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Surfactant Positive Airway Pressure and Pulse Oximetry Trial (SUPPORT)

Primary Purpose

Infant, Newborn, Diseases, Other Preterm Infants, Infant, Small for Gestational Age

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Surfactant
Continuous Positive Airway Pressure (CPAP)
Supplemental oxygen with target saturation of 85 to 89%
Supplemental oxygen with target saturation of 91 to 95%
Sponsored by
NICHD Neonatal Research Network
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infant, Newborn, Diseases focused on measuring NICHD Neonatal Research Network, Extremely Low Birth Weight (ELBW), Very Low Birth Weight (VLBW), Prematurity, Mechanical ventilation, Surfactant, Intubation, Neurodevelopmental impairment, Pulse oximetry, Oxygen saturation, Positive-Pressure Respiration

Eligibility Criteria

24 Weeks - 27 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Infants with a minimal gestational age of 24 weeks 0 days to 27 completed weeks (up to 27 6/7ths) by best obstetrical estimate Infants who will receive full resuscitation as necessary, i.e., no parental request or physician decision to forego resuscitation Infants whose parents/legal guardians have provided consent for enrollment, or Infants without known major congenital malformations Exclusion Criteria: Any infant transported to the center after delivery Infants whose parents/legal guardians refuse consent Infants born during a time when the research apparatus/study personnel are not available Infants < 24 weeks 0 days or > 28 weeks 0 days, completed weeks of gestation

Sites / Locations

  • University of Alabama at Birmingham
  • Stanford University
  • University of California at San Diego
  • Yale University
  • University of Miami
  • Emory University
  • Indiana University
  • University of Iowa
  • Tufts Medical Center
  • Wayne State University
  • University of New Mexico
  • University of Rochester
  • Wake Forest University
  • RTI International
  • Duke University
  • Cincinnati Children's Medical Center
  • Case Western Reserve University, Rainbow Babies and Children's Hospital
  • Brown University, Women & Infants Hospital of Rhode Island
  • University of Tennessee
  • University of Texas Southwestern Medical Center at Dallas
  • University of Texas Health Science Center at Houston
  • University of Utah

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Surfactant and Low Oxygen

Surfactant and High Oxygen

CPAP and Low Oxygen

CPAP and High Oxygen

Arm Description

Administration of surfactant by endotracheal tube and supplemental oxygen with target saturation of 85% to 89%

Administration of surfactant by endotracheal tube and supplemental oxygen with target saturationof 91% to 95%

Administration of continuous positive airway pressure (CPAP) and supplemental oxygen with target saturation of 85% to 89%

Administration of continuous positive airway pressure (CPAP)and supplemental oxygen with target saturation of 91% to 95%

Outcomes

Primary Outcome Measures

Survival Without Bronchopulmonary Dysplasia (BPD)
Survival Without Severe Retinopathy of Prematurity (ROP) (Threshold Disease or the Need for Surgery)

