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      <title>Pediatrics Subject Collection: Surgery</title>
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      <title>Pediatrics</title>
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   <item rdf:about="http://pediatrics.aappublications.org:80/cgi/content/short/124/1/241?rss=1">
      <title><![CDATA[Apolipoprotein E Genotype Modifies the Risk of Behavior Problems After Infant Cardiac Surgery [ARTICLES] ]]></title>
      <link>http://pediatrics.aappublications.org:80/cgi/content/short/124/1/241?rss=1</link>
      <description>OBJECTIVE: The goal was to evaluate polymorphisms of the APOE gene as modifiers of neurobehavioral outcomes for preschool-aged children with congenital heart defects, after cardiac surgery. 

METHODS: A prospective observational study with neurodevelopmental evaluation between the fourth and fifth birthdays was performed. Attention and behavioral skills were assessed through parental report. 

RESULTS: Parents of 380 children completed the neurobehavioral measures. Child Behavior Checklist scores for the pervasive developmental problem scale were in the at-risk or clinically significant range for 15% of the cohort, compared with 9% for the normative data (P &lt; .00001). Attention problem scores were in the at-risk or clinically significant range for 12% of the cohort, compared with 7% for the normative data (P = .0002). The Attention-Deficit/Hyperactivity Disorder Rating Scale-IV, Preschool Version, was completed for 378 children; 30% scored in the clinically significant range for inattention and 22% for impulsivity. After adjustment for covariates, the APOE {epsilon}2 allele was significantly associated with higher scores (worse problems) for multiple Child Behavior Checklist indices, including somatic complaints (P = .009), pervasive developmental problems (P = .032), and internalizing problems (P = .009). In each case, the {epsilon}4 allele was associated with a better outcome. APOE {epsilon}2 carriers had impaired social skills, compared with {epsilon}4 carriers (P = .009). 

CONCLUSIONS: For preschool-aged children with congenital heart defects requiring surgery, parental rating scales showed an increased prevalence of restricted behavior patterns, inattention, and impaired social interactions. The APOE {epsilon}2 allele was associated with increased behavior problems, impaired social interactions, and restricted behavior patterns.</description>
      <dc:creator>Gaynor, J. W.</dc:creator>
      <dc:creator>Nord, A. S.</dc:creator>
      <dc:creator>Wernovsky, G.</dc:creator>
      <dc:creator>Bernbaum, J.</dc:creator>
      <dc:creator>Solot, C. B.</dc:creator>
      <dc:creator>Burnham, N.</dc:creator>
      <dc:creator>Zackai, E.</dc:creator>
      <dc:creator>Heagerty, P. J.</dc:creator>
      <dc:creator>Clancy, R. R.</dc:creator>
      <dc:creator>Nicolson, S. C.</dc:creator>
      <dc:creator>Jarvik, G. P.</dc:creator>
      <dc:creator>Gerdes, M.</dc:creator>
      <dc:date>2009-07-01</dc:date>
      <dc:identifier>doi:10.1542/peds.2008-2281</dc:identifier>
      <dc:title>Apolipoprotein E Genotype Modifies the Risk of Behavior Problems After Infant Cardiac Surgery</dc:title>
      <dc:publisher>American Academy of Pediatrics</dc:publisher>
      <prism:number>1</prism:number>
      <prism:volume>124</prism:volume>
      <prism:endingPage>250</prism:endingPage>
      <prism:startingPage>241</prism:startingPage>
      <prism:publicationDate>2009-07-01</prism:publicationDate>
      <prism:section>ARTICLES</prism:section>
   </item>
   <item rdf:about="http://pediatrics.aappublications.org:80/cgi/content/short/123/5/1280?rss=1">
      <title><![CDATA[Impact of Age at Kasai Operation on Its Results in Late Childhood and Adolescence: A Rational Basis for Biliary Atresia Screening [ARTICLES] ]]></title>
      <link>http://pediatrics.aappublications.org:80/cgi/content/short/123/5/1280?rss=1</link>
      <description>BACKGROUND. Increased age at surgery has a negative impact on results of the Kasai operation for biliary atresia in infancy and early childhood. It remained unclear if an age threshold exists and if this effect persists with extended follow-up. In this study we examined the relationship between increased age at surgery and its results in adolescence. 

