DTaP and Apnea/Bradycardia in Preterm Infants (PIA)
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Purpose
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.
| Condition | Intervention |
|---|---|
|
Prolonged Apnea Prolonged Bradycardia |
Biological: Infanrix Biological: Pediatrix |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety Study Intervention Model: Parallel Assignment Masking: Single Blind Primary Purpose: Prevention |
| Official Title: | Prolonged Apnea and Prolonged Bradycardia Following DTaP Immunization in Preterm Infants: A Randomized Multicenter Study |
- 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). ]
| Enrollment: | 191 |
| Study Start Date: | September 2000 |
| Study Completion Date: | September 2004 |
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.
Eligibility| Ages Eligible for Study: | 56 Days to 60 Days |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
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.
Contacts and Locations| United States, Georgia | |
| Wellstar Cobb Hospital | |
| Austell, Georgia, United States, 30106 | |
| Kennestone Hospital | |
| Marietta, Georgia, United States, 30060 | |
| United States, New Jersey | |
| St. Peters Univ. Hospital | |
| Belle Mead, New Jersey, United States, 08502 | |
| United States, New York | |
| Brooklyn Hospital | |
| Brooklyn, New York, United States, 11201 | |
| St. Joseph's Hospital Health Ctr. | |
| Syracuse, New York, United States, 13203 | |
| United States, Ohio | |
| Toledo Children's Hospital | |
| Toledo, Ohio, United States, 43606 | |
| United States, Pennsylvania | |
| Thomas Jefferson University | |
| Philadelphia, Pennsylvania, United States, 19107 | |
| The Children's Home of Pittsburgh | |
| Pittsburgh, Pennsylvania, United States, 15232 | |
| Western Pennsylvania Hospital | |
| Pittsburgh, Pennsylvania, United States, 15224 | |
| United States, South Carolina | |
| Children’s Hospital | |
| Greenville, South Carolina, United States, 29605 | |
| Principal Investigator: | Tracy Carbone, MD | Valley Hospital, Ridgewood, NJ |
| Study Director: | Betty McEntire, PhD | American SIDS Institute |
More Information
No publications provided by American SIDS Institute
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| ClinicalTrials.gov Identifier: | NCT00482781 History of Changes |
| Other Study ID Numbers: | PIA-09012000 |
| Study First Received: | June 1, 2007 |
| Last Updated: | June 4, 2007 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by American SIDS Institute:
|
Apnea Bradycardia Preterm Infant Immunization DTaP |
Additional relevant MeSH terms:
|
Apnea Bradycardia Respiration Disorders Respiratory Tract Diseases Signs and Symptoms, Respiratory |
Signs and Symptoms Arrhythmias, Cardiac Heart Diseases Cardiovascular Diseases Pathologic Processes |
ClinicalTrials.gov processed this record on June 18, 2013