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A Rare Case of AICD Endocarditis caused by Staphylococcus Saprophyticus Treated Successfully with Antibiotics

机译:抗生素成功治疗由腐生葡萄球菌引起的AICD心内膜炎一例

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To date, there have been two cases of endocarditis caused by S. saprophyticus reported in the literature; both involved native valves and had serious to deadly courses. We report the first case of endocarditis of a prosthesis due to S. saprophyticus; it appeared to affect the right atrium and possibly the mitral valve as well. The infection did not occur as a result of urinary tract infection; it is assumed that the causative agent may have entered the body through a tunneled catheter for hemodyalisis, though the catheter insertion site exhibited no signs of infection. In addition, this case represents the first report of endocarditis caused by S. saprophyticus that was successfully treated with antibiotic therapy. This case illustrates the potential for infection of a prosthesis in addition to native valves caused by S. saprophyticus and also the potential for successful treatment with antibiotics. Introduction Staphylococcus saprophyticus is a coagulase-negative staphylococcus (CoNS) species that is most commonly associated in humans with uncomplicated urinary tract infections in young, sexually active females (1). Rarely, infections due to S. saprophyticus have progressed to become more serious, causing acute pyelonephritis (2), septicemia (3) and nephrolithiasis (4). To date, S. saprophyticus has been reported as the cause of endocarditis twice in the literature (5, 6). In both cases, a native valve was affected. One case required valve replacement (5) and the other resulted in death of the patient (6). Here we present the first reported case of endocarditis of a prosthesis due to S. saprophyticus, as well as the first case of endocarditis caused by S. saprophyticus which was successfully treated with antibiotic therapy. Case Report A 58-year-old female presented to the emergency room with fatigue, fever, chills, shortness of breath upon exertion, intermittent chest pain and dry cough for the previous four days. She denied any nausea, vomiting, abdominal pain, urinary symptoms or diarrhea. She was receiving hemodialysis for end stage renal failure via a right internal jugular tunneled catheter. A blood culture taken by the primary care physician two days prior to admission was positive for CoNS. The patient's medical history was positive for hypertension, diabetes mellitus, coronary artery disease with PCI and hypercholesterolemia. She had stent placement in the left anterior descending artery after myocardial infarction five years prior to the current admission and implantable cardiac defibrillator (AICD) placement 3-4 weeks prior to the current admission. The catheter site showed no signs of infection. The patient reported drug allergies to penicillin, tetracycline, vancomycin and tobramycin; therefore, she was started on quinupristin/dalfopristin and ciprofloxacin to treat possible tunneled catheter infection. Removal of the catheter was considered, but it was decided to wait to determine whether there was improvement in symptoms after beginning treatment. TEE revealed a 5x3 mm, highly echogenic density on the tip of the anterior leaflet of the mitral valve with a small amount of independent motion, suggestive of a vegetation versus a calcification of the leaflet (Figure 1). The right atrium (RA) showed a pedunculated, medium-sized, echogenic density with a tiny, more mobile surface excrescence at the junction of the inferior vena cava and the RA cavity consistent with a vegetation. There was also a 12x10 mm, fixed density with a mobile excrescence at the junction of the RA and the superior vena cava involving the catheter representing a vegetation or thrombus (Figure 2). There was moderate regurgitation of the mitral and tricuspid valves. Four blood cultures (from arm) taken on the first three days of admission grew Staphylococcus saprophyticus/CoNS that was resistant to ampicillin, cefazolin, cefepime, cefotaxime, ciprofloxacin, amoxicillin, gentamicin, imipenem and oxacillin. Treatment was switched to quinupristin/da
机译:迄今为止,文献中已有两例由腐生链球菌引起的心内膜炎病例。两者都涉及天然阀门,并具有严重到致命的过程。我们报告了第一例因腐生链球菌引起的假体心内膜炎;它似乎会影响右心房,甚至可能影响二尖瓣。尿路感染并未引起感染;尽管导管插入部位未显示感染迹象,但可以认为病因可能是通过隧道导管进入体内引起的血肿。此外,该病例代表了由腐生链球菌引起的心内膜炎的首例报道,已成功用抗生素治疗。该病例说明了除了由腐生链球菌引起的天然瓣膜外,还可能感染假体,并成功地使用了抗生素进行治疗。引言腐生葡萄球菌是一种凝固酶阴性葡萄球菌(CoNS)物种,在人类中,最常见的是伴有性行为活跃的年轻女性的简单尿路感染(1)。很少有由腐生链球菌引起的感染变得更加严重,从而引起急性肾盂肾炎(2),败血病(3)和肾结石(4)。迄今为止,已有文献报道腐生链球菌引起心内膜炎的原因有两次(5,6)。在这两种情况下,天然瓣膜均受影响。一例需要更换瓣膜(5),另一例导致患者死亡(6)。在这里,我们介绍了第一例因腐生链球菌引起的假体心内膜炎的病例,以及第一例由腐生链球菌引起的心内膜炎的病例,已成功用抗生素治疗。病例报告一名58岁的女性在前四天因疲劳,发烧,发冷,劳累时呼吸急促,间歇性胸痛和干咳出现在急诊室。她否认有任何恶心,呕吐,腹痛,泌尿症状或腹泻。她正在通过右颈内穿隧导管进行终末期肾衰竭的血液透析。入院前两天由初级保健医师进行的血液培养对CoNS呈阳性。患者的病史对高血压,糖尿病,冠状动脉疾病伴PCI和高胆固醇血症呈阳性。在本次入院前五年,在心肌梗塞后将她的支架放置在左前降支动脉中,并在本次入院前3-4周放置可植入式心脏除颤器(AICD)。导管部位未显示感染迹象。患者报告了对青霉素,四环素,万古霉素和妥布霉素的药物过敏。因此,她开始接受奎奴普丁/达福普汀和环丙沙星治疗可能的隧道感染。考虑了拔除导管,但是决定开始治疗后再等待以确定症状是否有所改善。 TEE在二尖瓣前小叶尖端显示5x3 mm的高回声密度,少量的独立运动,提示植物与小叶钙化(图1)。右心房(RA)显示出有蒂的中等大小的回声密度,在下腔静脉与RA腔的交界处与植物相一致的表面有微小的移动性。在RA和上腔静脉的交界处还存在一个12x10 mm的固定密度且活动性消退,涉及代表植物或血栓的导管(图2)。二尖瓣和三尖瓣有中度反流。在入院的前三天(从手臂开始)进行了四次血液培养,产生了对氨苄西林,头孢唑林,头孢吡肟,头孢噻肟,环丙沙星,阿莫西林,庆大霉素,亚胺培南和奥沙西林耐药的腐生葡萄球菌/ CoNS。治疗改为奎奴普丁/ da

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