METHODS. All patients with biliary atresia who were living in France and born between 1986 and 2002 were included. Median follow-up in survivors was 7 years. 

RESULTS. Included in the study were 743 patients with biliary atresia, 695 of whom underwent a Kasai operation; 2-, 5-, 10-, and 15-year survival rates with native liver were 57.1%, 37.9%, 32.4%, and 28.5%, respectively. Median age at Kasai operation was 60 days and was stable over the study period. Whatever the follow-up (2, 5, 10, or 15 years), survival rates with native liver decreased when age at surgery increased ([&amp;le;]30, 31-45, 46-60, 61-75, and 76-90 days). Accordingly, we estimated that if every patient with biliary atresia underwent the Kasai operation before 46 days of age, 5.7% of all liver transplantations performed annually in France in patients younger than 16 years could be spared. 

CONCLUSIONS. Increased age at surgery had a progressive and sustained deleterious effect on the results of the Kasai operation until adolescence. These findings indicate a rational basis for biliary atresia screening to reduce the need for liver transplantations in infancy and childhood.</description>
      <dc:creator>Serinet, M.-O.</dc:creator>
      <dc:creator>Wildhaber, B. E.</dc:creator>
      <dc:creator>Broue, P.</dc:creator>
      <dc:creator>Lachaux, A.</dc:creator>
      <dc:creator>Sarles, J.</dc:creator>
      <dc:creator>Jacquemin, E.</dc:creator>
      <dc:creator>Gauthier, F.</dc:creator>
      <dc:creator>Chardot, C.</dc:creator>
      <dc:date>2009-05-01</dc:date>
      <dc:identifier>doi:10.1542/peds.2008-1949</dc:identifier>
      <dc:title>Impact of Age at Kasai Operation on Its Results in Late Childhood and Adolescence: A Rational Basis for Biliary Atresia Screening</dc:title>
      <dc:publisher>American Academy of Pediatrics</dc:publisher>
      <prism:number>5</prism:number>
      <prism:volume>123</prism:volume>
      <prism:endingPage>1286</prism:endingPage>
      <prism:startingPage>1280</prism:startingPage>
      <prism:publicationDate>2009-05-01</prism:publicationDate>
      <prism:section>ARTICLES</prism:section>
   </item>
   <item rdf:about="http://pediatrics.aappublications.org:80/cgi/content/short/123/5/1377?rss=1">
      <title><![CDATA[Long-term Outcomes of Restorative Proctocolectomy in Children With Ulcerative Colitis [ARTICLES] ]]></title>
      <link>http://pediatrics.aappublications.org:80/cgi/content/short/123/5/1377?rss=1</link>
      <description>OBJECTIVE. Long-term outcomes of restorative proctocolectomy for pediatric-onset ulcerative colitis are unclear. 

METHODS. Questionnaires on health outcomes and quality of life were mailed to patients with childhood-onset ulcerative colitis who had undergone proctocolectomy with ileoanal anastomosis in 2 university hospitals between 1985 and 2005. Investigators not involved in the surgical management of the patients approached participants. Matched control children were randomly chosen from the Population Register Centre of Finland. 

RESULTS. Fifty-two (66%) patients and 117 (37%) controls responded. After a mean follow-up of 10 years, at least 1 surgical complication had occurred in 39 (75%) patients, and 28 (54%) had undergone reoperation. Only 1 failure of ileoanal anastomosis occurred. Ulcerative colitis had been reclassified as Crohn disease in 6 (12%) patients. Pouchitis occurred in 37 (73%) patients. The median stool frequency was 5 for day and 1 for night, but 46% used medication to control stool frequency. Nighttime soiling was reported by 56% of the patients. The mean overall quality-of-life score, the mean BMI (22 kg/m2 for both), and the number of subjects (aged &gt;20 years) with offspring (14% vs 15%) was similar to the population-based controls. 

