Evidence map›Paper›PMID 28583135›Full record

ArticleBMC infectious diseases2017

Outcomes and prognostic factors of non-HIV patients with pneumocystis jirovecii pneumonia and pulmonary CMV co-infection: A Retrospective Cohort Study.

Qing Yu, Peng Jia, Li Su, Hong Zhao, Chengli Que

Abstract read
In one paragraph

Article in BMC infectious diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 2 pooled it
–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

40 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Risk Factors of Mortality FromFrontiers in public health · 2021
    Pooled it
  3. Outcomes of concomitantAnnals of medicine · 2026
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  6. Clinical characteristics ofFrontiers in cellular and infection microbiology · 2026
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  7. Article
  8. iScience · 2025
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  14. Frontiers in medicine · 2024
    Article
  15. Article
  16. Article
  17. Article
  18. Pathogens (Basel, Switzerland) · 2023
    Review
  19. Machine Learning Models for Prediction of SevereDiagnostics (Basel, Switzerland) · 2023
    Article
  20. Article
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

5 authors.

Qing YuDepartment of Respiratory and Critical Care Medicine, Peking University First Hospital, Beijing, 100034, China.
Peng JiaDepartment of Respiratory and Critical Care Medicine, Peking University First Hospital, Beijing, 100034, China.
Li SuDepartment of Respiratory and Critical Care Medicine, Peking University First Hospital, Beijing, 100034, China.
Hong ZhaoDepartment of Infectious Disease, Peking University First Hospital, Beijing, 100034, China.
Chengli QueDepartment of Respiratory and Critical Care Medicine, Peking University First Hospital, Beijing, 100034, China. quechengli@bjmu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPneumocystis jirovecii pneumonia (PJP) and pulmonary cytomegalovirus (CMV) infection are common opportunistic infections among immunocompromised patients. However, few studies have evaluated their co-infection, especially among non-HIV patients. Therefore, we aimed to evaluate the outcomes and prognostic factors among non-HIV patients with PJP according to their CMV infection status.

methodsThis retrospective study evaluated non-HIV patients who were diagnosed with PJP between January 2009 and January2016.The patients were classified and compared according to their pulmonary CMV infection status (positive infection: bronchoalveolar lavage fluid [BALF] CMV DNA loads of >500copies/mL).

resultsAmong 70 non-HIV patients with PJP, we identified 38 patients (54.3%) with pulmonary CMV infection. There was no significant difference in the mortality rates for the two groups (p = 0.15). Pulmonary CMV infection was significantly more common among patients who were receiving glucocorticoids and immunosuppressants, compared to corticosteroids only (p = 0.02). Pulmonary CMV infection was also significantly associated with severe dyspnea, a lower PaO

conclusionsCombined therapy using corticosteroids and other immunosuppressants may be a risk factor for pulmonary CMV co-infection among patients with PJP. In addition, CMV pneumonia should be considered when centrilobular nodules and/or severe hypoxemia are observed in non-HIV patients with PJP. Furthermore, antiviral treatment should be promptly initiated for patients with a high CMV DNA load in BALF, based on their poor prognosis.

Indexed as

AdultAgedAntiviral AgentsBronchoalveolar Lavage FluidCoinfectionCytomegalovirus InfectionsFemaleGlucocorticoidsHIV InfectionsHumansImmunocompromised HostImmunosuppressive AgentsMaleMiddle AgedPneumocystis cariniiPneumonia, PneumocystisAntiviral AgentsGlucocorticoidsImmunosuppressive AgentsCMVDNA loadCytomegalovirusPneumocystis jiroveciipneumoniaPrognosis

Identifiers

PMID28583135
PMCPMC5460484

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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.