Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 48
Filter
1.
J Pediatr ; 164(1): 34-39.e2, 2014 Jan.
Article in English | MEDLINE | ID: mdl-23992673

ABSTRACT

OBJECTIVE: To evaluate the incidence of death or neurodevelopmental impairment (NDI) at 18-22 months corrected age in subjects enrolled in a trial of early dexamethasone treatment to prevent death or chronic lung disease in extremely low birth weight infants. STUDY DESIGN: Evaluation of infants at 18-22 months corrected age included anthropomorphic measurements, a standard neurological examination, and the Bayley Scales of Infant Development-II, including the Mental Developmental Index and the Psychomotor Developmental Index. NDI was defined as moderate or severe cerebral palsy, Mental Developmental Index or Psychomotor Developmental Index <70, blindness, or hearing impairment. RESULTS: Death or NDI at 18-22 months corrected age was similar in the dexamethasone and placebo groups (65% vs 66%, P = .99 among those with known outcome). The proportion of survivors with NDI was also similar, as were mean values for weight, length, and head circumference and the proportion of infants with poor growth (50% vs 41%, P = .42 for weight less than 10th percentile); 49% of infants in the placebo group received treatment with corticosteroid compared with 32% in the dexamethasone group (P = .02). CONCLUSION: The risk of death or NDI and rate of poor growth were high but similar in the dexamethasone and placebo groups. The lack of a discernible effect of early dexamethasone on neurodevelopmental outcome may be due to frequent clinical corticosteroid use in the placebo group.


Subject(s)
Child Development , Developmental Disabilities/prevention & control , Dexamethasone/administration & dosage , Infant, Extremely Low Birth Weight , Lung Diseases/prevention & control , Cause of Death/trends , Chronic Disease , Developmental Disabilities/epidemiology , Developmental Disabilities/etiology , Dose-Response Relationship, Drug , Double-Blind Method , Follow-Up Studies , Glucocorticoids/administration & dosage , Humans , Incidence , Infant , Injections, Intravenous , Lung Diseases/complications , Lung Diseases/epidemiology , Neurologic Examination , Retrospective Studies , Survival Rate/trends , Time Factors , Treatment Outcome , United States/epidemiology
2.
Neurotoxicol Teratol ; 33(5): 575-81, 2011.
Article in English | MEDLINE | ID: mdl-21849244

ABSTRACT

OBJECTIVE: To evaluate the impact of prenatal cocaine exposure and small-for-gestational-age (SGA) status on childhood growth. STUDY DESIGN: Cocaine exposure was defined by history or meconium metabolites. Hierarchical linear modeling was used to examine cocaine exposure and SGA status on growth, while controlling for exposure to other drugs and alcohol use. RESULTS: At birth cocaine-exposed infants (n=364) had significantly lower growth parameters compared to non-exposed children (n=771). At 6 years, weight was similar between exposed and unexposed children. SGA infants continued to be growth impaired. There was a significant interaction between prenatal cocaine exposure and SGA status at 6 years. The negative effects of cocaine on weight and height were greater among non-SGA than SGA children (432 vs. 280 gm, and 0.7 and 0.5 cm, respectively) while negative effects of SGA status on weight and height were larger in non-cocaine exposed compared to the exposed children (2.3 kg vs.1.6 kg and 2.2 and 1.0 cm). CONCLUSIONS: Children exposed to prenatal cocaine were similar in weight to non-exposed children at 6 years of age. Cocaine had an unexplained greater detrimental effect on non-SGA than SGA children. SGA status at birth has an independent detrimental effect on childhood growth.


Subject(s)
Child Development/physiology , Cocaine/toxicity , Infant, Small for Gestational Age/growth & development , Prenatal Exposure Delayed Effects/physiopathology , Body Height , Body Weight , Child , Child, Preschool , Female , Humans , Infant , Infant, Newborn , Infant, Small for Gestational Age/physiology , Male , Pregnancy
3.
Pediatrics ; 128(1): e112-20, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21669899

ABSTRACT

OBJECTIVE: To examine the predictive validity of the amplitude integrated electroencephalogram (aEEG) and stage of encephalopathy among infants with hypoxic-ischemic encephalopathy (HIE) eligible for therapeutic whole-body hypothermia. DESIGN: Neonates were eligible for this prospective study if moderate or severe HIE occurred at <6 hours and an aEEG was obtained at <9 hours of age. The primary outcome was death or moderate/severe disability at 18 months. RESULTS: There were 108 infants (71 with moderate HIE and 37 with severe HIE) enrolled in the study. aEEG findings were categorized as normal, with continuous normal voltage (n=12) or discontinuous normal voltage (n=12), or abnormal, with burst suppression (n=22), continuous low voltage (n=26), or flat tracing (n=36). At 18 months, 53 infants (49%) experienced death or disability. Severe HIE and an abnormal aEEG were related to the primary outcome with univariate analysis, whereas severe HIE alone was predictive of outcome with multivariate analysis. Addition of aEEG pattern to HIE stage did not add to the predictive value of the model; the area under the curve changed from 0.72 to 0.75 (P=.19). CONCLUSIONS: The aEEG background pattern did not significantly enhance the value of the stage of encephalopathy at study entry in predicting death and disability among infants with HIE.