CONCLUSIONS. Stool frequency after restorative proctocolectomy in children with ulcerative colitis is stable and comparable to those of adult patients. Although nighttime incontinence is common, general health status and overall quality of life are comparable to the normal population.</description>
      <dc:creator>Pakarinen, M. P.</dc:creator>
      <dc:creator>Natunen, J.</dc:creator>
      <dc:creator>Ashorn, M.</dc:creator>
      <dc:creator>Koivusalo, A.</dc:creator>
      <dc:creator>Turunen, P.</dc:creator>
      <dc:creator>Rintala, R. J.</dc:creator>
      <dc:creator>Kolho, K.-L.</dc:creator>
      <dc:date>2009-05-01</dc:date>
      <dc:identifier>doi:10.1542/peds.2008-2086</dc:identifier>
      <dc:title>Long-term Outcomes of Restorative Proctocolectomy in Children With Ulcerative Colitis</dc:title>
      <dc:publisher>American Academy of Pediatrics</dc:publisher>
      <prism:number>5</prism:number>
      <prism:volume>123</prism:volume>
      <prism:endingPage>1382</prism:endingPage>
      <prism:startingPage>1377</prism:startingPage>
      <prism:publicationDate>2009-05-01</prism:publicationDate>
      <prism:section>ARTICLES</prism:section>
   </item>
   <item rdf:about="http://pediatrics.aappublications.org:80/cgi/content/short/123/2/494?rss=1">
      <title><![CDATA[Timing of Delivery and Survival Rates for Infants With Prenatal Diagnoses of Congenital Diaphragmatic Hernia [ARTICLES] ]]></title>
      <link>http://pediatrics.aappublications.org:80/cgi/content/short/123/2/494?rss=1</link>
      <description>OBJECTIVES. The goal of the study was to test the hypothesis that infants with known congenital diaphragmatic hernias born at early term gestation (37-38 weeks) rather than later (39-41 weeks) had greater survival rates and less extracorporeal membrane oxygenation use. Primary outcomes were survival to hospital discharge or transfer and extracorporeal membrane oxygenation use. 

METHODS. A retrospective cohort study of term infants with prenatal diagnoses of congenital diaphragmatic hernia was performed with the Congenital Diaphragmatic Hernia Study Group Registry of patients with congenital diaphragmatic hernias who were treated between January 1995 and December 2006. 

RESULTS. Among 628 term infants at 37 to 41 weeks of gestation who had prenatal diagnoses of congenital diaphragmatic hernia and were free of major associated anomalies, early term birth (37 vs 39-41 weeks) and greater birth weight were associated independently with survival, whereas black race was related inversely to survival. Infants born at early term with birth weights at or above the group mean (3.1 kg) had the greatest survival rate (80%). Among infants born through elective cesarean delivery, infants born at 37 to 38 weeks of gestation, compared with 39 to 41 weeks, had less use of extracorporeal membrane oxygenation (22.0% vs 35.5%) and a trend toward a greater survival rate (75.0% vs 65.8%). 

CONCLUSIONS. The timing of delivery is an independent, potentially important factor in the consideration of elective delivery for infants diagnosed prenatally as having congenital diaphragmatic hernias. Among fetuses with prenatally diagnosed congenital diaphragmatic hernias and without major associated anomalies, early term delivery may confer advantage.</description>
      <dc:creator>Stevens, T. P.</dc:creator>
      <dc:creator>van Wijngaarden, E.</dc:creator>
      <dc:creator>Ackerman, K. G.</dc:creator>
      <dc:creator>Lally, P. A.</dc:creator>
      <dc:creator>Lally, K. P.</dc:creator>
      <dc:creator>for the Congenital Diaphragmatic Hernia Study Group,  </dc:creator>
      <dc:date>2009-02-01</dc:date>
      <dc:identifier>doi:10.1542/peds.2008-0528</dc:identifier>
      <dc:title>Timing of Delivery and Survival Rates for Infants With Prenatal Diagnoses of Congenital Diaphragmatic Hernia</dc:title>
      <dc:publisher>American Academy of Pediatrics</dc:publisher>
      <prism:number>2</prism:number>
      <prism:volume>123</prism:volume>
      <prism:endingPage>502</prism:endingPage>
      <prism:startingPage>494</prism:startingPage>
      <prism:publicationDate>2009-02-01</prism:publicationDate>
      <prism:section>ARTICLES</prism:section>
   </item>
   <item rdf:about="http://pediatrics.aappublications.org:80/cgi/content/short/123/1/199?rss=1">
      <title><![CDATA[Family Burden After Traumatic Brain Injury in Children [ARTICLES] ]]></title>
      <link>http://pediatrics.aappublications.org:80/cgi/content/short/123/1/199?rss=1</link>
      <description>OBJECTIVE. Traumatic brain injury has a substantial impact on caregivers. This study describes the burden experienced by caregivers of children with traumatic brain injury and examines the relationship between child functioning and family burden during the first year after injury. 

