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75例原发性心内膜弹力纤维增生症临床治疗的长期随访研究

[A long-term follow-up study on the clinical treatment of 75 cases with primary endocardial fibroelastosis].

作者信息

Jiao Meng, Han Ling, Wang Hui-ling, Jin Mei, Wang Xiao-fang, Zheng Ke, Liang Yong-mei, Xiao Yan-yan

机构信息

Department of Pediatric Cardiology, Beijing Anzhen Hospital, Beijing 100029, China.

出版信息

Zhonghua Er Ke Za Zhi. 2010 Aug;48(8):603-9.

PMID:21055306
Abstract

OBJECTIVE

To summarize and analyze the effects of treatment and prognosis of infants with endocardial fibroelastosis (EFE) in different states of the illness undergone relevant therapies, and to understand the roles of different treatments for improving the prognosis of the disease.

METHODS

Data of 75 cases with EFE admitted into Anzhen Hospital Affiliated to Capital Medical University from August 1984 to June 2006 were analyzed retrospectively.

RESULTS

(1) Of the 75 cases with EFE (40 males and 35 females), with the onset age ranged from 20-days to two years and eight months, 69 cases were treated normally and followed up in the Outpatient Department of the Hospital after discharge, the follow-up rate was 92%, with the follow-up span from six months to 23 years (5.7 years in average). During the follow-up, six cases (8.7%) died. (2) The total curative rate of EFE patients was 46.4% (32/69), while the improvement rate was 40.6% (28/69), the total rate of the cure and improvement was 87%. (3) The average value of ejection fraction (EF) of left ventricle of all the patients returned to normal two years after treatment (EF value was 55.86 ± 2.85), the percentage of patients with normal left ventricle EF at 1 year, 3 years, 5 years and 10 years after treatment was 42.6% (26/61), 64.4% (29/45), 70.7% (29/41) and 84.6% (22/26), respectively. The average value of cardiothoracic (C/T) ratio became normal three years after treatment through X ray examination (0.50 ± 0.01), however the average value of the LVDD had not been returned to normal 3 years after treatment. At 1 year, 3 years, 5 years and 10 years after treatment, the proportion of patients with normal LVDD was 0% (0/61), 13.3% (6/45), 53.7% (22/41) and 84.6% (22/26), respectively. (4) The average value of EF became normal one year after treatment in the glucocorticoid group (EF value 58.44 ± 5.10) in 37 cases scored < 22 at the first visit, while the average value of C/T normalized two years after treatment (0.50 ± 0.00); The average value of EF became normal three years after treatment in the glucocorticoid plus cyclophosphamide group (EF 57.33 ± 3.43) in 29 cases scored < 22 at the first visit, however the average value of the C/T and the LVDD did not return to normal 3 years after treatment. (5) Use of IVIG reduced the percentage of patients who received cyclophos-phamide. (6) The recovery of intimal thickness was slow in EFE patients, the span was four years on the average (1 - 8 years), the percentage of patients whose endocardium became normal 1 year, 3 years, 5 years and 10 years after treatment was 9.85% (6/61), 22.2% (10/45), 51.2% (21/41), 100% (29/29).

CONCLUSION

The long-term continuous normal treatment of patients with EFE showed good therapeutic effects. For severe and refractory cases, immunotherapy must be strengthened and maintained for longer time. For those who clinically recovered, the quantity of activity should be restricted after the treatment is discontinued, and the re-examination should be done timely for further management.

摘要

目的

总结分析不同病情状态的心内膜弹力纤维增生症(EFE)患儿经相关治疗后的疗效及预后情况,了解不同治疗方法对改善该病预后的作用。

方法

回顾性分析1984年8月至2006年6月首都医科大学附属安贞医院收治的75例EFE患儿的资料。

结果

(1)75例EFE患儿(男40例,女35例),发病年龄20天至2岁8个月,69例正规治疗后出院在门诊随访,随访率92%,随访时间6个月至23年(平均5.7年)。随访期间死亡6例(8.7%)。(2)EFE患儿总治愈率为46.4%(32/69),好转率为40.6%(28/69),治愈好转率合计87%。(3)所有患儿治疗后2年左心室射血分数(EF)平均值恢复正常(EF值为55.86±2.85),治疗后1年、3年、5年、10年左心室EF正常的患儿比例分别为42.6%(26/61)、64.4%(29/45)、70.7%(29/41)、84.6%(22/26)。经X线检查治疗后3年心胸比(C/T)平均值恢复正常(0.50±0.01),但治疗后3年左心室内径(LVDD)平均值未恢复正常。治疗后1年、3年、5年、10年LVDD正常的患儿比例分别为0%(0/61)、13.3%(6/45)、53.7%(22/41)、84.6%(22/26)。(4)初诊评分<22分的37例糖皮质激素组患儿治疗后1年EF平均值恢复正常(EF值58.44±5.10),治疗后2年C/T平均值恢复正常(0.50±0.00);初诊评分<22分的29例糖皮质激素加环磷酰胺组患儿治疗后3年EF平均值恢复正常(EF 57.33±3.43),但治疗后3年C/T及LVDD未恢复正常。(5)静脉注射免疫球蛋白(IVIG)的使用降低了接受环磷酰胺治疗的患儿比例。(6)EFE患儿内膜厚度恢复缓慢,平均恢复时间4年(1 - 8年),治疗后1年、3年、5年、10年内膜恢复正常的患儿比例分别为9.85%(6/61)、22.2%(10/45)、51.2%(21/41)、100%(29/29)。

结论

EFE患儿长期持续正规治疗疗效良好。对重症及难治性病例,必须加强免疫治疗并维持较长时间。对临床治愈者,停药后应限制活动量,并及时复查以进一步处理。

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