动力学和胰腺石蛋白和中区域肾上腺髓质素作为血液学恶性肿瘤患儿败血症和菌血症的预测因子。

Vasiliki Antari, Lemonia Skoura, Athanasios Tragiannidis, Emmanuel Hatzipantelis, Vasiliki-Regina Tsinopoulou, Konstantina Papakonstantinou, Efthimia Protonotariou, Assimina Galli-Tsinopoulou
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 Material and methods: We evaluated prospectively a total of 70 FN episodes in 70 children with acute leukemias and lymphomas. Levels of CRP, PSP and MR-proADM were measured at the onset of the febrile episode (day 1), on day 3 and on day 7. The outcome and survival of children were evaluated during the study period until day 28. The performance of each marker in identifying sepsis or severe sepsis was assessed as area under a receiver operating characteristic (ROC) curve. For each biomarker, ROC curves were used to derive cut-offs for sensitivity and specificity in distinguishing sepsis from non-sepsis.
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引用次数: 0

摘要

背景:探讨血液恶性肿瘤患儿发热性中性粒细胞减少症(FN)发作时胰石蛋白(PSP)和中期肾上腺髓质素原(MR-proADM)的动力学和预后价值。材料和方法:我们对70例急性白血病和淋巴瘤患儿共70例FN发作进行前瞻性评估。在发热发作开始时(第1天)、第3天和第7天测量CRP、PSP和MR-proADM水平。在研究期间直至第28天,对儿童的预后和生存进行评估。每个标志物在识别脓毒症或严重脓毒症方面的表现以受试者工作特征(ROC)曲线下的面积来评估。对于每种生物标志物,ROC曲线用于得出区分脓毒症与非脓毒症的敏感性和特异性的截止值。 结果:在2年的研究期间,70例血液学恶性肿瘤患儿的70例发热性中性粒细胞减少发作被纳入研究。在70例发热性中性粒细胞减少症中,17例(24%)记录有细菌/真菌感染。31例(44%)患者符合脓毒症标准,7例(10%)患者入PICU。所有生物标志物的中位值在第1天较高,并且在脓毒症患者和非脓毒症患者之间存在显著差异。PSP、MR-proADM、CRP特异性分别为0.82、0.70、0.57。PSP、MR-proADM、CRP的敏感性分别为0.84、0.74、0.88。 结论:PSP和MR-proADM都是早期诊断血液学恶性肿瘤患儿FN发作时败血症的有希望的生物标志物。PSP具有较高的敏感性和特异性。
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KINETICS AND ROLE OF PANCREATIC STONE PROTEIN AND MIDREGIONAL PROADRENOMEDULLIN AS PREDICTORS OF SEPSIS AND BACTEREMIA IN CHILDREN WITH HAEMATOLOGICAL MALIGNANCIES.
Background: To investigate the kinetics and prognostic value of pancreatic stone protein (PSP) and mid-regional proadrenomedullin (MR-proADM) during episodes of febrile neutropenia (FN) in children with haematological malignancies. Material and methods: We evaluated prospectively a total of 70 FN episodes in 70 children with acute leukemias and lymphomas. Levels of CRP, PSP and MR-proADM were measured at the onset of the febrile episode (day 1), on day 3 and on day 7. The outcome and survival of children were evaluated during the study period until day 28. The performance of each marker in identifying sepsis or severe sepsis was assessed as area under a receiver operating characteristic (ROC) curve. For each biomarker, ROC curves were used to derive cut-offs for sensitivity and specificity in distinguishing sepsis from non-sepsis. Results: During the 2-year study period, 70 febrile neutropenia episodes in 70 children with haematological malignancies were enrolled. Of 70 episodes of febrile neutropenia, in 17 (24%) a bacterial/fungal infection was documented. Criteria for sepsis were fulfilled for 31 (44%) and 7 (10%) patients were admitted to PICU. The median values of all biomarkers were higher on day 1 and differed significantly between patients with and without sepsis. The specificity of PSP, MR-proADM, and CRP were 0.82, 0.70, and 0.57, respectively. The sensitivity of PSP, MR-proADM and CRP were 0.84, 0.74, and 0.88, respectively. Conclusions: Both PSP and MR-proADM are promising biomarkers for early diagnosis of sepsis during FN episodes in children with haematological malignancies. PSP has the higher sensitivity and specificity.
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来源期刊
CiteScore
4.20
自引率
6.20%
发文量
113
审稿时长
12 weeks
期刊介绍: Reciprocal interdependence between infectious and hematologic diseases (malignant and non-malignant) is well known. This relationship is particularly evident in Mediterranean countries. Parasitosis as Malaria, Leishmaniosis, B Hookworms, Teniasis, very common in the southeast Mediterranean area, infect about a billion people and manifest prevalently with anemia so that they are usually diagnosed mostly by experienced hematologist on blood or bone marrow smear. On the other hand, infections are also a significant problem in patients affected by hematological malignancies. The blood is the primary vector of HIV infection, which otherwise manifest with symptoms related to a reduction in T lymphocytes. In turn, infections can favor the insurgency of hematological malignancies. The causative relationship between Epstein-Barr virus infection, Helicobacter pylori, hepatitis C virus, HIV and lymphoproliferative diseases is well known.
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