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13三体或18三体患者的强化心脏管理。

Intensive cardiac management in patients with trisomy 13 or trisomy 18.

作者信息

Kaneko Yukihiro, Kobayashi Jotaro, Yamamoto Yusuke, Yoda Hitoshi, Kanetaka Yuki, Nakajima Yayohi, Endo Daiichi, Tsuchiya Keiji, Sato Hajime, Kawakami Tadashi

机构信息

Department of Cardiovascular Surgery, Japanese Red Cross Medical Center, Tokyo, Japan.

出版信息

Am J Med Genet A. 2008 Jun 1;146A(11):1372-80. doi: 10.1002/ajmg.a.32311.

Abstract

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.

摘要

强化心脏管理,如针对动脉导管未闭的药物干预(使用吲哚美辛和/或甲芬那酸促进闭合,使用前列腺素E1维持开放)以及姑息性或矫正性手术,是先天性心脏缺陷的标准治疗方法。然而,对于13三体或18三体综合征患儿而言,这是否为一种治疗选择仍存在争议,因为尚未评估其对这些三体综合征患者生存的疗效。我们回顾性分析了2000年至2005年间在出生后6小时内入住我院新生儿病房的31例连续的13三体或18三体新生儿。在三个不同时期,机构管理政策有所不同。在第一个时期,药物性导管干预和心脏手术均未进行。在第二个时期,提供了药物性导管干预作为一种选择,但未进行心脏手术。在第三个时期,两种策略均可用。来自第一、第二和第三个时期的13例、9例和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,第三个时期的患者生存时间显著长于其他时期。在本系列研究中,由药物性导管通畅干预和心脏手术组成的强化心脏管理被证明可提高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综合征相关的心脏病变的一种治疗选择。这些数据有助于临床医生和家庭在对这些三体综合征患者进行最佳治疗时加以考虑。

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