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    <title>DSpace Собрание:</title>
    <link>http://ir.librarynmu.com/handle/123456789/18777</link>
    <description />
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        <rdf:li rdf:resource="http://ir.librarynmu.com/handle/123456789/15027" />
        <rdf:li rdf:resource="http://ir.librarynmu.com/handle/123456789/15025" />
        <rdf:li rdf:resource="http://ir.librarynmu.com/handle/123456789/15021" />
        <rdf:li rdf:resource="http://ir.librarynmu.com/handle/123456789/15019" />
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    <dc:date>2026-04-14T22:12:22Z</dc:date>
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  <item rdf:about="http://ir.librarynmu.com/handle/123456789/15027">
    <title>Impact of Alteplase on Mortality in Critically Ill Patients with COVID-19 and Pulmonary Embolism</title>
    <link>http://ir.librarynmu.com/handle/123456789/15027</link>
    <description>Название: Impact of Alteplase on Mortality in Critically Ill Patients with COVID-19 and Pulmonary Embolism
Авторы: Oliynyk, O.; Rorat, M.; Solyarik, S.; Lukianchuk, V.; Dubrov, S.; Guryanov, V.; Oliynyk, Y.; Yaroslavskaya, S.; Szalast, R.; Barg, W.
Краткий осмотр (реферат): COVID-19 is an independent risk factor for pulmonary embolism (PE). Little is known about alteplase therapy in this patient group. A retrospective study analyzed 74 patients with PE and acute respiratory distress syndrome (ARDS) due to COVID-19 who were hospitalized in the intensive care unit in 2021. Patients with or without confirmed right heart thrombi (RHT) were treated with unfractionated heparin or alteplase. The mortality rate in patients with RHT treated with heparin was 100% compared to 37.9% and 55.2% in those treated with alteplase without RHT and alteplase with RHT, respectively. The risk of death in the alteplase group increased with delayed thrombolysis (p = 0.009, odds ratio (OR) = 1.73 95% CI (confidence interval) 1.14–2.62), increased D dimer concentration (p = 0.02, OR = 1.43 95% CI 1.06–1.93), and decreased PaO2/FiO2 ratio (p = 0.001,&#xD;
OR = 0.56 95% CI 0.41–0.78). The receiver operating characteristic method determined that a 1-day delay in thrombolytic treatment, D-dimer concentration &gt;5.844 mg/L, and PaO2/FiO2 &lt;144 mmHg predicted a fatal outcome. The risk of death in patients with severe COVID-19 with ARDS and PE increases with higher D-dimer levels, decreased PaO2/FiO2 , and delayed thrombolytic treatment.&#xD;
Thrombolysis seems to be treatment of choice in severe COVID-19 with PE and RHT. It should be carried out as soon as possible after the diagnosis is established.</description>
    <dc:date>2023-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://ir.librarynmu.com/handle/123456789/15025">
    <title>Efficacy of Sildenafil in Patients with Severe COVID-19 and Pulmonary Arterial Hypertension</title>
    <link>http://ir.librarynmu.com/handle/123456789/15025</link>
    <description>Название: Efficacy of Sildenafil in Patients with Severe COVID-19 and Pulmonary Arterial Hypertension
Авторы: Oliynyk, O.; Rorat, M.; Strepetova, O.; Dubrov, S.; Guryanov, V.; Oliynyk, Y.; Kulivets, O.; Slifirczyk, A.; Barg, W.
Краткий осмотр (реферат): Pulmonary arterial hypertension (PAH) is common in severe coronavirus disease 2019 (COVID-19) and worsens the prognosis. Sildenafil, a phosphodiesterase-5 inhibitor, is approved for PAH treatment but little is known about its efficacy in cases of severe COVID-19 with PAH. This study aimed to investigate the clinical efficacy of sildenafil in patients with severe COVID-19 and PAH. Intensive care unit (ICU) patients were randomly assigned to receive sildenafil or a placebo, with 75 participants in each group. Sildenafil was administered orally at 0.25 mg/kg t.i.d. for one week in a placebo-controlled, double-blind manner as an add-on therapy alongside the patient’s routine treatment. The primary endpoint was one-week mortality, and the secondary endpoints were the one-week intubation rate and duration of ICU stay. The mortality rate was 4% vs. 13.3% (p = 0.078), the intubation rate was 8% and 18.7% (p = 0.09), and the length of ICU stay was 15 vs.&#xD;
19 days (p &lt; 0.001) for the sildenafil and placebo groups, respectively. If adjusted for PAH, sildenafil&#xD;
treatment significantly reduced mortality and intubation risks: OR = 0.21 (95% CI: 0.05–0.89) and OR = 0.26 (95% CI: 0.08–0.86), respectively. Sildenafil demonstrated some clinical efficacy in patients with severe COVID-19 and PAH and should be considered as an add-on therapy in these patients.</description>
    <dc:date>2023-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://ir.librarynmu.com/handle/123456789/15021">
    <title>Evaluation of bacterial contamination in the inanimate environment surfaces in acute care hospitals in Kyiv, Ukraine</title>
    <link>http://ir.librarynmu.com/handle/123456789/15021</link>
    <description>Название: Evaluation of bacterial contamination in the inanimate environment surfaces in acute care hospitals in Kyiv, Ukraine
Авторы: Salmanov, A.; Shchehlov, D.; Svyrydiuk, O.; Bortnik, I.; Mamonova, M.; Krylova, A.; Gudym, M.