PATIENTS AND METHODS. Children aged 5 to 15 years hospitalized for traumatic brain injury at 4 participating trauma centers were eligible. Caregivers completed baseline and 3- and 12-month telephone interviews measuring the child's health-related quality of life using the Pediatric Quality of Life Inventory. The emotional impact scale of the Child Health Questionnaire was used to identify caregivers with substantial distress, including general worry or interference with family routine. Caregiver perceptions of whether health care needs were met or unmet and days missed from work were also measured. 

RESULTS. A total of 330 subjects enrolled; follow-up was conducted with 312 at 3 months and 288 at 12 months. Most subjects were white (68%) and male (69%). Abnormal Pediatric Quality of Life Inventory subscores were related to substantial caregiver burden (either general worry or interference in routine). These abnormalities were reported by &gt;75% of patients at 3 months and persisted to 1 year in some patients. Parental perception of unmet health care needs was strongly related to family burden outcomes, with up to 69% of this subset of parents reporting substantial worry, and nearly one quarter reporting interference with daily routine/concentration 1 year after injury. Child dysfunction predicted parental burden at 3 and 12 months. Burden was greater when health care need was unmet. Abnormalities on the Pediatric Quality of Life Inventory predicted the amount of work missed by parents, especially in the presence of unmet needs. 

CONCLUSIONS. Caregivers are more likely to report family burden problems when child functioning is poorer and health care needs are unmet. Improved identification and provision of services is a potentially modifiable factor that may decrease family burden after pediatric traumatic brain injury.</description>
      <dc:creator>Aitken, M. E.</dc:creator>
      <dc:creator>McCarthy, M. L.</dc:creator>
      <dc:creator>Slomine, B. S.</dc:creator>
      <dc:creator>Ding, R.</dc:creator>
      <dc:creator>Durbin, D. R.</dc:creator>
      <dc:creator>Jaffe, K. M.</dc:creator>
      <dc:creator>Paidas, C. N.</dc:creator>
      <dc:creator>Dorsch, A. M.</dc:creator>
      <dc:creator>Christensen, J. R.</dc:creator>
      <dc:creator>MacKenzie, E. J.</dc:creator>
      <dc:creator>and the CHAT Study Group,  </dc:creator>
      <dc:date>2009-01-01</dc:date>
      <dc:identifier>doi:10.1542/peds.2008-0607</dc:identifier>
      <dc:title>Family Burden After Traumatic Brain Injury in Children</dc:title>
      <dc:publisher>American Academy of Pediatrics</dc:publisher>
      <prism:number>1</prism:number>
      <prism:volume>123</prism:volume>
      <prism:endingPage>206</prism:endingPage>
      <prism:startingPage>199</prism:startingPage>
      <prism:publicationDate>2009-01-01</prism:publicationDate>
      <prism:section>ARTICLES</prism:section>
   </item>
   <item rdf:about="http://pediatrics.aappublications.org:80/cgi/content/short/123/1/214?rss=1">
      <title><![CDATA[Reversal of Type 2 Diabetes Mellitus and Improvements in Cardiovascular Risk Factors After Surgical Weight Loss in Adolescents [ARTICLES] ]]></title>
      <link>http://pediatrics.aappublications.org:80/cgi/content/short/123/1/214?rss=1</link>
      <description>OBJECTIVES. Type 2 diabetes mellitus is associated with obesity, dyslipidemia, and hypertension, all well-known risk factors for cardiovascular disease. Surgical weight loss has resulted in a marked reduction of these risk factors in adults. We hypothesized that gastric bypass would improve parameters of metabolic dysfunction and cardiovascular risk in adolescents with type 2 diabetes mellitus. 

PATIENTS AND METHODS. Eleven adolescents who underwent Roux-en-Y gastric bypass at 5 centers were included. Anthropometric, hemodynamic, and biochemical measures and surgical complications were analyzed. Similar measures from 67 adolescents with type 2 diabetes mellitus who were treated medically for 1 year were also analyzed. 

