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首页> 外文期刊>American journal of medical genetics, Part A >Intensive cardiac management in patients with trisomy 13 or trisomy 18.
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Intensive cardiac management in patients with trisomy 13 or trisomy 18.

机译:13三体或18三体患者的强化心脏管理

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摘要

Intensive cardiac management such as pharmacological intervention for ductal patency (indomethacin and/or mefenamic acid for closure and prostaglandin E1 for maintenance) and palliative or corrective surgery is a standard treatment for congenital heart defects. However, whether it would be a treatment option for children with trisomy 13 or trisomy 18 syndrome is controversial because the efficacy on survival in patients with these trisomies has not been evaluated. We retrospectively reviewed 31 consecutive neonates with trisomy 13 or trisomy 18 admitted to our neonatal ward within 6 hr of birth between 2000 and 2005. The institutional management policies differed during three distinct periods. In the first period, both pharmacological ductal intervention and cardiac surgery were withheld. In the second, pharmacological ductal intervention was offered as an option, but cardiac surgery was withheld. Both strategies were available during the third period. The median survival times of 13, 9, and 9 neonates from the first, second, and third periods were 7, 24, and 243 days, respectively. Univariate and multivariate analyses confirmed that the patients in the third period survived significantly longer than the others. Intensive cardiac management consisting of pharmacological intervention for ductal patency and cardiac surgery was demonstrated to improve survival in patients with trisomy 13 or trisomy 18 in this series. Therefore, we suggest that this approach is a treatment option for cardiac lesions associated with these trisomies. These data are helpful for clinicians and families to consider in the optimal treatment of patients with these trisomies.
机译:强化心脏管理,例如导管通畅的药理干预(吲哚美辛和/或甲芬那酸用于封堵,前列腺素E1用于维持)和姑息或矫正手术是先天性心脏缺陷的标准治疗方法。但是,是否将其用于13三体综合征或18三体综合征的儿童仍存在争议,因为尚未评估这些三体综合征患者的生存疗效。我们回顾性研究了2000年至2005年之间出生的6个小时内入院的连续13例13三体或18三体的新生儿。在三个不同的时期,机构管理政策有所不同。在第一阶段,没有进行药理导管干预和心脏手术。在第二种方法中,可以选择药理导管干预,但是心脏手术被拒绝。两种策略在第三阶段都可用。第一,第二和第三期的13、9和9例新生儿的中位生存时间分别为7天,24天和243天。单因素和多因素分析证实,第三期患者的存活时间明显长于其他患者。在该系列研究中,由导管通畅的药物干预和心脏手术组成的强化心脏管理被证明可以改善13三体或18三体患者的生存率。因此,我们建议这种方法是与这些三体症相关的心脏病变的治疗选择。这些数据有助于临床医生和家庭考虑对这些三体症患者进行最佳治疗。

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