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Browsing by Author "Topalovic, Mirko (36616659900)"

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    Agreement between children and parents when reporting anxiety and depressive symptoms in pediatric epilepsy
    (2012)
    Stevanovic, Dejan (16313807500)
    ;
    Jancic, Jasna (35423853400)
    ;
    Topalovic, Mirko (36616659900)
    ;
    Tadic, Ivana (36617924700)
    The levels of agreement between self- and parent/proxy-reports of anxiety and depressive symptoms in pediatric epilepsy were evaluated. Data were drawn from 56 pairs of children with epilepsy and at least one parent. Anxiety symptoms were assessed using the Screen for Child Anxiety Related Emotional Disorders (SCARED), while depressive symptoms were assessed using the Mood and Feeling Questionnaire (MFQ). Moderate to substantial levels of agreement between raters when reporting various anxiety symptoms, such as panic/somatic disorder, generalized anxiety disorder, separation anxiety disorder, social phobia, and school phobia symptoms, were observed. Levels of agreement between raters were substantial when reporting depressive symptoms. However, levels of agreement differed if raw or criterion-referenced questionnaires' scores were used. In case of using raw questionnaire scores, substantial agreements appeared when reporting overall anxiety and depressive symptoms. On the other hand, moderate agreements appeared when reporting particular anxiety symptoms with raw questionnaire scores or when using criterion-referenced scores that indicate the presence of certain symptoms in a clinical range. Therefore, it is advisable to include both raters when assessing anxiety and depressive symptoms in pediatric epilepsy. © 2012 Elsevier Inc.
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    Agreement between children and parents when reporting anxiety and depressive symptoms in pediatric epilepsy
    (2012)
    Stevanovic, Dejan (16313807500)
    ;
    Jancic, Jasna (35423853400)
    ;
    Topalovic, Mirko (36616659900)
    ;
    Tadic, Ivana (36617924700)
    The levels of agreement between self- and parent/proxy-reports of anxiety and depressive symptoms in pediatric epilepsy were evaluated. Data were drawn from 56 pairs of children with epilepsy and at least one parent. Anxiety symptoms were assessed using the Screen for Child Anxiety Related Emotional Disorders (SCARED), while depressive symptoms were assessed using the Mood and Feeling Questionnaire (MFQ). Moderate to substantial levels of agreement between raters when reporting various anxiety symptoms, such as panic/somatic disorder, generalized anxiety disorder, separation anxiety disorder, social phobia, and school phobia symptoms, were observed. Levels of agreement between raters were substantial when reporting depressive symptoms. However, levels of agreement differed if raw or criterion-referenced questionnaires' scores were used. In case of using raw questionnaire scores, substantial agreements appeared when reporting overall anxiety and depressive symptoms. On the other hand, moderate agreements appeared when reporting particular anxiety symptoms with raw questionnaire scores or when using criterion-referenced scores that indicate the presence of certain symptoms in a clinical range. Therefore, it is advisable to include both raters when assessing anxiety and depressive symptoms in pediatric epilepsy. © 2012 Elsevier Inc.
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    Cardiac findings in pediatric patients with spinal muscular atrophy types 2 and 3
    (2021)
    Djordjevic, Stefan A. (57192951203)
    ;
    Milic-Rasic, Vedrana (6507653181)
    ;
    Brankovic, Vesna (57192421308)
    ;
    Kosac, Ana (55786067800)
    ;
    Vukomanovic, Goran (8252832300)
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    Topalovic, Mirko (36616659900)
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    Marinkovic, Dejan (7006275637)
    ;
    Mladenovic, Jelena (8310875700)
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    Pavlovic, Andrija S. (57204964008)
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    Bijelic, Maja (56807060700)
    ;
    Djukic, Milan (23988377500)
    ;
    Markovic-Denic, Ljiljana (55944510900)
    Background: It is unclear whether the heart is affected in pediatric patients with milder forms of spinal muscular atrophy (SMA). Therefore, we aimed to determine the presence of any cardiac abnormalities in these patients. Methods: We conducted a cross-sectional study of children and adolescents with SMA types 2 and 3 between July 2018 and July 2019. All patients underwent a comprehensive cardiac evaluation, including history-taking, physical examination, electrocardiography, echocardiography, measurement of cardiac biomarkers (cardiac troponin T [cTnT] and N-terminal pro–brain natriuretic peptide [NT-proBNP]), and 24-hour Holter monitoring. Results: In total, 42 patients were enrolled (27 and 15 with SMA type 2 and 3, respectively). No patient had structural heart disease, except for one with mitral valve prolapse. None had signs of ventricular dysfunction on echocardiography. Both cTnT and NT-proBNP levels were normal in all patients. Electrocardiography showed sinus tachycardia in seven patients (16.7%), and prolonged P-R interval in one (2.4%). Holter monitoring detected benign ventricular arrhythmias in two patients (4.8%), and rare supraventricular premature beats in one. The mean 24-hour heart rate was elevated in six patients (14.3%), whereas both the minimum 24-hour heart rate and the maximum R-R interval were increased in 23 (54.8%). Discussion: The prevalence of cardiac disease in pediatric patients with SMA types 2 and 3 is low; however, these patients may have increased resting heart rates. A complete cardiac history and physical examination are a useful screen. Additional cardiac investigations may be performed as needed. © 2020 Wiley Periodicals LLC
