837 results on '"Viral therapy"'
Search Results
2. Genetics of Viral Resistance: Clinical Relevance and Role in Viral Disease Outbreak
- Author
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Shenge, Juliet Adamma, Abia, Akebe Luther King, editor, and Essack, Sabiha Yusuf, editor
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- 2023
- Full Text
- View/download PDF
3. Leading Edge: Intratumor Delivery of Monoclonal Antibodies for the Treatment of Solid Tumors.
- Author
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Blanco, Ester, Chocarro, Luisa, Fernández-Rubio, Leticia, Bocanegra, Ana, Arasanz, Hugo, Echaide, Miriam, Garnica, Maider, Piñeiro-Hermida, Sergio, Kochan, Grazyna, and Escors, David
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MONOCLONAL antibodies , *TUMOR treatment , *IMMUNE checkpoint proteins , *GENE therapy , *TREATMENT effectiveness , *NANOMEDICINE - Abstract
Immunotherapies based on immune checkpoint blockade have shown remarkable clinical outcomes and durable responses in patients with many tumor types. Nevertheless, these therapies lack efficacy in most cancer patients, even causing severe adverse events in a small subset of patients, such as inflammatory disorders and hyper-progressive disease. To diminish the risk of developing serious toxicities, intratumor delivery of monoclonal antibodies could be a solution. Encouraging results have been shown in both preclinical and clinical studies. Thus, intratumor immunotherapy as a new strategy may retain efficacy while increasing safety. This approach is still an exploratory frontier in cancer research and opens up new possibilities for next-generation personalized medicine. Local intratumor delivery can be achieved through many means, but an attractive approach is the use of gene therapy vectors expressing mAbs inside the tumor mass. Here, we summarize basic, translational, and clinical results of intratumor mAb delivery, together with descriptions of non-viral and viral strategies for mAb delivery in preclinical and clinical development. Currently, this is an expanding research subject that will surely play a key role in the future of oncology. [ABSTRACT FROM AUTHOR]
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- 2023
- Full Text
- View/download PDF
4. The role of hyperbaric oxygenotherapy (HBOT) in the treatment of COVID-19 patients
- Author
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Sead Žiga, Dejan Andrić, Sanja Jurić Banai, Kristina Franjić, Dragan Vujović, Eva Pleško, Dživo Ljubičić, Nevenka Piskač Živković, and Marko Banić
- Subjects
covid-19 – complications ,therapy ,hyperbaric oxygenation ,pneumonia ,viral therapy ,hypoxia ,treatment outcome ,sars-cov-2 ,Medicine (General) ,R5-920 - Abstract
The COVID-19 pandemic has posed a major challenge to modern medicine. Despite significant efforts by the medical and scientific community, at the time of writing, there is still no targeted etiological treatment for acutely ill COVID-19 patients as well as patients with post-COVID syndrome. Hyperbaric oxygen therapy (HBOT) is a medically and scientifically recognized therapeutic procedure in the treatment of a number of acute and chronic conditions in which oxygen deficiency is pathophysiologically primary disorder. Given the several published series of cases that have shown a significant beneficial effect of HBOT in the treatment of patients with COVID-19 infection, and based on decades of experience in the use of HBOT in other fields, the need to conduct quality and well-structured studies arose with the aim to clearly examine the impact of HBOT use in the treatment of COVID-19 patients. According to available sources, nine such studies are being conducted worldwide.The mechanisms of the effect of HBOT in the treatment of COVID-19 patients are based on the correction of hypoxia, attenuation of the inflammatory response and “repayment of oxygen debt” in a short period of time, thus providing a window to aerobic metabolism in deeply hypoxic tissues and important organs.
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- 2021
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- View/download PDF
5. Novel Techniques and the Future of HIPEC (Immunotherapy, Viral Therapy)
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Beane, Joal D., Bartlett, David L., Fong, Yuman, editor, Gamblin, T. Clark, editor, Han, Ernest S., editor, Lee, Byrne, editor, and Zager, Jonathan S., editor
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- 2020
- Full Text
- View/download PDF
6. Immunotherapy in Glioblastoma: Current Approaches and Future Perspectives.
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Sener, Ugur, Ruff, Michael W., and Campian, Jian L.
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GENETIC vectors , *ELECTRIC field therapy , *GLIOBLASTOMA multiforme , *CHIMERIC antigen receptors , *BRAIN tumors , *IMMUNOTHERAPY , *CYTOTOXIC T cells - Abstract
Glioblastoma (GBM) is the most common malignant brain tumor. Despite multimodality treatment with surgical resection, radiation therapy, chemotherapy, and tumor treating fields, recurrence is universal, median observed survival is low at 8 months and 5-year overall survival is poor at 7%. Immunotherapy aims to generate a tumor-specific immune response to selectively eliminate tumor cells. In treatment of GBM, immunotherapy approaches including use of checkpoint inhibitors, chimeric antigen receptor (CAR) T-Cell therapy, vaccine-based approaches, viral vector therapies, and cytokine-based treatment has been studied. While there have been no major breakthroughs to date and broad implementation of immunotherapy for GBM remains elusive, multiple studies are underway. In this review, we discuss immunotherapy approaches to GBM with an emphasis on molecularly informed approaches. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
7. Glioblastoma: Pitfalls and Opportunities of Immunotherapeutic Combinations.
- Author
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Niedbała, Marcin, Malarz, Katarzyna, Sharma, Gitanjali, Kramer-Marek, Gabriela, and Kaspera, Wojciech
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IMMUNE checkpoint inhibitors , *GLIOBLASTOMA multiforme , *THERAPEUTICS , *TUMOR microenvironment , *VIRAL genes - Abstract
Glioblastoma multiforme (GBM) is the most common and aggressive primary central nervous system tumour in adults. It has extremely poor prognosis since the current standard of care, comprising of gross total resection and temozolomide (TMZ) chemoradiotherapy, prolongs survival, but does not provide a durable response. To a certain extent, this is due to GBM's heterogeneous, hostile and cold tumour microenvironment (TME) and the unique ability of GBM to overcome the host's immune responses. Therefore, there is an urgent need to develop more effective therapeutic approaches. This review provides critical insights from completed and ongoing clinical studies investigating novel immunotherapy strategies for GBM patients, ranging from the use of immune checkpoint inhibitors in different settings of GBM treatment to novel combinatorial therapies. In particular, we discuss how treatment regimens based on single antigen peptide vaccines evolved into fully personalised, polyvalent cell-based vaccines, CAR-T cell, and viral or gene therapies. Furthermore, the results of the most influential clinical trials and a selection of innovative preclinical studies aimed at activating the immunologically cold GBM microenvironment are reviewed. [ABSTRACT FROM AUTHOR]
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- 2022
- Full Text
- View/download PDF
8. Leading Edge: Intratumor Delivery of Monoclonal Antibodies for the Treatment of Solid Tumors
- Author
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Ester Blanco, Luisa Chocarro, Leticia Fernández-Rubio, Ana Bocanegra, Hugo Arasanz, Miriam Echaide, Maider Garnica, Sergio Piñeiro-Hermida, Grazyna Kochan, and David Escors
- Subjects
monoclonal antibodies (mAbs) ,intratumoral therapy ,viral therapy ,non-viral therapy ,Biology (General) ,QH301-705.5 ,Chemistry ,QD1-999 - Abstract
Immunotherapies based on immune checkpoint blockade have shown remarkable clinical outcomes and durable responses in patients with many tumor types. Nevertheless, these therapies lack efficacy in most cancer patients, even causing severe adverse events in a small subset of patients, such as inflammatory disorders and hyper-progressive disease. To diminish the risk of developing serious toxicities, intratumor delivery of monoclonal antibodies could be a solution. Encouraging results have been shown in both preclinical and clinical studies. Thus, intratumor immunotherapy as a new strategy may retain efficacy while increasing safety. This approach is still an exploratory frontier in cancer research and opens up new possibilities for next-generation personalized medicine. Local intratumor delivery can be achieved through many means, but an attractive approach is the use of gene therapy vectors expressing mAbs inside the tumor mass. Here, we summarize basic, translational, and clinical results of intratumor mAb delivery, together with descriptions of non-viral and viral strategies for mAb delivery in preclinical and clinical development. Currently, this is an expanding research subject that will surely play a key role in the future of oncology.
- Published
- 2023
- Full Text
- View/download PDF
9. Brd4 Inactivation Increases Adenoviral Delivery of BMP2 for Paracrine Stimulation of Osteogenic Differentiation as a Gene Therapeutic Concept to Enhance Bone Healing.
