IL-10 combined with procalcitonin improves early prediction of complications of febrile neutropenia in hematological patients

► IL-10 is an early predictor of complicated course of febrile neutropenia. ► Procalcitonin stays elevated for several days in complicated febrile neutropenia. ► Levels of IL-6 and IL-10 normalize more rapidly than that of procalcitonin. ► IL-10 combined with procalcitonin improves early prediction...

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Veröffentlicht in:Cytokine (Philadelphia, Pa.) Pa.), 2012-12, Vol.60 (3), p.787-792
Hauptverfasser: Vänskä, Matti, Koivula, Irma, Jantunen, Esa, Hämäläinen, Sari, Purhonen, Anna-Kaisa, Pulkki, Kari, Juutilainen, Auni
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container_issue 3
container_start_page 787
container_title Cytokine (Philadelphia, Pa.)
container_volume 60
creator Vänskä, Matti
Koivula, Irma
Jantunen, Esa
Hämäläinen, Sari
Purhonen, Anna-Kaisa
Pulkki, Kari
Juutilainen, Auni
description ► IL-10 is an early predictor of complicated course of febrile neutropenia. ► Procalcitonin stays elevated for several days in complicated febrile neutropenia. ► Levels of IL-6 and IL-10 normalize more rapidly than that of procalcitonin. ► IL-10 combined with procalcitonin improves early prediction of complications. Early diagnosis of complicated course in febrile neutropenia is cumbersome due to the non-specificity of clinical and laboratory signs of severe infection. This prospective study included 100 adult hematological patients with febrile neutropenia after intensive chemotherapy at the onset of fever (d0) and for 3days (d1–d3) thereafter. The study aim was to find early predictors for complicated course of febrile neutropenia, defined as bacteremia or septic shock. Interleukin 6 (IL-6), interleukin 10 (IL-10), procalcitonin (PCT) and C-reactive protein (CRP) all predicted complicated course of febrile neutropenia on d0, but only PCT was predictive throughout the study period. For IL-10 on d0–1 with cut-off 37ng/L, sensitivity was 0.71, specificity 0.82, positive predictive value 0.52 and negative predictive value 0.92. For PCT on d0–1 with cut-off 0.13μg/L, the respective measures were 0.95, 0.53, 0.36, and 0.98. For the combination of IL-10 and PCT on d0–1 with the same cut-offs, specificity improved to 0.85 and positive predictive value to 0.56. In conclusion, the present study confirms the high negative predictive value of PCT and provides new evidence for IL-10 as an early predictor for complicated course of febrile neutropenia in hematological patients. Combining IL-10 with PCT improves the early prediction for complicated course of febrile neutropenia.
doi_str_mv 10.1016/j.cyto.2012.07.023
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Early diagnosis of complicated course in febrile neutropenia is cumbersome due to the non-specificity of clinical and laboratory signs of severe infection. This prospective study included 100 adult hematological patients with febrile neutropenia after intensive chemotherapy at the onset of fever (d0) and for 3days (d1–d3) thereafter. The study aim was to find early predictors for complicated course of febrile neutropenia, defined as bacteremia or septic shock. Interleukin 6 (IL-6), interleukin 10 (IL-10), procalcitonin (PCT) and C-reactive protein (CRP) all predicted complicated course of febrile neutropenia on d0, but only PCT was predictive throughout the study period. For IL-10 on d0–1 with cut-off 37ng/L, sensitivity was 0.71, specificity 0.82, positive predictive value 0.52 and negative predictive value 0.92. For PCT on d0–1 with cut-off 0.13μg/L, the respective measures were 0.95, 0.53, 0.36, and 0.98. For the combination of IL-10 and PCT on d0–1 with the same cut-offs, specificity improved to 0.85 and positive predictive value to 0.56. In conclusion, the present study confirms the high negative predictive value of PCT and provides new evidence for IL-10 as an early predictor for complicated course of febrile neutropenia in hematological patients. 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Early diagnosis of complicated course in febrile neutropenia is cumbersome due to the non-specificity of clinical and laboratory signs of severe infection. This prospective study included 100 adult hematological patients with febrile neutropenia after intensive chemotherapy at the onset of fever (d0) and for 3days (d1–d3) thereafter. The study aim was to find early predictors for complicated course of febrile neutropenia, defined as bacteremia or septic shock. Interleukin 6 (IL-6), interleukin 10 (IL-10), procalcitonin (PCT) and C-reactive protein (CRP) all predicted complicated course of febrile neutropenia on d0, but only PCT was predictive throughout the study period. For IL-10 on d0–1 with cut-off 37ng/L, sensitivity was 0.71, specificity 0.82, positive predictive value 0.52 and negative predictive value 0.92. For PCT on d0–1 with cut-off 0.13μg/L, the respective measures were 0.95, 0.53, 0.36, and 0.98. 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Early diagnosis of complicated course in febrile neutropenia is cumbersome due to the non-specificity of clinical and laboratory signs of severe infection. This prospective study included 100 adult hematological patients with febrile neutropenia after intensive chemotherapy at the onset of fever (d0) and for 3days (d1–d3) thereafter. The study aim was to find early predictors for complicated course of febrile neutropenia, defined as bacteremia or septic shock. Interleukin 6 (IL-6), interleukin 10 (IL-10), procalcitonin (PCT) and C-reactive protein (CRP) all predicted complicated course of febrile neutropenia on d0, but only PCT was predictive throughout the study period. For IL-10 on d0–1 with cut-off 37ng/L, sensitivity was 0.71, specificity 0.82, positive predictive value 0.52 and negative predictive value 0.92. For PCT on d0–1 with cut-off 0.13μg/L, the respective measures were 0.95, 0.53, 0.36, and 0.98. For the combination of IL-10 and PCT on d0–1 with the same cut-offs, specificity improved to 0.85 and positive predictive value to 0.56. In conclusion, the present study confirms the high negative predictive value of PCT and provides new evidence for IL-10 as an early predictor for complicated course of febrile neutropenia in hematological patients. Combining IL-10 with PCT improves the early prediction for complicated course of febrile neutropenia.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>22902948</pmid><doi>10.1016/j.cyto.2012.07.023</doi><tpages>6</tpages></addata></record>
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identifier ISSN: 1043-4666
ispartof Cytokine (Philadelphia, Pa.), 2012-12, Vol.60 (3), p.787-792
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Adolescent
Adult
Aged
Bacteremia
Bacteremia - diagnosis
C-reactive protein
C-Reactive Protein - analysis
Calcitonin - blood
Calcitonin - metabolism
Calcitonin Gene-Related Peptide
Chemotherapy
Female
Fever
Fever - etiology
Humans
Infection
Interleukin 10
Interleukin 6
Interleukin-10 - blood
Interleukin-10 - metabolism
Interleukin-6 - blood
Interleukin-6 - metabolism
Leukemia, Myeloid, Acute - therapy
Male
Middle Aged
Neutropenia
Neutropenia - complications
Neutropenia - diagnosis
Neutropenic fever
Procalcitonin
Prognosis
Prospective Studies
Protein Precursors - blood
Protein Precursors - metabolism
Septic shock
Shock, Septic - diagnosis
Stem Cell Transplantation
Transplantation, Autologous
Young Adult
title IL-10 combined with procalcitonin improves early prediction of complications of febrile neutropenia in hematological patients
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