Callegari Alessia, Burkhardt Barbara, Relly Christa, Knirsch Walter, Christmann Martin
Pediatric Cardiology, Department of Surgery, Pediatric Heart Center, University Children's Hospital Zurich, Zurich, Switzerland.
Division of Infectious Diseases and Hospital Epidemiology, University Children's Hospital Zurich, Zurich, Switzerland.
Congenit Heart Dis. 2019 Jul;14(4):671-677. doi: 10.1111/chd.12830. Epub 2019 Aug 1.
Since routine clinical use of antibiotics as well as surgical and catheter-based closure of a patent arterial duct (PDA), PDA-associated infective endarteritis (PDA-IE) is rare but can still occur when the ductus is still open or as it closes. Thus, clinicians should maintain a high index of concern for patients with unexplained fever.
We report on a PDA-IE in a young infant shortly after potentially delayed obliteration of a PDA. We discuss this case report by reviewing the literature in regard to the pathogenesis (infection primary or secondary to PDA thrombus formation), clinical (new heart murmur) and diagnostic findings (transthoracic echocardiography, total body MRI, laboratory findings), and clinical outcome during mid-term follow-up after successful antibiotic treatment.
A 7-week-old term infant with Staphylococcus aureus sepsis and a new heart murmur was diagnosed with PDA-IE by transthoracic echocardiography at the pulmonary artery end of an obliterated PDA. Broad diagnostic workup excluded other reasons for sepsis. After 4 weeks of antibiotic treatment the vegetation reduced in size and the infant recovered completely. A review of all cases of PDA-IE (in pediatric and adult patients) previously published was performed.
Nowadays, a PDA-IE is an extremely rare, but still life-threating condition that may even affect patients with a nonpatent ductus arteriosus shortly after its obliteration and should be considered as infective complication in preterms, neonates, and small infants. Therefore, in septic neonates with bacteremia, transthoracic echocardiography may be integrated in the diagnostic workup, especially by fever without source and clinical signs of IE such as a new heart murmur.
自从抗生素在临床常规使用以及采用手术和经导管方法闭合动脉导管未闭(PDA)以来,PDA相关感染性心内膜炎(PDA-IE)虽罕见,但在动脉导管仍开放或闭合时仍可能发生。因此,临床医生应对不明原因发热的患者保持高度警惕。
我们报告了1例婴儿在PDA可能延迟闭合后不久发生的PDA-IE。我们通过回顾关于发病机制(感染原发或继发于PDA血栓形成)、临床(新出现的心杂音)和诊断结果(经胸超声心动图、全身MRI、实验室检查结果)以及成功抗生素治疗后中期随访期间的临床结局的文献来讨论该病例报告。
1例7周龄足月儿,患有金黄色葡萄球菌败血症且出现新的心杂音,经胸超声心动图在已闭合PDA的肺动脉端诊断为PDA-IE。广泛的诊断性检查排除了败血症的其他原因。抗生素治疗4周后赘生物缩小,婴儿完全康复。我们对先前发表的所有PDA-IE病例(儿科和成人患者)进行了回顾。
如今,PDA-IE是一种极其罕见但仍危及生命的疾病,甚至可能在动脉导管未闭闭合后不久影响到已闭合动脉导管的患者,在早产儿、新生儿和小婴儿中应被视为感染性并发症。因此,对于患有菌血症的败血症新生儿,经胸超声心动图可纳入诊断性检查,尤其是对于无明确病因的发热以及有IE临床体征如新出现的心杂音的情况。