免疫抑制剂在感染性心内膜炎相关性肾小球肾炎中的应用:系统综述。

IF 2.7 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Clinical Drug Investigation Pub Date : 2025-08-01 Epub Date: 2025-07-19 DOI:10.1007/s40261-025-01461-8
Reem Sayad, Ahmed Saad Elsaeidy, Muhammed Edib Mokresh, Mohamed Mohamed Shawqi, Yasmine Adel Mohammed, Eslam A Hawash, Ahmed Mostafa Ali, Danisha Kumar, Mostafa G Aly
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引用次数: 0

摘要

背景:感染性心内膜炎患者可发展为多种肾脏疾病,包括感染性心内膜炎相关的肾小球肾炎。抗生素对于根除感染是必不可少的。然而,对肾功能的预后仍然很差。本系统综述探讨了免疫抑制剂在感染性心内膜炎相关肾小球肾炎(GN)治疗中的作用。方法:对PubMed、Scopus、MedLine和Web of Science四个数据库进行全面检索,检索时间截止到2024年4月。我们纳入了那些接受免疫抑制剂治疗的感染性心内膜炎(IE)引起的任何类型GN的研究。使用标准化表格进行数据提取,并使用乔安娜布里格斯研究所(JBI)关键评估工具评估研究质量。结果:该综述纳入了55项研究,包括84例病例,其中65例为男性。中位年龄为46.5岁。总共有30例患者需要肾脏替代治疗。经免疫抑制治疗后,54例IE临床改善,9例病情恶化,3例无临床变化,18例资料不详。67例患者肾脏预后改善,9例病情恶化,3例无变化,3例出现部分或残余损害,2例肾脏预后无法获得。共有10例患者死亡,主要原因是败血症或感染相关并发症(5例),充血性或全身性心力衰竭(3例),肾功能衰竭伴相关代谢并发症(2例)。其他治疗包括血浆置换,其中9例接受血浆置换/血浆置换。其中8例患者肾功能明显改善,1例患者部分改善。3例患者还接受了静脉注射免疫球蛋白。结论:免疫抑制治疗在大多数病例中导致肾功能改善,提示其在治疗感染性心内膜炎相关肾小球肾炎方面的潜在益处。然而,反应的可变性和显著的死亡率突出了个性化治疗策略和进一步研究以优化管理的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Immunosuppressant Use in Infective Endocarditis-Associated Glomerulonephritis: A Systematic Review.

Immunosuppressant Use in Infective Endocarditis-Associated Glomerulonephritis: A Systematic Review.

Immunosuppressant Use in Infective Endocarditis-Associated Glomerulonephritis: A Systematic Review.

Immunosuppressant Use in Infective Endocarditis-Associated Glomerulonephritis: A Systematic Review.

Background: Patients with infective endocarditis can develop various renal diseases, including infective endocarditis-associated glomerulonephritis. Antibiotics are essential for eradicating the infection. However, the prognosis for renal function remains poor. This systematic review examines the role of immunosuppressants in managing infective endocarditis-associated glomerulonephritis (GN).

Methods: A comprehensive search was performed across four databases: PubMed, Scopus, MedLine, and Web of Science up to April 2024. We included studies that investigated patients with any type of GN due to infective endocarditis (IE) who were treated with immunosuppressants. Data extraction was conducted using a standardized sheet, and study quality was assessed using the Joanna Briggs Institute (JBI) critical appraisal tool.

Results: The review incorporated 55 studies encompassing 84 cases, 65 of whom were male. The median age was 46.5 years. A total of 30 cases required kidney replacement therapy. Following immunosuppressive therapy, clinical improvement of IE was observed in 54 cases, while 9 patients experienced worsening conditions, 3 patients had no clinical change, and data were unavailable in 18 cases. Renal outcomes showed improvement in 67 patients, with 9 cases showing worsening conditions, 3 patients showing no change, 3 experiencing partial or residual impairment, and renal outcome was unavailable in 2 cases. A total of ten patients died, primarily owing to sepsis or infection-related complications (five cases), congestive or global heart failure (three cases), and renal failure with associated metabolic complications (two cases). Additional treatments included plasma exchange, with nine cases receiving plasmapheresis/plasma exchange. Of these, eight patients showed marked renal function improvement, and one patient showed partial improvement. Three patients also received intravenous immunoglobulin.

Conclusions: Immunosuppressive therapy led to renal function improvement in the majority of cases, suggesting its potential benefit in managing infective endocarditis-associated glomerulonephritis. However, variability in response and significant mortality highlight the need for individualized treatment strategies and further research to optimize management.

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来源期刊
CiteScore
5.90
自引率
3.10%
发文量
108
审稿时长
6-12 weeks
期刊介绍: Clinical Drug Investigation provides rapid publication of original research covering all phases of clinical drug development and therapeutic use of drugs. The Journal includes: -Clinical trials, outcomes research, clinical pharmacoeconomic studies and pharmacoepidemiology studies with a strong link to optimum prescribing practice for a drug or group of drugs. -Clinical pharmacodynamic and clinical pharmacokinetic studies with a strong link to clinical practice. -Pharmacodynamic and pharmacokinetic studies in healthy volunteers in which significant implications for clinical prescribing are discussed. -Studies focusing on the application of drug delivery technology in healthcare. -Short communications and case study reports that meet the above criteria will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Clinical Drug Investigation may be accompanied by plain language summaries to assist readers who have some knowledge, but non in-depth expertise in, the area to understand important medical advances.
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