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  • 1
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2023
    In:  Clinical Infectious Diseases Vol. 76, No. 6 ( 2023-03-21), p. 1067-1073
    In: Clinical Infectious Diseases, Oxford University Press (OUP), Vol. 76, No. 6 ( 2023-03-21), p. 1067-1073
    Abstract: Tixagevimab and cilgavimab, a combined monoclonal antibody (Evusheld), was granted emergency use authorization for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) preexposure prophylaxis in individuals with immunocompromising conditions. In this study we used population-based real-world data to evaluate the effectiveness of Evusheld in immunocompromised patients. Methods Using the computerized database of the largest healthcare provider in Israel, we identified all adult immunocompromised patients who were eligible to receive Evusheld (150 mg tixagevimab and 150 mg cilgavimab) on 15 February 2022. Patients with a documentation of a prior SARS-CoV-2 infection were excluded. A total of 703 patients who received Evusheld were propensity score matched, using a ratio of 1:4, with 2812 patients who had not received Evusheld (control group). Patients were followed through 30 June 2022 for up to 90 days for the first documentation of SARS-CoV-2 infection and coronavirus disease 2019 (COVID-19)–related hospitalization. Results Overall, 72 patients in the Evusheld group and 377 patients in the control group had SARS-CoV-2 infection, reflecting an incidence rate of 4.18 and 5.64 per 100 person-months, respectively. The hazard ratios were 0.75 (95% confidence interval [CI]: .58–.96) for SARS-CoV-2 infection and 0.41 (95% CI: .19–.89) for COVID-19–related hospitalization in the Evusheld group compared to the control group. The magnitude of relative risk reduction of each outcome was greater in nonobese patients (P for interaction = .020 and .045, respectively). Conclusions This study suggests that Evusheld is effective in reducing the risk of SARS-CoV-2 infection and COVID-19 hospitalization in immunocompromised patients. The effectiveness of this dose appears to be greater in nonobese patients.
    Type of Medium: Online Resource
    ISSN: 1058-4838 , 1537-6591
    RVK:
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2023
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  • 2
    In: The Pharmacogenomics Journal, Springer Science and Business Media LLC, Vol. 21, No. 3 ( 2021-06), p. 402-408
    Type of Medium: Online Resource
    ISSN: 1470-269X , 1473-1150
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2021
    detail.hit.zdb_id: 2051501-7
    SSG: 15,3
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  • 3
    In: Heart, BMJ, Vol. 108, No. 4 ( 2022-02), p. 266-273
    Abstract: Clinical models such as the HAS-BLED (standing for Hypertension, Abnormal liver/renal function, Stroke history, Bleeding history or predisposition, Labile INR, Elderly, Drug/alcohol usage) were developed to predict risk of major bleeding on vitamin K antagonists/antiplatelet therapy. We aimed to develop a model that will improve the ability to predict major bleeding events in patients with non-valvular atrial fibrillation (AF) treated with new oral anticoagulants (NOACs). Methods Clalit Health Services is the largest of four integrated healthcare organisations in Israel, which insures 4.7 million patients (53% of the population). We identified in Clalit Health Services all patients with AF, new users of an NOAC (2013–2017), and followed them until first occurrence of a major bleeding event, death, switch to another oral anticoagulant, 30 days after discontinuation of NOAC or end of follow-up (31 December 2019). Importance of the candidate model variables was estimated by inclusion frequencies across forward selection algorithm applied to 50 bootstrap samples. Then, backward selection algorithm using the modified Bayesian Information Criterion for competing risks was applied to select predictors for the final model. Results 47 623 patients with AF prescribed NOAC were studied. 28 055 patients with AF, initiators of apixaban (mean age 78.7, SD 9.0), were included in the first phase and had 662 major bleeding events. Nine variables were selected for inclusion in a final points-based risk-scoring system: male sex, anaemia, thrombocytopaenia ( 〈 99×10 3 /µL), concurrent antiplatelet therapy, hypertension, prior major bleeding, risk factors for a fall, low cholesterol level and low estimated glomerular filtration rate, with apparent area-under-curve (AUC) of 0.6546. Applicability of the model was then shown for 14 118 and 5450 patients with AF, initiators of dabigatran and rivaroxaban, where the score achieved c indices of 0.62 and 0.61, respectively. Conclusions We present a novel and simple risk score for prediction of major bleeding in patients with non-valvular AF treated with NOACs. Validation in additional cohorts is warranted.
