Browsing by Author "Milošević, Ivana (58456808200)"
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Publication A pilot study in Serbia by European clostridium difficile infection surveillance network(2020) ;Jovanović, Milica (56765272500) ;van Dorp, Sofie M. (56549896100) ;Drakulović, Mitra (6507165169) ;Papić, Dubravka (57216824235) ;Pavić, Sladjana (6603595864) ;Jovanović, Snežana (7102384849) ;Lešić, Aleksandar (55409413400) ;Korać, Miloš (10040016700) ;Milošević, Ivana (58456808200)Kuijper, Ed J. (24429752400)Clostridium (Clostridioides) difficile infections (CDIs) are among the most frequent healthcare-associated infections in Serbia. In 2013, Serbia participated in the European Clostridium difficile Infection Surveillance Network (ECDIS-Net) who launched a pilot study to enhance laboratory capacity and standardize surveillance for CDI. Two clinics of Clinical Center of Serbia [Clinic for Infectious and Tropical Diseases (CITD) and Clinic of Orthopedic Surgery and Traumatology (COT)] from Belgrade and one general hospital from another metropolitan area of Serbia, Užice, participated. During a period of 3 months in 2013, all patients with diagnosed CDI were included. The CDI incidence rates in CITD, COT, and General Hospital Užice were 19.0, 12.2, and 3.9 per 10,000 patient-days, respectively. In total, 49 patients were enrolled in the study with average age of 72 years. A complicated course of CDI was found in 14.3% of all patients. Six (12.2%) of 49 patients died, but not attributable to CDI. Of 39 C. difficile isolates, available for ribotyping, 78.9% belonged to ribotype 027; other PCR ribotypes were 001, 015, 002, 005, 010, 014, and 276. Antimicrobial susceptibility testing revealed low levels of MIC50 and MIC90 for metronidazole (0.5 μg/ml both) and vancomycin (0.25 and 0.5 μg/ml), while 28 strains of ribotype 027 were resistant to moxifloxacin with MIC ≥4 μg/ml. National surveillance is important to obtain more insight in the epidemiology of CDI and to compare the results with other European countries. This study by ECDIS-Net gives bases for a national surveillance of CDI in Serbia. © 2019 Akadémiai Kiadó, Budapest. - Some of the metrics are blocked by yourconsent settings
Publication A pilot study in Serbia by European clostridium difficile infection surveillance network(2020) ;Jovanović, Milica (56765272500) ;van Dorp, Sofie M. (56549896100) ;Drakulović, Mitra (6507165169) ;Papić, Dubravka (57216824235) ;Pavić, Sladjana (6603595864) ;Jovanović, Snežana (7102384849) ;Lešić, Aleksandar (55409413400) ;Korać, Miloš (10040016700) ;Milošević, Ivana (58456808200)Kuijper, Ed J. (24429752400)Clostridium (Clostridioides) difficile infections (CDIs) are among the most frequent healthcare-associated infections in Serbia. In 2013, Serbia participated in the European Clostridium difficile Infection Surveillance Network (ECDIS-Net) who launched a pilot study to enhance laboratory capacity and standardize surveillance for CDI. Two clinics of Clinical Center of Serbia [Clinic for Infectious and Tropical Diseases (CITD) and Clinic of Orthopedic Surgery and Traumatology (COT)] from Belgrade and one general hospital from another metropolitan area of Serbia, Užice, participated. During a period of 3 months in 2013, all patients with diagnosed CDI were included. The CDI incidence rates in CITD, COT, and General Hospital Užice were 19.0, 12.2, and 3.9 per 10,000 patient-days, respectively. In total, 49 patients were enrolled in the study with average age of 72 years. A complicated course of CDI was found in 14.3% of all patients. Six (12.2%) of 49 patients died, but not attributable to CDI. Of 39 C. difficile isolates, available for ribotyping, 78.9% belonged to ribotype 027; other PCR ribotypes were 001, 015, 002, 005, 010, 014, and 276. Antimicrobial susceptibility testing revealed low levels of MIC50 and MIC90 for metronidazole (0.5 μg/ml both) and vancomycin (0.25 and 0.5 μg/ml), while 28 strains of ribotype 027 were resistant to moxifloxacin with MIC ≥4 μg/ml. National surveillance is important to obtain more insight in the epidemiology of CDI and to compare the results with other European countries. This study by ECDIS-Net gives bases for a national surveillance of CDI in Serbia. © 2019 Akadémiai Kiadó, Budapest. - Some of the metrics are blocked by yourconsent settings