- Author
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Paradise, Christopher R, De La Vega, Rodolfo E, Galvan, M Lizeth, Carrasco, Margarita E, Thaler, Roman, van Wijnen, Andre J, and Dudakovic, Amel
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GREEN fluorescent protein ,GENE expression ,HEALING ,TRANSGENE expression ,MESENCHYMAL stem cells ,BONE growth ,PARACRINE mechanisms ,HISTONES - Abstract
Bromodomain (BRD) proteins are histone code interpreters that recognize acetylated lysines and link the dynamic state of chromatin with the transcriptional machinery. Here, we demonstrate that ablation of the Brd4 gene in primary mouse bone marrow–derived mesenchymal stem cells via a conditional Brd4fl/fl allele suppresses osteogenic lineage commitment. Remarkably, loss of Brd4 function also enhances expression of genes in engineered adenoviral vectors, including Cre recombinase and green fluorescent protein (GFP). Similarly, vector‐based expression of BMP2 mRNA and protein levels are enhanced upon Brd4 depletion in cells transduced with an adenoviral vector that expresses BMP2 (Ad‐BMP2). Importantly, Brd4 depletion in MC3T3‐E1 and human adipose‐derived mesenchymal stem cells (AMSCs) transduced with Ad‐BMP2 enhances osteogenic differentiation of naïve MC3T3‐E1 cells via paracrine mechanisms based on transwell and conditioned medium studies. Our studies indicate that Brd4 depletion enhances adenoviral transgene expression in mammalian cells, which can be leveraged as a therapeutic strategy to improve viral vector‐based gene therapies. © 2021 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research. [ABSTRACT FROM AUTHOR]
- Published
- 2021
- Full Text
- View/download PDF
10. Brd4 Inactivation Increases Adenoviral Delivery of BMP2 for Paracrine Stimulation of Osteogenic Differentiation as a Gene Therapeutic Concept to Enhance Bone Healing
- Author
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Christopher R Paradise, Rodolfo E De La Vega, M Lizeth Galvan, Margarita E Carrasco, Roman Thaler, Andre J vanWijnen, and Amel Dudakovic
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ADENOVIRUS ,BMP2 ,BRD4 ,EPIGENETICS ,OSTEOGENESIS ,VIRAL THERAPY ,Orthopedic surgery ,RD701-811 ,Diseases of the musculoskeletal system ,RC925-935 - Abstract
ABSTRACT Bromodomain (BRD) proteins are histone code interpreters that recognize acetylated lysines and link the dynamic state of chromatin with the transcriptional machinery. Here, we demonstrate that ablation of the Brd4 gene in primary mouse bone marrow–derived mesenchymal stem cells via a conditional Brd4fl/fl allele suppresses osteogenic lineage commitment. Remarkably, loss of Brd4 function also enhances expression of genes in engineered adenoviral vectors, including Cre recombinase and green fluorescent protein (GFP). Similarly, vector‐based expression of BMP2 mRNA and protein levels are enhanced upon Brd4 depletion in cells transduced with an adenoviral vector that expresses BMP2 (Ad‐BMP2). Importantly, Brd4 depletion in MC3T3‐E1 and human adipose‐derived mesenchymal stem cells (AMSCs) transduced with Ad‐BMP2 enhances osteogenic differentiation of naïve MC3T3‐E1 cells via paracrine mechanisms based on transwell and conditioned medium studies. Our studies indicate that Brd4 depletion enhances adenoviral transgene expression in mammalian cells, which can be leveraged as a therapeutic strategy to improve viral vector‐based gene therapies. © 2021 The Authors. JBMR Plus published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research.
- Published
- 2021
- Full Text
- View/download PDF
11. Phase Ib Study of Axatilimab in Combination With Olaparib in BRCA1/2 and PALB2- Associated Metastatic HER2-negative Breast Cancer.
- Abstract
This document provides information about a clinical trial for the drug Axatilimab in the treatment of metastatic or unresectable HER2 negative breast cancer. The trial will use a Bayesian Optimal Interval design to determine the maximum tolerated dose of Axatilimab. Participants will undergo various assessments and must meet specific eligibility criteria to participate. The trial is not yet recruiting and is expected to be completed by March 2029. The study is being conducted by the Dana-Farber Cancer Institute in collaboration with Incyte Corporation. [Extracted from the article]
- Published
- 2024
12. Patent Application Titled "Methods For Determining Tumor Immune Status" Published Online (USPTO 20240180984).
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IMMUNITY ,PATENT applications ,IMMUNOLOGIC memory ,BONE marrow cells ,PATTERN perception receptors - Abstract
A patent application titled "Methods For Determining Tumor Immune Status" has been published online. The inventors have developed a novel immune competence blood test that can determine if cancer growth or standard cancer therapy compromises innate and adaptive immune function. The test involves measuring the level of inflammatory cytokines in a patient sample after exposure to an innate immune agonist. This information can predict the patient's responsiveness to immunotherapy. The method can also be used to select patients for oncolytic viral therapy based on the level of antibodies specific to a viral antigen in their serum sample. [Extracted from the article]
- Published
- 2024
13. Influence of Zika virus on the cytotoxicity, cell adhesion, apoptosis and inflammatory markers of glioblastoma cells.
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Marinowic, Daniel Rodrigo, Zanirati, Gabriele Goulart, Azevedo, Pamella Nunes, Zanatta, Ângela, Plentz, Ismael, Alcará, Allan Marinho, Morrone, Fernanda Bueno, Scheffel, Thamiris Becker, Cappellari, Angélica Regina, Roehe, Paulo Michel, Muterle Varela, Ana Paula, Machado, Denise Cantarelli, Spillari Viola, Fabiana, and Da Costa, Jaderson Costa
- Subjects
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PYROPTOSIS , *ZIKA virus , *CELL adhesion , *CYTOTOXINS , *ZIKA virus infections , *BRAIN tumors - Abstract
Glioblastoma (GBM) is one of the most common types of brain tumor in adults. Despite the availability of treatments for this disease, GBM remains one of the most lethal and difficult types of tumors to treat, and thus, a majority of patients die within 2 years of diagnosis. Infection with Zika virus (ZIKV) inhibits cell proliferation and induces apoptosis, particularly in developing neuronal cells, and thus could potentially be considered an alternative for GBM treatment. In the present study, two GBM cell lines (U-138 and U-251) were infected with ZIKV at different multiplicities of infection (0.1, 0.01 and 0.001), and cell viability, migration, adhesion, induction of apoptosis, interleukin levels and CD14/CD73 cell surface marker expression were analyzed. The present study demonstrated that ZIKV infection promoted loss of cell viability and increased apoptosis in U-138 cells, as measured by MTT and triplex assay, respectively. Changes in cell migration, as determined by wound healing assay, were not observed; however, the GBM cell lines exhibited an increase in cell adhesion when compared with non-tumoral cells (Vero). The Luminex immunoassay showed a significant increase in the expression levels of IL-4 specifically in U-251 cells (MOI 0.001) following exposure to ZIKV. There was no significant change in the expression levels of IFN-γ upon ZIKV infection in the cell lines tested. Furthermore, a marked increase in the percentage of cells expressing the CD14 surface marker was observed in both GBM cell lines compared with in Vero cells; and significantly increased CD73 expression was observed particularly in U-251 cells, when compared with uninfected cells. These findings indicate that ZIKV infection could lead to reduced cell viability, elevated CD73 expression, improved cellular adherence, and higher rates of apoptosis in glioblastoma cells. Further studies are required to explore the potential use of ZIKV in the treatment of GBM. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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14. Immunotherapy in Glioblastoma: Current Approaches and Future Perspectives
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Ugur Sener, Michael W. Ruff, and Jian L. Campian
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glioblastoma ,immunotherapy ,checkpoint inhibitor ,CAR T ,vaccine therapy ,viral therapy ,Biology (General) ,QH301-705.5 ,Chemistry ,QD1-999 - Abstract
Glioblastoma (GBM) is the most common malignant brain tumor. Despite multimodality treatment with surgical resection, radiation therapy, chemotherapy, and tumor treating fields, recurrence is universal, median observed survival is low at 8 months and 5-year overall survival is poor at 7%. Immunotherapy aims to generate a tumor-specific immune response to selectively eliminate tumor cells. In treatment of GBM, immunotherapy approaches including use of checkpoint inhibitors, chimeric antigen receptor (CAR) T-Cell therapy, vaccine-based approaches, viral vector therapies, and cytokine-based treatment has been studied. While there have been no major breakthroughs to date and broad implementation of immunotherapy for GBM remains elusive, multiple studies are underway. In this review, we discuss immunotherapy approaches to GBM with an emphasis on molecularly informed approaches.
- Published
- 2022
- Full Text
- View/download PDF
15. Viral Gene Therapy for Glioblastoma Multiforme: A Promising Hope for the Current Dilemma
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Junsheng Li, Wen Wang, Jia Wang, Yong Cao, Shuo Wang, and Jizong Zhao
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gene therapy ,viral therapy ,glioblastoma multiforme ,viral vector ,treatment strategy ,Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,RC254-282 - Abstract
Glioblastoma multiforme (GBM), as one of the most common malignant brain tumors, was limited in its treatment effectiveness with current options. Its invasive and infiltrative features led to tumor recurrence and poor prognosis. Effective treatment and survival improvement have always been a challenge. With the exploration of genetic mutations and molecular pathways in neuro-oncology, gene therapy is becoming a promising therapeutic approach. Therapeutic genes are delivered into target cells with viral vectors to act specific antitumor effects, which can be used in gene delivery, play an oncolysis effect, and induce host immune response. The application of engineering technology makes the virus vector used in genetics a more prospective future. Recent advances in viral gene therapy offer hope for treating brain tumors. In this review, we discuss the types and designs of viruses as well as their study progress and potential applications in the treatment of GBM. Although still under research, viral gene therapy is promising to be a new therapeutic approach for GBM treatment in the future.
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- 2021
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16. Immuno-Oncology: New Insights into Targets and Therapies.
- Author
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Schokrpur S, White MG, Roland CL, and Patel SP
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- Humans, Immunotherapy methods, Medical Oncology, T-Lymphocytes, Neoplasms therapy, Vaccines
- Abstract
The role of immunotherapy in the care of surgical oncology patients promises to expand as investigators and clinicians evaluate new targets and approaches. Currently active clinical trials evaluate new immune checkpoints, including lymphocyte activation gene 3, T cell immunoreceptor with Ig and ITIM domains, and killer Ig-like receptor 2DL1/2L3. Vaccines delivered through mRNA have demonstrated exciting results in early clinical trials and hold promise for expanded application. Investigational approaches include dendritic cell vaccines, peptide vaccines, cytokines therapies, and cellular therapies. These studies have the potential to revolutionize the management of surgical oncology patients and promote durable cures following surgical resection., Competing Interests: Disclosure The authors have nothing to disclose., (Copyright © 2023 Elsevier Inc. All rights reserved.)
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- 2024
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17. A Phase I/II Single-arm Trial of Azenosertib (ZN-c3) Combined With Carboplatin and Pembrolizumab in Patients With Metastatic Triple-negative Breast Cancer (ZAP-IT).