    Type of Medium: Online Resource
    ISSN: 1355-6037 , 1468-201X
    Language: English
    Publisher: BMJ
    Publication Date: 2022
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    detail.hit.zdb_id: 1475501-4
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  • 4
    In: Translational Oncology, Elsevier BV, Vol. 14, No. 1 ( 2021-01), p. 100934-
    Type of Medium: Online Resource
    ISSN: 1936-5233
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2021
    detail.hit.zdb_id: 2443840-6
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  • 5
    In: Blood, American Society of Hematology, Vol. 106, No. 11 ( 2005-11-16), p. 4672-4672
    Abstract: Bone marrow (BM) involvement in low grade NHL patients results in stage IV clinical classification and has a negative impact on survival. Standard practice includes morphologic examination of BM biopsy at diagnosis. In many institutions flow cytometry (FC) is also routinely performed on BM aspirates accompanying respective biopsies. FC is believed to increase the sensitivity of the morphologic analysis by detecting occult lymphoma cells evading the pathologist’s eyes. However, the prevalence of such finding and especially its clinical significance are largely unknown. In our institute BM biopsies of NHL patients conducted after 1993 were routinely accompanied by BM aspirates with FC analysis. We retrospectively reviewed the charts of all low grade NHL patients (small lymphocytic lymphoma, follicular small cleaved cell NHL, follicular mixed small and large cell, marginal zone B-cell lymphoma, mantle cell lymphoma and Waldenstrom macroglobulinemia) diagnosed or followed at the Hematology Unit (1994–2004), who had undergone BM biopsies and aspirates as part of their diagnostic workup or before treatment. FC results were considered positive if they showed either a ratio of immunoglobulin light chain expression of kappa: lambda 〉 3:1 or lambda: kappa 〉 2:1 in at least 2% of the gated population. Cell analysis included: CD5 versus CD19, CD20 versus CD10, and kappa light chain versus lambda light chain occasionally with the addition of CD19 or CD20. Lymphoma involving BM by morphology was found in the biopsies of 43 patients (61.4%) (BM+ group). Of the remaining 1 patient had inconclusive results and 26 patients had normal BM biopsies. Of these 27 patients the FC analysis was positive in 9 patients (BM-FC+ group) and negative in 18 (BM-FC- group). We could not compare the groups using FLIPI or IPI scores as a whole since both include the stage as one of the five summed parameters while BM involvement was different by definition between the groups. However, the groups had similar parameters that are prognostically important and are part of the FLIPI scoring system including age, hemoglobin and LDH levels and also the number of involved extranodal sites. Splenic involvement and number of involved nodal sites were higher in BM+ and BM-FC+ groups than in BM-FC- group. Significant differences in disease progression as indicated by time-to-treatment were observed. The median treatment-free period was shorter in the BM+ and BM-FC+ groups (1 month and 4 months, respectively) as compared with the BM-FC- group (31 months) (log rank test p=0.0195). BM-FC- patients had significantly longer survival time than BM+ and BM-FC+ groups. Median survival time was not reached for the BM-FC- patients while in the BM+ and BM-FC+ groups median survival times were 129 and 89 months respectively with no significant difference between them. (Log rank test=0.029 for the difference between BM-FC- and the two other groups). We conclude that the outcome of low grade NHL patients found to have malignant cells by FC analysis while their BM morphology is normal is the same as that of patients with histological involvement. This may imply that patients with localized disease who have BM involvement by FC should be regarded as advanced stage disease.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
    RVK:
