Evidence map›Paper›PMID 34688238›Full record

ArticleTurkish journal of medical sciences2022

SARS-COV-2 vaccine: first-month results of a six-month follow-up study.

Burak Mete, Ferdi Tanır, Hakan Demirhindi, Ertan Kara, Filiz Kibar, Salih Çetiner, Aslıhan Candevir, Rabia Dal

Open access · bronzeAbstract read
In one paragraph

Article in Turkish journal of medical sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 56% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

8 authors at 1 institution in 1 country.

Burak MeteDepartment of Public Health, Faculty of Medicine, Çukurova University, Adana, Turkey.
Ferdi TanırDepartment of Public Health, Faculty of Medicine, Çukurova University, Adana, Turkey.
Hakan DemirhindiDepartment of Public Health, Faculty of Medicine, Çukurova University, Adana, Turkey.
Ertan KaraDepartment of Public Health, Faculty of Medicine, Çukurova University, Adana, Turkey.
Filiz KibarDepartment of Medical Microbiology and Çukurova University Balcalı Hospital Central Laboratory, Faculty of Medicine, Çukurova University, Adana, Turkey.
Salih ÇetinerDepartment of Immunology and Çukurova University Balcalı Hospital Central Laboratory, Faculty of Medicine, ÇukurovaUniversity, Adana, Turkey.
Aslıhan CandevirDepartment of Infectious Diseases and Clinical Microbiology, Faculty of Medicine, Çukurova University, Adana, Turkey.
Rabia DalDepartment of Public Health, Faculty of Medicine, Çukurova University, Adana, Turkey.
Cukurova University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundVarious COVID-19 vaccines are being developed around the world. Important questions to be answered regarding vaccines are efficacy, safety, and whether antibodies are protective when used in different communities. This study aimed to determine seroconversion rates of the inactivated SARS-CoV-2 vaccine in healthcare workers in a hospital and short-term adverse events due to the vaccine.

methodsThe study carried out in Çukurova University, Turkey, comprised of 282 healthcare workers who received two doses of the inactivated SARS-CoV-2 vaccine administered in two 3 µg doses, 28 days apart. On day 28, after the second dose, antiS-RBD IgG and total anti-spike and anti-nucleocapsid IgM and IgG antibodies against SARS-CoV-2 were detected by using in vitro chemiluminescence immunoassay method.

resultsThe mean age of participants was 39.06±10.65 (min=21, max=65) with 43.6% males and 56.4% females. On day 28, after the second dose, the seroconversion rates were found to be 92.9% for total anti-spike and anti-nucleocapsid IgG and 15.2% for IgM and 98.2% for anti-S-RBD IgG antibodies and having natural COVID-19 prior to vaccination, age and comorbidity were found to be significant factors for immunogenicity. The incidence of at least one adverse event was found as 29.8% after the first dose and 24.1% after the second dose, with the most common adverse events of having pain at the injection site, weakness, fatigue, and headache.

Indexed as

COVID-19COVID-19 VaccinesFemaleFollow-Up StudiesHumansImmunoglobulin GImmunoglobulin MMaleSARS-CoV-2COVID-19 VaccinesImmunoglobulin GImmunoglobulin Madverse eventsimmunisationSARS-COV-2seroconversionvaccine

Identifiers

PMID34688238
PMCPMC10734823
OpenAlexW3209341797

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.