The Prognosis of Idiopathic Premature Ventricular Beats in Children with Structurally Normal Hearts.

IF 1.3 Q3 PEDIATRICS
Kürşat Çetin, Filiz Ekici, Fırat Kardelen, Muhammet Bulut, Şenay Akbay
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引用次数: 0

Abstract

Objective: The objective of this study is to evaluate the prognosis of idiopathic premature ventricular beats (PVBs) in children.

Materials and methods: We retrospectively evaluated 73 children (<18 years old) with idiopathic PVBs and structurally normal hearts. All patients were evaluated by 24-hour Holter electrocardiography (ECG) and echocardiography at the first admission and followed with a mean of 27 ± 7.6 months after diagnosis. Baseline Holter ECG and echocardiographic findings were compared to the last visit.

Results: The mean age of the patients was 11.1 ± 4.8 years, and half were symptomatic at initial examination. Baseline Holter showed complex beats in 35 cases, non-sustained ventricular tachycardia in 7 cases, and frequent PVBs in 19 cases. Complete recovery (CR) of PVBs was observed in 37 cases (50.7%) at a median of 15 (minimum: 5, maximum: 33) months after diagnosis. There were no significant differences in CR rates between patient groups with left bundle branch block (LBBB) vs. right bundle branch block (RBBB) morphology of PVBs, simple vs. complex PVBs, and daytime vs. nighttime dominance of PVBs (P > .05 for all parameters). The CR rate of PVBs was different among patients with infrequent, moderate, and frequent PVBs (62.8%, 36.4%, and 31.6%, respectively). Premature ventricular beats disappeared more often during follow-up in patients with infrequent PVBs (P = .045). However, the absolute decrease and disappearance rates of PVBs were similar across all groups (72.1%, 81.8%, and 89.5%, respectively; P = .319). The resolution rates of PVBs were not statistically different between the patient group who received pharmacological treatment and the group who followed up without treatment (P = .070). No myocardial dysfunction was observed in any patient during follow-up. No cases experienced major cardiac events.

Conclusion: Idiopathic PVBs usually regress in childhood regardless of frequency and complexity or receiving antiarrhythmic medication. The risk of ventricular dysfunction is low during childhood; however, they require careful evaluation and follow-up.

心脏结构正常儿童的特发性室性早搏预后。
目的:本研究旨在评估儿童特发性室性早搏(PVB)的预后:本研究旨在评估儿童特发性室性早搏(PVB)的预后:我们对 73 名儿童进行了回顾性评估:患者的平均年龄为(11.1 ± 4.8)岁,半数患者在初次检查时无症状。基线 Holter 显示,35 例为复杂搏动,7 例为非持续性室性心动过速,19 例为频繁 PVB。37 例患者(50.7%)在确诊后 15 个月(最短:5 个月,最长:33 个月)的中位数观察到 PVB 完全恢复(CR)。PVB形态为左束支传导阻滞(LBBB)与右束支传导阻滞(RBBB)、简单PVB与复杂PVB、白天PVB占主导地位与夜间PVB占主导地位的患者组之间的CR率无明显差异(所有参数的P>0.05)。不常发生、中度发生和频繁发生 PVB 的患者的 PVB CR 率不同(分别为 62.8%、36.4% 和 31.6%)。在随访期间,不常发生 PVB 的患者室性早搏消失的频率更高(P = 0.045)。然而,各组 PVB 的绝对减少率和消失率相似(分别为 72.1%、81.8% 和 89.5%;P = .319)。接受药物治疗的患者组和未接受治疗的随访组之间的 PVB 消除率没有统计学差异(P = .070)。随访期间未发现任何患者出现心肌功能障碍。没有病例发生重大心脏事件:结论:无论发病频率和复杂程度如何,或是否接受抗心律失常药物治疗,特发性 PVB 通常会在儿童期消退。儿童期发生心室功能障碍的风险较低;但需要对其进行仔细评估和随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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