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2.
Med Sci Monit ; 27: e935379, 2021 Dec 30.
Artículo en Inglés | MEDLINE | ID: covidwho-1593238

RESUMEN

BACKGROUND This retrospective study aimed to investigate outcomes and hospitalization rates in patients with a confirmed diagnosis of early COVID-19 treated at home with prescribed and non-prescribed treatments. MATERIAL AND METHODS The medical records of a cohort of 158 Italian patients with early COVID-19 treated at home were analyzed. Treatments consisted of indomethacin, low-dose aspirin, omeprazole, and a flavonoid-based food supplement, plus azithromycin, low-molecular-weight heparin, and betamethasone as needed. The association of treatment timeliness and of clinical variables with the duration of symptoms and with the risk of hospitalization was evaluated by logistic regression. RESULTS Patients were divided into 2 groups: group 1 (n=85) was treated at the earliest possible time (<72 h from onset of symptoms), and group 2 (n=73) was treated >72 h after the onset of symptoms. Clinical severity at the beginning of treatment was similar in the 2 groups. In group 1, symptom duration was shorter than in group 2 (median 6.0 days vs 13.0 days, P<0.001) and no hospitalizations occurred, compared with 19.18% hospitalizations in group 2. One patient in group 1 developed chest X-ray alterations and 2 patients experienced an increase in D-dimer levels, compared with 30 and 22 patients, respectively, in group 2. The main factor determining the duration of symptoms and the risk of hospitalization was the delay in starting therapy (P<0.001). CONCLUSIONS This real-world study of patients in the community showed that early diagnosis and early supportive patient management reduced the severity of COVID-19 and reduced the rate of hospitalization.


Asunto(s)
Tratamiento Farmacológico de COVID-19 , COVID-19/diagnóstico , Hospitalización/estadística & datos numéricos , Tiempo de Tratamiento/estadística & datos numéricos , Anciano , Anciano de 80 o más Años , Aspirina/uso terapéutico , Betametasona/uso terapéutico , Estudios de Cohortes , Suplementos Dietéticos , Diagnóstico Precoz , Femenino , Flavonoides/uso terapéutico , Estudios de Seguimiento , Heparina de Bajo-Peso-Molecular/uso terapéutico , Humanos , Indometacina/uso terapéutico , Italia , Masculino , Persona de Mediana Edad , Omeprazol/uso terapéutico , Gravedad del Paciente , Estudios Retrospectivos , Medición de Riesgo , SARS-CoV-2 , Tiempo , Resultado del Tratamiento
3.
BMC Pharmacol Toxicol ; 22(1): 61, 2021 10 21.
Artículo en Inglés | MEDLINE | ID: covidwho-1477468

RESUMEN

BACKGROUND: The emergence and rapid spread of SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) in thelate 2019 has caused a devastating global pandemic of the severe pneumonia-like disease coronavirus disease 2019 (COVID-19). Although vaccines have been and are being developed, they are not accessible to everyone and not everyone can receive these vaccines. Also, it typically takes more than 10 years until a new therapeutic agent is approved for usage. Therefore, repurposing of known drugs can lend itself well as a key approach for significantly expediting the development of new therapies for COVID-19. METHODS: We have incorporated machine learning-based computational tools and in silico models into the drug discovery process to predict Adsorption, Distribution, Metabolism, Excretion, and Toxicity (ADMET) profiles of 90 potential drugs for COVID-19 treatment identified from two independent studies mainly with the purpose of mitigating late-phase failures because of inferior pharmacokinetics and toxicity. RESULTS: Here, we summarize the cardiotoxicity and general toxicity profiles of 90 potential drugs for COVID-19 treatment and outline the risks of repurposing and propose a stratification of patients accordingly. We shortlist a total of five compounds based on their non-toxic properties. CONCLUSION: In summary, this manuscript aims to provide a potentially useful source of essential knowledge on toxicity assessment of 90 compounds for healthcare practitioners and researchers to find off-label alternatives for the treatment for COVID-19. The majority of the molecules discussed in this manuscript have already moved into clinical trials and thus their known pharmacological and human safety profiles are expected to facilitate a fast track preclinical and clinical assessment for treating COVID-19.


