Evidence map›Paper›PMID 36965894›Full record

ArticleTaiwanese journal of obstetrics & gynecology2023

Investigation of SARS-CoV-2 using RT-PCR in vaginal swab samples of female patients with a diagnosis of severe COVID-19.

Deniz Erdem, Bircan Kayaaslan, Esra Yakisik Cakir, Bedia Dinc, Dilek Asilturk, Fisun Kirca, Fatih Segmen, Isil Ozkocak Turan, Rahmet Guner

Open access · diamondAbstract read
In one paragraph

Article in Taiwanese journal of obstetrics & gynecology, 2023. 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
0.4field-weighted citation impact, top 36% 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

9 authors at 3 institutions in 1 country.

Deniz ErdemDepartment of Intensive Care Unıt, Univeristy of Health Sciences, Ankara City Hospital, Ankara, Turkey. Electronic address: dh2erdem@gmail.com.
Bircan KayaaslanInfectious Disease and Clinical Microbiology, Ankara Yildırım Beyazit University, Ankara City Hospital, Ankara, Turkey.
Esra Yakisik CakirDepartment of Intensive Care Unıt, Ankara City Hospital, Ankara, Turkey.
Bedia DincDepartment of Medical Microbiology, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.
Dilek AsilturkInfectious Disease and Clinical Microbiology, Ankara City Hospital, Ankara, Turkey.
Fisun KircaDepartment of Medical Microbiology, Ankara City Hospital, Ankara, Turkey.
Fatih SegmenDepartment of Intensive Care Unıt, Ankara City Hospital, Ankara, Turkey.
Isil Ozkocak TuranDepartment of Intensive Care Unıt, Univeristy of Health Sciences, Ankara City Hospital, Ankara, Turkey.
Rahmet GunerInfectious Disease and Clinical Microbiology, Ankara Yildırım Beyazit University, Ankara City Hospital, Ankara, Turkey.
Memorial Ankara Hospital · TRAnkara Yıldırım Beyazıt University · TRSağlık Bilimleri Üniversitesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIt is important to determine the presence of SARS-CoV-2 in the vaginal fluid samples of reproductive-aged women with severe disease during the acute stage of the disease and to determine the risks of transmission by sexual or vertical transmission. MATERIAL AND

methodsAdult women with confirmed severe COVID-19 who were admitted to Ankara City Hospital intensive care unit (ICU) between December 1st, 2020, and January 1st, 2021, were enrolled in the study. Vaginal swab samples were collected within 48 h in the ICU using Dacron or rayon swabs and tested for SARS-CoV-2 using reverse transcription real-time polymerase chain reaction (RT PCR).

resultsThirty women of reproductive age were included in the study, five (16.7%) of whom were pregnant. The mean age was 44.9 (±10.5) years. The most common symptoms were headache (100%), muscle soreness (86.7%), cough (76.7%), fever (60%), and nausea and vomiting (20%). Nineteen (63.3%) patients had underlying medical conditions. The time interval from obtaining vaginal swab samples to admission to the ICU was 48 h. The time between vaginal sampling and PCR positivity ranged from 2 to 18 days. SARS-CoV-2 was not detected in any vaginal samples.

conclusionOur study showed that women with severe COVID-19 did not have SARS-CoV-2 in their vaginal fluids. Investigation of the presence of SARS-CoV-2 in vaginal secretions may help in determining the risks of sexual transmission and vertical transmission from mother to baby. Information on this subject is still limited. Larger studies on comprehensive biological samples are needed.

Indexed as

COVID-19AdultCOVID-19 TestingFemaleHumansInfantMiddle AgedPregnancyReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionSARS-CoV-2VaginaCOVID-19Intensive careSARS-CoV-2Vaginal fluidVaginal sample

Identifiers

PMID36965894
PMCPMC9729648
OpenAlexW4311086161

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.