Publication A rare case of Candida parapsilosis endocarditis in a young healthy woman - case report(2013) ;Pelemiš, Mijomir (6507978433) ;Stevanović, Goran (15059280200) ;Lavadinović, Lidija (22941135800) ;Matić, Snežana (37049011100) ;Milošević, Ivana (58456808200) ;Korać, Miloš (10040016700) ;Pelemiš, Svetislav (55251583000) ;Nedeljković, Milan (7004488186)Prostran, Milica (7004009031)Disseminated fungal infections are still rare conditions, mostly caused by Candida spp. during immunosuppression. Infection of immunocompetent individuals is uncommon. Endocarditis is a rare manifestation during candidaemia, mostly in patients with prosthetic valves. Affection of previously unaltered valves is uncommon. We presented a case of a young, previously healthy female patient with endocarditis, caused by Candida parapsilosis. The initial symptom, fever, was present four months before hospital admittance. She was febrile without other symptoms and during observation in a local hospital. After her condition deteriorated, she was transferred to the Institute for infectious and tropical diseases, Belgrade. Clinical findings on admission include petechial skin rash and moderate hepatosplenomegaly. Newly developed systolic murmur was noted, and Candida parapsilosis was isolated in multiple blood cultures. Echocardiography revealed 15 × 14 mm vegetations on the right aortic vellum. She was treated with antifungal drugs (fluconasole, liposomal amphotericin B), and the affected valve was successfully replaced. The same strain of Candida parapsilosis was isolated from the intraoperative material of the valve. There were no markers of immunosuppression or other conditions which could affect the immune system. After a prolonged period of treatment she was successfully cured, and she received a long-term intermittent suppressive fluconasole therapy for the time being. © 2013 Pelemiš et al; licensee BioMed Central Ltd. - Some of the metrics are blocked by yourconsent settings
Publication A single-center experience of early administration of tocilizumab and corticosteroids in patients with COVID-19 pneumonia(2023) ;Milošević, Ivana (58456808200) ;Barać, Aleksandra (55550748700) ;Jovanović, Jaroslava (57220948637) ;Vujović, Ankica (57205475784) ;Stevanović, Goran (15059280200) ;Todorović, Nevena (58688792000)Milošević, Branko (57204639427)Background: We investigated the therapeutic response of tocilizumab (TCZ) therapy in patients with coronavirus disease 2019 (COVID-19) pneumonia. Methods: This observational retrospective study included 205 patients with confirmed COVID-19 pneumonia with SpO2˂93% and a markedly increased level of at least two biomarkers of inflammation. The TCZ was given in combination with corticosteroids. Clinical and laboratory results were analyzed and compared before TCZ therapy and 7 d after. Results: The mean value of C-reactive protein (CRP) was significantly lower (p=0.001) on the seventh day after administration of TCZ compared with before (10.7 and 173.6 mg/L, respectively). Only in 9/205 (4.3%) patients, the CRP level did not decrease during the week-long period, and this was related to disease progression. The mean level of interleukin-6 before TCZ administration was 88±113 pg/mL, while after it was 32.7±21.7 pg/mL (p=0.01). After 7 d of TCZ therapy, almost 50% of patients who needed high-flow oxygen or ventilation support started to receive low-flow oxygen, while 73/205 (35.6%) patients who received low-flow oxygen before TCZ administration did not receive further oxygen support anymore (p=0.001). Although they received TCZ treatment, 38/205 (18.5%) severely sick patients died. Conclusions: Tocilizumab improves clinical outcomes in hospitalized COVID-19 patients. These advantages were evident independent of the patient's comorbidities and were in addition to the advantages of systemic corticosteroids. In COVID-19 patients at risk of cytokine storms, TCZ appears to be an effective therapy choice. © 2023 The Author(s). Published by Oxford University Press on behalf of Royal Society of Tropical Medicine and Hygiene. - Some of the metrics are blocked by yourconsent settings
Publication A single-center experience of early administration of tocilizumab and corticosteroids in patients with COVID-19 pneumonia(2023) ;Milošević, Ivana (58456808200) ;Barać, Aleksandra (55550748700) ;Jovanović, Jaroslava (57220948637) ;Vujović, Ankica (57205475784) ;Stevanović, Goran (15059280200) ;Todorović, Nevena (58688792000)Milošević, Branko (57204639427)Background: We investigated the therapeutic response of tocilizumab (TCZ) therapy in patients with coronavirus disease 2019 (COVID-19) pneumonia. Methods: This observational retrospective study included 205 patients with confirmed COVID-19 pneumonia with SpO2˂93% and a markedly increased level of at least two biomarkers of inflammation. The TCZ was given in combination with corticosteroids. Clinical and laboratory results were analyzed and compared before TCZ therapy and 7 d