Subject(s)
Electroencephalography , Hypoxia-Ischemia, Brain/diagnosis , Neurologic Examination , Female , Follow-Up Studies , Humans , Infant, Newborn , Male , Predictive Value of Tests , Prospective Studies , Severity of Illness Index
4.
Clin Cardiol ; 34(2): 102-7, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21283998

ABSTRACT

BACKGROUND: Total and cardiac mortality rates in Los Angeles County, California, increased after the 1980 Super Bowl loss (SBL), but there was an overall reduction in total mortality after the 1984 Super Bowl win (SBW). HYPOTHESIS: We hypothesized that age, sex, and race may have played a role in the Super Bowl related differences in death rates. METHODS: We compared mortality rates for SB-related days with non-SB control days assessing differences in demographics. We ran regression models predicting daily death rates per 100,000 including SB variable versus non-SB control days for age, sex, race, and interactions for these covariates. RESULTS: After the SBL, daily death rates increased for both males and females. People aged ≥65 years had a larger absolute increase in all cause mortality during the SBL days compared with those aged <65 years, with significant interaction between age and SBL-variable for all-cause and cardiac-related mortality. Whites and Hispanics had increased death rates on SBL days. There were trends suggesting less death in older patients and females associated with the SBW. CONCLUSION: A SBL triggered increased deaths in both men and women and especially in older patients, whereas a SBW reduced death more in those aged ≥65 years and in women.


Subject(s)
Cardiovascular Diseases/mortality , Football , Racial Groups/statistics & numerical data , Stress, Psychological/mortality , Adaptation, Psychological , Age Factors , Aged , Analysis of Variance , California/epidemiology , Cardiovascular Diseases/epidemiology , Cardiovascular Diseases/ethnology , Death Certificates , Female , Humans , Male , Middle Aged , Mortality/trends , Sex Factors , Stress, Psychological/complications
5.
Acta Paediatr ; 100(7): 960-5, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21272067

ABSTRACT

AIM: To compare risk-adjusted outcomes at 18- to 22-month-corrected age for extremely low birth weight (ELBW) infants who never received phototherapy (NoPTx) to those who received any phototherapy (PTx) in the NICHD Neonatal Research Network randomized trial of Aggressive vs. Conservative Phototherapy. METHODS: Outcomes at 18 to 22-month-corrected age included death, neurodevelopmental impairment (NDI) and Bayley Scales Mental Developmental Index (MDI). Regression models evaluated the independent association of PTx with adverse outcomes controlling for centre and other potentially confounding variables. RESULTS: Of 1972 infants, 216 were NoPTx and 1756 were PTx. For the entire 501- to 1000-g-BW cohort, PTx was not independently associated with death or NDI (OR 0.85, 95% CI: 0.60-1.20), death or adverse neurodevelopmental endpoints. However, among infants 501-750 g BW, the rate of significant developmental impairment with MDI < 50 was significantly higher for NoPTx (29%) than PTx (12%) (p = 0.004). CONCLUSIONS: Phototherapy did not appear to be independently associated with death or NDI for the overall ELBW group. Whether PTx increases mortality could not be excluded because of bias from deaths before reaching conservative treatment threshold. The higher rate of MDI < 50 in the 501- to 750-g-BW NoPTx group is concerning and consistent with NRN Trial results.


Subject(s)
Developmental Disabilities/etiology , Infant, Extremely Low Birth Weight , Mental Disorders/etiology , Phototherapy/adverse effects , Developmental Disabilities/diagnosis , Humans , Infant , Infant, Newborn , Mental Disorders/diagnosis , Phototherapy/methods , Phototherapy/mortality , Psychomotor Performance , Risk Adjustment , Treatment Outcome
6.
J Child Neurol ; 26(3): 322-8, 2011 Mar.
Article in English | MEDLINE | ID: mdl-20921569

ABSTRACT

It remains controversial as to whether neonatal seizures have additional direct effects on the developing brain separate from the severity of the underlying encephalopathy. Using data collected from infants diagnosed with hypoxic-ischemic encephalopathy, and who were enrolled in an National Institute of Child Health and Human Development trial of hypothermia, we analyzed associations between neonatal clinical seizures and outcomes at 18 months of age. Of the 208 infants enrolled, 102 received whole body hypothermia and 106 were controls. Clinical seizures were generally noted during the first 4 days of life and rarely afterward. When adjustment was made for study treatment and severity of encephalopathy, seizures were not associated with death, or moderate or severe disability, or lower Bayley Mental Development Index scores at 18 months of life. Among infants diagnosed with hypoxic-ischemic encephalopathy, the mortality and morbidity often attributed to neonatal seizures can be better explained by the underlying severity of encephalopathy.


