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      Epidemiological and clinical characteristics of immunocompromised patients infected with Pneumocystis jirovecii in a twelve-year retrospective study from Norway

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          Abstract

          Background

          Pneumocystis pneumonia (PCP) severely menaces modern chemotherapy and immunosuppression. Detailed description of the epidemiology of Pneumocystis jirovecii today is needed to identify candidates for PCP-prophylaxis.

          Methods

          We performed a 12-year retrospective study of patients with P. jirovecii detected by polymerase chain reaction in Central Norway. In total, 297 patients were included. Comprehensive biological, clinical and epidemiological data were abstracted from patients’ medical records. Regional incidence rates and testing trends were also assessed.

          Results

          From 2007 to 2017 we found a 3.3-fold increase in testing for P. jirovecii accompanied by a 1.8-fold increase in positive results. Simultaneously, regional incidence rates doubled from 5.0 cases per 100,000 person years to 10.8. A majority of the study population had predisposing conditions other than human immunodeficiency virus (HIV). Hematological (36.0%) and solid cancers (25.3%) dominated. Preceding corticosteroids were a common denominator for 72.1%. Most patients (74.4%) presented with at least two cardinal symptoms; cough, dyspnea or fever. Main clinical findings were hypoxia, cytopenias and radiological features consistent with PCP. A total of 88 (29.6%) patients required intensive care and 121 (40.7%) suffered at least one complication. In-hospital mortality was 21.5%. Three patients (1.0%) had received prophylaxis.

          Conclusions

          P. jirovecii is re-emerging; likely due to increasing immunosuppressants use. This opportunistic pathogen threatens the life of heterogenous non-HIV immunosuppressed populations currently at growth. Corticosteroids seem to be a major risk factor. A strategy to increase prophylaxis is called for.

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s12879-021-06144-1.

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          Most cited references45

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          A new method of classifying prognostic comorbidity in longitudinal studies: Development and validation

          The objective of this study was to develop a prospectively applicable method for classifying comorbid conditions which might alter the risk of mortality for use in longitudinal studies. A weighted index that takes into account the number and the seriousness of comorbid disease was developed in a cohort of 559 medical patients. The 1-yr mortality rates for the different scores were: "0", 12% (181); "1-2", 26% (225); "3-4", 52% (71); and "greater than or equal to 5", 85% (82). The index was tested for its ability to predict risk of death from comorbid disease in the second cohort of 685 patients during a 10-yr follow-up. The percent of patients who died of comorbid disease for the different scores were: "0", 8% (588); "1", 25% (54); "2", 48% (25); "greater than or equal to 3", 59% (18). With each increased level of the comorbidity index, there were stepwise increases in the cumulative mortality attributable to comorbid disease (log rank chi 2 = 165; p less than 0.0001). In this longer follow-up, age was also a predictor of mortality (p less than 0.001). The new index performed similarly to a previous system devised by Kaplan and Feinstein. The method of classifying comorbidity provides a simple, readily applicable and valid method of estimating risk of death from comorbid disease for use in longitudinal studies. Further work in larger populations is still required to refine the approach because the number of patients with any given condition in this study was relatively small.
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            Pneumocystis pneumonia.

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              Colonization by Pneumocystis jirovecii and its role in disease.

              Although the incidence of Pneumocystis pneumonia (PCP) has decreased since the introduction of combination antiretroviral therapy, it remains an important cause of disease in both HIV-infected and non-HIV-infected immunosuppressed populations. The epidemiology of PCP has shifted over the course of the HIV epidemic both from changes in HIV and PCP treatment and prevention and from changes in critical care medicine. Although less common in non-HIV-infected immunosuppressed patients, PCP is now more frequently seen due to the increasing numbers of organ transplants and development of novel immunotherapies. New diagnostic and treatment modalities are under investigation. The immune response is critical in preventing this disease but also results in lung damage, and future work may offer potential areas for vaccine development or immunomodulatory therapy. Colonization with Pneumocystis is an area of increasing clinical and research interest and may be important in development of lung diseases such as chronic obstructive pulmonary disease. In this review, we discuss current clinical and research topics in the study of Pneumocystis and highlight areas for future research.
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                Author and article information

                Contributors
                stine.gronseth@ntnu.no
                Journal
                BMC Infect Dis
                BMC Infect Dis
                BMC Infectious Diseases
                BioMed Central (London )
                1471-2334
                7 July 2021
                7 July 2021
                2021
                : 21
                : 659
                Affiliations
                [1 ]GRID grid.5947.f, ISNI 0000 0001 1516 2393, Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, , NTNU - Norwegian University of Science and Technology, ; NO-7491 Trondheim, Norway
                [2 ]GRID grid.5947.f, ISNI 0000 0001 1516 2393, Department of Circulation and Medical Imaging, , NTNU, ; Trondheim, Norway
                [3 ]GRID grid.52522.32, ISNI 0000 0004 0627 3560, Department of Infectious Diseases, , St. Olavs hospital, Trondheim University Hospital, ; Trondheim, Norway
                [4 ]GRID grid.5947.f, ISNI 0000 0001 1516 2393, K.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, , NTNU, ; Trondheim, Norway
                [5 ]GRID grid.5947.f, ISNI 0000 0001 1516 2393, HUNT Research Center, Department of Public Health and Nursing, , NTNU, ; Levanger, Norway
                [6 ]GRID grid.52522.32, ISNI 0000 0004 0627 3560, Department of Endocrinology, , St. Olavs hospital, Trondheim University Hospital, ; Trondheim, Norway
                [7 ]GRID grid.52522.32, ISNI 0000 0004 0627 3560, Department of Medical Microbiology, , St. Olavs hospital, Trondheim University Hospital, ; Trondheim, Norway
                [8 ]GRID grid.5947.f, ISNI 0000 0001 1516 2393, Centre of Molecular Inflammation Research, , NTNU, ; Trondheim, Norway
                Article
                6144
                10.1186/s12879-021-06144-1
                8262122
                34233631
                508453fe-231c-4044-ad24-3185d1568c70
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 11 January 2021
                : 8 March 2021
                Categories
                Research
                Custom metadata
                © The Author(s) 2021

                Infectious disease & Microbiology
                pneumocystis jirovecii,pcp,pneumonia,immunosuppression,immunocompromised

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