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DTaP and Apnea/Bradycardia in Preterm Infants (PIA)

Primary Purpose

Prolonged Apnea, Prolonged Bradycardia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Infanrix
Pediatrix
Sponsored by
American SIDS Institute
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Prolonged Apnea focused on measuring Apnea, Bradycardia, Preterm Infant, Immunization, DTaP

Eligibility Criteria

56 Days - 60 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Born at a gestational age < 37 weeks.
  • Still in the hospital at time of study.
  • Between 56 - 60 days chronological age.

Exclusion Criteria:

  • Had active infections, were critically ill, or had unstable vital signs.
  • Requiring assisted ventilation or tracheostomy during the study.

Sites / Locations

  • Wellstar Cobb Hospital
  • Kennestone Hospital
  • St. Peters Univ. Hospital
  • Brooklyn Hospital
  • St. Joseph's Hospital Health Ctr.
  • Toledo Children's Hospital
  • Thomas Jefferson University
  • Western Pennsylvania Hospital
  • The Children's Home of Pittsburgh
  • Children's Hospital

Outcomes

Primary Outcome Measures

Bedside recording of apnea and bradycardia with events verified by 2 independent scorers who were blinded to the study phase and immunization status of the subject.

Secondary Outcome Measures

Full Information

First Posted
June 1, 2007
Last Updated
June 4, 2007
Sponsor
American SIDS Institute
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1. Study Identification

Unique Protocol Identification Number
NCT00482781
Brief Title
DTaP and Apnea/Bradycardia in Preterm Infants
Acronym
PIA
Official Title
Prolonged Apnea and Prolonged Bradycardia Following DTaP Immunization in Preterm Infants: A Randomized Multicenter Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2007
Overall Recruitment Status
Completed
Study Start Date
September 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
September 2004 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
American SIDS Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to examine the relationship between receipt of DTaP and the occurrence of prolonged episodes of apnea and bradycardia in preterm infants, while employing a random control study design and an objective assessment of cardiorespiratory events.
Detailed Description
The American Academy of Pediatrics (AAP) recommends the immunization of preterm infants at two months chronological age with the diphtheria-tetanus-acellular pertussis (DTaP) vaccine, regardless of birth weight and gestational age. However, several investigators, employing historical controls and subjective observations, have reported an increased incidence in prolonged apnea and bradycardia in preterm infants following immunization. Consequently, many primary care providers do not adhere to recommended AAP guidelines. The purpose of this study is to reexamine the relationship between receipt of DTaP and the occurrence of prolonged episodes of apnea and bradycardia in preterm infants, while employing a random control study design and an objective assessment of cardiorespiratory events. Ten participating hospitals will enroll infants < 37 completed weeks gestational age into the study when they are 56-60 days chronological age. Infants are randomly assigned into one of two groups: One group receives DTaP immunization and the control group does not (until study is completed). Physiological event recording monitors are used continuously during the next 2 days to document the incidence of prolonged apnea (respiratory pause of ≥20 sec in duration or >15 sec in duration if associated with bradycardia for ≥5 sec) and prolonged bradycardia (heart rate <80 bpm that lasted ≥10 sec) in all infants. The presence and number of episodes during the 48-hour period will be compared between the 2 groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prolonged Apnea, Prolonged Bradycardia
Keywords
Apnea, Bradycardia, Preterm Infant, Immunization, DTaP

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Randomized
Enrollment
191 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Biological
Intervention Name(s)
Infanrix
Intervention Type
Biological
Intervention Name(s)
Pediatrix
Primary Outcome Measure Information:
Title
Bedside recording of apnea and bradycardia with events verified by 2 independent scorers who were blinded to the study phase and immunization status of the subject.
Time Frame
Six days (Three 48-hour periods).

10. Eligibility

Sex
All
Minimum Age & Unit of Time
56 Days
Maximum Age & Unit of Time
60 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Born at a gestational age < 37 weeks. Still in the hospital at time of study. Between 56 - 60 days chronological age. Exclusion Criteria: Had active infections, were critically ill, or had unstable vital signs. Requiring assisted ventilation or tracheostomy during the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tracy Carbone, MD
Organizational Affiliation
Valley Hospital, Ridgewood, NJ
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Betty McEntire, PhD
Organizational Affiliation
American SIDS Institute
Official's Role
Study Director
Facility Information:
Facility Name
Wellstar Cobb Hospital
City
Austell
State/Province
Georgia
ZIP/Postal Code
30106
Country
United States
Facility Name
Kennestone Hospital
City
Marietta
State/Province
Georgia
ZIP/Postal Code
30060
Country
United States
Facility Name
St. Peters Univ. Hospital
City
Belle Mead
State/Province
New Jersey
ZIP/Postal Code
08502
Country
United States
Facility Name
Brooklyn Hospital
City
Brooklyn
State/Province
New York
ZIP/Postal Code
11201
Country
United States
Facility Name
St. Joseph's Hospital Health Ctr.
City
Syracuse
State/Province
New York
ZIP/Postal Code
13203
Country
United States
Facility Name
Toledo Children's Hospital
City
Toledo
State/Province
Ohio
ZIP/Postal Code
43606
Country
United States
Facility Name
Thomas Jefferson University
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States
Facility Name
Western Pennsylvania Hospital
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15224
Country
United States
Facility Name
The Children's Home of Pittsburgh
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15232
Country
United States
Facility Name
Children's Hospital
City
Greenville
State/Province
South Carolina
ZIP/Postal Code
29605
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18450851
Citation
Carbone T, McEntire B, Kissin D, Kelly D, Steinschneider A, Violaris K, Karamchandani N. Absence of an increase in cardiorespiratory events after diphtheria-tetanus-acellular pertussis immunization in preterm infants: a randomized, multicenter study. Pediatrics. 2008 May;121(5):e1085-90. doi: 10.1542/peds.2007-2059.
Results Reference
derived

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DTaP and Apnea/Bradycardia in Preterm Infants

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