Evidence map›Paper›PMID 36662716›Full record

Observational studyPloS one2023

Clinical characteristics and mortality risk among critically ill patients with COVID-19 owing to the B.1.617.2 (Delta) variant in Vietnam: A retrospective observational study.

Thanh Van Do, Toshie Manabe, Giap Van Vu, Vuong Minh Nong, Yuji Fujikura, Dung Phan, Thach The Pham, Cuong Duy Do, Tra Thu Doan, Nguyen Trung Nguyen and 15 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

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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

25 authors at 8 institutions in 3 countries.

Thanh Van DoCenter for Tropical Diseases, Bach Mai Hospital, Hanoi, Vietnam.
Toshie ManabeNagoya City University Graduate School of Medicine, Nagoya city, Aichi, Japan.ORCID 0000-0002-8208-8071
Giap Van VuHanoi Medical University, Hanoi, Vietnam.
Vuong Minh NongCenter for Tropical Diseases, Bach Mai Hospital, Hanoi, Vietnam.
Yuji FujikuraDepartment of Internal Medicine, National Defense Medical College, Tokorozawa, Saitama, Japan.
Dung PhanFaculty of Pharmacy and Pharmaceutical Sciences, Monash University, Parkville, Victoria, Australia.
Thach The PhamIntensive Care Center, Bach Mai Hospital, Hanoi, Vietnam.
Cuong Duy DoCenter for Tropical Diseases, Bach Mai Hospital, Hanoi, Vietnam.
Tra Thu DoanCenter for Tropical Diseases, Bach Mai Hospital, Hanoi, Vietnam.
Nguyen Trung NguyenPoison Control Center, Bach Mai Hospital, Hanoi, Vietnam.
Thai Quoc NguyenCenter for Tropical Diseases, Bach Mai Hospital, Hanoi, Vietnam.ORCID 0000-0002-7764-5822
Thanh Van DongOutpatient Department, Bach Mai Hospital, Hanoi, Vietnam.
Chinh Quoc LuongCenter for Emergency Medicine, Bach Mai Hospital, Hanoi, Vietnam.ORCID 0000-0002-6409-577X
Hiroki ManabeShitennoji University, Habikino city, Osaka, Japan.
Dan KambayashiNagoya City University Graduate School of Medicine, Nagoya city, Aichi, Japan.ORCID 0000-0002-3075-815X
Anh Viet HoangTraining and Direction of Healthcare Activities Center, Bach Mai Hospital, Hanoi, Vietnam.
Nhan Van VuTraining and Direction of Healthcare Activities Center, Bach Mai Hospital, Hanoi, Vietnam.
Giang Kim TrinhTraining and Direction of Healthcare Activities Center, Bach Mai Hospital, Hanoi, Vietnam.
Son Ngoc DoDepartment of Emergency and Critical Care Medicine, Hanoi Medical University, Hanoi, Vietnam.
Takeshi KamiyaNagoya City University Graduate School of Medicine, Nagoya city, Aichi, Japan.
Hirotaka OharaNagoya City University Graduate School of Medicine, Nagoya city, Aichi, Japan.
Chi Van NguyenCenter for Emergency Medicine, Bach Mai Hospital, Hanoi, Vietnam.
Tuan Quoc DangDepartment of Emergency and Critical Care Medicine, Hanoi Medical University, Hanoi, Vietnam.
Koichiro KudoYurin Hospital, Tokyo, Japan.
Co Xuan DaoDepartment of Emergency and Critical Care Medicine, Hanoi Medical University, Hanoi, Vietnam.
Bạch Mai Hospital · VNNagoya City University · JPHanoi Medical University · VNVietnam National University, Hanoi · VNMonash University · AUNational Defense Medical College Hospital · JPShitennoji University · JPWaseda University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSARS-CoV-2 Delta variant caused a large number of COVID-19 cases in many countries, including Vietnam. Understanding mortality risk factors is crucial for the clinical management of severe COVID-19.

methodsWe conducted a retrospective study at an intensive care center in Ho Chi Minh City that urgently built by Bach Mai Hospital during the COVID-19 outbreak in Vietnam, when the Delta variant predominated. Participants were laboratory-confirmed patients with SARS-CoV-2 infection, admitted in August 2021. Data on patients' demographic and clinical characteristics, radiographic and laboratory findings, treatment, and clinical time course were compared between survivors and non-survivors. Risk factors to mortality were assessed using logistic regression.

resultsAmong 504 eligible COVID-19 patients, case fatality was 52.2%. Unvaccinated patients accounted for 61.2% of non-survivors and 43.6% of survivors (p < 0.001). The time from onset to hospital admission was 8 days in non-survivors and 7 days in survivors (p = 0.004). Among non-survivors, 90.2% developed acute respiratory distress syndrome (ARDS). Oxygen therapy was administered for all patients, but antiviral agent was given to 51.7% of non-survivors. 54.2% of non-survivors tested positive for the bacterial infection using blood culture. The risk factors for mortality were diabetes mellitus, respiration rate, oxygen saturation, vaccination status, time from onset to admission, and older age.

conclusionsCritical patients with COVID-19 owing to the Delta variant in Vietnam had delayed hospital admission, leading to ARDS and death. Early availability of vaccines and preventing bacterial infections are crucial for reducing mortality of COVID-19, especially in low- and middle-income countries.

Indexed as

COVID-19Respiratory Distress SyndromeCritical IllnessHumansRetrospective StudiesSARS-CoV-2Vietnam

Identifiers

PMID36662716
PMCPMC9858045
OpenAlexW4317567376

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.