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肝结节病的临床管理:一项系统评价。

The clinical management of hepatic sarcoidosis: A systematic review.

作者信息

Sinnanaidu Ram Prasad, Kumar Vikneshwaran Chandra, Shunmugam Ranita Hisham, Mahadeva Sanjiv

机构信息

Gastroenterology Unit, Medical Department Universiti Malaya Medical Centre Kuala Lumpur Malaysia.

Hepatology Department Hospital Selayang Batu Caves Malaysia.

出版信息

JGH Open. 2024 Jun 20;8(6):e13076. doi: 10.1002/jgh3.13076. eCollection 2024 Jun.

Abstract

BACKGROUND

Hepatic sarcoidosis is an uncommon clinical condition in which clear recommendations are lacking in its treatment. We aimed to review systematically the literature on hepatic sarcoidosis treatment to guide clinicians.

METHODS

Using MEDLINE, PubMed, CINAHL, Cochrane Library, and Google Scholar databases, we searched original articles on clinical studies reporting the outcome of adult hepatic sarcoidosis patients following treatment with various pharmacological agents. The primary end point was focused on assessing symptomatic relief and biochemical improvement posttreatment.

RESULTS

Out of 614 retrieved references, 34 published studies were eligible, providing data for a total of 268 patients with hepatic sarcoidosis. First-line therapy with corticosteroids alone was reported in 187 patients, whilst ursodeoxycholic acid (UDCA) was used in 40 patients. Symptomatic and biochemical responses were reported among 113(60.4%) and 80(42.8%) cases of corticosteroids respectively, whereas UDCA showed a complete response in 23(57.5%) patients. Second-line therapy was used in steroid-refractory cases, with most cases being reported for azathioprine ( = 32) and methotrexate ( = 28). Notably, 15(46.9%) and 11(39.2%) patients showed both clinical and biochemical responses respectively. Biological therapy including anti-tumor necrosis factor (anti-TNF) was used as third line therapy in twelve cases with a 72.7% symptomatic and biochemical response rate each.

CONCLUSION

The quality of evidence for the treatment of hepatic sarcoidosis was poor. Nevertheless, it appears that corticosteroid or UDCA may be utilized as first-line therapy. For cases that are refractory to corticosteroids, steroid-sparing immunosuppressive agents and anti-TNF have shown some promising results, but further high-quality studies are required.

摘要

背景

肝结节病是一种临床罕见病,目前其治疗缺乏明确的推荐方案。我们旨在系统回顾关于肝结节病治疗的文献,以指导临床医生。

方法

我们使用MEDLINE、PubMed、CINAHL、Cochrane图书馆和谷歌学术数据库,检索了关于临床研究的原始文章,这些研究报告了成年肝结节病患者接受各种药物治疗后的结果。主要终点集中在评估治疗后症状缓解和生化指标改善情况。

结果

在检索到的614篇参考文献中,有34项已发表的研究符合要求,共提供了268例肝结节病患者的数据。187例患者报告单独使用皮质类固醇作为一线治疗,而40例患者使用了熊去氧胆酸(UDCA)。皮质类固醇治疗的病例中,分别有113例(60.4%)和80例(42.8%)出现了症状和生化反应,而UDCA在23例(57.5%)患者中显示出完全反应。对于类固醇难治性病例,使用二线治疗,大多数病例报告使用硫唑嘌呤(n = 32)和甲氨蝶呤(n = 28)。值得注意的是,分别有15例(46.9%)和11例(39.2%)患者出现了临床和生化反应。包括抗肿瘤坏死因子(抗TNF)在内的生物疗法在12例患者中用作三线治疗,症状和生化反应率均为72.7%。

结论

肝结节病治疗的证据质量较差。然而,皮质类固醇或UDCA似乎可作为一线治疗。对于皮质类固醇难治的病例,类固醇节省免疫抑制剂和抗TNF已显示出一些有前景的结果,但需要进一步的高质量研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f884/11187478/69570dfaf958/JGH3-8-e13076-g008.jpg

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