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肺气肿的外科治疗。

Surgical treatment for pulmonary emphysema.

作者信息

Delarue N C, Woolf C R, Sanders D E, Pearson F G, Henderson R D, Cooper J D, Nelems J M

出版信息

Can J Surg. 1977 May;20(3):222-31.

PMID:870155
Abstract

Three in-vivo observations stimulated interest in surgical treatment for emphysema: (a) the destructive changes are rarely generalized, (b) the central portions of the lungs are frequently less seriously affected, and (c) marginal folding produces obstructive change in the more normal lung tissue. If destroyed avascular space-occupying areas can be removed, the compressed lung tissue may be stretched to fill pleural space in a functionally effective fashion. Residual elastic tissue will them maintain patency of terminal bronchioles. Preoperatively the extent of the destructive change can be defined most accurately by pulmonary angiography, and zones of functioning capilary circulation can be identified. Forty-seven patients with multifocal space-occupying emphysematous change have been treated surgically. The postoperative mortality was 21% but worthwhile long-term improvement has been obtained in 45% of patients presenting with disabling dyspnea. In these patients, surgical treatment warrants consideration if significant space occupation accompanies the bullous disease, provided alveolar vascularization can be demonstrated in the compressed adjacent normal lung tissue. Limited resections that preserve all vascularized and potentially functioning lung tissue are preferable. It is essential that obliteration of the hemithorax be obtained promptly in view of the high incidence of postoperative complications requiring secondary operative procedures, if 'leaks' and residual spaces are allowed to persist. Postoperative care in a respiratory intensive care unit is mandatory.

摘要

三项体内观察结果激发了人们对肺气肿外科治疗的兴趣

(a)破坏性改变很少是全身性的;(b)肺的中央部分通常受影响较轻;(c)边缘折叠在较正常的肺组织中产生阻塞性改变。如果能够切除已破坏的无血管占位区域,受压的肺组织可能会被拉伸以有效地填充胸膜腔。残留的弹性组织将维持终末细支气管的通畅。术前,通过肺血管造影可以最准确地确定破坏性改变的范围,并识别出有功能的毛细血管循环区域。47例患有多灶性占位性肺气肿改变的患者接受了手术治疗。术后死亡率为21%,但在出现致残性呼吸困难的患者中,45%获得了值得的长期改善。对于这些患者,如果大疱性疾病伴有明显的占位,且受压的相邻正常肺组织能显示肺泡血管化,则手术治疗值得考虑。保留所有血管化且可能有功能的肺组织的有限切除术更为可取。鉴于术后并发症需要二次手术的发生率很高,如果允许“漏气”和残留腔隙持续存在,必须迅速实现半侧胸廓的闭塞。在呼吸重症监护病房进行术后护理是必需的。

相似文献

1
Surgical treatment for pulmonary emphysema.肺气肿的外科治疗。
Can J Surg. 1977 May;20(3):222-31.
2
Surgical therapy for chronic obstructive pulmonary disease.慢性阻塞性肺疾病的外科治疗
Semin Respir Crit Care Med. 2005 Apr;26(2):167-91. doi: 10.1055/s-2005-869537.
3
Effective surgical palliation of giant compressive bullous emphysema (vanishing lung syndrome): long-term follow-up.巨大压迫性肺大疱(消失肺综合征)的有效手术姑息治疗:长期随访
Am Surg. 1976 Mar;42(3):181-5.
4
[Bilateral lung volume reduction in patients with severe pulmonary emphysema].[重度肺气肿患者的双侧肺减容术]
Pneumologie. 1996 Jul;50(7):448-52.
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Persistent benefit from lung volume reduction surgery in patients with homogeneous emphysema.全小叶型肺气肿患者接受肺减容手术后的持续获益。
Ann Thorac Surg. 2009 Jan;87(1):229-36; discussion 236-7. doi: 10.1016/j.athoracsur.2008.10.012.
6
Long-term outcome of bilateral lung volume reduction in 250 consecutive patients with emphysema.250例连续性肺气肿患者双侧肺减容术的长期疗效
J Thorac Cardiovasc Surg. 2003 Mar;125(3):513-25. doi: 10.1067/mtc.2003.147.
7
[Surgery of large bullous emphysema--functional results].[大疱性肺气肿手术——功能结果]
Z Erkr Atmungsorgane. 1989;173(3):205-14.
8
Thoracoscopic lung volume reduction surgery for emphysema.用于治疗肺气肿的胸腔镜肺减容手术
Int Surg. 1996 Jul-Sep;81(3):229-34.
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[The surgical physiopathology of essential pulmonary emphysema and volume-reduction intervention].[特发性肺气肿的手术病理生理学与肺减容干预]
Minerva Chir. 1998 Nov;53(11):899-918.
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[Role of surgical lung volume reduction in the treatment of patients with severe emphysema].[外科肺减容术在重度肺气肿患者治疗中的作用]
Magy Seb. 2004 Dec;57(6):370-7.

引用本文的文献

1
Do pulmonary hemodynamics change after effective lung volume reduction surgery for emphysema?肺气肿患者接受有效肺减容手术后,肺血流动力学是否会发生变化?
Kaohsiung J Med Sci. 2004 Nov;20(11):533-7. doi: 10.1016/S1607-551X(09)70254-2.
2
Teflon strip pneumostasis for excision of giant emphysematous bullae.聚四氟乙烯条带肺固定术用于巨大气肿性肺大疱切除术
Thorax. 1987 Feb;42(2):144-8. doi: 10.1136/thx.42.2.144.