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右心梗阻患者的动脉导管相关近端肺动脉狭窄

Ductus-associated proximal pulmonary artery stenosis in patients with right heart obstruction.

作者信息

Moon-Grady Anita J, Teitel David F, Hanley Frank L, Moore Phillip

机构信息

Division of Pediatric Cardiology, University of California, San Francisco, 505 Parnassus Avenue Box 0214, San Francisco, CA 94143, United States.

出版信息

Int J Cardiol. 2007 Jan 2;114(1):41-5. doi: 10.1016/j.ijcard.2006.01.005. Epub 2006 Apr 27.

Abstract

Proximal pulmonary artery stenosis is a common acquired lesion in infants treated for congenital heart disease. We hypothesized that a large number of stenoses develop at the site of ductal insertion in patients with right ventricular outflow tract obstruction (RVOTO) and that these patients are at risk for developing hypoplasia of the ipsilateral pulmonary artery. The surgical and cardiac catheterization databases at our institution during the years 1988-2000 were searched for all patients under 1 year of age carrying a diagnosis of pulmonary atresia with intact ventricular septum (PA), tetralogy of Fallot (TOF) or pulmonary stenosis (PS), yielding 700 patients (62 PA, 373 TOF, 265 PS). The cardiac catheterization database was also searched for all patients with any diagnosis under 1 year of age found at catheterization to have proximal pulmonary artery stenosis. Proximal pulmonary artery stenosis associated with the ductal insertion site was diagnosed at catheterization in 33 infants (18 with PA, 5 with TOF, 6 with PS, 4 other diagnoses). This represents 29% of patients with PA, 1% with TOF and 2% with PS. Among patients with RVOTO and ductal insertion site-associated stenosis, there was a high prevalence (59%) of associated distal pulmonary arterial hypoplasia, defined as diameter of the stenosed vessel at first distal branch < or = 80% the diameter of the contralateral vessel. Symptomatology failed to identify this lesion; therefore, a high index of suspicion is necessary if proximal pulmonary artery stenosis is to be detected early in these patients.

摘要

近端肺动脉狭窄是先天性心脏病患儿常见的后天性病变。我们推测,右心室流出道梗阻(RVOTO)患者的大量狭窄发生在动脉导管插入部位,且这些患者有同侧肺动脉发育不全的风险。检索了我们机构1988年至2000年期间的外科手术和心导管检查数据库,查找所有诊断为室间隔完整的肺动脉闭锁(PA)、法洛四联症(TOF)或肺动脉狭窄(PS)的1岁以下患者,共找到700例患者(62例PA、373例TOF、265例PS)。还在心导管检查数据库中查找所有1岁以下在导管检查时发现有近端肺动脉狭窄的任何诊断患者。在33例婴儿(18例PA、5例TOF、6例PS、4例其他诊断)的心导管检查中诊断出与动脉导管插入部位相关的近端肺动脉狭窄。这分别占PA患者的29%、TOF患者的1%和PS患者的2%。在有RVOTO和与动脉导管插入部位相关狭窄的患者中,相关远端肺动脉发育不全(定义为狭窄血管在第一个远端分支处的直径≤对侧血管直径的80%)的患病率很高(59%)。症状学无法识别这种病变;因此,如果要在这些患者中早期发现近端肺动脉狭窄,必须高度怀疑。

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