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  1. Article ; Online: Secondary infections and long-term outcomes among hospitalized elderly and non-elderly patients with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and treated with baricitinib: a comparative study from the national centre of Hungary.

    Gáspár, Zsófia / Szabó, Bálint Gergely / Andrikovics, Hajnalka / Ceglédi, Andrea / Rajmon, Martin / Ábrahám, Anita / Várnai, Zsuzsanna / Kiss-Dala, Noémi / Szlávik, János / Sinkó, János / Vályi-Nagy, István / Lakatos, Botond

    GeroScience

    2024  Volume 46, Issue 3, Page(s) 2863–2877

    Abstract: Baricitinib is considered a first-line treatment for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-infected adult patients with an associated cytokine storm syndrome (CSS). Our objective was to compare rates of secondary infections and ... ...

    Abstract Baricitinib is considered a first-line treatment for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-infected adult patients with an associated cytokine storm syndrome (CSS). Our objective was to compare rates of secondary infections and long-term outcomes of elderly and non-elderly patients who received baricitinib for COVID-19. We conducted a single-centre observational study between November 2020 and September 2023, focusing on hospitalized adult SARS-CoV-2 patients with CSS, categorized as elderly (≥ 65 years) and non-elderly (< 65 years). Enrolment, severity stratification, and diagnosis of infectious complications followed predefined criteria. Outcomes of all-cause mortality and rates of non-severe and severe secondary infections were assessed at 1-year post-treatment initiation. Kaplan-Meier analysis was performed for survival analysis. In total, 490 patients were enrolled (median age 65 ± 23 (21-100) years (years, median ± IQR, min-max); 49.18% elderly; 59.59% male). Elderly patients were admitted to the hospital significantly earlier (7 ± 5 days vs. 8 ± 4 days; p = 0.02), experienced a higher occurrence of severe COVID-19 (121/241, 50.21% vs. 98/249, 39.36%; p = 0.02), and required the use of non-invasive ventilation at baseline (167/225, 74.22% vs. 153/236, 64.83%; p = 0.03). At 1 year, all-cause mortality was significantly higher in the elderly subgroup (111/241, 46.06% vs. 29/249, 11.65%; p < 0.01). At 90 days and 1 year, rates of any severe secondary infection were also more prevalent among the elderly (56/241, 23.24% vs. 37/249 14.86%; p = 0.02 and 58/241, 24.07% vs. 39/249, 15.66%; p = 0.02). In conclusion, elderly SARS-CoV-2-infected patients experience a more severe clinical course, higher secondary infection rates, and increased risk for long-term mortality, regardless of immunomodulatory therapy.
    MeSH term(s) Humans ; Male ; Aged ; Middle Aged ; Aged, 80 and over ; Female ; SARS-CoV-2 ; COVID-19 ; Coinfection ; Hungary ; COVID-19 Drug Treatment ; Azetidines ; Purines ; Pyrazoles ; Sulfonamides
    Chemical Substances baricitinib (ISP4442I3Y) ; Azetidines ; Purines ; Pyrazoles ; Sulfonamides
    Language English
    Publishing date 2024-02-17
    Publishing country Switzerland
    Document type Observational Study ; Journal Article
    ZDB-ID 2886586-8
    ISSN 2509-2723 ; 2509-2715
    ISSN (online) 2509-2723
    ISSN 2509-2715
    DOI 10.1007/s11357-024-01099-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Outcomes of high-risk adult outpatients treated with early remdesivir therapy during the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) omicron era: experiences from the national centre of Hungary.

    Gáspár, Zsófia / Szabó, Bálint Gergely / Ábrahám, Anita / Várnai, Zsuzsanna / Kiss-Dala, Noémi / Szlávik, János / Sinkó, János / Vályi-Nagy, István / Lakatos, Botond

    Naunyn-Schmiedeberg's archives of pharmacology

    2023  Volume 396, Issue 8, Page(s) 1857–1862

    Abstract: Emerging evidence suggests that remdesivir might improve clinical outcome of high-risk outpatients with coronavirus disease 2019 (COVID-19). Our aim was to evaluate characteristics and outcomes of nonhospitalised adults diagnosed with COVID-19 and ... ...