RESULTS. Adolescents who underwent Roux-en-Y gastric bypass were extremely obese (mean BMI of 50 {+/-} 5.9 kg/m2) with numerous cardiovascular risk factors. After surgery there was evidence of remission of type 2 diabetes mellitus in all but 1 patient. Significant improvements in BMI (-34%), fasting blood glucose (-41%), fasting insulin concentrations (-81%), hemoglobin A1c levels (7.3%-5.6%), and insulin sensitivity were also seen. There were significant improvements in serum lipid levels and blood pressure. In comparison, adolescents with type 2 diabetes mellitus who were followed during 1 year of medical treatment demonstrated stable body weight (baseline BMI: 35 {+/-} 7.3 kg/m2; 1-year BMI: 34.9 {+/-} 7.2 kg/m2) and no significant change in blood pressure or in diabetic medication use. Medically managed patients had significantly improved hemoglobin A1c levels over 1 year (baseline: 7.85% {+/-} 2.3%; 1 year: 7.1% {+/-} 2%). 

CONCLUSIONS. Extremely obese diabetic adolescents experience significant weight loss and remission of type 2 diabetes mellitus after Roux-en-Y gastric bypass. Improvements in insulin resistance, {beta}-cell function, and cardiovascular risk factors support Roux-en-Y gastric bypass as an intervention that improves the health of these adolescents. Although the long-term efficacy of Roux-en-Y gastric bypass is not known, these findings suggest that Roux-en-Y gastric bypass is an effective option for the treatment of extremely obese adolescents with type 2 diabetes mellitus.</description>
      <dc:creator>Inge, T. H.</dc:creator>
      <dc:creator>Miyano, G.</dc:creator>
      <dc:creator>Bean, J.</dc:creator>
      <dc:creator>Helmrath, M.</dc:creator>
      <dc:creator>Courcoulas, A.</dc:creator>
      <dc:creator>Harmon, C. M.</dc:creator>
      <dc:creator>Chen, M. K.</dc:creator>
      <dc:creator>Wilson, K.</dc:creator>
      <dc:creator>Daniels, S. R.</dc:creator>
      <dc:creator>Garcia, V. F.</dc:creator>
      <dc:creator>Brandt, M. L.</dc:creator>
      <dc:creator>Dolan, L. M.</dc:creator>
      <dc:date>2009-01-01</dc:date>
      <dc:identifier>doi:10.1542/peds.2008-0522</dc:identifier>
      <dc:title>Reversal of Type 2 Diabetes Mellitus and Improvements in Cardiovascular Risk Factors After Surgical Weight Loss in Adolescents</dc:title>
      <dc:publisher>American Academy of Pediatrics</dc:publisher>
      <prism:number>1</prism:number>
      <prism:volume>123</prism:volume>
      <prism:endingPage>222</prism:endingPage>
      <prism:startingPage>214</prism:startingPage>
      <prism:publicationDate>2009-01-01</prism:publicationDate>
      <prism:section>ARTICLES</prism:section>
   </item>
   <item rdf:about="http://pediatrics.aappublications.org:80/cgi/content/short/123/1/332?rss=1">
      <title><![CDATA[A Single-Blinded, Randomized Comparison of Laparoscopic Versus Open Hernia Repair in Children [ARTICLES] ]]></title>
      <link>http://pediatrics.aappublications.org:80/cgi/content/short/123/1/332?rss=1</link>
      <description>OBJECTIVE. The role of laparoscopic surgery in pediatric inguinal hernia repair is unclear. We aimed to compare day-case laparoscopic hernia repair with open repair. 

METHODS. A prospective, single-blinded randomized study in children aged 4 months to 16 years with unilateral inguinal hernia was performed. The primary outcome measure was the time to normal daily activities after surgery. Secondary outcome measures included postoperative pain, time in the operation room, results, and complications. 

RESULTS. Eighty-nine patients were enrolled (laparoscopic hernia repair: 47, open repair: 42). The mean number of days to normal activity after laparoscopic hernia repair and open repair was 2.4 and 2.5, respectively. Thirty-seven (79%) patients with laparoscopic hernia repair and 20 (42%) with open repair required rescue analgesia postoperatively. The median pain score in the second postoperative morning was significantly higher after laparoscopic hernia repair. The median times in the operation room for laparoscopic hernia repair and open repair were 63 and 38 minutes, respectively. Surgical and cosmetic results were similar at up to 2 years' follow-up. 

