Time to clinical response: An outcome of antibiotic therapy of febrile neutropenia with implications for quality and cost of care

被引:33
作者
Elting, LS [1 ]
Rubenstein, EB [1 ]
Rolston, K [1 ]
Cantor, SB [1 ]
Martin, CG [1 ]
Kurtin, D [1 ]
Rodriguez, S [1 ]
Lam, T [1 ]
Kanesan, K [1 ]
Bodey, G [1 ]
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Hlth Serv Res, Houston, TX 77030 USA
关键词
D O I
10.1200/JCO.2000.18.21.3699
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine whether antibiotic regimens with similar rates of response differ significantly in the speed of response and to estimate the impact of this difference on the cost of febrile neutropenia. Methods: The time point of clinical response wets defined by comparing the sensitivity, specificity, and predictive values of alternative objective and subjective definitions, Data from 488 episodes of febrile neutropenia, treated with either of two commonly used antibiotics (coded A or 8) during six clinical trials, were pooled to compare the median time to clinical response, days of antibiotic therapy and hospitalization, and estimated costs. Results: Response rates were similar; however, the median time to clinical response was significantly shorter with A-based regimens (5 days) compared with B-based regimens (7 days; P = .003). After 72 hours of therapy, 33% of patients who received A but only 18% of those who received B had responded (P = .01). These differences resulted in fewer days of antibiotic therapy and hospitalization with A-based regimens (7 and 9 days) compared with B-based regimens (9 and 12 days, respectively; P < .04) and in significantly lower estimated median casts ($8,491 v $11,133 per episode; P = .03), Early discharge at the time of clinical response should reduce the median cost from $10,752 to $8,162 (P < .001). Conclusion: Despite virtually identical Kites of response, time to clinical response and estimated cost of care varied significantly among regimens. An early discharge strategy based on our definition of the time point of clinical response may further reduce the cost of treating non-low-risk patients with febrile neutropenia, (C) 2000 by American Society of Clinical Oncology.
引用
收藏
页码:3699 / 3706
页数:8
相关论文
共 31 条
[1]   RANDOMIZED TRIAL OF BETA-LACTAM REGIMENS IN FEBRILE NEUTROPENIC CANCER-PATIENTS [J].
ANAISSIE, EJ ;
FAINSTEIN, V ;
BODEY, GP ;
ROLSTON, K ;
ELTING, L ;
KANTARJIAN, H ;
CABANILLAS, F ;
MCCREDIE, KB .
AMERICAN JOURNAL OF MEDICINE, 1988, 84 (03) :581-589
[2]  
BODEY GP, 1987, CANCER-AM CANCER SOC, V60, P255, DOI 10.1002/1097-0142(19870715)60:2<255::AID-CNCR2820600224>3.0.CO
[3]  
2-L
[4]  
BODEY GP, 1990, CANCER, V65, P9, DOI 10.1002/1097-0142(19900101)65:1<9::AID-CNCR2820650105>3.0.CO
[5]  
2-C
[6]   ANTIBIOTICS IN PATIENTS WITH NEUTROPENIA [J].
BODEY, GP .
ARCHIVES OF INTERNAL MEDICINE, 1984, 144 (09) :1845-1851
[7]  
CANTOR SB, 1997, P AN M AM SOC CLIN, V16, pA419
[8]   Outcomes of bacteremia in patients with cancer and neutropenia: Observations from two decades of epidemiological and clinical trials [J].
Elting, LS ;
Rubenstein, EB ;
Rolston, KVI ;
Bodey, GP .
CLINICAL INFECTIOUS DISEASES, 1997, 25 (02) :247-259
[9]  
FAINSTEIN V, 1983, J ANTIMICROB CHEMOTH, V12, pS101
[10]   Fever and neutropenia - How to use a new treatment strategy [J].
Finberg, RW ;
Talcott, JA .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (05) :362-363