Substantial concordance between transient elastography and APRI and FIB-4 combination amongst hepatitis C inmates with non advanced liver fibrosis

Q3 Medicine
E. Yela, N. Sole, S. Quintero
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引用次数: 1

Abstract

Abstract Objectives To establish concordance between transient elastography (TE) and non invasive markers (NIM) APRI and FIB-4 combination in cronic hepatitis C (HC) patients with non-advanced liver fibrosis (NALF). Material and method Multi-centre retrospective study carried out at two different Barcelona Prisons HC inmates who had the TE done at 2019. We compared the ET vs. NIM results. The NALF consideration was ≤2 (≤12.5 Kilopascal (kPa) in TE). In the NALF cases was calculated de NIM APRI and FIB-4 and the kappa index agreement was established between TE and NIM. Results 107 cases were included, but only 82 were assessable. The average age was 42 (DS: ±3.2) years. The 96.5% were men, 51.2% spanish, 70.7% drug users and 39% HIV co infected. The 45.1% of those HC infected had genotipe 1. The 90.2% of the evaluated patients by TE the ALD was not detected. The kappa index was 0.78. 65 (79.3%) studied inmates got HC treatment. The 20.7% could not be treated because the evaluation was not completed. Conclusion Most of the HC infected inmates have no ALD, and in such cases concordance between NIM/TE is substantial. The NIM can be used to shorten the evaluation time and prescribe the treatment faster, especially if the length of stay in prison is short and risk of transmission is high.
短暂弹性成像与APRI和FIB-4联合在丙型肝炎非晚期肝纤维化患者中的一致性
目的探讨瞬时弹性成像(TE)和非侵入性标志物(NIM)、APRI和FIB-4联合在慢性丙型肝炎(HC)合并非晚期肝纤维化(alf)患者中的一致性。材料和方法对两名不同的巴塞罗那监狱HC囚犯进行了多中心回顾性研究,他们于2019年完成了TE。我们比较了ET和NIM的结果。nff考虑≤2 (TE≤12.5千帕)。在nff病例中计算NIM的APRI和FIB-4,并在TE和NIM之间建立kappa指数一致性。结果共纳入107例,但可评估的病例只有82例。平均年龄42岁(DS:±3.2)岁。其中96.5%为男性,51.2%为西班牙人,70.7%为吸毒者,39%为艾滋病毒合并感染者。45.1%的HC感染者为基因1型。经TE评估的90.2%患者ALD未检出。kappa指数为0.78。65人(79.3%)接受了HC治疗。20.7%的患者因评估未完成而无法治疗。结论大多数HC感染的囚犯没有ALD,在这种情况下,NIM/TE的一致性是很大的。NIM可用于缩短评估时间并更快地开出治疗处方,特别是在监禁时间短且传播风险高的情况下。
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来源期刊
CiteScore
1.30
自引率
0.00%
发文量
11
审稿时长
15 weeks
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