Secondary Outcome Measures

Death or Neurodevelopmental Impairment
Duration of Mechanical Ventilation
The length in days that an individual was on mechanical ventilation which includes high frequency and conventional ventilation.
Survival Without Ventilation
Surviving the first 7 days of life without any need for ventilation by day 7
Received Surfactant Treatment
Received any surfactant treatment.
Number of Participants With Air Leaks
Number of participants with air leaks including pnemothorax, pulmonary interstitial emphysema (PIE), and pneumopericardium.
Physiological Bronchopulmonary Dysplasia
Infants who received support via ventilator or CPAP at 36 weeks PMA. Alternatively, infants who received low levels of supplemental oxygen (<30%) at 36 weeks PMA may have been eligible for a physiologic challenge in which there was an attempt to wean the infant to room air. Specifically, infants were eligible for the challenge if at 36 weeks PMA if they were receiving effective oxygen <27% and had majority saturation >90%, or they were receiving effective oxygen 27-30% and had majority saturation >96%, or they were receiving room air by nasal cannula. The challenge took place between 36 and 37 weeks PMA. Those who were not challenged because their level of support increased (support with CPAP or ventilation or increased oxygen) were considered to have BPD, as were those who failed the challenge.
Death
Participants who died by their follow-up visit at 18-22 months.
Severe Intraventricular Hemorrhage (IVH)
There are four grades of intraventricular hemorrhage: Grade I - echodensity/hemorrhage is confied to the germinal matrix. Grade II - echodensity/hemorrhage in the lateral ventricle(s) without distention. Grade III - echodensity/hemorrhage in the lateral ventricle(s) with distention. Grade IV - echodense lesion in the parenchyma. Severe IVH is defined as having IVH grades of III or IV.
Periventricular Leukomalacia (PVL)
Increased echogenicity or cysts in periventricular region.
Threshold Retinopathy of Prematurity (ROP) Requiring Surgery
Diagnosis of retinopathy of prematurity which resulted in requiring surgery.
Endotracheal Intubation
Insertion of a tube into the trachea to allow positive pressure ventilation for breathing.
Duration of Oxygen Supplementation
The length of time in days that a participant had oxygen supplementation.
Pulse Oximetry Values > 90%
Percentage of time spent above 90% oxygen saturation.
Blindness in at Least One Eye
Blindness in at least one eye by 18-22 months of life.
Received Postnatal Steroids
Participant received any doses or courses of systemic steroids to prevent or treat bronchopulmonary dysplasia/chronic lung disease.
Necrotizing Enterocolitis (NEC)
Proven necrotizing enterocolitis (NEC) diagnosis using the Modified Bell's Staging Criteria for NEC.
Cerebral Palsy
Incidence of cerebral palsy.

Full Information

First Posted
October 3, 2005
Last Updated
April 16, 2019
Sponsor
NICHD Neonatal Research Network
Collaborators
National Heart, Lung, and Blood Institute (NHLBI), National Center for Research Resources (NCRR), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
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1. Study Identification

Unique Protocol Identification Number
NCT00233324
Brief Title
Surfactant Positive Airway Pressure and Pulse Oximetry Trial
Acronym
SUPPORT
Official Title
Surfactant Positive Airway Pressure and Pulse Oximetry Trial (SUPPORT) in Extremely Low Birth Weight Infants
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
February 2005 (undefined)
Primary Completion Date
February 2009 (Actual)
Study Completion Date
August 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NICHD Neonatal Research Network
Collaborators
National Heart, Lung, and Blood Institute (NHLBI), National Center for Research Resources (NCRR), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study compared the use of continuous positive airway pressure initiated at birth with the early administration of surfactant administered through a tube in the windpipe within 1 hour of birth for premature infants born at 24 to 27 weeks gestation. In addition, these infants within 2 hours of birth, had a special pulse oximeter placed to continuously monitor their oxygen saturation in two different target ranges (85-89% or 91-95%). This study helped determine whether or not these two management strategies affect chronic lung disease and survival of premature infants.
