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<title>PEDIATRICS</title>
<url>http://pediatrics.aappublications.org/icons/banner/title.gif</url>
<link>http://pediatrics.aappublications.org</link>
</image>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0904v1?rss=1">
<title><![CDATA[Screening for Occult Abdominal Trauma in Children With Suspected Physical Abuse]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0904v1?rss=1</link>
<description><![CDATA[
<sec><st>Objectives:</st>
<p>The goals were (1) to determine the prevalence of occult abdominal trauma (OAT) in a sample of children with suspected physical abuse, (2) to assess the frequency of OAT screening, and (3) to assess factors associated with screening.</p>
</sec>
<sec><st>Methods:</st>
<p>Charts of children evaluated for abusive injury were identified through a search of hospital discharge codes. Identified charts were reviewed to determine whether OAT screening occurred. Data on results of screening tests, abusive injuries identified, family demographic features, and characteristics of the emergency department visit were collected.</p>
</sec>
<sec><st>Results:</st>
<p>Screening occurred for 51 (20%) of 244 eligible children. Positive results were identified for 41% of those screened and 9% of the total sample; 5% of children 12 to 23 months of age had OAT identified through imaging studies. Screening occurred more often in children presenting with probable abusive head trauma (odds ratio [OR]: 20.4 [95% confidence interval [CI]: 3.6&ndash;114.6]; <I>P</I> &lt; .01), compared with those presenting with other injuries. Consultation with the child protection team (OR: 8.5 [95% CI: 3.5&ndash;20.7]; <I>P</I> &lt; .01) and other subspecialists (OR: 24.3 [95% CI: 7.1&ndash;83.3]; <I>P</I> &lt; .01) also increased the likelihood that OAT screening would occur.</p>
</sec>
<sec><st>Conclusions:</st>
<p>Our findings support OAT screening with liver and pancreatic enzyme measurements for physically abused children. This study also supports the importance of subspecialty input, especially that of a child protection team. Although many identified injuries may not require treatment, their role in confirming or demonstrating increased severity of maltreatment may be critical.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Lane, W. G., Dubowitz, H., Langenberg, P.]]></dc:creator>
<dc:date>Mon, 23 Nov 2009 04:01:36 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-0904</dc:identifier>
<dc:title><![CDATA[Screening for Occult Abdominal Trauma in Children With Suspected Physical Abuse]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-23</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0165v1?rss=1">
<title><![CDATA[Energy Expenditure for Breastfeeding and Bottle-Feeding Preterm Infants]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0165v1?rss=1</link>
<description><![CDATA[
<sec><st>Objective:</st>
<p>We hypothesized that resting energy expenditure (REE) would be higher after breastfeeding than after bottle-feeding.</p>
</sec>
<sec><st>Methods:</st>
<p>Nineteen preterm infants (gestational age: 32 weeks) in stable condition who were nourished entirely with their mothers' breast milk were assigned randomly to feeding either by bottle or at the breast. Each infant served as his or her own control subject. REE was measured for 20 minutes after feeding. Breast milk quantity was evaluated with prefeeding and postfeeding weighing. REE values for bottle-feeding and breastfeeding were compared with paired <I>t</I> tests.</p>
</sec>
<sec><st>Results:</st>
<p>Contrary to our null hypothesis, the group's mean REE values after bottle-feeding and breastfeeding were very similar (284.7 &plusmn; 26.8 kJ/kg per day [68.3 &plusmn; 6.4 kcal/kg per day] vs 282.6 &plusmn; 28.5 kJ/kg per day [67.5 &plusmn; 6.8 kcal/kg per day]; not significant). The duration of feeding was significantly longer for breastfeeding than for bottle-feeding (20.1 &plusmn; 7.9 vs 7.8 &plusmn; 2.9 minutes; <I>P</I> &lt; .0001).</p>
</sec>
<sec><st>Conclusion:</st>
<p>There was no significant difference in REE when infants were breastfed versus bottle-fed. Longer feeding times at the breast did not increase REE. We speculate that it is safe to recommend feeding at the breast for infants born at &gt;32 weeks when they can tolerate oral feeding.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Berger, I., Weintraub, V., Dollberg, S., Kopolovitz, R., Mandel, D.]]></dc:creator>
<dc:date>Mon, 23 Nov 2009 04:01:34 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-0165</dc:identifier>
<dc:title><![CDATA[Energy Expenditure for Breastfeeding and Bottle-Feeding Preterm Infants]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-23</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0862v1?rss=1">
<title><![CDATA[Preschool-Aged Children's Television Viewing in Child Care Settings]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0862v1?rss=1</link>
<description><![CDATA[
<sec><st>Objective:</st>
<p>The goal was to quantify television viewing in day care settings and to investigate the characteristics of programs that predict viewing.</p>
</sec>
<sec><st>Methods:</st>
<p>A telephone survey of licensed child care programs in Michigan, Washington, Florida, and Massachusetts was performed. The frequency and quantity of television viewing for infants, toddlers, and preschool-aged children were assessed.</p>
</sec>
<sec><st>Results:</st>
<p>With the exception of infants, children in home-based child care programs were exposed to significantly more television on an average day than were children in center-based programs (infants: 0.2 vs 0 hours; toddlers: 1.6 vs 0.1 hours; preschool-aged children: 2.4 vs 0.4 hours). In a regression analysis of daily television time for preschool-aged children in child care, center-based programs were found to have an average of 1.84 fewer hours of television each day, controlling for the other covariates. Significant effect modification was found, in that the impact of home-based versus center-based child care programs differed somewhat depending on educational levels for staff members; having a 2- or 4-year college degree was associated with 1.41 fewer hours of television per day in home-based programs, but no impact of staff education on television use was observed in center-based programs.</p>
</sec>
<sec><st>Conclusions:</st>
<p>For many children, previous estimates of screen time significantly underestimated actual amounts. Pediatricians should council parents to minimize screen time in child care settings.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Christakis, D. A., Garrison, M. M.]]></dc:creator>
<dc:date>Mon, 23 Nov 2009 04:01:31 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-0862</dc:identifier>
<dc:title><![CDATA[Preschool-Aged Children's Television Viewing in Child Care Settings]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-23</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0738v1?rss=1">
<title><![CDATA[Association of Tobacco and Lead Exposures With Attention-Deficit/Hyperactivity Disorder]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0738v1?rss=1</link>
<description><![CDATA[
<sec><st>Objective:</st>
<p>The study objective was to determine the independent and joint associations of prenatal tobacco and childhood lead exposures with attention-deficit/hyperactivity disorder (ADHD), as defined by current diagnostic criteria, in a national sample of US children.</p>
</sec>
<sec><st>Methods:</st>
