Late onset of invasive aspergillus infection in bone marrow transplant patients at a university hospital

被引:145
作者
Grow, WB [1 ]
Moreb, JS [1 ]
Roque, D [1 ]
Manion, K [1 ]
Leather, H [1 ]
Reddy, V [1 ]
Khan, SA [1 ]
Finiewicz, KJ [1 ]
Nguyen, H [1 ]
Clancy, CJ [1 ]
Mehta, PS [1 ]
Wingard, JR [1 ]
机构
[1] Univ Florida, Shands Hosp, Coll Med, Gainesville, FL USA
关键词
aspergillosis; bone marrow transplant; fungal infections; corticosteroids;
D O I
10.1038/sj.bmt.1703332
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Despite new antifungal treatment strategies, invasive aspergillosis (IA) remains a principal cause of infectious mortality after bone marrow transplantation (BMT). We reviewed the medical records of 93 allogeneic and 149 autologous transplant recipients during a 20 month period, with attention to cases of proven or probable IA. No autologous transplant recipient developed IA, whereas IA was seen in 15.1% of allogeneic recipients (including two of five patients with a prior history of IA despite prophylaxis), for an overall incidence of 5.8%. The median time to occurrence was 92 days post transplant, with no de novo cases developing prior to engraftment. Survival 100 days from diagnosis was 29%. Risk factors for the development of IA included greater than or equal to21 days of corticosteroid therapy of greater than or equal to1 mg/kg/day and post-transplant cytomegalovirus (CMV) infection. These two risk factors were statistically linked. Our data illustrate a shift toward a later occurrence of post-transplant IA, suggesting a need for close, prolonged surveillance in the outpatient environment The contributory role of protracted corticosteroid use is also highlighted. These data have important implications in an era of alternate donor transplants and more intense immuno-suppression. Established strategies implementing newer, less toxic antifungal agents as prophylaxis in high-risk patients are needed.
引用
收藏
页码:15 / 19
页数:5
相关论文
共 15 条
  • [1] DIX SP, 1997, BLOOD MARROW TRANSPL, P100
  • [2] An EORTC international multicenter randomized trial (EORTC number 19923) comparing two dosages of liposomal amphotericin B for treatment of invasive aspergillosis
    Ellis, M
    Spence, D
    de Pauw, B
    Meunier, F
    Marinus, A
    Collette, L
    Sylvester, R
    Meis, J
    Boogaerts, M
    Selleslag, D
    Kremery, V
    von Sinner, W
    MacDonald, P
    Doyen, C
    Vandercam, B
    [J]. CLINICAL INFECTIOUS DISEASES, 1998, 27 (06) : 1406 - 1412
  • [3] RISK-FACTORS FOR FUNGAL INFECTION IN PATIENTS WITH MALIGNANT HEMATOLOGIC DISORDERS - IMPLICATIONS FOR EMPIRICAL THERAPY AND PROPHYLAXIS
    GUIOT, HFL
    FIBBE, WE
    VANTWOUT, JW
    [J]. CLINICAL INFECTIOUS DISEASES, 1994, 18 (04) : 525 - 532
  • [4] Cytomegalovirus infection is a risk factor for invasive aspergillosis in lung transplant recipients
    Husni, RN
    Gordon, SM
    Longworth, DL
    Arroliga, A
    Stillwell, PC
    Avery, RK
    Maurer, JR
    Mehta, A
    Kirby, T
    [J]. CLINICAL INFECTIOUS DISEASES, 1998, 26 (03) : 753 - 755
  • [5] Incidence and risk factors for invasive fungal infections in allogeneic BMT recipients
    Jantunen, E
    Ruutu, P
    Niskanen, L
    Volin, L
    Parkkali, T
    KoukilaKahkola, P
    Ruutu, T
    [J]. BONE MARROW TRANSPLANTATION, 1997, 19 (08) : 801 - 808
  • [6] PROGRESS IN THE DIAGNOSIS AND MANAGEMENT OF ASPERGILLOSIS IN BONE-MARROW TRANSPLANTATION - 13 YEARS EXPERIENCE
    MCWHINNEY, PHM
    KIBBLER, CC
    HAMON, MD
    SMITH, OP
    GANDHI, L
    BERGER, LA
    WALESBY, RK
    HOFFBRAND, AV
    PRENTICE, HG
    [J]. CLINICAL INFECTIOUS DISEASES, 1993, 17 (03) : 397 - 404
  • [7] MEYERS JD, 1990, SEMIN ONCOL, V17, P10
  • [8] NAVARRO E, 1990, 90 ANN M AM SOC MICR
  • [9] PREDICTION OF SYSTEMIC FUNGAL INFECTION IN ALLOGENEIC MARROW RECIPIENTS - IMPACT OF AMPHOTERICIN PROPHYLAXIS IN HIGH-RISK PATIENTS
    ODONNELL, MR
    SCHMIDT, GM
    TEGTMEIER, BR
    FAUCETT, C
    FAHEY, JL
    ITO, J
    NADEMANEE, A
    NILAND, J
    PARKER, P
    SMITH, EP
    SNYDER, DS
    STEIN, AS
    BLUME, KG
    FORMAN, SJ
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1994, 12 (04) : 827 - 834
  • [10] PRZEPIORKA D, 1995, BONE MARROW TRANSPL, V15, P825