Detailed Description
Study subjects were infants of 24 0/7ths to 27 6/7th weeks at birth for which a decision has been made to provide full resuscitation as required. Infants 27 weeks or less gestation (completed weeks by best obstetric estimate) were enrolled because more than 80% of such infants in the Network are intubated, usually early in their neonatal course. The feasibility trial demonstrated that the five NICHD centers involved could reduce intubation in the delivery room to less than 50% of such infants if they are not intubated for surfactant. We excluded infants of 23 weeks or less in view of their extremely high mortality and morbidity, and their almost universal need for delivery room intubation for resuscitation. Secondary studies included: neuroimaging/MRI, growth, and breathing outcomes. Strata: There were two randomization strata, infants of 24 0/7ths to 25 6/7ths weeks, and infants of 26 0/7ths-27 6/7ths weeks by best obstetrical estimate. Randomization: Randomization was stratified by gestational age group, occurred prior to delivery for consented deliveries, and was performed by utilizing specially prepared double-sealed envelopes. Deliveries were randomized as a unit, thus multiples, twins, triplets, etc. were randomized to the same arm of the trial. Informed Consent: Parents were approached prior to delivery for informed consent, and their infants enrolled at delivery. Study Intervention: Mode of Ventilatory Support The intervention began after birth when the infant was given to the resuscitation team. The conduct of the resuscitation followed usual guidelines, and once stabilized, all Control infants in both strata received prophylactic/early surfactant (within one hour of age), whereas all Treatment infants were placed on CPAP/PEEP following stabilization, and were intubated only for resuscitation indications. Pulse Oximeter Allocation: Infants were randomized to receive either a high- or low-saturation of peripheral oxygen (SpO2) as monitored by a study oximeter immediately following NICU admission, with a maximum allowable delay of two hours following admission. The SUPPORT Trial recruitment was temporarily paused on November 23, 2005 based on concern regarding pulse oximeter readings > 95% and due to concern regarding separation of the two arms of the oximetry portion of the study. Further analyses were performed which showed that infants on room air accounted for a significant portion of pulse oximetry saturations above 95%. Separation of the two groups was reanalyzed based on time spent in room air and the duration of time spent at individual SpO2 values, which both showed group differences. The trial was restarted on February 6, 2006. Follow-up: Subjects will be seen for a follow-up visit at 18-22 months corrected age to look at neurodevelopment. Extended follow-up: Subjects enrolled in the Neuroimaging/MRI secondary study will also be seen for a follow-up visit at 6-7 years to look at later school-age development. Subjects attending the 6-7 year follow-up visit will be invited to participate in this secondary study which will analyze the relationship of salivary cortisol and dehydroepiandrosterone (DHEA) to: (a) blood pressure and adiposity; (b) prenatal and postnatal growth; and (c) DNA methylation patterns.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infant, Newborn, Diseases, Other Preterm Infants, Infant, Small for Gestational Age, Premature Birth, Bronchopulmonary Dysplasia, Retinopathy of Prematurity
Keywords
NICHD Neonatal Research Network, Extremely Low Birth Weight (ELBW), Very Low Birth Weight (VLBW), Prematurity, Mechanical ventilation, Surfactant, Intubation, Neurodevelopmental impairment, Pulse oximetry, Oxygen saturation, Positive-Pressure Respiration

