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- IRMS - Nicolae Testemitanu SUMPh
- 1. COLECȚIA INSTITUȚIONALĂ
- MedEspera: International Medical Congress for Students and Young Doctors
- MedEspera 2016
Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12710/10987
Title: | Echocardiographic diagnosis of congenital heart malformations |
Authors: | Postolachi, Alina |
Keywords: | congenital heart defects;infant;echocardiography |
Issue Date: | 2016 |
Publisher: | MedEspera |
Citation: | POSTOLACHI, Alina. Echocardiographic diagnosis of congenital heart malformations. In: MedEspera: the 6th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2016, p.60. |
Abstract: | Introduction. Clinical analysis of profile of children with congenital heart disease at the age of
addressing as infant, depending on the type and severity of the heart defect, identifying those common
clinical features in diagnosis of MCC, the complications in their evolution, cardiac defects that
interventional or surgical correction was achieved, congenital anomalies Associated and the usefulness
echocardiography in the diagnosis of MCC.
Material and Methods. The lot in the study consisted of 159 infants (30 days - 12 months) with
MCC hospitalized in the Clinical Republican Hospital, Department of Surgery, in the period of Jan 2007
- Dec 2010. In this group were not included newborns with MCC, due to the particularities encountered
in newborns. We made a "Paper MCC" in which was noted retrospective and prospective medical
history, clinical, biological, radiological and echocardiographic investigations, treatment and outcomes
in each case. Radiological examinations were performed as it follows: cardiopulmonary Rx for 58 infants
and 79 infants followed echocardiographic examination. In our study we used specific research methods
which helped to achieve the results.Discussion results. MCC had a family history of 8 patients (11%). Depending on the presence
of other organ malformations, patients were divided: non-Associated malformations - 60%, 42 cases;
Associated malformations - 40%, 28 cases. In second group 18 cases (25%) were Associated with
malformations of other organs or systems, without falling into a syndrome: 10 cases (14%) had genetic
syndromes, 7 cases with Down syndrome (70%), 1 case of Proteus syndrome, 1 case of Potter syndrome,
1 case Werdnig Hoffemann syndrome. Regarding complications, seven developed heart failure (IC) (3
of those operated) and 4 pulmonary hypertension (PH) (2 of those operated). In evolution, five have
developed PAH / IC and one died. None were operated.
Conclusions. The incidence of congenital heart disease in types was different from other
statistics, ASD has met the highest percentage rather VSD and while both were above the rates found in
other studies. CAP, SP and had also TVM percent higher and, CAV, AT and DVPAP approached the
data found in the literature. MCC investigation which confirmed the diagnosis was EcoCG examination
which was performed in all cases in the study group, the "gold standard" in determining the MCC. |
URI: | http://repository.usmf.md/handle/20.500.12710/10987 |
ISBN: | 978-9975-3028-3-8. |
Appears in Collections: | MedEspera 2016
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