Evidence map›Paper›PMID 26030302›Full record

ArticleJAMA pediatrics2015

Adverse Events After Routine Immunization of Extremely Low-Birth-Weight Infants.

Stephen D DeMeo, Sudha R Raman, Christoph P Hornik, Catherine C Wilson, Reese Clark, P Brian Smith

Abstract readMulticenter Study
In one paragraph

Article in JAMA pediatrics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Underimmunization of very low birth weight infants at discharge from the neonatal intensive care unit.Journal of perinatology : official journal of the California Perinatal Association · 2024
    Article
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  8. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Stephen D DeMeoDepartment of Pediatrics, Duke University School of Medicine, Durham, North Carolina.
Sudha R RamanDuke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.
Christoph P HornikDepartment of Pediatrics, Duke University School of Medicine, Durham, North Carolina2Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.
Catherine C WilsonGreenville Hospital System, Greenville, South Carolina.
Reese ClarkPediatrix-Obstetrix Center for Research and Education, Sunrise, Florida.
P Brian SmithDepartment of Pediatrics, Duke University School of Medicine, Durham, North Carolina2Duke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina.
Duke University · USPrisma Health · US

Funding

Duke CTSA (Composite)UL1TR001117 · NCATS · DUKE UNIVERSITY · PI BOULWARE, LEIGH E, LI, JENNIFER S · 2013 to 2017
$41.3M
Duke CTSA (Composite)KL2TR001115 · NCATS · DUKE UNIVERSITY · PI BOULWARE, LEIGH E, KRAFT, MONICA · 2013 to 2017
$5.1M
ASPE HHS 1R18AE000028-01NCATS NIH HHS KL2 TR001115NCATS NIH HHS UL1 TR001117NCATS NIH HHS UL1TR001117NICHD NIH HHS HHSN267200700051CNICHD NIH HHS HHSN275201000003CNICHD NIH HHS HHSN275201000003INICHD NIH HHS L40 HD069892NIDDK NIH HHS HHSN267200700051C
6 · The paper itself

Abstract

importanceImmunization of extremely low-birth-weight (ELBW) infants in the neonatal intensive care unit (NICU) is associated with adverse events, including fever and apnea or bradycardia, in the immediate postimmunization period. These adverse events present a diagnostic dilemma for physicians, leading to the potential for immunization delay and sepsis evaluations.

objectiveTo compare the incidence of sepsis evaluations, need for increased respiratory support, intubation, seizures, and death among immunized ELBW infants in the 3 days before and after immunization. DESIGN, SETTING, AND

participantsIn this multicenter retrospective cohort study, we studied 13,926 ELBW infants born at 28 weeks' gestation or less who were discharged from January 1, 2007, through December 31, 2012, from 348 NICUs managed by the Pediatrix Medical Group. EXPOSURES: At least one immunization between the ages of 53 and 110 days. MAIN OUTCOMES AND MEASURES: Incidence of sepsis evaluations, need for increased respiratory support, intubation, seizures, and death.

resultsMost of the 13,926 infants (91.2%) received 3 or more immunizations. The incidence of sepsis evaluations increased from 5.4 per 1000 patient-days in the preimmunization period to 19.3 per 1000 patient-days in the postimmunization period (adjusted rate ratio [ARR], 3.7; 95% CI, 3.2-4.4). The need for increased respiratory support increased from 6.6 per 1000 patient-days in the preimmunization period to 14.0 per 1000 patient-days in the postimmunization period (ARR, 2.1; 95% CI, 1.9-2.5), and intubation increased from 2.0 per 1000 patient-days to 3.6 per 1000 patient-days (ARR, 1.7; 95% CI, 1.3-2.2). The postimmunization incidence of adverse events was similar across immunization types, including combination vaccines when compared with single-dose vaccines. Infants who were born at 23 to 24 weeks' gestation had a higher risk of sepsis evaluation and intubation after immunization. A prior history of sepsis was associated with higher risk of sepsis evaluation after immunization. CONCLUSIONS AND RELEVANCE: All ELBW infants in the NICU had an increased incidence of sepsis evaluations and increased respiratory support and intubation after routine immunization. Our findings provide no evidence to suggest that physicians should not use combination vaccines in ELBW infants. Further studies are needed to determine whether timing or spacing of immunization administrations confers risk for the developing adverse events and whether a prior history of sepsis confers risk for an altered immune response in ELBW infants.

Indexed as

Infant, Extremely Low Birth WeightIntubation, IntratrachealRespiration, ArtificialCohort StudiesFemaleHumansImmunizationInfant, NewbornMaleRetrospective StudiesSepsis

Identifiers

PMID26030302
PMCPMC4523398
OpenAlexW1816749787

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.