Chien Shao-Ju, Liang Chi-Di, Lin I-Chun, Lin Ying-Jui, Huang Chien-Fu
Section of Pediatric Cardiology, Departments of Pediatrics, Chang Gung Memorial Hospital-Kaohsiung Medical Center, Chang Gung University College of Medicine, Taiwan.
Pediatr Neonatol. 2008 Dec;49(6):218-22. doi: 10.1016/S1875-9572(09)60014-0.
Myocarditis complicated with complete atrioventricular block (CAVB) is rare in children. The purpose of this study was to report the outcome of myocarditis with CAVB in our institution.
Between June 1998 and June 2007, nine pediatric patients (aged from 1.5 to 16 years) were admitted, presenting with acute myocarditis with CAVB. We analyzed their clinical presentations, biochemistry and serology studies, chest X-rays, electrocardiograms, echocardiography, complications and outcomes.
Hypotension and Stokes-Adams seizures occurred in five and four of our patients, respectively. Cardiomegaly of chest X-ray was common in eight (89%) of our patients. Echocardiography revealed impaired left ventricular performance in three patients. Six patients suffered ventricular tachycardia (VT). Three cases of VT occurred before pacemaker implantation and the others occurred afterwards. Eight patients survived. Six of them regained sinus rhythm within 12 days (range 1-12 days), and two had a right bundle branch block at follow-up. Two patients had persistent CAVB, and one received permanent pacemaker implantation; the other received supportive care. One patient died due to persistent low cardiac output and a new onset of VT on the 4th admission day. During a follow-up period of 56+/-27 months, all eight surviving patients remained asymptomatic.
The outcome of CAVB complicated with myocarditis is variable. Most of our patients resumed normal heart function. The incidence of persistent CAVB was 22%. VT is a common and serious complication, but it can be effectively treated medically. Persistent low cardiac output after pacemaker implantation and late onset VT should be considered as risk factors of mortality.
儿童心肌炎合并完全性房室传导阻滞(CAVB)较为罕见。本研究旨在报告我院心肌炎合并CAVB的治疗结果。
1998年6月至2007年6月,收治9例儿科患者(年龄1.5至16岁),均表现为急性心肌炎合并CAVB。我们分析了他们的临床表现、生化及血清学检查、胸部X线、心电图、超声心动图、并发症及治疗结果。
分别有5例和4例患者出现低血压和斯托克斯-亚当斯发作。8例(89%)患者胸部X线显示心脏扩大。超声心动图显示3例患者左心室功能受损。6例患者发生室性心动过速(VT)。3例VT发生在起搏器植入前,其余发生在植入后。8例患者存活。其中6例在12天内(1至12天)恢复窦性心律,2例在随访时出现右束支传导阻滞。2例患者持续存在CAVB,1例接受了永久性起搏器植入;另1例接受支持治疗。1例患者因持续低心输出量及第4个住院日新发VT死亡。在56±27个月的随访期内,所有8例存活患者均无症状。
CAVB合并心肌炎的治疗结果各异。我们的大多数患者恢复了正常心功能。持续性CAVB的发生率为22%。VT是常见且严重的并发症,但药物治疗有效。起搏器植入后持续低心输出量及迟发性VT应被视为死亡危险因素。