Evidence map›Paper›PMID 39466071›Full record

ArticleHuman vaccines & immunotherapeutics2024

Surveillance for adverse events following immunization in Hebei Province, China, 2018-2020.

Li Sun, Shifan Wang, Yafei Wang, Yihan Wang, Jinghui Wang, Jing Li, Xiaomeng Xu, Junmian Zhang, Yanli Cong, Yu Guo

Abstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Observational
  2. Article
  3. Article
  4. Observational
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

10 authors.

Li SunImmunization Planning and Management Institute, Hebei Provincial Center For Disease Control And Prevention, Shijiazhuang, Hebei, China.
Shifan WangImmunization Planning and Management Institute, Hebei Provincial Center For Disease Control And Prevention, Shijiazhuang, Hebei, China.ORCID 0009-0007-5223-7359
Yafei WangImmunization Planning and Management Institute, Hebei Provincial Center For Disease Control And Prevention, Shijiazhuang, Hebei, China.
Yihan WangImmunization Planning and Management Institute, Hebei Provincial Center For Disease Control And Prevention, Shijiazhuang, Hebei, China.
Jinghui WangImmunization Planning and Management Institute, Hebei Provincial Center For Disease Control And Prevention, Shijiazhuang, Hebei, China.
Jing LiImmunization Planning and Management Institute, Hebei Provincial Center For Disease Control And Prevention, Shijiazhuang, Hebei, China.
Xiaomeng XuImmunization Planning and Management Institute, Hebei Provincial Center For Disease Control And Prevention, Shijiazhuang, Hebei, China.
Junmian ZhangImmunization Planning and Management Institute, Hebei Provincial Center For Disease Control And Prevention, Shijiazhuang, Hebei, China.
Yanli CongImmunization Planning and Management Institute, Hebei Provincial Center For Disease Control And Prevention, Shijiazhuang, Hebei, China.
Yu GuoImmunization Planning and Management Institute, Hebei Provincial Center For Disease Control And Prevention, Shijiazhuang, Hebei, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to analyze the incidence and characteristics of adverse events following immunization (AEFI) with post-licensure vaccines used in Hebei province from 2018 to 2020 and to evaluate the safety of vaccines. All information of AEFI was gained from national adverse event following immunization surveillance system (NAEFISS) in Hebei Province from 2018 to 2020. Descriptive epidemiology method was used to analyze the data about AEFI in Hebei province. Reporting rates of AEFI were calculated by sex, age, city, categories of AEFI, severity of AEFI, reaction categories, etc. A total of 35,999 AEFI were reported through NAEFISS, and the average annual rate was 47.64/100,000 doses. The reporting rates of common adverse reactions and rare adverse reactions were 46.37/100,000 doses and 1.05/100,000 doses. The male-to-female ratio was 1.26:1. Most of the AEFI were concentrated in the ≤1 year age group and were reported in the second quarter and third quarter. The majority of AEFI were reported to be recovered or improved, and about 62% of the AEFI occurred within 24 hours after vaccination. Vaccines associated with the highest reporting rate of AEFI were diphtheria, tetanus and acellular pertussis combined vaccine (DTaP, 170.45/100,000 doses). The reporting rate of allergic rash was found to be the highest in the adverse reactions (0.29/100,000 doses). The majority of AEFI cases were common adverse reactions, while serious rare adverse reactions caused by vaccines were extremely uncommon, and all vaccines used in Hebei Province were safe.

Indexed as

Adverse Drug Reaction Reporting SystemsDrug-Related Side Effects and Adverse ReactionsImmunizationAdolescentAdultAgedChildChild, PreschoolChinaFemaleHumansIncidenceInfantInfant, NewbornMaleMiddle AgedVaccinesAdverse events following immunizationincidence of adverse events following immunizationsafetysurveillancevaccine

Identifiers

PMID39466071
PMCPMC11520551

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.