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以先天性心脏传导阻滞为表现的新生儿红斑狼疮:临床特征及随访

Neonatal lupus erythematosus presenting with congenital heart block: clinical characteristics and follow-up.

作者信息

Sun Wenqiang, Zhou Minqian, Li Yihui, Sun Zexi, Zhu Xueping

机构信息

Department of Neonatology, Children's Hospital of Soochow University, Suzhou, China.

出版信息

Clin Rheumatol. 2025 Apr;44(4):1581-1587. doi: 10.1007/s10067-025-07381-4. Epub 2025 Mar 8.

Abstract

OBJECTIVE

Congenital heart block (CHB) in patients with neonatal lupus erythematosus (NLE) is usually irreversible. Our study aimed to investigate the clinical characteristics and prognostic follow-up results of patients with NLE presenting with CHB and to provide a reference for the clinical treatment and management of such patients.

METHODS

Six patients with NLE and CHB at the Children's Hospital of Soochow University between January 1, 2011, and December 31, 2023, were retrospectively analyzed. Prenatal maternal data, clinical characteristics, laboratory investigations, treatments, and follow-ups were analyzed using descriptive statistics.

RESULTS

Six patients with NLE and CHB-four females, two males, and five preterm infants-were included. Three patients had degree III CHB, one had degree II CHB, and two had degree I CHB. The diagnostic gestational age for CHB was 23.6 ± 2.7 weeks. Four patients experienced varying degrees of bradycardia during the fetal period. Of the six pregnant mothers, three had systemic lupus erythematosus, one had Sjogren's syndrome, and one was positive for the anti-SSA/Ro autoantibody after the postpartum patient was seropositive. All pregnant mothers with autoimmune diseases were in remission and stable before delivery. One case of mildly active lupus in early pregnancy resolved after low-dose oral steroid hormone administration. All six patients with NLE-related manifestations, except CHB, showed improvement in systemic symptoms within 6 months. One patient was implanted with a pacemaker for exercise intolerance and complete atrioventricular block (CAVB) at the age of 1 year and 5 months and is now tolerating activity well without abnormal cardiac rhythms. One of the six patients had a global developmental delay, and two had a motor developmental delay.

CONCLUSIONS

Fetal echocardiography should be performed in high-risk pregnancies between 16 weeks of gestation and 1 month after birth. Patients with NLE and CHB are prone to varying degrees of growth retardation. Pacemaker implantation is an effective treatment for children with CAVB. Key Points • CHB in patients with NLE is usually irreversible. • Patients with NLE and CHB are prone to varying degrees of growth retardation. • Implantation of a pacemaker is an effective treatment for children with CAVB.

摘要

目的

新生儿狼疮(NLE)患者的先天性心脏传导阻滞(CHB)通常是不可逆的。本研究旨在探讨患有CHB的NLE患者的临床特征及预后随访结果,为这类患者的临床治疗和管理提供参考。

方法

回顾性分析2011年1月1日至2023年12月31日期间苏州大学附属儿童医院收治的6例患有NLE合并CHB的患者。使用描述性统计方法分析产前母亲的数据、临床特征、实验室检查、治疗及随访情况。

结果

纳入6例患有NLE合并CHB的患者,其中4例女性,2例男性,5例为早产儿。3例患者为III度CHB,1例为II度CHB,2例为I度CHB。CHB的诊断孕周为23.6±2.7周。4例患者在胎儿期经历了不同程度的心动过缓。6例孕妇中,3例患有系统性红斑狼疮,1例患有干燥综合征,1例在产后患者血清学阳性后抗SSA/Ro自身抗体呈阳性。所有患有自身免疫性疾病的孕妇在分娩前病情缓解且稳定。1例孕早期轻度活动的狼疮患者在给予低剂量口服类固醇激素治疗后病情缓解。除CHB外,所有6例有NLE相关表现的患者在6个月内全身症状均有改善。1例患者在1岁5个月时因运动不耐受和完全性房室传导阻滞(CAVB)植入起搏器,目前活动耐受良好,心律无异常。6例患者中有1例存在全面发育迟缓,2例存在运动发育迟缓。

结论

应在妊娠16周后至出生后1个月内对高危妊娠进行胎儿超声心动图检查。患有NLE合并CHB的患者容易出现不同程度的生长发育迟缓。起搏器植入是治疗CAVB患儿的有效方法。要点:•NLE患者的CHB通常是不可逆的。•患有NLE合并CHB的患者容易出现不同程度的生长发育迟缓。•起搏器植入是治疗CAVB患儿的有效方法。

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