ/L thereafter) until 12 months CA. For the purposes of this evaluation, infants were categorized into four mutually exclusive feeding groups: 1) predominantly human milk fed until term CA (PHM-T, n = 43); 2) ≥ 50% energy from human milk before hospital discharge (≥ 50% HM, n = 98); 3) < 50% of energy from human milk before hospital discharge (< 50% HM, n = 203); or 4) predominantly formula fed until term CA (PFF-T, n = 119).ResultsPFF-T infants weighed approximately 500 g more at term CA than did PHM-T infants. This absolute difference persisted until 6 months CA. PFF-T infants were also longer (1.0–1.5 cm) and had larger head circumferences (0.3–1.1 cm) than both PHM-T and ≥ 50% HM infants at term CA. There was a positive association between duration of human milk feeding and the Bayley Mental Index at 12 months CA (P= 0.032 full andP= 0.073 reduced, statistical models) after controlling for the confounding variables of home environment and maternal intelligence. Infants with chronic lung disease fed ≥ 50% HM until term CA (n = 22) had a mean Bayley Motor Index about 11 points higher at 12 months CA compared with infants PFF-T (n = 24,P= 0.033 full model).ConclusionOur data suggest that, despite a slower early growth rate, human milk fed LBW infants have development at least comparable to that of infants fed nutrient-enriched formula. Exploratory analysis suggests that some subgroups of human milk fed LBW infants may have enhanced development, although this needs to be confirmed in future studies.
ISSN:0277-2116
出版商:OVID
年代:2003
数据来源: OVID
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9. |
Maternal Education and the Incidence and Duration of Breast Feeding: A Prospective Study |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 37,
Issue 4,
2003,
Page 447-452
Giovanna Bertini,
Silvia Perugi,
Carlo Dani,
Marco Pezzati,
Michele Tronchin,
Firmino Rubaltelli,
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摘要:
IntroductionDuration of breast feeding and factors possibly affecting duration were studied in a population of 2174 newborn infants, with gestational age of >37 weeks, who were born in the Department of Obstetrics and Gynaecology at the University of Florence Hospital between November 15, 1997, and November 14, 1998.Patients and MethodsNine hundred mothers agreed to participate in the study. Five questionnaires were completed at the end of the 1st, 3rd, 6th, 9th, and 12th postpartum month. These dealt with infant feeding practices, including breast feeding during the previous week. Breast feeding duration was defined as short (1 month); medium-short (>1 month–<3 months); medium (>3–<6 months); medium-long (>6–<9 months), and long (>9 months).ResultsThe authors found that 76.3%, 64.7%, 42.3%, 26.4%, and 17% of mothers were still breast feeding at 1, 3, 6, 9, and 12 months after delivery, respectively. The multivariate analysis of the correspondence shows that lack of breast feeding is associated with a birth weight of less than 3000 g, a low level of maternal education, and maternal profession as a housewife or blue collar worker in the commercial sector. A period of breast feeding defined as short or medium-short is associated with mothers who smoke, primiparous mothers, and absence of maternal allergy. The survival curves highlight how the single factor of smoking is an element that leads to a significant difference in the duration of breast feeding. The multiple Cox regression analysis shows a significant negative influence associated with birth weight of less than 3000 g, maternal smoking, and first parity. Above all, among low–birth-weight infants of mothers who smoke, there is a strong correlation with a shorter duration of breast feeding.DiscussionThere is still a need for programs that support and encourage breast feeding, focusing particularly on mothers with a low level of education who give birth to a low-weight infant, primiparous mothers, and smokers.
ISSN:0277-2116
出版商:OVID
年代:2003
数据来源: OVID
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10. |
Dietary Nucleotides Accelerate Changes in Intestinal Lymphocyte Maturation in Weanling Mice |
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Journal of Pediatric Gastroenterology and Nutrition,
Volume 37,
Issue 4,
2003,
Page 453-461
Manuel Manzano,
Ana Clara Abadía-Molina,
Enrique-García Olivares,
Angel Gil,
Ricardo Rueda,
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摘要:
ObjectiveNucleotides, the building blocks of nucleic acids, are normal components of the mammalian diet. These molecules have been implicated in biologic processes, such as the stimulation of the immunologic response. Nucleotides have also been considered as conditionally essential nutrients for infant formulas. The authors evaluated the influence of dietary nucleotides on the expression of several surface antigens by different intestinal lymphocyte populations in weanling mice.MethodsMice at weaning were fed a semipurified diet with or without 3 g/kg of each of the following nucleotides: adenosine monophosphate, cytosine monophosphate, guanosine monophosphate, and uridine monophosphate. Animals were killed at different times (0, 4, 7, 12, and 18 days) after weaning, and lymphocytes from intestinal Peyer's patches, epithelium, and lamina propria were isolated. The expression of different antigens (CD3, CD4, CD8&agr;, CD8&bgr;, TCR&agr;&bgr;, TCR&ggr;&dgr;, CD5, CD22 and CD45R) was analyzed by flow cytometry.ResultsThe expression of these antigens changed parallel to the maturation of the lymphocytes from Peyer's patches, epithelium, and lamina propria. However, developmental changes of expression for most of the antigens occurred sooner in the animals fed the diet supplemented with nucleotides. The expression of T and B antigens was different in the lymphocyte populations analyzed and also changed according to the diet within each population. In general, nucleotides promoted the expression of B- and T-helper cell antigens.ConclusionsThe authors conclude that dietary nucleotides may affect the process of maturation and differentiation of intestinal lymphocytes, which usually takes place at weaning.
ISSN:0277-2116
出版商:OVID
年代:2003
数据来源: OVID
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