Subject(s)
Developmental Disabilities/physiopathology , Hypothermia, Induced/methods , Hypoxia-Ischemia, Brain/complications , Seizures/etiology , Disability Evaluation , Electroencephalography , Female , Humans , Hypoxia-Ischemia, Brain/therapy , Infant , Male , National Institute of Child Health and Human Development (U.S.)/standards , Seizures/therapy , Time Factors , Treatment Outcome , United States
7.
N Engl J Med ; 362(21): 1959-69, 2010 May 27.
Article in English | MEDLINE | ID: mdl-20472937

ABSTRACT

BACKGROUND: Previous studies have suggested that the incidence of retinopathy is lower in preterm infants with exposure to reduced levels of oxygenation than in those exposed to higher levels of oxygenation. However, it is unclear what range of oxygen saturation is appropriate to minimize retinopathy without increasing adverse outcomes. METHODS: We performed a randomized trial with a 2-by-2 factorial design to compare target ranges of oxygen saturation of 85 to 89% or 91 to 95% among 1316 infants who were born between 24 weeks 0 days and 27 weeks 6 days of gestation. The primary outcome was a composite of severe retinopathy of prematurity (defined as the presence of threshold retinopathy, the need for surgical ophthalmologic intervention, or the use of bevacizumab), death before discharge from the hospital, or both. All infants were also randomly assigned to continuous positive airway pressure or intubation and surfactant. RESULTS: The rates of severe retinopathy or death did not differ significantly between the lower-oxygen-saturation group and the higher-oxygen-saturation group (28.3% and 32.1%, respectively; relative risk with lower oxygen saturation, 0.90; 95% confidence interval [CI], 0.76 to 1.06; P=0.21). Death before discharge occurred more frequently in the lower-oxygen-saturation group (in 19.9% of infants vs. 16.2%; relative risk, 1.27; 95% CI, 1.01 to 1.60; P=0.04), whereas severe retinopathy among survivors occurred less often in this group (8.6% vs. 17.9%; relative risk, 0.52; 95% CI, 0.37 to 0.73; P<0.001). There were no significant differences in the rates of other adverse events. CONCLUSIONS: A lower target range of oxygenation (85 to 89%), as compared with a higher range (91 to 95%), did not significantly decrease the composite outcome of severe retinopathy or death, but it resulted in an increase in mortality and a substantial decrease in severe retinopathy among survivors. The increase in mortality is a major concern, since a lower target range of oxygen saturation is increasingly being advocated to prevent retinopathy of prematurity. (ClinicalTrials.gov number, NCT00233324.)


Subject(s)
Infant Mortality , Infant, Premature/blood , Oxygen Inhalation Therapy/methods , Oxygen/blood , Retinopathy of Prematurity/prevention & control , Continuous Positive Airway Pressure , Female , Hospital Mortality , Humans , Infant, Newborn , Intubation, Intratracheal , Kaplan-Meier Estimate , Male , Oximetry , Oxygen/administration & dosage , Oxygen Inhalation Therapy/adverse effects , Proportional Hazards Models , Pulmonary Surfactants/therapeutic use , Reference Values , Retinopathy of Prematurity/epidemiology
8.
N Engl J Med ; 362(21): 1970-9, 2010 May 27.
Article in English | MEDLINE | ID: mdl-20472939

ABSTRACT

BACKGROUND: There are limited data to inform the choice between early treatment with continuous positive airway pressure (CPAP) and early surfactant treatment as the initial support for extremely-low-birth-weight infants. METHODS: We performed a randomized, multicenter trial, with a 2-by-2 factorial design, involving infants who were born between 24 weeks 0 days and 27 weeks 6 days of gestation. Infants were randomly assigned to intubation and surfactant treatment (within 1 hour after birth) or to CPAP treatment initiated in the delivery room, with subsequent use of a protocol-driven limited ventilation strategy. Infants were also randomly assigned to one of two target ranges of oxygen saturation. The primary outcome was death or bronchopulmonary dysplasia as defined by the requirement for supplemental oxygen at 36 weeks (with an attempt at withdrawal of supplemental oxygen in neonates who were receiving less than 30% oxygen). RESULTS: A total of 1316 infants were enrolled in the study. The rates of the primary outcome did not differ significantly between the CPAP group and the surfactant group (47.8% and 51.0%, respectively; relative risk with CPAP, 0.95; 95% confidence interval [CI], 0.85 to 1.05) after adjustment for gestational age, center, and familial clustering. The results were similar when bronchopulmonary dysplasia was defined according to the need for any supplemental oxygen at 36 weeks (rates of primary outcome, 48.7% and 54.1%, respectively; relative risk with CPAP, 0.91; 95% CI, 0.83 to 1.01). Infants who received CPAP treatment, as compared with infants who received surfactant treatment, less frequently required intubation or postnatal corticosteroids for bronchopulmonary dysplasia (P<0.001), required fewer days of mechanical ventilation (P=0.03), and were more likely to be alive and free from the need for mechanical ventilation by day 7 (P=0.01). The rates of other adverse neonatal outcomes did not differ significantly between the two groups. CONCLUSIONS: The results of this study support consideration of CPAP as an alternative to intubation and surfactant in preterm infants. (ClinicalTrials.gov number, NCT00233324.)


