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Treatment and outcome of autoimmune hepatitis: Audit of 28 UK centres

机译:自身免疫性肝炎的治疗和结果:对28个英国中心的审计

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Abstract Background With few data regarding treatment and outcome of patients with AIH outside of large centres we present such a study of patients with AIH in 28 UK hospitals of varying size and facilities. Methods Patients with AIH were identified in 14 University and 14 District General hospitals; incident cases during 2007–2015 and prevalent cases, presenting 2000–2015. Treatment and outcomes were analysed. Results In 1267 patients with AIH, followed up for 3.8 (0–15) years, 5‐ and 10‐year death/transplant rates were 7.1?±?0.8 and 10.1?±?1.3 (all‐cause) and 4.0?±?0.6 and 5.9?±?1 (liver related) respectively. Baseline parameters independently associated with death/transplantation for all causes were: older age, vascular/respiratory co‐morbidity, cirrhosis, decompensation, platelet count, attending transplant centre and for liver related: the last four of these and peak bilirubin. All‐cause and liver‐related death/transplantation was independently associated with: non‐treatment with corticosteroids, non‐treatment with a steroid‐sparing agent (SSA), non‐treatment of asymptomatic or non‐cirrhotic patients and initial dose of Prednisolone >35?mg/0.5?mg/kg/day (all‐cause only), but not with type of steroid (Prednisolone vs. Budesonide) or steroid duration beyond 12?months. Subsequent all‐cause and liver‐death/transplant rates showed independent associations with smaller percentage fall in serum ALT after 1 and 3?months, but not with failure to normalise levels over 12?months. Conclusions We observed higher death/transplant rates in patients with AIH who were untreated with steroids (including asymptomatic or non‐cirrhotic subgroups), those receiving higher Prednisolone doses and those who did not receive an SSA. Similar death/transplant rates were seen in those receiving Prednisolone or Budesonide, those continuing steroids after 12?months and patients attaining normal ALT within 12?months versus not.
机译:摘要 背景:由于在大型中心之外,关于自身免疫性肝炎患者的治疗和结果的数据很少,我们在28家不同规模和设施的英国医院中对自身免疫性肝炎患者进行了这样的研究。方法 在14所大学医院和14家区综合医院中发现自身免疫性肝炎患者;2007-2015 年的事件案例和 2000-2015 年的流行案例。分析了治疗和结局。结果 1267例自身免疫性肝炎患者随访3.8(0–15)年,5年和10年死亡/移植率分别为7.1±0.8%和10.1±1.3%(全因)和4.0?±?0.6%和5.9?±?1%(肝脏相关)。与所有原因的死亡/移植独立相关的基线参数是:高龄、血管/呼吸系统合并症、肝硬化、失代偿、血小板计数、就诊移植中心和肝脏相关:其中最后四个和胆红素峰值。全因和肝脏相关死亡/移植与以下因素独立相关:未使用皮质类固醇治疗、未使用类固醇保留剂 (SSA) 治疗、未治疗无症状或非肝硬化患者和泼尼松龙初始剂量 >35?mg/0.5?mg/kg/天(仅全因),但与类固醇类型(泼尼松龙与布地奈德)或类固醇持续时间超过 12 个月无关。随后的全因死亡率和肝死亡/移植率显示,1 个月和 3 个月后血清 ALT 下降百分比较小,但与 12 个月后血清 ALT 水平未能正常化无关。结论 我们观察到未接受类固醇治疗的自身免疫性肝炎患者(包括无症状或非肝硬化亚组)、接受较高泼尼松龙剂量的患者和未接受SSA的患者的死亡/移植率较高。在接受泼尼松龙或布地奈德治疗的患者、12 个月后继续使用类固醇的患者以及 12 个月内达到正常 ALT 的患者中观察到相似的死亡/移植率。

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