after. Results: The mean value of C-reactive protein (CRP) was significantly lower (p=0.001) on the seventh day after administration of TCZ compared with before (10.7 and 173.6 mg/L, respectively). Only in 9/205 (4.3%) patients, the CRP level did not decrease during the week-long period, and this was related to disease progression. The mean level of interleukin-6 before TCZ administration was 88±113 pg/mL, while after it was 32.7±21.7 pg/mL (p=0.01). After 7 d of TCZ therapy, almost 50% of patients who needed high-flow oxygen or ventilation support started to receive low-flow oxygen, while 73/205 (35.6%) patients who received low-flow oxygen before TCZ administration did not receive further oxygen support anymore (p=0.001). Although they received TCZ treatment, 38/205 (18.5%) severely sick patients died. Conclusions: Tocilizumab improves clinical outcomes in hospitalized COVID-19 patients. These advantages were evident independent of the patient's comorbidities and were in addition to the advantages of systemic corticosteroids. In COVID-19 patients at risk of cytokine storms, TCZ appears to be an effective therapy choice. © 2023 The Author(s). Published by Oxford University Press on behalf of Royal Society of Tropical Medicine and Hygiene. - Some of the metrics are blocked by yourconsent settings
Publication Actinomycotic hepatic abscess in woman with longstanding intrauterine contraceptive device(2018) ;Basarić, Dragan (6506303741) ;Lekić, Nebojša (57191481699) ;Đorđević, Vladimir (7003704287) ;Ćeranić, Miljan (6507036900) ;Barać, Aleksandra (55550748700) ;Stevanović, Goran (15059280200)Milošević, Ivana (58456808200)We present a case of a 50 year-old female bearing an intrauterine contraceptive device for 20 years who was diagnosed with abdominopelvic actinomycosis with liver dissemination. The patient was successfully treated by a combination of surgical resection and a 3-month course of amoxicillin. © 2018 Basarić et al. - Some of the metrics are blocked by yourconsent settings
Publication Actinomycotic hepatic abscess in woman with longstanding intrauterine contraceptive device(2018) ;Basarić, Dragan (6506303741) ;Lekić, Nebojša (57191481699) ;Đorđević, Vladimir (7003704287) ;Ćeranić, Miljan (6507036900) ;Barać, Aleksandra (55550748700) ;Stevanović, Goran (15059280200)Milošević, Ivana (58456808200)We present a case of a 50 year-old female bearing an intrauterine contraceptive device for 20 years who was diagnosed with abdominopelvic actinomycosis with liver dissemination. The patient was successfully treated by a combination of surgical resection and a 3-month course of amoxicillin. © 2018 Basarić et al. - Some of the metrics are blocked by yourconsent settings
Publication Atypical course of COVID-19 in patient with Bruton agammaglobulinemia(2020) ;Milošević, Ivana (58456808200) ;Jovanović, Jaroslava (57220948637)Stevanović, Olja (57201195181)We present atypical course of the novel coronavirus disease (COVID-19) in 34-year man with Bruton agammaglobulinemia. The patient was successfully treated by a combination of available drugs, including convalescent plasma and interleukin-6 (IL-6) inhibitor. © 2020 Journal of Infection in Developing Countries. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Atypical course of COVID-19 in patient with Bruton agammaglobulinemia(2020) ;Milošević, Ivana (58456808200) ;Jovanović, Jaroslava (57220948637)Stevanović, Olja (57201195181)We present atypical course of the novel coronavirus disease (COVID-19) in 34-year man with Bruton agammaglobulinemia. The patient was successfully treated by a combination of available drugs, including convalescent plasma and interleukin-6 (IL-6) inhibitor. © 2020 Journal of Infection in Developing Countries. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Bilateral facial nerve palsy in a patient with West Nile neuroinvasive disease(2024) ;Nikolić, Nataša (58288723700) ;Filipović, Ana (58487006900) ;Todorović, Nevena (58688792000) ;Grgurović, Mirjana Jakšić (59522176000) ;Mitrović, Nikola (55110096400) ;Malinić, Jovan (57190970697)Milošević, Ivana (58456808200)Introduction: Bilateral facial nerve palsy (FNP) is a rare condition that is idiopathic in only 20%. FNP is the most common cranial neuropathy in West Nile neuroinvasive disease (WNND) but is usually unilateral and only a few cases of bilateral FNP have been reported. Case: We present a case of a 65-year-old woman with confirmed WNND and simultaneous bilateral FNP. Results: In August 2022, the patient presented with ataxia, gait instability, tremor, fever, and vomiting. Following admission, due to her cerebrospinal fluid analyses she was diagnosed with WNV encephalitis. Her