CONCLUSIONS. Recovery and outcome were similar after open repair and laparoscopic hernia repair in children. Laparoscopic hernia repair was associated with increased theater time and postoperative pain.</description>
      <dc:creator>Koivusalo, A. I.</dc:creator>
      <dc:creator>Korpela, R.</dc:creator>
      <dc:creator>Wirtavuori, K.</dc:creator>
      <dc:creator>Piiparinen, S.</dc:creator>
      <dc:creator>Rintala, R. J.</dc:creator>
      <dc:creator>Pakarinen, M. P.</dc:creator>
      <dc:date>2009-01-01</dc:date>
      <dc:identifier>doi:10.1542/peds.2007-3752</dc:identifier>
      <dc:title>A Single-Blinded, Randomized Comparison of Laparoscopic Versus Open Hernia Repair in Children</dc:title>
      <dc:publisher>American Academy of Pediatrics</dc:publisher>
      <prism:number>1</prism:number>
      <prism:volume>123</prism:volume>
      <prism:endingPage>337</prism:endingPage>
      <prism:startingPage>332</prism:startingPage>
      <prism:publicationDate>2009-01-01</prism:publicationDate>
      <prism:section>ARTICLES</prism:section>
   </item>
   <item rdf:about="http://pediatrics.aappublications.org:80/cgi/content/short/122/6/1218?rss=1">
      <title><![CDATA[Surgical Repair of Pectus Excavatum Markedly Improves Body Image and Perceived Ability for Physical Activity: Multicenter Study [ARTICLES] ]]></title>
      <link>http://pediatrics.aappublications.org:80/cgi/content/short/122/6/1218?rss=1</link>
      <description>OBJECTIVE. This study evaluated changes in both physical and psychosocial quality of life reported by the parent and child after surgical repair of pectus excavatum. 

METHODS. As part of a multicenter study of pectus excavatum, a previously validated tool called the Pectus Excavatum Evaluation Questionnaire was administered by the research coordinator, via telephone, to parents and patients (8-21 years of age) before and 1 year after surgery. Eleven North American children's hospitals participated. From 2001 to 2006, 264 patients and 291 parents completed the initial questionnaire, and 247 patients and 274 parents completed the postoperative questionnaire. Responses used a Likert-type scale of 1 to 4, reflecting the extent or frequency of a particular experience, with higher values conveying less-desirable experience. 

RESULTS. Preoperative psychosocial functioning was unrelated to objective pectus excavatum severity (computed tomographic index). Patients and their parents reported significant positive postoperative changes. Improvements occurred in both physical and psychosocial functioning, including less social self-consciousness and a more-favorable body image. For children, the body image component improved from 2.30 {+/-} 0.62 (mean {+/-} SD) to 1.40 {+/-} 0.42 after surgery and the physical difficulties component improved from 2.11 {+/-} 0.82 to 1.37 {+/-} 0.44. For the parent questionnaire, the child's emotional difficulties improved from 1.81 {+/-} 0.70 to 1.24 {+/-} 0.36, social self-consciousness improved from 2.86 {+/-} 1.03 to 1.33 {+/-} 0.68, and physical difficulties improved from 2.14 {+/-} 0.75 to 1.32 {+/-} 0.39. Ninety-seven percent of patients thought that surgery improved how their chest looked. 

