TY  - JOUR
A1  - Lüsebrink, Natalia
A1  - Kieslich, Matthias
A1  - Rabenau, Holger
A1  - Schlößer, Rolf Lambert
A1  - Buxmann, Horst
T1  - Retrospectively diagnosing congenital cytomegalovirus infections in symptomatic infants is challenging
T2  - Acta Paediatrica
N2  - Aim: Our aim was to analyse the diagnostic workup of hospitalised infants with symptoms of congenital cytomegalovirus (CMV) infections.
Methods: This retrospective study was carried out at the University Hospital Frankfurt, Germany, from 2008 to 2017 on infants aged 4 weeks to 12 months presenting with neurological symptoms consistent with congenital CMV infections.
Results: We studied 117 infants, and workup data for CMV infections were available for 84%. Of these, 54% were immunoglobulin G‐ and immunoglobulin M‐seronegative for CMV or immunoglobulin G‐seropositive with no viral shedding. Congenital CMV infection was excluded in these cases. In 16%, the CMV workup was incomplete, precluding a definitive diagnosis. Dried blood spots (DBS) were requested from 30%. CMV polymerase chain reaction was negative in 19 of these 29 infants, and CMV deoxyribonucleic acid detection confirmed congenital CMV infections in six patients. DBS had been destroyed in line with German law in four cases. Congenital CMV infections were diagnosed (5%) or excluded (62%) in 67% of patients and unanswered in the remaining 33%.
Conclusion: Diagnoses of congenital CMV infections were widely considered and found in 5%. CMV was not stringently investigated in all patients or remained elusive due to German law on destroying DBS.
KW  - cytomegalovirus
KW  - infectious diseases
KW  - neurological impairment
KW  - neonatology
KW  - newborn screening
Y1  - 2020
UR  - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/57073
UR  - https://nbn-resolving.org/urn:nbn:de:hebis:30:3-570738
SN  - 0365-1436
VL  - 2020
PB  - Wiley-Blackwell
CY  - Oxford
ER  -