Evidence map›Paper›PMID 35765569›Full record

ArticlePediatric quality & safety

Improving Hepatitis B Vaccination Rates among At-risk Children and Adolescents with Inflammatory Bowel Disease.

Megan Megan McNicol, Amy Donegan, Kate Hawa, Angelique E Boutzoukas, Barb Drobnic, Melanie Oates, Maudie Orraca-Tetteh, Hilary K Michel, Ross M Maltz, Jennifer L Dotson and 3 more

Erratum issuedAbstract read
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Article in Pediatric quality & safety. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–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

7 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Megan Megan McNicolDepartment of Pharmacy, Department of Pediatrics, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio.
Amy DoneganDivision of Gastroenterology, Hepatology, and Nutrition, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio.
Kate HawaGeneral Pediatrics Residency Program, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio.
Angelique E BoutzoukasGeneral Pediatrics Residency Program, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio.
Barb DrobnicDivision of Gastroenterology, Hepatology, and Nutrition, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio.
Melanie OatesDivision of Gastroenterology, Hepatology, and Nutrition, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio.
Maudie Orraca-TettehDivision of Gastroenterology, Hepatology, and Nutrition, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio.
Hilary K MichelDivision of Gastroenterology, Hepatology, and Nutrition, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio.
Ross M MaltzDivision of Gastroenterology, Hepatology, and Nutrition, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio.
Jennifer L DotsonDivision of Gastroenterology, Hepatology, and Nutrition, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio.
Don BuckinghamCenter for Clinical Excellence, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio.
Brendan BoyleDivision of Gastroenterology, Hepatology, and Nutrition, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio.
Monica I ArduraDivision of Infectious Diseases and Host Defense Program, Nationwide Children's Hospital and The Ohio State University, Columbus, Ohio.

Funding

Unified Program for Therapeutics in Children (UPTiC)T32HD094671 · NICHD · DUKE UNIVERSITY · PI Ian J Davis, Kanecia Obie Zimmerman · 2019 to 2026
$2.9M
NICHD NIH HHS T32 HD094671
6 · The paper itself

Abstract

Patients with inflammatory bowel disease (IBD) receiving tumor necrosis factor alpha inhibitors (TNFai) may be at higher risk for hepatitis B virus (HBV) infection. We conducted a quality improvement (QI) initiative to improve HBV vaccination rates in seronegative children with IBD. Methods: This QI initiative implemented an HBV vaccination strategy from September 2018 to March 2020 in patients with newly diagnosed IBD with hepatitis B surface antibody (HBsAb) <10 mIU/mL. The project aimed to (1) increase HBV vaccination rates in seronegative patients and (2) document immunogenicity after completing a three-dose vaccine series. Outcome measures included the percentage of seronegative patients who received HBV vaccines (dose 1 and three-dose series). Interventions included applying a standardized vaccination protocol, and creating a vaccine workflow in two clinical areas, previsit planning and stakeholder engagement. Results: One hundred seventy-four children and adolescents with IBD were evaluated during the study period, and 132 (76%) were HBsAb negative. After plan-do-study-act (PDSA) 1, the proportion of eligible patients who received HBV vaccine dose 1 increased from a baseline of 7% to 100% and was sustained for over 12 months. During PDSA 2, the proportion of patients completing the three-dose vaccine series improved from a baseline of 0% to 82% (n = 100); among 93 children in this subgroup who had repeat serology performed, 86 (92%) demonstrated serologic evidence of HBV protection. Conclusions: A multidisciplinary approach applying QI methodology allowed for improved and sustained HBV vaccination rates in at-risk seronegative children and adolescents with IBD. A three-dose HBV vaccine series proved immunogenic in 92% of eligible patients.

Identifiers

PMID35765569
PMCPMC9225488

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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.