CONCLUSIONS. Surgical repair of pectus excavatum can significantly improve the body image difficulties and limitations on physical activity experienced by patients. These results should prompt physicians to consider the physiologic and psychological implications of pectus excavatum just as they would any other physical deformity known to have such consequences.</description>
      <dc:creator>Kelly, R. E.</dc:creator>
      <dc:creator>Cash, T. F.</dc:creator>
      <dc:creator>Shamberger, R. C.</dc:creator>
      <dc:creator>Mitchell, K. K.</dc:creator>
      <dc:creator>Mellins, R. B.</dc:creator>
      <dc:creator>Lawson, M. L.</dc:creator>
      <dc:creator>Oldham, K.</dc:creator>
      <dc:creator>Azizkhan, R. G.</dc:creator>
      <dc:creator>Hebra, A. V.</dc:creator>
      <dc:creator>Nuss, D.</dc:creator>
      <dc:creator>Goretsky, M. J.</dc:creator>
      <dc:creator>Sharp, R. J.</dc:creator>
      <dc:creator>Holcomb, G. W.</dc:creator>
      <dc:creator>Shim, W. K. T.</dc:creator>
      <dc:creator>Megison, S. M.</dc:creator>
      <dc:creator>Moss, R. L.</dc:creator>
      <dc:creator>Fecteau, A. H.</dc:creator>
      <dc:creator>Colombani, P. M.</dc:creator>
      <dc:creator>Bagley, T.</dc:creator>
      <dc:creator>Quinn, A.</dc:creator>
      <dc:creator>Moskowitz, A. B.</dc:creator>
      <dc:date>2008-12-01</dc:date>
      <dc:identifier>doi:10.1542/peds.2007-2723</dc:identifier>
      <dc:title>Surgical Repair of Pectus Excavatum Markedly Improves Body Image and Perceived Ability for Physical Activity: Multicenter Study</dc:title>
      <dc:publisher>American Academy of Pediatrics</dc:publisher>
      <prism:number>6</prism:number>
      <prism:volume>122</prism:volume>
      <prism:endingPage>1222</prism:endingPage>
      <prism:startingPage>1218</prism:startingPage>
      <prism:publicationDate>2008-12-01</prism:publicationDate>
      <prism:section>ARTICLES</prism:section>
   </item>
   <item rdf:about="http://pediatrics.aappublications.org:80/cgi/content/short/122/6/e1236?rss=1">
      <title><![CDATA[Effect of Ursodeoxycholic Acid on Liver Function in Children After Successful Surgery for Biliary Atresia [ARTICLES] ]]></title>
      <link>http://pediatrics.aappublications.org:80/cgi/content/short/122/6/e1236?rss=1</link>
      <description>OBJECTIVES. Although ursodeoxycholic acid has been used to treat various cholestatic liver diseases in children, few data are available about its efficacy in biliary atresia. The aim of this study was to assess the effect of ursodeoxycholic acid treatment on liver function in children who underwent successful surgery for biliary atresia. 

PATIENTS AND METHODS. We prospectively studied 16 children with biliary atresia who underwent successful portoenterostomies (postoperative conjugated bilirubin concentration: &lt;34 {micro}mol/L) and were treated with ursodeoxycholic acid for at least 18 months after surgery. Ursodeoxycholic acid treatment was then discontinued. Clinical and biological assessment was performed at the time of discontinuation of ursodeoxycholic acid treatment (T0), at follow-up (T1) and, if the clinical or biological status worsened, after resumption of ursodeoxycholic acid treatment (T2). 

RESULTS. Ursodeoxycholic acid treatment was resumed in 13 cases. In 1 patient, jaundice recurred after ursodeoxycholic acid therapy was discontinued but abated after resumption of treatment. In 13 children, liver function worsened significantly when ursodeoxycholic acid was discontinued. T1 versus T0 concentrations expressed as multiples of the upper limit of the normal range (in parentheses) were as follows: alanine aminotransferase, 3.0 xN (0.8-7.0) vs 1.5 xN (0.5-5.4); {gamma} glutamyl transpeptidase, 8.0 xN (1.8-30.2) vs 4.2 xN (0.5-27.4); and aspartate aminotransferase, 1.7 xN (0.7-6.0) vs 1.3 xN (0.6-3.4). When ursodeoxycholic acid treatment was resumed, liver function had improved in all patients by T2. Concentrations of endogenous bile acids tended to be elevated at T1 (not significant) and were significantly decreased at T2. 

