Nesbitt J C, Carrasco H
Department of Thoracic and Cardiovascular Surgery, University of Texas M.D. Anderson Cancer Center, Houston, USA.
Chest Surg Clin N Am. 1996 May;6(2):305-28.
Expandable metallic stents are effective in selected patients with malignant or benign airway stenoses. When used for malignant lesions, the primary purpose of the stent is to improve the quality of life; stents are usually chosen for palliation of symptoms in recognition of the low likelihood of success for other therapy. For patients with benign stenoses, the stents provide a permanent source of structural support to alleviate the narrowed segment. The advantages of the expandable metallic stents are as follows: (1) they can be inserted through an endotracheal tube or under local anesthesia with relative simplicity under fluoroscopic guidance; (2) they do not impair the drainage of sputum because ciliary movement is not interrupted; (3) over a period of a few weeks, the meshwork is gradually covered with mucosa as the stent becomes incorporated into the airway wall; (4) ventilation usually is not impaired if the metallic mesh stent covers another nonstenosed bronchus, because the interstices of the stent are nonobstructive; and (5) they are dynamic and continue to expand over time, particularly if concurrent treatment achieves an effect on the lesion that caused stenosis. Disadvantages of the expandable stent include (1) they often are only temporarily effective for tracheobronchial stenosis due to intraluminal tumor or granulation tissue, both of which can grow between the wires; (2) they are considered permanent stents because removal is difficult; and (3) they can be poorly positioned during placement or can become displaced by progressive migration after placement, and they cannot be repositioned. A relative contraindication to insertion is an inflammatory process or infection that can predispose to granulation formation, particularly at the points of maximal contact pressure of the stent to the airway mucosa. In the presence of inflammation, it may be better to use a silicone prosthesis until the inflammatory process subsides and fibrosis occurs. Granulation tissue is less likely to occur in areas of established scar than in areas of acute inflammation. In circumstances in which it is essential that a stent remain only temporarily, an expandable stent should not be inserted in favor of a silicone stent, which can be removed. In the future, expandable stents may have silicone coverings or may be constructed of materials that facilitate removal. Until that time, expandable stents should be considered permanent and nonremovable. Subtle differences exist among the available stents. Standard is low-profile expandable construction from wire mesh. A relatively minor difference is the slightly wider expansibility of the Gianturco stent, a quality that makes it the best suited of the three stents for lesions that involve tracheomalacia. Perhaps the only major difference between the Wallstent and the Gianturco and Palmaz stents is its better ability to conform to tortuous lesions. In an acutely angled stricture, a Wallstent offers a better opportunity for successful placement than other stents. The filamentous meshwork of the Wallstent allows it to bend and conform better to distorted airways. The Gianturco and Palmaz stents have little longitudinal elasticity, which makes them less effective in a tortuous or highly angulated airway stenosis. Expandable stents have demonstrated their efficacy and exposed their limitations in the treatment of airway stenoses. Refinements in design should help to lessen specific disadvantages and problems. Covered expandable stents, a realistic prospect, have specific advantages over standard expandable stents; they will be removable and prevent tumor ingrowth. Current investigative work with such prostheses for the vascular system may provide the foundation for their investigative use in the airway. In essence, two categories of expandable stents are evolving, covered and uncovered, each having unique features adaptable to the specific clinical needs.
可扩张金属支架对某些患有恶性或良性气道狭窄的患者有效。用于恶性病变时,支架的主要目的是改善生活质量;鉴于其他治疗成功的可能性较低,通常选择支架来缓解症状。对于良性狭窄患者,支架提供永久性的结构支撑源,以缓解狭窄段。可扩张金属支架的优点如下:(1)它们可以通过气管内导管插入,或在透视引导下相对简单地在局部麻醉下插入;(2)它们不会妨碍痰液引流,因为纤毛运动未被中断;(3)在几周的时间里,随着支架融入气道壁,网孔逐渐被黏膜覆盖;(4)如果金属网状支架覆盖另一个无狭窄的支气管,通气通常不会受到影响,因为支架的间隙不会造成阻塞;(5)它们具有动态性,会随着时间持续扩张,特别是如果同时进行的治疗对导致狭窄的病变产生效果时。可扩张支架的缺点包括:(1)由于腔内肿瘤或肉芽组织,它们对气管支气管狭窄通常只是暂时有效,这两者都可能在金属丝之间生长;(2)它们被视为永久性支架,因为取出困难;(3)它们在放置过程中可能定位不佳,或者放置后可能因渐进性移位而移位,且无法重新定位。插入的相对禁忌证是炎症过程或感染,这可能易导致肉芽形成,特别是在支架与气道黏膜最大接触压力点处。存在炎症时,在炎症过程消退且出现纤维化之前,使用硅胶假体可能更好。与急性炎症区域相比,在已形成瘢痕的区域肉芽组织不太可能发生。在必须使支架仅暂时留置的情况下,不应插入可扩张支架,而应选择可取出的硅胶支架。未来,可扩张支架可能会有硅胶覆盖层,或者可能由便于取出的材料制成。在此之前,可扩张支架应被视为永久性且不可取出的。现有支架之间存在细微差异。标准的是由金属丝网制成的低轮廓可扩张结构。一个相对较小的差异是Gianturco支架的扩张性稍宽,这一特性使其成为三种支架中最适合涉及气管软化病变的支架。Wallstent支架与Gianturco支架和Palmaz支架之间可能唯一的主要差异在于其对扭曲病变的更好顺应能力。在锐角狭窄中,Wallstent支架比其他支架有更好的成功放置机会。Wallstent支架的丝状网孔使其能够更好地弯曲并顺应变形的气道。Gianturco支架和Palmaz支架几乎没有纵向弹性,这使得它们在扭曲或高度成角的气道狭窄中效果较差。可扩张支架在气道狭窄治疗中已证明其疗效并暴露了其局限性。设计的改进应有助于减少特定的缺点和问题。带覆膜可扩张支架是一个现实的前景,与标准可扩张支架相比有特定优势;它们将是可取出的,并可防止肿瘤向内生长。目前针对血管系统此类假体的研究工作可能为其在气道中的研究应用提供基础。本质上,两类可扩张支架正在发展,带覆膜的和无覆膜的,每类都有适应特定临床需求的独特特征。