Gordon Victoria, Adhikary Ratul, Appleby Victoria, Das Debasish, Day James, Delahooke Toby, Dixon Selena, Elphick David, Hardie Claire, Heneghan Michael A, Hoeroldt Barbara, Hooper Patricia, Hutchinson John, Jones Rebecca, Khan Faisal, Aithal Guruprasad P, Metcalf Jane, Nkhoma Alick, Pelitari Stavroula, Prince Martin, Prosser Annell, Sathyanarayana Vinay, Saksena Sushma, Vani Deven, Yeoman Andrew, Abouda George, Nelson Andrew, Gleeson Dermot
University Hospitals Coventry and Warwickshire.
Calderdale Royal Hospital.
Liver Int. 2022 Mar 14. doi: 10.1111/liv.15241.
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.
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.
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 >35mg/0.5mg/kg/day (all-cause only), but not with type of steroid (Prednisolone versus 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.
We observed higher death/transplant rates in patients with AIH who were untreated with steroids (including asymptomatic or non-cirrhotic sub-groups), 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.
除大型中心外,关于自身免疫性肝炎(AIH)患者的治疗及预后的数据较少,我们在此呈现一项针对英国28家规模和设施各异的医院中AIH患者的研究。
在14家大学医院和14家区综合医院中识别出AIH患者;纳入2007 - 2015年的新发病例以及2000 - 2015年的现患病例。对治疗情况及预后进行分析。
1267例AIH患者,随访3.8(0 - 15)年,全因死亡/移植率的5年和10年分别为7.1 + 0.8%和10.1 + 1.3%,肝脏相关死亡/移植率的5年和10年分别为4.0 + 0.6%和5.9 + 1%。与全因死亡/移植独立相关的基线参数有:年龄较大、血管/呼吸合并症、肝硬化、失代偿、血小板计数、就诊于移植中心;与肝脏相关死亡/移植独立相关的基线参数为上述最后四项以及胆红素峰值。全因和肝脏相关死亡/移植与以下因素独立相关:未接受皮质类固醇治疗、未接受类固醇节省剂(SSA)治疗、未对无症状或非肝硬化患者进行治疗以及泼尼松龙初始剂量>35mg/0.5mg/kg/天(仅全因相关),但与类固醇类型(泼尼松龙与布地奈德)或超过12个月的类固醇使用时长无关。后续全因和肝脏相关死亡/移植率与1个月和3个月后血清ALT下降百分比较小独立相关,但与12个月内未恢复正常水平无关。
我们观察到,未接受类固醇治疗的AIH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以及未接受SSA治疗的患者,其死亡/移植率较高。接受泼尼松龙或布地奈德治疗的患者、1年后继续使用类固醇的患者以及12个月内ALT恢复正常的患者与未恢复正常的患者相比,死亡/移植率相似。