Maurer U
Medical University of Graz
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Publication
Featured researches published by Maurer U.
The Journal of Pediatrics | 1996
Berndt Urlesberger; Gerfried Zobel; Zenz W; Kuttnig-Haim M; Maurer U; F. Reiterer; Michael Riccabona; Drago Dacar; Siegfried Gallistl; Bettina Leschnik; Wolfgang Muntean
OBJECTIVES To determine the degree of clotting activation that occurs with the usual anticoagulation regimen with systemic heparinization. METHODS To allow a standardized comparison of the patients, this study focused on the first 48 hours of extracorporeal membrane oxygenation (ECMO) in term newborn infants. The ECMO perfusion circuit consisted of a roller pump, silicone membrane lungs, and silicone rubber tubing. Coagulation was controlled routinely by measuring prothrombin time, fibrinogen, antithrombin III, and reptilase time. Platelet counts, activated clotting time, and heparin concentration were controlled regularly. The following specific activation markers of the clotting system were measured: prothrombin activation fragment 1 + 2(F1+2), thrombin-antithrombin III complexes, and D-dimer. Measurements were done before the start of ECMO, after 5 minutes, and at hours 1, 2, 3, 4, 6, 12, 24 and 48. RESULTS All seven term infants had excessively high levels of clotting activation markers within the first 2 hours of ECMO: F1+2, 11.6(+/- O.9) nmol/L (mean +/- SEM); thrombin-antithrombin, 920(+/- 2.2) microg/L; D-dimer, 15.522(+/- 3.689) ng/L. During the next 46 hours of ECMO, F1+2 and thrombin-antithrombin III complexes decreased from those high values, whereas D-dimer did not. The increase of activation markers was accompanied by low fibrinogen, low platelet counts. and prolongation of reptilase time. CONCLUSIONS These findings fit the pattern of consumptive coagulopathy during neonatal ECMO, especially in the first 24 hours.
Early Human Development | 2002
J. Kutschera; J. Tomaselli; Berndt Urlesberger; Maurer U; M Häusler; E Gradnitzer; K Burmucic; W. Müller
UNLABELLED The objective of this study was to examine the cognitive, neurological and somatic developments of children who had in utero an absent or reversed end-diastolic blood flow (ARED) in the umbilical artery or an abnormal cerebroplacental ratio (ABF). METHODS 16 children with ARED blood flow and 15 children with ABF were each matched to children with the same gestational age, appropriate for gestational age, the same sex and born within 4 months. Data were assessed at the age of 3-6 years. Children with asphyxia, neonatal infection, malformation or major surgical interventions in the neonatal period were excluded. Each child underwent a neuropediatrical examination; furthermore, a Kaufman Assessment Battery for Children, a Snijders-Oomen Intelligence Scale for Children and a Man-Drawing Test were used to evaluate cognitive development. The socioeconomic status was also assessed. RESULTS Children in the ARED group remained lighter and had a higher frequency of microcephaly. In the Kaufman Assessment Battery for Children and the Snijders-Oomen Intelligence Scale for Young Children, cognitive development was impaired in the ARED and the ABF groups compared to the control group. The ARED and the ABF groups, however, showed no differences. The Man-Drawing Test and the Denver Development Test did not show any differences. DISCUSSION ARED blood flow and ABF showed impaired cognitive development. The degree of impairment was the same in the ARED and the ABF groups. Long-term follow-up studies until adulthood are necessary to see if impaired cognitive development remains significant in these groups of patients.
European Radiology | 1997
Michael Riccabona; Kuttnig-Haim M; Drago Dacar; Berndt Urlesberger; F. Reiterer; Maurer U; Gerfried Zobel
The purpose of our study was to evaluate thrombosis of venous vessels during and after extracorporeal membrane oxygenation (ECMO) using color Doppler sonography. We prospectively performed serial color Doppler sonography investigations in 30 ECMO patients [age: newborn to 3 years, male:female = 20:10, venoarterial (VA) ECMO = 18, venovenous (VV) ECMO = 12]. During ECMO obstruction and/or thrombosis of the superior vena cava (SVC) was observed in 2 neonates on VA ECMO. Furthermore, a thrombotic clot from an initially open duct of Arantii with partial portal vein thrombosis, reaching into the inferior vena cava (IVC), occurred despite adequate heparinization. After ECMO, late septic SVC thrombus occurred in one neonate. IVC thrombus was observed in two pediatric VV ECMO patients. The overall incidence of venous clots was 20 % (6 of 30). Routine color Doppler sonography monitoring of vessels in children on and after ECMO was found to be useful for early detection of venous thrombosis. It enabled consequent administration of appropriate therapy as well as follow-up after decannulation and reconstruction.
Acta Paediatrica | 2006
J. Kutschera; Johanna Tomaselli; Maurer U; Gerhard Pichler; Gerold Schwantzer; Berndt Urlesberger
Aim: To determine, using strict exclusion criteria, whether transient periventricular echodensities (TPE) in very‐low‐birthweight infants lead to minor neurological dysfunction and problems in cognitive and somatic development in children without major neurological impairments. Methods: 23 children with TPE were matched to 23 children without TPE. Exclusion criteria were small for gestational age, microcephaly at birth, diplegia, asphyxia, psychomotor retardation, intraventricular haemorrhage grade III/IV, major surgical interventions and malformations. The Kaufman Assessment Battery for Children, Draw‐a‐Man Test and neuropaediatric examination were used for evaluation. Results: There were no differences in demographic data, growth and socio‐economic status. Significant differences with lower results in the TPE group were found in fine motor skills and in the Draw‐a‐Man Test. In the Kaufman Assessment Battery for Children, all subscales were below average in the TPE group, except the sequential processing scale. In the control group, all subscales were within the average range.
Zeitschrift Fur Geburtshilfe Und Neonatologie | 2002
J. Kutschera; Berndt Urlesberger; Maurer U; W. Müller
Klinische Padiatrie | 2003
Kreuzer C; Berndt Urlesberger; Maurer U; W. Müller
Wiener Klinische Wochenschrift | 1998
W. Müller; Berndt Urlesberger; Maurer U; Kuttnig-Haim M; F. Reiterer; Moradi G; Gerhard Pichler
Early Human Development | 2005
J. Kutschera; J. Tomaselli; Maurer U; Wilhelm Mueller; Berndt Urlesberger
Wiener Klinische Wochenschrift | 1997
F. Reiterer; Kuttnig-Haim M; Gerfried Zobel; Berndt Urlesberger; Maurer U; Michael Riccabona; Drago Dacar; W. Müller
Klinische Padiatrie | 1994
F. Reiterer; Kuttnig-Haim M; Maurer U; Berndt Urlesberger; M. Ricabbona; Gerfried Zobel; Wilhelm Müller; Drago Dacar