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METASTATIC breast cancer ,TRIPLE-negative breast cancer ,PEMBROLIZUMAB ,HORMONE receptor positive breast cancer ,DRUG side effects ,AIDS-related opportunistic infections ,AIDS - Abstract
This document provides information about a clinical trial (NCT06351332) conducted by the Dana-Farber Cancer Institute in collaboration with Merck Sharp & Dohme LLC and Zentalis Pharmaceuticals. The trial aims to investigate the effects of a drug called azenosertib on cancer treatment. Participants must meet certain criteria, such as being 18 years or older and having a history of treated central nervous system metastases. The document also includes contact information for the primary investigator and information about data sharing. [Extracted from the article]
- Published
- 2024
18. Open-label, Single Center, Single-arm, Phase 2 Study of Neoadjuvant Pembrolizumab in Combination With Carboplatin and Paclitaxel in Patients With Stage 1 cT1b-T1cN0M0 Triple Negative Breast Cancer.
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TRIPLE-negative breast cancer ,PEMBROLIZUMAB ,CARBOPLATIN ,DRUG side effects ,PACLITAXEL - Abstract
This article provides information about a clinical trial, NCT06318897, conducted at the M.D. Anderson Cancer Center, which aims to study the effectiveness of pembrolizumab, carboplatin, and paclitaxel in patients with stage 1 cT1b-T1cN0M0 Triple Negative Breast Cancer. The trial's primary objective is to estimate the rate of pathological complete response (pCR) in patients after neoadjuvant therapy, with secondary objectives including assessing safety and toxicity and exploring patient-reported outcomes. The trial is currently ongoing and is expected to be completed by September 2025. Additionally, the document is a verification report from March 2024 about the Anderson Cancer Center, which claims to deliver fact-based news of research and discoveries from around the world. [Extracted from the article]
- Published
- 2024
19. Nutritional therapy optimization in COVID-19 critically ill patients
- Author
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Francisco G Yanowsky-Escatell and Iván Armando Osuna-Padilla
- Subjects
medicine.medical_specialty ,Coronavirus disease 2019 (COVID-19) ,business.industry ,Critically ill ,MEDLINE ,General Medicine ,medicine.disease ,Pneumonia ,Critical illness ,Pandemic ,Viral therapy ,Medicine ,Medical nutrition therapy ,business ,Intensive care medicine - Published
- 2023
20. Assessment of efficacy of dendritic cell therapy and viral therapy in high grade glioma clinical trials. A meta-analytic review.
- Author
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Vatu, Bogdan Ionel, Artene, Stefan-Alexandru, Staicu, Adeline-Georgiana, Turcu-Stiolica, Adina, Folcuti, Catalin, Dragoi, Alexandra, Cioc, Catalina, Baloi, Stefania-Carina, Tataranu, Ligia Gabriela, Silosi, Cristian, and Dricu, Anica
- Subjects
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DENDRITIC cells , *CELLULAR therapy , *GLIOMAS , *CLINICAL trials , *META-analysis - Abstract
In recent years, immunotherapy has raised the interest of many studies and provided different perspectives for the therapeutic management of high grade glioma. Our meta-analysis focused on the effectiveness of dendritic cell (DC) therapy and viral therapy (VT) in clinical trials. Fourteen eligible studies have been evaluated and the results suggest the improvement of both OS (HR = 0.65) (p < 0.0001) and PFS (HR = 0.59) (p = 0.01) for patients receiving DC therapy. The data for VT showed a slight improvement in terms of OS (HR = 0.81), while PFS was similar to the control arms (HR = 1.06) (p = 0.41). [ABSTRACT FROM AUTHOR]
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- 2019
- Full Text
- View/download PDF
21. Viral hepatitis: A global burden needs future directions for the management
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Henu Kumar, Verma, Kiran, Prasad, Pramod, Kumar, and Bhaskar, Lvks
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Liver Cirrhosis ,Hepatitis, Viral, Human ,Acute ,Chronic ,Vaccination ,Viral Hepatitis ,Viral Therapy ,Liver Neoplasms ,Gastroenterology ,Humans ,General Medicine ,Hepatitis A - Abstract
Viral hepatitis is an acute or chronic liver disease due to the infection from Hepatitis A, B, C, D and E viruses. It can cause severe liver damage such as cirrhosis, liver failure and liver cancer. To avoid such fatal complications, hepatitis patients must be diagnosed, pathologized and treated as soon as possible. Furthermore, these hepatitis viruses infect through different routes, resulting in distinct disease pathologies, severity and even the need for specific treatment strategies to combat the infection.
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- 2022
22. Phase II, Single Arm, Open Label, Study of the Combination of Pembrolizumab and Tazemetostat to Overcome Immune Tolerance Following ASCT or CAR T-Cell Therapy in Patients With Aggressive B-Cell Non-Hodgkin's Lymphoma.
- Subjects
NON-Hodgkin's lymphoma ,CHRONIC hepatitis B ,INTERSTITIAL lung diseases ,IMMUNOLOGICAL tolerance ,T cells ,DIFFUSE large B-cell lymphomas ,THERAPEUTICS - Abstract
This document provides information about a clinical trial that is investigating the effectiveness of pembrolizumab and tazemetostat in treating patients with aggressive B-cell non-Hodgkin's lymphoma who have undergone autologous stem cell transplantation or chimeric antigen receptor T-cell therapy. The trial aims to evaluate various outcomes such as survival rates, safety, and immune cell changes. The trial is not yet recruiting participants and is expected to be completed by April 2028. Eligibility criteria for participants are outlined, and the trial is being conducted by Northwestern University with collaboration from the National Cancer Institute. [Extracted from the article]
- Published
- 2024
23. Whole Body HER3 Quantification With Radiolabelled Patritumab Deruxtecan (HER3-DXd) PET/CT.
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SARCOIDOSIS ,DIGESTIVE system diseases ,SKIN cancer ,RESPIRATORY diseases ,MEDICAL research ,BLOOD proteins ,GENETICS - Abstract
A clinical trial, NCT06222489, is being conducted to investigate the effectiveness of patritumab deruxtecan (HER3-DXd) in patients with HER3 expressing breast cancer and EGFR TKI refractory EGFR mutation positive NSCLC. The trial aims to use positron emission tomography (PET) imaging with radiolabelled antibodies to assess HER3 expression and biodistribution of patritumab deruxtecan. The document provides eligibility criteria for the trial, including age, performance status, bone marrow and organ function, laboratory values, and the need for a tumor tissue specimen. The trial is not yet recruiting and is expected to be completed by April 2028. [Extracted from the article]
- Published
- 2024
24. Phase I/II Clinical Trial of Allogeneic Cytomegalovirus-specific T Cells in Combination With Pembrolizumab for Recurrent and Newly Diagnosed Glioblastoma Multiforme.
- Subjects
GLIOBLASTOMA multiforme ,T cells ,AIDS ,DIGESTIVE system diseases ,CLINICAL trials - Abstract
This document provides information about a clinical trial for the treatment of glioblastoma, a type of brain cancer. The trial is investigating the use of a drug called pembrolizumab in combination with other therapies. The document outlines the eligibility criteria for participants, including factors such as serology status, performance status, organ function, and availability of specific T cells. It also lists the exclusion criteria, such as previous treatment with certain drugs, active infections, and certain medical conditions. The document includes contact information for the primary investigator and provides administrative details about the trial. [Extracted from the article]
- Published
- 2023
25. The role of hyperbaric oxygenotherapy (HBOT) in the treatment of COVID-19 patients
- Author
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Žiga, Sead, Andrić, Dejan, Jurić Banai, Sanja, Franjić, Kristina, Vujović, Dragan, Pleško, Eva, Ljubičić, Dživo, Piskač Živković, Nevenka, and Banić, Marko
- Subjects
BIOMEDICINA I ZDRAVSTVO. Kliničke medicinske znanosti. Interna medicina ,covid-19 – complications ,Medicine (General) ,ISHOD LIJEČENJA ,HYPOXIA ,viral therapy ,hypoxia ,treatment outcome ,sars-cov-2 ,SARS-COV-2 ,PANDEMIJA ,BIOMEDICINE AND HEALTHCARE. Clinical Medical Sciences. Infectology ,therapy ,hyperbaric oxygenation ,pneumonia ,R5-920 ,COVID-19 – komplikacije, liječenje ,SARS-CoV-2, PANDEMICS ,VIRUSNA PNEUMONIJA – liječenje ,HYPERBARIC OXYGENATION ,PNEUMONIA, VIRAL therapy ,HIPERBARIČNA OKSIGENOTERAPIJA ,BIOMEDICINA I ZDRAVSTVO. Kliničke medicinske znanosti. Infektologija ,BIOMEDICINE AND HEALTHCARE. Clinical Medical Sciences. Internal Medicine ,COVID-19 – complications, therapy ,TREATMENT OUTCOME ,HIPOKSIJA - Abstract
Pandemija COVID-19 postavila je velik izazov suvremenoj medicini. Unatoč značajnim naporima medicinske i znanstvene zajednice, do trenutka pisanja ovog članka i dalje ne postoji ciljano etiološko liječenje bolesnika akutno oboljelih od COVID-19, kao i bolesnika s post-COVID sindromom. Hiperbarična oksigenoterapija (HBOT) jest medicinski i znanstveno priznat terapijski postupak u liječenju brojnih akutnih i kroničnih stanja u kojima je nedostatak kisika osnovni patofiziološki poremećaj. S obzirom na nekoliko publiciranih serija slučajeva koji su pokazali značajan povoljni učinak primjene HBOT-a u liječenju pacijenata oboljelih od infekcije COVID-19 te na osnovi višedesetljetnog iskustva u primjeni HBOT-a u drugim poljima, rodila se potreba za provođenjem kvalitetnih i dobro strukturiranih studija kojima je cilj jasno ispitati utjecaj primjene HBOT-a u liječenju oboljelih od COVID-19. Prema dostupnim izvorima trenutno se u svijetu provodi 9 takvih istraživanja. Mehanizmi učinka primjene HBOT-a u liječenju oboljelih od COVID-19 zasnivaju se na korekciji hipoksije, atenuaciji upalnog odgovora te „otplate duga kisika“ u kratkom vremenskom razdoblju, na taj način osiguravajući prozor aerobnom metabolizmu u duboko hipoksičnim tkivima i važnim organima., The COVID-19 pandemic has posed a major challenge to modern medicine. Despite significant efforts by the medical and scientific community, at the time of writing, there is still no targeted etiological treatment for acutely ill COVID-19 patients as well as patients with post-COVID syndrome. Hyperbaric oxygen therapy (HBOT) is a medically and scientifically recognized therapeutic procedure in the treatment of a number of acute and chronic conditions in which oxygen deficiency is pathophysiologically primary disorder. Given the several published series of cases that have shown a significant beneficial effect of HBOT in the treatment of patients with COVID-19 infection, and based on decades of experience in the use of HBOT in other fields, the need to conduct quality and well-structured studies arose with the aim to clearly examine the impact of HBOT use in the treatment of COVID-19 patients. According to available sources, nine such studies are being conducted worldwide.The mechanisms of the effect of HBOT in the treatment of COVID-19 patients are based on the correction of hypoxia, attenuation of the inflammatory response and “repayment of oxygen debt” in a short period of time, thus providing a window to aerobic metabolism in deeply hypoxic tissues and important organs.
