Pagano L, Antinori A, Ammassari A, Mele L, Nosari A, Melillo L, Martino B, Sanguinetti M, Equitani F, Nobile F, Carotenuto M, Morra E, Morace G, Leone G
Istituto di Semeiotica Medica, Università Cattolica Sacro Cuore, Rome, Italy.
Eur J Haematol. 1999 Aug;63(2):77-85. doi: 10.1111/j.1600-0609.1999.tb01120.x.
A retrospective study of 76 episodes of candidemia in 73 patients with underlying hematological malignancy, from 1988 until 1997, has been conducted to evaluate the clinical characteristics and to ascertain the variables related to the onset and the outcome of candidemia. The most frequent malignancy was acute myeloid leukemia (29 episodes). Candidemia developed mainly during aplasia in patients refractory to chemotherapy (42%). In 65 episodes (86%) the patients were neutropenic (ANC <1 x 10(9)/l) before the candidemia diagnosis for a median time of 13 d, and in 53 episodes (70%) at microbiological diagnosis of candidemia ANC was <1 x 10(9)/l. Candida albicans was the most frequently isolated etiologic agent (31 episodes), but C. non-albicans species sustained the majority of candidemia. Seventeen candidemias developed during azoles prophylaxis. One month after the diagnosis of candidemia, 26 patients died. In 19 cases, death was attributable to candidemia. The case-control study demonstrated, at univariate analysis, that the colonization with Candida. spp. (p=0.004), antimycotic prophylaxis (p=0.01), presence of central venous catheter (p=0.01), neutropenia (p=0.002), and the use of glycopeptide (p=0.0001) increased the risk of candidemia. Using multivariate regression analysis only colonization with Candida spp. and the previous therapy with glycopeptide were associated with a significantly increased risk. Acute mortality, expressed by a cumulative probability of survival at 30 d from diagnosis of candidemia, was 0.67 (95% C.I. 0.55-0.77) and was significantly reduced in patients with neutrophils <1 x 10(9)/l when compared to those with neutrophils >1 x 10(9)/l (p at Mantel-Cox=0.029). Overall cumulative probability of survival at 1 yr was 0.38 (95% C.I. 0.27-0.49) and only the treatment with Amfotericin B significantly reduced the risk of death.
对1988年至1997年间73例患有潜在血液系统恶性肿瘤的患者发生的76次念珠菌血症发作进行了一项回顾性研究,以评估其临床特征,并确定与念珠菌血症的发生及转归相关的变量。最常见的恶性肿瘤是急性髓系白血病(29次发作)。念珠菌血症主要发生在化疗难治性患者的再生障碍期(42%)。在65次发作(86%)中,患者在念珠菌血症诊断前中性粒细胞减少(中性粒细胞绝对值<1×10⁹/L),中位时间为13天,在53次发作(70%)中,在念珠菌血症微生物学诊断时中性粒细胞绝对值<1×10⁹/L。白色念珠菌是最常分离出的病原体(31次发作),但非白色念珠菌属导致了大多数念珠菌血症。17次念珠菌血症发生在唑类预防期间。念珠菌血症诊断后1个月,26例患者死亡。在19例中,死亡归因于念珠菌血症。病例对照研究在单因素分析中表明,念珠菌属定植(p=0.004)、抗真菌预防(p=0.01)、中心静脉导管的存在(p=0.01)、中性粒细胞减少(p=0.002)以及糖肽的使用(p=0.0001)增加了念珠菌血症的风险。使用多因素回归分析,只有念珠菌属定植和先前使用糖肽治疗与风险显著增加相关。从念珠菌血症诊断起30天的累积生存概率表示的急性死亡率为0.67(95%置信区间0.55-0.77),与中性粒细胞绝对值>1×10⁹/L的患者相比,中性粒细胞绝对值<1×10⁹/L的患者急性死亡率显著降低(Mantel-Cox检验p=0.029)。1年时的总体累积生存概率为0.38(95%置信区间0.27-0.49),只有两性霉素B治疗显著降低了死亡风险。