Beáta Rosdy
Boston Children's Hospital
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Featured researches published by Beáta Rosdy.
Epilepsy Research | 2006
Béla Clemens; Andrea Ménes; Pálma Piros; Mónika Bessenyei; Anna Altmann; Judit Jerney; Katalin Kollár; Beáta Rosdy; Margit Rózsavölgyi; Katalin Steinecker; Katalin Hollódy
UNLABELLED Quantitative EEG (QEEG) effects of therapeutic doses of carbamazepine (CBZ), oxcarbazepine (OXC), valproate (VA) and lamotrigine (LA) monotherapy were investigated in patients with beginning epilepsy. Baseline waking EEG (EEG1) was recorded in the untreated state, the second EEG (EEG2) was done after 8 weeks of reaching the therapeutic dose. Left occipital data were used for analysis. QEEG target parameters were absolute band-power (delta: AD, theta: AT, alpha: AA, beta: AB), and alpha mean frequency (AMF). Group effects (untreated versus treated condition in the CBZ, VA, OXC, LA groups) were computed for each target parameter. One group with benign rolandic epilepsy remained untreated for clinical reasons and served to estimate the QEEG test-retest differences. In addition, the individual QEEG response to each drug was calculated as (EEG2-EEG1). RESULTS statistically significant (p<0.05) group differences indicated the QEEG domain systematically affected by the drugs. CBZ caused AT increase and AMF decrease. OXC caused AMF decrease. VA and LA did not decrease AMF (LA even increased it), but reduced broad-band power. Individual power and AMF changes showed considerable variability in each group. >0.5 Hz AMF decrease (that was reported to predict cognitive impairment in prior studies) occurred in 10/41 patients in the CBZ group but never in the OXC, VA, LA groups. The results may be utilized in planning further studies addressing the relationship between antiepileptic drugs and their CNS effects. In addition, the relationship of AED-related cognitive impairment and AMF changes was discussed.
European Archives of Oto-rhino-laryngology | 2013
Zsuzsanna Csákányi; Beáta Rosdy; Katalin Kollár; Judit Móser; Éva Kovács; Gábor Katona
The objective of this study was to evaluate long-term clinical and radiological outcomes in children treated with lateral sinus thrombosis secondary to acute mastoiditis considering also contralateral sinus hypoplasia. This study was a retrospective chart review, conducted in tertiary pediatric hospital. Medical reports of eight children with acute mastoiditis and lateral sinus thrombosis from 1998 to 2011 were examined in terms of therapy, clinical recovery and radiological proof of lateral sinus recanalization. Three children presented hypoplasia of contralateral venous drainage system. Condition of sinuses was regularly monitored with MRI. Otologically and neurologically, all children recovered fully. All received antibiotics; six received additional low molecular weight heparin therapy. Mastoidectomy was performed on six cases. Incision and thrombectomy were applied in the other two, one involving internal jugular vein ligation. This latter case presented also contralateral venous hypoplasia; visual impairment proved permanent. The other two children with contralateral sinus hypoplasia recovered fully after steroid, dehydration and low molecular weight heparin therapy. Recanalization occurred in all children except the one with internal jugular vein ligation, in whom good collateral circulation was observed. There were no bleeding complications. Anatomical variations of cerebral venous drainage system can frequently be observed and should be considered in treatment planning. Mastoidectomy with antibiotics and additional low molecular weight heparin treatment is a safe, promising alternative to thrombectomy and internal jugular vein ligation in children with lateral sinus thrombosis following acute mastoiditis, also having contralateral sinus hypoplasia. Recanalization can be expected within two to five months.