<p>Data are from the 2001&ndash;2004 National Health and Nutrition Examination Survey, a cross-sectional, nationally representative sample of the US population. Participants were 8 to 15 years of age (<I>N</I> = 2588). Prenatal tobacco exposure was measured by report of maternal cigarette use during pregnancy. Lead exposure was assessed by using current blood lead levels. The Diagnostic Interview Schedule for Children was used to ascertain the presence of ADHD in the past year, on the basis of <I>Diagnostic and Statistical Manual of Mental Disorders</I>, <I>Fourth Edition</I>, criteria.</p>
</sec>
<sec><st>Results:</st>
<p>A total of 8.7% (95% confidence interval [CI]: 7.3%&ndash;10.1%) of children met criteria for ADHD. Prenatal tobacco exposure (adjusted odds ratio [aOR]: 2.4 [95% CI: 1.5&ndash;3.7]) and higher current blood lead concentrations (aOR for third versus first tertile: 2.3 [95% CI: 1.5&ndash;3.8]) were independently associated with ADHD. Compared with children with neither exposure, children with both exposures (prenatal tobacco exposure and third-tertile lead levels) had an even greater risk of ADHD (aOR: 8.1 [95% CI: 3.5&ndash;18.7]) than would be expected if the independent risks were multiplied (tobacco-lead exposure interaction term, <I>P</I> &lt; .001).</p>
</sec>
<sec><st>Conclusions:</st>
<p>Prenatal tobacco and childhood lead exposures are associated with ADHD in US children, especially among those with both exposures. Reduction of these common toxicant exposures may be an important avenue for ADHD prevention.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Froehlich, T. E., Lanphear, B. P., Auinger, P., Hornung, R., Epstein, J. N., Braun, J., Kahn, R. S.]]></dc:creator>
<dc:date>Mon, 23 Nov 2009 04:01:27 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-0738</dc:identifier>
<dc:title><![CDATA[Association of Tobacco and Lead Exposures With Attention-Deficit/Hyperactivity Disorder]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-23</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0674v1?rss=1">
<title><![CDATA[Prevalence of Sexually Transmitted Infections Among Female Adolescents Aged 14 to 19 in the United States]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0674v1?rss=1</link>
<description><![CDATA[
<sec><st>Objective:</st>
<p>Most young women initiate sexual activity during adolescence; risk for sexually transmitted infections (STIs) accompanies this initiation. In this study we estimated the prevalence of the most common STIs among a representative sample of female adolescents in the United States.</p>
</sec>
<sec><st>Methods:</st>
<p>Data were analyzed from 838 females who were aged 14 to 19 and participating in the nationally representative National Health and Nutrition Examination Survey 2003&ndash;2004. After interview and examination, survey participants provided biological specimens for laboratory testing. The main outcome was weighted prevalence of at least 1 of 5 STIs: <I>Neisseria gonorrhoeae</I>, <I>Chlamydia trachomatis</I>, <I>Trichomonas vaginalis</I>, herpes simplex virus type 2, and human papillomavirus (HPV) (any of 23 high-risk types or type 6 or 11).</p>
</sec>
<sec><st>Results:</st>
<p>Prevalence of any of the 5 STIs was 24.1% among all and 37.7% among sexually experienced female adolescents. HPV (23 high-risk types or type 6 or 11) was the most common STI among all female adolescents (prevalence: 18.3%), followed by <I>C trachomatis</I> infection (prevalence: 3.9%). Prevalence of any of the STIs was 25.6% among those whose age was the same or 1 year greater than their age at sexual initiation and 19.7% among those who reported only 1 lifetime sex partner.</p>
</sec>
<sec><st>Conclusions:</st>
<p>The prevalence of STIs among female adolescents is substantial, and STIs begin to be acquired soon after sexual initiation and with few sex partners. These findings support early and comprehensive sex education, routine HPV vaccination at the age of 11 to 12 years, and <I>C trachomatis</I> screening of sexually active female adolescents.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Forhan, S. E., Gottlieb, S. L., Sternberg, M. R., Xu, F., Datta, S. D., McQuillan, G. M., Berman, S. M., Markowitz, L. E.]]></dc:creator>
<dc:date>Mon, 23 Nov 2009 04:01:24 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-0674</dc:identifier>
<dc:title><![CDATA[Prevalence of Sexually Transmitted Infections Among Female Adolescents Aged 14 to 19 in the United States]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-23</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0233v1?rss=1">
<title><![CDATA[Spatial Accessibility to Providers and Vaccination Compliance Among Children With Medicaid]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0233v1?rss=1</link>
<description><![CDATA[
<sec><st>Objective:</st>
<p>We examined the relationship between spatial accessibility to pediatric immunization providers and vaccination compliance in a low-income, urban population of children.</p>
</sec>
<sec><st>Methods:</st>
<p>In 2007, we accessed the Washington, DC, Immunization Information System (IIS) to collect data on the immunization statuses and residential addresses of children who were aged 19 to 35 months and had Medicaid insurance. In addition, we calculated each child's spatial accessibility to pediatric vaccination providers by assessing the provider-to-population ratio at each residential address. Spatial accessibility was divided into tertiles (low, medium, and high) of access. The relationship between spatial accessibility to providers and vaccination compliance was examined by using logistic regression analysis adjusting for age, type of vaccination provider, and enrollment in child care status.</p>
</sec>
<sec><st>Results:</st>
<p>Overall for our cohort of 4195 children, 80.5% of the children were up-to-date with vaccinations. Vaccination coverage ranged from 61.6% to 100% (median: 79.2%) among different neighborhoods. Having the highest level of access to pediatric vaccination providers was associated with 36% higher odds of being up-to-date as compared with having the lowest level of access. The middle tertile of access was associated with 25% higher odds of being up-to-date.</p>
</sec>
<sec><st>Conclusions:</st>
<p>Within our low-income, urban population, children with higher spatial accessibility to pediatric vaccination providers were more likely to be up-to-date with vaccinations. This association may guide future studies and efforts to ensure adequate immunization coverage for children regardless of where they live.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Fu, L. Y., Cowan, N., McLaren, R., Engstrom, R., Teach, S. J.]]></dc:creator>
<dc:date>Mon, 23 Nov 2009 04:01:21 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-0233</dc:identifier>
<dc:title><![CDATA[Spatial Accessibility to Providers and Vaccination Compliance Among Children With Medicaid]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-23</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0041v1?rss=1">
<title><![CDATA[Transition to Adult Care for Youths With Diabetes Mellitus: Findings From a Universal Health Care System]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0041v1?rss=1</link>
<description><![CDATA[
<sec><st>Objectives:</st>
<p>The goals were (1) to describe rates of diabetes mellitus (DM)-related hospitalizations and retinopathy screening before and after transition to adult care and (2) to test whether different methods of transfer of care were associated with improved outcomes.</p>
</sec>
<sec><st>Methods:</st>
<p>In a retrospective cohort study, we included 1507 young adults with DM of &ge;5-year duration and tracked these patients until 20 years of age.</p>
</sec>
<sec><st>Results:</st>
