Evidence map›Paper›PMID 35248497›Full record

ArticleJournal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy2022

Adverse effect investigation using application software after vaccination against SARS-CoV-2 for healthcare workers.

Shingo Yamazaki, Kenta Watanabe, Yoshio Okuda, Misao Urushihara, Hiromi Koshikawa, Hitoshi Chiba, Misuzu Yahaba, Toshibumi Taniguchi, Taka-Aki Nakada, Hiroshi Nakajima and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 52% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

12 authors at 2 institutions in 1 country.

Shingo YamazakiDivision of Pharmacy, Chiba University Hospital, Chiba, Japan. Electronic address: s-yamazaki@chiba-u.jp.
Kenta WatanabeDivision of Pharmacy, Chiba University Hospital, Chiba, Japan.
Yoshio OkudaDivision of Infection Control, Chiba University Hospital, Chiba, Japan.
Misao UrushiharaDivision of Infection Control, Chiba University Hospital, Chiba, Japan.
Hiromi KoshikawaDivision of Infection Control, Chiba University Hospital, Chiba, Japan; Chiba University Hospital COVID-19 Vaccine Center, Chiba University, Japan.
Hitoshi ChibaDivision of Infection Control, Chiba University Hospital, Chiba, Japan.
Misuzu YahabaDivision of Infection Control, Chiba University Hospital, Chiba, Japan.
Toshibumi TaniguchiDivision of Infection Control, Chiba University Hospital, Chiba, Japan.
Taka-Aki NakadaDepartment of Emergency and Critical Care Medicine, Graduate School of Medicine, Chiba University, Japan.
Hiroshi NakajimaDepartment of Allergy and Clinical Immunology, Chiba University Hospital, Chiba, Japan; Chiba University Hospital COVID-19 Vaccine Center, Chiba University, Japan.
Itsuko IshiiDivision of Pharmacy, Chiba University Hospital, Chiba, Japan.
Hidetoshi IgariDivision of Infection Control, Chiba University Hospital, Chiba, Japan; Chiba University Hospital COVID-19 Vaccine Center, Chiba University, Japan.
Chiba University Hospital · JPChiba University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe usefulness of smartphone-based application software as a way to manage adverse events (AEs) after vaccination is well known. The purpose of this study is to clarify the usefulness and precautions of employing a smartphone application for collecting AEs after the administration of Comirnaty®️.

methodsHealthcare workers (HCWs) who were vaccinated with Comirnaty®️ were asked to register for the application software and to report AEs for 14 days after vaccination. AEs were self-reported according to severity. The software was set to output an alert in case of fever.

resultsThe number of HCWs who received the first dose was 2,551, and 2,406 (94.3%) reported their vaccinations. 2,547 received the second dose, and 2,347 (92.1%) reported their vaccinations. With the first dose, the reporting rate stayed above 83.3% until the final day. On the other hand, that of the second dose decreased rapidly after 6 days. The most frequent symptom was "pain at injection site" (more than 70%). Severe AEs were 6.6% after the second dose, with 0.6% visiting a clinic. Many AEs peaked on the day after administration and disappeared within 1 week. There were few reports of fever.

conclusionSmartphone applications can be used to collect information on AEs after vaccination. Application settings and dissemination are necessary to maintain the reporting rate of HCWs.

Indexed as

COVID-19Drug-Related Side Effects and Adverse ReactionsCOVID-19 VaccinesHealth PersonnelHumansSARS-CoV-2SoftwareVaccinationCOVID-19 VaccinesAdverse eventApplication softwareSARS-CoV2Vaccine

Identifiers

PMID35248497
PMCPMC8885303
OpenAlexW4214549844

What OpenQuestion holds

Textmetadata
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.