    Abstract Emerging evidence suggests that remdesivir might improve clinical outcome of high-risk outpatients with coronavirus disease 2019 (COVID-19). Our aim was to evaluate characteristics and outcomes of nonhospitalised adults diagnosed with COVID-19 and treated with early remdesivir therapy during the omicron wave. A single-centre prospective cohort study was performed among adult patients between February and June 2022, during the circulation of phylogenetic assignment of named global outbreak (PANGO) subvariants BA.2, BA.4, and BA.5 in Hungary. Patients were enrolled based on pre-defined criteria. Clinical characteristics (demography, comorbidities, vaccination status, imaging, treatment, and disease course) and outcomes (COVID-19 related hospitalisation, oxygen supplementation, intensive care support, and all-cause death) were assessed at 28 days post-treatment. A subgroup analysis of patients with and without active haematological malignancies was also carried out. Altogether, 127 patients were enrolled: 51.2% (65/127) were female with a median age of 59 (IQR: 22, range: 21‒92) years, and 48.8% (62/127) had active haematological malignancy. At 28 days post-treatment, 7.1% (9/127) of patients required COVID-19-related hospitalisation, 2.4% (3/127) required oxygen supplementation, 1.6% (2/127) required intensive care, and 0.8% (1/127) died due to a non-COVID-19-related secondary infection at the intensive care unit, all with haematological malignancies. Early remdesivir treatment might be a feasible strategy among high-risk outpatients with COVID-19 during the omicron wave.
    MeSH term(s) Humans ; Adult ; Female ; Young Adult ; Middle Aged ; Aged ; Aged, 80 and over ; Male ; SARS-CoV-2 ; COVID-19 ; Outpatients ; Hungary ; Phylogeny ; Prospective Studies ; COVID-19 Drug Treatment ; Hematologic Neoplasms
    Chemical Substances remdesivir (3QKI37EEHE)
    Language English
    Publishing date 2023-03-09
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 121471-8
    ISSN 1432-1912 ; 0028-1298
    ISSN (online) 1432-1912
    ISSN 0028-1298
    DOI 10.1007/s00210-023-02456-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: A nyugat-nílusi vírus kimutatása humán betegmintákból: nyomon követéses vizsgálatok a 2015. évi szezonális időszakban.

    Nagy, Anna / Nagy, Orsolya / Bán, Enikő / Molnár, Eszter / Müller, Zsófia / Orbán, Márton / Kecskés, Borbála / Harsányi, Emese Henriett / Kővágó, Levente / Jobbágy, Lajos / Németh, Zoltán / Várnai, Zsuzsanna / Takács, Mária

    Orvosi hetilap

    2017  Volume 158, Issue 20, Page(s) 791–796

    Abstract: Introduction: West Nile virus, a mosquito-borne viral zoonosis is responsible for human infections in Hungary. Laboratory diagnosis is based on serological tests, however the application of molecular methods has been appreciated.: Aim: The aim of the ...

    Title translation Detection of West Nile virus in human samples: follow-up studies during the 2015 seasonal period.
    Abstract Introduction: West Nile virus, a mosquito-borne viral zoonosis is responsible for human infections in Hungary. Laboratory diagnosis is based on serological tests, however the application of molecular methods has been appreciated.
    Aim: The aim of the study was to investigate blood, cerebrospinal-fluid and urine samples of acutely ill patients and to follow-up PCR positive cases to ascertain the length of virus excretion.
    Method: Clinical specimens were examined by indirect-immunofluorescent, haemagglutination-inhibition, two PCR tests and Sanger-sequencing. Virus isolation in case of two patients was successful.
    Results: A follow-up study could be carried out in case of 5 patients. Viral nucleic acid was detectable in urine even for several weeks after symptom onset and viral RNA was present at higher concentration compared with other samples.
    Conclusions: PCR analysis of urine could provide useful epidemiological and diagnostic information. Therefore, it is recommended to collect urine samples in order to supplement the serological diagnosis. Orv Hetil. 2017; 158(20): 791-796.
    MeSH term(s) Antibodies, Viral/blood ; Follow-Up Studies ; Humans ; Hungary ; RNA, Viral/blood ; RNA, Viral/urine ; Seasons ; West Nile Fever/blood ; West Nile Fever/urine ; West Nile Fever/virology ; West Nile virus/isolation & purification
    Chemical Substances Antibodies, Viral ; RNA, Viral
    Language Hungarian
    Publishing date 2017-05
    Publishing country Hungary
    Document type Journal Article
    ZDB-ID 123879-6
    ISSN 1788-6120 ; 0030-6002
    ISSN (online) 1788-6120
    ISSN 0030-6002
    DOI 10.1556/650.2017.30760
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Role of favipiravir in the treatment of adult patients with moderate to severe COVID-19: a single-center, prospective, observational, sequential cohort study from Hungary

