Lipid formulations of amphotericin B preserve and stabilize renal function in HSCT recipients

被引:25
作者
Miller, CB
Waller, EK
Klingemann, HG
Dignani, MC
Anaissie, EJ
Cagnoni, PJ
McSweeney, P
Fleck, PR
Fruchtman, SM
McGuirk, J
Chao, NJ
机构
[1] Duke Univ, Med Ctr, BMT Program, Durham, NC 27710 USA
[2] St Agnes Healthcare, Durham, NC USA
[3] Emory Univ, Durham, NC USA
[4] Rush Presbyterian St Lukes Med Ctr, Durham, NC USA
[5] Univ Arkansas Med Sci, Durham, NC USA
[6] Univ Colorado, Ctr Hlth Sci, Durham, NC USA
[7] Cincinnati Transplant Inst, Durham, NC USA
[8] Mt Sinai Med Ctr, Durham, NC USA
[9] Oncol & Hematol Associates Kansas City, Durham, NC USA
关键词
amphotericin B; amBisome; fungal infections; hematopoietic stem cell transplant; nephrotoxicity; renal function;
D O I
10.1038/sj.bmt.1704408
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The current study assessed renal function based on medical records in adult hematopoietic stem cell transplant (HSCT) recipients with proven or probable invasive fungal infection (IFI) transplanted between 1995 and 2000. We confirm that amphotericin B deoxycholate (AmB-d) is nephrotoxic in a large percentage of HSCT recipients. Due to nephrotoxicity, defined as serum creatinine (SCr) >2.5 mg/dl or a 100% increase in SCr from baseline, 88% of patients treated with AmB-d were switched to a lipid formulation of amphotericin B (LFAB). In total, 53% of patients initiated on AmB-d were switched within the first week of therapy. Significantly more patients (70.6%) treated with AmB-d experienced a 100% increase in SCr from baseline compared to patients treated with either AmBisome (44.4%) or Abelcet (41.2%). A Cox Proportional Hazards Model revealed that, compared to patients initiated on AmBisome or Abelcet, the risk of nephrotoxicity (RR = 1.5 vs AmBisome; RR = 1.7 vs Abelcet), dialysis (RR = 2.4 vs AmBisome; RR = 1.4 vs Abelcet), and death (RR = 2.0 vs AmBisome; RR = 1.1 vs Abelcet) were all increased for patients initiated on AmB-d. Study results suggest that renal function improves and mortality declines when an LFAB is given to HSCT patients as initial therapy rather than as second-line therapy, the current practice.
引用
收藏
页码:543 / 548
页数:6
相关论文
共 27 条
[1]   A systematic review of the antifungal effectiveness and tolerability of amphotericin B formulations [J].
Barrett, JP ;
Vardulaki, KA ;
Conlon, C ;
Cooke, J ;
Daza-Ramirez, P ;
Evans, EGV ;
Hawkey, PM ;
Herbrecht, R ;
Marks, DI ;
Moraleda, JM ;
Park, GR ;
Senn, SJ ;
Viscoli, C .
CLINICAL THERAPEUTICS, 2003, 25 (05) :1295-1320
[2]   Mortality and costs of acute renal failure associated with amphotericin B therapy [J].
Bates, DW ;
Su, L ;
Yu, DT ;
Chertow, GM ;
Seger, DL ;
Gomes, DRJ ;
Dasbach, EJ ;
Platt, R .
CLINICAL INFECTIOUS DISEASES, 2001, 32 (05) :686-693
[3]   AmBisome (Liposomal amphotericin B): A comparative review [J].
Boswell, GW ;
Buell, D ;
Bekersky, I .
JOURNAL OF CLINICAL PHARMACOLOGY, 1998, 38 (07) :583-592
[4]   Pharmacoeconomic analysis of liposomal amphotericin B versus conventional amphotericin B in the empirical treatment of persistently febrile neutropenic patients [J].
Cagnoni, PJ ;
Walsh, TJ ;
Prendergast, MM ;
Bodensteiner, D ;
Hiemenz, S ;
Greenberg, RN ;
Arndt, CAS ;
Schuster, M ;
Seibel, N ;
Yeldandi, V ;
Tong, KB .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (12) :2476-2483
[5]  
CLEMENTS JS, 1990, AM J MED, V88, pN22
[6]   NIAID MYCOSES STUDY-GROUP MULTICENTER TRIAL OF ORAL ITRACONAZOLE THERAPY FOR INVASIVE ASPERGILLOSIS [J].
DENNING, DW ;
LEE, JY ;
HOSTETLER, JS ;
PAPPAS, P ;
KAUFFMAN, CA ;
DEWSNUP, DH ;
GALGIANI, JN ;
GRAYBILL, JR ;
SUGAR, AM ;
CATANZARO, A ;
GALLIS, H ;
PERFECT, JR ;
DOCKERY, B ;
DISMUKES, WE ;
STEVENS, DA .
AMERICAN JOURNAL OF MEDICINE, 1994, 97 (02) :135-144
[7]   Amphotericin B nephrotoxicity [J].
Deray, G .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 49 :37-41
[8]  
GALLIS HA, 1990, REV INFECT DIS, V12, P308
[9]  
Graybill JR, 2000, MED MYCOL, V38, P323, DOI 10.1080/mmy.38.s1.323.333
[10]   Characterizing and predicting amphotericin B-associated nephrotoxicity in bone marrow or peripheral blood stem cell transplant recipients [J].
Gubbins, PO ;
Penzak, SR ;
Polston, S ;
McConnell, SA ;
Anaissie, E .
PHARMACOTHERAPY, 2002, 22 (08) :961-971