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Randomized Controlled Trial
. 2025 Feb;167(2):362-373.
doi: 10.1016/j.chest.2024.07.144. Epub 2024 Jul 25.

Effect of Metagenomic Next-Generation Sequencing on Clinical Outcomes of Patients With Severe Community-Acquired Pneumonia in the ICU: A Multicenter, Randomized Controlled Trial

Xiaojing Wu  1 , Ting Sun  2 , Hangyong He  3 , Lihua Xing  4 , Zhenshun Cheng  5 , Shuang Geng  6 , Dexiang Xu  7 , Hong Luo  8 , Cheng Chen  9 , Mingyan Jiang  10 , Guopeng Hou  11 , Tianshu Zhai  3 , Ying Cai  3 , Yijie Liu  12 , Junlu Li  4 , Lan Ni  5 , Xueying Li  6 , Binbin Qu  7 , Cheng Lei  8 , Yang Wang  9 , Zi Gu  10 , Peng Zhang  11 , Xu Huang  3 , Min Li  3 , Jingen Xia  3 , Lian He  13 , Qingyuan Zhan  14
Affiliations
Randomized Controlled Trial

Effect of Metagenomic Next-Generation Sequencing on Clinical Outcomes of Patients With Severe Community-Acquired Pneumonia in the ICU: A Multicenter, Randomized Controlled Trial

Xiaojing Wu et al. Chest. 2025 Feb.

Abstract

Background: Metagenomic next-generation sequencing (mNGS) was previously established as a method that can increase the pathogen identification rate in patients with severe community-acquired pneumonia (SCAP).

Research question: What is the impact on clinical outcomes of mNGS of BAL fluid (BALF) in patients with SCAP in the ICU?

Study design and methods: A multicenter randomized controlled open-label clinical trial was conducted in 10 ICUs. Patients were randomized in a 1:1 ratio to undergo BALF assessment with conventional microbiological tests (CMTs) only (ie, the CMT group) or BALF assessment with both mNGS and CMTs (ie, the mNGS group). The primary outcome was the time to clinical improvement, defined as the time from randomization to either an improvement of two points on a six-category ordinal scale or discharge from the ICU, whichever occurred first.

Results: A total of 349 patients were randomized to treatment between January 1, 2021, and November 18, 2022; 170 were assigned to the CMT group and 179 to the mNGS group. In the intention-to-treat analysis, the time to clinical improvement was better in the mNGS group than in the CMT group (10 days vs 13 days; difference, -2.0 days; 95% CI, -3.0 to 0.0 days). Similar results were obtained in the per-protocol analysis. The proportion of patients with clinical improvement within 14 days was significantly higher in the mNGS group (62.0%) than in the CMT group (46.5%). There was no significant difference in other secondary outcomes.

Interpretation: We found that compared with the use of CMTs alone, mNGS combined with CMTs reduced the time to clinical improvement for patients with SCAP.

Clinical trial registration: Chinese Clinical Trial Registry, ChiCTR; www.chictr.org.cn/index.html; ChiCTR2000037894.

Keywords: ICUs; clinical outcomes; metagenomic next-generation sequencing; severe community-acquired pneumonia.

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Conflict of interest statement

Financial/Nonfinancial Disclosures None declared.

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