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  • 1
    In: Fetal Diagnosis and Therapy, S. Karger AG, Vol. 20, No. 5 ( 2005), p. 371-376
    Abstract: 〈 i 〉 Objective: 〈 /i 〉 Computerized fetal heart rate (FHR) analysis revealed that antenatal corticosteroids transiently suppress multiple parameters of fetal well-being, potentially leading to the erroneous diagnosis of fetal distress and to unnecessary iatrogenic delivery of premature infants. Our aim was to determine whether clinicians who visually analyze FHR tracings detect these suppressive effects, thereby potentially affecting their clinical management decisions. 〈 i 〉 Methods: 〈 /i 〉 Singleton pregnancies admitted for preterm labor between 26 and 34 weeks’ gestation received two doses of betamethasone, 24 h apart, and were monitored daily between 16:00 and 19:00 h for 5 days. FHR tracings were randomly coded and presented in a non-consecutive order to four clinicians, who were unaware of the time of steroid administration. FHR baseline, FHR variability, number of accelerations and amplitude of maximal FHR acceleration were determined. Variability was scored semiquantitatively based on a modified Hon score. Analysis of variance (ANOVA) with repeated measures was used for primary analysis and followed up with the Wald test of significance. Corrections for multiple comparisons were made and only p 〈 0.005 considered significant. ANOVA was also used to assess the uniformity of trend in the interpretation by the four examiners for each given day. 〈 i 〉 Results: 〈 /i 〉 Baseline FHR was elevated, FHR variability was decreased, and the number of accelerations decreased on day 1 (p 〈 0.0001; p 〈 0.0001; p 〈 0.0001) and day 2 (p 〉 0.0001; p 〈 0.0001; p 〈 0.0001) in comparison to day 0. On day 3, the FHR baseline, variability and number of accelerations returned to pre-exposure values (p = NS). The maximal amplitude of FHR accelerations showed a trend towards reduction (p = 0.08). Subgroup analysis by gestational age (group I = 26–30 weeks and group II = 30–34 weeks) showed the same response patterns and significance levels for both groups. 〈 i 〉 Conclusions: 〈 /i 〉 Betamethasone causes profound, but transient, suppression of FHR parameters, which can mimic fetal distress. This effect is clinically recognized by visual FHR analysis. Clinicians need to be aware of this phenomenon, in order to avoid unwarranted iatrogenic delivery.
    Type of Medium: Online Resource
    ISSN: 1015-3837 , 1421-9964
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2005
    detail.hit.zdb_id: 1482292-1
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  • 2
    Online Resource
    Online Resource
    S. Karger AG ; 2022
    In:  Acta Haematologica Vol. 145, No. 4 ( 2022), p. 440-447
    In: Acta Haematologica, S. Karger AG, Vol. 145, No. 4 ( 2022), p. 440-447
    Abstract: 〈 b 〉 〈 i 〉 Background: 〈 /i 〉 〈 /b 〉 Tocilizumab has been proposed as an effective treatment for severe COVID-19. We aimed to investigate whether tocilizumab administration is associated with increased availability of serum iron which may possibly be associated with adverse effects on clinical outcomes. 〈 b 〉 〈 i 〉 Methods: 〈 /i 〉 〈 /b 〉 We performed an observational, retrospective cohort study. We included adults, who were hospitalized in ICU with the diagnosis of severe COVID-19 infection eligible for tocilizumab treatment. Laboratory data including serum iron, ferritin, transferrin saturation, hemoglobin, and C-reactive protein levels of all patients were collected shortly before and 24 h, 48 h, and 72 h after tocilizumab administration. 〈 b 〉 〈 i 〉 Results: 〈 /i 〉 〈 /b 〉 During the study period, 15 patients fulfilled the inclusion criteria and were eligible to receive tocilizumab treatment. Tocilizumab therapy was associated with a prominent increase in serum iron and transferrin saturation levels (26 ± 13 μg/dL and 15 ± 8% before treatment and 79 ± 32 μg/dL and 41 ± 15% 72 h after treatment, respectively, 〈 i 〉 p 〈 /i 〉 & #x3c; 0.001) and decrease in serum ferritin levels (1,921 ± 2,071 ng/mL before and 1,258 ± 1,140 ng/mL 72 h after treatment, 〈 i 〉 p 〈 /i 〉 = 0.027). 〈 b 〉 〈 i 〉 Conclusion: 〈 /i 〉 〈 /b 〉 Treatment of severe COVID-19 patients with tocilizumab is associated with a profound increase in serum iron and ferritin saturation levels along with a decrease in ferritin levels. This may represent an undesirable side effect that may potentiate viral replication.
