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急性B型主动脉壁内血肿的内科及外科治疗

Medical and surgical management of acute type B aortic intramural hematoma.

作者信息

Brown James A, Arnaoutakis George J, Kilic Arman, Gleason Thomas G, Aranda-Michel Edgar, Sultan Ibrahim

机构信息

Division of Cardiac Surgery, Department of Cardiothoracic Surgery, University of Pittsburgh, Pittsburgh, Pennsylvania.

Division of Thoracic and Cardiovascular Surgery, University of Florida, Gainesville, Florida.

出版信息

J Card Surg. 2020 Sep;35(9):2324-2330. doi: 10.1111/jocs.14823. Epub 2020 Jul 15.

DOI:10.1111/jocs.14823
PMID:32668075
Abstract

Type B acute aortic dissection (AAD) and intramural hematoma (IMH) can both present as potentially catastrophic lesions of the descending aorta. IMH is distinguished from AAD by the absence of an intimal tear and flap. With short-term outcomes being similar to type B AAD, IMH is treated identically to AAD in the corresponding segment of the aorta. While all patients with any acute aortic syndrome of the descending aorta receive prompt anti-impulse therapy, thoracic endovascular aortic repair (TEVAR) is reserved for patients presenting with certain complications, namely malperfusion, rupture, or periaortic hematoma. Technical aspects of TEVAR for IMH include maximal endograft oversizing of 10% with 20 mm landing zones of the healthy aorta, revascularization of the left subclavian artery when covered, use of cerebrospinal fluid drainage with extensive coverage, and restoration of branch vessel perfusion. With respect to disease evolution, IMH may progress to classic AD, frank rupture, or aneurysmal dilation; yet, IMH may also regress and be completely resorbed. However, since the natural history of IMH is unpredictable, TEVAR is being used more aggressively to improve long-term survival, rates of secondary reintervention, and positive aortic remodeling. Much remains unknown for acute type B IMH, including the use of prophylactic TEVAR for stable uncomplicated presentations, as well as the optimal timing of intervention and certain technical aspects of TEVAR. As such, IMH remains a diagnostic and therapeutic challenge for cardiovascular surgeons.

摘要

B型急性主动脉夹层(AAD)和壁内血肿(IMH)都可能表现为降主动脉的潜在灾难性病变。IMH与AAD的区别在于不存在内膜撕裂和内膜瓣。由于其短期预后与B型AAD相似,IMH在主动脉相应节段的治疗方式与AAD相同。虽然所有降主动脉急性主动脉综合征患者都接受迅速的抗冲击治疗,但胸主动脉腔内修复术(TEVAR)仅适用于出现某些并发症的患者,即灌注不良、破裂或主动脉周围血肿。针对IMH的TEVAR技术要点包括:移植物最大超尺寸10%,在健康主动脉设置20 mm的锚定区;覆盖左锁骨下动脉时进行血管重建;广泛覆盖时使用脑脊液引流;恢复分支血管灌注。关于疾病演变,IMH可能进展为典型主动脉夹层、明显破裂或动脉瘤样扩张;然而,IMH也可能消退并完全吸收。然而,由于IMH的自然病程不可预测,TEVAR正被更积极地用于提高长期生存率、二次干预率和主动脉正向重塑率。对于急性B型IMH,仍有许多未知之处,包括对于稳定且无并发症表现的患者使用预防性TEVAR,以及TEVAR的最佳干预时机和某些技术要点。因此,IMH仍然是心血管外科医生面临的诊断和治疗挑战。

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