Piperacillin tazobactam - An updated review of its use in the treatment of bacterial infections

被引:137
作者
Perry, CM [1 ]
Markham, A [1 ]
机构
[1] Adis Int Ltd, Auckland 10, New Zealand
关键词
D O I
10.2165/00003495-199957050-00017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Piperacillin/tazobactam is a beta-lactam/beta-lactamase inhibitor combination with a broad spectrum of antibacterial activity encompassing most Gram-positive and Gram-negative aerobic bacteria and anaerobic bacteria, including many pathogens producing beta-lactamases. Evidence from clinical trials in adults has shown that piperacillin/tazobactam, administered in an 8 : 1 ratio, is an effective treatment for patients with lower respiratory tract, intra-abdominal, urinary tract, gynaecological and skin/soft tissue infections, and for fever in patients with neutropenia. Combination regimens of piperacillin/tazobactam plus an aminoglycoside are used to treat patients with severe nosocomial (hospital-acquired) infections. In clinical trials, piperacillin/tazobactam was significantly more effective than ticarcillin/clavulanic acid in terms of clinical and microbiological outcome in patients with community-acquired pneumonia. In patients with intra-abdominal infections, clinical and bacteriological response rates were significantly higher with piperacillin/tazobactam than with imipenem/cilastatin (administered at a dosage lower than is recommended in countries outside Scandinavia). Piperacillin/tazobactam in combination with amikacin was at least as effective as ceftazidime plus amikacin in the treatment of ventilator-associated pneumonia and was significantly more effective than ceftazidime plus amikacin in the empirical treatment of febrile episodes in patients with neutropenia or granule; cytopenia. In other trials, the efficacy of piperacillin/tazobactam was similar to that of standard aminoglycoside-containing and other treatment regimens in patients with intra-abdominal, skin/soft tissue or gynaecological infections. Piperacillin/tazobactam is generally well tolerated. The most frequent adverse events are gastrointestinal symptoms (most commonly diarrhoea) and skin reactions. The incidence of adverse events with piperacillin/tazobactam is higher when the combination is given in combination with an aminoglycoside than when given as monotherapy. Conclusion: Because of the broad spectrum of antibacterial activity provided by piperacillin/tazobactam, it is useful for the treatment of patients with polymicrobial infections caused by aerobic or anaerobic beta-lactamase-producing bacteria. Piperacillin/tazobactam appears to have a particularly useful role in the treatment of patients with intra-abdominal infections and, in combination with amikacin, in the treatment of patients with febrile neutropenia, especially given the current prevalence of Gram-positive infections in this group.
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页码:805 / 843
页数:39
相关论文
共 167 条
[1]   A 5-YEAR MULTICENTER STUDY OF THE SUSCEPTIBILITY OF THE BACTEROIDES-FRAGILIS GROUP ISOLATES TO CEPHALOSPORINS, CEPHAMINS, PENICILLINS, CLINDAMYCIN, AND METRONIDAZOLE IN THE UNITED-STATES [J].
ALDRIDGE, KE ;
GELFAND, M ;
RELLER, LB ;
AYERS, LW ;
PIERSON, CL ;
SCHOENKNECHT, F ;
TILTON, RC ;
WILKINS, J ;
HENDERBERG, A ;
SCHIRO, DD ;
JOHNSON, M ;
JANNEY, A ;
SANDERS, CV .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1994, 18 (04) :235-241
[2]   An open, multicenter clinical trial of piperacillin tazobactam in the treatment of pediatric patients with intra-abdominal infections [J].
Arguedas, A ;
SifuentesOsornio, J ;
Loaiza, C ;
Herrera, M ;
Corrales, JC ;
Mohs, E .
JOURNAL OF CHEMOTHERAPY, 1996, 8 (02) :130-136
[3]   Imipenem/cilastatin - An update of its antibacterial activity, pharmacokinetics and therapeutic efficacy in the treatment of serious infections [J].
Balfour, JA ;
Bryson, HM ;
Brogden, RN .
DRUGS, 1996, 51 (01) :99-136
[4]  
BARIE PS, 1994, EUR J SURG, P61
[5]   NATIONAL SURVEY OF THE IN-VITRO SPECTRUM OF PIPERACILLIN-TAZOBACTAM TESTED AGAINST MORE THAN 40,000 AEROBIC CLINICAL ISOLATES FROM 236 MEDICAL-CENTERS [J].
BARON, EJ ;
JONES, RN .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1995, 21 (03) :141-151
[6]  
BETRIU C, 1997, REV ESP QUIM, V10, P161
[7]  
BISCHOFF M, 1997, ONKOLOGIE S1, V20, P132
[8]  
Böhme A, 1998, BRIT J HAEMATOL, V102, P94
[9]   Tazobactam is a potent inactivator of selected inhibitor-resistant class A beta-lactamases [J].
Bonomo, RA ;
Rudin, SA ;
Shlaes, DM .
FEMS MICROBIOLOGY LETTERS, 1997, 148 (01) :59-62
[10]   Evaluation of in vitro activity of a new fluoroquinolone trovafloxacin (cp-99,219) compared with other anti-anaerobic antimicrobials against members of the Bacteroides fragilis group [J].
Borobio, MV ;
Suarez, AI ;
Ramirez, E ;
Perea, EJ .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 1997, 8 (04) :249-252