Subject(s)
Bronchopulmonary Dysplasia/epidemiology , Continuous Positive Airway Pressure , Infant Mortality , Infant, Extremely Low Birth Weight , Intubation, Intratracheal , Oxygen Inhalation Therapy/methods , Pulmonary Surfactants/therapeutic use , Apgar Score , Female , Hospital Mortality , Humans , Infant, Newborn , Infant, Premature , Intention to Treat Analysis , Male , Oximetry , Oxygen/administration & dosage , Oxygen/blood , Retinopathy of Prematurity/epidemiology
9.
J Hypertens ; 28(6): 1166-75, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20486281

ABSTRACT

BACKGROUND: Prenatal cocaine exposure has been linked to intrauterine growth retardation and poor birth outcomes; little is known about the effects on longer-term medical outcomes, such as overweight status and hypertension in childhood. Our objective was to examine the association between prenatal cocaine exposure and BMI and blood pressure at 9 years of age among children followed prospectively in a multisite longitudinal study evaluating the impact of maternal lifestyle during pregnancy on childhood outcome. DESIGN/METHODS: This analysis includes 880 children (277 cocaine exposed and 603 with no cocaine exposure) with blood pressure, height, and weight measurements at 9 years of age. Regression analyses were conducted to explore the relationship between prenatal cocaine exposure and BMI and blood pressure at 9 years of age after controlling for demographics, other drug exposure, birthweight, maternal weight, infant postnatal weight gain, and childhood television viewing, exercise, and dietary habits at 9 years. Path analyses were used to further explore these relationships. RESULTS: At 9 years of age, 15% of the children were prehypertensive and 19% were hypertensive; 16% were at risk for overweight status and 21% were overweight. A small percentage of women were exposed to high levels of prenatal cocaine throughout pregnancy. A higher BMI was noted in children born to these women. Path analysis suggested that high cocaine exposure has an indirect effect on systolic and diastolic blood pressures that is mediated through its effect on BMI. CONCLUSION: High levels of in-utero cocaine exposure are a marker for elevated BMI and blood pressure among children born full term.


Subject(s)
Blood Pressure , Body Mass Index , Cocaine/administration & dosage , Prenatal Exposure Delayed Effects , Child , Energy Intake , Exercise , Female , Humans , Longitudinal Studies , Male , Pregnancy
11.
Am J Cardiol ; 103(12): 1647-50, 2009 Jun 15.
Article in English | MEDLINE | ID: mdl-19539070

ABSTRACT

The purpose of this study was to determine whether there were changes in death rates when a local football team participated in the Super Bowl. Los Angeles (LA) played in the Super Bowl twice: on January 20, 1980 (LA Rams vs Pittsburgh Steelers, which LA lost), and on January 22, 1984 (LA Raiders vs Washington Redskins, which LA won). Data from LA County were analyzed for all-cause and circulatory death rates for the Super Bowl and the following 14 days when LA played (Super Bowl-related days) and control days (from January 15 to the end of February for 1980 to 1983 and 1984 to 1988). The Super Bowl-related days during LA's losing 1980 game were associated with higher daily death rates in LA County (per 100,000 population) for all deaths (2.4482 vs 2.0968 for control days, p <0.0001), circulatory deaths (1.3024 vs 1.0665 for control days, p <0.0001), deaths from ischemic heart disease (0.8551 vs 0.7143 for control days, p <0.0001), and deaths from acute myocardial infarctions (0.2710 vs 0.2322 for control days, p = 0.0213). In contrast, the Super Bowl-related days during the winning 1984 game were associated with a lower rate of all-cause death (2.1870 vs 2.3205 for control days, p = 0.0302). In conclusion, the emotional stress of loss and/or the intensity of a game played by a sports team in a highly publicized rivalry such as the Super Bowl can trigger total and cardiovascular deaths.


