Browsing by Author "Cetkovic, A. (15729111700)"
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Publication Fetal Ventriculomegalies during pregnancy course, outcome, and psychomotor development of bom children(2016) ;Dukanac Stamenkovic, J. (57170807300) ;Steric, M. (36192097800) ;Srbinovic, L. (57273906200) ;Janjic, T. (56362345500) ;Vrzic Petronijevic, S. (14520050800) ;Petronijevic, M. (21739995200)Cetkovic, A. (15729111700)Purpose: The objectives of this study were as follows: to present the course and outcome of pregnancies complicated with fetal ventriculomegaly, determine the association between prenatal ultrasound diagnoses and definitive postnatal diagnosis or diagnoses after autopsy and additional analysis, and to monitor the psychomotor development of children bom with ventriculomegaly. Materials and Methods: The survey was designed as retrospective study and included 62 pregnant women who were attending a regular ultrasound examinations at the Department of Gynecology and Obstetrics, Clinical Center of Serbia, or patients who were referred from other institutions in Serbia. Results: Ventriculomegalies were divided into three groups: mild, moderate, and severe or hydrocephalus. The most common were severe ventriculomegalies, with 34 cases (55%). Of all pregnancies complicated with ventriculomegalies, 61% were terminated. Among those continued, 88% had normal psychomotor development. In 97% ultrasonographic diagnosis was confirmed. Conclusion: Majority of pregnancies complicated with ventriculomegaly were continued and most of the children bom with anomalies had normal psychomotor development. - Some of the metrics are blocked by yourconsent settings
Publication Peripartum cardiomyopathy: A case of patient with triplet pregnancy(2016) ;Kastratovic Kotlica, B. (55623374800) ;Cetkovic, A. (15729111700) ;Plešinac, S. (55920049900) ;Macut, D. (35557111400)Ašanin, M. (8603366900)Peripartum cardiomyopathy (PPCM) is a rare but potentially devastating complication of pregnancy associated with heart failure due to left ventricular systolic dysfunction occurring within the last month of pregnancy and five month postpartum with no obvious other cause of heart failure and no pre-existing heart disease. In the present case report the authors present a woman who developed PPCM on the day after she delivered by cesarean section in 35th weeks of gestation of triplet pregnancy conceived after ovarian stimulation and insemination. A treatment with diuretics, ACE inhibitors, antiarrhythmics, low weight heparin, antibiotics and bromocriptine was applied and resulted in complete recovery. In conclusion, timely detection and initiation of treatment are important factors for complete recovery of patients with PPCM. - Some of the metrics are blocked by yourconsent settings
Publication The outcome and course of pregnancies complicated with fetal neural tube defects(2015) ;Steric, M. (36192097800) ;Stamenkovic, J. Dukanac (54414801300) ;Srbinovic, L. (57273906200) ;Janjic, T. (56362345500) ;Petronijevic, S. Vrzic (56545626100) ;Petronijevic, M. (21739995200)Cetkovic, A. (15729111700)Purpose: The objectives of this study were as follows: to present the course and outcome of pregnancies complicated with neural tube defects, determine the association between prenatal ultrasound diagnoses, and definitive diagnoses after autopsy. Matherial and Methods: The survey was designed as a retrospective study and included 24 pregnant women who were attending a regular ultrasound examinations at the Department of Gynecology and Obstetrics, Clinical Center of Serbia, or patients who were referred from other institutions in Serbia. Results: Neural tube defects are divided into five subgroups: spina bifida, meningocele, myelomeningocele, acranius, and anencephaly. The most frequent in the present study was spina bifida with 67%. All pregnancies complicated with neural tube defects were terminated. Conclusion: Their clinical severity and uncertain cause make them priorities for further research, whether to better target primary preventive measures, to improve in-utero surgery for prenatal repair, or to identify the causative genes to provide an objective basis for individual genetic counselling.