initial symptoms subsided, but on the 17th day of the disease, right FNP was observed. Three days later bilateral FNP developed, predominantly on the right side, with bilateral otalgia. Further diagnostic was performed but no other aetiology that could contribute to FNP was found. The patient was treated with a 3-day metilprednisolone course, followed by 60 mg of prednisone with dose tapering for 12 days. One month later she was discharged with significant regression of the left and slight regression of the right FNP. Subsequent physical therapy was conducted. The patient’s neurological status gradually improved and 4 months after the first symptoms onset, her neurological examination was normal. Conclusions: WNND should be included in the differential diagnosis of acquired bilateral FNP. It can result in full recovery, but unfavorable course is also possible. © 2024 Nikolić et al. - Some of the metrics are blocked by yourconsent settings
Publication Bilateral facial nerve palsy in a patient with West Nile neuroinvasive disease(2024) ;Nikolić, Nataša (58288723700) ;Filipović, Ana (58487006900) ;Todorović, Nevena (58688792000) ;Grgurović, Mirjana Jakšić (59522176000) ;Mitrović, Nikola (55110096400) ;Malinić, Jovan (57190970697)Milošević, Ivana (58456808200)Introduction: Bilateral facial nerve palsy (FNP) is a rare condition that is idiopathic in only 20%. FNP is the most common cranial neuropathy in West Nile neuroinvasive disease (WNND) but is usually unilateral and only a few cases of bilateral FNP have been reported. Case: We present a case of a 65-year-old woman with confirmed WNND and simultaneous bilateral FNP. Results: In August 2022, the patient presented with ataxia, gait instability, tremor, fever, and vomiting. Following admission, due to her cerebrospinal fluid analyses she was diagnosed with WNV encephalitis. Her initial symptoms subsided, but on the 17th day of the disease, right FNP was observed. Three days later bilateral FNP developed, predominantly on the right side, with bilateral otalgia. Further diagnostic was performed but no other aetiology that could contribute to FNP was found. The patient was treated with a 3-day metilprednisolone course, followed by 60 mg of prednisone with dose tapering for 12 days. One month later she was discharged with significant regression of the left and slight regression of the right FNP. Subsequent physical therapy was conducted. The patient’s neurological status gradually improved and 4 months after the first symptoms onset, her neurological examination was normal. Conclusions: WNND should be included in the differential diagnosis of acquired bilateral FNP. It can result in full recovery, but unfavorable course is also possible. © 2024 Nikolić et al. - Some of the metrics are blocked by yourconsent settings
Publication Clinical characteristics of imported malaria: An 11-year experience in a Serbian referral center(2016) ;Poluga, Jasmina (6507116358) ;Milošević, Ivana (58456808200) ;Jordović, Jelena (57190498051) ;Dakić, Zorica (35186070500) ;Lavadinović, Lidija (22941135800) ;Stevanović, Goran (15059280200) ;Milošević, Branko (57204639427) ;Jevtović, Đorđe (55410443900)Pavlović, Milorad (7202542036)Introduction: Due to intercontinental traffic, population migration trends, natural disasters, and climate change, imported malaria remains important to consider in a febrile returning traveler. This study aims to raise awareness about malaria and help European clinicians maintain a working knowledge of this disease by reviewing the most important clinical characteristics in a non-endemic setting. Methodology: Using medical records, a retrospective study was performed on clinical and laboratory data in order to analyze 103 malaria cases managed at the Clinic for Infectious and Tropical Diseases in Belgrade, from 2000 to 2010. Descriptive statistics, Chi-squared test, Spearman's rank correlation, and analysis of variance were used. Results: Patients were predominantly male (89.3%) with a mean age of 46.66 ± 12.45 years, and most (98.06%) returned from Africa without having taken chemoprophylaxis (72.88%). Fever, arthralgia, myalgia, headache, vomiting, dark urine, and cough were common at presentation. Hepatosplenomegaly, jaundice, neurological and pulmonary findings, and thrombocytopenia were dominant findings on physical and laboratory examinations. Most (73.48%) were infected with P. falciparum. Few patients (17.55%) who were hyperparasitemic had significantly higher values of bilirubin and more frequent neurological complications. All patients were treated with artemisinin-based drug combinations regardless of Plasmodium species. Three (2.9%) patients succumbed to P. falciparum malaria. Conclusion: We suggest a high index of suspicion of malaria be maintained when evaluating febrile patients returning from endemic regions, especially if thrombocytopenia and hemolysis are present. Hyperparasitemia, high bilirubin levels, and neurological symptoms are associated with severe malaria. The importance of adequate malaria chemoprophylaxis cannot be overstated. © 2016 Poluga et al. - Some of the metrics are blocked by yourconsent settings
