Walti Laura N, Ng Chun Fai, Kaur Simran, Almansour Sarah, Mazzulli Tony, Bitterman Roni, Sidhu Aman, Keshavjee Shaf, Chaparro Cecilia, Martinu Tereza, Tikkanen Jussi, Del Sorbo Lorenzo, Husain Shahid
Transplant Infectious Diseases, Toronto General Hospital, University Health Network, University of Toronto, Toronto, Canada.
Department of Infectious Diseases, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Clin Infect Dis. 2025 Feb 22. doi: 10.1093/cid/ciaf078.
Hyperammonemia syndrome (HS) is a rare but potentially fatal complication of Lung Transplantation (LT). Optimal screening methods are unknown: Here we investigated serum ammonia screening (SAS) for HS and compared it with PCR for Mollicutes (ureaplasma-producing bacteria).
All LT recipients from 07/2019-02/2020 and 10/2021-11/2022 with available donor bronchial wash samples from the LT biobank were included. Mollicute-PCR was performed using two commercially available kits. Daily ammonia serum levels were measured for the first 14 days. Recipients were prospectively followed for HS for 30 days post-LT. HS was defined by new neurological symptoms and the presence of elevated serum ammonium (>1x >70 µmol/l).
Of 241 LT recipients, 5 (2%) developed HS within the first month post-LT. Median time to HS was 8 days (IQR 5-10). All HS were diagnosed within the first 14 days post-LT, while daily SAS was in place.Ammonia was confirmed elevated (>1x >70µmol/l) in 4% (9/241) during follow-up however, outside of HS, 4 were found to be liver disease-related. Donor Mollicute-PCR was positive in 8% (19/241), recipient M-PCR in 1% (1/72) at transplant. Donor Mollicute-PCR, in contrast to recipient Mollicute-PCR, was associated with HS but only in 2 of the 5 HS cases. No HS patient died within 90 days post-LT.
HS was a rare complication in our LT cohort. Daily post-LT SAS might add to early HS diagnosis and treatment and is potentially associated with improved outcome. Donor screening with Mollicute-PCR has limited predictive value for HS post-LT.
高氨血症综合征(HS)是肺移植(LT)罕见但可能致命的并发症。最佳筛查方法尚不清楚:在此,我们研究了用于HS的血清氨筛查(SAS),并将其与支原体(产脲原体细菌)的聚合酶链反应(PCR)进行比较。
纳入2019年7月至2020年2月以及2021年10月至2022年11月期间所有可从LT生物样本库获取供体支气管灌洗样本的LT受者。使用两种市售试剂盒进行支原体PCR检测。在最初14天内每日测量血清氨水平。LT受者在LT后30天内接受HS的前瞻性随访。HS定义为出现新的神经症状且血清铵升高(>1倍>70µmol/l)。
241例LT受者中,5例(2%)在LT后第一个月内发生HS。发生HS的中位时间为8天(四分位间距5 - 10天)。所有HS均在LT后14天内确诊,此时每日SAS检测正在进行。随访期间4%(9/241)的患者氨被确认升高(>1倍>70µmol/l),然而,在HS之外,发现4例与肝脏疾病相关。移植时供体支原体PCR阳性率为8%(19/241),受者M-PCR阳性率为1%(1/72)。与受者支原体PCR不同,供体支原体PCR与HS相关,但仅在5例HS病例中的2例中出现。没有HS患者在LT后90天内死亡。
HS是我们LT队列中的罕见并发症。LT后每日进行SAS检测可能有助于早期HS诊断和治疗,并可能改善预后。用支原体PCR进行供体筛查对LT后HS的预测价值有限。