Malik Vikas, Nichani Jaya, Rothera Michael P, Wraith James Edmond, Jones Simon A, Walker Robert, Bruce Iain A
Paediatric ENT Department, Royal Manchester Children's Hospital, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK.
Int J Pediatr Otorhinolaryngol. 2013 Jul;77(7):1204-8. doi: 10.1016/j.ijporl.2013.05.002. Epub 2013 May 31.
Patients with mucopolysaccharidosis type II (MPS II) may develop progressive multi-level upper airway obstruction. Despite the unique challenges presented by these complex patients, tracheostomy remains an important intervention to safeguard the airway when other interventions have failed or when the airway obstruction involves multiple sites. Airway involvement is largely responsible for the significant anaesthetic risk seen in MPS II. We reviewed our tertiary unit's experience of tracheostomies in patients with MPS II.
Retrospective study.
Case note review of MPS II patients requiring tracheostomy at our tertiary institution. The primary outcome measure used for this study was complications following tracheostomy.
We identified 10 MPS II patients requiring tracheostomy to manage upper airway obstruction. Mean age at which tracheostomy was 11 years 2 months (range 4 years 6 months to 28 years 10 months). Tracheostomy insertion was indicated in 3 scenarios: (1) to safeguard an anticipated difficult airway prior to a planned non-ENT surgical procedure, (2) to treat refractory progressive upper airway obstruction and (3) emergency airway management. Complications recorded included infratip and suprastomal granulations, local wound infection and skin ulceration from mechanical trauma. There were no immediate postoperative complications.
Progressive upper airway obstruction is common in children with MPS II. Tracheostomy is an effective way of managing airway obstruction when less invasive interventions are no longer adequate. Tracheostomy in these patients can be technically difficult and although the complications of tracheostomy in MPS II do not significantly differ from other patient groups, the implications and management complexity vary considerably. The impact of ERT on airway obstruction is not yet fully understood, with tracheostomies likely to remain an important airway adjunct in some patients who fail to respond to ERT, or in those patients surviving into adulthood. It is vital that a multidisciplinary team, comprising clinicians with experience in managing such patients, are involved in airway management of patients with MPS II to enable the best standard of care to be given. The significant additional implications of a tracheostomy in a patient with MPS II, in terms of safety, aftercare and potentially life-threatening complications must be discussed in detail with the patient's family and/or carers.
2c.
II型黏多糖贮积症(MPS II)患者可能会出现进行性多平面上气道梗阻。尽管这些复杂患者存在独特的挑战,但当其他干预措施失败或气道梗阻累及多个部位时,气管切开术仍是保障气道的重要干预手段。气道受累在很大程度上导致了MPS II患者面临的重大麻醉风险。我们回顾了我们三级医疗单位对MPS II患者进行气管切开术的经验。
回顾性研究。
对在我们三级医疗机构需要气管切开术的MPS II患者的病历进行回顾。本研究使用的主要结局指标是气管切开术后的并发症。
我们确定了10例需要气管切开术来处理上气道梗阻的MPS II患者。气管切开术时的平均年龄为11岁2个月(范围为4岁6个月至28岁10个月)。气管切开术适用于3种情况:(1)在计划进行非耳鼻喉外科手术前保障预期的困难气道,(2)治疗难治性进行性上气道梗阻,(3)紧急气道管理。记录的并发症包括鼻尖下和造口上肉芽、局部伤口感染以及机械创伤导致的皮肤溃疡。术后无即刻并发症。
进行性上气道梗阻在MPS II患儿中很常见。当侵入性较小的干预措施不再足够时,气管切开术是处理气道梗阻的有效方法。对这些患者进行气管切开术在技术上可能具有挑战性,尽管MPS II患者气管切开术的并发症与其他患者群体没有显著差异,但其影响和管理复杂性差异很大。酶替代疗法(ERT)对气道梗阻的影响尚未完全了解,对于一些对ERT无反应的患者或存活至成年的患者,气管切开术可能仍然是重要的气道辅助手段。至关重要的是,由有管理此类患者经验的临床医生组成的多学科团队应参与MPS II患者的气道管理,以便提供最佳的护理标准。必须与患者家属和/或护理人员详细讨论气管切开术对MPS II患者在安全性、术后护理以及潜在危及生命的并发症方面的重大额外影响。
2c。