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Published on: May 22, 2014
[Anesthetic management of an 18-trisomy neonate with high frequency ventilation]
Michiyo Kimoto1, Kohei Murao, Makiko Yamada
1Department of Anesthesiology, Kansai Medical University Hospital, Moriguchi.
Insights
Neonates with trisomy 18 syndrome often have poor prognoses. This case demonstrates successful anesthetic management and high-frequency ventilation for a neonate with trisomy 18, improving survival rates.
Area of Science:
- Anesthesiology
- Neonatology
- Medical Genetics
Background:
- Trisomy 18 syndrome (Edwards syndrome) is associated with significant congenital anomalies and historically poor one-year survival rates (<10%).
- Active treatment is often not recommended due to these low survival rates.
- Improved survival rates have been observed in some centers, necessitating effective anesthetic strategies for surgical interventions.
Observation:
- A male neonate diagnosed with trisomy 18 syndrome presented for immediate radical repair of an umbilical hernia.
- The neonate exhibited difficult tracheal intubation due to airway anomalies (cleft lip, cleft palate, macrognathia) and facial dysmorphism.
- Conventional ventilation proved insufficient for adequate carbon dioxide elimination and oxygenation, complicated by pulmonary hypoplasia and intracardiac shunts.
Findings:
- High-frequency ventilation was employed as an alternative anesthetic technique.
- This ventilation strategy significantly improved both carbon dioxide elimination and oxygenation in the neonate.
- The patient survived beyond five years, indicating the potential efficacy of tailored anesthetic management.
Implications:
- This case highlights the feasibility and benefits of advanced anesthetic techniques, such as high-frequency ventilation, in neonates with trisomy 18 syndrome.
- It suggests that improved survival rates may be achievable with appropriate perioperative care and ventilation strategies.
- Further research into anesthetic management protocols for trisomy 18 neonates undergoing surgery is warranted.
Abstract:
Neonates with 18-trisomy syndrome have various anomalies including cardiac and facial anomalies. Active treatments for them have not been recommended due to a low survival over one year which is less than 10%. However, the survival over one year in our institute between 1985 and 2003 is higher at 22%, and we had a patient with survival of over 5 years. We report a case of anesthetic management in a male 18-trisomy neonate who received a radical repair of umbilical hernia immediately after his birth. Tracheal intubation was difficult due to small airway and facial anomalies; cleft clip, cleft palate, and macrognathia. Conventional ventilation was ineffective for elimination of carbon dioxide and oxygenation due to pulmonary hypoplasia and intra- and extra-cardiac shunts. A high frequency ventilation improved elimination of carbon dioxide and oxygenation.
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