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1316 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Surfactant and Low Oxygen
Arm Type
Experimental
Arm Description
Administration of surfactant by endotracheal tube and supplemental oxygen with target saturation of 85% to 89%
Arm Title
Surfactant and High Oxygen
Arm Type
Experimental
Arm Description
Administration of surfactant by endotracheal tube and supplemental oxygen with target saturationof 91% to 95%
Arm Title
CPAP and Low Oxygen
Arm Type
Experimental
Arm Description
Administration of continuous positive airway pressure (CPAP) and supplemental oxygen with target saturation of 85% to 89%
Arm Title
CPAP and High Oxygen
Arm Type
Experimental
Arm Description
Administration of continuous positive airway pressure (CPAP)and supplemental oxygen with target saturation of 91% to 95%
Intervention Type
Drug
Intervention Name(s)
Surfactant
Intervention Description
Intubation and administration of surfactant by 1 hour of age.
Intervention Type
Device
Intervention Name(s)
Continuous Positive Airway Pressure (CPAP)
Other Intervention Name(s)
CPAP
Intervention Description
Continuous Positive Airway Pressure/Positive End Expiratory Pressure (CPAP/PEEP) begun in the delivery room and continuing in the NICU
Intervention Type
Drug
Intervention Name(s)
Supplemental oxygen with target saturation of 85 to 89%
Other Intervention Name(s)
Low oxygen
Intervention Description
Supplemental oxygen in the range of 85% to 89% until the infant is no longer requiring ventilatory support or oxygen
Intervention Type
Drug
Intervention Name(s)
Supplemental oxygen with target saturation of 91 to 95%
Other Intervention Name(s)
High oxygen
Intervention Description
Supplemental oxygen in the range of 91% to 95% until the infant is no longer requiring ventilatory support or oxygen.
Primary Outcome Measure Information:
Title
Survival Without Bronchopulmonary Dysplasia (BPD)
Time Frame
36 weeks
Title
Survival Without Severe Retinopathy of Prematurity (ROP) (Threshold Disease or the Need for Surgery)
Time Frame
55 weeks
Secondary Outcome Measure Information:
Title
Death or Neurodevelopmental Impairment
Time Frame
18-22 months
Title
Duration of Mechanical Ventilation
Description
The length in days that an individual was on mechanical ventilation which includes high frequency and conventional ventilation.
Time Frame
Entire NICU stay, up to 120 days
Title
Survival Without Ventilation
Description
Surviving the first 7 days of life without any need for ventilation by day 7
Time Frame
From birth through first 7 days of life.
Title
Received Surfactant Treatment
Description
Received any surfactant treatment.
Time Frame
From birth through 120 days of life.
Title
Number of Participants With Air Leaks
Description
Number of participants with air leaks including pnemothorax, pulmonary interstitial emphysema (PIE), and pneumopericardium.
Time Frame
From birth through first 14 days of life.
Title
Physiological Bronchopulmonary Dysplasia
Description
Infants who received support via ventilator or CPAP at 36 weeks PMA. Alternatively, infants who received low levels of supplemental oxygen (<30%) at 36 weeks PMA may have been eligible for a physiologic challenge in which there was an attempt to wean the infant to room air. Specifically, infants were eligible for the challenge if at 36 weeks PMA if they were receiving effective oxygen <27% and had majority saturation >90%, or they were receiving effective oxygen 27-30% and had majority saturation >96%, or they were receiving room air by nasal cannula. The challenge took place between 36 and 37 weeks PMA. Those who were not challenged because their level of support increased (support with CPAP or ventilation or increased oxygen) were considered to have BPD, as were those who failed the challenge.
Time Frame
36 weeks post menstrual age.
Title
Death
Description
Participants who died by their follow-up visit at 18-22 months.
Time Frame
18-22 months
Title
Severe Intraventricular Hemorrhage (IVH)
Description
There are four grades of intraventricular hemorrhage: Grade I - echodensity/hemorrhage is confied to the germinal matrix. Grade II - echodensity/hemorrhage in the lateral ventricle(s) without distention. Grade III - echodensity/hemorrhage in the lateral ventricle(s) with distention. Grade IV - echodense lesion in the parenchyma. Severe IVH is defined as having IVH grades of III or IV.
Time Frame
From birth through first 120 days of life.
Title
Periventricular Leukomalacia (PVL)
Description
Increased echogenicity or cysts in periventricular region.
Time Frame
From birth through first 120 days of life.
Title
Threshold Retinopathy of Prematurity (ROP) Requiring Surgery
Description
Diagnosis of retinopathy of prematurity which resulted in requiring surgery.
Time Frame
From birth through first 120 days of life.
Title
Endotracheal Intubation
Description
Insertion of a tube into the trachea to allow positive pressure ventilation for breathing.
Time Frame
Delivery Room, post-delivery
Title
Duration of Oxygen Supplementation
Description
The length of time in days that a participant had oxygen supplementation.
Time Frame
From birth through first 120 days of life.
Title
Pulse Oximetry Values > 90%
Description
Percentage of time spent above 90% oxygen saturation.
Time Frame
From birth through first 120 days of life.
Title
Blindness in at Least One Eye
Description
Blindness in at least one eye by 18-22 months of life.
Time Frame
18-22 months
