3 results on '"Sogol Koolaji"'
Search Results
2. Dissection of non-pharmaceutical interventions implemented by Iran, South Korea, and Turkey in the fight against COVID-19 pandemic
- Author
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Bagher Larijani, Negar Rezaei, Yosef Farzi, Shaghayegh Zokaei, Reyhaneh Kalantar, Arya Aminorroaya, Nazila Rezaei, Erfan Ghasemi, Mohammad Keykhaei, Rosa Haghshenas, Sahar Saeedi Moghaddam, Sogol Koolaji, Esmaeil Mohammadi, Sina Rashedi, Sina Azadnajafabad, and Farshad Farzadfar
- Subjects
Economic growth ,medicine.medical_specialty ,Turkey ,business.industry ,Non-pharmaceutical interventions ,Endocrinology, Diabetes and Metabolism ,Social distance ,Corporate governance ,Public health ,Scopus ,Psychological intervention ,COVID-19 ,Review Article ,Iran ,South Korea ,Pandemic ,Internal Medicine ,medicine ,business ,Personal protective equipment ,Contact tracing - Abstract
Purpose The novel coronavirus disease 2019 (COVID-19) has imposed a great global burden on public health. As one of the most affected countries, Iran has tackled emerging challenges in the path to overcoming the epidemic, with three peaks of the disease propagation as of February 19, 2020. To flatten the curve of the COVID-19 pandemic, most countries have implemented bundles of intrusive, sometimes extremely stringent non-pharmaceutical interventions (NPIs). In this communication, we have dissected the effectiveness of NPIs and compared the strategies implemented by Iran, Turkey, and South Korea to mitigate the disease’s spread. Methods We searched online databases via PubMed, Web of Knowledge, and Scopus. Titles/abstracts and full-texts were screened by two reviewers and discrepancies were resolved upon discussion. Results Our results provide insights into five domains: prevention, screening, in-patient and out-patient facilities, governance, and management of diabetes mellitus. Analysis of previous efforts put in place illustrates that by fostering efficient social distancing measures, increasing the capability to perform prompt polymerase chain reaction tests, applying smart contact tracing, and supplying adequate personal protective equipment, Turkey and South Korea have brought the epidemic sub-optimally under control. Conclusion From the perspective of policymakers, these achievements are of utmost importance given that attaining the aspirational goals in the management of the COVID-19 necessities a suitable adjustment of previous successful strategies. Hence, policymakers should be noticed that a suitable combination of NPIs is necessary to stem the disease’s propagation.
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- 2021
- Full Text
- View/download PDF
3. Safety and effectiveness of high-dose vitamin C in patients with COVID-19: a randomized open-label clinical trial
- Author
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Fatemeh Jafari, Faeze Salahshour, Ladan Abbasian, Fereshteh Ghiasvand, Mohsen Meidani, Sara Ghaderkhani, Besharat Zarezade, Sogol Koolaji, Mohamadreza Salehi, Malihe Hasannezhad, Mohammad Tabarestani, Ehsan Sekhavati Moghadam, Seyed Ali Dehghan Manshadi, SeyedAhmad SeyedAlinaghi, Navid Manafi, Abolfazl Zendehdel, Saeidreza Jamalimoghadamsiahkali, and University of Manitoba
- Subjects
Male ,medicine.medical_specialty ,lcsh:Medicine ,SARS-COV-2 ,Ascorbic Acid ,Antiviral Agents ,Lopinavir ,Body Temperature ,law.invention ,03 medical and health sciences ,0302 clinical medicine ,Pharmacotherapy ,Randomized controlled trial ,law ,Internal medicine ,Humans ,Medicine ,Vitamin C ,030212 general & internal medicine ,Respiratory Distress Syndrome ,Ritonavir ,business.industry ,Research ,lcsh:R ,COVID-19 ,030208 emergency & critical care medicine ,Hydroxychloroquine ,Pneumonia ,General Medicine ,Length of Stay ,Middle Aged ,Intensive care unit ,COVID-19 Drug Treatment ,Oxygen ,Clinical trial ,Intensive Care Units ,Regimen ,Treatment Outcome ,2019-nCoV ,Female ,business ,medicine.drug - Abstract
Background Vitamin C is an essential water-soluble nutrient that functions as a key antioxidant and has been proven to be effective for boosting immunity. In this study, we aimed to assess the efficacy of adding high-dose intravenous vitamin C (HDIVC) to the regimens for patients with severe COVID-19 disease. Methods An open-label, randomized, and controlled trial was conducted on patients with severe COVID-19 infection. The case and control treatment groups each consisted of 30 patients. The control group received lopinavir/ritonavir and hydroxychloroquine and the case group received HDIVC (6 g daily) added to the same regimen. Results There were no statistically significant differences between two groups with respect to age and gender, laboratory results, and underlying diseases. The mean body temperature was significantly lower in the case group on the 3rd day of hospitalization (p = 0.001). Peripheral capillary oxygen saturations (SpO2) measured at the 3rd day of hospitalization was also higher in the case group receiving HDIVC (p = 0.014). The median length of hospitalization in the case group was significantly longer than the control group (8.5 days vs. 6.5 days) (p = 0.028). There was no significant difference in SpO2 levels at discharge time, the length of intensive care unit (ICU) stay, and mortality between the two groups. Conclusions We did not find significantly better outcomes in the group who were treated with HDIVC in addition to the main treatment regimen at discharge. Trial registration irct.ir (IRCT20200411047025N1), April 14, 2020
- Published
- 2021
- Full Text
- View/download PDF
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