Couetil J P, Tolan M J, Loulmet D F, Guinvarch A, Chevalier P G, Achkar A, Birmbaum P, Carpentier A F
Department of Cardiothoracic Surgery, Broussais Hospital, Paris, France.
J Thorac Cardiovasc Surg. 1997 Mar;113(3):529-37. doi: 10.1016/s0022-5223(97)70366-0.
The scarcity of small donors has significantly limited lung transplantation for pediatric and small adult patients. Use of single lobes procured from size-unmatched donors has overcome this difficulty, but only in a few selected cases and, in addition, it represents a waste of lung tissue. In an animal model we have shown that it is possible to divide one lung with careful partitioning of the vascular and bronchial structures and thus obtain two viable lobar grafts suitable for bilateral implantation in a smaller animal. We have now applied this procedure clinically in seven patients operated on between May 1993 and November 1994. The indications were cystic fibrosis in three children, primary pulmonary hypertension in two adults, bronchiectasis in one, and idiopathic pulmonary fibrosis in one. There were three children aged 13 to 17 years (median 14) and four adults aged 40 to 53 years (median 45). There was a 46% to 50% discrepancy for weight between recipient and donor and a 12% to 17% discrepancy for height. The surgical technique consisted of careful partitioning of the left donor lung, bilateral anterior thoracotomy in the recipient, and, with the use of cardiopulmonary bypass, implantation of the lower lobe in the left hemithorax and the upper lobe in the right hemithorax. Vascular and bronchial connections were facilitated by leaving a long pedicle on the recipient side. The pulmonary artery anastomosis for the donor left upper lobe was done with the "fissure" side of the artery to ensure an anastomosis without tension. An end-to-end bronchial anastomosis overcame the problem of size discrepancy. Six patients are alive and well 10 to 27 months (median 19) after operation. One patient with cystic fibrosis died of systemic aspergillosis infection. All were discharged from the hospital within the first or second postoperative month. No technical problems were identified: repeated bronchoscopy has demonstrated satisfactory healing without early stricture formation. All patients remain well subjectively with good exercise tolerance and all patients achieve greater than 70% of predicted values of forced expiratory volume in 1 second. Perfect adaptation of the transplanted lobes to the recipient pleural space has been demonstrated by postoperative computed tomographic scan. In conclusion, bilateral lobar transplantation from a single donor lung is possible in small adults or children when there is a large size discrepancy with the donor. This may help resolve the problem of donor availability in the pediatric population.
小供体的稀缺显著限制了儿科和成年小患者的肺移植。使用来自大小不匹配供体的单叶肺克服了这一困难,但仅在少数特定病例中可行,此外,这还造成了肺组织的浪费。在动物模型中,我们已表明通过仔细划分血管和支气管结构来分割一侧肺,从而获得两个适合在较小动物体内双侧植入的存活叶状移植物是可行的。我们现已将此手术应用于1993年5月至1994年11月期间接受手术的7例患者。适应证为3例儿童的囊性纤维化、2例成人的原发性肺动脉高压、1例支气管扩张症和1例特发性肺纤维化。有3例13至17岁(中位数14岁)的儿童和4例40至53岁(中位数45岁)的成人。受体与供体之间的体重差异为46%至50%,身高差异为12%至17%。手术技术包括仔细分割供体左肺、受体双侧前开胸,并在体外循环辅助下,将下叶植入左半胸,上叶植入右半胸。通过在受体侧保留长蒂来促进血管和支气管连接。供体左肺上叶的肺动脉吻合在动脉的“裂面”进行,以确保无张力吻合。端对端支气管吻合克服了大小差异问题。6例患者术后10至27个月(中位数19个月)存活且状况良好。1例囊性纤维化患者死于全身性曲霉菌感染。所有患者均在术后第一个月或第二个月内出院。未发现技术问题:反复支气管镜检查显示愈合良好,无早期狭窄形成。所有患者主观感觉良好,运动耐量良好,所有患者第一秒用力呼气量均达到预测值的70%以上。术后计算机断层扫描显示移植的肺叶与受体胸膜腔完美适配。总之,当受体与供体存在较大大小差异时,在成年小患者或儿童中进行单供体肺的双侧叶移植是可行的。这可能有助于解决儿科人群供体可用性的问题。