Evidence map›Paper›PMID 35299062›Full record

ArticleJournal of infection and public health2022

Overview of clinical outcome and therapeutic effectiveness of Favipiravir in patients with COVID-19 admitted to intensive care unit, Riyadh, Saudi Arabia.

Abbas Al Mutair, Jinan Shamou, Saad Alhumaid, Laila Layqah, Gasmelseed Y Ahmed, Koritala Thoyaja, Mohammed Al Mohaini, Sana Almahmoud, Mazin Barry, Amjad Khan and 4 more

Abstract read
In one paragraph

Article in Journal of infection and public health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

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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

14 authors.

Abbas Al MutairAlmoosa Specialist Hospital, Alhassa, Saudi Arabia; School of Nursing, University of Wollongong, Wollongong, Australia; Princess Norah Bint Abdulrhamn University, Riyadh, Saudi Arabia. Electronic address: abbas.almutair@almoosahospital.com.
Jinan ShamouDepartment of Medicine, King Abdulaziz Medical City, Riyadh, Saudi Arabia.
Saad AlhumaidAdministration of Pharmaceutical Care, Al-Ahsa Health Cluster, Ministry of Health, Al-Ahsa, Saudi Arabia.
Laila LayqahResearch Office, King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
Gasmelseed Y AhmedAlmoosa Specialist Hospital, Alhassa, Saudi Arabia; Almoosa Specialit Hospital, Al-ahsa, Saudi Arabia College of Medicine and Health sciences. Almanagil University, Sudan.
Koritala ThoyajaDepartment of Internal Medicine, Mayo Clinic Health System, Mankato, MN, USA.
Mohammed Al MohainiBasic Sciences Department, College of Applied Medical Sciences, King Saud Bin Abdulaziz University for Health Sciences, Al-ahsa, Saudi Arabia; King Abdullah International Medical Research Center, Al-ahsa, Saudi Arabia.
Sana AlmahmoudDepartment of Administration, College of Nursing, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
Mazin BarryDivision of Infectious Diseases, College of Medicine, King Saud University, Riyadh, Saudi Arabia.
Amjad KhanDepartment of Public Health/Nutrition, The University of Haripur, Pakistan.
Kuldeep DhamaDivision of Pathology, ICAR-Indian Veterinary, Bareilly, Uttar Pradesh, India.
Lamiaa Hamad Al-JameaVice Deanship of Postgraduate Studies and Research, Prince Sultan Military College of Health Sciences, Dhahran, Saudi Arabia.
Alxeander WoodmanVice Deanship of Postgraduate Studies and Research, Prince Sultan Military College of Health Sciences, Dhahran, Saudi Arabia.
Ali A RabaanMolecular Diagnostics Laboratory, Johns Hopkins Aramco Healthcare, Dhahran, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrior to the availability of the current COVID-19 vaccine, the need to control the pandemic worldwide was focused on management of the disease using previously approved antivirals, including Favipiravir which inhibits viral replication through the RNA dependent RNA polymerase enzyme. Favipiravir's efficacy against different viral infections has made it a potential treatment for COVID-19. We are aiming in this study to assess the therapeutic efficacy and safety of Favipiravir in treating critically ill patients admitted with COVID-19 to Intensive Care Units (ICUs).

methodsThis is a retrospective cohort study was conducted in five tertiary hospitals in Riyadh, Kingdom of Saudi Arabia (KSA). The studied sample was randomized from a huge pool of data collected primarily for critically ill COVID-19 patients admitted to (ICUs) during the period between April 2020 to March 2021. Two groups of patients matched 1: 1 for age and body mass index (BMI) was enrolled in the study; one group received Favipiravir and another comparison group received other antimicrobial medications, not including Favipiravir.

resultsA total data of 538 COVID-19 patients were analyzed, 269 (50.%) received Favipiravir and 269 (50%) the control group received different treatments. More than two-thirds 201 (74.7%) were Saudi citizens, the majority 177 (65.8%) were males and the mean age and (BMI) were; (57.23 ± 15.16) years and (31.61 ± 7.33) kg/m2 respectively. The most frequent symptoms of presentation were shortness of breath (SOB), fever, and cough, and the most frequent comorbidity was diabetes mellitus, hypertension, and ischemic heart disease. In the supplemental therapy, corticosteroid, tocilizumab and chloroquine were statistically significant (P = 0.001) when combined in the FVP group more than in the comparison group. Severe acute respiratory distress syndrome (ARDS) was more frequent among Favipiravir group, while the overall mortality rate among the Favipiravir group was not statistically significant (p-value 0.4).

conclusionAccording to the study's results revealing FVP is not superior to other antivirals, patients who received Favipiravir presented with more severe symptoms, more comorbidities, more complications, and is not effective in controlling the cytokine storm which negatively impact the efficacy of Favipiravir. FVP therapy had no influence on ICU and hospital length of stay in comparison with the control group as well as in the overall mortality rate among the FVP group was not statistically significant. further research is needed to understand how FVP along with other treatments can improve the length of stay among COVID-19 patients admitted to the ICU.

Indexed as

COVID-19 Drug TreatmentAmidesAntiviral AgentsCOVID-19 VaccinesCritical IllnessHumansIntensive Care UnitsMalePyrazinesRetrospective StudiesSARS-CoV-2Saudi ArabiaAmidesAntiviral AgentsCOVID-19 VaccinesfavipiravirPyrazinesCOVID-19Critically illEfficacy and safetyFavipiravirICUSaudi Arabia

Identifiers

PMID35299062
PMCPMC8845266

What OpenQuestion holds

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Registered trials

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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.