- Published
- 2021
26. ASSESSING THE RATE OF ANTIRETRO VIRAL THERAPY ADHERENCE AMONG PEOPLE LIVING WITH HIV/AIDS IN THE ATWIMA NWABIAGYA MUNICIPAL - ASHANTI REGION
- Author
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Ernest Boateng and Emmanuel Kumah
- Subjects
Acquired immunodeficiency syndrome (AIDS) ,business.industry ,Environmental health ,medicine ,Viral therapy ,medicine.disease ,business - Abstract
At the end of 2018, HIV remains a significant worldwide medical problem and has claimed over 32 million lives. Around 37.9 million individuals were living with the condition at the end of 2018. The pervasiveness of HIV among African adults (15–49 years) was 3–multiple times higher in 2018. When properly followed, ART has been shown to slow the progression of HIV and enable HIV-positive people to live longer, more productive lives. A treatment regimen of at least three antiretroviral (ARV) medications is typically used. Adherence to antiretroviral therapy (ART) is insufficient. Therefore, the study aimed to assess the ART adherence among PLHIV in the Atwima Nwabiagya Municipality to suggest efficient and effective strategies to maximize adherence. A cross-sectional study was employed using quantitative methods to assess the associations between ART adherence and socio-demographic and socioeconomic factors. The site for this study was the ART Clinic at Nkawie Government Hospital, with a study population of all AIDS patients at the ART Clinic. The 450 PLHIV sample included females (n = 323, or 71.8%), while the males were 127 (28.2). Of the 450 participants, 215 (47.8%) reported adherence of 95%. The mean adherence index was 91.3%. Again, the study showed that those who took a single (137; 30.4%) ART dose was more comfortable than those who took multiple doses (313; 69.6%). Discomfort with the ART regimen, financial restrictions, forgetting to take medicine, lack of family support, social stigma, and antiretroviral therapy side effects were all major barriers to adherence in this study. Adherence, as stated by the participants, appeared to be below. Non-adherence is linked to both medical and behavioural factors, such as pausing ART or feeling ART discomfort. Atwima Nwabiagya Municipality, adherence to antiretroviral therapy is low. Before starting antiretroviral treatment, all patients can receive intensive adherence counselling.
- Published
- 2021
27. Cancer terminator viruses (<italic>CTV</italic>): A better solution for viral‐based therapy of cancer.
- Author
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Emdad, Luni, Das, Swadesh K., Wang, Xiang‐Yang, Sarkar, Devanand, and Fisher, Paul B.
- Subjects
- *
CANCER treatment , *GENE therapy , *METASTASIS , *VIRAL tropism , *CANCER cells , *ADENOVIRUSES - Abstract
In principle, viral gene therapy holds significant potential for the therapy of solid cancers. However, this promise has not been fully realized and systemic administration of viruses has not proven as successful as envisioned in the clinical arena. Our research is focused on developing the next generation of efficacious viruses to specifically treat both primary cancers and a major cause of cancer lethality, metastatic tumors (that have spread from a primary site of origin to other areas in the body and are responsible for an estimated 90% of cancer deaths). We have generated a chimeric tropism‐modified type 5 and 3 adenovirus that selectively replicates in cancer cells and simultaneously produces a secreted anti‐cancer toxic cytokine, melanoma differentiation associated gene‐7/Interleukin‐24 (
mda‐7/IL‐24 ), referred to as a Cancer Terminator Virus (CTV) (Ad.5/3‐CTV). In preclinical animal models, injection into a primary tumor causes selective cell death and therapeutic activity is also observed in non‐injected distant tumors, that is, “bystander anti‐tumor activity.” To enhance the impact and therapeutic utility of the CTV, we have pioneered an elegant approach in which viruses are encapsulated in microbubbles allowing “stealth delivery” to tumor cells that when treated with focused ultrasound causes viral release killing tumor cells through viral replication, and producing and secreting MDA‐7/IL‐24, which stimulates the immune system to attack distant cancers, inhibits tumor angiogenesis and directly promotes apoptosis in distant cancer cells. This strategy is called UTMD (ultrasound‐targeted microbubble‐destruction). This novel CTV and UTMD approach hold significant promise for the effective therapy of primary and disseminated tumors. [ABSTRACT FROM AUTHOR]- Published
- 2018
- Full Text
- View/download PDF
28. Researchers from University of Gondar Detail New Studies and Findings in the Area of HIV/AIDS (Determinates of anemia among Human Immune Deficiency Virus positive children on Anti-retro Viral Therapy in selected health facilities, Northwest...).
- Abstract
Keywords: Anemia; Antivirals; Clinical Research; Clinical Trials and Studies; Drugs and Therapies; HIV/AIDS; Health and Medicine; Hematologic Diseases and Conditions; Hemic and Lymphatic Diseases and Conditions; Immune System Diseases and Conditions; Pediatrics; Pharmaceuticals; Primate Lentiviruses; RNA Viruses; Retroviridae; Therapy; Vertebrate Viruses; Viral; Viral Inhibition Therapy; Viral Sexually Transmitted Diseases and Conditions; Viral Therapy; Virology; Virus; World Health Organization EN Anemia Antivirals Clinical Research Clinical Trials and Studies Drugs and Therapies HIV/AIDS Health and Medicine Hematologic Diseases and Conditions Hemic and Lymphatic Diseases and Conditions Immune System Diseases and Conditions Pediatrics Pharmaceuticals Primate Lentiviruses RNA Viruses Retroviridae Therapy Vertebrate Viruses Viral Viral Inhibition Therapy Viral Sexually Transmitted Diseases and Conditions Viral Therapy Virology Virus World Health Organization 175 175 1 09/11/23 20230911 NES 230911 2023 SEP 11 (NewsRx) -- By a News Reporter-Staff News Editor at AIDS Weekly -- Research findings on HIV/AIDS are discussed in a new report. According to the news reporters, the research concluded: "The present study found that CD4 count, WHO clinical stage, cotrimoxazole prophylaxis therapy and MUAC were significantly associated with anaemia in children on ART. Anemia, Antivirals, Clinical Research, Clinical Trials and Studies, Drugs and Therapies, HIV/AIDS, Health and Medicine, Hematologic Diseases and Conditions, Hemic and Lymphatic Diseases and Conditions, Immune System Diseases and Conditions, Pediatrics, Pharmaceuticals, Primate Lentiviruses, RNA Viruses, Retroviridae, Therapy, Vertebrate Viruses, Viral, Viral Inhibition Therapy, Viral Sexually Transmitted Diseases and Conditions, Viral Therapy, Virology, Virus, World Health Organization. [Extracted from the article]
- Published
- 2023
29. Long-term clinical benefit of Peg-IFNα and NAs sequential anti-viral therapy on HBV related HCC
- Author
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Qian Zhang, Yan Xu, Ping Zhao, Changyu Zhou, Lin Liu, Wenqian Qi, Yu Sun, Hong-hua Guo, Xu Wang, and Jiangbin Wang
- Subjects
Oncology ,Hepatitis B virus ,Cancer Research ,medicine.medical_specialty ,Carcinoma, Hepatocellular ,Cumulative Survival Rate ,medicine.disease_cause ,Antiviral Agents ,Polyethylene Glycols ,Peg ifnα ,Internal medicine ,medicine ,Carcinoma ,Humans ,Viral therapy ,In patient ,Survival rate ,business.industry ,Liver Neoplasms ,Antiviral therapy ,Interferon-alpha ,Nucleosides ,Hepatitis B ,medicine.disease ,Recombinant Proteins ,digestive system diseases ,Treatment Outcome ,Neoplasm Recurrence, Local ,business - Abstract
Analysis of the value of long-term antiviral therapy using sequential Peg-IFN therapy and nucleos(t)ide analogues (NAs) improves the prognosis of HBV-related HCC. HBV-related HCC patients were classified into sequential therapy with Peg-IFNα-2a and NAs, and NAs therapy alone. All patients were followed up for 5 years. The survival rate, HCC recurrence rate, Child-Pugh score, and side effects of drugs were evaluated. Firstly, the early and late cumulative survival rate was higher in patients receiving antiviral therapy compared with the control patients (p0.05). Patients receiving sequential therapy with Peg-IFNα-2a and NAs showed a higher late cumulative survival rate and significantly reduced early and late recurrence rate, compared to those in the NA-alone group (p0.05). Single NAs therapy only reduced the late recurrence rate in HCC-patients. Secondly, NAs therapy significantly increased the Child-Pugh score after five years of therapy (five-year therapy 7.03±1.50 vs. initial score 6.63±0.85; p0.05), whereas the sequential therapy with Peg-IFNα-2a and NAs did not greatly alter the Child-Pugh score (6.88±1.26; p0.05). Compared to the control patients, patients receiving antiviral therapy (NAs alone or sequential therapy with Peg-IFNα-2a and NAs) exhibited a significantly decreased Child-Pugh score (p0.05). Compared to NAs alone, sequential therapy with Peg-IFNα-2a and NAs provided a more efficient strategy for improving both the five-year survival rate and the two-year or five-year recurrence rate in patients.
