V-A ECMO 治疗新生儿柯萨奇病毒 B 型暴发性心肌炎:病例报告和文献综述

Xingchao Li, Li Sun, Shibing Xi, Yaofei Hu, Zhongqin Yu, Hui Liu, Hui Sun, Weili Jing, Li Yuan, Hongyan Liu, Tao Li
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引用次数: 0

摘要

新生儿(肠道病毒)心肌炎(NM/NEM)虽然罕见,但却具有不可预知性和破坏性,死亡率和发病率都很高。我们报告了一例新生儿柯萨奇病毒 B(CVB)暴发性心肌炎病例,该病例经静脉-动脉体外膜氧合(V-A ECMO)治疗后获得成功。一名 7 天大的健康男孩因发热 4 天后出现进行性心功能不全(心音减弱、肝肿大、肺水肿、腹水和少尿)、左室射血分数(LVEF)和缩短分数(FS)下降、一过性心室颤动、肌酸激酶-MB 急剧升高(405.8 U/L)、心肌肌钙蛋白 I(25.85 ng/ml)、N-末端前脑钠尿肽(NT-proBNP > 35,000 ng/L)和血 CVB 核糖核酸阳性表明新生儿 CVB 暴发性心肌炎。在住院的前四天(DOH 1-4),机械通气、液体复苏、肌注、皮质类固醇、静脉注射免疫球蛋白和利尿剂均无效。在 ECMO 解除后的头 4 天内(DOH 10-13),随着机械通气的撤除、LVEF > 60% 和 FS > 30%,他的病情继续好转。在随后的 4 天内(DOH 14-17),他的 LVEF 和 FS 分别降至 52% 和 25%,并在接下来的 2 天内(DOH 18-19)进一步降至 37%-38% 和 17%。除了心脏肿大和阵发性呼吸急促外,没有其他恶化情况。通过加强液体限制和利尿以及改善心肺功能,他的病情恢复稳定。最后,尽管NT-proBNP升高(>35,000 ng/L)、心脏肿大、LVEF(40%-44%)和FS(18%-21%)水平较低,他还是在出院后3周内停用口服药物,于DOH 26出院。在近三年的随访中,他的情况并无异常,但有室间隔高回声灶和轻度二尖瓣/三尖瓣反流。通过实时超声心动图进行动态心功能监测对 NM/NEM 的诊断和治疗非常有用。作为一种挽救生命的疗法,ECMO 可以提高 NM/NEM 患者的存活率。然而,ECMO 后的 "蜜月期 "可能会造成康复的假象。无论 NM/NEM 幸存者是否接受了 ECMO,长期密切随访对及时发现和干预异常情况至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
V-A ECMO for neonatal coxsackievirus B fulminant myocarditis: a case report and literature review
Neonatal (enteroviral) myocarditis (NM/NEM) is rare but unpredictable and devastating, with high mortality and morbidity. We report a case of neonatal coxsackievirus B (CVB) fulminant myocarditis successfully treated with veno-arterial extracorporeal membrane oxygenation (V-A ECMO).A previously healthy 7-day-old boy presented with fever for 4 days. Progressive cardiac dysfunction (weak heart sounds, hepatomegaly, pulmonary edema, ascites, and oliguria), decreased left ventricular ejection fraction (LVEF) and fractional shortening (FS), transient ventricular fibrillation, dramatically elevated creatine kinase-MB (405.8 U/L), cardiac troponin I (25.85 ng/ml), and N-terminal pro-brain natriuretic peptide (NT-proBNP > 35,000 ng/L), and positive blood CVB ribonucleic acid indicated neonatal CVB fulminating myocarditis. It was refractory to mechanical ventilation, fluid resuscitation, inotropes, corticosteroids, intravenous immunoglobulin, and diuretics during the first 4 days of hospitalization (DOH 1–4). The deterioration was suppressed by V-A ECMO in the next 5 days (DOH 5–9), despite the occurrence of bilateral grade III intraventricular hemorrhage on DOH 7. Within the first 4 days after ECMO decannulation (DOH 10–13), he continued to improve with withdrawal of mechanical ventilation, LVEF > 60%, and FS > 30%. In the subsequent 4 days (DOH 14–17), his LVEF and FS decreased to 52% and 25%, and further dropped to 37%–38% and 17% over the next 2 days (DOH 18–19), respectively. There was no other deterioration except for cardiomegaly and paroxysmal tachypnea. Through strengthening fluid restriction and diuresis, and improving cardiopulmonary function, he restabilized. Finally, notwithstanding NT-proBNP elevation (>35,000 ng/L), cardiomegaly, and low LVEF (40%–44%) and FS (18%–21%) levels, he was discharged on DOH 26 with oral medications discontinued within 3 weeks postdischarge. In nearly three years of follow-up, he was uneventful, with interventricular septum hyperechogenic foci and mild mitral/tricuspid regurgitation.Dynamic cardiac function monitoring via real-time echocardiography is useful for the diagnosis and treatment of NM/NEM. As a lifesaving therapy, ECMO may improve the survival rate of patients with NM/NEM. However, the “honeymoon period” after ECMO may cause the illusion of recovery. Regardless of whether the survivors of NM/NEM have undergone ECMO, close long-term follow-up is paramount to the prompt identification and intervention of abnormalities.
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