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1.
Revista Ibérica de Sistemas e Tecnologias de Informação ; - (E54):52-64, 2022.
Article in Portuguese | ProQuest Central | ID: covidwho-2319066

ABSTRACT

The objective of the research was to identify the barriers to telehealth adoption from the perspective of health professionals from the Military Police of the state of Pará in the Amazon. The analysis of evidence showed that of the seven aspects identified as barriers to the adoption of telehealth, the organizational issue was the most strongly pointed out. The main contribution of this research was the construction of a framework on the barriers to telehealth implementation in the view of health managers who serve regions with large territorial extensions. O Hospital Militar de Área de Sao Paulo (HMASP) já vem adotando essa prática realizando teleconsultas em campanha e até mesmo transmissao de cirurgias ao vivo.

2.
Emerg Infect Dis ; 29(3): 569-575, 2023 03.
Article in English | MEDLINE | ID: covidwho-2231947

ABSTRACT

We estimated comparative primary and booster vaccine effectiveness (VE) of SARS-CoV-2 Omicron BA.5 and BA.2 lineages against infection and disease progression. During April-June 2022, we implemented a case-case and cohort study and classified lineages using whole-genome sequencing or spike gene target failure. For the case-case study, we estimated the adjusted odds ratios (aORs) of vaccination using a logistic regression. For the cohort study, we estimated VE against disease progression using a penalized logistic regression. We observed no reduced VE for primary (aOR 1.07 [95% CI 0.93-1.23]) or booster (aOR 0.96 [95% CI 0.84-1.09]) vaccination against BA.5 infection. Among BA.5 case-patients, booster VE against progression to hospitalization was lower than that among BA.2 case-patients (VE 77% [95% CI 49%-90%] vs. VE 93% [95% CI 86%-97%]). Although booster vaccination is less effective against BA.5 than against BA.2, it offers substantial protection against progression from BA.5 infection to severe disease.


Subject(s)
COVID-19 Vaccines , COVID-19 , Humans , Portugal , Cohort Studies , SARS-CoV-2 , Disease Progression
3.
Adv Drug Deliv Rev ; 191: 114570, 2022 Dec.
Article in English | MEDLINE | ID: covidwho-2060294

ABSTRACT

Currently, there are over 100 antibody-based therapeutics on the market for the treatment of various diseases. The increasing importance of antibody treatment is further highlighted by the recent FDA emergency use authorization of certain antibody therapies for COVID-19 treatment. Protein-based materials have gained momentum for antibody delivery due to their biocompatibility, tunable chemistry, monodispersity, and straightforward synthesis and purification. In this review, we discuss progress in engineering the molecular features of protein-based biomaterials, in particular recombinant protein polymers, for introducing novel functionalities and enhancing the delivery properties of antibodies and related binding protein domains.


Subject(s)
COVID-19 Drug Treatment , Polymers , Humans , Polymers/chemistry , Nanotechnology , Biocompatible Materials/chemistry , Recombinant Proteins , Antibodies
4.
Revista Ibérica de Sistemas e Tecnologias de Informação ; - (E45):372-385, 2021.
Article in Portuguese | ProQuest Central | ID: covidwho-1777170

ABSTRACT

The heating of the market boosted the demand for professionals in the IT area, causing a movement of evasion of employees in search of more attractive jobs and offers. The Brazilian public sector had been hit hard by this phenomenon, suffering the loss of hired employees and occupants of commissioned positions in the information technology area. Keywords: Evasion of Professionals, Information Technology, Courts of Accounts, Covid. 1.Introduçao 0 surgimento do cenário de pandemia causado pelo Covid-19 fez com que diversas empresas investissem de forma mais acentuada no setor de tecnología e inovaçao como forma de prover seus serviços sob paralisaçao das atividades físicas. Uma pesquisa realizada por BR Angels/HSM/LearningVillage, Cenário Pós-Vacina denominada "o que podemos esperar dos negócios"4 , foi realizada durante o mes de março de 2021 e coletou respostas de 3.220 empresários e executivos do alto escalão de empresas de segmentos variados, como industria, varejo, serviços, startups e ONGs.