Title
Received Postnatal Steroids
Description
Participant received any doses or courses of systemic steroids to prevent or treat bronchopulmonary dysplasia/chronic lung disease.
Time Frame
From birth through first 120 days of life.
Title
Necrotizing Enterocolitis (NEC)
Description
Proven necrotizing enterocolitis (NEC) diagnosis using the Modified Bell's Staging Criteria for NEC.
Time Frame
From birth through first 120 days of life.
Title
Cerebral Palsy
Description
Incidence of cerebral palsy.
Time Frame
18-22 months
Other Pre-specified Outcome Measures:
Title
Apgar Scores at 5 Minutes
Description
Apgar stands for "Appearance, Pulse, Grimace, Activity, and Respiration" and scores range from 1 (worst) to 10 (best) indicating a baby's condition 5 minutes after birth.
Time Frame
5 minutes after birth.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
24 Weeks
Maximum Age & Unit of Time
27 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Infants with a minimal gestational age of 24 weeks 0 days to 27 completed weeks (up to 27 6/7ths) by best obstetrical estimate Infants who will receive full resuscitation as necessary, i.e., no parental request or physician decision to forego resuscitation Infants whose parents/legal guardians have provided consent for enrollment, or Infants without known major congenital malformations Exclusion Criteria: Any infant transported to the center after delivery Infants whose parents/legal guardians refuse consent Infants born during a time when the research apparatus/study personnel are not available Infants < 24 weeks 0 days or > 28 weeks 0 days, completed weeks of gestation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Abbot R. Laptook, MD
Organizational Affiliation
Brown University, Women & Infants Hospital of Rhode Island
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Michele C. Walsh, MD MS
Organizational Affiliation
Case Western Reserve University, Rainbow Babies and Children's Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ronald N. Goldberg, MD
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Barbara J. Stoll, MD
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Brenda B. Poindexter, MD MS
Organizational Affiliation
Indiana University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Abhik Das, PhD
Organizational Affiliation
RTI International
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Krisa P. Van Meurs, MD
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ivan D. Frantz III, MD
Organizational Affiliation
Tufts Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Neil N. Finer, MD
Organizational Affiliation
University of California, San Diego
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kurt Schibler, MD
Organizational Affiliation
Children's Hospital Medical Center, Cincinnati
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Waldemar A. Carlo, MD
Organizational Affiliation
University of Alabama at Birmingham
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Edward F. Bell, MD
Organizational Affiliation
University of Iowa
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kristi L. Watterberg, MD
Organizational Affiliation
University of New Mexico
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Pablo J. Sanchez, MD
Organizational Affiliation
University of Texas, Southwestern Medical Center at Dallas
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kathleen A. Kennedy, MD MPH
Organizational Affiliation
The University of Texas Health Science Center, Houston
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Roger G. Faix, MD
Organizational Affiliation
University of Utah
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Seetha Shankaran, MD
Organizational Affiliation
Wayne State University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Richard A. Ehrenkranz, MD
Organizational Affiliation
Yale University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alabama at Birmingham
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233
Country
United States
Facility Name
Stanford University
City
Palo Alto
State/Province
California
ZIP/Postal Code
94304
Country
United States
Facility Name
University of California at San Diego
City
San Diego
State/Province
California
ZIP/Postal Code
92103-8774
Country
United States
Facility Name
Yale University
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06504
Country
United States
Facility Name
University of Miami
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States
Facility Name
Emory University
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30303
Country
United States
Facility Name
Indiana University
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States
Facility Name
University of Iowa
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States
Facility Name
Tufts Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02111
Country
United States
Facility Name
Wayne State University
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States
Facility Name
University of New Mexico
City
Albuquerque
State/Province
New Mexico
ZIP/Postal Code
87131
Country
United States
Facility Name
University of Rochester
City
Rochester
State/Province
New York
ZIP/Postal Code
14642
Country
United States
Facility Name
Wake Forest University
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
27157
Country
United States
Facility Name
RTI International
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27705
Country
United States
