Mortality and admission to intensive care units after febrile neutropenia in patients with cancer

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Mortality and admission to intensive care units after febrile neutropenia in patients with cancer. / Aagaard, Theis; Reekie, Joanne; Jørgensen, Mette; Roen, Ashley; Daugaard, Gedske; Specht, Lena; Sengeløv, Henrik; Mocroft, Amanda; Lundgren, Jens; Helleberg, Marie.

I: Cancer Medicine, Bind 9, Nr. 9, 05.2020, s. 3033-3042.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Aagaard, T, Reekie, J, Jørgensen, M, Roen, A, Daugaard, G, Specht, L, Sengeløv, H, Mocroft, A, Lundgren, J & Helleberg, M 2020, 'Mortality and admission to intensive care units after febrile neutropenia in patients with cancer', Cancer Medicine, bind 9, nr. 9, s. 3033-3042. https://doi.org/10.1002/cam4.2955

APA

Aagaard, T., Reekie, J., Jørgensen, M., Roen, A., Daugaard, G., Specht, L., Sengeløv, H., Mocroft, A., Lundgren, J., & Helleberg, M. (2020). Mortality and admission to intensive care units after febrile neutropenia in patients with cancer. Cancer Medicine, 9(9), 3033-3042. https://doi.org/10.1002/cam4.2955

Vancouver

Aagaard T, Reekie J, Jørgensen M, Roen A, Daugaard G, Specht L o.a. Mortality and admission to intensive care units after febrile neutropenia in patients with cancer. Cancer Medicine. 2020 maj;9(9):3033-3042. https://doi.org/10.1002/cam4.2955

Author

Aagaard, Theis ; Reekie, Joanne ; Jørgensen, Mette ; Roen, Ashley ; Daugaard, Gedske ; Specht, Lena ; Sengeløv, Henrik ; Mocroft, Amanda ; Lundgren, Jens ; Helleberg, Marie. / Mortality and admission to intensive care units after febrile neutropenia in patients with cancer. I: Cancer Medicine. 2020 ; Bind 9, Nr. 9. s. 3033-3042.

Bibtex

@article{a5301de2e0f14011b001325d922931d7,
title = "Mortality and admission to intensive care units after febrile neutropenia in patients with cancer",
abstract = "Febrile neutropenia (FN) is a critical complication of chemotherapy associated with increased in-hospital mortality. However, associations with increased mortality and intensive care unit (ICU) admissions during longer follow-up are not established. Patients treated with standard first-line chemotherapy for solid cancers at Rigshospitalet, Denmark in 2010-2016 were included. Incidence rate ratios (IRR) of all-cause, infectious and cardiovascular mortality, and ICU admissions after FN were analyzed by Poisson regression. Risk factors at the time of FN were analyzed in the subpopulation of patients with FN; all-cause mortality was further stratified by the time periods 0-30, 31-365, and 366+ days after FN. We included 9018 patients with gastric (14.4%) and breast (13.1%) cancer being the most common, 51.2% had locally advanced or disseminated disease and the patients had a median Charlson Comorbidity Index score of 0 (interquartile range, 0-0). During follow-up, 845 (9.4%) experienced FN and 4483 (49.7%) died during 18 775 person-years of follow-up. After adjustment, FN was associated with increased risk of all-cause mortality, infectious mortality, and ICU admissions with IRRs of 1.39 (95% CI, 1.24-1.56), 1.94 (95% CI, 1.43-2.62), and 2.28 (95% CI, 1.60-3.24). Among those with FN, having a positive blood culture and low lymphocytes were associated with excess risk of death and ICU admissions (predominantly the first 30 days after FN), while elevated C-reactive protein and low hemoglobin predicted mortality the first year after FN. The risk of death varied according to the time since FN; adjusted IRR per additional risk factor present for the time periods 0-30, 31-365, and 366+ days after FN were 2.00 (95% CI, 1.45-2.75), 1.36 (95% CI, 1.17-1.57), and 1.17 (95% CI, 0.98-1.41). FN was associated with increased mortality and risk of ICU admissions. An objectively identifiable subgroup of patients among those with FN carried this excess risk.",
author = "Theis Aagaard and Joanne Reekie and Mette J{\o}rgensen and Ashley Roen and Gedske Daugaard and Lena Specht and Henrik Sengel{\o}v and Amanda Mocroft and Jens Lundgren and Marie Helleberg",
note = "{\textcopyright} 2020 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.",
year = "2020",
month = may,
doi = "10.1002/cam4.2955",
language = "English",
volume = "9",
pages = "3033--3042",
journal = "Cancer Medicine",
issn = "2045-7634",
publisher = "JohnWiley & Sons Ltd",
number = "9",