5.
Revista Ibérica de Sistemas e Tecnologias de Informação ; - (E45):358-371, 2021.
Article in Portuguese | ProQuest Central | ID: covidwho-1776991

ABSTRACT

A partir da triangulaçâo dos dados primários, da revisâo da literatura e do levantamento de dados estatísticos secundários, foi possível perceber que nao existe relaçâo positiva entre o grau de instruçâo dos usuários de smartphones e a confiabilidade imposta nas soluçoes mobiles disponibilizadas por Órgaos Públicos e privados, além dos dispositivos colaborativos, o que caracteriza a potencialidade e acessibilidade deste instrumento para a gestao remota da saúde em tempos de restriçoes sanitarias de contato social. : The unfolding of the Covid-19 Global Crisis directly impacted healthcare organizations around the world, leveraging technological innovations focused on care and remote medical monitoring, being important tools for crisis management. From the triangulation of primary data, the literature review, and the survey of secondary statistical data, it was possible to realize that there is no positive relationship between the level of education of smartphone users and the reliability imposed on mobile solutions made available by public and private agencies, as well as collaborative devices, which encourages the characterization of the potentiality and accessibility of this instrument for remote health management in times of sanitary restrictions on social contact. Keywords: Smartphone Applications;Remote Health Monitoring;Reliability;Crisis Management. 1.Introduçao A crise na saúde mundial causada pela propagaçao pandémica do vírus da Covid 19 vem marcando a humanidade de forma devastadora, produzindo desafios no gerenciamento de um cenário hostil e intimidador.

6.
Braz J Otorhinolaryngol ; 88(6): 982-989, 2022.
Article in English | MEDLINE | ID: covidwho-1525706

ABSTRACT

OBJECTIVE: Goiters and benign nodules detected in the thyroid are growing lesions and the COVID-19 pandemic have negatively impacted on their surgical treatment. The appropriate selection of patients to treatment will improve the overall health status. This article review will focus on the impact of the COVID-19 pandemic on treatment of benign conditions of the thyroid gland and their implications. METHODS: This review pointed out the status of the health system in developing country and the problems to treat benign surgical diseases of thyroid. Aspects of epidemiology, incidence, clinical presentation and surgical treatment of goiters, economic and health status impact were cited. RESULTS: All surgical treatment of goiter and other benign conditions were postponed, forced to redirect, and reschedule all benign surgeries, situation aggravated by poor public management and closure of hospital beds. These conditions have caused deterioration in patients' physical (decompensated thyroid disease) and mental health status, increasing work disabilities and burdening society by increasing the social and health cost. The overall situation could be catastrophic in emergent countries where this increased disease-related social expenditure on surgical treatment may increase the risk of national impoverishment as increase the treatment cost. Brazilian Society Head and Neck Surgery related some recommendations and new suggestions were made to safely treat these high potential hazard surgical conditions. CONCLUSIONS: Surgeries for goiter and benign thyroid conditions can be performed during the COVID-19 pandemic, following strict safety protocols for the patient and the medical team, reducing the negative economic and on patient health impact.


Subject(s)
COVID-19 , Goiter , Thyroid Diseases , Humans , Pandemics , Public Health , Thyroid Diseases/surgery , Goiter/surgery
7.
Br J Clin Pharmacol ; 87(9): 3425-3438, 2021 09.
Article in English | MEDLINE | ID: covidwho-1494607

ABSTRACT

AIMS: We propose the use of in silico mathematical models to provide insights that optimize therapeutic interventions designed to effectively treat respiratory infection during a pandemic. A modelling and simulation framework is provided using SARS-CoV-2 as an example, considering applications for both treatment and prophylaxis. METHODS: A target cell-limited model was used to quantify the viral infection dynamics of SARS-CoV-2 in a pooled population of 105 infected patients. Parameter estimates from the resulting model were used to simulate and compare the impact of various interventions against meaningful viral load endpoints. RESULTS: Robust parameter estimates were obtained for the basic reproduction number, viral release rate and infected-cell mortality from the infection model. These estimates were informed by the largest dataset currently available for SARS-CoV-2 viral time course. The utility of this model was demonstrated using simulations, which hypothetically introduced inhibitory or stimulatory drug mechanisms at various target sites within the viral life-cycle. We show that early intervention is crucial to achieving therapeutic benefit when monotherapy is administered. In contrast, combination regimens of two or three drugs may provide improved outcomes if treatment is initiated late. The latter is relevant to SARS-CoV-2, where the period between infection and symptom onset is relatively long. CONCLUSIONS: The use of in silico models can provide viral load predictions that can rationalize therapeutic strategies against an emerging viral pathogen.


