Covid19 Clinical Trial
Official title:
Corona Virus (COVID-19) Disease Duration and Gastrointestinal Tract (GIT) Manifestations; Can be New Disease Severity Classification. A Pilot Egyptian Single National Center Experience
The present study conducted to correlate symptoms not only constitutional and respiratory, but GIT as a principle presentation, with laboratory markers and COVID-19 severe acute respiratory syndrome (SARS-COV2) disease outcomes, as the duration of symptoms varies substantially between patients; the investigators undertook this study to determine the optimal time to predict COVID-19 outcomes based on real-time experience.
This observational retrospective cohort single center national study was conducted on
patients who tested positive COVID-19 infection by the polymerase chain reaction (PCR) of
nasopharyngeal sample in the period from first June to the med of July 2020. Patients were
recruited from Kasr Al-Aini School of medicine, COVID-19 out-patient clinic, Cairo University
hospitals.
The diagnosis and classification of severity of COVID-19 infection were made according to the
clinical management of COVID-19, released by the World Health Organization (WHO), mild and
moderate case were recruited, the treatment protocol used was according to the Egyptian
ministry of health treatment recommendations, which met in part the criteria that was later
on published by the national institute of health, Mild and moderate cases once diagnosed by
PCR received hydroxychloroquine 400 mg twice daily first day and maintained on 200 mg twice
daily for 6 days in mild cases and 10 days in moderate cases. Also they received
anticoagulants, vitamin c and zinc. In case of secondary bacterial infection, empiric
antibiotics are started till result of sputum culture and sensitivity. Steroids were
initiated in hypoxic cases that required supplemental oxygen and in cases of persistent
symptoms.
Any adult patient (age ≥18 years) suffering from mild or moderate COVID-19 infection was
included in this study. While severe cases according to WHO classifications and patients aged
less than18 were excluded from the study.
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