Clinical course, treatment and outcome of Pneumocystis pneumonia in immunocompromised adults: a retrospective analysis over 17 years

Standard

Clinical course, treatment and outcome of Pneumocystis pneumonia in immunocompromised adults: a retrospective analysis over 17 years. / Schmidt, Julius J; Lueck, Catherina; Ziesing, Stefan; Stoll, Matthias; Haller, Hermann; Gottlieb, Jens; Eder, Matthias; Welte, Tobias; Hoeper, Marius M; Scherag, André; David, Sascha.

in: CRIT CARE, Jahrgang 22, Nr. 1, 19.11.2018, S. 307.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Schmidt, JJ, Lueck, C, Ziesing, S, Stoll, M, Haller, H, Gottlieb, J, Eder, M, Welte, T, Hoeper, MM, Scherag, A & David, S 2018, 'Clinical course, treatment and outcome of Pneumocystis pneumonia in immunocompromised adults: a retrospective analysis over 17 years', CRIT CARE, Jg. 22, Nr. 1, S. 307. https://doi.org/10.1186/s13054-018-2221-8

APA

Schmidt, J. J., Lueck, C., Ziesing, S., Stoll, M., Haller, H., Gottlieb, J., Eder, M., Welte, T., Hoeper, M. M., Scherag, A., & David, S. (2018). Clinical course, treatment and outcome of Pneumocystis pneumonia in immunocompromised adults: a retrospective analysis over 17 years. CRIT CARE, 22(1), 307. https://doi.org/10.1186/s13054-018-2221-8

Vancouver

Bibtex

@article{41ec9200b29d49f0b8d86224c6e43a9e,
title = "Clinical course, treatment and outcome of Pneumocystis pneumonia in immunocompromised adults: a retrospective analysis over 17 years",
abstract = "BACKGROUND: Despite modern intensive care with standardized strategies against acute respiratory distress syndrome (ARDS), Pneumocystis pneumonia (PcP) remains a life-threatening disease with a high mortality rate. Here, we analyzed a large mixed cohort of immunocompromised patients with PcP, with regard to clinical course and treatment, and aimed at identifying predictors of outcome.METHODS: This was a single-center retrospective analysis in a tertiary care institution across 17 years. Diagnosis of PcP required typical clinical features and microbiological confirmation of Pneumocystis jirovecii. Epidemiological, clinical, laboratory and outcome data were collected from patient records.RESULTS: A total of 52,364 specimens from 7504 patients were sent for microbiological assessment (3653 with clinical suspicion of Pneumocystis pneumonia). PcP was confirmed in 240 patients, about half of them HIV positive (52%). The remaining subjects were either solid organ transplant recipients (16.3%) or suffered from malignancy (15.8%) or autoimmune diseases (11.7%). Of note, 95% of patients with PcP were not receiving chemoprophylaxis. Overall in-hospital mortality was 25.4%, increasing to 58% if ICU admission was required. Multivariable regression identified lactate dehydrogenase (LDH) as predictor of in-hospital mortality (adjusted OR 1.17 (95% CI 1.09-1.27), p < 0.0001). Mortality in LDH quartiles increased from 8% to 49%, and a cutoff value of 495 U/L predicted mortality with sensitivity and specificity of 70%. With regard to treatment, 40% of patients received trimethoprim-sulfamethoxazole at doses that were lower than recommended, and these patients had a higher mortality risk (HR 1.80 (95% CI 1.10-3.44), p = 0.02).CONCLUSIONS: PcP remains a life-threatening disease among immunocompromised patients. About half of patients with PcP do not have HIV infection. Initial LDH values might serve as a stratifying tool to identify those patients at high risk of death among patients with HIV and without HIV infection.",
keywords = "Adult, Area Under Curve, Cohort Studies, Female, HIV Infections/complications, Hospital Mortality, Humans, Immunocompromised Host, Kaplan-Meier Estimate, Male, Middle Aged, Odds Ratio, Pneumocystis carinii/pathogenicity, Pneumonia, Pneumocystis/complications, Proportional Hazards Models, ROC Curve, Regression Analysis, Retrospective Studies, Treatment Outcome",
author = "Schmidt, {Julius J} and Catherina Lueck and Stefan Ziesing and Matthias Stoll and Hermann Haller and Jens Gottlieb and Matthias Eder and Tobias Welte and Hoeper, {Marius M} and Andr{\'e} Scherag and Sascha David",
year = "2018",
month = nov,
day = "19",
doi = "10.1186/s13054-018-2221-8",
language = "English",
volume = "22",
pages = "307",
journal = "CRIT CARE",
issn = "1364-8535",
publisher = "Springer Science + Business Media",
number = "1",

}

RIS

TY - JOUR

T1 - Clinical course, treatment and outcome of Pneumocystis pneumonia in immunocompromised adults: a retrospective analysis over 17 years