- Published
- 2021
30. Hypothalamus Specific Re-Introduction of SNORD116 into Otherwise Snord116 Deficient Mice Increased Energy Expenditure.
- Author
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Qi, Y., Purtell, L., Fu, M., Zhang, L., Zolotukhin, S., Campbell, L., and Herzog, H.
- Subjects
- *
HYPOTHALAMUS , *GENE clusters , *GENETIC disorders , *METABOLIC disorders , *PHENOTYPES - Abstract
The Snord116 gene cluster has been recognised as a critical contributor to the Prader-Willi syndrome ( PWS), with mice lacking Snord116 displaying many classical PWS phenotypes, including low postnatal body weight, reduced bone mass and increased food intake. However, these mice do not develop obesity as a result of increased energy expenditure. To understand the physiological function of SNORD116 better and potentially rescue the altered metabolism of Snord116−/− mice, we used an adeno-associated viral ( AAV) approach to reintroduce the product of the Snord116 gene into the hypothalamus in Snord116−/− mice at different ages. The results obtained show that mid-hypothalamic re-introduction of SNORD116 in 6-week-old Snord116−/− mice leads to significantly reduced body weight and weight gain, which is associated with elevated energy expenditure. Importantly, when the intervention targets other areas such as the anterior region of the hypothalamus or the reintroduction occurs in older mice, the positive effects on energy expenditure are diminished. These data indicate that the metabolic symptoms of PWS develop gradually and the Snord116 gene plays a critical role during this process. Furthermore, when we investigated the consequences of SNORD116 re-introduction under conditions of thermoneutrality where the mild cold stress influences are avoided, we also observed a significant increase in energy expenditure. In conclusion, the rescue of mid-hypothalamic Snord116 deficiency in young Snord116 germline deletion mice increases energy expenditure, providing fundamental information contributing to potential virus-mediated genetic therapy in PWS. [ABSTRACT FROM AUTHOR]
- Published
- 2017
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- View/download PDF
31. Oncolytic Virotherapy for the Treatment of Malignant Glioma.
- Author
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Foreman, Paul, Friedman, Gregory, Cassady, Kevin, Markert, James, Foreman, Paul M, Friedman, Gregory K, Cassady, Kevin A, and Markert, James M
- Subjects
GLIOMA treatment ,BRAIN tumor treatment ,ENTEROVIRUSES ,VIRUSES ,CLINICAL trials ,MICROBIOLOGY ,PHENOMENOLOGICAL biology ,GLIOMAS ,BRAIN tumors ,TREATMENT effectiveness ,GENES ,IMPACT of Event Scale ,RESEARCH funding ,RNA viruses ,ONCOLYTIC virotherapy ,ANIMALS - Abstract
Malignant glioma is the most common primary brain tumor and carries a grim prognosis, with a median survival of just over 14 months. Given the poor outcomes with standard-of-care treatments, novel treatment strategies are needed. The concept of virotherapy for the treatment of malignant tumors dates back more than a century and can be divided into replication-competent oncolytic viruses and replication-deficient viral vectors. Oncolytic viruses are designed to selectively target, infect, and replicate in tumor cells, while sparing surrounding normal brain. A host of oncolytic viruses has been evaluated in early phase human trials with promising safety results, but none has progressed to phase III trials. Despite the 25 years that has passed since the initial publication of genetically engineered oncolytic viruses for the treatment of glioma, much remains to be learned about the use of this therapy, including its mechanism of action, optimal treatment paradigm, appropriate targets, and integration with adjuvant agents. Oncolytic viral therapy for glioma remains promising and will undoubtedly impact the future of patient care. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
- View/download PDF
32. Características, evolución clínica y factores asociados a la mortalidad en UCI de los pacientes críticos infectados por SARS-CoV-2 en España: estudio prospectivo, de cohorte y multicéntrico
- Author
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M. Gómez-Rojo, Javier Fernández, Pablo Monedero, J. Ripollés, Á. Candela, C. Morcillo, G. Muñoz, E. Bassas, F.J. Redondo, L. Zattera, A. Martín, Alfredo Gea, A. Margarit, G. Ángeles, R. Mellado-Artigas, Emilio Maseda, Cesar Aldecoa, Carlos Ferrando, Fernando Ramasco, Gonzalo Tamayo, M.L. Hernández-Sanz, A. Jacas, A. Martínez, N. García, Pedro Castro, María Hernández-Tejero, C. Deiros, P. Casas, J. Mercadal, A. Nieto, E. Arruti, R. Adalia, and A. Bordell
- Subjects
Male ,Severe Acute Respiratory Syndrome ,Critical Care and Intensive Care Medicine ,0302 clinical medicine ,Risk Factors ,Odds Ratio ,Medicine ,Hospital Mortality ,Prospective Studies ,030212 general & internal medicine ,Unitats de cures intensives -- Mortalitat ,Hypoxia ,APACHE ,Age Factors ,Shock ,General Medicine ,Acute Kidney Injury ,Middle Aged ,Intensive Care Units ,Regression Analysis ,Original Article ,Female ,COVID-19 (Malaltia) -- Mortalitat ,Coronavirus Infections ,Respiratory Therapy ,2019-20 coronavirus outbreak ,Coronavirus disease 2019 (COVID-19) ,Critical Illness ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Pneumonia, Viral ,Hospital mortality ,Antiviral Agents ,Article ,Andorra ,Betacoronavirus ,03 medical and health sciences ,Humans ,Viral therapy ,Pandemics ,Aged ,SARS-CoV-2 ,business.industry ,COVID-19 ,Arrhythmias, Cardiac ,030208 emergency & critical care medicine ,Length of Stay ,Oxygen ,Anesthesiology and Pain Medicine ,Multicenter study ,Spain ,Critical illness ,business ,Humanities - Abstract
Antecedentes: No se ha reportado plenamente la evolución clínica de los pacientes críticos de COVID-19 durante su ingreso en la unidad de cuidados intensivos (UCI), incluyendo las complicaciones médicas e infecciosas y terapias de soporte, así como su asociación con la mortalidad en UCI. Objetivo: El objetivo de este estudio es describir las características clínicas y la evolución de los pacientes ingresados en UCI por COVID-19 y determinar los factores de riesgo de la mortalidad en UCI de dichos pacientes. Métodos: Estudio prospectivo, multicéntrico y de cohorte, que incluyó a los pacientes críticos de COVID-19 ingresados en 30 UCI de España y Andorra. Se incluyó a los pacientes consecutivos del 12 de marzo al 26 de mayo del 2020 si habían fallecido o habían recibido el alta de la UCI durante el periodo de estudio. Se reportaron los datos demográficos, los síntomas, los signos vitales, los marcadores de laboratorio, las terapias de soporte, terapias farmacológicas y las complicaciones médicas e infecciosas, realizándose una comparación entre los pacientes fallecidos y los pacientes dados de alta. Resultados: Se incluyó a un total de 663 pacientes. La mortalidad general en UCI fue del 31% (203 pacientes). Al ingreso en UCI los no supervivientes eran más hipoxémicos (SpO2 con mascarilla de no reinhalación, de 90 [RIC 83-93] vs. 91 [RIC 87-94]; p < 0,001] y con mayor puntuación en la escala SOFA-Evaluación de daño orgánico secuencial (SOFA, 7 [RIC 5-9] vs. 4 [RIC 3-7]; p
- Published
- 2020
33. Return Hospital Admissions Among 1419 COVID‐19 Patients Discharged from Five U.S. Emergency Departments
- Author
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Austin S. Kilaru, David A. Asch, M. Kit Delgado, Kathleen Lee, Zachary F. Meisel, Nandita Mitra, and Christopher K. Snider
- Subjects
2019-20 coronavirus outbreak ,Coronavirus disease 2019 (COVID-19) ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Pneumonia, Viral ,Patient Readmission ,Betacoronavirus ,03 medical and health sciences ,0302 clinical medicine ,Research Letter ,medicine ,Humans ,Viral therapy ,Decompensation ,Pandemics ,SARS-CoV-2 ,business.industry ,COVID-19 ,030208 emergency & critical care medicine ,General Medicine ,medicine.disease ,Research Letters ,Patient Discharge ,United States ,Hospital admission ,Emergency Medicine ,Medical emergency ,Coronavirus Infections ,Emergency Service, Hospital ,business - Abstract
Although many ED patients with known or suspected Covid‐19 require hospital admission, the majority are discharged home. Concern for surges in hospital occupancy compel emergency providers to preserve inpatient resources and discern which patients benefit most from admission. Even in the absence of surge conditions, patients may prefer to recover at home if safe to do so. However, some patients with Covid‐19 experience delayed decompensation.
