The global pandemic of novel coronavirus disease 2019 (COVID-19) began in Wuhan, China, in December 2019, and has since spread worldwide. The disease is mild in 85% of cases but the remaining 15% requires hospitalization and/or intensive care. Recent publications show that a significant number of COVID-19 patients are co-infected with one or more pathogens. Most co-infections occurred within 1-4 days of onset of COVID-19 disease and a considerable number of patients arrive to the Emergency rooms with mild-moderate respiratory symptoms compatible with pneumonia of presumed bacterial origin and not severe enough for requiring hospitalization. It therefore seems reasonable to adopt therapeutic strategies for these patients that are effective and easy to follow in the outpatient setting. Cefditoren (CDN) is a third-generation cephalosporin for oral administration. CDN has a broad spectrum of activity and is particularly active against the bacterial pathogens involved in community respiratory tract infections. Besides that, the use of CDN has been associated with a marked decrease in circulating levels of IL-6 and other pro-inflammatory cytokines and mediators of epithelial damage. The aim of this study is to demonstrate that CDN improves clinical condition in patients with mild-moderate COVID-19 and symptoms of bacterial pneumonia.
The global pandemic of novel coronavirus disease 2019 (COVID-19) began in Wuhan, China, in
December 2019, and has since spread worldwide. The novel coronavirus is now referred to as
severe and critical acute respiratory syndrome coronavirus-2 (SARS-CoV-2). The disease is
mild in 85% of cases but the remaining 15% requires hospitalization and/or intensive care.
Recent publications show that a variable number of COVID-19 patients are co-infected with one
or more pathogens. Most co-infections occurred within 1-4 days of onset of COVID-19 disease
and in a retrospective study, secondary infection was observed in 50% of non-survivor
patients.
In COVID-19 patients the elevated inflammatory cytokines and other inflammatory mediators
present suggest that a cytokine storm, also known as cytokine release syndrome (CRS), may
play a major role in the pathology of this disease. The elevated cytokine levels,
specifically IL-6, may also be responsible for the lethal complications of COVID-19.
Therefore, the interleukin-6 (IL-6) blockade has been proposed as one of the strategies to
manage COVID-19-induced CRS.
A considerable number of COVID-19 patients arrive to the Emergency rooms with mild-moderate
respiratory symptoms compatible with pneumonia of presumed bacterial origin not severe enough
for requiring hospitalization. It therefore seems reasonable to adopt therapeutic strategies
for these patients that are effective and easy to follow in the outpatient setting to avoid
overloading the Health System.
Cefditoren (CDN) is a third-generation cephalosporin for oral administration. CDN has a broad
spectrum of activity and is particularly active against the bacterial pathogens involved in
community respiratory tract infections. The results of clinical trials with CDN on
community-acquired pneumonia showed percentages of clinical and microbiological efficacy
around 85%. On the other hand, the use of CDN has been associated with a marked decrease in
circulating levels of IL-6 and other pro-inflammatory cytokines and mediators of epithelial
damage such as Krebs von den Lungen-6 (KL-6).
Considering the above and the current estate of knowledge against SARS-CoV-2, we have
considered of relevance to study the efficacy of CDN in a series of patients with
mild-moderate COVID-19 and with symptoms compatible with pneumonia of presumed bacterial
origin, seen at the Emergency room of a public hospital and followed on outpatient basis.
Drug: Cefditoren pivoxil 400mg
Cefditoren pivoxil 400mg bid for 7 days
Other Name: CDN-PI 400mg
Inclusion Criteria:
- Adult ≥18 years
- Positive for SARS CoV-2
- Radiological and clinical signs of mild-moderate pneumonia
- Fever ≥37.7 ºC
- Sat O2> 94% and respiratory rate <24 on admission
- Able of taking oral medication
- HIV negative
- Written and signed consent
Exclusion Criteria:
- Concomitant treatments with drugs of demonstrated or potential action against SARS
CoV-2 within the previous 24 hours.
- Alanine aminotransferase (ALT) or Aspartate aminotransferase (AST) > 5 times the upper
limit
- corrected QT (QTc) interval prolongation> 450 msg,
- Moderate or severe renal impairment (creatinine<50ml/min)
- Severe hepatic impairment (Child-Pugh C)
- Pregnancy or childbearing
- Allergy to penicillin or any other beta-lactam
- Primary carnitine deficiency
- Malabsorption or swallowing problems
- Inability to understand and follow study procedures
HU Henares
Coslada, Madrid, Spain
Cristóbal Rodríguez Leal, Dr, Principal Investigator
HU Henares