Universal antifungal therapy is not needed in persistent febrile neutropenia: a tailored diagnostic and therapeutic approach

被引:29
作者
Aguilar-Guisado, Manuela [1 ,2 ]
Martin-Pena, Almudena [1 ,2 ]
Espigado, Ildefonso [2 ,3 ]
Ruiz Perez de Pipaon, Maite [1 ]
Falantes, Jose [3 ]
de la Cruz, Fatima [3 ]
Cisneros, Jose M. [1 ,2 ]
机构
[1] Univ Hosp Virgen del Rocio, Serv Infect Dis Clin Microbiol & Prevent Med, Seville 41013, Spain
[2] Univ Hosp Virgen del Rocio, Spanish Network Res Infect Dis, Seville 41013, Spain
[3] Hematol Serv, Seville, Spain
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2012年 / 97卷 / 03期
关键词
persistent febrile neutropenia; invasive fungal infection; selective antifugal therapy; empirical antifugal therapy; INVASIVE FUNGAL-INFECTION; LIPOSOMAL AMPHOTERICIN-B; CLINICAL-PRACTICE GUIDELINES; HEMATOLOGIC MALIGNANCIES; DISEASES SOCIETY; HIGH-RISK; FEVER; CASPOFUNGIN; ASPERGILLOSIS; CANCER;
D O I
10.3324/haematol.2011.049999
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Giving antifungal therapy exclusively to selected patients with persistent febrile neutropenia may avoid over-treatment without increasing mortality. The aim of this study was to validate an innovative diagnostic and therapeutic approach based on assessing patients' risk profile and clinical criteria in order to select those patients requiring antifungal therapy. The efficacy of this approach was compared to that of universal empirical antifungal therapy. Design and Methods This was a prospective study which included all consecutive adult hematology patients with neutropenia and fever refractory to 5 days of empirical antibacterial therapy admitted to a teaching hospital in Spain over a 2-year period. A diagnostic and therapeutic approach based on clinical criteria and risk profile was applied in order to select patients for antifungal therapy. The sensitivity, specificity and negative predictive value of this approach and also the overall success rate, according to the same criteria of efficacy described in classical clinical trials, were analyzed. Results Eighty-five episodes were included, 35 of them (41.2%) in patients at high risk of invasive fungal infections. Antifungal therapy was not indicated in 33 episodes (38.8%). The overall incidence of proven and probable invasive fungal infections was 14.1%, all of which occurred in patients who had received empirical antifungal therapy. The 30-day crude mortality rate was 15.3% and the invasive fungal infection-related mortality rate was 2.8% (2/72). The overall success rate following the diagnostic and therapeutic approach was 36.5% compared with 33.9% and 33.7% obtained in the trial by Walsh et al. The sensitivity, specificity and negative predictive value of the study approach were 100%, 52.4% and 100%, respectively. Conclusions Based on the high negative predictive value of this diagnostic and therapeutic approach in persistent febrile neutropenia patients with hematologic malignancies or patients who have received a hematopoietic stem cell transplant, the approach is useful for identifying patients who are not likely to develop invasive fungal infection and do not, therefore, require antifungal therapy. The effectiveness of the strategy is similar to that of universal empirical antifungal therapy reported in controlled trials.
引用
收藏
页码:464 / 471
页数:8
相关论文
共 29 条
[1]   Empirical antifungal therapy in selected patients with persistent febrile neutropenia [J].
Aguilar-Guisado, M. ;
Espigado, I. ;
Cordero, E. ;
Noguer, M. ;
Parody, R. ;
Pachon, J. ;
Cisneros, J. M. .
BONE MARROW TRANSPLANTATION, 2010, 45 (01) :159-164
[2]   Defining opportunistic invasive fungal infections in immunocompromised patients with cancer and hematopoietic stem cell transplants: An international consensus [J].
Ascioglu, S ;
Rex, JH ;
de Pauw, B ;
Bennett, JE ;
Bille, J ;
Crokaert, F ;
Denning, DW ;
Donnelly, JP ;
Edwards, JE ;
Erjavec, Z ;
Fiere, D ;
Lortholary, O ;
Maertens, J ;
Meis, JF ;
Patterson, TF ;
Ritter, J ;
Selleslag, D ;
Shah, PM ;
Stevens, DA ;
Walsh, TJ .