<p>DM-related hospitalization rates increased from 7.6 to 9.5 cases per 100 patient-years in the 2 years after transition to adult care (<I>P</I> = .03). Previous DM-related hospitalizations, lower income, female gender, and living in areas with low physician supply were associated with higher admission rates. With controlling for all other factors, individuals who were transferred to a new allied health care team with no change in physician were 23% less likely (relative risk: 0.23 [95% confidence interval: 0.05&ndash;0.79]) to be hospitalized after the transition than were those transferred to a new physician with either a new or no allied health care team. The rates of eye examinations were stable across the transition to adult care (72% vs 70%; <I>P</I> = .06). Female patients, patients with higher income, and patients with previous eye care were more likely to have an eye care visit after transfer.</p>
</sec>
<sec><st>Conclusions:</st>
<p>During the transition to adult health care, there is increased risk of DM-related hospitalizations, although this may be attenuated in youths for whom there is physician continuity. Eye care visits were not related to transition; however, rates were below evidence-based guideline recommendations.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Nakhla, M., Daneman, D., To, T., Paradis, G., Guttmann, A.]]></dc:creator>
<dc:date>Mon, 23 Nov 2009 04:01:19 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-0041</dc:identifier>
<dc:title><![CDATA[Transition to Adult Care for Youths With Diabetes Mellitus: Findings From a Universal Health Care System]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-23</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-3645v1?rss=1">
<title><![CDATA[Booster Vaccinations: Can Immunologic Memory Outpace Disease Pathogenesis?]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-3645v1?rss=1</link>
<description><![CDATA[
<p>Almost all current vaccines work by the induction of antibodies in serum or on the mucosa to block adherence of pathogens to epithelial cells or interfere with microbial invasion of the bloodstream. However, antibody levels usually decline after vaccination to undetectable amounts if further vaccination does not occur. Persistence of vaccine-induced antibodies usually goes well beyond the time when they should have decayed to undetectable levels because of ongoing "natural" boosting or other immunologic mechanisms. The production of memory B and T cells is of clear importance, but the likelihood that a memory response will be fast enough in the absence of a protective circulating antibody level likely depends on the pace of pathogenesis of a specific organism. This concept is discussed with regard to <I>Haemophilus influenzae</I> type b, <I>Streptococcus pneumoniae</I>, and <I>Neisseria meningitidis</I>; hepatitis A and B; diphtheria, tetanus, and pertussis; polio, measles, mumps, rubella, and varicella; rotavirus; and human papilloma virus. With infectious diseases for which the pace of pathogenesis is less rapid, some individuals will contract infection before the memory response is fully activated and implemented. With infectious diseases for which the pace of pathogenesis is slow, immune memory should be sufficient to prevent disease.</p>
]]></description>
<dc:creator><![CDATA[Pichichero, M. E.]]></dc:creator>
<dc:date>Mon, 23 Nov 2009 04:01:16 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2008-3645</dc:identifier>
<dc:title><![CDATA[Booster Vaccinations: Can Immunologic Memory Outpace Disease Pathogenesis?]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-23</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-3074v1?rss=1">
<title><![CDATA[Relative Impact of Influenza and Respiratory Syncytial Virus in Young Children]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-3074v1?rss=1</link>
<description><![CDATA[
<sec><st>Objective:</st>
<p>We measured the relative impact of influenza and respiratory syncytial virus (RSV) infections in young children in terms of emergency department (ED) visits, clinical care requirements, and overall resource use.</p>
</sec>
<sec><st>Methods:</st>
<p>Patients who were aged &le;7 years and treated in the ED of a tertiary care pediatric hospital for an acute respiratory infection were enrolled during 2 winter seasons between 2003 and 2005. We quantified health care resource use for children with influenza or RSV infections, and extrapolated results to estimate the national resource use associated with influenza and RSV infections.</p>
</sec>
<sec><st>Results:</st>
<p>Nationally, an estimated 10.2 ED visits per 1000 children were attributable to influenza and 21.5 visits per 1000 to RSV. Children who were aged 0 to 23 months and infected with RSV had the highest rate of ED visits with 64.4 visits per 1000 children. Significantly more children required hospitalization as a result of an RSV infection compared with influenza, with national hospitalization rates of 8.5 and 1.4 per 1000 children, respectively. The total number of workdays missed yearly by caregivers of children who required ED care was 246965 days for influenza infections and 716404 days for RSV infections.</p>
</sec>
<sec><st>Conclusion:</st>
<p>For young children, RSV is associated with higher rates of ED visits, hospitalization, and caregiver resource use than is influenza. Our results provide data on the large number of children who receive outpatient care for influenza and RSV illnesses and serve to inform analyses of prevention programs and treatments for both influenza and RSV disease.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Bourgeois, F. T., Valim, C., McAdam, A. J., Mandl, K. D.]]></dc:creator>
<dc:date>Mon, 23 Nov 2009 04:01:13 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2008-3074</dc:identifier>
<dc:title><![CDATA[Relative Impact of Influenza and Respiratory Syncytial Virus in Young Children]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-23</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-2771v1?rss=1">
<title><![CDATA[Antiretroviral Exposure and Lymphocyte mtDNA Content Among Uninfected Infants of HIV-1-Infected Women]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-2771v1?rss=1</link>
<description><![CDATA[
<sec><st>Objective:</st>
<p>Concern for potential adverse effects of antiretroviral (ARV) chemotherapy used to prevent mother-to-child HIV transmission has led the US Public Health Service to recommend long-term follow-up of ARV-exposed children. Nucleoside reverse transcriptase inhibitor ARV agents can inhibit DNA polymerase , impairing mitochondrial DNA (mtDNA) synthesis and resulting in depletion or dysfunction.</p>
</sec>
<sec><st>Methods:</st>
<p>We measured the mtDNA content of stored peripheral blood mononuclear cells (PBMCs) of 411 healthy children who were born to HIV-uninfected women and 213 uninfected infants who were born to HIV-infected women with or without in utero and neonatal ARV exposure. Cryopreserved PBMC mtDNA was quantified by using the Primagen Retina Mitox assay.</p>
</sec>
<sec><st>Results:</st>
<p>Geometric mean PBMC mtDNA levels were lower at birth in infants who were born to HIV-infected women. Among HIV-exposed children, mtDNA levels were lowest in those who were not exposed to ARVs, higher in those with exposure to zidovudine alone, and higher still in those with combination nucleoside reverse transcriptase inhibitor exposure. A similar pattern was observed in the corresponding women. Levels of mtDNA increased during the first 5 years of life in all HIV-exposed children but achieved normal levels only in those with ARV exposure.</p>
</sec>
<sec><st>Conclusions:</st>
