Browsing by Author "Stajević, Mila (8392548400)"
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Publication Cardiac tumors in the pediatric population – surgical experience of four decades(2023) ;Stajević, Mila (8392548400) ;Ilić, Slobodan (57212487618) ;Parezanović, Vojislav (14325763000) ;Prijić, Sergej (20734985500) ;Milovanović, Vladimir (36935585800) ;Kuzmanović, Miloš (6602721300) ;Đuričić, Slaviša (22940480000) ;Dizdarević, Ivan (57216609439) ;Popović, Saša (57200324005)Bisenić, Dejan (57246618300)Introduction/Objective Although cardiac tumors in the pediatric population are found infrequently, their occurrence is constant and with occasional variations. The purpose of this study is to show our experience with surgical options of these masses in two leading national university-level pediatric centers over four decades. Methods This retrospective study is presenting a total number of 24 surgically treated pediatric patients who have been operated on 1998–2020. There were 16 children with primary masses and eight children with metastatic cardiac tumors. Two patients with tumor-like intracardiac masses were not included in the series but had been mentioned as diagnostic challenges. Our patients did not have cardiac transplantation options. Results The average age of our patients was five and a half years, and the most frequent operated tumor was the cardiac myxoma. Four children had neurological symptoms. There were two deaths, one in the primary tumor group and one metastatic patient misdiagnosed as a primary tumor in the early ages of our department. We had two recurrent cases, a girl with Carney complex, and an infant with an extremely rare form of cardiac malignancy after a myxoma extraction. One child required a permanent pacemaker insertion. Conclusion Although rare, the pediatric cardiac tumors can be a source of different life-threatening conditions and lifelong sequelae. Therefore, special considerations should be paid to the diagnostic and surgical modalities of their treatment. © 2023, Serbia Medical Society. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Does colchicine substitute corticosteroids in treatment of idiopathic and viral pediatric pericarditis?(2019) ;Vukomanovic, Vladislav (55881072000) ;Prijic, Sergej (20734985500) ;Krasic, Stasa (57192096021) ;Borovic, Ruzica (57211070403) ;Ninic, Sanja (51864038300) ;Nesic, Dejan (26023585700) ;Bjelakovic, Bojko (15070010000) ;Popovic, Sasa (57200324005) ;Stajević, Mila (8392548400)Petrović, Gordana (57211071996)Background and Objectives: Recurrence of pericarditis (ROP) is an important complication of the acute pericarditis. The aim of this study was to analyse the influence of aetiology, clinical findings and treatment on the outcome of acute pericarditis. Methods: Data were retrospectively collected from medical records of patients treated from 2011 to 2019 at a tertiary referent heart paediatric center. Results: Our investigation included 56 children with idiopathic and viral pericarditis. Relapse was registered in 8/56 patients, 2/29 (7.41%) treated with nonsteroidal anti-inflammatory drugs (NSAID) and 6/27 (28.57%) treated with corticosteroids (CS) and NSAID. Independent risk factors for ROP were viral pericarditis (p = 0.01, OR 31.46), lack of myocardial affection (p = 0.03, OR 29.15), CS use (p = 0.02, OR 29.02) and ESR = 50 mm/h (p = 0.03, OR 25.23). In 4/8 patients the first recurrence was treated with NSAID and colchicine, while treatment of 4/8 patients included CS. Children with ROP treated with CS had higher median number of recurrence (5, IQR: 2-15) than those treated with colchicine (0, IQR: 0-0.75). Conclusions: Independent risk factors for recurrence are CS treatment, viral aetiology, pericarditis only and ESR = 50 mm/h. Acute pericarditis should be treated with NSAID. Colchicine and NSAID might be recommended in children with the first ROP. © 2019 by the authors. Licensee MDPI, Basel, Switzerland. - Some of the metrics are blocked by yourconsent settings
Publication Early and midterm results after surgical repair of anomalous origin of the left coronary artery from the pulmonary artery(2019) ;Prijić, Sergej (20734985500) ;Krasić, Staša (57192096021) ;Košutić, Jovan (55928740700) ;Stajević, Mila (8392548400) ;Ninić, Sanja (51864038300) ;Popović, Saša (57200324005) ;Bjelaković, Bojko (15070010000) ;Mahmutović, Meho (57191586729)Vukomanović, Vladislav (55881072000)Introduction/Objective The anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is rare congenital disease, which causes myocardial ischemia and subsequent heart failure in infants. The aim is early and mid-term follow up evaluation of the heart function after surgical repair of ALCAPA. Methods Investigation was retrospective and included medical records of the ALCAPA patients treated surgically, between 2009 and 2017, at the tertiary referent heart center. Results Five patients (four girls) with coronary anomaly were included in the study. All patients had significantly increased left ventricular end diastolic diameter (z-score 6.6 ± 2.43) and left atria size (z-score 3.09 ± 0.37), along with decreased systolic function (ejection fraction 34.8 ± 7.4% and fractional shortening 15.5 ± 3.4%). The surgery was performed on average at the age of 8.2 ± 7.8 months. Operative treatment was associated with early improvement in echocardiographic parameters (except the size of the left atria). Patients were followed for 4.5 ± 2.6 years. Improvement in echocardiographic parameters was age-related. Patients under four months had recovery early after surgery, those treated at 5.5–6 months of age had normalization after 12 months, and patient who was recognized in the second year of life had late recovery (after ≥ 24 months). Conclusion Operative treatment in the first 3–4 months of life is related with the most favorable prognosis and rapid normalization of the echocardiographic parameters. © 2019, Serbia Medical Society. All rights reserved. - Some of the metrics are blocked by yourconsent settings
Publication Video-assisted thoracoscopic surgery for primary hyperparathyroidism with ectopic parathyroid adenoma in thymus(2021) ;Jokić, Radoica (22979996700) ;Antić, Jelena (55305523400) ;Vorgučin, Ivana (24924004500) ;Stajević, Mila (8392548400) ;Nikin, Zoran (35488550200) ;Žeravica, Radmila (16320233000)Lukić, Ivana (57211574349)Introduction Primary hyperparathyroidism is rare pathology in children (2–5:100,000). In more than 85% of patients, a single adenoma is present, and its extirpation is usually the only treatment a patient requires. In approximately 15–80% of cases, ectopic mediastinal parathyroid tissue can be found inside the thymus. Case outline Our patient was a 13-year-old boy, who presented with multiple bone fractures in the previous period of time, and fatigue. Parathyroid hormone levels preoperatively were extremely high (1320 pg/ml – more than 19 times higher than normal). Serum calcium was also elevated (total 3.55 mmol/l; ionized 1.41 mmol/l). He was examined and diagnosed as primary hyperparathyroidism by a pediatric endocri-nologist. Imaging procedures for the preoperative localization of parathyroid adenomas were done (99mTc sestamibi scintigraphy and magnetic resonance imaging suggested ectopic mediastinal parathyroid adenoma). The patient underwent video-assisted thoracoscopic surgery procedure. After exploration of the mediastinum and chest, no ectopic parathyroid tissue was found, so total thoracoscopic thymectomy was performed. Final pathological section confirmed parathyroid adenoma inside the thymus. Conclusion We believe that if no parathyroid tissue is found during surgical exploration of mediastinum, in a child with preoperatively detected parathyroid adenoma in anterior mediastinum, recommendation is to think about possible intrathymic localization and consider removing the thymus. Greater sample size is necessary for higher reliability of this statement. © 2021, Serbia Medical Society. All rights reserved.
