Developmental Impact of NICU Exposures (DINE)

Brief Summary
The DINE study will test the hypothesis that potentially avoidable NICU-based exposures contribute to the neuro-cognitive and somatic impairments prevalent among NICU graduates. This hypothesis is drawn from the documented impact of phthalate exposure on early development in term-born children, and the acknowledged presence of these toxic chemicals in the NICU. Third trimester in utero exposure to phthalates have been linked to poorer childhood performance in cognition, motor function, attention, hyperactivity and social behavior. Phthalate exposure is also associated with altered onset of puberty and asthma. The multi-site cohort and approach will clarify the role of NICU-based phthalate exposure on high-prevalence clinical outcomes.
Brief Title
Developmental Impact of NICU Exposures (DINE)
Detailed Description
Background: Each year in the United States, over 300,000 preterm infants are admitted to neonatal intensive care units (NICUs) where they are exposed to a chemical-intensive hospital environment during a developmentally vulnerable period. Many life-saving and supportive respiratory, nutritional, hematologic and pharmaceutical therapies in the NICU expose preterm infants to potentially harmful chemicals during a life stage analogous to the third trimester of gestation. The NIH-funded DINE study capitalizes on the infrastructure, biorepositories, and extensive clinical databases of four existing preterm cohorts to explore the hypothesis that early life exposure to phthalates adversely impacts neurodevelopment, lung function, growth, adiposity, and pubertal development in childhood.

The scientific premise of the DINE study is that early life exposure to phthalates, a class of chemical plasticizers ubiquitous in the NICU, has long-lasting harmful effects on child health and development, and that these harmful effects are magnified in children born preterm. This premise is based on strong evidence of multisystem adverse health effects in term-born children who are exposed to phthalates in utero during the third trimester of pregnancy or in early infancy. In preterm infants, however, rigorously obtained data on the health effects of phthalates are scant. Dermal, inhalational and intravenous exposures to phthalates are widespread in some NICUs, where preterm infants are cared for during the sensitive "third trimester" developmental window. Moreover, premature infants experience a high prevalence of the adverse health effects that are associated with early life exposures to phthalates in term-born children, including altered neurodevelopment, poor pulmonary function, and maladapted growth. A rigorous, well-designed, sufficiently powered study of NICU-based phthalate exposures and long-term health outcomes of preterm infants has the potential to change care practices, promote regulatory policy changes and lead to mitigation of phthalate exposures in the NICU.

Significance: The proposed research is expected to identify modifiable sources of developmental risk for NICU patients that can inform and improve hospital care and long-term outcome. Moreover, our findings could lead to relatively inexpensive NICU interventions, such as use of non-phthalate containing medical materials, dosing guidelines for elemental metals and guidance for parents and staff on infant stress-reduction, and policy changes (e.g. regulation of the phthalates used in medical devices or changes to the trace metal content of parenteral nutrition) with significant positive potential impacts on life-long morbidities common among NICU graduates. Information gleaned from studying our highly-exposed, highly-vulnerable population may elucidate health impacts of early life exposures that translate to risk reduction in the general population.
Completion Date
Completion Date Type
Actual
Conditions
Prematurity
Eligibility Criteria
Inclusion Criteria:

* Children who were study participants in one of the four extant preterm cohorts (PROP, TOLSURF, NICU-HEALTH, and PENUT) that comprise the combined DINE cohort and who were followed to study endpoint at one of the clinical sites in DINE.
* Newly recruited preterm infants admitted to the NICU at the Icahn School of Medicine at Mount Sinai
* Newly recruited preterm and term infants who participated in the PRISM study at University of Rochester
* Parents agreed to be re-contacted or local Institutional Review Board (IRB) grants permission to recontact families to obtain consent to participate in DINE.

Exclusion Criteria:

* Family requested that they not be contacted after their child completed the parent study
* Family is unlikely to be available for long-term follow-up
Inclusion Criteria
Inclusion Criteria:

* Children who were study participants in one of the four extant preterm cohorts (PROP, TOLSURF, NICU-HEALTH, and PENUT) that comprise the combined DINE cohort and who were followed to study endpoint at one of the clinical sites in DINE.
* Newly recruited preterm infants admitted to the NICU at the Icahn School of Medicine at Mount Sinai
* Newly recruited preterm and term infants who participated in the PRISM study at University of Rochester
* Parents agreed to be re-contacted or local Institutional Review Board (IRB) grants permission to recontact families to obtain consent to participate in DINE.

