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Outcomes and prognostic factors of non-HIV patients with pneumocystis jirovecii pneumonia and pulmonary CMV co-infection: A Retrospective Cohort Study.
- Source :
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BMC infectious diseases [BMC Infect Dis] 2017 Jun 05; Vol. 17 (1), pp. 392. Date of Electronic Publication: 2017 Jun 05. - Publication Year :
- 2017
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Abstract
- Background: Pneumocystis 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.<br />Methods: This 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).<br />Results: Among 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 <subscript>2</subscript> /FiO <subscript>2</subscript> , and the presence of centrilobular nodules (p = 0.008). Higher CMV DNA loads in the BALF were positively associated with mortality (p = 0.012).<br />Conclusions: Combined 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.
- Subjects :
- Adult
Aged
Antiviral Agents therapeutic use
Bronchoalveolar Lavage Fluid virology
Coinfection drug therapy
Coinfection mortality
Cytomegalovirus Infections mortality
Female
Glucocorticoids therapeutic use
HIV Infections
Humans
Immunocompromised Host
Immunosuppressive Agents adverse effects
Male
Middle Aged
Pneumocystis carinii pathogenicity
Pneumonia, Pneumocystis mortality
Prognosis
Retrospective Studies
Risk Factors
Treatment Outcome
Cytomegalovirus Infections drug therapy
Cytomegalovirus Infections virology
Immunosuppressive Agents therapeutic use
Pneumonia, Pneumocystis drug therapy
Pneumonia, Pneumocystis virology
Subjects
Details
- Language :
- English
- ISSN :
- 1471-2334
- Volume :
- 17
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- BMC infectious diseases
- Publication Type :
- Academic Journal
- Accession number :
- 28583135
- Full Text :
- https://doi.org/10.1186/s12879-017-2492-8