Subject(s)
Cardiovascular Diseases/mortality , Football , California/epidemiology , Cardiovascular Diseases/etiology , Cause of Death/trends , Humans , Retrospective Studies , Risk Factors , Stress, Psychological/complications , Stress, Psychological/mortality , Survival Rate/trends
12.
Pediatrics ; 123(2): e220-7, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19139085

ABSTRACT

OBJECTIVE: The purpose of this work was to compare the risk-adjusted incidence of death or neurodevelopmental impairment at 18 to 22 months' corrected age between twin and singleton extremely low birth weight infants. We hypothesized that twin gestation is independently associated with increased risk of death or adverse neurodevelopmental outcomes at 18 to 22 months' corrected age in these infants. METHODS: We conducted a retrospective study of inborn extremely low birth weight infants admitted to Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network units between 1997 and 2005, who either died or had follow-up data available at 18 to 22 months' corrected age. Neurodevelopmental impairment, the primary outcome variable, was defined as the presence of any 1 of the following: moderate or severe cerebral palsy, severe bilateral hearing loss, bilateral blindness, Bayley Mental Developmental Index or Psychomotor Developmental Index of <70. Death was included with neurodevelopmental impairment as a composite outcome. Results were compared for both twins, twin A, twin B, same-gender twins, unlike-gender twins, and singleton infants. Logistic regression analysis was performed to control for demographic and clinical factors that were different among the groups. RESULTS: The cohort of infants who either died or were assessed for neurodevelopmental impairment consisted of 7630 singleton infants and 1376 twins. Logistic regression adjusting for clinical and sociodemographic risk factors showed an increased risk of death or neurodevelopmental impairment for twins as a group when compared with the singletons. On analyzing twin A and B separately as well, risk of death or neurodevelopmental impairment was increased in both twin A and twin B. CONCLUSIONS: Twin gestation in extremely low birth weight infants is associated with an independent increased risk of death or neurodevelopmental impairment at 18 to 22 months' corrected age compared with singleton-gestation infants. Both first- and second-born twins are at increased risk.


Subject(s)
Developmental Disabilities/epidemiology , Infant, Extremely Low Birth Weight , Nervous System Diseases/epidemiology , Twins , Diseases in Twins/mortality , Female , Humans , Infant, Newborn , Infant, Newborn, Diseases/mortality , Male , Retrospective Studies
13.
J Pediatr ; 154(4): 498-503.e2, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19111322

ABSTRACT

OBJECTIVES: To compare the rates of adverse neurodevelopmental outcome or death at 18 to 22 months among extremely low birth weight (ELBW) infants born to mothers >or=4 0 years to the corresponding rates among infants of younger mothers. STUDY DESIGN: Prospective evaluation of ELBW infants to quantify the relative risks of maternal age and multiple birth for death or adverse neurodevelopmental outcome. RESULTS: The sample consisted of 14 671 live ELBW births divided into maternal age groups: <20, 20 to 29, 30 to 39, and >or= 40 years. Of infants born to mothers >or= 40 years, 20% were multiples. Mothers >or= 40 years had high rates of obstetric interventions and medical morbidities compared with mothers <40 years. ELBW live births of mothers >or= 40 years were 22% more likely to survive and had a 13% decreased risk of neurodevelopmental impairment or death compared with mothers <20. Multiple birth, however, was associated with a 10% greater risk of neurodevelopmental impairment or death. CONCLUSION: Although mothers >or= 40 years had high pregnancy-related morbidities, we found no overall increased risk of the composite outcome of death or NDI. Multiple birth, however, was a predictor of all adverse outcomes examined, regardless of maternal age.


Subject(s)
Central Nervous System Diseases/epidemiology , Developmental Disabilities/epidemiology , Infant Mortality , Infant, Very Low Birth Weight , Maternal Age , Adult , Female , Humans , Infant , Infant, Newborn , Male , Pregnancy , Pregnancy Complications/epidemiology , Pregnancy, Multiple , Prospective Studies , Regression Analysis , Risk Factors , United States/epidemiology
14.
N Engl J Med ; 359(18): 1885-96, 2008 Oct 30.
Article in English | MEDLINE | ID: mdl-18971491

