Beierle E A, Langham M R, Cassin S
Department of Surgery, University of Florida College of Medicine, Gainesville, USA.
J Pediatr Surg. 1996 Jan;31(1):141-6; discussion 146-7. doi: 10.1016/s0022-3468(96)90337-1.
The observation that tracheal ligation produces pulmonary hyperplasia even in animals with surgically induced diaphragmatic hernia (DH) has led to rapid application of the technique to human fetuses with DH. The aim of this study was to determine how rapidly fetal lung volume increases after creation of a high-grade tracheal stenosis in fetal sheep with surgically created DH. Twenty-three fetal sheep were prepared with a left thoracotomy at 90 days' gestational. Six had creation of a DH with tracheal stenosis (DHTS) over an 18-gauge cannula, which was then removed. Ten had DH alone, and seven control animals (CT) had a thoracotomy without DH. Thirty days later, vascular and tracheal loop catheters were inserted in all animals and tunneled out the ewes' flank. Between 125 and 140 days' gestation, lung volumes and lung liquid production were measured in awake, unanesthetized animals using a standard double-marker dilution technique. Average lung volumes (in milliliters) were 150.9 +/- 13.9 for CT, 29.3 +/- 4.4 for DH, and 414.5 +/- 88 for DHTS (p < 0.01). Mean lung liquid production varied from 6.00 +/- 2.23 mL/h in DH animals before 130 days to 16.69 +/- 8.29 mL/h in DHTS animals after 135 days' gestation. DH animals had lower lung liquid production (8.51 +/- 1.4 mL/h) than CT (12.4 +/- 0.8 mL/h) or DHTS animals (12.4 +/- 2.2 mL/h)(P < .01). The rate constant gamma (h-1) for lung liquid production was significantly higher in DH animals than in either CT or DHTS animals (P < .01). Tracheal stenosis in this model causes rapid lung growth before 130 days' gestation. The authors speculate that short periods of incomplete stenosis might reverse the pulmonary hypoplasia associated with DH. To achieve this goal, the timing and duration of treatment and the optimal degree of stenosis must be defined.
气管结扎即使在患有手术诱导膈疝(DH)的动物中也会导致肺增生,这一观察结果使得该技术迅速应用于患有DH的人类胎儿。本研究的目的是确定在通过手术制造DH的胎羊中造成高度气管狭窄后,胎儿肺体积增加的速度有多快。23只胎羊在妊娠90天时进行左胸切开术。6只通过18号套管制造了伴有气管狭窄的DH(DHTS),然后移除套管。10只仅有DH,7只对照动物(CT)进行了无DH的胸切开术。30天后,在所有动物中插入血管和气管环导管,并从母羊侧腹引出。在妊娠125至140天期间,使用标准双标记稀释技术在清醒、未麻醉的动物中测量肺体积和肺液生成量。CT组的平均肺体积(毫升)为150.9±13.9,DH组为29.3±4.4,DHTS组为414.5±88(p<0.01)。平均肺液生成量在妊娠130天前的DH动物中为6.00±2.23毫升/小时,在妊娠135天后的DHTS动物中为16.69±8.29毫升/小时。DH动物的肺液生成量(8.51±1.4毫升/小时)低于CT组(12.4±0.8毫升/小时)或DHTS动物(12.4±2.2毫升/小时)(P<0.01)。DH动物肺液生成的速率常数γ(h-1)显著高于CT组或DHTS动物(P<0.01)。该模型中的气管狭窄在妊娠130天前导致肺快速生长。作者推测,短时间的不完全狭窄可能会逆转与DH相关的肺发育不全。为实现这一目标,必须确定治疗的时机和持续时间以及最佳狭窄程度。