Cargando…
Analyzing the Difference in the Length of Stay (LOS) in Moderate to Severe COVID-19 Patients Receiving Hydroxychloroquine or Favipiravir
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, b...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9785070/ https://www.ncbi.nlm.nih.gov/pubmed/36558907 http://dx.doi.org/10.3390/ph15121456 |
_version_ | 1784857963587960832 |
---|---|
author | Alosaimi, Bandar Alshanbari, Huda M. Alturaiqy, Muath AlRawi, Halah Z. Alamri, Saad Albujaidy, Asma Bin Sabaan, Aljawharah Alrashed, Ahmed A. Alamer, Ahmad Alghofaili, Fayez Al-Duraymih, Khaled Alshalani, Abdulaziz J. Alturaiki, Wael |
author_facet | Alosaimi, Bandar Alshanbari, Huda M. Alturaiqy, Muath AlRawi, Halah Z. Alamri, Saad Albujaidy, Asma Bin Sabaan, Aljawharah Alrashed, Ahmed A. Alamer, Ahmad Alghofaili, Fayez Al-Duraymih, Khaled Alshalani, Abdulaziz J. Alturaiki, Wael |
author_sort | Alosaimi, Bandar |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9785070 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97850702022-12-24 Analyzing the Difference in the Length of Stay (LOS) in Moderate to Severe COVID-19 Patients Receiving Hydroxychloroquine or Favipiravir Alosaimi, Bandar Alshanbari, Huda M. Alturaiqy, Muath AlRawi, Halah Z. Alamri, Saad Albujaidy, Asma Bin Sabaan, Aljawharah Alrashed, Ahmed A. Alamer, Ahmad Alghofaili, Fayez Al-Duraymih, Khaled Alshalani, Abdulaziz J. Alturaiki, Wael Pharmaceuticals (Basel) Article 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. MDPI 2022-11-24 /pmc/articles/PMC9785070/ /pubmed/36558907 http://dx.doi.org/10.3390/ph15121456 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Alosaimi, Bandar Alshanbari, Huda M. Alturaiqy, Muath AlRawi, Halah Z. Alamri, Saad Albujaidy, Asma Bin Sabaan, Aljawharah Alrashed, Ahmed A. Alamer, Ahmad Alghofaili, Fayez Al-Duraymih, Khaled Alshalani, Abdulaziz J. Alturaiki, Wael Analyzing the Difference in the Length of Stay (LOS) in Moderate to Severe COVID-19 Patients Receiving Hydroxychloroquine or Favipiravir |
title | Analyzing the Difference in the Length of Stay (LOS) in Moderate to Severe COVID-19 Patients Receiving Hydroxychloroquine or Favipiravir |
title_full | Analyzing the Difference in the Length of Stay (LOS) in Moderate to Severe COVID-19 Patients Receiving Hydroxychloroquine or Favipiravir |
title_fullStr | Analyzing the Difference in the Length of Stay (LOS) in Moderate to Severe COVID-19 Patients Receiving Hydroxychloroquine or Favipiravir |
title_full_unstemmed | Analyzing the Difference in the Length of Stay (LOS) in Moderate to Severe COVID-19 Patients Receiving Hydroxychloroquine or Favipiravir |
title_short | Analyzing the Difference in the Length of Stay (LOS) in Moderate to Severe COVID-19 Patients Receiving Hydroxychloroquine or Favipiravir |
title_sort | analyzing the difference in the length of stay (los) in moderate to severe covid-19 patients receiving hydroxychloroquine or favipiravir |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9785070/ https://www.ncbi.nlm.nih.gov/pubmed/36558907 http://dx.doi.org/10.3390/ph15121456 |
work_keys_str_mv | AT alosaimibandar analyzingthedifferenceinthelengthofstaylosinmoderatetoseverecovid19patientsreceivinghydroxychloroquineorfavipiravir AT alshanbarihudam analyzingthedifferenceinthelengthofstaylosinmoderatetoseverecovid19patientsreceivinghydroxychloroquineorfavipiravir AT alturaiqymuath analyzingthedifferenceinthelengthofstaylosinmoderatetoseverecovid19patientsreceivinghydroxychloroquineorfavipiravir AT alrawihalahz analyzingthedifferenceinthelengthofstaylosinmoderatetoseverecovid19patientsreceivinghydroxychloroquineorfavipiravir AT alamrisaad analyzingthedifferenceinthelengthofstaylosinmoderatetoseverecovid19patientsreceivinghydroxychloroquineorfavipiravir AT albujaidyasma analyzingthedifferenceinthelengthofstaylosinmoderatetoseverecovid19patientsreceivinghydroxychloroquineorfavipiravir AT binsabaanaljawharah analyzingthedifferenceinthelengthofstaylosinmoderatetoseverecovid19patientsreceivinghydroxychloroquineorfavipiravir AT alrashedahmeda analyzingthedifferenceinthelengthofstaylosinmoderatetoseverecovid19patientsreceivinghydroxychloroquineorfavipiravir AT alamerahmad analyzingthedifferenceinthelengthofstaylosinmoderatetoseverecovid19patientsreceivinghydroxychloroquineorfavipiravir AT alghofailifayez analyzingthedifferenceinthelengthofstaylosinmoderatetoseverecovid19patientsreceivinghydroxychloroquineorfavipiravir AT alduraymihkhaled analyzingthedifferenceinthelengthofstaylosinmoderatetoseverecovid19patientsreceivinghydroxychloroquineorfavipiravir AT alshalaniabdulazizj analyzingthedifferenceinthelengthofstaylosinmoderatetoseverecovid19patientsreceivinghydroxychloroquineorfavipiravir AT alturaikiwael analyzingthedifferenceinthelengthofstaylosinmoderatetoseverecovid19patientsreceivinghydroxychloroquineorfavipiravir |