COVID-EC Study: Clinical Characteristics of Patients With COVID-19 in Guayaquil, Ecuador

Design: Retrospective cohort study that will review the data of patients seen in participating centers with a confirmed or probable diagnosis of COVID-19 between March and April 2020. Those patients who test positive for nasopharyngeal exudate for SARS-CoV-2 will be considered a confirmed case using the real-time reverse transcriptase polymerase chain reaction (RT-PCR) technique. A patient with a severe acute respiratory infection (with fever and who needs to be hospitalized), and without another etiology that fully explains the clinical manifestations, and who has traveled to or resided in China in the 14 days prior to the onset of symptoms, or a patient with any acute respiratory illness and in whom at least one of the following conditions is met in the last 14 days prior to the onset of symptoms: having contact with a confirmed or probable case of infection with the COVID-19 virus, or having worked or been in a health care facility where patients with confirmed or probable infection with the COVID-19 virus were being treated, according to WHO criteria. Cases with nasopharyngeal exudate for SARS-CoV-2 negative are excluded from the study.

Ambit: Emergency, hospitalization and intensive care services at participating centers.

Subjects to study: Patients older than 18 years with a confirmed or suspected diagnosis of COVID-19 that required admission at participating centers.

Study variables:

• Demographic variables: Age, Sex, Personal history (hypertension, diabetes, previous cardiovascular disease, previous chronic lung disease, active smoking, obesity, etc.).
• Clinical variables: previous contact with a confirmed or suspected COVID-19 patient, days of onset of symptoms until the first consultation, symptoms (fever, asthenia / deterioration of general condition, cough, dyspnea, anosmia, ageusia, diarrhea, nausea, headache), signs present in the first recorded physical examination (blood pressure, saturation, temperature, heart rate, respiratory rate, auscultation, edema, weight and height).
• Laboratory variables: blood count, C-reactive protein (PCR), procalcitonin (PCT), lactate dehydrogenase (LDH), D-dimer, Ferritin, AST, ALT, GGT, Alkaline phosphatase, coagulation times, creatinine, urea, sodium, potassium . Arterial blood gas when available.
• Radiological variables: findings on plain radiography and chest computed tomography (CT).
• Microbiological variables: nasopharyngeal exudate for SARS-CoV-2, sputum culture, bronchoalveolar lavage, blood cultures, urine culture.
• Prognostic variables: need for hospitalization, length of hospital stay, need for admission to the Intensive Surveillance Unit (LVU), length of stay at LVU, need for invasive or non-invasive mechanical ventilation (MV), development of respiratory distress syndrome (ARDS), pneumonia, severity of pneumonia (CURB-65), sepsis (qSOFA), renal failure, electrolytic disturbances, stroke, ischemic heart disease, pulmonary embolism (PE) or deep vein thrombosis (DVT) and death.
• Therapeutic variables: treatment administered (Hydroxychloroquine, Chloroquine, Azithromycin, Lopinavir / Ritonavir, Oseltamivir, Tocilizumab, Corticosteroids, Ivermectin, Nitaxozanide, Enoxaparin or other low molecular weight heparin), dose administered, drug combination, time of administration, (counting the days from the onset of symptoms), registered adverse effects.

Definitions: Fever is defined as axillary temperature greater than 37.5ºC. Lymphopenia is defined as the presence of <1500 cells / mm3. Thrombocytopenia is defined as the presence of <150,000 platelets / mm3. ARDS will be defined according to the Berlin criteria, CID according to the ISTH criteria, Pneumonia will be defined according to SEPAR criteria and its severity will be based on the CURB-65 scale. The rest of the variables that require a definition will be defined according to standard clinical practice.

Statistic analysis: The data will be collected in a Microsoft Excel database, and will be exported to the SPSS statistical package for mathematical analysis. The mean and standard deviation (SD) will be used as measures of centralization and dispersion, respectively, in the case of quantitative variables with normal distribution. In case of variables that do not present normal distribution, the median and the interquartile range (RIQ) will be used. The study of the normality of the distributions will be carried out using the Kolmogorov-Smirnov test. Qualitative variables will be expressed as percentages.

-Inferential: The independent means will be compared using the Student's t test for variables that follow a normal distribution, otherwise the Mann-Whitney U test will be used. The Wilcoxon test will be used for paired data. The association between qualitative variables will be evaluated by means of the Chi square test (χ2) (or Fisher's test, if applicable). In the hypothesis test it will require an error α less than 0.05 to reject the null hypothesis.

Ethical aspects: In the process and development of the present study, patients will not be contacted and only the information collected in the medical records will be accessed. These medical records will be used solely and exclusively for the purposes of the study.

The study presented here will follow the standards of Good Clinical Practice, the principles of the Declaration of Helsinki (Seoul 2013), and the Oviedo Convention (1997). No identifying or clinical data of the patients will be provided and the investigators will work on an anonymized and password protected file that does not allow traceability of the people included in the registry. Likewise, the handling of data will be carried out in accordance with the provisions of the Law on data protection and the Law on the rights and protection of the patient.

Informed consent: The investigators will request exemption from informed consent as it is considered disproportionate measures to call or make appointments for each of the patients or their families, taking into account that this is a retrospective study based on the review of medical records. The database will be anonymized in compliance with current legal regulations.