Is monotherapy for febrile neutropenia still a viable alternative?

被引:32
作者
Ramphal, R [1 ]
机构
[1] Univ Florida, Dept Med, Div Infect Dis, Gainesville, FL 32610 USA
关键词
D O I
10.1086/598623
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Monotherapy for empirical treatment of febrile neutropenia is effective and often less costly than combination therapy but remains controversial. The controversy results from observations that combination therapy for Pseudomonas aeruginosa improved outcomes, and this approach became a standard. Many subsequent publications, including the Infectious Diseases Society of America guidelines for febrile neutropenia, now support monotherapy. However, changes in the pathogens involved in febrile neutropenia and in their resistance prompt a reevaluation In the evaluation of new antibiotics, recent trials comparing either cefepime or meropenem with combination therapy or with ceftazidime confirm that monotherapy remains a viable therapeutic approach, with infectious mortality in the 5% range in all arms. The choice of monotherapy should, however, be made on the basis of resistance patterns seen in an institution. The agent selected should be very active against the organisms that are likely to cause rapidly fatal infections,and clinicians must be prepared to modify monotherapy as appropriate.
引用
收藏
页码:508 / 514
页数:7
相关论文
共 42 条
[1]  
[Anonymous], 1978, J INFECT DIS
[2]   CARBENICILLIN THERAPY FOR PSEUDOMONAS INFECTIONS [J].
BODEY, GP ;
WHITECAR, JP ;
MIDDLEMAN, E ;
RODRIGUEZ, V .
JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1971, 218 (01) :62-+
[3]  
BOOGAERTS MA, 1995, J ANTIMICROB CHEMOTH, V36, P185
[4]  
Breen J, 1997, FEBRILE NEUTROPENIA, P63
[5]  
CALANDRA T, 1987, NEW ENGL J MED, V317, P1692
[6]   BACTEREMIA DUE TO VIRIDANS STREPTOCOCCI THAT ARE HIGHLY RESISTANT TO PENICILLIN - INCREASE AMONG NEUTROPENIC PATIENTS WITH CANCER [J].
CARRATALA, J ;
ALCAIDE, F ;
FERNANDEZSEVILLA, A ;
CORBELLA, X ;
LINARES, J ;
GUDIOL, F .
CLINICAL INFECTIOUS DISEASES, 1995, 20 (05) :1169-1173
[7]   PIPERACILLIN-TAZOBACTAM PLUS AMIKACIN VERSUS CEFTAZIDIME PLUS AMIKACIN AS EMPIRIC THERAPY FOR FEVER IN GRANULOCYTOPENIC PATIENTS WITH CANCER [J].
COMETTA, A ;
ZINNER, S ;
DEBOCK, R ;
CALANDRA, T ;
GAYA, H ;
KLASTERSKY, J ;
LANGENAEKEN, J ;
PAESMANS, M ;
VISCOLI, C ;
GLAUSER, MP ;
GIBSON, B ;
SANZ, M ;
HANN, IM ;
FOLLATH, F ;
FATIO, R ;
FERSTER, A ;
VANHOOF, A ;
VANLANDUYT, H ;
ARENDT, V ;
HEMMER, R ;
PEETERMANS, M ;
PADMOS, A ;
SEITANIDES, B ;
HATZIYANNI, M ;
LOPEZ, A ;
PORCELLINI, A ;
GREK, V ;
CABALLERO, D ;
TOGNI, P ;
GALLAGHER, JG ;
GARAVENTA, A ;
MASSIMO, L ;
SUGAR, A ;
LEGRAND, JC ;
OPPENHEIM, B ;
PETRIKKOS, G ;
BEYTOUT, J ;
NIKOSKELAINEN, J ;
SHAPIRO, M ;
ESTAVOYER, JM ;
KERN, W .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (02) :445-452
[8]   Monotherapy with meropenem versus combination therapy with ceftazidime plus amikacin as empiric therapy for fever in granulocytopenic patients with cancer [J].
Cometta, AF ;
Calandra, T ;
Gaya, H ;
Zinner, SH ;
deBock, R ;
DelFavero, A ;
Bucaneve, G ;
Crokaert, F ;
Kern, WV ;
Klastersky, J ;
Langenaeken, J ;
Micozzi, A ;
Padmos, A ;
Paesmans, M ;
Viscoli, C ;
Glauser, MP ;
Martino, P ;
Caballero, D ;
Engelhard, D ;
Shapiro, M ;
Castagnola, E ;
Massimo, L ;
Giacchino, R ;
Sanz, M ;
Gigium, M ;
Carotenuto, M ;
Lopez, A ;
Andrien, JM ;
Paulus, R ;
Martino, B ;
Nobile, F ;
Togni, P ;
Ferster, A ;
Cudillo, L ;
Legrand, JC ;
Dinota, A ;
Cajozzo, A ;
Quintini, G ;
MartinezDalmau, A ;
Nosari, A ;
Bucaneve, GP ;
Cometta, A ;
Galazzo, M ;
Giddey, M ;
Bille, J ;
Blaser, J .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (05) :1108-1115
[9]  
DEJONGH CA, 1986, AM J MED, V80, P96
[10]   RANDOMIZED STUDY OF CEFTAZIDIME VERSUS GENTAMICIN PLUS CEFOTAXIME FOR INFECTIONS IN SEVERE GRANULOCYTOPENIC PATIENTS [J].
DEPAUW, BE ;
KAUW, F ;
MUYTJENS, H ;
WILLIAMS, KJ ;
BOTHOF, T .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1983, 12 :93-99