Evidence map›Paper›PMID 23776114›Full record

ArticlePediatrics2013

Effectiveness of monovalent and pentavalent rotavirus vaccine.

Margaret M Cortese, Lilly Cheng Immergluck, Melissa Held, Shabnam Jain, Trisha Chan, Alexandra P Grizas, Saadia Khizer, Carol Barrett, Osbourne Quaye, Slavica Mijatovic-Rustempasic and 6 more

Abstract readComparative Study
In one paragraph

Article in Pediatrics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 7 pooled it
–field-weighted citation impact
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

59 citing papers in PubMed, 7 syntheses or guidelines pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Margaret M CorteseDivision of Viral Diseases, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, GA, USA. mcortese@cdc.gov
Lilly Cheng Immergluck
Melissa Held
Shabnam Jain
Trisha Chan
Alexandra P Grizas
Saadia Khizer
Carol Barrett
Osbourne Quaye
Slavica Mijatovic-Rustempasic
Rashi Gautam
Michael D Bowen
Jessica Moore
Jacqueline E Tate
Umesh D Parashar
Marietta Vázquez

Funding

Research Desogn and Biostatistics CoreU54MD007588 · NIMHD · MOREHOUSE SCHOOL OF MEDICINE · PI MAYBERRY, ROBERT M · 2012 to 2018
$24.8M
DVD&DBD Rotavirus/PCV (ACA) EIPU01CI000307 · CI · CONNECTICUT STATE DEPT OF PUBLIC HEALTH · PI CARTTER, MATTHEW LEWIS · 2005 to 2011
$19.3M
Renewal Application for Clinical Research Education and Career Development (CRECDR25MD007589 · NIMHD · MOREHOUSE SCHOOL OF MEDICINE · PI PRISCILLA E PEMU, Alexander Quarshie · 2012 to 2026
$5.4M
NCPDCID CDC HHS U01CI0000307-05NCPDCID CDC HHS U01 CI000307NIMHD NIH HHS 8R25MD007589-10NIMHD NIH HHS R25 MD007589NIMHD NIH HHS U54 MD007588PHS HHS U0I000312
6 · The paper itself

Abstract

objectivePrevious US evaluations have not assessed monovalent rotavirus vaccine (RV1, a G1P[8] human rotavirus strain) effectiveness, because of its later introduction (2008). Using case-control methodology, we measured the vaccine effectiveness (VE) of the 2-dose RV1 and 3-dose pentavalent vaccine (RV5) series against rotavirus disease resulting in hospital emergency department or inpatient care.

methodsChildren were eligible for enrollment if they presented to 1 of 5 hospitals (3 in Georgia, 2 in Connecticut) with diarrhea of ≤10 days' duration during January through June 2010 or 2011, and were born after RV1 introduction. Stools were collected; immunization records were obtained from providers and state electronic immunization information system (IIS). Case-subjects (children testing rotavirus antigen-positive) were compared with 2 control groups: children testing rotavirus negative and children selected from IIS.

resultsOverall, 165 rotavirus-case subjects and 428 rotavirus-negative controls were enrolled. Using the rotavirus-negative controls, RV1 VE was 91% (95% confidence interval [CI] 80 to 95) and RV5 VE was 92% (CI 75 to 97) among children aged ≥8 months. The RV1 VE against G2P[4] disease was high (94%, CI 78 to 98), as was that against G1P[8] disease (89%, CI 70 to 96). RV1 effectiveness was sustained among children aged 12 through 23 months (VE 91%; CI 75 to 96). VE point estimates using IIS controls were similar to those using rotavirus-negative controls.

conclusionsRV1 and RV5 were both highly effective against severe rotavirus disease. RV1 conferred sustained protection during the first 2 years of life and demonstrated high effectiveness against G2P[4] (heterotypic) disease.

Indexed as

Case-Control StudiesConfidence IntervalsDiarrhea, InfantileEmergency Service, HospitalFemaleGeorgiaHospitals, PediatricHumansImmunization, SecondaryInfantMalePatient AdmissionRotavirus InfectionsRotavirus VaccinesTreatment OutcomeUtilization ReviewRIX4414 vaccineRotaTeqRotavirus VaccinesVaccines, Attenuateddiarrheagastroenteritisimmunizationrotavirusrotavirus vaccinevaccine effectiveness

Identifiers

PMID23776114
PMCPMC4074617

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.