Nygren David, Elf Johan, Torisson Gustav, Holm Karin
Division of Infection Medicine, Department for Clinical Sciences Lund, Lund University, Lund, Sweden.
Center of Thrombosis and Haemostasis, Skåne University Hospital, Malmö, Sweden.
Open Forum Infect Dis. 2020 Nov 29;8(1):ofaa585. doi: 10.1093/ofid/ofaa585. eCollection 2021 Jan.
Lemierre's syndrome is typically caused by where an oropharyngeal infection is followed by septic internal jugular vein thrombophlebitis with subsequent septic embolization. Yet, the pathogenesis of septic thrombophlebitis, differences dependent on the presence of jugular vein thrombosis, and the role of anticoagulant therapy are insufficiently understood.
Patients with invasive infection with and Lemierre's syndrome who had been investigated for jugular vein thrombosis were included from a previous population-based observational study in Sweden. Medical records were reviewed and compared in patients with and without jugular vein thrombosis. Then, patients with jugular vein thrombosis were compared by exposure to therapeutic, prophylactic, or no anticoagulation. Outcomes examined were thrombosis progression, early or late peripheral septic complications, chronic major sequelae, 30-day mortality, and major bleeding.
Fifty-one of 82 (62%) radiologically investigated patients with Lemierre's syndrome had jugular vein thrombosis. Patients with jugular vein thrombosis had lower platelet levels (median, 76 vs 112 ×10/L; = .04) on presentation and more days to defervesence (12 vs 7 days; = .03) yet similar rates of major sequelae and 30-day mortality. No significant differences in outcomes were seen between patients with jugular vein thrombosis exposed to therapeutic, prophylactic, or no anticoagulation therapy, yet study outcomes were rare.
Patients with Lemierre's syndrome with jugular vein thrombosis were more severely affected, yet had similar prognosis. Most patients with jugular vein thrombosis recovered well without therapeutic anticoagulation therapy, though adverse events were similarly rare in anticoagulated patients. The observational design and rarity of study outcomes require cautious interpretation.
勒米尔综合征通常由口咽感染后继发化脓性颈内静脉血栓性静脉炎及随后的脓毒性栓塞引起。然而,化脓性血栓性静脉炎的发病机制、取决于颈静脉血栓形成的差异以及抗凝治疗的作用尚未得到充分了解。
从瑞典之前一项基于人群的观察性研究中纳入患有侵袭性感染和勒米尔综合征且已接受颈静脉血栓形成调查的患者。对有或无颈静脉血栓形成的患者的病历进行回顾和比较。然后,对接受治疗性、预防性或未进行抗凝治疗的颈静脉血栓形成患者进行比较。检查的结局包括血栓进展、早期或晚期外周脓毒性并发症、慢性主要后遗症、30天死亡率和大出血。
82例接受放射学检查的勒米尔综合征患者中有51例(62%)患有颈静脉血栓形成。颈静脉血栓形成患者就诊时血小板水平较低(中位数,76对112×10/L;P = .04),退热天数更多(12天对7天;P = .03),但主要后遗症发生率和30天死亡率相似。接受治疗性、预防性或未进行抗凝治疗的颈静脉血栓形成患者在结局方面未见显著差异,但研究结局少见。
患有颈静脉血栓形成的勒米尔综合征患者受影响更严重,但预后相似。大多数颈静脉血栓形成患者在未接受治疗性抗凝治疗的情况下恢复良好,尽管抗凝患者的不良事件同样少见。观察性设计和研究结局的少见性需要谨慎解读。