Facility Name
Duke University
City
Durham
State/Province
North Carolina
ZIP/Postal Code
27710
Country
United States
Facility Name
Cincinnati Children's Medical Center
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45267
Country
United States
Facility Name
Case Western Reserve University, Rainbow Babies and Children's Hospital
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Facility Name
Brown University, Women & Infants Hospital of Rhode Island
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02905
Country
United States
Facility Name
University of Tennessee
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38163
Country
United States
Facility Name
University of Texas Southwestern Medical Center at Dallas
City
Dallas
State/Province
Texas
ZIP/Postal Code
75235
Country
United States
Facility Name
University of Texas Health Science Center at Houston
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States
Facility Name
University of Utah
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84108
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
2674614
Citation
Deuticke B. Monocarboxylate transport in red blood cells: kinetics and chemical modification. Methods Enzymol. 1989;173:300-29. doi: 10.1016/s0076-6879(89)73020-2. No abstract available.
Results Reference
background
PubMed Identifier
20472937
Citation
SUPPORT Study Group of the Eunice Kennedy Shriver NICHD Neonatal Research Network; Carlo WA, Finer NN, Walsh MC, Rich W, Gantz MG, Laptook AR, Yoder BA, Faix RG, Das A, Poole WK, Schibler K, Newman NS, Ambalavanan N, Frantz ID 3rd, Piazza AJ, Sanchez PJ, Morris BH, Laroia N, Phelps DL, Poindexter BB, Cotten CM, Van Meurs KP, Duara S, Narendran V, Sood BG, O'Shea TM, Bell EF, Ehrenkranz RA, Watterberg KL, Higgins RD. Target ranges of oxygen saturation in extremely preterm infants. N Engl J Med. 2010 May 27;362(21):1959-69. doi: 10.1056/NEJMoa0911781. Epub 2010 May 16.
Results Reference
result
PubMed Identifier
20472939
Citation
SUPPORT Study Group of the Eunice Kennedy Shriver NICHD Neonatal Research Network; Finer NN, Carlo WA, Walsh MC, Rich W, Gantz MG, Laptook AR, Yoder BA, Faix RG, Das A, Poole WK, Donovan EF, Newman NS, Ambalavanan N, Frantz ID 3rd, Buchter S, Sanchez PJ, Kennedy KA, Laroia N, Poindexter BB, Cotten CM, Van Meurs KP, Duara S, Narendran V, Sood BG, O'Shea TM, Bell EF, Bhandari V, Watterberg KL, Higgins RD. Early CPAP versus surfactant in extremely preterm infants. N Engl J Med. 2010 May 27;362(21):1970-9. doi: 10.1056/NEJMoa0911783. Epub 2010 May 16. Erratum In: N Engl J Med. 2010 Jun 10;362(23):2235.
Results Reference
result
PubMed Identifier
20587676
Citation
Rich WD, Auten KJ, Gantz MG, Hale EC, Hensman AM, Newman NS, Finer NN; National Institute of Child Health and Human Development Neonatal Research Network. Antenatal consent in the SUPPORT trial: challenges, costs, and representative enrollment. Pediatrics. 2010 Jul;126(1):e215-21. doi: 10.1542/peds.2009-3353. Epub 2010 Jun 29.
Results Reference
result
PubMed Identifier
22738947
Citation
Di Fiore JM, Walsh M, Wrage L, Rich W, Finer N, Carlo WA, Martin RJ; SUPPORT Study Group of Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network. Low oxygen saturation target range is associated with increased incidence of intermittent hypoxemia. J Pediatr. 2012 Dec;161(6):1047-52. doi: 10.1016/j.jpeds.2012.05.046. Epub 2012 Jun 26.
Results Reference
result
PubMed Identifier
22371462
Citation
Rich W, Finer NN, Gantz MG, Newman NS, Hensman AM, Hale EC, Auten KJ, Schibler K, Faix RG, Laptook AR, Yoder BA, Das A, Shankaran S; SUPPORT and Generic Database Subcommittees of the Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network. Enrollment of extremely low birth weight infants in a clinical research study may not be representative. Pediatrics. 2012 Mar;129(3):480-4. doi: 10.1542/peds.2011-2121. Epub 2012 Feb 27.
Results Reference
result
PubMed Identifier
25425651
Citation
Ambalavanan N, Carlo WA, Wrage LA, Das A, Laughon M, Cotten CM, Kennedy KA, Laptook AR, Shankaran S, Walsh MC, Higgins RD; SUPPORT Study Group of the NICHD Neonatal Research Network. PaCO2 in surfactant, positive pressure, and oxygenation randomised trial (SUPPORT). Arch Dis Child Fetal Neonatal Ed. 2015 Mar;100(2):F145-9. doi: 10.1136/archdischild-2014-306802. Epub 2014 Nov 25.
Results Reference
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PubMed Identifier
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Citation
Navarrete CT, Wrage LA, Carlo WA, Walsh MC, Rich W, Gantz MG, Das A, Schibler K, Newman NS, Piazza AJ, Poindexter BB, Shankaran S, Sanchez PJ, Morris BH, Frantz ID 3rd, Van Meurs KP, Cotten CM, Ehrenkranz RA, Bell EF, Watterberg KL, Higgins RD, Duara S; Eunice Kennedy Shriver National Institute of Child Health and Human Development Neonatal Research Network. Growth Outcomes of Preterm Infants Exposed to Different Oxygen Saturation Target Ranges from Birth. J Pediatr. 2016 Sep;176:62-68.e4. doi: 10.1016/j.jpeds.2016.05.070. Epub 2016 Jun 22.
Results Reference
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Links:
URL
http://neonatal.rti.org/
Description
NICHD Neonatal Research Network site
URL
https://www.nichd.nih.gov/about/org/der/branches/ppb/Pages/projects.aspx
Description
NICHD Pregnancy & Perinatology Branch

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Surfactant Positive Airway Pressure and Pulse Oximetry Trial

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