Publication Clinical characteristics of imported malaria: An 11-year experience in a Serbian referral center(2016) ;Poluga, Jasmina (6507116358) ;Milošević, Ivana (58456808200) ;Jordović, Jelena (57190498051) ;Dakić, Zorica (35186070500) ;Lavadinović, Lidija (22941135800) ;Stevanović, Goran (15059280200) ;Milošević, Branko (57204639427) ;Jevtović, Đorđe (55410443900)Pavlović, Milorad (7202542036)Introduction: Due to intercontinental traffic, population migration trends, natural disasters, and climate change, imported malaria remains important to consider in a febrile returning traveler. This study aims to raise awareness about malaria and help European clinicians maintain a working knowledge of this disease by reviewing the most important clinical characteristics in a non-endemic setting. Methodology: Using medical records, a retrospective study was performed on clinical and laboratory data in order to analyze 103 malaria cases managed at the Clinic for Infectious and Tropical Diseases in Belgrade, from 2000 to 2010. Descriptive statistics, Chi-squared test, Spearman's rank correlation, and analysis of variance were used. Results: Patients were predominantly male (89.3%) with a mean age of 46.66 ± 12.45 years, and most (98.06%) returned from Africa without having taken chemoprophylaxis (72.88%). Fever, arthralgia, myalgia, headache, vomiting, dark urine, and cough were common at presentation. Hepatosplenomegaly, jaundice, neurological and pulmonary findings, and thrombocytopenia were dominant findings on physical and laboratory examinations. Most (73.48%) were infected with P. falciparum. Few patients (17.55%) who were hyperparasitemic had significantly higher values of bilirubin and more frequent neurological complications. All patients were treated with artemisinin-based drug combinations regardless of Plasmodium species. Three (2.9%) patients succumbed to P. falciparum malaria. Conclusion: We suggest a high index of suspicion of malaria be maintained when evaluating febrile patients returning from endemic regions, especially if thrombocytopenia and hemolysis are present. Hyperparasitemia, high bilirubin levels, and neurological symptoms are associated with severe malaria. The importance of adequate malaria chemoprophylaxis cannot be overstated. © 2016 Poluga et al. - Some of the metrics are blocked by yourconsent settings
Publication Clostridioides difficile ribotype distribution in a large teaching hospital in Serbia(2020) ;Korać, Milos&caron (10040016700) ;Rupnik, Maja (7003833037) ;Nikolić, Nataša (58288723700) ;Jovanović, Milica (56765272500) ;Tošić, Tanja (8326509800) ;Malinić, Jovan (57190970697) ;Mitrović, Nikola (55110096400) ;Marković, Marko (57534497700) ;Vujović, Ankica (57205475784) ;Peruničić, Sanja (57191926042) ;Bojović, Ksenija (6505585757) ;Djordjević, Vladimir (56019682600) ;Barać, Aleksandra (55550748700)Milošević, Ivana (58456808200)Background: The global epidemic of nosocomial diarrhea caused by Clostridioides (Clostridium) difficile started in 2000, with high mortality rates and emergence of a new hypervirulent strain NAP1/BI/027. The aim of this study was to assess the presence of ribotype 027 and other C. difficile ribotypes in a Serbian University Hospital, compare the temporal variability of ribotypes 3 years apart, as well as to compare clinical, demographic and laboratory characteristics and disease outcome among patients infected with 027 and non-027 ribotype. This was a prospective observational cohort study addressing 4-month intervals during 2014/2015 and 2017/2018. Results: Ribotyping was performed in 64 non-duplicate C. difficile strains. Ribotype 027 was the most prevalent, and was detected in 53 (82.8%) patients (43/45 and 10/19 patients in 2014-2015 and 2017/2018, respectively). Other detected ribotypes were 001/072 in 4 (6.3%), 002 in 4 (6.3%), 014/020 in 2 (3.1%) and 176 in 1 (1.5%) patient. The percentage of the patients infected with ribotype 027 significantly decreased during the 3-year period, from 95.6 to 52.6% (p < 0.001). Ribotype 027 infection was associated with fluoroquinolone treatment more frequently than infection with other ribotypes [33 (62.3%) vs. 2 (18.2%), p = 0.010)]. A severe C. difficile infection was diagnosed more often in patients with the detected ribotype 027 compared to those infected with non-027 ribotypes (p = 0.006). No significant difference in the mortality and recurrence rates was found between the patients infected with ribotype 027 and those infected with other ribotypes [10/53 (18.8%) vs. 2/11 (18.2%), p = 0.708, and 10/35 (28.6%) vs. 0/2 (0%), p = 1.000, respectively]. Conclusion: Clostridium difficile ribotype 027 was the most prevalent ribotype among patients in a large Serbian hospital, but there is a clear decreasing trend. © 2020 The Author(s). - Some of the metrics are blocked by yourconsent settings