CONCLUSION. Our study demonstrates the beneficial effect of ursodeoxycholic acid on liver function in children after successful surgery for biliary atresia.</description>
      <dc:creator>Willot, S.</dc:creator>
      <dc:creator>Uhlen, S.</dc:creator>
      <dc:creator>Michaud, L.</dc:creator>
      <dc:creator>Briand, G.</dc:creator>
      <dc:creator>Bonnevalle, M.</dc:creator>
      <dc:creator>Sfeir, R.</dc:creator>
      <dc:creator>Gottrand, F.</dc:creator>
      <dc:date>2008-12-01</dc:date>
      <dc:identifier>doi:10.1542/peds.2008-0986</dc:identifier>
      <dc:title>Effect of Ursodeoxycholic Acid on Liver Function in Children After Successful Surgery for Biliary Atresia</dc:title>
      <dc:publisher>American Academy of Pediatrics</dc:publisher>
      <prism:number>6</prism:number>
      <prism:volume>122</prism:volume>
      <prism:endingPage>1241</prism:endingPage>
      <prism:startingPage>1236</prism:startingPage>
      <prism:publicationDate>2008-12-01</prism:publicationDate>
      <prism:section>ARTICLES</prism:section>
   </item>
   <item rdf:about="http://pediatrics.aappublications.org:80/cgi/content/short/peds.2008-0986v1?rss=1">
      <title><![CDATA[Effect of Ursodeoxycholic Acid on Liver Function in Children After Successful Surgery for Biliary Atresia [ARTICLES] ]]></title>
      <link>http://pediatrics.aappublications.org:80/cgi/content/short/peds.2008-0986v1?rss=1</link>
      <description>OBJECTIVES. Although ursodeoxycholic acid has been used to treat various cholestatic liver diseases in children, few data are available about its efficacy in biliary atresia. The aim of this study was to assess the effect of ursodeoxycholic acid treatment on liver function in children who underwent successful surgery for biliary atresia. 

PATIENTS AND METHODS. We prospectively studied 16 children with biliary atresia who underwent successful portoenterostomies (postoperative conjugated bilirubin concentration: &lt;34 {micro}mol/L) and were treated with ursodeoxycholic acid for at least 18 months after surgery. Ursodeoxycholic acid treatment was then discontinued. Clinical and biological assessment was performed at the time of discontinuation of ursodeoxycholic acid treatment (T0), at follow-up (T1) and, if the clinical or biological status worsened, after resumption of ursodeoxycholic acid treatment (T2). 

RESULTS. Ursodeoxycholic acid treatment was resumed in 13 cases. In 1 patient, jaundice recurred after ursodeoxycholic acid therapy was discontinued but abated after resumption of treatment. In 13 children, liver function worsened significantly when ursodeoxycholic acid was discontinued. T1 versus T0 concentrations expressed as multiples of the upper limit of the normal range (in parentheses) were as follows: alanine aminotransferase, 3.0 xN (0.8-7.0) vs 1.5 xN (0.5-5.4); {gamma} glutamyl transpeptidase, 8.0 xN (1.8-30.2) vs 4.2 xN (0.5-27.4); and aspartate aminotransferase, 1.7 xN (0.7-6.0) vs 1.3 xN (0.6-3.4). When ursodeoxycholic acid treatment was resumed, liver function had improved in all patients by T2. Concentrations of endogenous bile acids tended to be elevated at T1 (not significant) and were significantly decreased at T2. 

CONCLUSION. Our study demonstrates the beneficial effect of ursodeoxycholic acid on liver function in children after successful surgery for biliary atresia.</description>
      <dc:creator>Willot, S.</dc:creator>
      <dc:creator>Uhlen, S.</dc:creator>
      <dc:creator>Michaud, L.</dc:creator>
      <dc:creator>Briand, G.</dc:creator>
      <dc:creator>Bonnevalle, M.</dc:creator>
      <dc:creator>Sfeir, R.</dc:creator>
      <dc:creator>Gottrand, F.</dc:creator>
      <dc:date>2008-11-24</dc:date>
      <dc:identifier>doi:10.1542/peds.2008-0986</dc:identifier>
      <dc:title>Effect of Ursodeoxycholic Acid on Liver Function in Children After Successful Surgery for Biliary Atresia</dc:title>
      <dc:publisher>American Academy of Pediatrics</dc:publisher>
      <prism:number>2008</prism:number>
      <prism:volume>0</prism:volume>
      <prism:endingPage>1241</prism:endingPage>
      <prism:startingPage>200809861</prism:startingPage>
      <prism:publicationDate>2008-11-24</prism:publicationDate>
      <prism:section>ARTICLES</prism:section>
   </item>
</rdf:RDF>