ABSTRACT

BACKGROUND: It is unclear whether aggressive phototherapy to prevent neurotoxic effects of bilirubin benefits or harms infants with extremely low birth weight (1000 g or less). METHODS: We randomly assigned 1974 infants with extremely low birth weight at 12 to 36 hours of age to undergo either aggressive or conservative phototherapy. The primary outcome was a composite of death or neurodevelopmental impairment determined for 91% of the infants by investigators who were unaware of the treatment assignments. RESULTS: Aggressive phototherapy, as compared with conservative phototherapy, significantly reduced the mean peak serum bilirubin level (7.0 vs. 9.8 mg per deciliter [120 vs. 168 micromol per liter], P<0.01) but not the rate of the primary outcome (52% vs. 55%; relative risk, 0.94; 95% confidence interval [CI], 0.87 to 1.02; P=0.15). Aggressive phototherapy did reduce rates of neurodevelopmental impairment (26%, vs. 30% for conservative phototherapy; relative risk, 0.86; 95% CI, 0.74 to 0.99). Rates of death in the aggressive-phototherapy and conservative-phototherapy groups were 24% and 23%, respectively (relative risk, 1.05; 95% CI, 0.90 to 1.22). In preplanned subgroup analyses, the rates of death were 13% with aggressive phototherapy and 14% with conservative phototherapy for infants with a birth weight of 751 to 1000 g and 39% and 34%, respectively (relative risk, 1.13; 95% CI, 0.96 to 1.34), for infants with a birth weight of 501 to 750 g. CONCLUSIONS: Aggressive phototherapy did not significantly reduce the rate of death or neurodevelopmental impairment. The rate of neurodevelopmental impairment alone was significantly reduced with aggressive phototherapy. This reduction may be offset by an increase in mortality among infants weighing 501 to 750 g at birth. (ClinicalTrials.gov number, NCT00114543.)


Subject(s)
Hyperbilirubinemia, Neonatal/therapy , Infant, Extremely Low Birth Weight , Phototherapy/methods , Bayes Theorem , Bilirubin/blood , Birth Weight , Developmental Disabilities/epidemiology , Developmental Disabilities/etiology , Developmental Disabilities/prevention & control , Female , Humans , Hyperbilirubinemia, Neonatal/complications , Infant Mortality , Infant, Extremely Low Birth Weight/blood , Infant, Newborn , Male , Phototherapy/adverse effects , Treatment Outcome
15.
Pediatrics ; 122(3): 491-9, 2008 Sep.
Article in English | MEDLINE | ID: mdl-18762517

ABSTRACT

OBJECTIVE: The goal was to determine whether the risk of death or moderate/severe disability in term infants with hypoxic-ischemic encephalopathy increases with relatively high esophageal or skin temperature occurring between 6 and 78 hours after birth. METHODS: This was an observational secondary study within the National Institute of Child Health and Human Development Neonatal Research Network randomized trial comparing whole-body cooling and usual care (control) for term infants with hypoxic-ischemic encephalopathy. Esophageal and skin temperatures were recorded serially for 72 hours. Each infant's temperatures for each site were rank ordered. The high temperature was defined for each infant as the mean of all temperature measurements in the upper quartile. The low temperature was similarly defined as the mean of the lower quartile. Outcomes were related to temperatures in 3 logistic regression analyses for the high, median, and low temperatures at each temperature site for each group, with adjustment for the level of encephalopathy, gender, gestational age, and race. RESULTS: In control infants, the mean esophageal temperature was 37.2 +/- 0.7 degrees C over the 72-hour period, and 63%, 22%, and 8% of all temperatures were >37 degrees C, >37.5 degrees C, and >38 degrees C, respectively. The mean skin temperature was 36.5 +/- 0.8 degrees C, and 12%, 5%, and 2% of all temperatures were >37 degrees C, >37.5 degrees C, and >38 degrees C, respectively. The odds of death or disability were increased 3.6-4 fold for each 1 degrees C increase in the highest quartile of skin or esophageal temperatures. There were no associations between temperatures and outcomes in the cooling-treated group. CONCLUSIONS: Relatively high temperatures during usual care after hypoxia-ischemia were associated with increased risk of adverse outcomes. The results may reflect underlying brain injury and/or adverse effects of temperature on outcomes.


Subject(s)
Body Temperature/physiology , Fever/etiology , Hypothermia, Induced/methods , Hypoxia-Ischemia, Brain/physiopathology , Female , Fever/physiopathology , Fever/therapy , Follow-Up Studies , Humans , Hypoxia-Ischemia, Brain/complications , Hypoxia-Ischemia, Brain/prevention & control , Infant, Newborn , Male , Time Factors , Treatment Outcome
16.
Arch Pediatr Adolesc Med ; 162(8): 748-55, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18678807