Краткий осмотр (реферат): The aim: To evaluate the quality of cleaning and disinfection of surfaces scheduled for daily cleaning and degree of bacterial contamination of hospital rooms and the patients’ inanimate environment in Kyiv acute care hospitals, Ukraine.&#xD;
Materials and methods: We performed a multicenter prospectively study of the quality of cleaning and disinfection of surfaces scheduled for daily cleaning in 9 acute care hospitals by use of an ultraviolet fluorescence targeting method and microbial methods.&#xD;
Results: A total 9,104 environmental samples from were collected and tested. The cleaning and disinfection of surfaces were not being performed properly in most cases. Complete removal of the mark was 49.1%, partial removal was 37,5%, and mark was still visible, i.e. this area had not been processed was 13,4% when the ultraviolet fluorescence targeting method procedures were used, respectively. The predominant bacterial agents in hospital environment surfaces were: Escherichia coli, Enterobacter spp., Pseudomonas aeruginosa, Klebsiella pneumoniae, Proteus spp., Citrobacter spp., Acinetobacter spp., and Enterococcus spp. The overall proportion of extended spectrum beta-lactamase (ESBL) production among Enterobacteriaceae was 31.5% and of methicillin-resistance in Staphylococcus aureus (MRSA) 14.9%. Vancomycin resistance was observed in 5.2% of isolated enterococci (VRE). Resistance to third-generation cephalosporins was observed in 12.7% E.coli isolates and was in 11.2% K. pneumoniae isolates. Carbapenem resistance was identified in 24.7% of P.aeruginosa isolates and 59.3% of Acinetibacter spp. isolates.&#xD;
Conclusions: In a hospital rooms, patient environmental surfaces can be a vehicle for the transmission of multidrug-resistant (MDR) bacterial agents that cause healthcare-associatedinfections.</description>
    <dc:date>2022-01-01T00:00:00Z</dc:date>
  </item>
  <item rdf:about="http://ir.librarynmu.com/handle/123456789/15019">
    <title>Results of the Treatment and Evaluation of Quality of Life in Patients  with High-Grade Cerebral Arteriovenous Malformations  after Endovascular Embolization</title>
    <link>http://ir.librarynmu.com/handle/123456789/15019</link>
    <description>Название: Results of the Treatment and Evaluation of Quality of Life in Patients  with High-Grade Cerebral Arteriovenous Malformations  after Endovascular Embolization
Авторы: Shchehlov, D.; Svyrydiuk, O.; Vyval, M.; Chebanyuk, S.; Altman, I.; Mamonova, M.
Краткий осмотр (реферат): Introduction. Treatment options for cerebral arteriovenous malformations (cAVMs) may include radiosurgery,&#xD;
endovascular embolization, microsurgical removal, or a combination thereof. However, treatment of high-grade&#xD;
(Spetzler–Martin grades IV and V) cAVMs remains extremely challenging when aiming complete occlusion.&#xD;
The aim. To study the safety of the endovascular embolization in patients with high-grade cAVMs and its impact&#xD;
on the quality of life (QoL).&#xD;
Materials and methods. Between 2012 and 2022, 174 patients with cAVMs were endovascularly treated at&#xD;
Research and Practical Center for Endovascular Neuroradiology of the National Academy of Medical Sciences of Ukraine with an average follow-up of more than 9 months. Of these patients, 11 (6.3%) and 6 (3.4%) had Spetzler–Martin grade IV and grade V cAVM, respectively. Outcomes after surgical procedures were assessed and QoL was evaluated using standardized EQ-5D-3L questionnaire.&#xD;
Results. Five (29.4%) patients had intracerebral hemorrhage, 6 (35.3%) had seizures, 5 (29.4%) had other&#xD;
non-hemorrhagic manifestations and 1 (5.9%) patient had a neurological deficit as a result of cerebral steal. In&#xD;
17 patients, 28 embolization sessions were performed, and in nearly all of them (96%) N-butyl cyanoacrylate was used as the preferred embolic agent. There were no procedural complications. After embolization, three (17.6%) patients had neurologic deterioration (temporary in 2 patients and persistent in 1 patient).&#xD;
All the patients were alive at the nearest follow-up. After embolization, 2 (11.7%) patients had recurrent&#xD;
hemorrhage, but without additional morbidity. Two of the five patients after cAVM rupture had some degree of&#xD;
disability. With regard to non-hemorrhagic debut, 8 (72%) patients reported symptom reduction. QoL assessment with EQ-5D-3L questionnaire revealed that severe problems were present in 2 (33.3%) of 6 patients after intracerebral hemorrhage and 2 (18.2%) of 11 patients with non-hemorrhagic manifestation. The mean Visual Analogue Scale score for the hemorrhagic group was 76.4 ± 15 points, while the non-hemorrhagic group’s score was 85.2 ± 14 points.&#xD;
Conclusions. Endovascular embolization, which aims to occlude the bleeding site or improve cerebral steal with&#xD;
a manageable consequence profile, can be used safely in carefully selected patients with high-grade cAVMs. Our experience shows that QoL can be satisfactory in 3/4 of patients after high-grade cAVM embolization, and more data from real-world practice are highly needed to determine the best method and time for improving patient outcomes</description>
    <dc:date>2023-01-01T00:00:00Z</dc:date>
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