International Journal of Pediatric Otorhinolaryngology | 2014
Beáta Rosdy; Zsuzsanna Csákányi; Katalin Kollár; Judit Móser; Mónika Mellár; Andrea Kulcsár; Éva Kovács; György Várallyay; Gábor Katona
OBJECTIVES Otogenic lateral sinus thrombosis is a rare complication of acute otitis media whose clinical presentation has changed with the early use of antibiotics. The aim of this study was to analyze the changing clinical signs, vaccination status, therapeutic management and outcome of these patients. METHODS Retrospective chart review of 10 children treated with otogenic lateral sinus thrombosis in a tertiary level teaching hospital in Budapest, Hungary, from January 1998 till August 2013. RESULTS Patients were divided into Early and Late presenting groups. In the Early presenting group, sepsis developed within one week after the onset of acute otitis media. At admission otological symptoms were predominant. The Late presenting group experienced acute otitis media several weeks prior to presentation and in this group neurologic symptoms dominated the clinical picture at admission. All patients received antibiotics. Eight of them were also treated with low molecular weight heparin. All children underwent cortical mastoidectomy. After surgery, the clinical signs of elevated intracranial pressure transiently worsened. This manifested as progression of papilledema in seven children, causing severe visual disturbance in two cases. After medical treatment and serial lumbar punctures all patients except one recovered. This child has permanent visual acuity failure of 0.5D unilaterally. At one year follow up complete and partial recanalization were noted in five and two patients, respectively. CONCLUSIONS After mastoidectomy the signs of elevated intracranial pressure can transiently worsen, papilledema can progress. Daily bedside monitoring of visual acuity and regular ophthalmoscopy with neurologic examination is recommended during hospitalization. Close follow up is advised up to one year. When the dominant sinus is occluded, the clinical scenario is more protracted and severe.
European Journal of Paediatric Neurology | 2015
Beáta Rosdy; Katalin Kollár; Judit Móser; M. Mellár; Éva Kovács; G. Várallyay
Objective Posttraumatic dural sinus thrombosis is a rare complication of traumatic head injury in children. Before the new anticoagulation guidelines (AHA/ASA 2011) the majority of patients were conservatively managed and their recoveries were mostly uneventful. However there are a few case reports where severe complications and even death occurred. According to the new guidelines pharmacological treatment of posttraumatic dural sinovenous thrombosis consists of administering low molecular weight heparin, (LMWH) or venous heparin. In situations, where systemic anticoagulation is contraindicated, local thrombolysis is allowed. Case report A 14 year old child suffered moderate traumatic head injury. Subgaleal and epidural hematomas were diagnosed on CT, and the suspicion of superior sagittal sinus thrombosis was raised. MR venography verified an incomplete superior sagittal sinus (SSS) thrombosis. Weighting the risk of progression of the thrombosis to further bleeding full dose LMWH was administered. Results The patient remained stable, but the hematomas started to grow. Neuroradiological counselling revealed suturolysis of the corona sutures on both sides, and fracture of the inner table of the skull at the sagittal superior suture on CT. A small epidural hematoma over the superior sagittal sinus was diagnosed, compressing the vein. The dose of LMWH was lowered to preventive dosage, and was administered for four month. On the follow up MRI examination the hematomas were absorbed, and the SSS recanalised. Conclusion Treating traumatic sinodural thrombosis in children with intra and extra cranial hematomas remains controversial. The decision in these situations must be individualized and during the clinical course frequently re-evaluated
Ideggyogyaszati Szemle-clinical Neuroscience | 2005
Péter Halász; Anna Kelemen; Béla Clemens; Judit Saracz; Beáta Rosdy; György Rásonyi; Anna Szucs
Ideggyogyaszati Szemle-clinical Neuroscience | 2006
Magdolna Neuwirth; Judit Saracz; Márta Hegyi; Eva Paraicz; Katalin Kollár; Judit Móser; Beáta Rosdy; Ágnes Herczegfalvi; András Fogarasi
Ideggyogyaszati Szemle-clinical Neuroscience | 2009
Judit Móser; Liptai Z; Veres E; Beáta Rosdy; Katalin Kollár
Ideggyogyaszati Szemle-clinical Neuroscience | 2009
Katalin Kollár; Liptai Z; Beáta Rosdy; Judit Móser
Ideggyogyaszati Szemle-clinical Neuroscience | 2009
Beáta Rosdy; Katalin Kollár; Judit Móser; Várallyay G; Kordas M
European Journal of Paediatric Neurology | 2008
Katalin Kollár; Beáta Rosdy; I. Szikora; Z. Harkányi; Judit Móser; G. Várallyay