Publication Clostridioides difficile ribotype distribution in a large teaching hospital in Serbia(2020) ;Korać, Milos&caron (10040016700) ;Rupnik, Maja (7003833037) ;Nikolić, Nataša (58288723700) ;Jovanović, Milica (56765272500) ;Tošić, Tanja (8326509800) ;Malinić, Jovan (57190970697) ;Mitrović, Nikola (55110096400) ;Marković, Marko (57534497700) ;Vujović, Ankica (57205475784) ;Peruničić, Sanja (57191926042) ;Bojović, Ksenija (6505585757) ;Djordjević, Vladimir (56019682600) ;Barać, Aleksandra (55550748700)Milošević, Ivana (58456808200)Background: The global epidemic of nosocomial diarrhea caused by Clostridioides (Clostridium) difficile started in 2000, with high mortality rates and emergence of a new hypervirulent strain NAP1/BI/027. The aim of this study was to assess the presence of ribotype 027 and other C. difficile ribotypes in a Serbian University Hospital, compare the temporal variability of ribotypes 3 years apart, as well as to compare clinical, demographic and laboratory characteristics and disease outcome among patients infected with 027 and non-027 ribotype. This was a prospective observational cohort study addressing 4-month intervals during 2014/2015 and 2017/2018. Results: Ribotyping was performed in 64 non-duplicate C. difficile strains. Ribotype 027 was the most prevalent, and was detected in 53 (82.8%) patients (43/45 and 10/19 patients in 2014-2015 and 2017/2018, respectively). Other detected ribotypes were 001/072 in 4 (6.3%), 002 in 4 (6.3%), 014/020 in 2 (3.1%) and 176 in 1 (1.5%) patient. The percentage of the patients infected with ribotype 027 significantly decreased during the 3-year period, from 95.6 to 52.6% (p < 0.001). Ribotype 027 infection was associated with fluoroquinolone treatment more frequently than infection with other ribotypes [33 (62.3%) vs. 2 (18.2%), p = 0.010)]. A severe C. difficile infection was diagnosed more often in patients with the detected ribotype 027 compared to those infected with non-027 ribotypes (p = 0.006). No significant difference in the mortality and recurrence rates was found between the patients infected with ribotype 027 and those infected with other ribotypes [10/53 (18.8%) vs. 2/11 (18.2%), p = 0.708, and 10/35 (28.6%) vs. 0/2 (0%), p = 1.000, respectively]. Conclusion: Clostridium difficile ribotype 027 was the most prevalent ribotype among patients in a large Serbian hospital, but there is a clear decreasing trend. © 2020 The Author(s). - Some of the metrics are blocked by yourconsent settings
Publication Correlation between serum quantitative HBsAg and HBV DNA levels in chronic hepatitis B patients; [Korelacija između nivoa serumskog kvantitativnog HBsAg i HBV DNK kod bolesnika sa hroničnim hepatitisom B](2023) ;Pete, Maria (57191373359) ;Ružić, Maja (24768227700) ;Kovačević, Nadica (7006810324) ;Petrić, Vedrana (55801211600) ;Milošević, Ivana (58456808200)Preveden, Tomislav (6602244852)Background/Aim. Quantitative hepatitis B virus (HBV) surface antigen (qHBsAg) has become increasingly widespread in the last few years in both diagnostic and therapeutic protocols for HBV infection. Numerous studies have proposed it as a surrogate marker for covalently closed circular DNA (cccDNA). The aim of the study was to determine the correlation between qHBsAg and HBV DNA viremia in untreated patients. Methods. The study included 112 untreated patients diagnosed with chronic HBV infection. Demographic and other data from medical records and laboratory analyses, taken as part of routine chronic HBV infection diagnosis with the determination of qHBsAg and HBV DNA viremia, were recorded for all patients. Results. The average age of the patients included in the study was 48.27 ± 15.14 years; males (58%) were more represented. qHBsAg levels had a high-intensity positive correlation with HBV DNA viremia. The concentration of qHBsAg, HBV DNA viremia, and the concentrations of alanine aminotransferase and aspartate aminotransferase showed statistically significantly higher values in HBV e antigen (HBeAg)-positive than in HBeAg-negative patients. Conclusion. Our study showed that qHBsAg has a high-intensity positive correlation with HBV DNA viremia. The use of qHBsAg is essential for determining the phase of chronic HBV infection, assessment of the success and length of treatment, as well as for safe discontinuation of antiviral therapy with a lower risk of relapse. © 2023 Inst. Sci. inf., Univ. Defence in Belgrade. