Motoyama Etsuro K, Deeney Vincent F, Fine Gavin F, Yang Charles I, Mutich Rebecca L, Walczak Stephen A, Moreland Morey S
Department of Anesthesiology, Children's Hospital of Pittsburgh and University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
Spine (Phila Pa 1976). 2006 Feb 1;31(3):284-90. doi: 10.1097/01.brs.0000197203.76653.d0.
Longitudinal study of intraoperative pulmonary function in young children with thoracic hypoplasia and scoliosis undergoing multiple expansion thoracoplasty using the vertical expandable prosthetic titanium ribs (VEPTRs).
To test the long-term efficacy of VEPTR multiple expansion thoracoplasty.
To our knowledge, no direct measurements of pulmonary function have been reported with VEPTR expansion thoracoplasty.
There were 10 children with thoracic insufficiency syndrome, secondary to thoracic hypoplasia with progressive scoliosis, studied. A mobile pulmonary function laboratory unit was used to study forced vital capacity (FVC), maximum expiratory flow volume curves, and respiratory system compliance (Crs) with the patient under general anesthesia immediately before and after expansion thoracoplasty. Studies were repeated every 6 months at each subsequent operation for expansion thoracoplasty for the duration up to 33 months.
At the baseline studies, FVC showed a moderate-to-severe decrease (69% of predicted values), indicating the presence of significant restrictive lung defect. Only 1 of 10 children had severe airway obstruction. The baseline Crs was markedly decreased in part because of the presence of significant atelectasis. Crs increased with an average of 42% after repeated hyperinflation (deep sighs). There was no change in lung volume or function immediately before versus after completion of expansion thoracoplasty. FVC increased significantly over time, with an average rate of 26.8% per year, the rate of increase similar to that of healthy children of comparative ages. In terms of percent-predicted values, FVC did not change significantly between the baseline and last test, indicating that in most children studied, lung growth kept up with body growth.
Although it is difficult to assess the extent of the efficacy without a proper or historical control group for comparison, the present study indicates that in children with severe thoracic insufficiency syndrome, the insertion of VEPTRs with multiple expansion thoracoplasties is beneficial over time, by allowing the lungs to expand with body growth without further deterioration in lung function.
对患有胸廓发育不全和脊柱侧弯的幼儿在接受使用垂直可扩张人工钛肋骨(VEPTR)进行的多次扩张胸廓成形术时的术中肺功能进行纵向研究。
测试VEPTR多次扩张胸廓成形术的长期疗效。
据我们所知,尚无关于VEPTR扩张胸廓成形术对肺功能直接测量的报道。
对10例因胸廓发育不全继发进行性脊柱侧弯而患有胸廓功能不全综合征的儿童进行研究。使用移动肺功能实验室装置,在扩张胸廓成形术前后立即在全身麻醉下研究患者的用力肺活量(FVC)、最大呼气流量容积曲线和呼吸系统顺应性(Crs)。在随后每次进行扩张胸廓成形术时,每6个月重复进行研究,持续时间长达33个月。
在基线研究时,FVC显示中度至重度下降(为预测值的69%),表明存在明显的限制性肺缺陷。10名儿童中只有1名有严重气道阻塞。基线Crs明显降低,部分原因是存在明显肺不张。重复过度充气(深呼吸)后,Crs平均增加42%。扩张胸廓成形术完成前后肺容量和功能无变化。FVC随时间显著增加,平均每年增加26.8%,增加速率与同龄健康儿童相似。就预测值百分比而言,基线和最后一次测试之间FVC无显著变化,表明在大多数研究儿童中,肺生长与身体生长同步。
尽管没有合适的或历史对照组进行比较很难评估疗效程度,但本研究表明,对于患有严重胸廓功能不全综合征的儿童,随着时间推移,插入VEPTR并进行多次扩张胸廓成形术是有益的,可使肺随身体生长而扩张,且肺功能不会进一步恶化。