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漏斗胸的当前治疗方法。

Current management of pectus excavatum.

作者信息

Fonkalsrud Eric W

出版信息

World J Surg. 2003 May;27(5):502-8. doi: 10.1007/s00268-003-7025-5. Epub 2003 Apr 28.

Abstract

Pectus excavatum (PE) is one of the most common anomalies of childhood. It occurs in approximately 1 in every 400 births, with males afflicted 5 times more often than females. PE is usually recognized in infancy, becomes much more severe during adolescent growth years, and remains constant throughout adult life. Symptoms are infrequent during early childhood, but become increasingly severe during adolescent years with easy fatigability, dyspnea with mild exertion, decreased endurance, pain in the anterior chest, and tachycardia. The heart is deviated into the left chest to varying degrees causing reduction in stroke volume and cardiac output. Pulmonary expansion is confined, causing a restrictive defect. Repair is recommended for patients who are symptomatic and who have a markedly elevated pectus severity index as determined by chest X-ray or computed tomography scan. Repair using the highly modified Ravitch technique is usually performed after the age of 8 years. The optimal age for repair is between 12 and 16 years. Repair can be performed on adults with similar good results. Recent modifications in the Ravitch technique remove minimal cartilage and routinely use a temporary internal support bar for 6 months. Operation rarely takes more than 3 hours, and hospitalization rarely exceeds 3 days. Pain is mild and complications are rare, with 97% of patients experiencing a good to excellent result. The new minimally invasive Nuss repair avoids cartilage resection and takes less operating time, but is associated with more severe pain, longer hospitalization and a higher complication rate, with the bar remaining for 2 or more years. This technique is less applicable to older patients and those with asymmetric deformities. Long-term follow-up will be necessary to determine which operation may be best for any specific patient.

摘要

漏斗胸(PE)是儿童期最常见的畸形之一。每400例出生中约有1例发生,男性患病几率是女性的5倍。漏斗胸通常在婴儿期被发现,在青春期生长阶段会变得更加严重,并在成年期保持不变。幼儿期症状不常见,但在青春期会越来越严重,表现为容易疲劳、轻度运动时呼吸困难、耐力下降、前胸疼痛和心动过速。心脏不同程度地向左胸偏移,导致每搏输出量和心输出量减少。肺扩张受限,导致限制性缺陷。对于有症状且经胸部X光或计算机断层扫描确定漏斗胸严重指数明显升高的患者,建议进行修复手术。使用高度改良的Ravitch技术进行修复通常在8岁以后进行。最佳修复年龄在12至16岁之间。也可以对成年人进行修复,效果同样良好。Ravitch技术最近的改进是去除最少的软骨,并常规使用临时内部支撑杆6个月。手术很少超过3小时,住院时间很少超过3天。疼痛轻微,并发症罕见,97%的患者效果良好至极佳。新的微创Nuss修复术避免了软骨切除,手术时间更短,但疼痛更严重,住院时间更长,并发症发生率更高,支撑杆要保留2年或更长时间。这种技术不太适用于老年患者和有不对称畸形的患者。需要长期随访以确定哪种手术对任何特定患者可能是最佳选择。

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