首页> 外文期刊>Intensive care medicine >Airway obstruction and ventilator dependency in young children with congenital cardiac defects: a role for self-expanding metal stents.
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Airway obstruction and ventilator dependency in young children with congenital cardiac defects: a role for self-expanding metal stents.

机译:先天性心脏缺陷幼儿的气道阻塞和呼吸机依赖性:自膨胀金属支架的作用。

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OBJECTIVE: Young children with congenital cardiac defect and airway obstruction leading to ventilator dependency present a significant clinical challenge with uncertain outcome. DESIGN: Retrospective review of our experience with self-expanding metal stents in these young children between 1996-2000. RESULTS: Airway stenting has been undertaken in five such children (four boys, one girl) at our institution. Their mean age was 7.4 months (range 2-14 months), and four of the five had undergone congenital cardiac surgery and could not be weaned from the ventilator following surgery. These five children were ventilator dependent for a mean of 112 days (range 40-210 days, median 71). A total of ten self-expanding metal stents were inserted (4-11 mm in diameter and 15-33 mm in length). The sites stented included the trachea (two stents), the left main bronchus (three stents) and the bronchus intermedius (five stents). Four of these five children were successfully weaned from the ventilator and extubated after a mean time interval of 6 days (range 2-11 days, median 5.5) after stenting. One child failed to wean from the ventilator, required tracheostomy and is ventilator dependent after 8 months. There was one death 2 months after extubation but unrelated to the airway. Three children remain well and asymptomatic 24, 36 and 54 months after stenting. CONCLUSIONS: Airway stenting in such young children is an infrequent procedure often undertaken in dire circumstances. We have found it valuable in enabling ventilator-dependent children to be extubated with encouraging early results. Their long-term outlook remains uncertain and is dependent on the underlying cardiac status.
机译:目的:患有先天性心脏缺陷和气道阻塞导致呼吸机依赖性的幼儿面临重大临床挑战,且结果不确定。设计:回顾性回顾我们在1996年至2000年间对这些年幼儿童使用自膨胀金属支架的经验。结果:我们机构中有五个这样的孩子(四个男孩,一个女孩)进行了气道支架置入术。他们的平均年龄为7.4个月(2到14个月不等),五名患者中有四名接受了先天性心脏手术,并且在手术后无法从呼吸机上断奶。这五个孩子平均依赖呼吸机112天(范围40-210天,中位数71)。总共插入十个自扩张金属支架(直径4-11毫米,长度15-33毫米)。支架部位包括气管(两个支架),左主支气管(三个支架)和中间支气管(五个支架)。这五名儿童中有四名成功从呼吸机断奶,并在置入支架后平均间隔6天(范围2-11天,中位数5.5)后拔管。 1名儿童未能从呼吸机断奶,需要进行气管切开术,并且在8个月后依赖呼吸机。拔管后2个月有1例死亡,但与气道无关。三名儿童在置入支架后24、36和54个月仍保持健康且无症状。结论:在这种幼儿中,气道支架置入术是一种罕见的手术,通常在严峻的情况下进行。我们发现它对使依赖呼吸机的儿童拔管以鼓励早期结果非常有价值。他们的长期前景仍然不确定,并取决于潜在的心脏状况。

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