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一期序贯双侧胸廓扩张术治疗窒息性胸廓发育不良(朱恩综合征)

One-stage sequential bilateral thoracic expansion for asphyxiating thoracic dystrophy (Jeune syndrome).

作者信息

Muthialu Nagarajan, Mussa Shafi, Owens Catherine M, Bulstrode Neil, Elliott Martin J

机构信息

Department of Cardiothoracic Surgery, Great Ormond Street Hospital NHS Trust, London, UK

Department of Cardiothoracic Surgery, Great Ormond Street Hospital NHS Trust, London, UK.

出版信息

Eur J Cardiothorac Surg. 2014 Oct;46(4):643-7. doi: 10.1093/ejcts/ezu074. Epub 2014 Mar 5.

Abstract

OBJECTIVES

Jeune syndrome (asphyxiating thoracic dystrophy) is a rare disorder characterized by skeletal dysplasia, reduced diameter of the thoracic cage and extrathoracic organ involvement. Fatal, early respiratory insufficiency may occur. Two-stage lateral thoracic expansion has been reported, addressing each side sequentially over 3-12 months. While staged repair theoretically provides less invasive surgery in a small child with respiratory distress, we utilized a single stage, bilateral procedure aiming to rapidly maximize lung development. Combined bilateral surgery also offered the chance of rapid recovery, and reduced hospital stay. We present our early experience of this modification of existing surgical treatment for an extremely rare condition, thought to be generally fatal in early childhood.

METHODS

Nine children (6 males, 3 females; median age 30 months [3.5-75]) underwent thoracic expansion for Jeune syndrome in our centre. All patients required preoperative respiratory support (5 with tracheostomy, 8 requiring positive pressure ventilation regularly within each day/night cycle). Two children underwent sequential unilateral (2-month interval between stages) and 7 children bilateral thoracic expansion by means of staggered osteotomies of third to eighth ribs and plate fixation of fourth to fifth rib and sixth to seventh rib, leaving the remaining ribs floating.

RESULTS

There was no operative mortality. There were 2 deaths within 3 months of surgery, due to pulmonary hypertension (1 following two-stage and 1 following single-stage thoracic expansion). At the median follow-up of 11 months (1-15), 3 children have been discharged home from their referring unit and 2 have significantly reduced respiratory support. One child remains on non-invasive ventilation and another is still ventilated with a high oxygen requirement.

CONCLUSION

Jeune syndrome is a difficult condition to manage, but bilateral thoracic expansion offers an effective reduction in ventilator requirements in these children. While two-stage repair has been described previously, this is the first report of single-stage bilateral thoracic expansion. Single-stage repair is feasible and may offer better resource management and significant cost savings by potentially reducing theatre usage and overall length of stay (intensive care and hospital) without compromising clinical outcomes.

摘要

目的

约内综合征(窒息性胸廓发育不良)是一种罕见疾病,其特征为骨骼发育异常、胸廓直径减小以及胸外器官受累。可能会出现致命的早期呼吸功能不全。已有报道采用两阶段胸廓外侧扩展术,在3至12个月内依次处理每一侧胸廓。虽然分期修复理论上对患有呼吸窘迫的幼儿手术侵入性较小,但我们采用了单阶段双侧手术,旨在迅速最大限度地促进肺部发育。双侧联合手术还提供了快速康复和缩短住院时间的机会。我们介绍了对这种极其罕见疾病现有手术治疗方法进行改良后的早期经验,这种疾病在幼儿期通常被认为是致命的。

方法

我们中心有9名儿童(6名男性,3名女性;中位年龄30个月[3.5 - 75个月])因约内综合征接受胸廓扩展术。所有患者术前均需要呼吸支持(5例行气管切开术,8例每天/夜间周期内定期需要正压通气)。2名儿童接受了序贯单侧胸廓扩展术(两阶段间隔2个月),7名儿童通过对第三至第八肋骨进行交错截骨以及对第四至第五肋骨和第六至第七肋骨进行钢板固定进行双侧胸廓扩展术,其余肋骨保持浮动。

结果

无手术死亡病例。术后3个月内有2例死亡,原因是肺动脉高压(1例为两阶段胸廓扩展术后,1例为单阶段胸廓扩展术后)。中位随访时间为11个月(1 - 15个月),3名儿童已从转诊单位出院回家,2名儿童的呼吸支持显著减少。1名儿童仍需无创通气,另1名儿童仍需高氧需求通气。

结论

约内综合征是一种难以处理的疾病,但双侧胸廓扩展术能有效减少这些儿童对呼吸机的需求。虽然此前已描述过两阶段修复术,但这是单阶段双侧胸廓扩展术的首次报告。单阶段修复是可行的,并且通过潜在地减少手术时间和总体住院时间(重症监护和住院),在不影响临床结果的情况下,可能提供更好的资源管理并显著节省成本。

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