Gender
All
Gender Based
false
Keywords
children's environmental health
prematurity
preterm birth
phthalates
NICU
stress
lung health
neurodevelopment
growth
Last Update Submit Date
Maximum Age
12 Years
NCT Id
NCT03061890
Org Class
Other
Org Full Name
Albert Einstein College of Medicine
Org Study Id
2016-7369
Overall Status
Completed
Primary Completion Date
Primary Completion Date Type
Actual
Official Title
Developmental Impact of Neonatal Intensive Care Unit (NICU) Exposures: Environmental Influences on Child Health Outcomes (ECHO)
Primary Outcomes
Outcome Description
Brief Respiratory Questionnaire to determine association between exposure and lung health
Outcome Measure
Association between NICU environmental exposures and lung health and asthma measured by Brief Respiratory Questionnaire
Outcome Time Frame
One time between the ages of 3 to 4
Outcome Description
PROMISĀ® (Patient-Reported Outcomes Measurement Information System) Parent Proxy Asthma Impact item bank to determine association between exposure and asthma
Outcome Measure
Associations between NICU environmental exposures and lung health and asthma measured by the PROMISĀ® (Patient-Reported Outcomes Measurement Information System) Parent Proxy Asthma Impact item bank
Outcome Time Frame
One time between the ages of 5 to 6
Outcome Description
PhenX (consensus measures for Phenotypes and eXposures) Toolkit measures of spirometry and bronchodilator responsiveness to determine association between exposure and asthma
Outcome Measure
Associations between NICU environmental exposures and lung health and asthma measured by PhenX (consensus measures for Phenotypes and eXposures) Toolkit measures of spirometry and bronchodilator responsiveness
Outcome Time Frame
Twice between the ages of 8 to 12
Outcome Description
PROMIS Pediatric Asthma Impact item bank to determine the association between exposures and asthma
Outcome Measure
Associations between NICU environmental exposures and lung health and asthma measured by the PROMIS Pediatric Asthma Impact item bank.
Outcome Time Frame
Twice between the ages of 8 to 12
Outcome Description
NIH Toolbox Early Childhood Cognition Battery to determine the associations between exposures and neurocognitive behavioral development
Outcome Measure
Associations between NICU environmental exposures and neurocognitive behavioral development measured by NIH Toolbox Early Childhood Cognition Battery
Outcome Time Frame
Twice within 24 months between the ages of 3 to 5
Outcome Description
NIH Toolbox Cognition Battery to determine the associations between exposures and neurocognitive behavioral development
Outcome Measure
Associations between NICU environmental exposures and neurocognitive behavioral development measured by NIH Toolbox Cognition Battery
Outcome Time Frame
Twice within 24 months between the ages of 7 to 9
Outcome Description
NIH Toolbox Early Childhood Motor Battery to determine the associations between exposures and neurocognitive behavioral development
Outcome Measure
Associations between NICU environmental exposures and neurocognitive behavioral development measured by NIH Toolbox Early Childhood Motor Battery
Outcome Time Frame
Twice within 24 months between the ages of 4 to 6
Outcome Description
NIH Toolbox Motor Battery to determine the associations between exposures and neurocognitive behavioral development
Outcome Measure
Associations between NICU environmental exposures and neurocognitive behavioral development measured by NIH Toolbox Motor Battery
Outcome Time Frame
Twice between the ages of 8 to 12
Outcome Description
Child Behavior Checklist (CBCL) to determine the associations between exposures and neurocognitive behavioral development
Outcome Measure
Associations between NICU environmental exposures and neurocognitive behavioral development measured by Child Behavior Checklist (CBCL)
Outcome Time Frame
One time between the ages of 3 to 4
Outcome Description
PROMIS Cognitive Item bank to determine the associations between exposures and neurocognitive behavioral development
Outcome Measure
Associations between NICU environmental exposures and neurocognitive behavioral development measured by PROMIS Cognitive Item bank
Outcome Time Frame
Three times between the ages of 5 to 12
Outcome Description
PROMIS Pediatric Mobility Item bank to determine the associations between exposures and neurocognitive behavioral development
Outcome Measure
Associations between NICU environmental exposures and neurocognitive behavioral development measured by PROMIS Pediatric Mobility Item bank
Outcome Time Frame
Three times between the ages of 5 to 12
Outcome Description
PROMIS Pediatric Upper Extremity Item to determine the associations between exposures and neurocognitive behavioral development
Outcome Measure
Associations between NICU environmental exposures and neurocognitive behavioral development measured by PROMIS Pediatric Upper Extremity Item bank
Outcome Time Frame
Three times between the ages of 5 to 12
Outcome Description
Measurement of height, weight, head circumference, mid-upper arm circumference and bioimpedence scale to determine associations between exposures and heathy growth and obesity
Outcome Measure
Associations between NICU environmental exposures and growth and obesity as measured by height, weight, head circumference, mid-upper arm circumference and bioimpedence
Outcome Time Frame
Annually, up to 12 years
Outcome Description
Parent reported height and weight to determine associations between exposures and healthy growth and obesity
Outcome Measure
Associations between NICU environmental exposures and growth and obesity as measured by parent report height and weight
Outcome Time Frame
Annually, up to 12 years
Outcome Description
PhenX Assessment of Pubertal Development to determine associations between exposures and pubertal development
Outcome Measure
Associations between NICU environmental exposures and pubertal development measured by PhenX Assessment of Pubertal Development
Outcome Time Frame
Annually, up to 12 years
Secondary Ids
Secondary Id
UG3OD023320
Secondary Id
UH3OD023320
Start Date
Start Date Type
Actual
Status Verified Date
First Submit Date
First Submit QC Date
Study Population
Former preterm infants who were participants hospitalized in the NICU of one of the 8 clinical sites participating in the UH3 phase of the ECHO and DINE studies and whose parents had consented to participate in one of the 4 extent cohorts of the following NIH-supported studies: Prematurity and Respiratory Outcomes Program (PROP), the Trial of Late Surfactant (TOLSURF), the NICU Hospital Exposures and Long-Term Health (NICU-HEALTH) study and the Preterm Erythropoietin Neuroprotection Trial (PENUT) study and agreed to longitudinal follow up of infants as part of DINE
Std Ages
Child
Maximum Age Number (converted to Years and rounded down)
12
Minimum Age Number (converted to Years and rounded down)
0
Investigators
Investigator Type
Principal Investigator
Investigator Name
Judy Aschner
Investigator Email
judy.aschner@einsteinmed.org
Investigator Phone
718-741-2499