ABSTRACT

OBJECTIVE: To determine special outpatient services (SOS) use, need, associated factors, and neurodevelopmental and functional outcomes among extremely preterm infants at 18 to 22 months' corrected age. DESIGN: Retrospective analysis. SETTING: National Institute of Child Health and Human Development (NICHD) Neonatal Research Network. PARTICIPANTS: Infants younger than 28 weeks' gestational age who had been born weighing less than 1000 g at an NICHD Neonatal Research Network center from January 1, 1997, to December 31, 2000, and who were receiving follow-up at 18 to 22 months' corrected age. INTERVENTIONS: Questionnaires were administered at the 18- to 22-month follow-up visit regarding SOS use since hospital discharge and the current need for SOS (social work, visiting nurse, medical specialty, early intervention, speech and language services, occupational therapy and physical therapy, and neurodevelopmental and behavioral services). MAIN OUTCOME MEASURES: The use of and need for SOS were analyzed by gestational age. Logistic regression analysis identified factors independently associated with the use of more than 5 services and with the need for any services. RESULTS: Of 2315 infants, 54.7% used more than 3 SOS by 18 to 22 months, and 19.1% used 6 to 7 SOS. The need for any SOS was reported by approximately 37%. The following variables that were commonly associated with adverse neurodevelopmental outcomes were also associated with the use of more than 5 SOS: sepsis, birth weight, postnatal corticosteroid use, bronchopulmonary dysplasia, and cystic periventricular leukomalacia or grade 3 or 4 intraventricular hemorrhage. Male sex was associated with the need for any SOS. Although high SOS use was more likely among children with adverse neurodevelopmental outcomes, a reported need for SOS was common even among those with mild developmental impairment (39.7%) and mild cerebral palsy (42.2%). CONCLUSIONS: High SOS use is common, has identifiable neonatal risk factors, and is associated with neurodevelopmental impairment. Extremely preterm survivors have substantial need for community supports regardless of their impairment level. Efforts to improve comprehensive delivery of family-centered community-based services are urgently needed.


Subject(s)
Ambulatory Care/standards , Child Health Services/standards , Community Health Services/standards , Developmental Disabilities/therapy , Infant, Extremely Low Birth Weight , Survivors/statistics & numerical data , Ambulatory Care/statistics & numerical data , Child , Child Health Services/statistics & numerical data , Child, Preschool , Community Health Services/statistics & numerical data , Confidence Intervals , Continuity of Patient Care/standards , Continuity of Patient Care/statistics & numerical data , Developmental Disabilities/diagnosis , Developmental Disabilities/epidemiology , Disability Evaluation , Female , Humans , Infant , Infant, Newborn , Infant, Premature , Infant, Premature, Diseases/diagnosis , Infant, Premature, Diseases/mortality , Infant, Premature, Diseases/therapy , Intensive Care Units, Neonatal , Logistic Models , Male , Multivariate Analysis , Needs Assessment , Odds Ratio , Quality of Health Care , Retrospective Studies , Risk Assessment , United States
17.
Infant Ment Health J ; 29(6): 570-587, 2008 Nov 01.
Article in English | MEDLINE | ID: mdl-19779585

ABSTRACT

Effects on a family of a child with chronic illness have been described. The Impact on Family Scale (IOF) was developed to measure these effects. The impact of extremely low birth weight (ELBW) infants with neurodevelopmental impairment on families is unknown. This study determined IOF scores for families of ELBW infants with increasing degree of impairment at 18 months and identified factors that increase vulnerability to impact. A total of 3,849 ELBW infant survivors born at the 16 centers of the National Institute of Child Health and Human Development Neonatal Research Network between January 1993 and February 2001 were assessed at 18 to 22 months. Infants were divided into four groups by degree of impairment. IOF scores were analyzed by impairment group. Multivariate analyses assessed effects of impairment, social/demographic factors, unmet service needs, and resource utilization on the IOF. A total of 1,624 (42.2%) infants had moderate/severe impairment. Increasing severity of impairment was associated with higher IOF scores. Severity of impairment contributed 6% of variance to the IOF scores. Twenty-one percent of variance was contributed by additional medical needs, low socioeconomic status (SES), and lack of social support. Although increasing severity of impairment impacts families of ELBW infants, significantly more impact is contributed by additional medical needs, low SES, and lack of social support.

18.
Pediatrics ; 120(6): e1512-9, 2007 Dec.
Article in English | MEDLINE | ID: mdl-17984212

ABSTRACT

BACKGROUND: Studies of growth and neurodevelopmental impairment in extremely low birth weight infants often exclude infants with major congenital anomalies; thus, there are few outcome data available on these infants. OBJECTIVES: The purpose of this work was to compare growth and neurodevelopmental outcomes of extremely low birth weight infants with major anomalies to extremely low birth weight infants without these findings. It was hypothesized that infants with severe anomalies would have worse growth, neurodevelopmental, and survival outcomes. METHODS: A retrospective cohort analysis was performed on 5920 extremely low birth weight infants surviving beyond 12 hours of life at 19 neonatal network centers between 1998 and 2001. Infants with significant anomalies were more likely to die before 18 to 22 months' corrected age. A total of 3705 children underwent neurodevelopmental and anthropometric evaluation at 18 to 22 months' corrected age. Statistical significance for unadjusted comparisons was determined by Wilcoxon tests for continuous variables and chi2 or Fisher's exact tests for categorical variables. Regression models were used to compare the outcomes after adjusting for potential confounders. RESULTS: Children with major congenital anomalies were more likely to have Bayley Mental Development Index scores of < or = 70, Psychomotor Development Index scores of < or = 70, neurodevelopmental impairment, moderate-to-severe cerebral palsy, length in the < or = 10th percentile, head circumference in the < or = 10th percentile, more rehospitalizations, and higher rates of early intervention use at 18 to 22 months' corrected age. CONCLUSIONS: At 18 to 22 months' corrected age, extremely low birth weight infants born with major anomalies have nearly twice the risk for neurodevelopmental impairment, increased risk of poor growth, and > 3 times greater risk of rehospitalization when compared with extremely low birth weight infants without major anomalies. This information may be valuable for counseling parents regarding the outcomes of these infants and for the facilitation of appropriate support and intervention services.


