Procalcitonin levels in plasma in oncohaematologic patients with and without bacterial infections

被引:15
作者
Ciaccio, M
Fugardi, G
Titone, L
Romano, A
Giordano, S
Bivona, G
Scarlata, F
Vocca, L
Di Gangi, M
机构
[1] Univ Palermo, Fac Med, Inst Infect Pathol & Virol, I-90127 Palermo, Italy
[2] Univ Palermo, Fac Med, Inst Pediat, I-90127 Palermo, Italy
[3] Univ Palermo, Fac Med, Chair Clin Biochem, I-90127 Palermo, Italy
关键词
procalcitonin; marker; infection;
D O I
10.1016/j.cccn.2003.10.014
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 [基础医学];
摘要
Background: The flogosis markers currently in use show both low sensitivity and specificity, particularly in neoplastic and degenerative diseases. Procalcitonin (PCT) is a pro-peptide of calcitonin produced mainly but not only in the C-cells of the thyroid glands and, as several studies show, PCT levels in plasma increase during infections. Bacterial infections are also the main cause of death in oncological patients. Furthermore, in patients with leukaemia in chemotherapy recovery, infections often induce relapses. The aim of the present study is to detect PCT levels in plasma in oncohaematologic patients with and without infections. Methods: The study was carried out on 54 patients by a quantitative automated immunoassay. Results: PCT plasma levels greater than or equal to0.5 ng were detected in 27 out of 30 patients (90,0%) with bacterial infections; 8 out of 9 patients (88,9%) with viral infections and in 12 out of 15 patients in the control group without statistically significant differences. Conclusions: The results, which differ from those in the literature, are discussed. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:149 / 152
页数:4
相关论文
共 18 条
[1]
HIGH SERUM PROCALCITONIN CONCENTRATIONS IN PATIENTS WITH SEPSIS AND INFECTION [J].
ASSICOT, M ;
GENDREL, D ;
CARSIN, H ;
RAYMOND, J ;
GUILBAUD, J ;
BOHUON, C .
LANCET, 1993, 341 (8844) :515-518
[2]
CALCITONIN-GENE EXPRESSION IN NORMAL HUMAN LIVER [J].
BRACQ, S ;
MACHAIRAS, M ;
CLEMENT, B ;
PIDOUX, E ;
ANDREOLETTI, M ;
MOUKHTAR, MS ;
JULLIENNE, A .
FEBS LETTERS, 1993, 331 (1-2) :15-18
[3]
Brunkhorst FM, 2000, INTENS CARE MED, V26, pS148, DOI 10.1007/BF02900728
[4]
Procalcitonin for discrimination between activity of systemic autoimmune disease and systemic bacterial infection [J].
Brunkhorst, R ;
Eberhardt, OK ;
Haubitz, M ;
Brunkhorst, FM .
INTENSIVE CARE MEDICINE, 2000, 26 :S199-S201
[5]
Di Filippo A, 2002, Minerva Chir, V57, P59
[6]
Alveolar and serum procalcitonin - Diagnostic and prognostic value in ventilator-associated pneumonia [J].
Duflo, F ;
Debon, R ;
Monneret, G ;
Bienvenu, J ;
Chassard, D ;
Allaouchiche, B .
ANESTHESIOLOGY, 2002, 96 (01) :74-79
[7]
Procalcitonin - a sensitive inflammation marker of febrile episodes in neutropenic children with cancer [J].
Fleischhack, G ;
Cipic, D ;
Juettner, J ;
Hasan, C ;
Bode, U .
INTENSIVE CARE MEDICINE, 2000, 26 :S202-S211
[8]
Procalcitonin as a marker of bacterial infection [J].
Gendrel, D ;
Bohuon, C .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2000, 19 (08) :679-688
[9]
Postnatal increase of procalcitonin in premature newborns is enhanced by chorioamnionitis and neonatal sepsis [J].
Janota, J ;
Stranák, Z ;
Belohlávková, S ;
Mudra, K ;
Simák, J .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2001, 31 (11) :978-983
[10]
Martinot M, 2001, PRESSE MED, V30, P1091