Barlow病合并表皮葡萄球菌性心内膜炎1例报告

Iulia Grigore, N. Popa-Fotea, M. Micheu
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引用次数: 0

摘要

感染性心内膜炎(IE)如果不及时治疗,死亡率高,并伴有许多并发症,如:脓毒性栓塞、脓肿、瓣膜破裂或充血性心力衰竭。我们在此报告一名69岁男性患者,因用力性呼吸困难、不适和疲劳而就诊于急诊室,症状持续数月并逐渐恶化。心脏检查突出二尖瓣收缩期杂音,超声心动图显示严重的二尖瓣反流,伴有二尖瓣变性黏液瘤样表现,提示Barlow病,同时二尖瓣上有高回声肿块。经验性治疗是在三次血培养后开始静脉注射万古霉素和庆大霉素。血培养呈表皮葡萄球菌阳性,鉴于抗生素谱对万古霉素和达托霉素敏感,随后仅用万古霉素继续治疗。虽然凝固酶阴性葡萄球菌(如表皮葡萄球菌)通常在有瓣膜假体、植入式装置、血液透析或血管内导管等危险因素的患者中发现,但在本病例中,患者没有这些危险因素,而是在原生退化的瓣膜上发展为IE。患者被转诊至心血管外科医生,随后植入假体二尖瓣和三尖瓣环成形术。恢复顺利,随访6个月,患者无症状,无并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BARLOW’S DISEASE IN NATIVE VALVE ENDOCARDITIS WITH STAPHYLOCOCCUS EPIDERMIDIS - A CASE REPORT
Infective endocarditis (IE) is associated with high mortality if left untreated and is associated with many complications such as: septic emboli, abscesses, valvular rupture or congestive heart failure. We present below the case of a 69-year-old male who presented to the emergency room for exertional dyspnea, malaise and fatigue, symptoms that started for several months with progressive worsening. The cardiac examination highlighted a systolic murmur in the mitral area in concordance with the echocardiographic findings that revealed severe mitral regurgitation along with a degenerative-myxomatous appearance of the mitral valve, suggestive for Barlow’s disease, as well as a hyperechogenic mass on the mitral valve. Empirical therapy was initiated intravenously with vancomycin and gentamicin after three blood cultures were harvested. The blood cultures were positive for Staphylococcus (S.) epidermidis and given the antibiogram’s susceptibility to vancomycin and daptomycin, the treatment was subsequently continued only with vancomycin. Albeit coagulase negative staphylococci such as S. epidermidis are usually found at patients with risk factors: valvular prostheses, implantable devices, hemodialysis or intravascular catheters, in our case the patient had no such risk factors, but instead developed IE on a native, degenerated valve. The patient was referred to the cardiovascular surgeon and subsequently, a prosthetic, bidisc mitral valve was implanted along with tricuspid annuloplasty. The recovery was uneventful and at 6 months of follow-up the patient was asymptomatic with no complications.
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