AU - Schmidt, Julius J

AU - Lueck, Catherina

AU - Ziesing, Stefan

AU - Stoll, Matthias

AU - Haller, Hermann

AU - Gottlieb, Jens

AU - Eder, Matthias

AU - Welte, Tobias

AU - Hoeper, Marius M

AU - Scherag, André

AU - David, Sascha

PY - 2018/11/19

Y1 - 2018/11/19

N2 - BACKGROUND: Despite modern intensive care with standardized strategies against acute respiratory distress syndrome (ARDS), Pneumocystis pneumonia (PcP) remains a life-threatening disease with a high mortality rate. Here, we analyzed a large mixed cohort of immunocompromised patients with PcP, with regard to clinical course and treatment, and aimed at identifying predictors of outcome.METHODS: This was a single-center retrospective analysis in a tertiary care institution across 17 years. Diagnosis of PcP required typical clinical features and microbiological confirmation of Pneumocystis jirovecii. Epidemiological, clinical, laboratory and outcome data were collected from patient records.RESULTS: A total of 52,364 specimens from 7504 patients were sent for microbiological assessment (3653 with clinical suspicion of Pneumocystis pneumonia). PcP was confirmed in 240 patients, about half of them HIV positive (52%). The remaining subjects were either solid organ transplant recipients (16.3%) or suffered from malignancy (15.8%) or autoimmune diseases (11.7%). Of note, 95% of patients with PcP were not receiving chemoprophylaxis. Overall in-hospital mortality was 25.4%, increasing to 58% if ICU admission was required. Multivariable regression identified lactate dehydrogenase (LDH) as predictor of in-hospital mortality (adjusted OR 1.17 (95% CI 1.09-1.27), p < 0.0001). Mortality in LDH quartiles increased from 8% to 49%, and a cutoff value of 495 U/L predicted mortality with sensitivity and specificity of 70%. With regard to treatment, 40% of patients received trimethoprim-sulfamethoxazole at doses that were lower than recommended, and these patients had a higher mortality risk (HR 1.80 (95% CI 1.10-3.44), p = 0.02).CONCLUSIONS: PcP remains a life-threatening disease among immunocompromised patients. About half of patients with PcP do not have HIV infection. Initial LDH values might serve as a stratifying tool to identify those patients at high risk of death among patients with HIV and without HIV infection.

AB - BACKGROUND: Despite modern intensive care with standardized strategies against acute respiratory distress syndrome (ARDS), Pneumocystis pneumonia (PcP) remains a life-threatening disease with a high mortality rate. Here, we analyzed a large mixed cohort of immunocompromised patients with PcP, with regard to clinical course and treatment, and aimed at identifying predictors of outcome.METHODS: This was a single-center retrospective analysis in a tertiary care institution across 17 years. Diagnosis of PcP required typical clinical features and microbiological confirmation of Pneumocystis jirovecii. Epidemiological, clinical, laboratory and outcome data were collected from patient records.RESULTS: A total of 52,364 specimens from 7504 patients were sent for microbiological assessment (3653 with clinical suspicion of Pneumocystis pneumonia). PcP was confirmed in 240 patients, about half of them HIV positive (52%). The remaining subjects were either solid organ transplant recipients (16.3%) or suffered from malignancy (15.8%) or autoimmune diseases (11.7%). Of note, 95% of patients with PcP were not receiving chemoprophylaxis. Overall in-hospital mortality was 25.4%, increasing to 58% if ICU admission was required. Multivariable regression identified lactate dehydrogenase (LDH) as predictor of in-hospital mortality (adjusted OR 1.17 (95% CI 1.09-1.27), p < 0.0001). Mortality in LDH quartiles increased from 8% to 49%, and a cutoff value of 495 U/L predicted mortality with sensitivity and specificity of 70%. With regard to treatment, 40% of patients received trimethoprim-sulfamethoxazole at doses that were lower than recommended, and these patients had a higher mortality risk (HR 1.80 (95% CI 1.10-3.44), p = 0.02).CONCLUSIONS: PcP remains a life-threatening disease among immunocompromised patients. About half of patients with PcP do not have HIV infection. Initial LDH values might serve as a stratifying tool to identify those patients at high risk of death among patients with HIV and without HIV infection.

KW - Adult

KW - Area Under Curve

KW - Cohort Studies

KW - Female

KW - HIV Infections/complications

KW - Hospital Mortality

KW - Humans

KW - Immunocompromised Host

KW - Kaplan-Meier Estimate

KW - Male

KW - Middle Aged

KW - Odds Ratio

KW - Pneumocystis carinii/pathogenicity

KW - Pneumonia, Pneumocystis/complications

KW - Proportional Hazards Models

KW - ROC Curve

KW - Regression Analysis

KW - Retrospective Studies

KW - Treatment Outcome

U2 - 10.1186/s13054-018-2221-8

DO - 10.1186/s13054-018-2221-8

M3 - SCORING: Journal article

C2 - 30454031

VL - 22

SP - 307

JO - CRIT CARE

JF - CRIT CARE

SN - 1364-8535

IS - 1

ER -