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Therapeutic efficacy of macrolides in management of patients with mild COVID-19.
Rashad, Alaa; Nafady, Asmaa; Hassan, Mohammed H; Mansour, Haggagy; Taya, Usama; Bazeed, Shamardan Ezzeldin S; Aref, Zaki F; Sayed, Mennatallah Ali Abdelrhman; Nafady-Hego, Hanaa; Abdelmaksoud, Aida A.
Afiliação
  • Rashad A; Department of Chest Diseases and Tuberculosis, Faculty of Medicine, South Valley-University, Qena, Egypt.
  • Nafady A; Department of Clinical Pathology, Faculty of Medicine, Assiut University, Assiut, Egypt.
  • Hassan MH; Department of Clinical and Chemical Pathology, Faculty of Medicine, South Valley University, Qena, Egypt.
  • Mansour H; Department of Medical Biochemistry, Faculty of Medicine, South Valley University, Qena, 83523, Egypt. Mohammedhosnyhassaan@yahoo.com.
  • Taya U; Department of Chest Diseases and Tuberculosis, Faculty of Medicine, South Valley-University, Qena, Egypt.
  • Bazeed SES; ENT Department, Faculty of Medicine, South Valley University, Qena, Egypt.
  • Aref ZF; Tropical Medicine and Gastroenterology Department, Faculty of Medicine, South Valley University, Qena, Egypt.
  • Sayed MAA; ENT Department, Faculty of Medicine, South Valley University, Qena, Egypt.
  • Nafady-Hego H; King Salman International University, Sharm El-Sheikh, Egypt.
  • Abdelmaksoud AA; Department of Microbiology and Immunology, Faculty of Medicine, Assiut University, Assiut, Egypt.
Sci Rep ; 11(1): 16361, 2021 08 11.
Article em En | MEDLINE | ID: mdl-34381155
Evidence on the efficacy of adding macrolides (azithromycin or clarithromycin) to the treatment regimen for COVID-19 is limited. We testify whether adding azithromycin or clarithromycin to a standard of care regimen was superior to standard of supportive care alone in patients with mild COVID-19.This randomized trial included three groups of patients with COVID-19. The azithromycin group included, 107 patients who received azithromycin 500 mg/24 h for 7 days, the clarithromycin group included 99 patients who received clarithromycin 500 /12 h for 7 days, and the control group included 99 patients who received standard care only. All three groups received only symptomatic treatment for control of fever and cough .Clinical and biochemical evaluations of the study participants including assessment of the symptoms duration, real-time reverse transcription-polymerase chain reaction (rRT-PCR), C-reactive protein (CRP), serum ferritin, D-dimer, complete blood count (CBC), in addition to non-contrast chest computed tomography (CT), were performed. The overall results revealed significant early improvement of symptoms (fever, dyspnea and cough) in patients treated with either azithromycin or clarithromycin compared to control group, also there was significant early conversion of SARS-CoV-2 PCR to negative in patients treated with either azithromycin or clarithromycin compared to control group (p < 0.05 for all).There was no significant difference in time to improvement of fever, cough, dyspnea, anosmia, gastrointestinal tract "GIT" symptoms and time to PCR negative conversion between patients treated with azithromycin compared to patients treated with clarithromycin (p > 0.05 for all). Follow up chest CT done after 2 weeks of start of treatment showed significant improvement in patients treated with either azithromycin or clarithromycin compared to control group (p < 0.05 for all).Adding Clarithromycin or azithromycin to the therapeutic protocols for COVID-19 could be beneficial for early control of fever and early PCR negative conversion in Mild COVID-19.Trial registration: (NCT04622891) www.ClinicalTrials.gov retrospectively registered (November 10, 2020).
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Claritromicina / Azitromicina / Tratamento Farmacológico da COVID-19 Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Claritromicina / Azitromicina / Tratamento Farmacológico da COVID-19 Idioma: En Ano de publicação: 2021 Tipo de documento: Article