Asunto(s)
Antivirales/toxicidad , Tratamiento Farmacológico de COVID-19 , Descubrimiento de Drogas , Reposicionamiento de Medicamentos , Animales , Antivirales/efectos adversos , Captopril/uso terapéutico , Cardiotoxinas/toxicidad , Catecoles/uso terapéutico , Biología Computacional , Sistema Enzimático del Citocromo P-450/metabolismo , Descubrimiento de Drogas/métodos , Humanos , Indometacina/uso terapéutico , Linezolid/uso terapéutico , Hígado/efectos de los fármacos , Ratones , Modelos Biológicos , Nitrilos/uso terapéutico , Ratas , Reproducción/efectos de los fármacos , Programas Informáticos , Ácido Valproico/uso terapéutico
4.
Expert Rev Anti Infect Ther ; 20(3): 383-390, 2022 Mar.
Artículo en Inglés | MEDLINE | ID: covidwho-1462214

RESUMEN

INTRODUCTION: COVID-19, a dreadful pandemic that has impacted human life like no other pathogenic invasion, has claimed the lives of over 100 million people. The need for effective treatment strategies is still a subject of intense research considering the rapidly evolving genome and continental diversity. Indomethacin is administered mostly as co-treatment for affected patients as a non-steroidal anti-inflammatory drug (NSAID). However, the underlying mechanism of action is unresolved. This study explores the basal mechanism of indomethacin and potency in alleviating the damage caused by SARS-CoV-2 and discusses the experimental and clinical efficacy in recent studies. AREAS COVERED: The literature search and system biology-based network formation were employed to describe the potent effects and risks associated with indomethacin in in-vitro, in-vivo, and clinical studies. This study also highlights the plausible mechanism of antiviral action of indomethacin with its apparent viral protein targets. The SARS-CoV-2 protein, the interacting host proteins, and the effect of indomethacin on this interactome as a standalone treatment or as part of a co-therapy strategy are particularly emphasized using network modeling. EXPERT OPINION: Indomethacin has demonstrated excellent clinical endpoint characteristics in several studies, and we recommend that it be utilized in the treatment of mild-to-moderate COVID patients.


Asunto(s)
Antivirales , Tratamiento Farmacológico de COVID-19 , Interacciones Huésped-Patógeno , Indometacina , SARS-CoV-2/efectos de los fármacos , Antivirales/farmacología , Antivirales/uso terapéutico , Humanos , Indometacina/farmacología , Indometacina/uso terapéutico
5.
Acta Neurol Belg ; 122(2): 465-469, 2022 Apr.
Artículo en Inglés | MEDLINE | ID: covidwho-1427443

RESUMEN

BACKGROUND: COVID-19, a disease caused by SARS-CoV-2, manifests with headache, both in the acute phase and as a post-infection symptom, which may be refractory to usual analgesics. OBJECTIVES: Investigate the therapeutic response of refractory COVID or post-COVID headache to indomethacin. METHODS: This was an observational, retrospective, open and uncontrolled. A sample of 37 patients diagnosed with COVID-19 presenting headache during the acute phase or after the resolution of the disease, with refractoriness to the usual symptomatic medication was treated with indomethacin. RESULTS: Of the 37 patients (24 women and 13 men), 29 were migraineurs and 8 had no previous history of headache. The average age was 40.4 ± 9.4 years, ranging from 19 to 65 years. In 26 (70.3%) patients, the onset of headache occurred within 72 h, and in 11 (29.7%), after 10 days of positivity for Sars-CoV-2. After treatment with indomethacin, 36 patients reported greater than 50% headache relief from the third day and 5 became asymptomatic on the fifth day. CONCLUSIONS: In patients with migraine or no prior history of headache who present with refractory COVID or post-COVID headache to common analgesics, anti-inflammatory drugs, and/or triptans, indomethacin should be considered a therapeutic option.


Asunto(s)
COVID-19 , Adulto , Analgésicos , COVID-19/complicaciones , Femenino , Cefalea/tratamiento farmacológico , Cefalea/etiología , Humanos , Indometacina/uso terapéutico , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , SARS-CoV-2
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