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支气管肺泡灌洗液宏基因组下一代测序在特发性肺纤维化急性加重中的价值:基于微生物证据的个体化治疗方案。

Value of bronchoalveolar lavage fluid metagenomic next-generation sequencing in acute exacerbation of fibrosing interstitial lung disease: an individualized treatment protocol based on microbiological evidence.

机构信息

Department of Respiratory and Critical Care Medicine, Tianjin Medical University General Hospital, Tianjin, 300052, China.

出版信息

BMC Pulm Med. 2024 Aug 20;24(1):400. doi: 10.1186/s12890-024-03216-1.

Abstract

BACKGROUND

Acute exacerbation of fibrosing interstitial lung diseases (AE-ILD) is a serious life-threatening event per year. Methylprednisolone and/or immunosuppressive agents (ISA) are a mainstay in any regimen, under the premise that pulmonary infection has been promptly identified and controlled. We investigated the value of bronchoalveolar lavage fluid (BALF) metagenomic next-generation sequencing (mNGS) on the treatment adjustment of AE-ILD.

METHODS

We conducted a cross-sectional observational study. All data were collected prospectively and retrospectively analyzed. We included fifty-six patients with AE-ILD and nineteen stable ILD who underwent BALF mNGS at the beginning of admission.

RESULTS

Patients with a variety of ILD classification were included. Connective-tissue disease related ILD (CTD-ILD) occupy the most common underlying non-idiopathic pulmonary fibrosis (non-IPF). The infection-triggered AE accounted for 39.29%, with the majority of cases being mixed infections. The microorganisms load in the AE-ILD group was significantly higher. After adjusted by mNGS, the therapy coverage number of pathogens was significantly higher compared to the initial treatment (p < 0.001). After treatment, the GGO score and the consolidation score were significantly lower during follow up in survivors (1.57 ± 0.53 vs. 2.38 ± 0.83 with p < 0.001, 1.11 ± 0.24 vs. 1.49 ± 0.47 with p < 0.001, respectively). Some detected microorganisms, such as Tropheryma whipplei, Mycobacterium, Aspergillus, and mixed infections were difficult to be fully covered by empirical medication. BALF mNGS was also very helpful for excluding infections and early administration of methylprednisolone and/or ISA.

CONCLUSIONS

mNGS has been shown to be a useful tool to determine pathogens in patients with AE-ILD, the results should be fully analyzed. The comprehensive treatment protocol based on mNGS has been shown crucial in AE-ILD patients.

摘要

背景

纤维性间质性肺病(ILD)的急性加重(AE-ILD)每年都是严重危及生命的事件。在及时识别和控制肺部感染的前提下,甲泼尼龙和/或免疫抑制剂(ISA)是任何治疗方案的基础。我们研究了支气管肺泡灌洗液(BALF)宏基因组下一代测序(mNGS)在 AE-ILD 治疗调整中的价值。

方法

我们进行了一项横断面观察性研究。所有数据均前瞻性和回顾性收集并进行分析。我们纳入了 56 例 AE-ILD 患者和 19 例稳定期 ILD 患者,他们在入院时均进行了 BALF mNGS 检查。

结果

纳入了各种ILD 分类的患者。结缔组织疾病相关 ILD(CTD-ILD)占最常见的非特发性肺纤维化(非-IPF)。感染触发的 AE 占 39.29%,大多数为混合感染。AE-ILD 组的微生物负荷明显更高。经 mNGS 校正后,与初始治疗相比,病原体治疗覆盖率明显更高(p<0.001)。治疗后,在存活者中随访时 GGO 评分和实变评分明显降低(1.57±0.53 与 2.38±0.83,p<0.001,1.11±0.24 与 1.49±0.47,p<0.001)。一些检测到的微生物,如 Whipple 螺旋体、分枝杆菌、曲霉菌和混合感染,难以通过经验性药物充分覆盖。BALF mNGS 对于排除感染和早期给予甲泼尼龙和/或 ISA 也非常有帮助。

结论

mNGS 已被证明是确定 AE-ILD 患者病原体的有用工具,应充分分析结果。基于 mNGS 的综合治疗方案已被证明对 AE-ILD 患者至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a082/11337881/0f7cabb5e273/12890_2024_3216_Fig1_HTML.jpg

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