- Published
- 2020
34. Ethics Roundtable: Distribution of Critical Care Resources in the Setting of a COVID-19 Surge
- Author
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Steven J. Baumrucker, Gregory T. Carter, Gregg VandeKieft, Matt Stolick, Russel W Adkins, and Cheryl Perkins
- Subjects
2019-20 coronavirus outbreak ,Critical Care ,Coronavirus disease 2019 (COVID-19) ,Attitude of Health Personnel ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Clinical Decision-Making ,Pneumonia, Viral ,Distribution (economics) ,Betacoronavirus ,Humans ,Medicine ,Viral therapy ,Ethics, Medical ,Surge ,Pandemics ,Ventilators, Mechanical ,Surge Capacity ,SARS-CoV-2 ,business.industry ,COVID-19 ,General Medicine ,Intensive Care Units ,Engineering ethics ,Coronavirus Infections ,business - Published
- 2020
35. Cancer Research: The Lessons to Learn from COVID-19
- Author
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Charles Swanton, Christopher Bailey, and James R M Black
- Subjects
0301 basic medicine ,2019-20 coronavirus outbreak ,Biomedical Research ,Time Factors ,Coronavirus disease 2019 (COVID-19) ,Cancer clinical trial ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Pneumonia, Viral ,Medical Oncology ,Betacoronavirus ,03 medical and health sciences ,0302 clinical medicine ,Neoplasms ,Pandemic ,Humans ,Viral therapy ,Medicine ,Pandemics ,Clinical Trials as Topic ,Health Care Rationing ,SARS-CoV-2 ,business.industry ,COVID-19 ,Neoplasms therapy ,Timeline ,3. Good health ,030104 developmental biology ,Oncology ,030220 oncology & carcinogenesis ,Cancer research ,Coronavirus Infections ,business ,Forecasting - Abstract
Summary: The COVID-19 pandemic has caused widespread disruption of cancer clinical trials due to the restrictions on nonessential services and the reallocation of resources, and at the same time the urgent global effort toward discovering therapies that treat or prevent COVID-19 infection has led to shortening of traditional regulatory timelines. This experience should stimulate similar urgency in the way future cancer research is conducted.
- Published
- 2020
36. Telemedicine for Chronic Pain in the COVID-19 Era and Beyond
- Author
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Susan Jarquin, Trent Emerick, Cheryl D. Bernstein, Kevin Luong, Ajay D. Wasan, Shannon Morrisseyand, Benedict J. Alter, and Scott Brancolini
- Subjects
2019-20 coronavirus outbreak ,medicine.medical_specialty ,Telemedicine ,Coronavirus disease 2019 (COVID-19) ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Pneumonia, Viral ,Clinical Neurology ,Betacoronavirus ,Humans ,Pain Management ,Medicine ,Viral therapy ,Intensive care medicine ,Pandemics ,SARS-CoV-2 ,business.industry ,Perspective & Commentary ,Chronic pain ,COVID-19 ,General Medicine ,medicine.disease ,Anesthesiology and Pain Medicine ,Commentary ,Neurology (clinical) ,Chronic Pain ,Erratum ,Coronavirus Infections ,AcademicSubjects/MED00010 ,business - Published
- 2020
37. Estimating the Maximum Capacity of COVID-19 Cases Manageable per Day Given a Health Care System's Constrained Resources
- Author
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Nathan M. Stall, Deepit Bhatia, Vasily Giannakeas, Matthew T. Warkentin, and Isaac I. Bogoch
- Subjects
2019-20 coronavirus outbreak ,Coronavirus disease 2019 (COVID-19) ,SARS-CoV-2 ,business.industry ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Pneumonia, Viral ,COVID-19 ,General Medicine ,Letters: Observations ,Hospital Medicine ,Betacoronavirus ,Age groups ,Health care ,Internal Medicine ,Humans ,Medicine ,Viral therapy ,Age distribution ,Operations management ,Coronavirus Infections ,business ,Pandemics - Published
- 2020
38. Staffing and Orientation During the <scp>COVID</scp> ‐19 Pandemic
- Author
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Kimberly J. Retzlaff
- Subjects
2019-20 coronavirus outbreak ,Coronavirus disease 2019 (COVID-19) ,SARS-CoV-2 ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Pneumonia, Viral ,Personnel Staffing and Scheduling ,Staffing ,COVID-19 ,Perioperative Leadership Strategies: COVID‐19 ,Organizational Policy ,Betacoronavirus ,Medical–Surgical Nursing ,Special Reports ,Nursing ,Orientation (mental) ,Political science ,Medical–Surgical ,Pandemic ,Special Report: Perioperative Leadership Strategies: COVID‐19 ,Humans ,Viral therapy ,Coronavirus Infections ,Pandemics ,Personal Protective Equipment ,Occupational Health - Published
- 2020
39. Bleeding prevalence in COVID-19 patients receiving intensive antithrombotic prophylaxis
- Author
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Gabriele Casso, Alessandro Felice Chiesa, Daniela Demundo, Giuseppe Colucci, Marco Conti, Elisa Stoira, Marco Previsdomini, Georg Stussi, Luca Spinedi, Michael Llamas, Alberto Pagnamenta, Chiara Kessler, H. Stricker, Bernhard Gerber, Davide Rossi, Luigia Elzi, Rita Monotti, Giorgia Bianchi, Elisa Valenti, University of Zurich, and Gerber, Bernhard
- Subjects
Adult ,Male ,2019-20 coronavirus outbreak ,medicine.medical_specialty ,Time Factors ,Coronavirus disease 2019 (COVID-19) ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,2720 Hematology ,Pneumonia, Viral ,Treatment outcome ,610 Medicine & health ,Hemorrhage ,11171 Cardiocentro Ticino ,2705 Cardiology and Cardiovascular Medicine ,Betacoronavirus ,Young Adult ,Fibrinolytic Agents ,Risk Factors ,Internal medicine ,Antithrombotic ,Prevalence ,medicine ,Humans ,Viral therapy ,Young adult ,Letter to the Editor ,Pandemics ,Aged ,Aged, 80 and over ,SARS-CoV-2 ,business.industry ,Anticoagulants ,COVID-19 ,Thrombosis ,Hematology ,Middle Aged ,medicine.disease ,Pneumonia ,Treatment Outcome ,Host-Pathogen Interactions ,Female ,Coronavirus Infections ,Cardiology and Cardiovascular Medicine ,business ,Switzerland - Published
- 2020
40. <scp>COVID</scp> ‐19 pandemic and the tension between the need to act and the need to know
- Author
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Ian A Scott
- Subjects
2019-20 coronavirus outbreak ,Coronavirus disease 2019 (COVID-19) ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Clinical Decision-Making ,Pneumonia, Viral ,Outcome assessment ,Betacoronavirus ,Need to know ,Outcome Assessment, Health Care ,Pandemic ,Internal Medicine ,Humans ,Viral therapy ,Medicine ,Pandemics ,Clinical Trials as Topic ,SARS-CoV-2 ,business.industry ,Editorials ,COVID-19 ,Standard of Care ,Public relations ,Data Accuracy ,Patient Care Management ,Editorial ,Needs assessment ,Coronavirus Infections ,business ,Needs Assessment - Published
- 2020
41. Nutrición Clínica en tiempos de COVID-19
- Author
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Irene Bretón Lesmes and María Dolores Ballesteros Pomar
- Subjects
medicine.medical_specialty ,Nutrition and Dietetics ,business.industry ,Endocrinology, Diabetes and Metabolism ,Decision Trees ,Pneumonia, Viral ,MEDLINE ,COVID-19 ,medicine.disease ,Article ,Pneumonia ,Endocrinology ,Diabetes mellitus ,Pandemic ,Humans ,Medicine ,Viral therapy ,Nutrition Therapy ,Medical nutrition therapy ,Coronavirus Infections ,business ,Intensive care medicine ,Pandemics - Published
- 2020
42. Oncology Care Delivery in the COVID-19 Pandemic: An Opportunity to Study Innovations and Outcomes
- Author
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James O. Armitage, John Cox, Linda D. Bosserman, Sagar Lonial, Apar Kishor Ganti, Pelin Cinar, Jeffery C. Ward, Kathleen Bickel, Sandra L. Wong, Monika K. Krzyzanowska, and Arif H. Kamal
- Subjects
medicine.medical_specialty ,2019-20 coronavirus outbreak ,Coronavirus disease 2019 (COVID-19) ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Pneumonia, Viral ,MEDLINE ,Medical Oncology ,Betacoronavirus ,Neoplasms ,Pandemic ,medicine ,Humans ,Viral therapy ,Intensive care medicine ,Pandemics ,SARS-CoV-2 ,Oncology (nursing) ,Viral Epidemiology ,business.industry ,Health Policy ,COVID-19 ,medicine.disease ,Pneumonia ,Oncology ,Coronavirus Infections ,business - Published
- 2020
43. 30-Year-Old Woman With Cough, Dyspnea, and Anosmia
- Author
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Harmon, David M., McDonald, Nicholas M., and Beckman, Thomas J.