Subject(s)
COVID-19 Drug Treatment , SARS-CoV-2 , Computer Simulation , Humans , Pandemics , SARS-CoV-2/drug effects , Viral Load
8.
Nat Commun ; 12(1): 6097, 2021 10 20.
Article in English | MEDLINE | ID: covidwho-1475295

ABSTRACT

Effective treatments against Severe Acute Respiratory Syndrome coronavirus 2 (SARS-CoV-2) are urgently needed. Monoclonal antibodies have shown promising results in patients. Here, we evaluate the in vivo prophylactic and therapeutic effect of COVA1-18, a neutralizing antibody highly potent against the B.1.1.7 isolate. In both prophylactic and therapeutic settings, SARS-CoV-2 remains undetectable in the lungs of treated hACE2 mice. Therapeutic treatment also causes a reduction in viral loads in the lungs of Syrian hamsters. When administered at 10 mg kg-1 one day prior to a high dose SARS-CoV-2 challenge in cynomolgus macaques, COVA1-18 shows very strong antiviral activity in the upper respiratory compartments. Using a mathematical model, we estimate that COVA1-18 reduces viral infectivity by more than 95% in these compartments, preventing lymphopenia and extensive lung lesions. Our findings demonstrate that COVA1-18 has a strong antiviral activity in three preclinical models and could be a valuable candidate for further clinical evaluation.


Subject(s)
Antibodies, Monoclonal/administration & dosage , Antibodies, Neutralizing/administration & dosage , Antiviral Agents/administration & dosage , COVID-19 Drug Treatment , SARS-CoV-2/immunology , Angiotensin-Converting Enzyme 2/genetics , Animals , Antibodies, Monoclonal/pharmacokinetics , Antiviral Agents/pharmacokinetics , COVID-19/blood , COVID-19/immunology , COVID-19/virology , Disease Models, Animal , Drug Evaluation, Preclinical , Female , Humans , Lung/metabolism , Lung/virology , Macaca fascicularis , Male , Mesocricetus , Mice , Mice, Transgenic , SARS-CoV-2/isolation & purification , Tissue Distribution , Viral Load
9.
Laryngoscope Investig Otolaryngol ; 6(5): 1044-1048, 2021 Oct.
Article in English | MEDLINE | ID: covidwho-1437063

ABSTRACT

BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and the resulting coronavirus disease 2019 (COVID-19) have afflicted hundreds of millions of people in a worldwide pandemic. During this pandemic, otolaryngologists have sought to better understand risk factors associated with COVID-19 contamination during surgical procedures involving the airways such as tracheostomies. OBJECTIVE: This study provides a standardized technique of performing an ultrasound (US)-guided percutaneous dilatational tracheostomy (PDT) on COVID-19 patients in the intensive care unit (ICU). It also outlines safety strategies for health care providers that includes proper use of personal protective equipment (PPE) and regular testing of otolaryngologists for COVID-19 contamination. METHODS: This study analyzed data from 44 PDT procedures performed on COVID-19 patients in the ICU of hospitals in Sao Paulo and Santos, Brazil. The PDT procedures were conducted between April 2020 and August 2020, which coincided with a peak of the COVID-19 pandemic in São Paulo, Brazil. Surgeons were tested for COVID-19 using a two-stage serological enzyme-linked immunosorbent assay specific for SARS-CoV-2 antigens. CONCLUSION: This study describes a safe standardized technique of US-guided PDT for COVID-19 patients in the ICU using a method that also decreases the risk of surgeon contamination.

