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肾移植后感染所致迟发性高氨血症综合征

A late-onset hyperammonemia syndrome caused by infection after kidney transplantation.

作者信息

Wu Jing, Hu Yunjian

机构信息

Department of Laboratory Medicine, Beijing Children's Hospital, Capital Medical University, National Centre for Children's Health, Beijing, China.

Department of Laboratory Medicine, Beijing Hospital, National Centre for Gerontology, Beijing, China.

出版信息

Heliyon. 2024 May 28;10(11):e32134. doi: 10.1016/j.heliyon.2024.e32134. eCollection 2024 Jun 15.

DOI:10.1016/j.heliyon.2024.e32134
PMID:38912440
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11190536/
Abstract

Hyperammonemia syndrome has a high mortality rate in the immunosuppressed population due to its association with mental status changes. Recently studies have shown that organisms' infection can lead to hyperammonemia in post-transplant patients. Symptoms typically occur within 30 days postoperatively. However, the late-onset hyperammonemia caused by infection after kidney transplantation has never been reported. In this case study, a 64-year-old Chinese male presented with symptoms such as nausea, vomiting, trouble sleeping, and deteriorating mental status 81 days after kidney transplantation. His plasma ammonia level was significantly elevated, and there was no evidence of liver synthetic dysfunction. Although common methods for ammonia clearance, such as haemodialysis and oral lactulose were initiated, his serum ammonia levels remained high. Metagenomic sequencing of serum determined infection. Levofloxacin and minocycline were administered respectively, which resulted in a decrease in ammonia levels, but normalization was not achieved. The computed tomographic scan revealed the presence of cerebral edema. Unfortunately, the patient eventually became brain dead with multiple organ failure. This case highlights that can cause late-onset hyperammonemia in kidney transplant patients. Once the mental status changes are identified, immediate empiric treatments should be initiated without waiting for a confirmed diagnosis of spp. infection.

摘要

高氨血症综合征在免疫抑制人群中死亡率很高,因为它与精神状态改变有关。最近的研究表明,生物体感染可导致移植后患者发生高氨血症。症状通常在术后30天内出现。然而,肾移植后由感染引起的迟发性高氨血症从未有过报道。在本病例研究中,一名64岁的中国男性在肾移植81天后出现恶心、呕吐、睡眠障碍和精神状态恶化等症状。他的血浆氨水平显著升高,且没有肝合成功能障碍的证据。尽管启动了诸如血液透析和口服乳果糖等常见的氨清除方法,但他的血清氨水平仍然很高。血清宏基因组测序确定了感染情况。分别给予左氧氟沙星和米诺环素,氨水平有所下降,但未恢复正常。计算机断层扫描显示存在脑水肿。不幸的是,患者最终因多器官衰竭而脑死亡。该病例突出表明,[原文此处有缺失内容]可导致肾移植患者发生迟发性高氨血症。一旦发现精神状态改变,应立即开始经验性治疗,而不必等待确诊[原文此处有缺失内容]属感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b59/11190536/cec6c1aab0e7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b59/11190536/84beb4185187/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b59/11190536/cec6c1aab0e7/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b59/11190536/84beb4185187/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b59/11190536/cec6c1aab0e7/gr2.jpg

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本文引用的文献

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Trends Microbiol. 2024 Feb;32(2):142-150. doi: 10.1016/j.tim.2023.08.006. Epub 2023 Sep 7.
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Successful management of noncirrhotic hyperammonemia syndrome after kidney transplantation from putative Ureaplasma infection.肾移植后疑似解脲脲原体感染致非肝硬化性高氨血症综合征的成功治疗。
Transpl Infect Dis. 2020 Oct;22(5):e13332. doi: 10.1111/tid.13332. Epub 2020 Jun 13.
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Hyperammonemia syndrome due to Ureaplasma urealyticum in a kidney transplant recipient: A case of disseminated disease from a fluoroquinolone-resistant isolate.尿素分解支原体导致肾移植受者高氨血症综合征:氟喹诺酮耐药分离株引起的播散性疾病病例。
Transpl Infect Dis. 2020 Oct;22(5):e13328. doi: 10.1111/tid.13328. Epub 2020 Jun 2.
7
Hyperammonemia syndrome due to Ureaplasma infection after liver-kidney transplant.肝移植术后解脲脲原体感染致高氨血症综合征。
Transpl Infect Dis. 2020 Jun;22(3):e13298. doi: 10.1111/tid.13298. Epub 2020 Apr 30.
8
Era of molecular diagnosis for pathogen identification of unexplained pneumonia, lessons to be learned.不明原因肺炎病原体鉴定的分子诊断时代:经验教训。
Emerg Microbes Infect. 2020 Mar 16;9(1):597-600. doi: 10.1080/22221751.2020.1738905. eCollection 2020.
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Ureaplasma parvum causes hyperammonemia presenting as refractory status epilepticus after kidney transplant.解脲脲原体导致高氨血症,在肾移植后表现为难治性癫痫持续状态。
J Crit Care. 2020 Jun;57:79-83. doi: 10.1016/j.jcrc.2020.02.003. Epub 2020 Feb 5.
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Acute diffuse edematous-hemorrhagic Epstein-Barr virus meningoencephalitis: A case report.急性弥漫性水肿-出血性爱泼斯坦-巴尔病毒脑膜脑炎:一例报告
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