}

RIS

TY - JOUR

T1 - Mortality and admission to intensive care units after febrile neutropenia in patients with cancer

AU - Aagaard, Theis

AU - Reekie, Joanne

AU - Jørgensen, Mette

AU - Roen, Ashley

AU - Daugaard, Gedske

AU - Specht, Lena

AU - Sengeløv, Henrik

AU - Mocroft, Amanda

AU - Lundgren, Jens

AU - Helleberg, Marie

N1 - © 2020 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

PY - 2020/5

Y1 - 2020/5

N2 - Febrile neutropenia (FN) is a critical complication of chemotherapy associated with increased in-hospital mortality. However, associations with increased mortality and intensive care unit (ICU) admissions during longer follow-up are not established. Patients treated with standard first-line chemotherapy for solid cancers at Rigshospitalet, Denmark in 2010-2016 were included. Incidence rate ratios (IRR) of all-cause, infectious and cardiovascular mortality, and ICU admissions after FN were analyzed by Poisson regression. Risk factors at the time of FN were analyzed in the subpopulation of patients with FN; all-cause mortality was further stratified by the time periods 0-30, 31-365, and 366+ days after FN. We included 9018 patients with gastric (14.4%) and breast (13.1%) cancer being the most common, 51.2% had locally advanced or disseminated disease and the patients had a median Charlson Comorbidity Index score of 0 (interquartile range, 0-0). During follow-up, 845 (9.4%) experienced FN and 4483 (49.7%) died during 18 775 person-years of follow-up. After adjustment, FN was associated with increased risk of all-cause mortality, infectious mortality, and ICU admissions with IRRs of 1.39 (95% CI, 1.24-1.56), 1.94 (95% CI, 1.43-2.62), and 2.28 (95% CI, 1.60-3.24). Among those with FN, having a positive blood culture and low lymphocytes were associated with excess risk of death and ICU admissions (predominantly the first 30 days after FN), while elevated C-reactive protein and low hemoglobin predicted mortality the first year after FN. The risk of death varied according to the time since FN; adjusted IRR per additional risk factor present for the time periods 0-30, 31-365, and 366+ days after FN were 2.00 (95% CI, 1.45-2.75), 1.36 (95% CI, 1.17-1.57), and 1.17 (95% CI, 0.98-1.41). FN was associated with increased mortality and risk of ICU admissions. An objectively identifiable subgroup of patients among those with FN carried this excess risk.

AB - Febrile neutropenia (FN) is a critical complication of chemotherapy associated with increased in-hospital mortality. However, associations with increased mortality and intensive care unit (ICU) admissions during longer follow-up are not established. Patients treated with standard first-line chemotherapy for solid cancers at Rigshospitalet, Denmark in 2010-2016 were included. Incidence rate ratios (IRR) of all-cause, infectious and cardiovascular mortality, and ICU admissions after FN were analyzed by Poisson regression. Risk factors at the time of FN were analyzed in the subpopulation of patients with FN; all-cause mortality was further stratified by the time periods 0-30, 31-365, and 366+ days after FN. We included 9018 patients with gastric (14.4%) and breast (13.1%) cancer being the most common, 51.2% had locally advanced or disseminated disease and the patients had a median Charlson Comorbidity Index score of 0 (interquartile range, 0-0). During follow-up, 845 (9.4%) experienced FN and 4483 (49.7%) died during 18 775 person-years of follow-up. After adjustment, FN was associated with increased risk of all-cause mortality, infectious mortality, and ICU admissions with IRRs of 1.39 (95% CI, 1.24-1.56), 1.94 (95% CI, 1.43-2.62), and 2.28 (95% CI, 1.60-3.24). Among those with FN, having a positive blood culture and low lymphocytes were associated with excess risk of death and ICU admissions (predominantly the first 30 days after FN), while elevated C-reactive protein and low hemoglobin predicted mortality the first year after FN. The risk of death varied according to the time since FN; adjusted IRR per additional risk factor present for the time periods 0-30, 31-365, and 366+ days after FN were 2.00 (95% CI, 1.45-2.75), 1.36 (95% CI, 1.17-1.57), and 1.17 (95% CI, 0.98-1.41). FN was associated with increased mortality and risk of ICU admissions. An objectively identifiable subgroup of patients among those with FN carried this excess risk.

U2 - 10.1002/cam4.2955

DO - 10.1002/cam4.2955

M3 - Journal article

C2 - 32144897

VL - 9

SP - 3033

EP - 3042

JO - Cancer Medicine

JF - Cancer Medicine

SN - 2045-7634

IS - 9

ER -

ID: 251643318