Shanghai Children's Medical Center, Shanghai Jiao Tong University, School of Medicine, Shanghai, China.
J Pediatr Surg. 2012 Dec;47(12):2189-93. doi: 10.1016/j.jpedsurg.2012.09.007.
Children with portal vein cavernous transformation (PVCT) can develop life-threatening variceal hemorrhage from progressive portal hypertension. While spleno-renal shunt ± splenectomy is the most common portosystemic decompression surgery performed in children, we have adopted a modified spleno-adrenal (SA) shunt for complicated PVCT. We describe our 10 year experience focusing on technique evolution and treatment efficacy.
Between 2001 and 2011, 15 children (9 girls and 6 boys, ages 3-11 years, median: 6 years) with PVCT, portal hypertension, and hypersplenism were treated with SA shunt with splenectomy in Shanghai Children's Medical Center. All children in the study had endoscopy proven active esophageal variceal bleeding requiring multiple transfusions (mean: 4.2 units) with failed sclerotherapy (mean: 2.6 times). Greater omental vein pressure (GVP) approximating portal venous pressure was measured pre- and post-SA shunt. Pre- and post-operative ammonia levels were obtained. Follow-up ranged from 6 months to 10 years (mean: 4.2 ± 2 years).
Intra-operative adrenal vein diameter and length ranged from 0.7 to 1.8 cm and 2 to 3 cm, respectively. Intra-operative GVPs pre-and post-SA shunt were (30 ± 11) and (22 ± 7) mmHg, respectively (p<0.01). On follow-up, there have been no recurrences of GI bleeding. Liver function tests remained normal in all children with the exception of elevated post-operative mean blood ammonia levels [Pre (18 ± 7) mmol/L, post (60 ± 17) mmol/L (p<0.05)] in all children. Ammonia levels normalized in all cases on outpatient follow-up. There have been no cases of hepatic encephalopathy, and all have normal age appropriate neurodevelopment (Bayley's assessment). Barium swallow and/or upper endoscopy showed interval resolution of esophageal varices in all children, and vascular ultrasound showed patent shunt anastomosis without stricture in 14 (93%).
The left adrenal vein is a viable conduit for effective selective portosystemic decompression. Similar to the more traditional spleno-renal shunt, SA appears also to have the advantage of preventing hepatic encephalopathy preserving neurodevelopment, although the rise in post-operative ammonia levels was unexpected. Longer follow-up is needed to look for late signs of encephalopathy assessing neurodevelopment long term.
患有门静脉海绵样变性(PVCT)的儿童可能会因进行性门静脉高压而发生危及生命的静脉曲张出血。虽然脾-肾分流术±脾切除术是儿童最常见的门体减压手术,但我们采用了改良的脾-肾上腺(SA)分流术来治疗复杂的 PVCT。我们描述了我们 10 年的经验,重点介绍了技术演变和治疗效果。
2001 年至 2011 年,上海儿童医学中心采用 SA 分流术加脾切除术治疗 15 例(9 名女性和 6 名男性,年龄 3-11 岁,中位数:6 岁)PVCT、门静脉高压和脾功能亢进的儿童。所有研究中的儿童均经内镜证实有活动性食管静脉曲张出血,需要多次输血(平均:4.2 单位),且硬化治疗失败(平均:2.6 次)。SA 分流术前和术后测量大网膜静脉压(GVP)接近门静脉压力。获取术前和术后的血氨水平。随访时间为 6 个月至 10 年(平均:4.2±2 年)。
术中肾上腺静脉直径和长度分别为 0.7-1.8cm 和 2-3cm。SA 分流术前和术后的 GVP 分别为(30±11)和(22±7)mmHg(p<0.01)。在随访中,没有再发生 GI 出血。除所有儿童术后平均血氨水平升高[术前(18±7)mmol/L,术后(60±17)mmol/L(p<0.05)]外,所有儿童肝功能检查均正常。所有病例在门诊随访中血氨水平均恢复正常。无肝性脑病病例,所有儿童的神经发育均正常(贝利评估)。钡餐和/或上消化道内镜显示所有儿童食管静脉曲张间隔缓解,血管超声显示 14 例(93%)分流吻合口通畅无狭窄。
左肾上腺静脉是一种有效的选择性门体减压的有效通道。与更传统的脾-肾分流术类似,SA 似乎也具有预防肝性脑病和保护神经发育的优势,尽管术后血氨水平升高是出乎意料的。需要更长时间的随访来寻找迟发性脑病的迹象,以评估长期的神经发育。