Evidence map›Paper›PMID 36326342›Full record

ArticleTurkish journal of medical sciences2022

Determination of COVID-19 PCR positivity and mutation status in coronaVac vaccinated individuals in Turkey.

Ahmet Çalışkan, Mücahit Seçme, İlknur Kalelı, Tuğba Sarı, Sedef Zeliha Öner, Saniye Küçükakın Yakın, Büşra Dönmez

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. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 91% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 2 institutions in 2 countries.

Ahmet ÇalışkanDepartment of Medical Microbiology, Faculty of Medicine, Pamukkale University, Denizli, Turkey.
Mücahit SeçmeDepartment of Medical Biology, Faculty of Medicine, Pamukkale University, Denizli, Turkey.
İlknur KalelıDepartment of Medical Microbiology, Faculty of Medicine, Pamukkale University, Denizli, Turkey.
Tuğba SarıDepartment of Infectious Diseases and Clinical Microbiology, Faculty of Medicine, Pamukkale University, Denizli, Turkey.
Sedef Zeliha ÖnerDepartment of Medical Microbiology, Faculty of Medicine, Pamukkale University, Denizli, Turkey.
Saniye Küçükakın YakınDepartment of Medical Microbiology, Faculty of Medicine, Pamukkale University, Denizli, Turkey.
Büşra DönmezDepartment of Medical Microbiology, Faculty of Medicine, Pamukkale University, Denizli, Turkey.
Czech Academy of Sciences, Institute of Microbiology · CZPamukkale University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoronaVac is an inactivated virus-based COVID-19 vaccine used in Turkey and approved for emergency use by the World Health Organization (WHO). In this study, it was aimed to retrospectively evaluate the mutation status and clinical status in individuals who received two doses of CoronaVac vaccine and were infected with COVID-19 at least two weeks after the second dose.

methods164 people were included in the study and COVID-19 diagnosis and mutation analyses were determined by RT-PCR using the Bioseepdy SARS CoV-2 Double Gene RT-qPCR Kit and the Biospeedy SARS-CoV-2 Variant Plus kit in accordance with the protocol determined by the manufacturer.

results116 (70.7%) UK (Alpha, B.1.1.7) mutation and 3 (1.8%) South Africa (Beta, B.1.351), Brazil (Gamma, P.1) mutations were determined in 164 double doses CoronaVac vaccinated patients; 45 (27.5%) patients were mutation negative. Nine patients (5.5%) developed pneumonia. Eight patients (4.9%) had CT findings compatible with corona virus infection. Seven (4.3%) of the patients received treatment in the intensive care unit, and 5 (3%) of the patients were intubated. DISCUSSION: In conclusion, people who receive two doses of CoronaVac vaccine can be reinfected with mutant viruses, vaccine significantly reduces the need for hospitalization, CT findings and intensive care.

Indexed as

COVID-19VaccinesAntibodies, ViralCOVID-19 TestingCOVID-19 VaccinesHumansMutationPolymerase Chain ReactionRetrospective StudiesSARS-CoV-2TurkeyAntibodies, ViralCOVID-19 VaccinesVaccinesCoronaVac vaccineSarsCov-2SinovacTurkeyvariant virus

Identifiers

PMID36326342
PMCPMC10390140
OpenAlexW4285140271

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LicenceCC BY
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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.