<p>Levels of mtDNA are lower than normal in HIV-exposed children. Contrary to expectation, PBMC mtDNA levels are significantly higher in ARV-exposed, HIV-uninfected infants and their infected mothers compared with ARV-unexposed infants and women. By 5 years, levels of PBMC mtDNA rise to normal concentrations in ARV-exposed children but remain depressed in ARV-unexposed children.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Aldrovandi, G. M., Chu, C., Shearer, W. T., Li, D., Walter, J., Thompson, B., McIntosh, K., Foca, M., Meyer, W. A., Ha, B. F., Rich, K. C., Moye, J.]]></dc:creator>
<dc:date>Mon, 23 Nov 2009 04:01:10 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2008-2771</dc:identifier>
<dc:title><![CDATA[Antiretroviral Exposure and Lymphocyte mtDNA Content Among Uninfected Infants of HIV-1-Infected Women]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-23</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-1210v1?rss=1">
<title><![CDATA[Food Allergy Among Children in the United States]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-1210v1?rss=1</link>
<description><![CDATA[
<sec><st>Objectives:</st>
<p>The goals were to estimate the prevalence of food allergy and to describe trends in food allergy prevalence and health care use among US children.</p>
</sec>
<sec><st>Methods:</st>
<p>A cross-sectional survey of data on food allergy among children &lt;18 years of age, as reported in the 1997&ndash;2007 National Health Interview Survey, 2005&ndash;2006 National Health and Nutrition Examination Survey, 1993&ndash;2006 National Hospital Ambulatory Medical Care Survey and National Ambulatory Medical Care Survey, and 1998&ndash;2006 National Hospital Discharge Survey, was performed. Reported food allergies, serum immunoglobulin E antibody levels for specific foods, ambulatory care visits, and hospitalizations were assessed.</p>
</sec>
<sec><st>Results:</st>
<p>In 2007, 3.9% of US children &lt;18 years of age had reported food allergy. The prevalence of reported food allergy increased 18%  (<I>z</I> = 3.4; <I>P</I> &lt; .01) from 1997 through 2007. In 2005&ndash;2006, serum immunoglobulin E antibodies to peanut were detectable for an estimated 9% of US children. Ambulatory care visits tripled between 1993 and 2006  (<I>P</I> &lt; .01). From 2003 through 2006, an estimated average of 317000 food allergy-related, ambulatory care visits per year (95% confidence interval: 195000&ndash;438000 visits per year) to emergency and outpatient departments and physician's offices were reported. Hospitalizations with any recorded diagnoses related to food allergy also increased between 1998&ndash;2000 and 2004&ndash;2006, from an average of 2600 discharges per year to 9500 discharges per year (<I>z</I> = 3.4; <I>P</I> &lt; .01), possibly because of increased use of food allergy V codes.</p>
</sec>
<sec><st>Conclusion:</st>
<p>Several national health surveys indicate that food allergy prevalence and/or awareness has increased among US children in recent years.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Branum, A. M., Lukacs, S. L.]]></dc:creator>
<dc:date>Mon, 16 Nov 2009 04:01:23 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-1210</dc:identifier>
<dc:title><![CDATA[Food Allergy Among Children in the United States]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-16</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-1207v1?rss=1">
<title><![CDATA[Promoting Early Literacy in Pediatric Practice: Twenty Years of Reach Out and Read]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-1207v1?rss=1</link>
<description><![CDATA[
<p>Reach Out and Read (ROR) is the first pediatric, evidence-based strategy to prevent problems of early childhood development and learning. With a start in a single clinic in Boston City Hospital in 1989, doctors working in &gt;4000 clinics and practices gave ~5.7 million new books to &gt;3.5 million children in all 50 states in 2008. ROR also has become a model for a different way of thinking about parent education during primary care encounters, based less on telling and more on creating real-time learning experiences. ROR flourished because of (1) the growth of pediatric interest in child development, (2) local leadership of pediatric champions as well as nonmedical supporters, coordinators, and volunteers, (3) evidence of effectiveness, and (4) public financial support attributable to strong bipartisan support in Congress, led by Senator Edward Kennedy. Since ROR started, an increasing amount of research confirms the importance of reading aloud for the development of language and other emergent literacy skills, which in turn helps children get ready for school and leads to later success in reading. Future goals include continued growth until all low-income children are reached with pediatric advice and books, a national campaign led by physicians encouraging all parents to read to their children every day, additional evidence-based, parent information to increase the effectiveness of parents reading to children, quality-improvement efforts to achieve the full potential, and global expansion.</p>
]]></description>
<dc:creator><![CDATA[Zuckerman, B.]]></dc:creator>
<dc:date>Mon, 16 Nov 2009 04:01:20 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-1207</dc:identifier>
<dc:title><![CDATA[Promoting Early Literacy in Pediatric Practice: Twenty Years of Reach Out and Read]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-16</prism:publicationDate>
<prism:section>Special Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0952v1?rss=1">
<title><![CDATA[Best-Practice Guidelines for Physical Activity at Child Care]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0952v1?rss=1</link>
<description><![CDATA[
<p>Research has indicated that the child care center is a very strong predictor of preschool-aged children's physical activity levels, making this an important setting to help young children obtain physical activity that is appropriate for their health and development. However, some evidence suggests that organized child care may not adequately support children's physical activity needs. Although many organizations provide recommendations, guidelines, or standards for motor skill development and physical activity opportunities, no set of guidelines exist that directly target the overall physical activity environment at child care. Because of the lack of comprehensive recommendations, the Nutrition and Physical Activity Self-assessment for Child Care best-practice guidelines for healthy weight development were created on the basis of an extensive review of existing guidelines, research evidence, and expert review. The purpose of this article is to present these physical activity best-practice guidelines and provide data on how these guidelines compare to current practice in a large sample (<I>N</I> = 96) of child care centers in North Carolina. These best-practice guidelines include recommendations for 8 unique components of the child care environment, including active opportunities, fixed play environment, portable play environment, sedentary opportunities, sedentary environment, staff behavior, staff training/education, and physical activity policies. Our results showed that only a few of the best-practice guidelines were achieved by a majority of the 96 North Carolina child care centers that participated in this study. Establishing comprehensive guidelines for physical activity at child care could result in higher activity levels and healthier children, but more research is needed.</p>
]]></description>
<dc:creator><![CDATA[McWilliams, C., Ball, S. C., Benjamin, S. E., Hales, D., Vaughn, A., Ward, D. S.]]></dc:creator>
