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      COVID‐19 pneumonia suspected to be co‐infection with Mycoplasma pneumoniae and improved by early administration of favipiravir and ciclesonide

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          Abstract

          A female nurse in her 40s caring for a patient with severe coronavirus disease 2019 (COVID‐19) pneumonia treated with a high‐flow nasal cannula (HFNC) presented with fever, cough and dyspnoea. Based on imaging findings and a positive reverse transcription‐polymerase chain reaction (RT‐PCR) for severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2), COVID‐19 pneumonia was diagnosed, although her cohabiting family had similar symptoms and their RT‐PCR tests were negative. Laboratory results showed Mycoplasma antigen (+). She was started on ciclesonide 1200 μg/day and favipiravir (3600 mg/day on the first day and 1600 mg/day from Day 2). As Mycoplasma antigen was positive on admission and her family had similar symptoms, levofloxacin 500 mg/day was started. The patient recovered and was discharged on Day 10. The patient did not have Mycoplasma infection because the Mycoplasma antibody measured by particle agglutination (PA) method was increased only up to 80 times after 4 weeks. This case highlights that healthcare workers wearing full personal protective equipment can nevertheless acquire COVID‐19 from patients treated with HFNCs.

          Abstract

          We present the case of a patient with coronavirus disease 2019 (COVID‐19) pneumonia who was suspected to have co‐infection with Mycoplasma pneumoniae and a nosocomial infection from a patient treated with a high‐flow nasal cannula, and who did not worsen and was relieved by early administration of favipiravir and ciclesonide.

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          Most cited references5

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          Practical recommendations for critical care and anesthesiology teams caring for novel coronavirus (2019-nCoV) patients

          A global health emergency has been declared by the World Health Organization as the 2019-nCoV outbreak spreads across the world, with confirmed patients in Canada. Patients infected with 2019-nCoV are at risk for developing respiratory failure and requiring admission to critical care units. While providing optimal treatment for these patients, careful execution of infection control measures is necessary to prevent nosocomial transmission to other patients and to healthcare workers providing care. Although the exact mechanisms of transmission are currently unclear, human-to-human transmission can occur, and the risk of airborne spread during aerosol-generating medical procedures remains a concern in specific circumstances. This paper summarizes important considerations regarding patient screening, environmental controls, personal protective equipment, resuscitation measures (including intubation), and critical care unit operations planning as we prepare for the possibility of new imported cases or local outbreaks of 2019-nCoV. Although understanding of the 2019-nCoV virus is evolving, lessons learned from prior infectious disease challenges such as Severe Acute Respiratory Syndrome will hopefully improve our state of readiness regardless of the number of cases we eventually manage in Canada.
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            Efficacy of favipiravir in COVID-19 treatment: a multi-center randomized study

            No specific antiviral drugs have been approved for the treatment of COVID-19. This study aimed to evaluate the efficacy of favipiravir in treatment of COVID-19. This was a multicenter randomized controlled study including 96 patients with COVID- 19 who were randomly assigned into a chloroquine (CQ) group and a favipiravir group. None of the patients in the favipiravir group needed mechanical ventilation (p = 0.129). One patient (2.3%) in the favipiravir group and two patients (4.2%) in the CQ group died (p = 1.00). Favipiravir is a promising drug for COVID-19 that decreases the hospital stay and the need for mechanical ventilation. ClinicalTrials.gov Identifier NCT04351295.
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              High-flow nasal cannula oxygen therapy to treat patients with hypoxemic acute respiratory failure consequent to SARS-CoV-2 infection

              This observational study aims to assess the outcome and safety of O 2 -therapy by high-flow nasal cannula (HFNC) in 28 consecutive patients with severe hypoxemic acute respiratory failure (hARF) consequent to SARS-CoV-2 infection, unresponsive to conventional O 2 -therapy. Nineteen patients had a positive response. Nine patients required escalation of treatment to non-invasive ventilation (five subsequently intubated). None of the staff had a positive swab testing during the study period and the following 14 days. Severity of hypoxemia and C reactive protein level were correlated with HFNC failure. These data suggest HFNC to be a safe treatment for less severe patients with SARS-CoV-2 hARF and efficacy will need to be assessed as part of a clinical trial.
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                Author and article information

                Contributors
                keimaito4869@gmail.com
                Journal
                Respirol Case Rep
                Respirol Case Rep
                10.1002/(ISSN)2051-3380
                RCR2
                Respirology Case Reports
                John Wiley & Sons, Ltd (Chichester, UK )
                2051-3380
                03 August 2021
                September 2021
                : 9
                : 9 ( doiID: 10.1002/rcr2.v9.9 )
                : e0821
                Affiliations
                [ 1 ] Department of Respiratory Medicine, Allergy and Clinical Immunology Nagoya City University Graduate School of Medical Sciences Nagoya Japan
                [ 2 ] Department of Respiratory Medicine Asahi Rosai Hospital Owariasahi Japan
                Author notes
                [*] [* ] Correspondence

                Keima Ito, Department of Respiratory Medicine, Allergy and Clinical Immunology, Nagoya City University Graduate School of Medical Sciences, 1, Kawasumi, Mizuho‐cho, Mizuho‐ku, Nagoya, Aichi, Japan.

                Email: keimaito4869@ 123456gmail.com

                Author information
                https://orcid.org/0000-0002-9217-6956
                Article
                RCR2821
                10.1002/rcr2.821
                8333772
                34377494
                fbca42f0-268f-4b46-87e2-9efdbcd0fe45
                © 2021 The Authors. Respirology Case Reports published by John Wiley & Sons Australia, Ltd on behalf of The Asian Pacific Society of Respirology.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 19 July 2021
                : 02 July 2021
                : 20 July 2021
                Page count
                Figures: 3, Tables: 0, Pages: 4, Words: 1641
                Categories
                Case Report
                Case Reports
                Custom metadata
                2.0
                September 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.4 mode:remove_FC converted:04.08.2021

                ciclesonide,covid‐19,favipiravir,high‐flow nasal cannula,mycoplasma pneumoniae

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