10.
Br J Clin Pharmacol ; 87(9): 3439-3450, 2021 09.
Article in English | MEDLINE | ID: covidwho-1373788

ABSTRACT

AIM: We hypothesized that viral kinetic modelling could be helpful to prioritize rational drug combinations for COVID-19. The aim of this research was to use a viral cell cycle model of SARS-CoV-2 to explore the potential impact drugs, or combinations of drugs, that act at different stages in the viral life cycle might have on various metrics of infection outcome relevant in the early stages of COVID-19 disease. METHODS: Using a target-cell limited model structure that has been used to characterize viral load dynamics from COVID-19 patients, we performed simulations to inform on the combinations of therapeutics targeting specific rate constants. The endpoints and metrics included viral load area under the curve (AUC), duration of viral shedding and epithelial cells infected. Based on the known kinetics of the SARS-CoV-2 life cycle, we rank ordered potential targeted approaches involving repurposed, low-potency agents. RESULTS: Our simulations suggest that targeting multiple points central to viral replication within infected host cells or release from those cells is a viable strategy for reducing both viral load and host cell infection. In addition, we observed that the time-window opportunity for a therapeutic intervention to effect duration of viral shedding exceeds the effect on sparing epithelial cells from infection or impact on viral load AUC. Furthermore, the impact on reduction on duration of shedding may extend further in patients who exhibit a prolonged shedder phenotype. CONCLUSIONS: Our work highlights the use of model-informed drug repurposing approaches to better rationalize effective treatments for COVID-19.


Subject(s)
COVID-19 Drug Treatment , Drug Repositioning , SARS-CoV-2 , Drug Combinations , Humans , Kinetics , SARS-CoV-2/drug effects
11.
PLoS Comput Biol ; 17(3): e1008785, 2021 03.
Article in English | MEDLINE | ID: covidwho-1181165

ABSTRACT

Non-human primates infected with SARS-CoV-2 exhibit mild clinical signs. Here we used a mathematical model to characterize in detail the viral dynamics in 31 cynomolgus macaques for which nasopharyngeal and tracheal viral load were frequently assessed. We identified that infected cells had a large burst size (>104 virus) and a within-host reproductive basic number of approximately 6 and 4 in nasopharyngeal and tracheal compartment, respectively. After peak viral load, infected cells were rapidly lost with a half-life of 9 hours, with no significant association between cytokine elevation and clearance, leading to a median time to viral clearance of 10 days, consistent with observations in mild human infections. Given these parameter estimates, we predict that a prophylactic treatment blocking 90% of viral production or viral infection could prevent viral growth. In conclusion, our results provide estimates of SARS-CoV-2 viral kinetic parameters in an experimental model of mild infection and they provide means to assess the efficacy of future antiviral treatments.


Subject(s)
COVID-19/virology , Macaca fascicularis/virology , SARS-CoV-2/physiology , Animals , Antiviral Agents/pharmacology , Basic Reproduction Number , COVID-19/blood , COVID-19/prevention & control , Cytokines/blood , Disease Models, Animal , Nasopharynx/virology , SARS-CoV-2/drug effects , Trachea/virology , Viral Load , Virus Replication/drug effects
12.
Euro Surveill ; 26(10)2021 03.
Article in English | MEDLINE | ID: covidwho-1136424

ABSTRACT

We show that the SARS-CoV-2 B.1.1.7 lineage is highly disseminated in Portugal, with the odds of B.1.1.7 proportion increasing at an estimated 89% (95% confidence interval: 83-95%) per week until week 3 2021. RT-PCR spike gene target late detection (SGTL) can constitute a useful surrogate to track B.1.1.7 spread, besides the spike gene target failure (SGTF) proxy. SGTL/SGTF samples were associated with statistically significant higher viral loads, but not with substantial shift in age distribution compared to non-SGTF/SGTL cases.


Subject(s)
COVID-19/virology , SARS-CoV-2/genetics , COVID-19/transmission , Humans , Portugal/epidemiology , Spike Glycoprotein, Coronavirus/genetics
13.
PLoS Comput Biol ; 17(3): e1008752, 2021 03.
Article in English | MEDLINE | ID: covidwho-1110080

