Surgical Correction of Congenital Heart Disease In 18 Trisomy / 소아과
Korean Journal of Pediatrics
;
: 462-464, 2004.
Article
in Korean
| WPRIM
| ID: wpr-178716
ABSTRACT
18 trisomy(Edwards syndrome) is a fatal disease with a congenital heart anomaly. Patients usually receive less aggressive care because caregivers expect them to die very young. Although they have a very poor prognosis due to severe multi-organ dysfunction, symptomatic simple cardiac anomaly with left to right shunt can be repaired. We experienced a case of 18 trisomy with ventricular septal defect and patent ductus arteriosus. He showed prolonged dyspnea and tachypnea after the ligation of patent ductus arteriosus in a previous hospital. In our hospital, the ventricular septal defect was closed because his parents insisted on aggressive treatment. After surgery, the symptoms were relieved and he was discharged in a condition satisfactory to his parents and the medical team.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Parents
/
Prognosis
/
Trisomy
/
Caregivers
/
Ductus Arteriosus, Patent
/
Dyspnea
/
Tachypnea
/
Heart
/
Heart Defects, Congenital
/
Heart Septal Defects, Ventricular
Type of study:
Prognostic study
Limits:
Humans
Language:
Korean
Journal:
Korean Journal of Pediatrics
Year:
2004
Type:
Article
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