Study of renal safety in amphotericin B lipid complex-treated patients

被引:46
作者
Alexander, BD
Wingard, JR
机构
[1] Duke Univ, Med Ctr, Div Infect Dis & Int Hlth, Durham, NC 27710 USA
[2] Univ Florida, Shands Canc Ctr, Gainesville, FL USA
关键词
D O I
10.1086/429335
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To investigate the renal safety of amphotericin B lipid complex ( ABLC), records from 3514 ABLC- treated patients with fungal infections were reviewed. The median change in predicted creatinine clearance ( C (Cr)) from baseline to the end of therapy was - 3 mL/ min ( range, - 119 to 118 mL/ min); doubling of serum creatinine ( S- Cr) level occurred in 13% of patients, and new dialysis was needed for 3% of patients. Patients with underlying renal disease who had received prior antifungal therapy demonstrated a median C-Cr of 0.5 mL/ min ( range, - 107 to 52 mL/ min). Despite increased risk for renal impairment in allogeneic hematopoietic stem- cell transplant recipients, only 17% of patients demonstrated end- of- therapy doubling of S- Cr levels, and the median change in C-Cr was - 10 mL/ min ( range, -107 to 108 mL/ min). In ABLC- treated patients, concomitant treatment with potentially nephrotoxic agents and a baseline S- Cr level of <2 mg/ dL were factors predisposing for the development of nephrotoxicity. These data provide evidence that ABLC may be used safely to treat patients who are at increased risk for renal impairment.
引用
收藏
页码:S414 / S421
页数:8
相关论文
共 25 条
  • [1] [Anonymous], 35 INT C ANT AG CHEM
  • [2] Mortality and costs of acute renal failure associated with amphotericin B therapy
    Bates, DW
    Su, L
    Yu, DT
    Chertow, GM
    Seger, DL
    Gomes, DRJ
    Dasbach, EJ
    Platt, R
    [J]. CLINICAL INFECTIOUS DISEASES, 2001, 32 (05) : 686 - 693
  • [3] Liposomal amphotericin B versus conventional amphotericin B in the empirical treatment of persistently febrile neutropenic patients
    Cagnoni, PJ
    [J]. JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 49 : 81 - 86
  • [4] A prospective and retrospective analysis of the nephrotoxicity and efficacy of lipid-based amphotericin B formulations
    Cannon, JP
    Garey, KW
    Danziger, LH
    [J]. PHARMACOTHERAPY, 2001, 21 (09): : 1107 - 1114
  • [5] Introduction to antifungal drugs
    Dismukes, WE
    [J]. CLINICAL INFECTIOUS DISEASES, 2000, 30 (04) : 653 - 657
  • [6] Comparison of amphotericin B lipid complex (ABLC) vs. AmBisome in the treatment of suspected or documented fungal infections in patients with leukemia
    Fleming, RV
    Kantarjian, HM
    Husni, R
    Rolston, K
    Lim, J
    Raad, I
    Pierce, S
    Cortes, J
    Estey, E
    [J]. LEUKEMIA & LYMPHOMA, 2001, 40 (5-6) : 511 - 520
  • [7] GALLIS HA, 1990, REV INFECT DIS, V12, P308
  • [8] Characterizing and predicting amphotericin B-associated nephrotoxicity in bone marrow or peripheral blood stem cell transplant recipients
    Gubbins, PO
    Penzak, SR
    Polston, S
    McConnell, SA
    Anaissie, E
    [J]. PHARMACOTHERAPY, 2002, 22 (08): : 961 - 971
  • [9] The epidemiology of nephrotoxicity associated with conventional amphotericin B therapy
    Harbarth, S
    Pestotnik, SL
    Lloyd, JF
    Burke, JP
    Samore, MH
    [J]. AMERICAN JOURNAL OF MEDICINE, 2001, 111 (07) : 528 - 534
  • [10] Retrospective study of the renal effects of amphotericin B lipid complex when used at higher-than-recommended dosages and longer durations compared with lower dosages and shorter durations in patients with systemic fungal infections
    Hooshmand-Rad, R
    Reed, MD
    Chu, A
    Gotz, V
    Morris, JA
    Weinberg, J
    Dominguez, EA
    [J]. CLINICAL THERAPEUTICS, 2004, 26 (10) : 1652 - 1662