CLINICAL INFECTIOUS DISEASES, 2002, 34 (01) :7-14
[3]   Intravenous and oral itraconazole versus intravenous amphotericin B deoxycholate as empirical antifungal therapy for persistent fever in neutropenic patients with cancer who are receiving broad-spectrum antibacterial therapy - A randomized, controlled trial [J].
Boogaerts, M ;
Winston, DJ ;
Bow, EJ ;
Garber, G ;
Reboli, AC ;
Schwarer, AP ;
Novitzky, N ;
Boehme, A ;
Chwetzoff, E ;
De Beule, K .
ANNALS OF INTERNAL MEDICINE, 2001, 135 (06) :412-422
[4]   Antifungal therapy in patients with hematological malignancies:: how to avoid overtreatment? [J].
Cherif, Honar ;
Kalin, Mats ;
Bjorkholm, Magnus .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2006, 77 (04) :288-292
[5]   Empirical antifungal therapy in selected patients with persistent fever and neutropenia [J].
Cisneros, JM ;
Espigado, I ;
Rivero, A ;
de León, FL ;
Parra, J ;
Collado, AR ;
Lomas, JM ;
Pachón, J .
ENFERMEDADES INFECCIOSAS Y MICROBIOLOGIA CLINICA, 2005, 23 (10) :609-614
[6]   Empirical versus Preemptive Antifungal Therapy for High-Risk, Febrile, Neutropenic Patients: A Randomized, Controlled Trial [J].
Cordonnier, Catherine ;
Pautas, Cecile ;
Maury, Sebastien ;
Vekhoff, Anne ;
Farhat, Hassan ;
Suarez, Felipe ;
Dhedin, Nathalie ;
Isnard, Francoise ;
Ades, Lionel ;
Kuhnowski, Frederique ;
Foulet, Francoise ;
Kuentz, Mathieu ;
Maison, Patrick ;
Bretagne, Stephane ;
Schwarzinger, Michael .
CLINICAL INFECTIOUS DISEASES, 2009, 48 (08) :1042-1051
[7]   Value of Serial Quantification of Fungal DNA by a Real-Time PCR-Based Technique for Early Diagnosis of Invasive Aspergillosis in Patients with Febrile Neutropenia [J].
Cuenca-Estrella, Manuel ;
Meije, Yolanda ;
Diaz-Pedroche, Carmen ;
Gomez-Lopez, Alicia ;
Buitrago, Maria J. ;
Bernal-Martinez, Leticia ;
Grande, Carlos ;
Juan, Rafael San ;
Lizasoain, Manuel ;
Rodriguez-Tudela, Juan L. ;
Aguado, Jose M. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2009, 47 (02) :379-384
[8]   Surviving Sepsis Campaign guidelines for management of severe sepsis and septic shock [J].
Dellinger, RP ;
Carlet, JM ;
Masur, H ;
Gerlach, H ;
Calandra, T ;
Cohen, J ;
Gea-Banacloche, J ;
Keh, D ;
Marshall, JC ;
Parker, MM ;
Ramsay, G ;
Zimmerman, JL ;
Vincent, JL ;
Levy, MM .
CRITICAL CARE MEDICINE, 2004, 32 (03) :858-873
[9]   An early CT-diagnosis-based treatment strategy for invasive fungal infection in allogeneic transplant recipients using caspofungin first line: an effective strategy with low mortality [J].
Dignan, F. L. ;
Evans, S. O. ;
Ethell, M. E. ;
Shaw, B. E. ;
Davies, F. E. ;
Dearden, C. E. ;
Treleaven, J. G. ;
Riley, U. B. G. ;
Morgan, G. J. ;
Potter, M. N. .
BONE MARROW TRANSPLANTATION, 2009, 44 (01) :51-56
[10]   Polymerase chain reaction for diagnosing invasive aspergillosis: Getting closer but still a ways to go [J].
Donnelly, JP .
CLINICAL INFECTIOUS DISEASES, 2006, 42 (04) :487-489