- Subjects
Adult ,2019-20 coronavirus outbreak ,Pediatrics ,medicine.medical_specialty ,Coronavirus disease 2019 (COVID-19) ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Pneumonia, Viral ,Anosmia ,MEDLINE ,Article ,Olfaction Disorders ,COVID-19 Testing ,Pandemic ,medicine ,Humans ,Viral therapy ,Pandemics ,Clinical Laboratory Techniques ,business.industry ,COVID-19 ,General Medicine ,medicine.disease ,COVID-19 Drug Treatment ,Pneumonia ,Dyspnea ,Cough ,Female ,medicine.symptom ,Coronavirus Infections ,business - Published
- 2020
44. Industry update: the latest developments in the field of therapeutic delivery, March 2020
- Author
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Peter Timmins
- Subjects
DNA metabolism ,2019-20 coronavirus outbreak ,Engineering management ,Coronavirus disease 2019 (COVID-19) ,Government regulation ,business.industry ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Pharmaceutical Science ,Viral therapy ,Medicine ,business ,Drug industry ,Product Approvals - Published
- 2020
45. Physiological Changes During Prone Positioning in COVID-19 Acute Respiratory Distress Syndrome
- Author
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Rui Min Lee, Sanjay H. Chotirmall, Chiaw Yee Choy, Geak Poh Tan, Hui Ling Tan, Jee Jian See, Li Min Ling, Ser Hon Puah, Yu Lin Wong, and John Abisheganaden
- Subjects
Adult ,Male ,medicine.medical_specialty ,2019-20 coronavirus outbreak ,Critical Care ,Coronavirus disease 2019 (COVID-19) ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Pneumonia, Viral ,Treatment outcome ,Acute respiratory distress ,Patient Positioning ,Betacoronavirus ,Internal medicine ,Prone Position ,medicine ,Humans ,Viral therapy ,Pandemics ,Aged ,Retrospective Studies ,Respiratory Distress Syndrome ,SARS-CoV-2 ,business.industry ,COVID-19 ,General Medicine ,Length of Stay ,Middle Aged ,medicine.disease ,Respiratory Function Tests ,Pneumonia ,Prone position ,Treatment Outcome ,Cardiology ,Female ,Coronavirus Infections ,business - Published
- 2020
46. Traditional Chinese medicine for combating COVID-19
- Author
-
Kaixian Chen and Hongzhuan Chen
- Subjects
China ,2019-20 coronavirus outbreak ,Coronavirus disease 2019 (COVID-19) ,International Cooperation ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Pneumonia, Viral ,MEDLINE ,Traditional Chinese medicine ,Betacoronavirus ,Preventive Health Services ,Humans ,Medicine ,Viral therapy ,Medicine, Chinese Traditional ,Mortality ,Practice Patterns, Physicians' ,Drug Approval ,Pandemics ,Traditional medicine ,SARS-CoV-2 ,business.industry ,Disease progression ,COVID-19 ,General Medicine ,Editorial ,Disease Progression ,Comprehensive Health Care ,Coronavirus Infections ,business ,Drugs, Chinese Herbal - Published
- 2020
47. Comprehensive Review on Current Interventions, Diagnostics, and Nanotechnology Perspectives against SARS-CoV-2
- Author
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Murali M. Yallapu, Deepak S. Chauhan, Subhash C. Chauhan, Rajendra Prasad, Rohit Srivastava, and Meena Jaggi
- Subjects
2019-20 coronavirus outbreak ,Coronavirus disease 2019 (COVID-19) ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Pneumonia, Viral ,Biomedical Engineering ,Psychological intervention ,Pharmaceutical Science ,Bioengineering ,Nanotechnology ,Biosensing Techniques ,Review ,02 engineering and technology ,01 natural sciences ,Pandemic ,Humans ,Viral therapy ,Pandemics ,Pharmacology ,010405 organic chemistry ,Extramural ,Chemistry ,Organic Chemistry ,COVID-19 ,021001 nanoscience & nanotechnology ,COVID-19 Drug Treatment ,0104 chemical sciences ,Coronavirus Infections ,0210 nano-technology ,Biotechnology ,Healthcare system - Abstract
The coronavirus disease 2019 (COVID-19) has dramatically challenged the healthcare system of almost all countries. The authorities are struggling to minimize the mortality along with ameliorating the economic downturn. Unfortunately, until now, there has been no promising medicine or vaccine available. Herein, we deliver perspectives of nanotechnology for increasing the specificity and sensitivity of current interventional platforms toward the urgent need of quickly deployable solutions. This review summarizes the recent involvement of nanotechnology from the development of a biosensor to fabrication of a multifunctional nanohybrid system for respiratory and deadly viruses, along with the recent interventions and current understanding about severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
- Published
- 2020
48. Reply to: Oncolytic Viral Therapy for Malignant Pleural Mesothelioma
- Author
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Clément Meiller, Nicolas Boisgerault, Tiphaine Delaunay, Marc Grégoire, Marion Grard, Stefano Caruso, Jean-François Fonteneau, Jaafar Bennouna, Didier Jean, Frédéric Tangy, Emanuela Felley-Bosco, Christophe Blanquart, Centre de Recherche des Cordeliers (CRC (UMR_S_1138 / U1138)), École pratique des hautes études (EPHE), Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Université de Paris (UP), Immunogenic Cell Death and Mesothelioma Therapy (CRCINA-ÉQUIPE 4), Centre de Recherche en Cancérologie et Immunologie Nantes-Angers (CRCINA), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE), Université de Nantes (UN)-Université de Nantes (UN)-Centre hospitalier universitaire de Nantes (CHU Nantes)-Centre National de la Recherche Scientifique (CNRS)-Université d'Angers (UA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Nantes - UFR de Médecine et des Techniques Médicales (UFR MEDECINE), Université de Nantes (UN)-Université de Nantes (UN)-Centre hospitalier universitaire de Nantes (CHU Nantes)-Centre National de la Recherche Scientifique (CNRS)-Université d'Angers (UA), University hospital of Zurich [Zurich], Service de pneumologie [Nantes], Université de Nantes (UN)-Centre hospitalier universitaire de Nantes (CHU Nantes), Epidémiologie et Physiopathologie des Virus Oncogènes / Oncogenic Virus Epidemiology and Pathophysiology (EPVO (UMR_3569 / U-Pasteur_3)), Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS)-Université de Paris (UP), ANR-16-CE18-0016,OncoMeVax,Un virus de la rougeole modifié pour traiter le cancer(2016), ANR-11-LABX-0016,IGO,Immunothérapies Grand Ouest(2011), Bernardo, Elizabeth, Un virus de la rougeole modifié pour traiter le cancer - - OncoMeVax2016 - ANR-16-CE18-0016 - AAPG2016 - VALID, Laboratoires d'excellence - Immunothérapies Grand Ouest - - IGO2011 - ANR-11-LABX-0016 - LABX - VALID, Université Paris sciences et lettres (PSL)-Université Paris sciences et lettres (PSL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Université Paris Cité (UPCité), Université d'Angers (UA)-Université de Nantes (UN)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre hospitalier universitaire de Nantes (CHU Nantes)-Université d'Angers (UA)-Université de Nantes (UN)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Centre hospitalier universitaire de Nantes (CHU Nantes), Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), University of Zurich, Jean, Didier, and École Pratique des Hautes Études (EPHE)
- Subjects
Mesothelioma ,Pulmonary and Respiratory Medicine ,Lung Neoplasms ,10255 Clinic for Thoracic Surgery ,Pleural Neoplasms ,610 Medicine & health ,[SDV.CAN]Life Sciences [q-bio]/Cancer ,Measles virus ,03 medical and health sciences ,0302 clinical medicine ,[SDV.CAN] Life Sciences [q-bio]/Cancer ,MESH: Oncolytic immunotherapy ,Humans ,Medicine ,Viral therapy ,ComputingMilieux_MISCELLANEOUS ,Sequence Deletion ,030304 developmental biology ,0303 health sciences ,MESH: Type I interferon ,MESH: Mesothelioma ,biology ,business.industry ,Pleural mesothelioma ,Homozygote ,MESH: Gene homozygous deletion ,biology.organism_classification ,Oncolytic virus ,Oncolytic Viruses ,Oncology ,2740 Pulmonary and Respiratory Medicine ,030220 oncology & carcinogenesis ,Interferon Type I ,Cancer research ,2730 Oncology ,business ,MESH: Measles virus ,Interferon type I ,medicine.drug - Abstract
International audience
- Published
- 2020
49. 'COVID-19: diagnosis, management and prognosis': a new topical collection of Internal and Emergency Medicine
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Riccardo Polosa, Domenico Prisco, and Michele Spinicci
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2019-20 coronavirus outbreak ,Coronavirus disease 2019 (COVID-19) ,business.industry ,SARS-CoV-2 ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Pneumonia, Viral ,MEDLINE ,COVID-19 ,medicine.disease ,Prognosis ,Betacoronavirus ,Diagnosis management ,medicine ,Emergency Medicine ,Internal Medicine ,Viral therapy ,Humans ,Medical emergency ,business ,Coronavirus Infections ,Pandemics ,Editor's Page - Abstract
At the dawn of 2020, the planet woke up with an unexpected shocking public health threat. A novel zoonotic coronavirus, later named severe acute respiratory syndrome 2 (SARS-CoV-2), genetically close to SARS-CoV responsible for the outbreak in 2003, emerged as causative agent of a multifaceted syndrome, known as coronavirus disease 2019 (COVID-19) [1]. The outbreak rapidly spread from the Wuhan City, Hubei Province, China, where the first cases of SARS-CoV-2 infection occurred in early December 2019, toward western countries, resulting in an unprecedented challenge for the health systems worldwide. On 11th March 2020, the World Health Organization declared the outbreak of SARS-CoV-2 a pandemic. As of the 8th of July 2020 globally more than 11 million cases of SARS-CoV-2 infections had been confirmed, and 545,398 COVID-19 related fatalities had occurred globally [2]. The body of knowledge about biologic SARS-CoV-2 and clinical features of COVID-19 has been increasing exponentially. Nonetheless, conflicting opinions and confusing issues still dominate the scientific debate. The topical collection ofInternal and Emergency Medicine, titled “COVID-19: diagnosis, management and prognosis” was launched to better inform researchers, academics, physicians and healthcare professionals about the evolving understanding of the topic. Ethical issues are at the forefront of the debate, as it deserves for an event of such magnitude, to whom healthcare workers (HCWs) paid a heavy price. In their fascinating letter, Lippi et al. offered a historical perspective of doctors’ role in the past epidemics, stuck between professional duties, based on the Hippocratic Oath, and the need to protect themselves, through adequate measures and equipment [3]. More to the point, Arora et al. identified ethics key issues in the COVID-19 era, such as the long-term implications of non-urgent care cancelled, how to make priority decisions on patients’ treatment escalation and how clinicians should act when adequate personal protective equipment (PPE) is not available [4]. Indeed, as highlighted by Russo et al., the pandemic storm has been not only a clinical challenge but also an organizational crisis for our health systems [5]. Shortage of PPE for frontline HCWs was one of the more worrisome aspects of the early pandemic. Tsilingiris et al. went into the debate on the appropriate use of medical masks and respirators for HCWs and revised available evidence on the topic [6]. The theme of COVID-19 as diversion and deterrent from the care of patients with chronic conditions, causing possible negative consequences in the near future, returned in the point of view by Viganò et al.: in their Emergency Department, the admissions dropped in March and April 2020 by 53% and 63%, respectively, with respect to the period December 2019–February 2020 [7]. Two nice papers