<dc:date>Mon, 16 Nov 2009 04:01:18 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-0952</dc:identifier>
<dc:title><![CDATA[Best-Practice Guidelines for Physical Activity at Child Care]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-16</prism:publicationDate>
<prism:section>Special Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0727v1?rss=1">
<title><![CDATA[Cardiopulmonary Resuscitation for Bradycardia With Poor Perfusion Versus Pulseless Cardiac Arrest]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0727v1?rss=1</link>
<description><![CDATA[
<sec><st>Objective:</st>
<p>The objective of this study was to assess whether pediatric inpatients who receive cardiopulmonary resuscitation (CPR) for bradycardia with poor perfusion are more likely to survive to hospital discharge than pediatric inpatients who receive CPR for pulseless arrest (asystole/pulseless electrical activity [PEA]), after controlling for confounding characteristics.</p>
</sec>
<sec><st>Methods:</st>
<p>A prospective cohort from the National Registry of Cardiopulmonary Resuscitation was enrolled between January 4, 2000, and February 23, 2008. Patients who were younger than 18 years and had an in-hospital event that required chest compressions for &gt;2 minutes were eligible. Patients were divided into 2 groups on the basis of initial rhythm and pulse state: bradycardia/poor perfusion and asystole/PEA. Patient characteristics, event characteristics, and clinical characteristics were analyzed as possible confounders. Univariate analysis between bradycardia and asystole/PEA patient groups was performed. Multivariable logistic regression was used to determine whether an initial state of bradycardia/poor perfusion was independently associated with survival to discharge.</p>
</sec>
<sec><st>Results:</st>
<p>A total of 6288 patients who were younger than 18 years were reported; 3342 met all inclusion criteria. A total of 1853 (55%) patients received chest compressions for bradycardia/poor perfusion compared with 1489 (45%) for asystole/PEA. Overall, 755 (40.7%) of 1353 patients with bradycardia survived to hospital discharge, compared with 365 (24.5%) of 1489 patients with asystole/PEA. After controlling for known confounders, CPR for bradycardia with poor perfusion was associated with increased survival to hospital discharge.</p>
</sec>
<sec><st>Conclusions:</st>
<p>Pediatric inpatients with chest compressions initiated for bradycardia and poor perfusion before onset of pulselessness were more likely to survive to discharge than pediatric inpatients with chest compressions initiated for asystole or PEA.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Donoghue, A., Berg, R. A., Hazinski, M. F., Praestgaard, A. H., Roberts, K., Nadkarni, V. M., for the American Heart Association National Registry of CPR Investigators]]></dc:creator>
<dc:date>Mon, 16 Nov 2009 04:01:15 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-0727</dc:identifier>
<dc:title><![CDATA[Cardiopulmonary Resuscitation for Bradycardia With Poor Perfusion Versus Pulseless Cardiac Arrest]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-16</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0582v1?rss=1">
<title><![CDATA[Severe Thrombocytopenia in the NICU]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0582v1?rss=1</link>
<description><![CDATA[
<sec><st>Objective:</st>
<p>Severe thrombocytopenia (platelets &le; 50000/&micro;L) in a NICU patient can have significant consequences; however, previous reports have not focused exclusively on NICU patients with counts this low.</p>
</sec>
<sec><st>Methods:</st>
<p>We identified all patients with severe thrombocytopenia who were cared for in the Intermountain Healthcare level III NICUs from 2003&ndash;2007.</p>
</sec>
<sec><st>Results:</st>
<p>Among 11281 NICU admissions, severe thrombocytopenia was identified in 273 (2.4%). Just over 30% of these presented in the first three days of life. Half presented by day 10, 75% by day 27, and 95% by day 100. The prevalence was inversely related to birth weight. Cutaneous bleeding was more common in patients with platelet counts of &lt;20000/&micro;L; however, no statistically significant correlation was found between platelet counts and pulmonary, gastrointestinal, or intraventricular bleeding. The most common explanations for severe thrombocytopenia were acquired varieties of consumptive thrombocytopenia. Platelet transfusions (median 5, range 0&ndash;76) were administered to 86% of the patients. No deaths were ascribed to exsanguinations. The mortality rate did not correlate with the lowest platelet count but was proportionate to the number of platelet transfusions.</p>
</sec>
<sec><st>Conclusion:</st>
<p>The prevalence of severe thrombocytopenia in the NICU is inversely proportional to birth weight and most cases are acquired consumptive thrombocytopenias. We speculate that very low platelet counts are a causal factor in cutaneous bleeding, but pulmonary, gastrointestinal, and intraventricular bleeding are less influenced by the platelet count and occur primarily from causes other than severe thrombocytopenia. The lowest platelet count does not predict the mortality rate but the number of platelet transfusions received does.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Baer, V. L., Lambert, D. K., Henry, E., Christensen, R. D.]]></dc:creator>
<dc:date>Mon, 16 Nov 2009 04:01:12 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-0582</dc:identifier>
<dc:title><![CDATA[Severe Thrombocytopenia in the NICU]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-16</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-3822v1?rss=1">
<title><![CDATA[Pediatric Robotic Surgery: Early Assessment]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-3822v1?rss=1</link>
<description><![CDATA[
<sec><st>Objectives:</st>
<p>This article reviews the evidence regarding the feasibility, safety, benefits, limitations, and costs of robotically assisted surgery in children, evaluates how the technology compares with other pediatric surgical techniques, and provides insights about the near and more-distant future of the technology.</p>
</sec>
<sec><st>Methods:</st>
<p>The peer-reviewed medical pediatric literature was searched for studies that provided evidence of the feasibility and safety of robotic surgery in children and for studies that compared pediatric robotic surgery with conventional laparoscopic surgery or open surgery.</p>
</sec>
<sec><st>Results:</st>
<p>A total of 8 case series and 5 studies comparing robotic surgery with open or conventional laparoscopic surgery met the selection criteria for review. A few small studies that focused on rare complex surgical procedures also were reviewed. All studies were designed to evaluate the feasibility and safety of robotic surgery in children. None of the studies was randomized, and some studies had a retrospective design. These studies demonstrated that a number of routine, robotically assisted, laparoscopic and thoracic procedures were feasible and safe when performed by surgeons experienced in the technique, although robotic surgery did not provide superior outcomes, compared with traditional laparoscopic and open surgery. The advantages of the robotic system were best seen in complex procedures that involved areas that were difficult to access and in procedures in which dissection of delicate, anatomic structures was required.</p>
</sec>
<sec><st>Conclusions:</st>
<p>Robotic surgery is feasible and safe for a number of pediatric surgical procedures, but evidence that it offers better clinical outcomes than conventional open or laparoscopic techniques is lacking.</p>
</sec>
]]></description>