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Covid-19-associated pulmonary aspergillosis in patients with acute leukemia: A single-center study(2021) ;Rajic, Jovan (57435044600) ;Gmizic, Ivana (57205466405) ;Gunjak, Tara (57314224900) ;Milosevic, Violeta (24399200100) ;Pantic, Nikola (57221630977) ;Sabljic, Nikica (57221634280) ;Mitrovic, Mirjana (54972086700) ;Stefanovic, Aleksandra Djuric (59026442300) ;Lazic, Ljubica (36093093100) ;Jovanovic, Snezana (7102384849) ;Milošević, Ivana (58456808200) ;Barac, Aleksandra (55550748700)Vidovic, Ana (6701313789)Patients with coronavirus disease 19 (COVID-19) have increased susceptibility to secondary respiratory infections including invasive pulmonary aspergillosis (IPA). COVID-19-associated pulmonary aspergillosis (CAPA) is difficult to diagnose and can be associated with increased mortality especially in severe immunodeficiency such as hematological malignancies. Our study evaluates IPA in COVID-19 patients defined as COVID-19-CAPA among patients with acute leukemia (AL). A retrospective single-center study analyzed 46 patients with COVID-19 infection and acute leukemia, admitted to the Clinic for Haematology, Clinical Center of Serbia, Belgrade between the 2 April 2020 and 15 May 2021. During hospitalization, all participants were diagnosed with probable IPA according to the previous consensus definitions. Positive serology and galactomannan (GM) detection values in bronchoalveolar lavage (BAL) and serum were used as microbiological criteria. COVID-19 associated probable IPA was found in 22% (9/41) tested patients, where serum GM and IgM anti-Aspergillus antibodies were positive in 12% (5/41) and 10% (4/41) had positive serology for aspergillosis. One patient died while eight recovered during follow-up. Our study showed that COVID-19 might be a risk factor for IPA development in patients with AL. Early diagnosis and prompt treatment are required as reported mortality rates are high. © 2021 by the authors. Licensee MDPI, Basel, Switzerland. - Some of the metrics are blocked by yourconsent settings
Publication Covid-19-associated pulmonary aspergillosis in patients with acute leukemia: A single-center study(2021) ;Rajic, Jovan (57435044600) ;Gmizic, Ivana (57205466405) ;Gunjak, Tara (57314224900) ;Milosevic, Violeta (24399200100) ;Pantic, Nikola (57221630977) ;Sabljic, Nikica (57221634280) ;Mitrovic, Mirjana (54972086700) ;Stefanovic, Aleksandra Djuric (59026442300) ;Lazic, Ljubica (36093093100) ;Jovanovic, Snezana (7102384849) ;Milošević, Ivana (58456808200) ;Barac, Aleksandra (55550748700)Vidovic, Ana (6701313789)Patients with coronavirus disease 19 (COVID-19) have increased susceptibility to secondary respiratory infections including invasive pulmonary aspergillosis (IPA). COVID-19-associated pulmonary aspergillosis (CAPA) is difficult to diagnose and can be associated with increased mortality especially in severe immunodeficiency such as hematological malignancies. Our study evaluates IPA in COVID-19 patients defined as COVID-19-CAPA among patients with acute leukemia (AL). A retrospective single-center study analyzed 46 patients with COVID-19 infection and acute leukemia, admitted to the Clinic for Haematology, Clinical Center of Serbia, Belgrade between the 2 April 2020 and 15 May 2021. During hospitalization, all participants were diagnosed with probable IPA according to the previous consensus definitions. Positive serology and galactomannan (GM) detection values in bronchoalveolar lavage (BAL) and serum were used as microbiological criteria. COVID-19 associated probable IPA was found in 22% (9/41) tested patients, where serum GM and IgM anti-Aspergillus antibodies were positive in 12% (5/41) and 10% (4/41) had positive serology for aspergillosis. One patient died while eight recovered during follow-up. Our study showed that COVID-19 might be a risk factor for IPA development in patients with AL. Early diagnosis and prompt treatment are required as reported mortality rates are high. © 2021 by the authors. Licensee MDPI, Basel, Switzerland. - Some of the metrics are blocked by yourconsent settings