rose concern on how pandemic can represent an additional complication for the management of cardiac emergencies, both inside and outside the hospitals [8,9]. The experience of the first 5weeks of COVID-19 epidemic in a referral centre in the epicentre of the Italian epidemic represented an effective strategy of Emergency Medicine network, able to manage an increased amount of calls and requests, by integrating “out-of-hospital” and “hospital” efforts [10]. Within the hospitals, physicians from disparate specialities were called to change their habits, when their facilities and wards were converted to COVID-19 areas, in response to an overwhelming flow of affected patients. At best, it was an occasion to put in place an unexpected teamwork cooperation and to share different skills and experiences [11]. The correct identification of COVID-19 cases remains the cornerstone for the control of the epidemic, allowing to confine infected patients and prevent SARS-CoV-2 spread. At the hospital level, an effective triage strategy is of paramount importance to avoid nosocomial outbreaks amongst HCWs and patients with other diseases than COVID-19. Poggiali et al. described their flowchart, applied in the heart of the Italian epidemic storm [12]. Polymerase chain reaction (PCR) testing on respiratory samples, i.e., nasopharyngeal swab, sputum or bronchoalveolar lavage, is the gold standard for a confirmed diagnosis of SARS-CoV-2 infection. However, physicians soon learned that in some cases, a typical clinical and radiological picture should drive the diagnosis, regardless of a negative microbiological result. As an example, in the case report by Song et al. a patient with fever, respiratory symptoms and evocative mixed ground-glass opacity at the computed tomography (CT), had negative PCR on seven consecutive sputum sample, before achieving the diagnosis of SARS-CoV-2 infection on the eighth sample [13]. Typical and atypical clinical features of COVID-19 patients, as well as risk factors with possible impact on COVID-19 outcome, are outlined in several papers of this Topical Collection. Bertolino et al. tried to summarize the evidences on key clinical features to differentiate COVID-19 case from upper respiratory and/or influenza-like illnesses of other aetiology, providing a practical guide for internists [14]. According to data collected by Lapostolle et al. among 1487 outpatients diagnosed with COVID-19 in the Greater Paris region, dry cough and fever were the most frequent symptoms reported (more than 90% of cases), in association with general symptoms, such as body aches/myalgia, headache, and asthenia, and a considerable quote of anosmia and ageusia [15]. Nevertheless, the clinical presentation can be sometimes atypical, respiratory symptoms can be less pronounced, and other sites targeted, such as the digestive tract, the cardiovascular system and central nervous system. For instance, a number of neurologic manifestation, from unspecific symptoms such as headache, altered mental status, and anosmia, up to cerebrovascular accidents and Guillain–Barré syndrome have occurred in many patients with Covid-19 [16,17]. Morjaria et al. described two cases of unusual neurological complications, i.e. bilateral lower limbs weakness, possibly related to cerebrovascular accidents, in critically ill patients with prolonged hospital stays [18]. Great interest exists on whether patients presenting with atypical symptoms are at increased risk to evolve toward severe forms of COVID-19. Henry et al. revised the available literature about common gastrointestinal symptoms and found that abdominal pain, nausea and vomiting, but not diarrhoea, were significantly associated with an increased odds of severe COVID-19 [19]. Moreover, myocardial injury was often observed in SARS-CoV-2 patients, especially those with severe to critical disease, in need of intensive care treatment. Preliminary data by Violi et al. on a limited sample of patients suggested that patients who show troponin elevation may be at higher risk of mortality [20]. As for other predictors of outcome in COVID-19 patients, Sciacqua et al. explored the potential causative factors of poor outcome in elderly people, such as immunosenescence, reduced resilience and the coexistence of multiple comorbidities, and focused on impaired nutritional status and sarcopenia, commonly due to inadequate food and calorie intake and an unmet increased protein demand [21]. Pantanetti et al. reviewed the pathophysiologic basis related to an excess of disease severity in diabetic patients and suggested a possible use of dipeptidyl peptidase-4 inhibitors as immunomodulatory drugs in COVID-19 [22]. Surprisingly, a systematic review by Farsalinos et al. found that smoking had a protective effect against COVID-19, based on an unexpected low prevalence of current smokers among Chinese patients hospitalized with COVID-19 [23]. Despite confidence issues on the accuracy about data collection methods for reporting smoking status, similar findings have been reported from other countries, allowing to speculate on pharmaceutical nicotine as a potential treatment option in COVID-19 [24]. To date, there is no established treatment for COVID-19. In recent days, remdesivir was the first antiviral drug approved by U.S. Food and Drug Administration (FDA) and European Medicine Agency (EMA) for the treatment of hospitalized adults with evidence of SARS-CoV-2 lower respiratory tract involvement, in virtue of the positive results obtained in a double-blind, randomized, placebo-controlled trial [25]. So far, remdesivir has been available only for compassionate use or within the randomized clinical trial and therapeutic strategies have largely relied on off-label use of old drugs, such as antimalarial drugs chloroquine (CQ) and hydroxychloroquine (HCQ) and antiretroviral lopinavir/ritonavir and darunavir/cobicistat [26]. Unfortunately, conclusive data about the real impact of these compounds on the outcome on Covid-19 patients are still lacking, albeit a constant flow of published data from clinical experiences, mostly biased by methodological flaws. Fanin et al. analysed ins and outs of a well-known open-label non-randomized clinical trial by Gautret et al. on the efficacy of the combination use of hydroxychloroquine and azithromycin, which had great resonance and influenced treatment strategies worldwide, despite important limitations [27,28]. Depfenhart et al. revised pharmacodynamics basis of antiviral drugs available so far, and suggested bromhexine, an FDA-approved ingredient in mucolytic cough suppressants, as a potential new option, due to its TMPRSS2 inhibitor activity [29]. However, overall management of Covid-19 patients exceeds the administration of antiviral drugs. Immune-modulant drugs and anti-thrombotic prophylaxis are pillars of the treatment of severe forms. Both arterial and venous thrombotic events frequently complicated the course of patients with COVID-19, especially in those critically ill, leading to the definition of Coronavirus-associated coagulopathy (CAC) by the International Society on Thrombosis and Haemostasis [30,31]. An interesting Spanish case series of non-ICU hospitalized COVID-19 patients diagnosed with pulmonary embolism, without evidence of concomitant deep–vein thrombosis of the lower limbs, suggested a predominance of small-vessel thrombosis secondary to inflammatory and immune responses [32]. Understanding mechanism underlying CAC is crucial to put in place appropriate therapeutic measures: observed hemostatic alternations—increasedD-dimer, normal or slightly deranged prothrombin time and within range platelets count—differ from those usually observed during the disseminated intravascular coagulopathy. Bazzan et al. found reduced levels of ADAMTS-13 and higher levels of von Willebrand factor in a cohort of COVID-19 patients, in comparison with healthy controls, and also in fatal COVID-19 cases, when compared to patients with the non-fatal outcome. These alterations, similar to those observed in patients with thrombotic thrombocytopenic purpura, may lean more to a thrombotic microangiopathy origin of CAC, rather than a consumption coagulopathy [33]. Moreover, the infusion of hyperimmune plasma from donors recovered from SARS-CoV-2 infection emerged as an attractive option. Perotti et al. presented the COVID-19 PLASMA trial, the first proof-of-concept interventional trial using hyperimmune plasma with a high titre of specific neutralizing antibodies for treating critical patients with COVID-19 [34]. Supportive care includes supplemental oxygen and ventilatory management of patients with respiratory distress. Privitera et al. proposed a flowchart for non-invasive ventilation support in COVID-19 patients, as a first approach in the Emergency Department [35]. Management of chronic therapies was also challenging. The role of ACE-2 receptor in SARS-CoV-2 cell entry process produced a lively debate on the potential impact of angiotensin-converting enzyme inhibitors (ACE-Is) and angiotensin II receptor blockers (ARBs), extensively used for the treatment of hypertension and other cardiovascular diseases, on the natural history of SARS-Cov-2 infection. Two papers of the Topical Collection explored the potential implication of ACE-Is and ARBs use in Covid-19 patients [36,37]. Finally, Testa et al. addressed the management of Covid-19 patients on oral anticoagulant drugs, and the high risk of over/under treatment due to the multiple pharmacological interactions, and the possible necessity of mechanical ventilation, and suggested replacing oral anticoagulant therapies with parenteral low-molecular-weight heparin or unfractionated heparin [38]. On the other hand, a paper by Poli et al. provided some advice aimed at improving the outpatient management of people on anticoagulant treatment during COVID-19 pandemic, with particular regard to the lockdown and reopening periods [39]. In the authors’ view, this new Topical Collection will contribute significantly to stimulate the scientific debate and to advance the current body of knowledge of the medical community about the pandemic and its ethical, organizational, and clinical challenges. Given the importance of the topic to the active role that internists and general physicians play in assisting the many patients directly or indirectly affected by COVID-19,Internal and Emergency Medicineremains committed to further expanding the current knowledge base and advancing the scientific debate about the impact of SARS-CoV-2 on human health worldwide.
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- 2020
50. Modifying Practices in GI Oncology in the Face of COVID-19: Recommendations From Expert Oncologists on Minimizing Patient Risk
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Scott Kopetz, Emil Lou, Veena Shankaran, Emily K. Bergsland, S. Yousuf Zafar, Cathy Eng, Alok A. Khorana, Shaalan Beg, Sam J. Lubner, and Leonard B. Saltz
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medicine.medical_specialty ,2019-20 coronavirus outbreak ,Coronavirus disease 2019 (COVID-19) ,Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) ,Patient risk ,Pneumonia, Viral ,MEDLINE ,Medical Oncology ,Risk Assessment ,Betacoronavirus ,Neoplasms ,Humans ,Medicine ,Viral therapy ,Medical physics ,Pandemics ,Oncologists ,SARS-CoV-2 ,Oncology (nursing) ,business.industry ,Health Policy ,COVID-19 ,Neoplasms therapy ,Oncology ,Coronavirus Infections ,business ,Risk assessment - Published
- 2020
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