Subject(s)
Abnormalities, Multiple , Developmental Disabilities/epidemiology , Developmental Disabilities/etiology , Growth Disorders/epidemiology , Growth Disorders/etiology , Infant, Extremely Low Birth Weight , Nervous System/growth & development , Abnormalities, Multiple/mortality , Cohort Studies , Female , Humans , Infant , Infant, Newborn , Male , Retrospective Studies , Risk Factors , Severity of Illness Index , Survival Rate
19.
Pediatrics ; 120(4): e953-9, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17908750

ABSTRACT

BACKGROUND: We previously reported beneficial effects of breast milk ingestion by infants with extremely low birth weight in the NICU on developmental outcomes at 18 months' corrected age. The objective of this study was to determine whether these effects of breast milk in infants with extremely low birth weight persisted at 30 months' corrected age. METHODS: Nutrition data, including enteral and parenteral feeds, were prospectively collected, and 30 months' corrected age follow-up assessments were completed on 773 infants with extremely low birth weight who participated in the National Institute of Child Health and Human Development Neonatal Research Network Glutamine Trial. A total of 593 ingested some breast milk during the neonatal hospitalization, and 180 ingested none. Neonatal feeding characteristics and morbidities and 30-month interim history, neurodevelopmental outcomes, and growth parameters were analyzed. Children were divided into quintiles of breast milk volume to evaluate the effects of volume of human milk ingested during the NICU hospitalization. RESULTS: At 30 months, increased ingestion of breast milk was associated with higher Bayley Mental Developmental Index scores, higher Bayley behavior score percentiles for emotional regulation, and fewer rehospitalizations between discharge and 30 months. There were no differences in growth parameters or cerebral palsy. For every 10 mL/kg per day increase in breast milk, the Mental Developmental Index increased by 0.59 points, the Psychomotor Developmental Index by 0.56 points, and the total behavior percentile score by 0.99 points, and the risk of rehospitalization between discharge and 30 months decreased by 5%. CONCLUSIONS: Beneficial effects of ingestion of breast milk in the NICU persist at 30 months' corrected age in this vulnerable extremely low birth weight population. Continued efforts must be made to offer breast milk to all extremely low birth weight infants both in the NICU and after discharge.


Subject(s)
Child Development , Infant, Extremely Low Birth Weight , Intensive Care Units, Neonatal , Milk, Human , Adult , Child, Preschool , Female , Follow-Up Studies , Humans , Infant, Newborn , Neuropsychological Tests , Patient Readmission/statistics & numerical data , Prospective Studies
20.
Pediatrics ; 120(1): 1-9, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17606555

ABSTRACT

OBJECTIVES: Our goal was to analyze the association between human milk intake and severe retinopathy of prematurity in extremely low birth weight infants. PATIENTS AND METHODS: This study is a secondary analysis of data collected for a trial of glutamine supplementation in extremely low birth weight infants (birth weight <1000 g). Among the 1433 participants in that trial, data are available regarding human milk intake and the occurrence of severe retinopathy of prematurity (defined in this study as retinopathy of prematurity treated surgically) for 1057 infants. The volume of human milk intake was expressed as the mean volume (milliliters per kilogram per day) and the mean proportional volume (proportion of total nutritional intake) from birth to discharge or transfer. Using logistic regression, we estimated odds ratios and 95% confidence intervals for any human milk intake and, among infants who received human milk, for each 10 mL/kg per day and each 10% increase in volume. RESULTS: Of the 1057 infants included in this cohort, 788 infants (75%) received at least some human milk. Among these milk-fed infants, the median volume of human milk intake was 30 mL/kg per day (interquartile range: 6-83 mL/kg per day), and the median proportional volume of human milk intake was 0.18 (interquartile range: 0.03-0.66). One hundred sixty-three infants (15%) developed severe retinopathy of prematurity. CONCLUSIONS: In extremely low birth weight infants, human milk intake was not associated with a decreased risk of severe retinopathy of prematurity.


Subject(s)
Infant, Extremely Low Birth Weight , Milk, Human , Retinopathy of Prematurity/prevention & control , Breast Feeding , Female , Glutamine/administration & dosage , Humans , Infant, Newborn , Male , Milk, Human/chemistry , Retinopathy of Prematurity/surgery
SELECTION OF CITATIONS
SEARCH DETAIL