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土耳其产前诊断先天性心脏异常的咨询与结果

Counseling and outcomes of antenatally diagnosed congenital heart anomalies in Turkey.

作者信息

Gedikbaşı Ali, Oztarhan Kazım, Yıldırım Gökhan, Gül Ahmet, Ceylan Yavuz

机构信息

Clinic of Obstetrics and Gynecology, İstanbul Bakırköy Maternity and Children Diseases Hospital, İstanbul, Turkey.

出版信息

Anadolu Kardiyol Derg. 2011 Mar;11(2):137-45. doi: 10.5152/akd.2011.035. Epub 2011 Feb 23.

Abstract

OBJECTIVE

To determine the clinical outcomes and decisions of families of fetuses with prenatally-diagnosed cardiac abnormalities.

METHODS

Prenatally diagnosed cases (n=155) with congenital heart disease were retrospectively categorized according to the Allan-Huggon grading system: Group A (cardiac disease associated with severe / lethal extracardiac disease); Group B1 (low risk with a postnatal prognosis); Group B2 (moderate risk, amenable to surgical repair with a low mortality); and Group B3 (high risk, associated with high mortality after surgery). Neonatal outcomes, including termination of pregnancy, were recorded for 18 months of follow-up after counseling the parents. Student's t-test, Mann-Whitney U, Pearson's Chi-square test and Fischer's exact Chi-square test were used for statistical analyses.

RESULTS

One hundred forty-five cases completed follow up. Thirty-nine cases (Group A) were associated with extracardiac lethal defects and the pregnancies were terminated; these cases were excluded from statistical evaluation. Twenty parents in Group B3 opted also for termination. The survival rates of ongoing pregnancies after 18 months of follow-up between the three cardiac abnormality Groups (Group B1, n=37; Group B2, n=12; and Group B3, n=37) were 89.2%, 66.7%, and 13.5%, respectively. Significance was present between the survival rates of the three Groups [Group B3 vs. Group B1: p=0.0001; OR: 52.8 (12.9-214.5); Group B3 vs. Group B2: p=0.0009; OR: 12.8 (2.8-58.9); Group B2 vs. Group B1: p=0.087; OR: 4.12 (0.84-20.2)].

CONCLUSION

Our practice and the findings reported herein support the efficacy of this staging system and counseling parents of fetuses for congenital heart diseases.

摘要

目的

确定产前诊断为心脏异常的胎儿家庭的临床结局及决策。

方法

对产前诊断为先天性心脏病的病例(n = 155),根据艾伦 - 哈贡分级系统进行回顾性分类:A组(与严重/致命性心外疾病相关的心脏病);B1组(产后预后低风险);B2组(中度风险,可通过手术修复且死亡率低);B3组(高风险,手术后死亡率高)。在为父母提供咨询后,记录18个月随访期内的新生儿结局,包括终止妊娠情况。采用学生t检验、曼 - 惠特尼U检验、皮尔逊卡方检验和费舍尔精确卡方检验进行统计分析。

结果

145例完成随访。39例(A组)与心外致命缺陷相关,妊娠终止;这些病例被排除在统计评估之外。B3组中有20名父母也选择终止妊娠。三个心脏异常组(B1组,n = 37;B2组,n = 12;B3组,n = 37)在随访18个月后继续妊娠的存活率分别为89.2%、66.7%和13.5%。三组存活率之间存在显著差异[B3组与B1组:p = 0.0001;OR:52.8(12.9 - 214.5);B3组与B2组:p = 0.0009;OR:12.8(2.8 - 58.9);B2组与B1组:p = 0.087;OR:4.12(0.84 - 20.2)]。

结论

我们的实践及本文报告的研究结果支持该分期系统的有效性,以及为先天性心脏病胎儿的父母提供咨询的有效性。

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