Evidence map›Paper›PMID 30945037›Full record

Observational studyDigestive diseases and sciences2019

Improved Antibody Response to Three Additional Hepatitis B Vaccine Doses Following Primary Vaccination Failure in Patients with Inflammatory Bowel Disease.

Perry K Pratt, David Nunes, Michelle T Long, Francis A Farraye

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in Digestive diseases and sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Observational
  4. Article
  5. Review
  6. [Viral Hepatitis in Patients with Inflammatory Bowel Disease].The Korean journal of gastroenterology = Taehan Sohwagi Hakhoe chi · 2022
    Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. A comprehensive review of vaccination in patients with inflammatory bowel diseases:  An Indian perspective.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2020
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 3 institutions in 1 country.

Perry K PrattDivision of Gastroenterology and Hepatology, University of Connecticut Health, Farmington, CT, USA.
David NunesSection of Gastroenterology, Boston University Medical Center, 85 East Concord Street, Boston, MA, 02118, USA.
Michelle T LongSection of Gastroenterology, Boston University Medical Center, 85 East Concord Street, Boston, MA, 02118, USA.
Francis A FarrayeSection of Gastroenterology, Boston University Medical Center, 85 East Concord Street, Boston, MA, 02118, USA. francis.farraye@bmc.org.
Boston Medical Center · USBoston University · USUConn Health · US

Funding

Identifying clinical and genetic correlates of hepatic fibrosis from fatty liver disease in the communityK23DK113252 · NIDDK · BOSTON MEDICAL CENTER · PI LONG, MICHELLE T · 2018 to 2022
$944k
NIDDK NIH HHS K23 DK113252NIDDK NIH HHS L30 DK106778
6 · The paper itself

Abstract

backgroundStudies have shown the efficacy of hepatitis B (HBV) vaccination in patients with inflammatory bowel disease (IBD) is impaired, but few data exist regarding the effectiveness of revaccination strategies following primary vaccination failure. Our aim was to analyze the association between administration of additional vaccine doses and hepatitis B surface antibody (HBsAb) seroconversion.

methodsThis is a retrospective cohort study. Inclusion criteria are as follows: age ≥ 18, diagnosis of Crohn's disease (CD) or ulcerative colitis (UC), inadequate HBsAb < 10 IU/L following initial HBV vaccination series, subsequent administration of 1-3 additional doses of HBV vaccine with follow-up serum HBsAb measurements. Patients were stratified into groups of ≤ 2 or 3 doses received. Primary outcome was achieving HBsAb > 10 IU/L. Outcomes were stratified by age ≥ or < 40 years. We performed logistic and linear multivariable regression analyses for categorical and continuous data.

resultsThe study cohort consists of (n = 149) 54.4% women; 77.9% white; 72.6% with CD, with mean age: 46.2. Patients of all ages and age ≥ 40 years, who received 3 additional doses of vaccine, were more likely to achieve seroprotective HBsAb levels than patients who received 1 or 2 doses (OR 1.77, P = 0.01; OR 1.9, P = 0.03, respectively, after adjusting for age, sex, race, immunosuppressive medication exposure, time between vaccine/titer).

conclusionsFollowing initial HBV vaccination failure, patients with IBD of all ages are more likely to develop seroprotective levels of HBsAb following 3 additional vaccine doses, rather than 1 or 2 alone. In patients who fail primary HBV vaccination, providers should consider a more aggressive revaccination strategy with an additional 3-dose series.

Indexed as

ImmunizationImmunogenicity, VaccineAdrenal Cortex HormonesAdultBiomarkersColitis, UlcerativeCrohn DiseaseFemaleHepatitis B AntibodiesHepatitis B VaccinesHumansImmunocompromised HostImmunosuppressive AgentsMaleMiddle AgedRetrospective StudiesAdrenal Cortex HormonesBiomarkersHepatitis B AntibodiesHepatitis B VaccinesImmunosuppressive AgentsTumor Necrosis Factor InhibitorsBoosterCrohn’s diseaseHepatitis B virus immunityHepatitis B virus vaccination failureInflammatory bowel diseaseRevaccinationUlcerative colitis

Identifiers

PMID30945037
PMCPMC6764090
OpenAlexW2933203182

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.