Ye Li-yan, Yu Zi-hua, Huang Zu-xiong, Chen Xin-min, Ren Rong-na, Chen Guang-ming, Wang Cheng-feng, Xia Gui-zhi, Huang Juan, Wang Fang-jian
Department of Pediatrics, Fuzhou General Hospital of Nanjing Millitary Command, Fuzhou 350025, China.
Zhonghua Er Ke Za Zhi. 2006 Mar;44(3):206-9.
Hemolytic uremic syndrome (HUS) is a common primary disease that can cause acute renal failure in childhood. Renal disease is the most important long-term complication in patients who survived the acute stage of HUS. Use of angiotensin-converting enzyme inhibitors (ACEI) and a restricted protein intake may be beneficial to the patients. However, it is not established whether such patients should be treated with steroids and immunosuppressors. The present study aimed to probe into the benefit of using steroid and immunosuppressor in patients after acute stage of HUS.
The subjects included 17 patients (aged 9 months to 15 years, 12 males, 5 females) with HUS. Thirteen patients recovered from the acute stage of HUS, and underwent continuative treatment and follow-up. All the patients were treated with ACEI and early restriction of protein intake. Additionally, 2 children manifested as glomerulonephritis, one was treated with triperygium glycosides. Other 11 children who manifested as nephrotic syndrome were treated with prednisone, among them 5 children had no response or had incomplete response to prednisone, for these children short-term high dose cyclophosphamide or methylprednisolone pulse treatment were added; in 3 of the children short-term high dose methylprednisolone treatment was applied additionally for membranoproliferative glomerulonephritis and/or focal segmental glomerulosclerosis and crescentic glomerulonephritis.
After follow-up for 2 months to 8 years, 4 patients with milder disease recovered, their blood pressure, renal function and urinalysis became normal, but 1 patient had recurrence. Among 9 patients with severe disease, 6 maintained normal blood pressure, recovered renal function and urinalysis, the other 3 patients failed to comply with treatment protocol and died during the 3rd, 9th and 13th month. The remainder (4 cases) gave up therapy and died on the 27th to 48th days of the course.
The treatment applied in this study could improve the prognosis of patients after acute phase of HUS evidently by using the steroid and immuno suppressor according to clinical classification and pathological findings. It is recommended that triperygium glycosides is beneficial to children with glomerulonephritis, proteinuria and hematuria after acute stage of HUS. Adjustment of therapeutic schedule based on pathological findings after renal biopsy is helpful. To the patients with progressive renal failure who have no response to the steroid and immunosuppressors, steroid and immunosuppressor should be discontinued and dialysis treatment should be applied. Protocol compliance is also an important factor.
溶血尿毒综合征(HUS)是一种常见的可导致儿童急性肾衰竭的原发性疾病。肾脏疾病是HUS急性期存活患者最重要的长期并发症。使用血管紧张素转换酶抑制剂(ACEI)和限制蛋白质摄入可能对患者有益。然而,此类患者是否应使用类固醇和免疫抑制剂治疗尚未确定。本研究旨在探讨在HUS急性期后使用类固醇和免疫抑制剂对患者的益处。
研究对象包括17例HUS患者(年龄9个月至15岁,男12例,女5例)。13例患者从HUS急性期康复,并接受持续治疗和随访。所有患者均接受ACEI治疗并早期限制蛋白质摄入。此外,2例表现为肾小球肾炎的患儿,1例接受雷公藤多苷治疗。其他11例表现为肾病综合征的患儿接受泼尼松治疗,其中5例对泼尼松无反应或反应不完全,对这些患儿加用短期大剂量环磷酰胺或甲泼尼龙冲击治疗;3例患儿因膜增生性肾小球肾炎和/或局灶节段性肾小球硬化及新月体性肾小球肾炎额外接受短期大剂量甲泼尼龙治疗。
随访2个月至8年,4例病情较轻的患者康复,血压、肾功能和尿常规恢复正常,但1例复发。9例病情严重的患者中,6例血压维持正常,肾功能和尿常规恢复,另外3例未遵守治疗方案,分别在第3、9和13个月死亡。其余4例放弃治疗,在病程第27至48天死亡。
本研究应用的治疗方法根据临床分类和病理结果使用类固醇和免疫抑制剂,可明显改善HUS急性期后患者预后。推荐雷公藤多苷对HUS急性期后患有肾小球肾炎、蛋白尿和血尿的患儿有益。根据肾活检病理结果调整治疗方案是有帮助的。对于对类固醇和免疫抑制剂无反应的进行性肾衰竭患者,应停用类固醇和免疫抑制剂并应用透析治疗。遵守治疗方案也是一个重要因素。