ABSTRACT

Repurposed drugs that are safe and immediately available constitute a first line of defense against new viral infections. Despite limited antiviral activity against SARS-CoV-2, several drugs are being tested as medication or as prophylaxis to prevent infection. Using a stochastic model of early phase infection, we evaluate the success of prophylactic treatment with different drug types to prevent viral infection. We find that there exists a critical efficacy that a treatment must reach in order to block viral establishment. Treatment by a combination of drugs reduces the critical efficacy, most effectively by the combination of a drug blocking viral entry into cells and a drug increasing viral clearance. Below the critical efficacy, the risk of infection can nonetheless be reduced. Drugs blocking viral entry into cells or enhancing viral clearance reduce the risk of infection more than drugs that reduce viral production in infected cells. The larger the initial inoculum of infectious virus, the less likely is prevention of an infection. In our model, we find that as long as the viral inoculum is smaller than 10 infectious virus particles, viral infection can be prevented almost certainly with drugs of 90% efficacy (or more). Even when a viral infection cannot be prevented, antivirals delay the time to detectable viral loads. The largest delay of viral infection is achieved by drugs reducing viral production in infected cells. A delay of virus infection flattens the within-host viral dynamic curve, possibly reducing transmission and symptom severity. Thus, antiviral prophylaxis, even with reduced efficacy, could be efficiently used to prevent or alleviate infection in people at high risk.


Subject(s)
Antiviral Agents/therapeutic use , COVID-19 Drug Treatment , COVID-19/prevention & control , SARS-CoV-2 , Antiviral Agents/administration & dosage , Basic Reproduction Number/statistics & numerical data , COVID-19/transmission , COVID-19/virology , Computational Biology , Drug Repositioning , Drug Therapy, Combination , Host Microbial Interactions/drug effects , Host Microbial Interactions/immunology , Humans , Models, Biological , Pandemics/prevention & control , Primary Prevention/methods , Risk Factors , SARS-CoV-2/drug effects , SARS-CoV-2/pathogenicity , SARS-CoV-2/physiology , Stochastic Processes , Time Factors , Treatment Outcome , Viral Load/drug effects , Virus Internalization/drug effects , Virus Replication/drug effects
14.
Revista Ibérica de Sistemas e Tecnologias de Informação ; - (E41):221-231, 2021.
Article in Portuguese | ProQuest Central | ID: covidwho-1102986

ABSTRACT

The results found in this research were unanimous regarding the lack of user involvement in the system, the very low formal training, the impact on the quality and waste of information due to the lack of integration between systems and the high risk of their degradation. In the current moment of COVID-19, the only resource that manages to connect people to their needs is technology not only as a collaboration tool, but as an information system, reducing the gap and becoming a critical success factor. Keywords: Resistance, Hospital Information System, COVID-19. 1.Introdução Os efeitos da nova pandemia mundial, o COVID 19, transformará definitivamente a maneira como a medicina é praticada hoje. Information System Resistance e os filtros: "open acess", "all years", "open access", "subject áreas": computer science, business management e decision sciences tendo sido encontrados 11 artigos.

15.
Am J Otolaryngol ; 41(6): 102694, 2020.
Article in English | MEDLINE | ID: covidwho-731702

ABSTRACT

PURPOSE: Head and neck surgeons are among the highest risk for COVID-19 exposure, which also brings great risk to their mental wellbeing. In this study, we aim to evaluate mental health symptoms among head and neck surgeons in Brazil surrounding the time it was declared the epicenter of the virus. MATERIALS AND METHODS: A cross-sectional, survey-based study evaluating burnout, anxiety, distress, and depression among head and neck surgeons in Brazil, assessed through the single-item Mini-Z burnout assessment, 7-item Generalized Anxiety Disorder scale, 22-item Impact of Event Scale-Revised, and 2-item Patient Health Questionnaire, respectively. RESULTS: 163 physicians completed the survey (74.2% males). Anxiety, distress, burnout, and depression symptoms were reported in 74 (45.5%), 43 (26.3%), 24 (14.7%), and 26 (16.0%) physicians, respectively. On multivariable analysis, female physicians were more likely to report a positive screening for burnout compared to males (OR 2.88, CI [1.07-7.74]). Physicians 45 years or older were less likely to experience anxiety symptoms than those younger than 45 years (OR 0.40, CI [0.20-0.81]). Physicians with no self-reported prior psychiatric conditions were less likely to have symptoms of distress compared to those with such history (OR 0.11, CI [0.33-0.38]). CONCLUSION: Head and neck surgeons in Brazil reported symptoms of burnout, anxiety, distress and depression during our study period within the COVID-19 pandemic. Institutions should monitor these symptoms throughout the pandemic. Further study is required to assess the long-term implications for physician wellness.