<dc:creator><![CDATA[van Haasteren, G., Levine, S., Hayes, W.]]></dc:creator>
<dc:date>Mon, 16 Nov 2009 04:01:10 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2008-3822</dc:identifier>
<dc:title><![CDATA[Pediatric Robotic Surgery: Early Assessment]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-16</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-2969v1?rss=1">
<title><![CDATA[Risk Factors Associated With Deformational Plagiocephaly]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-2969v1?rss=1</link>
<description><![CDATA[
<sec><st>Objective:</st>
<p>This study was designed to statistically evaluate the independent and interacting effects of biological and environmental risk factors that influence lateralization of deformational plagiocephaly (DP) in an attempt to provide future guidance for clinical treatment.</p>
</sec>
<sec><st>Methods:</st>
<p>A database of &gt;20000 children treated for DP was examined by using 2- and 3-way factor analyses for categorical frequency data, representing the largest statistical analysis of DP to date. Data on parity, zygosity, intrauterine presentation, birth number and weight, sleep position, lateralization, and sex were collected from parents of children with DP who were treated at Cranial Technologies, Inc, from 1990 to 2007.</p>
</sec>
<sec><st>Results:</st>
<p>As with most DP studies, male patients were significantly overrepresented. Nonetheless, after statistically accounting for sex in our analyses, DP is significantly correlated with primiparity, fewer vertex but more breech and transverse intrauterine presentations, twinning (specifically, dizygosity), and, finally, right-sided lateralization. Additional analyses revealed that several factors correlated with DP, such as intrauterine presentation, sleep position, and lateralization, are not easily explained by an underlying biological factor. Instead, sleep position was the single greatest predictor of lateralization.</p>
</sec>
<sec><st>Conclusion:</st>
<p>Although previous studies have argued for both environmental and underlying biological factors associated with DP, we found that lateralization in children with DP could be largely explained by environmental factors such as sleep position.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Joganic, J. L., Lynch, J. M., Littlefield, T. R., Verrelli, B. C.]]></dc:creator>
<dc:date>Mon, 16 Nov 2009 04:01:07 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2008-2969</dc:identifier>
<dc:title><![CDATA[Risk Factors Associated With Deformational Plagiocephaly]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-16</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-2711v1?rss=1">
<title><![CDATA[Association of Maternal Smoking Status With Breastfeeding Practices: Missouri, 2005]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-2711v1?rss=1</link>
<description><![CDATA[
<sec><st>Objective:</st>
<p>We sought to determine the association of smoking status as a risk factor for reduced initiation and duration of breastfeeding.</p>
</sec>
<sec><st>Methods:</st>
<p>The Missouri Pregnancy Related Assessment and Monitoring System collected a stratified sample of new mothers in 2005. Surveys were mailed, with telephone follow-up, and completed within 2 to 12 months after delivery. Respondents were classified as nonsmokers, smokers who quit during pregnancy, light smokers (&le;10 cigarettes per day), or moderate/heavy smokers (&gt;10 cigarettes per day). Multivariable binomial regression and Cox proportional hazards models were used to assess breastfeeding initiation and duration according to smoking status.</p>
</sec>
<sec><st>Results:</st>
<p>Overall, 1789 women participated (weighted response rate: 61%). Approximately 74% of the women ever breastfed; 31% of the women ever smoked while pregnant. Compared with nonsmokers, the moderate/heavy smokers and light smokers were less likely to initiate breastfeeding, after controlling for sociodemographic characteristics, the presence of other smokers in the household, alcohol use, mode of delivery, and infant hospitalization. Compared with nonsmokers, the moderate/heavy smokers, light smokers, and smokers who quit during pregnancy were more likely to wean over time, controlling for the same covariates. There were no significant differences between nonsmokers and smokers regarding reasons for not initiating or ceasing breastfeeding.</p>
</sec>
<sec><st>Conclusions:</st>
<p>Mothers who smoked initiated breastfeeding less often and weaned earlier than nonsmoking mothers. Incorporating knowledge of the association between smoking and breastfeeding into existing smoking-cessation and breastfeeding programs could provide opportunities to reduce perinatal exposure to tobacco smoke, improve interest in breastfeeding, and address other barriers to breastfeeding that smoking mothers may face.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Weiser, T. M., Lin, M., Garikapaty, V., Feyerharm, R. W., Bensyl, D. M., Zhu, B.-P.]]></dc:creator>
<dc:date>Mon, 16 Nov 2009 04:01:05 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2008-2711</dc:identifier>
<dc:title><![CDATA[Association of Maternal Smoking Status With Breastfeeding Practices: Missouri, 2005]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-16</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0825v1?rss=1">
<title><![CDATA[Recurrent Abdominal Pain in Childhood Urolithiasis]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0825v1?rss=1</link>
<description><![CDATA[
<sec><st>Objective:</st>
<p>Our goal was to establish the clinical presentation and features of pain attacks in children with recurrent abdominal pain (RAP) and urolithiasis.</p>
</sec>
<sec><st>Methods:</st>
<p>We compared the rate of previous appendectomy among 100 consecutive patients with that of 270 control subjects. We also compared the frequency of pain attacks with that reported by children with functional or organic gastrointestinal RAP.</p>
</sec>
<sec><st>Results:</st>
<p>Fifty-three patients had no history of dysuria or gross hematuria, and only 35 had hematuria at the first visit; 41 patients were evaluated for urolithiasis only because of a family history of kidney stones associated with RAP. Twenty-nine patients had been previously hospitalized for abdominal symptoms. Sixteen patients and 4 control subjects (1.5%) had undergone a previous appendectomy (<I>P</I> &lt; .0001). Two to 28 months before the diagnosis of urolithiasis, 37 patients underwent abdominal ultrasonography, which did not show urinary stones. Sixty-nine percent of subjects younger than 8 years of age had central/diffuse abdominal pain. The mean frequency of pain attacks was 4 to 9 times lower than in patients with functional or organic gastrointestinal RAP.</p>
</sec>
<sec><st>Conclusions:</st>
<p>Because of the inconstant occurrence of dysuria and hematuria, the location of pain in areas other than the flank, and the lack of calculi shown on imaging studies performed after pain attacks, the urologic origin of pain may be overlooked and ineffective procedures performed. The possibility of urolithiasis should be considered in children with RAP who have a family history of urolithiasis and/or infrequent pain attacks, even when dysuria and hematuria are lacking, and in younger children even when pain is not lateral.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Polito, C., La Manna, A., Signoriello, G., Marte, A.]]></dc:creator>
<dc:date>Mon, 09 Nov 2009 04:01:11 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-0825</dc:identifier>
<dc:title><![CDATA[Recurrent Abdominal Pain in Childhood Urolithiasis]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-09</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0679v1?rss=1">
