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先天性孤立性马蹄内翻足的预后。

Outcome of prenatally diagnosed isolated clubfoot.

机构信息

Department of Medical Genetics, Children's and Women's Hospital of British Columbia, University of British Columbia, Vancouver, BC, Canada.

出版信息

Ultrasound Obstet Gynecol. 2010 Jun;35(6):708-14. doi: 10.1002/uog.7558.

Abstract

OBJECTIVES

To analyze the aneuploidy risk and treatment outcome of prenatally diagnosed isolated clubfoot, to determine the false-positive rate (FPR) of ultrasound diagnosis and to calculate the risk of diagnostic revision to complex clubfoot.

METHODS

By chart review, 65 patients were retrospectively ascertained to have unilateral or bilateral clubfeet diagnosed prenatally. We calculated the rates of false positives, aneuploidy and diagnostic revision to complex clubfoot, and used an ad hoc scoring system to determine orthopedic outcome. Published rates of aneuploidy were pooled and evaluated.

RESULTS

Prenatally diagnosed isolated clubfoot FPR (defined as 1 - positive predictive value) was 10.5% (95% CI, 5.8-18%) (calculated per foot). After a minimum of 1-year postnatal follow-up, 13% (95% CI, 6-26%) of patients had revised diagnoses of complex clubfoot. No patients had aneuploidy identified by cytogenetic analysis or clinical assessment. Of the 34 patients with 2-year postnatal follow-up, 76.5% were treated with serial casting with or without Botox. All children with isolated clubfoot were walking and had an average outcome score of 'very good' to 'excellent'.

CONCLUSIONS

When counseling women regarding prenatally diagnosed isolated clubfoot, it is important to tell them that approximately 10% of individuals will have a normal foot or positional foot deformity requiring minimal treatment. Conversely, 10-13% of prenatally diagnosed cases of isolated clubfoot will have complex clubfoot postnatally, based on the finding of additional structural or neurodevelopmental abnormalities. Although this study did not identify an increased risk of fetal aneuploidy associated with isolated clubfoot, a review of the literature indicates a risk of 1.7-3.6% with predominance of sex chromosome aneuploidy.

摘要

目的

分析产前诊断孤立性马蹄足的非整倍体风险和治疗结果,确定超声诊断的假阳性率(FPR),并计算诊断为复杂性马蹄足的修正风险。

方法

通过病历回顾,共确定了 65 例单侧或双侧马蹄足产前诊断的患者。我们计算了假阳性率、非整倍体率和诊断为复杂性马蹄足的修正率,并使用特定的评分系统来确定矫形结果。评估了已发表的非整倍体率。

结果

产前诊断孤立性马蹄足的 FPR(定义为 1-阳性预测值)为 10.5%(95%CI,5.8-18%)(按足计算)。在至少 1 年的产后随访后,13%(95%CI,6-26%)的患者被修正为复杂性马蹄足诊断。没有通过细胞遗传学分析或临床评估发现非整倍体。在 34 例有 2 年产后随访的患者中,76.5%接受了连续石膏固定加或不加肉毒毒素治疗。所有孤立性马蹄足的儿童都能行走,平均结局评分为“非常好”到“优秀”。

结论

在向女性提供产前诊断孤立性马蹄足的咨询时,重要的是要告诉她们,大约 10%的个体将有正常的足部或位置性足部畸形,需要进行最小的治疗。相反,根据发现的其他结构或神经发育异常,10-13%的产前孤立性马蹄足病例在产后会出现复杂性马蹄足。尽管本研究未发现孤立性马蹄足与胎儿非整倍体风险增加相关,但文献综述表明,其风险为 1.7-3.6%,以性染色体非整倍体为主。

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