Neonatal symptomatic thromboembolism in Germany: two year survey
a Departments of Paediatrics, University Hospital of
Münster, b University Hospital of Munich, c University Hospital of Düsseldorf
Correspondence to: Dr Ulrike Nowak-Göttl Department of Paediatric Haematology/Oncology, University Children's Hospital, Westfälische Wilhelms-University, Albert-Schweitzer- Str. 33, D-48149 Münster, Germany.
Accepted 2
January 1997
AIMS
To determine the incidence of neonatal
thromboembolism in Germany.
METHODS
Diagnostic imaging techniques, therapeutic
modalities, and short term outcome were evaluated in a prospective
nationwide two year case registry study.
RESULTS
The reported incidence of symptomatic
neonatal thromboembolism, diagnosed in most cases with Doppler
ultrasonography, was 5.1 per 100 000 births, with a total of 79 cases
registered: renal venous thrombosis (n=35); venous thrombosis (n=25);
and arterial vascular occlusion (n=19). Fifty seven of 79 thromboses
were associated with additional risk factors (central line n=25,
asphyxia n=13, septicaemia n=11, dehydration n=6, maternal diabetes
n=2, cardiac disease n=1). Inherited thrombophilia was also diagnosed
in seven out of 35 cases investigated. Twenty three children received
supportive treatment: 42 received heparin and in 13 neonates
thrombolytic agents were administered. Most neonates (91%) survived;
seven died.
CONCLUSION
Controlled multicentre studies are
needed to obtain more information on treatment efficacy.
© 1997 by Archives of Disease in Childhood
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