Publication FIB-4 and APRI scores for predicting severe fibrosis in chronic hepatitis C - A developing country’s perspective in DAA era(2018) ;Karić, Uroš (57201195591) ;Pešić-Pavlović, Ivana (36473869000) ;Stevanović, Goran (15059280200) ;Korać, Miloš (10040016700) ;Nikolić, Nataša (58288723700) ;Radovanović-Spurnić, Aleksandra (57191847101) ;Barać, Aleksandra (55550748700) ;Mitrović, Nikola (55110096400) ;Marković, Aleksandar (57198206234) ;Marković, Marko (57534497700) ;Petković, Anita (57201547687) ;Ostojić, Ivana (56005428100) ;Peruničić, Sanja (57191926042) ;Kekić, Natalija (57201548083) ;Glidžić, Martina (57201551635) ;Đonin-Nenezić, Miljana (57201195027) ;Brmbolić, Branko (6701712863)Milošević, Ivana (58456808200)Introduction: Chronic Hepatitis C Virus (HCV) infection leads to progressive fibrosis making fibrosis staging necessary in the evaluation of such patients. Different fibrosis scores are emerging as possible non-invasive alternatives for liver biopsy. The Fibrosis-4 Index (FIB-4) and AST to Platelet Ratio Index (APRI) scores are the most widely used and the most extensively tested. This study aims to determine if it was possible to accurately use these to identify patients that are unlikely to have severe fibrosis. Methodology: One hundred and forty-two patients with chronic hepatitis C infection who underwent liver biopsy since January 1st 2014 until May 31st 2017 at the Hospital for Infectious and Tropical Diseases in Belgrade were analyzed. The FIB-4 and APRI scores were calculated for each patient and compared to histologically determined fibrosis stage. Results: A comprehensive statistical analysis was conducted in order to compare patients with and without severe fibrosis and to evaluate the accuracy of the fibrosis scores. Patients with non-severe fibrosis were younger, had higher platelet counts and lower transaminase levels. FIB-4 had an AUC of 0.875 and the APRI score had an AUC of 0.861. No patients with severe fibrosis or cirrhosis had a FIB-4 lower than 1.08. FIB-4 was superior to APRI in identifying patients with severe fibrosis in the study cohort. Conclusion: FIB-4 was superior to APRI in the recognition of severe fibrosis. FIB-4 may prove very useful in identifying patients without advanced liver disease, especially if other non-invasive methods are inaccessible. © 2018 Karić et al. - Some of the metrics are blocked by yourconsent settings
Publication FIB-4 and APRI scores for predicting severe fibrosis in chronic hepatitis C - A developing country’s perspective in DAA era(2018) ;Karić, Uroš (57201195591) ;Pešić-Pavlović, Ivana (36473869000) ;Stevanović, Goran (15059280200) ;Korać, Miloš (10040016700) ;Nikolić, Nataša (58288723700) ;Radovanović-Spurnić, Aleksandra (57191847101) ;Barać, Aleksandra (55550748700) ;Mitrović, Nikola (55110096400) ;Marković, Aleksandar (57198206234) ;Marković, Marko (57534497700) ;Petković, Anita (57201547687) ;Ostojić, Ivana (59954448700) ;Peruničić, Sanja (57191926042) ;Kekić, Natalija (57201548083) ;Glidžić, Martina (57201551635) ;Đonin-Nenezić, Miljana (57201195027) ;Brmbolić, Branko (6701712863)Milošević, Ivana (58456808200)Introduction: Chronic Hepatitis C Virus (HCV) infection leads to progressive fibrosis making fibrosis staging necessary in the evaluation of such patients. Different fibrosis scores are emerging as possible non-invasive alternatives for liver biopsy. The Fibrosis-4 Index (FIB-4) and AST to Platelet Ratio Index (APRI) scores are the most widely used and the most extensively tested. This study aims to determine if it was possible to accurately use these to identify patients that are unlikely to have severe fibrosis. Methodology: One hundred and forty-two patients with chronic hepatitis C infection who underwent liver biopsy since January 1st 2014 until May 31st 2017 at the Hospital for Infectious and Tropical Diseases in Belgrade were analyzed. The FIB-4 and APRI scores were calculated for each patient and compared to histologically determined fibrosis stage. Results: A comprehensive statistical analysis was conducted in order to compare patients with and without severe fibrosis and to evaluate the accuracy of the fibrosis scores. Patients with non-severe fibrosis were younger, had higher platelet counts and lower transaminase levels. FIB-4 had an AUC of 0.875 and the APRI score had an AUC of 0.861. No patients with severe fibrosis or cirrhosis had a FIB-4 lower than 1.08. FIB-4 was superior to APRI in identifying patients with severe fibrosis in the study cohort. Conclusion: FIB-4 was superior to APRI in the recognition of severe fibrosis. FIB-4 may prove very useful in identifying patients without advanced liver disease, especially if other non-invasive methods are inaccessible. © 2018 Karić et al.