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    Cardiac findings in pediatric patients with spinal muscular atrophy types 2 and 3
    (2021)
    Djordjevic, Stefan A. (57192951203)
    ;
    Milic-Rasic, Vedrana (6507653181)
    ;
    Brankovic, Vesna (57192421308)
    ;
    Kosac, Ana (55786067800)
    ;
    Vukomanovic, Goran (8252832300)
    ;
    Topalovic, Mirko (36616659900)
    ;
    Marinkovic, Dejan (7006275637)
    ;
    Mladenovic, Jelena (8310875700)
    ;
    Pavlovic, Andrija S. (57204964008)
    ;
    Bijelic, Maja (56807060700)
    ;
    Djukic, Milan (23988377500)
    ;
    Markovic-Denic, Ljiljana (55944510900)
    Background: It is unclear whether the heart is affected in pediatric patients with milder forms of spinal muscular atrophy (SMA). Therefore, we aimed to determine the presence of any cardiac abnormalities in these patients. Methods: We conducted a cross-sectional study of children and adolescents with SMA types 2 and 3 between July 2018 and July 2019. All patients underwent a comprehensive cardiac evaluation, including history-taking, physical examination, electrocardiography, echocardiography, measurement of cardiac biomarkers (cardiac troponin T [cTnT] and N-terminal pro–brain natriuretic peptide [NT-proBNP]), and 24-hour Holter monitoring. Results: In total, 42 patients were enrolled (27 and 15 with SMA type 2 and 3, respectively). No patient had structural heart disease, except for one with mitral valve prolapse. None had signs of ventricular dysfunction on echocardiography. Both cTnT and NT-proBNP levels were normal in all patients. Electrocardiography showed sinus tachycardia in seven patients (16.7%), and prolonged P-R interval in one (2.4%). Holter monitoring detected benign ventricular arrhythmias in two patients (4.8%), and rare supraventricular premature beats in one. The mean 24-hour heart rate was elevated in six patients (14.3%), whereas both the minimum 24-hour heart rate and the maximum R-R interval were increased in 23 (54.8%). Discussion: The prevalence of cardiac disease in pediatric patients with SMA types 2 and 3 is low; however, these patients may have increased resting heart rates. A complete cardiac history and physical examination are a useful screen. Additional cardiac investigations may be performed as needed. © 2020 Wiley Periodicals LLC
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    Oral propranolol for infantile hemangiomas: a prospective study on the role of 48-hour Holter monitoring in additional safety assessment
    (2017)
    Petrovic, Jelena (57207943674)
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    Trifunovic, Branislav (8269362700)
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    Vukomanovic, Goran (8252832300)
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    Topalovic, Mirko (36616659900)
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    Trajkovic, Goran (9739203200)
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    Parezanović, Vojislav (14325763000)
    Purpose: Oral propranolol has been recently approved for infantile hemangiomas (IHs), but potential side effects stay a challenge. We sought to make an additional assessment on oral propranolol safety for this indication. Materials and methods: Prospective study included 108 infants consecutively treated for IHs at the University Children’s Hospital Tirsova, Belgrade from January 2010 to December 2013. Propranolol was administered orally at a daily dose of 0.5 mg/kg and doubled every 48 hours in the absence of side effects until reaching the maximum dose of 2 mg/kg daily. Systolic and diastolic blood pressure and heart rate were measured every 48 hours with clinical observation. Heart rate was monitored by standard electrocardiogram (ECG) and 48-hour Holter ECG. Results: Statistically significant, but asymptomatic decreases in systolic blood pressure and heart rate recorded by Holter ECG were observed during the first doubling of dose and then remained stable. Arrhythmias were not detected. Despite mild sleep disturbance observed in 31% of infants in the hospital milieu, Holter monitoring indicated circadian rhythm maintenance. Conclusions: Oral propranolol for IHs does not remarkably affect heart rhythm including circadian variations throughout hospital initiation. Therefore, there is no necessity for Holter monitoring in additional safety assessment. © 2017 Informa UK Limited, trading as Taylor & Francis Group.
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    Two rare conditions in an Eisenmenger patient: Left main coronary artery compression and Ortner's syndrome due to pulmonary artery dilatation
    (2013)
    Andjelkovic, Kristina (55778189900)
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    Kalimanovska-Ostric, Dimitra (6603414966)
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    Djukic, Milan (23988377500)
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    Vukcevic, Vladan (15741934700)
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    Menkovic, Nemanja (57113304600)
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    Mehmedbegovic, Zlatko (55778381000)
    ;
    Topalovic, Mirko (36616659900)
    ;
    Tesic, Milorad (36197477200)
    The left-main coronary artery extrinsic compression due to enlarged pulmonary artery has been described in several case series. Ortner's syndrome is also a rare condition in some cardiovascular disorders. There have been no reports about these two rare conditions in the same patient. Hence, we report a very rare case of an Eisenmenger patient with severe pulmonary hypertension and dilated pulmonary artery which has compressed the left main coronary artery, severely narrowing it, and the left laryngeal recurrent nerve with subsequent Ortner's syndrome and brief literature review. © 2013 Elsevier Inc.

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