骨科实践中万古霉素潮红综合征1例报告。

IF 2 Q2 ORTHOPEDICS
Fawaz M Al-Anii, Mir Sadat-Ali, Khalid Waleed Al-Tabash, Ahmad I AlMulhim, Sulaiman A AlMousa, Abdulaziz M AlHawas
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引用次数: 0

摘要

背景:万古霉素潮红综合征(VFS),又称红人综合征,是一种对万古霉素的过敏反应。静脉注射万古霉素后,通常表现为面部、颈部和上半身出现皮疹。VFS归咎于治疗期间快速静脉输注万古霉素,很少在局部使用后发生。对文献的回顾显示,在过去的23年里,有4例这样的病例被报道。在这里,我们又增加了一例万古霉素在水泥珠中局部缓慢吸收后发生的VFS。病例总结:一名44岁男性,已知高血压病例,无药物过敏史,右胫骨慢性骨髓炎病史,腿前外侧有排出窦。脓液培养培养出对克林霉素和万古霉素敏感的金黄色葡萄球菌。患者行冲洗和清创术,植入万古霉素水泥珠,万古霉素水泥珠由4 g万古霉素粉末和40 g聚甲基丙烯酸甲酯制成。术后3小时,患者出现瘙痒、红斑、黄斑皮疹,主要出现在面部、颈部、胸部和下肢,上肢轻度出现。诊断为VFS,并成功治疗西替利嗪(10 mg,口服)和琥珀酸甲泼尼龙钠(125 mg,静脉注射)。患者持续瘙痒并伴有面部皮疹12小时后逐渐改善。随着病人病情的持续好转,医生决定不移除这些珠子。96 h后皮疹逐渐消失,无其他后遗症。结论:快速静脉注射万古霉素后可发生VFS,也可局部释放,如本病例。由于骨科医生在慢性骨髓炎和翻修关节成形术中常规使用万古霉素和聚甲基丙烯酸甲酯,他们应该意识到这种并发症的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vancomycin flushing syndrome in orthopaedic practice: A case report.

Background: Vancomycin flushing syndrome (VFS), also known as red man syndrome, is an allergic reaction to vancomycin. It typically presents as a rash on the face, neck, and upper torso after intravenous administration of vancomycin. VFS is blamed on rapid intravenous infusion of vancomycin during management and rarely happens after local use. A review of the literature showed that in the last 23 years, 4 such cases have been reported. Here, we add another case of VFS developed after slow local absorption of vancomycin in cement beads.

Case summary: A 44-year-old male with a known case of hypertension, no history of allergies to medications, and a history of chronic osteomyelitis of the right tibia with discharging sinus over the anterolateral aspect of the leg. The pus culture grew Staphylococcus aureus, which was sensitive to clindamycin and vancomycin. The patient underwent irrigation and debridement with the placement of vancomycin cement beads made from 4 g of vancomycin powder and 40 g of polymethyl methacrylate. Three hours postoperatively, the patient developed a pruritic, erythematous, macular rash predominantly on his face, neck, chest, and lower extremities and to a lesser extent his upper extremities. A diagnosis of VFS was made and was successfully treated with cetirizine (10 mg, oral) and methylprednisolone sodium succinate (125 mg, intravenous). The patient continued to have itching with a facial rash for 12 h with gradual improvement. A decision was made to not remove the beads as the patient continued to improve. Gradually, the rash disappeared after 96 h with no further sequela.

Conclusion: VFS can occur not only after rapid intravenous injection of vancomycin but also with local release, as in our case. As orthopaedic surgeons routinely use vancomycin with polymethyl methacrylate in chronic osteomyelitis and revision arthroplasty, they should be aware of such a complication occurring.

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