    Type of Medium: Online Resource
    ISSN: 0001-5792 , 1421-9662
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2022
    detail.hit.zdb_id: 1481888-7
    detail.hit.zdb_id: 80008-9
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  • 3
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2009
    In:  Journal of Neural Transmission Vol. 116, No. 2 ( 2009-2), p. 151-160
    In: Journal of Neural Transmission, Springer Science and Business Media LLC, Vol. 116, No. 2 ( 2009-2), p. 151-160
    Type of Medium: Online Resource
    ISSN: 0300-9564 , 1435-1463
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2009
    detail.hit.zdb_id: 1481655-6
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  • 4
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2007
    In:  Journal of Molecular Neuroscience Vol. 31, No. 3 ( 2007-03), p. 307-307
    In: Journal of Molecular Neuroscience, Springer Science and Business Media LLC, Vol. 31, No. 3 ( 2007-03), p. 307-307
    Type of Medium: Online Resource
    ISSN: 0895-8696 , 1559-1166
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2007
    detail.hit.zdb_id: 2071508-0
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  • 5
    Online Resource
    Online Resource
    Frontiers Media SA ; 2022
    In:  Frontiers in Neurology Vol. 12 ( 2022-2-14)
    In: Frontiers in Neurology, Frontiers Media SA, Vol. 12 ( 2022-2-14)
    Abstract: Elevated blood pressure (BP) in acute ischemic stroke is common. A raised BP is related to mortality and disability, yet excessive BP lowering can be detrimental. The optimal BP management in acute ischemic stroke remains insufficient and relies on expert consensus statements. Permissive hypertension is recommended during the first 24-h after stroke onset, yet there is ongoing uncertainty regarding the most appropriate blood BP management in the acute phase of ischemic stroke. This study aims to develop a decision support tool for improving the management of extremely high BP during the first 24 h after acute ischemic stroke by using machine learning (ML) tools. Methods This diagnostic accuracy study used retrospective data from MIMIC-III and eICU databases. Decision trees were constructed by a hierarchical binary recursive partitioning algorithm to predict the BP-lowering of 10–30% off the maximal value when antihypertensive treatment was given in patients with an extremely high BP (above 220/110 or 180/105 mmHg for patients receiving thrombolysis), according to the American Heart Association/American Stroke Association (AHA/ASA), the European Society of Cardiology, and the European Society of Hypertension (ESC/ESH) guidelines. Regression trees were used to predict the time-weighted average BP. Implementation of synthetic minority oversampling technique was used to balance the dataset according to different antihypertensive treatments. The model performance of the decision tree was compared to the performance of neural networks, random forest, and logistic regression models. Results In total, 7,265 acute ischemic stroke patients were identified. Diastolic BP (DBP) is the main variable for predicting BP reduction in the first 24 h after a stroke. For patients receiving thrombolysis with DBP & lt;120 mmHg, Labetalol and Amlodipine are effective treatments. Above DBP of 120 mmHg, Amlodipine, Lisinopril, and Nicardipine are the most effective treatments. However, successful treatment depends on avoiding hyponatremia and on kidney functions. Conclusion This is the first study to address BP management in the acute phase of ischemic stroke using ML techniques. The results indicate that the treatment choice should be adjusted to different clinical and BP parameters, thus, providing a better decision-making approach.
