Demirel Aslıhan, Tabak Fehmi, Ar M Cem, Mete Bilgül, Öngören Şeniz, Yemişen Mücahit, Özaras Reşat, Eşkazan Emre, Başlar Zafer, Mert Ali, Soysal Teoman, Ferhanoğlu Burhan, Aydın Yıldız, Öztürk Recep
Turk J Haematol. 2015 Sep;32(3):243-50. doi: 10.4274/tjh.2013.0422.
Febrile neutropenic episodes (FNEs) are among major causes of mortality in patients with hematological malignancies. Secondary infections develop either during the empirical antibiotic therapy or one week after cessation of therapy for a FNE. The aim of the study was to investigate the risk factors associated with secondary infections in febrile neutropenic patients.
We retrospectively analyzed 750 FNEs in 473 patients between January 2000 and December 2006.
Secondary infections were diagnosed in 152 (20%) of 750 FNEs. The median time to develop secondary infection was 10 days (range 2-34 days). The duration of neutropenia over 10 days significantly increased the risk of secondary infections (p<0.001). The proportion of patients with microbiologically documented infections was found to be higher in primary infections (271/750, 36%) compared to secondary infections (43/152, 28%) (p=0.038). Age, sex, underlying disease, antibacterial, antifungal or antiviral prophylaxis, blood transfusion or bone marrow transplantation, central venous catheter or severity of neutropenia did not differ significantly between primary and secondary infections (p>0.05) While fever of unknown origin (FUO) (p=0.005) and catheter-related bacteremia (p<0.001) were less frequently observed in secondary infections, the frequency of microbiologically (p=0.003) and clinically (p<0.001) documented infections, fungal pneumonias (p<0.001), infections related with gram positive bacteria (p=0.04) and fungi (p<0.001) and 30-day mortality rate (p<0.001) were significantly higher in secondary infections (p<0.001).
Secondary infections should be regarded as life-threatening complications of febrile neutropenia. Secondary infections represent a more severe and mortal complication and cannot be regarded just as another febrile neutropenic episode.
发热性中性粒细胞减少症(FNE)是血液系统恶性肿瘤患者死亡的主要原因之一。继发性感染在经验性抗生素治疗期间或FNE治疗停止后一周内发生。本研究的目的是调查发热性中性粒细胞减少患者继发性感染的相关危险因素。
我们回顾性分析了2000年1月至2006年12月期间473例患者的750次FNE。
750次FNE中有152次(20%)被诊断为继发性感染。发生继发性感染的中位时间为10天(范围2 - 34天)。中性粒细胞减少持续超过10天显著增加了继发性感染的风险(p<0.001)。发现微生物学确诊感染的患者比例在原发性感染中(271/750,36%)高于继发性感染(43/152,28%)(p = 0.038)。原发性和继发性感染在年龄、性别、基础疾病、抗菌、抗真菌或抗病毒预防、输血或骨髓移植、中心静脉导管或中性粒细胞减少的严重程度方面无显著差异(p>0.05)。虽然继发性感染中不明原因发热(FUO)(p = 0.005)和导管相关菌血症(p<0.001)的发生率较低,但继发性感染中微生物学确诊(p = 0.003)和临床确诊(p<0.001)感染、真菌性肺炎(p<0.001)、革兰氏阳性菌(p = 0.04)和真菌(p<0.001)相关感染以及30天死亡率(p<0.001)显著更高(p<0.001)。
继发性感染应被视为发热性中性粒细胞减少症危及生命的并发症。继发性感染是一种更严重且致命的并发症,不能仅仅被视为另一次发热性中性粒细胞减少发作。