Subject(s)
Anxiety/epidemiology , Burnout, Professional/epidemiology , Coronavirus Infections/epidemiology , Depression/epidemiology , Occupational Stress/epidemiology , Otolaryngologists/psychology , Pneumonia, Viral/epidemiology , Surgeons/psychology , Adult , Age Factors , Aged , Betacoronavirus , Brazil/epidemiology , COVID-19 , Cross-Sectional Studies , Female , Humans , Male , Middle Aged , Pandemics , SARS-CoV-2 , Sex Factors , Stress, Psychological/epidemiology , Surveys and Questionnaires
16.
Nature ; 585(7826): 584-587, 2020 09.
Article in English | MEDLINE | ID: covidwho-664587

ABSTRACT

Coronavirus disease 2019 (COVID-19) has rapidly become a global pandemic and no antiviral drug or vaccine is yet available for the treatment of this disease1-3. Several clinical studies are ongoing to evaluate the efficacy of repurposed drugs that have demonstrated antiviral efficacy in vitro. Among these candidates, hydroxychloroquine (HCQ) has been given to thousands of individuals infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-the virus that causes COVID-19-worldwide but there is no definitive evidence that HCQ is effective for treating COVID-194-7. Here we evaluated the antiviral activity of HCQ both in vitro and in SARS-CoV-2-infected macaques. HCQ showed antiviral activity in African green monkey kidney cells (Vero E6) but not in a model of reconstituted human airway epithelium. In macaques, we tested different treatment strategies in comparison to a placebo treatment, before and after peak viral load, alone or in combination with azithromycin (AZTH). Neither HCQ nor the combination of HCQ and AZTH showed a significant effect on viral load in any of the analysed tissues. When the drug was used as a pre-exposure prophylaxis treatment, HCQ did not confer protection against infection with SARS-CoV-2. Our findings do not support the use of HCQ, either alone or in combination with AZTH, as an antiviral drug for the treatment of COVID-19 in humans.


Subject(s)
Betacoronavirus/drug effects , Coronavirus Infections/drug therapy , Coronavirus Infections/virology , Hydroxychloroquine/therapeutic use , Pneumonia, Viral/drug therapy , Pneumonia, Viral/virology , Animals , Azithromycin/pharmacology , Azithromycin/therapeutic use , COVID-19 , Chlorocebus aethiops , Coronavirus Infections/pathology , Coronavirus Infections/physiopathology , Cytokines/blood , Disease Models, Animal , Female , Humans , Hydroxychloroquine/pharmacokinetics , Hydroxychloroquine/pharmacology , In Vitro Techniques , Kinetics , Macaca fascicularis , Male , Pandemics , Pneumonia, Viral/pathology , Pneumonia, Viral/physiopathology , Pre-Exposure Prophylaxis , Respiratory Mucosa/cytology , Respiratory Mucosa/drug effects , Respiratory Mucosa/virology , SARS-CoV-2 , Time Factors , Treatment Failure , Vero Cells , Viral Load/drug effects , COVID-19 Drug Treatment
17.
CPT Pharmacometrics Syst Pharmacol ; 9(9): 509-514, 2020 09.
Article in English | MEDLINE | ID: covidwho-603799

ABSTRACT

We modeled the viral dynamics of 13 untreated patients infected with severe acute respiratory syndrome-coronavirus 2 to infer viral growth parameters and predict the effects of antiviral treatments. In order to reduce peak viral load by more than two logs, drug efficacy needs to be > 90% if treatment is administered after symptom onset; an efficacy of 60% could be sufficient if treatment is initiated before symptom onset. Given their pharmacokinetic/pharmacodynamic properties, current investigated drugs may be in a range of 6-87% efficacy. They may help control virus if administered very early, but may not have a major effect in severely ill patients.


Subject(s)
Antiviral Agents/therapeutic use , COVID-19 Drug Treatment , SARS-CoV-2/physiology , Antiviral Agents/pharmacology , Humans , Lopinavir/pharmacology , Lopinavir/therapeutic use , Models, Theoretical , Ritonavir/pharmacology , Ritonavir/therapeutic use , SARS-CoV-2/drug effects , Severity of Illness Index , Singapore , Treatment Outcome , Viral Load/drug effects
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