Evidence map›Paper›PMID 36558907›Full record

ArticlePharmaceuticals (Basel, Switzerland)2022

Analyzing the Difference in the Length of Stay (LOS) in Moderate to Severe COVID-19 Patients Receiving Hydroxychloroquine or Favipiravir.

Bandar Alosaimi, Huda M Alshanbari, Muath Alturaiqy, Halah Z AlRawi, Saad Alamri, Asma Albujaidy, Aljawharah Bin Sabaan, Ahmed A Alrashed, Ahmad Alamer, Fayez Alghofaili and 3 more

Abstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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.

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

13 authors.

Bandar AlosaimiResearch Center, King Fahad Medical City, Riyadh Second Health Cluster, Riyadh 11525, Saudi Arabia.ORCID 0000-0003-4719-2655
Huda M AlshanbariDepartment of Mathematical Sciences, College of Science, Princess Nourah bint Abdulrahman University, Riyadh 11671, Saudi Arabia.ORCID 0000-0001-5154-7477
Muath AlturaiqyDepartment of Internal Medicine, Alzulfi General Hospital, Riyadh Second Health Cluster, Riyadh 11525, Saudi Arabia.
Halah Z AlRawiResearch Center, King Fahad Medical City, Riyadh Second Health Cluster, Riyadh 11525, Saudi Arabia.ORCID 0000-0001-6761-9519
Saad AlamriResearch Center, King Fahad Medical City, Riyadh Second Health Cluster, Riyadh 11525, Saudi Arabia.
Asma AlbujaidyDepartment of Clinical Pharmacy Service, Prince Mohammed bin Abdulaziz Hospital, Riyadh Second Health Cluster, Riyadh 11525, Saudi Arabia.
Aljawharah Bin SabaanPharmacy College, Almaarifa University, Riyadh 11597, Saudi Arabia.
Ahmed A AlrashedDepartment of Pharmaceutical Services, Main Hospital, King Fahad Medical City, Riyadh Second Health Cluster, Riyadh 11525, Saudi Arabia.
Ahmad AlamerDepartment of Clinical Pharmacy, Prince Sattam Bin Abdulaziz University, Alkharj 11942, Saudi Arabia.ORCID 0000-0002-2091-1376
Fayez AlghofailiDepartment of Medical Laboratory Sciences, College of Applied Medical Sciences, Majmaah University, Majmaah 11952, Saudi Arabia.ORCID 0000-0002-1505-3581
Khaled Al-DuraymihMain Laboratory and Blood Bank, Alzulfi General Hospital, Riyadh Second Health Cluster, Riyadh 11525, Saudi Arabia.
Abdulaziz J AlshalaniAlzulfi General Hospital, Riyadh Second Health Cluster, Riyadh 11525, Saudi Arabia.
Wael AlturaikiDepartment of Medical Laboratory Sciences, College of Applied Medical Sciences, Majmaah University, Majmaah 11952, Saudi Arabia.ORCID 0000-0002-6947-7582

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The coronavirus 2019 (COVID-19) disease, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus led to a global pandemic. HCQ and FPV were used early in the pandemic as a treatment modality for COVID-19. Various studies evaluated the HCQ and FPV effectiveness, based on the mortality endpoint and showed conflicting results. We hypothesize that analyzing the difference in the LOS as a significant endpoint would be of a major interest, especially for healthcare providers, to prevent a lengthy hospitalization and disease progression. Methods: This is a retrospective observational study, conducted via a medical chart review of COVD-19 patients who were admitted between April 2020 and March 2021 with a moderate to severe illness. The LOS endpoint was tested using the paired Wilcoxon signed-rank (WSR) model. Prior to using the WSR model, the balance between the HCQ and FPV groups, the propensity score matching, the LOS distribution, and the normality assumptions were tested. Two sensitivity statistical analyses were conducted to confirm the results (stratified log-rank test and U Welch test after transforming the LOS by the squared root values). Results: A total of 200 patients were included for the analysis: 83 patients in the HCQ group and 117 patients in the FPV group. Thirty-seven patients were matched in each group. The LOS data was positively skewed and violated the normality (Shapiro−Wilk p < 0.001) and had an unequal variance (Levene’s test, p = 0.019). The WSR test showed no statistical significance in the LOS endpoint, with a median of −0.75 days (95% confidence interval: −4.0 to 2.5, p = 0.629), in favor of the HCQ group (four days), in comparison to seven days of the FPV group. The WSR findings were further confirmed with the stratified log rank test (p = 740) and the U Welch test (p = 391). Conclusions: The study concluded that the HCQ and FPV treatments have a comparable effectiveness in terms of the LOS in the moderate to severe COVID-19 patients. This study highlights the importance of analyzing the LOS as a relevant endpoint, in order to prevent the costs of a lengthy hospitalization and disease progression. The current study also emphasizes the importance of applying the appropriate statistical testing when dealing with two-sample paired data and analyzing non-parametric data such as the LOS.

Indexed as

COVID-19effectivenessfavipiravirhydroxychloroquinelength of staySARS-CoV-2statistical analysis

Identifiers

PMID36558907
PMCPMC9785070

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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.