Evidence map›Paper›PMID 39725980›Full record

ArticleJournal of translational medicine2024

Epidemiological and clinical characteristics of ammonia-producing microorganisms in the lungs of patients with severe pneumonia: a multicentre cohort study.

Jun Xu, Xindie Ren, Xiaohan Huang, Yue Jin, Mingqiang Wang, Lin Zhong, Guojun He, Shengfeng Wang, Qianqian Wang, Muhua Dai and 9 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Jun Xu *Department of Critical Care Medicine, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Xindie Ren *Department of Critical Care Medicine, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Xiaohan Huang *Department of Critical Care Medicine, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Yue Jin *Department of Critical Care Medicine, Xinxiang Medical University, Henan Provincial People's Hospital, Zhengzhou, China.
Mingqiang WangDepartment of Critical Care Medicine, Xinxiang Medical University, Henan Provincial People's Hospital, Zhengzhou, China.
Lin ZhongDepartment of Critical Care Medicine, The First People's Hospital of Pinghu, Pinghu, China.
Guojun HeDepartment of Critical Care Medicine, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Shengfeng WangDepartment of Critical Care Medicine, The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Qianqian WangDepartment of Critical Care Medicine, The First Hospital of Jiaxing, Jiaxing, China.
Muhua DaiDepartment of Critical Care Medicine, Tongde Hospital of Zhejiang Province, Hangzhou, China.
Yonghui XiongDepartment of Critical Care Medicine, Lanxi Hospital of Traditional Chinese Medicine, Lanxi, China.
Yinghe XuDepartment of Critical Care Medicine, Taizhou Hospital of Zhejiang Province Affiliated to Wenzhou Medical University, Taizhou, China.
Xuwei HeDepartment of Critical Care Medicine, Lishui People's Hospital, Lishui, China.
Yujie PanDepartment of Critical Care Medicine, Wenzhou Central Hospital, Wenzhou, China.
Hongyu WangDepartment of Emergency Intensive Care Unit, The Fifth Clinical Medical College of Henan University of Chinese Medicine, Zhengzhou, China.
Qi XiaState Key Laboratory for Diagnosis and Treatment of Infectious Diseases, National Clinical Research Center for Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China. xiaqi@zju.edu.cn.
Huanzhang ShaoDepartment of Critical Care Medicine, Xinxiang Medical University, Henan Provincial People's Hospital, Zhengzhou, China. shaohuanzhang001@126.com.
Lingtong HuangDepartment of Critical Care Medicine, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China. lingtonghuang@zju.edu.cn.
Hongliu CaiDepartment of Critical Care Medicine, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China. 1193001@zju.edu.cn.

Funding

the National Natural Science Foundation of China 82202356the Zhejiang Provincial Natural Science Fund LTGY24H190001
6 · The paper itself

Abstract

backgroundUreaplasma urealyticum, Ureaplasma parvum, and Mycoplasma hominis were widely known as ammonia-producing microorganisms and can cause hyperammonemia, leading to cerebral edema and altered consciousness, which represent serious complications in lung transplant recipients. However, there is limited knowledge on the epidemiology and outcomes of infections caused by U. urealyticum, U. parvum, and M. hominis in non-transplant patients with severe pneumonia in the ICU.

methodsPatients with severe pneumonia who underwent clinical metagenomics of bronchoalveolar lavage fluid (BALF) at the intensive care units (ICUs) of 17 medical centers from January 2019 to March 2023 were enrolled. All cases were divided into the positive group and the negative group based on whether U. urealyticum, U. parvum, or M. hominis was detected in lower respiratory tract. The clinical characteristics and outcomes were compared among the groups. The survival analysis after propensity score matching (PSM) was used to evaluate whether the mortality rate of U. urealyticum, U. parvum, and M. hominis positive patients were increased. Multivariate logistic regression was used to evaluate whether these microbials positivity were a risk factor for central nervous system dysfunction.

resultsIn a total number of 1737 patients, 55 patients (3.17%) in the positive group and 1682 patients (96.83%) in the negative group. Patients in the positive group were younger, had a greater proportion of male patients, and had a longer time from ICU admission to clinical metagenomics testing. In contrast, the negative group had a higher proportion of patients with cerebrovascular disease. After PSM, there was no statistically significant difference in 28-day mortality following ICU admission between the two groups (hazard ratio [HR], 0.842; 95% confidence interval [CI], 0.489-1.451; p = 0.536). Multivariate logistic regression analysis showed an association between the detection of U. urealyticum, U. parvum, or M. hominis and neurological dysfunction (odds ratio [OR], 1.84; 95% CI 1.04-3.24; p = 0.035).

conclusionThe detection of U. urealyticum, U. parvum, or M. hominis in the lungs of patients is associated with neurological dysfunction.

Indexed as

LungPneumoniaAgedAmmoniaBronchoalveolar Lavage FluidCohort StudiesFemaleHumansIntensive Care UnitsMaleMiddle AgedRisk FactorsUreaplasmaAmmoniaHyperammonemiaMycoplasma hominisNeurological dysfunctionSevere pneumoniaUreaplasma parvumUreaplasma urealyticum

Identifiers

PMID39725980
PMCPMC11673322

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.