k 2016

Congenital diaphragmatic hernia in the neonates-review od 10-year experience

PINKASOVÁ, Tereza; Linda SKUTKOVÁ; Jan PAPEŽ; Petr JABANDŽIEV; Ladislav PLÁNKA et al.

Základní údaje

Originální název

Congenital diaphragmatic hernia in the neonates-review od 10-year experience

Vydání

WOFAPS 2016, 2016

Další údaje

Jazyk

angličtina

Typ výsledku

Prezentace na konferencích

Obor

30209 Paediatrics

Stát vydavatele

Spojené státy

Utajení

není předmětem státního či obchodního tajemství

Označené pro přenos do RIV

Ano

Kód RIV

RIV/00216224:14110/16:00091370

Organizační jednotka

Lékařská fakulta

Klíčová slova anglicky

Congenital diaphragmatic hernia

Štítky

Změněno: 27. 10. 2016 14:23, Soňa Böhmová

Anotace

V originále

AIM: The prognosis of the children with CDH remains unsatisfactory despite recent advances in medical and surgical treatment including gore-tex patches. In our poster we would like to point to the importance of interdisciplinary collaboration including gynecologist, obstertician, neonatologist and surgeon. METHODS: We retrospectively reviewed medical records of neonates with CDH admitted to the University Hospital Brno. Prenatal and postnatal factors, birth details, managment were studied. RESULTS: We admitted 29 neonates with CDH who fullified the study criterias. 28 patients /97%/ had left-sided Bochdalek hernia, only 1 patient had right-sided Morgagni hernia. The mean gestational age was 37,5 weeks /range 31.-41.wA 9 neonates /33%/were prenatally diagnosed by using ultrasound or MRI and therefore they were delivered in the tertiary perinatal centre. The operation was performed in almost all of the patiens the first day. Average duration of the mechanical ventilation was 8,5 days, a severe pulmonary hypertension developed in 5 patients with the need of high frequency oscilatory ventilation. Two neonates died in early postoperative period. The reoperation was needed in 3 patients during the neonatal period. CONCLUSION: The surgery after birth is not an emergency and is usually performed when the baby has stabilized. In our review the size of the defect wasn't the determing factor for the mortality rate which was 7% in our case. We have learned that the severity and outcome is determined by 3 factors - other associated malformations, pulmonary hypertension and low gestational age .