1. 伴气道梗阻的颈部淋巴管畸形患儿 产前产后程序化管理.
- Author
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吴强, 钟微, 吕俊健, 林土连, 侯龙龙, 夏波, 顾圆圆, 牛传强, and 何秋明
- Abstract
Objective To summarize the clinical experiences of managing cervical lymphatic malformation with airway obstruction ( CLMAO) from prenatal assessments to postnatal interventions. Methods Retrospective analysis was conducted for clinical data of 22 hospitalized CLMAO infants from July 2015 to March 2023. Nine cases were born at our hospital while another 13 infants were transferred from other hospitals. They were assigned into two groups of early surgical treatment ( n = 6) and protocol treatment (n = 16 ). Fetal assessments, intrapartum managements and postnatal interventions were recorded. Surgical complications, duration of mechanical ventilation, length of hospital stay and other prognostic factors were compared between two groups. Results Nine infants born at our hospital were examined by prenatal magnetic resonance imaging( MRI) for assessing tracheoescphageal displacement index( TEDI) or amniotic fluid volume. Eight infants had TEDI> 12 mm or polyhydramnios. Ex-utero intrapartum treatment( EXIT) was offered for postnatal dyspnea. One case of TEDI≤ 12 mm and normal anmiotic fluid volume had dyspnea after umbilical cord clamping and underwent tracheal intubation. The accuracy of prenatal assessment for airway obstruction was 88. 9% ( 8/9). Three cases were operated in protocol treatment group. As compared with early treatment group, no significant inter-group differences existed in proportion of tracheostomy, duration of mechanical ventilation or length of hospital stay. During a follow-up period of ( 6 - 39) months, there was no significant difference in cure rate or improvement rate. Conclusion Fetuses with suspected CLMAO should be evaluated for TEDI and amniotic fluid volume. As compared with early surgery, programmed therapy may obtain comparable outcomes. It offers a novel therapeutic option for CLMAO. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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