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    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2005
    detail.hit.zdb_id: 1468538-3
    detail.hit.zdb_id: 80069-7
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  • 6
    Online Resource
    Online Resource
    Bioscientifica ; 2018
    In:  Endocrine Abstracts ( 2018-05-08)
    In: Endocrine Abstracts, Bioscientifica, ( 2018-05-08)
    Type of Medium: Online Resource
    ISSN: 1479-6848
    Language: Unknown
    Publisher: Bioscientifica
    Publication Date: 2018
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  • 7
    In: The American Journal of Medicine, Elsevier BV, ( 2023-8)
    Type of Medium: Online Resource
    ISSN: 0002-9343
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2023
    detail.hit.zdb_id: 2003338-2
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  • 8
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2023
    In:  Clinical Infectious Diseases Vol. 76, No. 3 ( 2023-02-08), p. e342-e349
    In: Clinical Infectious Diseases, Oxford University Press (OUP), Vol. 76, No. 3 ( 2023-02-08), p. e342-e349
    Abstract: Paxlovid was granted an Emergency Use Authorization for the treatment of mild to moderate coronavirus disease 2019 (COVID-19), based on the interim analysis of the Evaluation of Protease Inhibition for COVID-19 in High-Risk Patients (EPIC-HR) trial. Paxlovid effectiveness needs to be assessed in a noncontrolled setting. In this study we used population-based real-world data to evaluate the effectiveness of Paxlovid. Methods The database of the largest healthcare provider in Israel was used to identify all adults aged 18 years or older with first-ever positive test for severe acute respiratory syndrome coronavirus 2 between January and February 2022, who were at high risk for severe COVID-19 and had no contraindications for Paxlovid use. Patients were included irrespective of their COVID-19 vaccination status. Cox hazard regression was used to estimate the 28-day hazard ratio (HR) for severe COVID-19 or mortality with Paxlovid examined as time-dependent variable. Results Overall, 180 351 eligible patients were included; of these, only 4737 (2.6%) were treated with Paxlovid, and 135 482 (75.1%) had adequate COVID-19 vaccination status. Both Paxlovid and adequate COVID-19 vaccination status were associated with significant decrease in the rate of severe COVID-19 or mortality with adjusted HRs of 0.54 (95% confidence interval [CI] , .39–.75) and 0.20 (95% CI, .17–.22), respectively. Paxlovid appears to be more effective in older patients, immunosuppressed patients, and patients with underlying neurological or cardiovascular disease (interaction P & lt; .05 for all). No significant interaction was detected between Paxlovid treatment and COVID-19 vaccination status. Conclusions This study suggests that in the era of Omicron and in real-life settings, Paxlovid is highly effective in reducing the risk of severe COVID-19 or mortality.
    Type of Medium: Online Resource
    ISSN: 1058-4838 , 1537-6591
    RVK:
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2023
    detail.hit.zdb_id: 2002229-3
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  • 9
    Online Resource
    Online Resource
    Elsevier BV ; 2016
    In:  The American Journal of Medicine Vol. 129, No. 8 ( 2016-08), p. 843-849
    In: The American Journal of Medicine, Elsevier BV, Vol. 129, No. 8 ( 2016-08), p. 843-849
    Type of Medium: Online Resource
    ISSN: 0002-9343
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2016
    detail.hit.zdb_id: 2003338-2
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  • 10
    Online Resource
    Online Resource
    Elsevier BV ; 2022
    In:  European Journal of Pharmacology Vol. 932 ( 2022-10), p. 175209-
    In: European Journal of Pharmacology, Elsevier BV, Vol. 932 ( 2022-10), p. 175209-
    Type of Medium: Online Resource
    ISSN: 0014-2999
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2022
    detail.hit.zdb_id: 1483526-5
    SSG: 15,3
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