Gonzalez Blanca E, Teruya Jun, Mahoney Donald H, Hulten Kristina G, Edwards Rachael, Lamberth Linda B, Hammerman Wendy A, Mason Edward O, Kaplan Sheldon L
Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.
Pediatrics. 2006 May;117(5):1673-9. doi: 10.1542/peds.2005-2009.
Venous thrombosis (VT) in children with Staphylococcus aureus osteomyelitis occurs rarely. We describe clinical features of infections and molecular characterization of isolates of children at Texas Children's Hospital with S aureus osteomyelitis and VT.
We reviewed records and imaging studies (chest radiographs, ultrasound, computed tomography, and MRI) of 9 patients at Texas Children's Hospital with acute S aureus osteomyelitis and new onset VT between August 1999 and December 2004. Isolates were fingerprinted by pulsed-field gel electrophoresis and tested for the presence of genes encoding selective virulence factors.
The mean age of the patients was 10.6 years. All 9 of the patients had osteomyelitis with sites of infection adjacent to the VT. The femoral and popliteal veins were most commonly affected. Two patients had VTs develop on the same side in which a central line had been in place. Four patients had chest radiographs consistent with septic emboli; inferior vena cava filters were placed in 3. Evaluation for hypercoagulable state revealed 3 patients with lupus anticoagulant, 1 with anticardiolipin IgG antibody, and 5 with no defect. Most laboratory abnormalities had resolved at follow-up. Seven patients had infections caused by methicillin-resistant S aureus belonging to the same clonal group (USA300); all were community acquired. Seven isolates carried the Panton-Valentine leukocidin (luk-S-PV and luk-F-PV) genes.
The predominant community-acquired, methicillin-resistant S aureus clone in Houston, Texas, (USA300) may have a unique propensity to cause VT in association with osteomyelitis. Management of the venous thrombosis in this setting may be complicated by the rapid evolution of septic emboli.
金黄色葡萄球菌骨髓炎患儿发生静脉血栓形成(VT)的情况很少见。我们描述了德克萨斯儿童医院患有金黄色葡萄球菌骨髓炎和VT的患儿的感染临床特征及分离菌株的分子特征。
我们回顾了1999年8月至2004年12月期间德克萨斯儿童医院9例急性金黄色葡萄球菌骨髓炎并新发VT患儿的病历和影像学检查(胸部X线片、超声、计算机断层扫描和磁共振成像)。通过脉冲场凝胶电泳对分离菌株进行指纹图谱分析,并检测编码选择性毒力因子的基因的存在情况。
患者的平均年龄为10.6岁。所有9例患者均患有骨髓炎,感染部位与VT相邻。股静脉和腘静脉最常受累。2例患者在留置中心静脉导管的同一侧发生VT。4例患者的胸部X线片与脓毒性栓子相符;3例患者放置了下腔静脉滤器。对高凝状态的评估显示,3例患者有狼疮抗凝物,1例有抗心磷脂IgG抗体,5例无缺陷。大多数实验室异常在随访时已消失。7例患者的感染由属于同一克隆群(USA300)的耐甲氧西林金黄色葡萄球菌引起;均为社区获得性感染。7株分离菌携带杀白细胞素(luk-S-PV和luk-F-PV)基因。
德克萨斯州休斯顿主要的社区获得性耐甲氧西林金黄色葡萄球菌克隆株(USA300)可能具有与骨髓炎相关的导致VT的独特倾向。在这种情况下,静脉血栓形成的管理可能因脓毒性栓子的快速演变而复杂化。