<title><![CDATA[HIV Risk Reduction Among Detained Adolescents: A Randomized, Controlled Trial]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0679v1?rss=1</link>
<description><![CDATA[
<sec><st>Objectives:</st>
<p>Criminally involved adolescents engage in high levels of alcohol-related risky sex. A theory-based sexual and alcohol risk-reduction intervention was designed, implemented, and evaluated in juvenile detention facilities.</p>
</sec>
<sec><st>Participants and Methods.</st>
<p>In a randomized, controlled trial, 484 detained adolescents received 1 of 3 group-based interventions: combined sexual and alcohol risk reduction (group psychosocial intervention [GPI] + group motivational enhancement therapy [GMET]); sexual risk reduction only (GPI); or HIV/sexually transmitted disease prevention information only (group information-only intervention [GINFO]). Follow-up data were obtained 3, 6, 9, and 12 months after the intervention. Behavioral outcomes were condom-use behavior, frequency of intercourse while drinking, and alcohol-related problems.</p>
</sec>
<sec><st>Results:</st>
<p>Condom-use behavior measured as frequency of condom use during sex (ranging from never to always) decreased over time, although the GPI and GPI + GMET interventions mitigated this tendency at the 3-, 6-, and 9-month follow-up assessments. Although both active interventions were significantly more successful than the GINFO condition and the pattern of effects favored the GPI + GMET, there were no statistically significant differences between the GPI and GPI + GMET interventions.</p>
</sec>
<sec><st>Conclusions:</st>
<p>Findings support the feasibility of integrating alcohol-specific sexual risk content into a theory-based sexual risk-reduction intervention and provide additional evidence that theory-based interventions are effective at reducing risky sex in this population. There was limited evidence of intervention effects on alcohol-use outcomes. Future research should focus on strengthening the GPI + GMET to most effectively target risky sexual behavior among at-risk adolescents.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Bryan, A. D., Schmiege, S. J., Broaddus, M. R.]]></dc:creator>
<dc:date>Mon, 09 Nov 2009 04:01:09 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-0679</dc:identifier>
<dc:title><![CDATA[HIV Risk Reduction Among Detained Adolescents: A Randomized, Controlled Trial]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-09</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-3704v1?rss=1">
<title><![CDATA[Natural History of Spinal Anomalies and Scoliosis Associated With Esophageal Atresia]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-3704v1?rss=1</link>
<description><![CDATA[
<sec><st>Objective:</st>
<p>Clinical characteristics of spinal deformities that commonly occur in patients with esophageal atresia (EA) are unclear. The objective of this study was to assess the incidence and natural history of spinal anomalies and scoliosis in patients with EA.</p>
</sec>
<sec><st>Methods:</st>
<p>A population-based cohort of 100 adults who had an operation for EA in our hospital were examined clinically and radiographically for spinal deformities. The results were compared with data obtained from normal population-based controls.</p>
</sec>
<sec><st>Results:</st>
<p>Vertebral anomalies were observed in 45 patients, predominating in the cervical spine in 38 patients. Any additional anomaly was the most significant risk factor (odds ratio [OR]: 27 [95% confidence interval (CI): 8&ndash;100]) for the occurrence of vertebral anomalies. Scoliosis of &gt;10&deg; was observed in 56 patients, &gt;20&deg; in 11 patients, and &gt;45&deg; in 1 patient. The risk for scoliosis of &gt;10&deg; was 13-fold (OR: 13 [95% CI: 8.3&ndash;21]), and the risk for scoliosis of &gt;20&deg; was 38-fold (OR: 38 [95% CI: 14&ndash;106]) compared with those in the normal population. Thoracotomy-induced rib fusions (OR: 3.6 [95% CI: 0.7&ndash;19]) and other associated anomalies (OR: 2.1 [95% CI: 0.9&ndash;2.9]) were the strongest predictive factors for scoliosis. The general clinical course of spinal deformities was mild, and none of the patients had undergone spinal surgery.</p>
</sec>
<sec><st>Conclusions:</st>
<p>The risk of scoliosis is 13-fold after repair of EA in relation to general population. Nearly half of the patients have vertebral anomalies predominating in the cervical spine. Most of these deformities were not diagnosed primarily or during growth. Spinal surgery is rarely indicated.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Sistonen, S. J., Helenius, I., Peltonen, J., Sarna, S., Rintala, R. J., Pakarinen, M. P.]]></dc:creator>
<dc:date>Mon, 09 Nov 2009 04:01:05 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2008-3704</dc:identifier>
<dc:title><![CDATA[Natural History of Spinal Anomalies and Scoliosis Associated With Esophageal Atresia]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-09</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-0999v1?rss=1">
<title><![CDATA[Multidisciplinary Management of Hunter Syndrome]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2008-0999v1?rss=1</link>
<description><![CDATA[
<p>Hunter syndrome is a rare, X-linked disorder caused by a deficiency of the lysosomal enzyme iduronate-2-sulfatase. In the absence of sufficient enzyme activity, glycosaminoglycans accumulate in the lysosomes of many tissues and organs and contribute to the multisystem, progressive pathologies seen in Hunter syndrome. The nervous, cardiovascular, respiratory, and musculoskeletal systems can be involved in individuals with Hunter syndrome. Although the management of some clinical problems associated with the disease may seem routine, the management is typically complex and requires the physician to be aware of the special issues surrounding the patient with Hunter syndrome, and a multidisciplinary approach should be taken. Subspecialties such as otorhinolaryngology, neurosurgery, orthopedics, cardiology, anesthesiology, pulmonology, and neurodevelopment will all have a role in management, as will specialty areas such as physiotherapy, audiology, and others. The important management topics are discussed in this review, and the use of enzyme-replacement therapy with recombinant human iduronate-2-sulfatase as a specific treatment for Hunter syndrome is presented.</p>
]]></description>
<dc:creator><![CDATA[Muenzer, J., Beck, M., Eng, C. M., Escolar, M. L., Giugliani, R., Guffon, N. H., Harmatz, P., Kamin, W., Kampmann, C., Koseoglu, S. T., Link, B., Martin, R. A., Molter, D. W., Munoz Rojas, M. V., Ogilvie, J. W., Parini, R., Ramaswami, U., Scarpa, M., Schwartz, I. V., Wood, R. E., Wraith, E.]]></dc:creator>
<dc:date>Mon, 09 Nov 2009 04:01:02 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2008-0999</dc:identifier>
<dc:title><![CDATA[Multidisciplinary Management of Hunter Syndrome]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-09</prism:publicationDate>
<prism:section>Special Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0473v1?rss=1">
<title><![CDATA[Pediatric Hospital Adherence to the Standard of Care for Acute Gastroenteritis]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0473v1?rss=1</link>
<description><![CDATA[
<sec><st>Background:</st>
<p>Adherence to published care guidelines for the management of acute gastroenteritis (AGE) is unknown.</p>
</sec>
<sec><st>Objectives:</st>
<p>To evaluate the association of AGE guideline adherence with outcomes and resource use at pediatric hospitals.</p>
</sec>
<sec><st>Design/Methods:</st>
