Neild G H
Dept. of Renal Medicine, Institute of Urology, UCMSM, St Philip's Hospital, London, U.K.
APMIS Suppl. 1990;19:56-60. doi: 10.1111/j.1600-0463.1990.tb05739.x.
Patients with microscopic polyarteritis and Wegener's granulomatosis are often elderly. At present 10-20% of these patients will die from infection in the first three months of immunosuppressive treatment. Therapeutic strategies initially must maximize anti-inflammatory and immunosuppressive effects and minimize the later in the longer term. Regimens with pulse MP combined with low dose prednisolone (ie 20 mg/day), together with oral or pulsed cyclophosphamide in the first weeks followed by maintenance treatment with azathioprine and prednisolone are suggested--with PE reserved for those requiring dialysis, lung haemorrhage, or uncontrolled vasculitis.
显微镜下多血管炎和韦格纳肉芽肿患者往往年事已高。目前,这些患者中有10% - 20%会在免疫抑制治疗的头三个月死于感染。治疗策略最初必须使抗炎和免疫抑制作用最大化,并在长期内将后期影响最小化。建议采用脉冲式甲泼尼龙联合低剂量泼尼松龙(即20毫克/天)的方案,在最初几周内加用口服或脉冲式环磷酰胺,随后用硫唑嘌呤和泼尼松龙进行维持治疗——血浆置换仅用于那些需要透析、肺出血或血管炎控制不佳的患者。