Absence of an increase in cardiorespiratory events after diphtheria-tetanus-acellular pertussis immunization in

Tracy Carbone1, Betty McEntire, Dmitry Kissin

  • 1Center for Pediatric Sleep Disorders, Valley Hospital, 505 Goffle Rd, Ridgewood, NJ 07450, USA. tcarbon@valleyhealth.com

Pediatrics
|May 3, 2008
PubMed

Insights

Diphtheria-tetanus-acellular pertussis (DTaP) immunization at 2 months chronological age is safe for preterm infants. This study found no increased risk of cardiorespiratory events like apnea or bradycardia in vaccinated preterm infants compared to controls.

Area of Science:

  • Pediatrics
  • Immunology
  • Neonatology

Background:

  • The American Academy of Pediatrics recommends DTaP immunization for preterm infants at 2 months chronological age.
  • Concerns exist regarding potential cardiorespiratory events following immunization in preterm infants, leading to inconsistent adherence to guidelines.
  • This study aimed to objectively assess the relationship between DTaP vaccination and cardiorespiratory events in this population.

Purpose of the Study:

  • To reevaluate the association between diphtheria-tetanus-acellular pertussis (DTaP) vaccination and cardiorespiratory events in preterm infants.
  • To utilize a randomized controlled study design with objective cardiorespiratory monitoring.
  • To provide evidence-based data to support or refute current immunization recommendations for preterm infants.

Main Methods:

  • A randomized controlled trial was conducted across ten hospitals involving 191 preterm infants (<37 weeks gestational age) at 56-60 days chronological age.
  • Infants were randomly assigned to receive DTaP immunization (n=93) or serve as a control group (n=98).
  • Continuous monitoring for 48 hours post-vaccination/assignment documented prolonged apnea and bradycardia, with statistical comparisons (chi-squared and t-tests) between groups.

Main Results:

  • 16.1% of the DTaP group experienced prolonged apnea versus 20.4% in the control group.
  • Prolonged bradycardia occurred in 58.1% of the DTaP group and 56.1% of the control group.
  • No significant differences in the frequency or mean number of prolonged apnea (0.5 episodes in both groups) or bradycardia episodes (2.6 vs. 2.7) were observed between the immunized and control groups.

Conclusions:

  • Preterm infants receiving DTaP immunization at 2 months chronological age are not at increased risk for prolonged apnea or bradycardia.
  • The findings support the American Academy of Pediatrics' recommendation for timely DTaP immunization in preterm infants.
  • Objective assessment confirms the safety profile of DTaP vaccination in this vulnerable population.
Abstract

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