<p>We studied children aged 6 months to 6 years with an <I>International Classification of Diseases</I>, <I>Ninth Edition</I> (ICD-9) discharge code indicative of AGE and without comorbid conditions in the emergency department, observation setting, or hospital. Laboratory studies, antiemetic use, and antibiotic use were evaluated, and the length of stay, mean adjusted total charges, and readmission proportion were documented. Multiple analysis of variance determined if the variance of adjusted charges, length of stay, and diagnostic studies were hospital-related. A regression analysis determined the association between guideline adherence and outcomes.</p>
</sec>
<sec><st>Results:</st>
<p>There were a total of 188873 patients; 174594 (92.4%) were not admitted, and 14279 (7.6%) were admitted. There was substantial variation in resource use among hospitals. The mean adjusted total charge for all patients was $863 (SD: 1336). The mean adjusted total charge for nonadmitted patients was $591 (SD: 636). Individual hospitals contributed to the variance of mean length of stay, total adjusted charges, and use of diagnostic studies after controlling for covariates (<I>P</I> &lt; .001). Guideline adherence was associated with a mean decrease in the average adjusted cost ($591) for nonadmitted patients of $296 (95% confidence interval: &ndash;399 to &ndash;193).</p>
</sec>
<sec><st>Conclusions:</st>
<p>Guideline-adherent hospitals demonstrated 50% lower charges for emergency department or observation patients with uncomplicated AGE without adversely affecting outcomes. Use of resources not routinely recommended by published AGE guidelines remains common in pediatric hospitals.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Tieder, J. S., Robertson, A., Garrison, M. M.]]></dc:creator>
<dc:date>Mon, 02 Nov 2009 11:01:18 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-0473</dc:identifier>
<dc:title><![CDATA[Pediatric Hospital Adherence to the Standard of Care for Acute Gastroenteritis]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-02</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0207v1?rss=1">
<title><![CDATA[Association Between Adherence and Glycemic Control in Pediatric Type 1 Diabetes: A Meta-analysis]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-0207v1?rss=1</link>
<description><![CDATA[
<sec><st>Context:</st>
<p>Although adherence has been identified in practice guidelines for youth with type 1 diabetes to promote optimal glycemic control, there has been no systematic integration of studies investigating the adherence-glycemic control link. This recommendation partly stemmed from the Diabetes Control and Complications Trial (DCCT); however, this trial did not comprehensively measure adherence and had only 195 adolescents.</p>
</sec>
<sec><st>Objective:</st>
<p>Our goal was to determine the magnitude of the adherence-glycemic control link in pediatric type 1 diabetes and evaluate its correlates.</p>
</sec>
<sec><st>Methods:</st>
<p>Our data sources were PubMed (1950&ndash;2008), Scopus (1950&ndash;2008), and references from reviews in pediatric type 1 diabetes. Studies that included youth under age 19 with type 1 diabetes and a reported association between adherence and glycemic control were eligible for inclusion. Articles were not included if they contained youth with type 2 diabetes, had study samples that overlapped with other studies, or the results came from intervention studies. Of the eligible 26 studies, 21 had sufficient statistical data. Two authors independently extracted information by using a standardized protocol. Agreement between coders was high.</p>
</sec>
<sec><st>Results:</st>
<p>The mean effect size across 21 studies, including 2492 youth with type 1 diabetes, was &ndash;0.28 (95% confidence interval: &ndash;0.32 to &ndash;0.24). As adherence increases, A1c values decrease. No sample or disease characteristics were correlates of the adherence-glycemic control link. Pre-DCCT studies had a mean effect size of &ndash;0.32 (8 studies; 1169 participants) compared with &ndash;0.25 in post-DCCT studies (13 studies; 1323 participants).</p>
</sec>
<sec><st>Conclusions:</st>
<p>This meta-analysis supports the adherence-glycemic control link in pediatric type 1 diabetes. The weaker post-DCCT association suggests that the approach to intensive diabetes management has shortcomings. We conclude that this is because of a mismatch between what scientists and clinicians know is the best way to manage pediatric type 1 diabetes and the capabilities of youth and their families.</p>
</sec>
]]></description>
<dc:creator><![CDATA[Hood, K. K., Peterson, C. M., Rohan, J. M., Drotar, D.]]></dc:creator>
<dc:date>Mon, 02 Nov 2009 11:01:14 PST</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-0207</dc:identifier>
<dc:title><![CDATA[Association Between Adherence and Glycemic Control in Pediatric Type 1 Diabetes: A Meta-analysis]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-11-02</prism:publicationDate>
<prism:section>Articles</prism:section>
</item>

<item rdf:about="http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-2345v1?rss=1">
<title><![CDATA[Policy Statement--Modified Recommendations for Use of Palivizumab for Prevention of Respiratory Syncytial Virus Infections]]></title>
<link>http://pediatrics.aappublications.org/cgi/content/abstract/peds.2009-2345v1?rss=1</link>
<description><![CDATA[
<p>Palivizumab was licensed in June 1998 by the US Food and Drug Administration for prevention of serious lower respiratory tract disease caused by respiratory syncytial virus (RSV) in pediatric patients who are at increased risk of severe disease. Safety and efficacy have been established for infants born at or before 35 weeks' gestation with or without chronic lung disease of prematurity and for infants and children with hemodynamically significant heart disease. The American Academy of Pediatrics (AAP) published a policy statement on the use of palivizumab in November 1998 (American Academy of Pediatrics, Committee on Infectious Diseases and Committee on Fetus and Newborn. <I>Pediatrics.</I> 1998;102[5]:1211&ndash;1216) and revised it in December 2003 (American Academy of Pediatrics, Committee on Infectious Diseases and Committee on Fetus and Newborn. <I>Pediatrics.</I> 2003;112[6 pt 1]:1442&ndash;1446), and an AAP technical report on palivizumab was published in 2003 (Meissner HC, Long SS; American Academy of Pediatrics, Committee on Infectious Diseases and Committee on Fetus and Newborn. <I>Pediatrics.</I> 2003;112[6 pt 1]:1447&ndash;1452). On the basis of the availability of additional data regarding seasonality of RSV disease as well as the limitations in available data on risk factors for identifying children who are at increased risk of serious RSV lower respiratory tract disease, AAP recommendations for immunoprophylaxis have been updated in an effort to ensure optimal balance of benefit and cost from this expensive intervention. This statement updates and replaces the 2003 AAP statement and the 2006 <I>Red Book</I> and is consistent with the 2009 <I>Red Book</I> recommendations.</p>
]]></description>
<dc:creator><![CDATA[COMMITTEE ON INFECTIOUS DISEASES]]></dc:creator>
<dc:date>Mon, 07 Sep 2009 04:01:33 PDT</dc:date>
<dc:identifier>info:doi/10.1542/peds.2009-2345</dc:identifier>
<dc:title><![CDATA[Policy Statement--Modified Recommendations for Use of Palivizumab for Prevention of Respiratory Syncytial Virus Infections]]></dc:title>
<dc:publisher>American Academy of Pediatrics</dc:publisher>
<prism:publicationDate>2009-09-07</prism:publicationDate>
<prism:section>AMERICAN ACADEMY OF PEDIATRICS</prism:section>
</item>

</rdf:RDF>