    SZABO, Balint Gergely / LENART, Katalin Szidonia / PETRIK, Borisz / GASPAR, Zsofia / BALOGH, Zsofia / BANYAI, Zsuzsanna / BANYASZ, Emese / BUDAI, Jozsef / CZEL, Eszter / FRIED, Katalin / HANUSKA, Adrienn / KISS-DALA, Noemi / LORINCZI, Csaba / NEMESI, Krisztina / KADAR, Janos / NAGY, Eva Livia / OSVALD, Akos / PETROVICZ, Edina / RICZU, Alexandra /
    SZANKA, Judit / SZATHMARY, Beata / SZOMBATI, Andrea / TOTH, Szilvia / VARNAI, Zsuzsanna / WOLLER, Orsolya / SZLAVIK, Janos / LAKATOS, Botond

    medRxiv

    Abstract: Background: Preliminary data suggests that favipiravir (FVP) might have a role in COVID-19 treatment. Methods: A single-center, prospective, observational, sequential cohort study was performed among consecutive adults hospitalized with PCR-confirmed ... ...

    Abstract Background: Preliminary data suggests that favipiravir (FVP) might have a role in COVID-19 treatment. Methods: A single-center, prospective, observational, sequential cohort study was performed among consecutive adults hospitalized with PCR-confirmed COVID-19 between March-July,2020. Patients were screened for inclusion by a priori criteria, and were included in the favipiravir cohort if standard-of-care (SOC)+FVP, or the non-favipiravir group if SOC+other antiviral medications without FVP were administered for >48 hours. Treatment allocation was done per national guidelines. For COVID-19 diagnosis and severity, ECDC and WHO definitions were utilized, and daily per protocol hospital follow-up was done. Primary composite end-point was disease progression (14-day all-cause death, need for mechanical ventilation, or immunomodulatory therapy). For statistical comparison, Fisher9s exact test and Mann-Whitney U-test were used. Results: In all, 75 patients were included per cohort. In the FVP cohort, chronic heart disease (36/75, 48.0% vs. 16/75, 21.3%, p<0.01) and diabetes mellitus (23/75, 30.7% vs. 10/75, 13.3%, p<0.01) were more prevalent, hospital LOS (18.5+/-15.5 days vs. 13.0+/-8.5 days, p<0.01) was higher. Disease progression (17/75, 22.7% vs. 10/75, 13.3%, p=0.13), 14-day all-cause death (9/75, 12.0% vs. 10/75, 13.3%, p=0.8) and need for mechanical ventillation (8/75, 10.7% vs. 4/75, 5.3%, p=0.22) were similar between groups. Immunomodulatory therapies were administered frequently among patients receiving FVP (10/75, 13.3% vs. 1/75, 1.3%, p<0.01). Conclusions: In this study, favipiravir did not seem to affect disease progression. Further data are needed to position this drug among the anti-SARS-CoV-2 armamentarium.
    Keywords covid19
    Language English
    Publishing date 2020-12-09
    Publisher Cold Spring Harbor Laboratory Press
    Document type Article ; Online
    DOI 10.1101/2020.11.26.20238014
    Database COVID19

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