    Type of Medium: Online Resource
    ISSN: 1664-2295
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2022
    detail.hit.zdb_id: 2564214-5
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  • 6
    Online Resource
    Online Resource
    Elsevier BV ; 2019
    In:  European Journal of Internal Medicine Vol. 63 ( 2019-05), p. 34-41
    In: European Journal of Internal Medicine, Elsevier BV, Vol. 63 ( 2019-05), p. 34-41
    Type of Medium: Online Resource
    ISSN: 0953-6205
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2019
    detail.hit.zdb_id: 2026166-4
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  • 7
    Online Resource
    Online Resource
    Mary Ann Liebert Inc ; 2006
    In:  Antioxidants & Redox Signaling Vol. 8, No. 11-12 ( 2006-11), p. 1987-1995
    In: Antioxidants & Redox Signaling, Mary Ann Liebert Inc, Vol. 8, No. 11-12 ( 2006-11), p. 1987-1995
    Type of Medium: Online Resource
    ISSN: 1523-0864 , 1557-7716
    Language: English
    Publisher: Mary Ann Liebert Inc
    Publication Date: 2006
    detail.hit.zdb_id: 2039747-1
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  • 8
    In: Otorhinolaryngology-Head and Neck Surgery, Open Access Text Pvt, Ltd., Vol. 5, No. 6 ( 2020)
    Type of Medium: Online Resource
    ISSN: 2398-4937
    Language: Unknown
    Publisher: Open Access Text Pvt, Ltd.
    Publication Date: 2020
    detail.hit.zdb_id: 2872629-7
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  • 9
    In: International Journal of Molecular Sciences, MDPI AG, Vol. 18, No. 8 ( 2017-08-01), p. 1666-
    Abstract: Neuroinflammation contributes to amyotrophic lateral sclerosis (ALS) progression. TLR4, a transmembrane protein that plays a central role in activation of the innate immune system, has been shown to induce microglial activation in ALS models. TLR4 is up-regulated in the spinal cords of hSOD1G93A mice. We aimed to examine the effects of specific TLR4 inhibition on disease progression and survival in the hSOD1G93A mouse model of ALS. Immunologic effect of TLR4 inhibition in vitro was measured by the effect of TAK-242 treatment on LPS-induced splenocytes proliferation. hSOD1G93A transgenic mice were treated with TAK-242, a selective TLR4 inhibitor, or vehicle. Survival, body weight, and motor behavior were monitored. To evaluate in vivo immunologic modifications associated with TAK-242 treatment, we measured serum IL-1β in the plasma, as well as IL-1β and TNF-α mRNAs in the spinal cord in wild-type mice and in TAK-242-treated and vehicle-treated early symptomatic hSOD1G93A mice. Immunohistochemical analysis of motor neurons, astrocytes, and microglial reactivity in the spinal cords were performed on symptomatic (100 days old) TAK-242-treated and vehicle-treated hSOD1G93A mice. In vitro, splenocytes taken from 100 days old hSOD1G93A mice showed significantly increased proliferation when exposed to LPS (p = 0.0002), a phenomenon that was reduced by TAK-242 (p = 0.0179). TAK-242 treatment did not attenuate body weight loss or significantly affect survival. However, TAK-242-treated hSOD1G93A mice showed temporary clinical delay in disease progression evident in the ladder test and hindlimb reflex measurements. Plasma IL-1β levels were significantly reduced in TAK-242-treated compared to vehicle-treated hSOD1G93A mice (p = 0.0023). TAK-242 treatment reduced spinal cord astrogliosis and microglial activation and significantly attenuated spinal cord motor neuron loss at early disease stage (p = 0.0259). Compared to wild-type animals, both IL-1β and TNF-α mRNAs were significantly upregulated in the spinal cords of hSOD1G93A mice. Spinal cord analysis in TAK-242-treated hSOD1G93A mice revealed significant attenuation of TNF-α mRNA (p = 0.0431), but no change in IL-1β mRNA. TLR4 inhibition delayed disease progression, attenuated spinal cord astroglial and microglial reaction, and reduced spinal motor neuron loss in the ALS hSOD1G93A mouse model. However, this effect did not result in increased survival. To our knowledge, this is the first report on TAK-242 treatment in a neurodegenerative disease model. Further studies are warranted to assess TLR4 as a therapeutic target in ALS.
    Type of Medium: Online Resource
    ISSN: 1422-0067
    Language: English
    Publisher: MDPI AG
    Publication Date: 2017
    detail.hit.zdb_id: 2019364-6
    SSG: 12
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  • 10
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2007
    In:  Journal of Neurology Vol. 254, No. S5 ( 2007-9), p. 19-26
    In: Journal of Neurology, Springer Science and Business Media LLC, Vol. 254, No. S5 ( 2007-9), p. 19-26
    Type of Medium: Online Resource
    ISSN: 0340-5354 , 1432-1459
    RVK:
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2007
    detail.hit.zdb_id: 1421299-7
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