CONTINUOUS INFUSION TOBRAMYCIN COMBINED WITH CARBENICILLIN FOR INFECTIONS IN CANCER-PATIENTS

被引:20
作者
ISSELL, BF [1 ]
KEATING, MJ [1 ]
VALDIVIESO, M [1 ]
BODEY, GP [1 ]
机构
[1] UNIV TEXAS,MD ANDERSON HOSP & TUMOR INST,DEPT DEV THERAPEUT,HOUSTON,TX 77030
关键词
D O I
10.1097/00000441-197905000-00010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The cure rate of infections in cancer patients is adversely affected by neutropenia (< 1,000/mm3). In particular, patients with severe neutropenia (<100/mm3) have shown a poor response to antibiotics. To overcome the adverse effects of neutropenia, tobramycin was given by continuous infusion and combined with intermittent carbenicillin. Tobramycin was given to a total daily dose of 300 mg/m2 and carbenicillin was given at a dose of 5 gm every four hours. There were 125 infectious episodes in 116 cancer patients receiving myelosuppressive chemotherapy. The overall cure rate was 70%. Pneumonia was the most common infection and 61% of 59 episodes were cured. Gram-negative bacilli were the most common causative organisms and 69% of these infections were cured. The most common pathogen was Klebsiella pneumoniae and this, together with Escherichia coli and Pseudomonas aeruginosa, accounted for 74% of all gram-negative bacillary infections. Response was not influenced by the initial neutrophil count, with a 62% cure rate for 39 episodes associated with severe neutropenia. However, failure of the neutrophil count to increase during therapy adversely affected response. Azotemia was the major side effect recognized, and it occurred in 11% of episodes. Major azotemia (serum creatinine > 2.5 mg/dl or BUN >50 mg/dl) occurred in only 2%. Azotemia was not related to duration of therapy or serum tobramycin concentration. This antibiotic regimen showed both therapeutic efficacy and acceptable renal toxicity for these patients.
引用
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页码:311 / 318
页数:8
相关论文
共 22 条
  • [1] SUSCEPTIBILITY OF PSEUDOMONAS-AERUGINOSA TO TOBRAMYCIN OR GENTAMICIN ALONE AND COMBINED WITH CARBENICILLIN
    ANDERSON, EL
    GRAMLING, PK
    VESTAL, PR
    FARRAR, WE
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1975, 8 (03) : 300 - 304
  • [2] BLOOMFIELD CD, 1974, CANCER-AM CANCER SOC, V34, P431, DOI 10.1002/1097-0142(197408)34:2<431::AID-CNCR2820340229>3.0.CO
  • [3] 2-9
  • [4] AMIKACIN FOR TREATMENT OF INFECTIONS IN PATIENTS WITH MALIGNANT DISEASES
    BODEY, GP
    RODRIGUEZ, V
    VALDIVIESO, M
    FELD, R
    [J]. JOURNAL OF INFECTIOUS DISEASES, 1976, 134 : S421 - S427
  • [5] BODEY GP, 1972, CANCER-AM CANCER SOC, V29, P1697, DOI 10.1002/1097-0142(197206)29:6<1697::AID-CNCR2820290638>3.0.CO
  • [6] 2-K
  • [7] FEASIBILITY OF ADMINISTERING AMINOGLYCOSIDE ANTIBIOTICS BY CONTINUOUS INTRAVENOUS-INFUSION
    BODEY, GP
    CHANG, HY
    RODRIGUEZ, V
    STEWART, D
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1975, 8 (03) : 328 - 333
  • [8] INFECTIONS IN CANCER-PATIENTS
    BODEY, GP
    [J]. CANCER TREATMENT REVIEWS, 1975, 2 (02) : 89 - +
  • [9] BODEY GP, 1969, AM J MED SCI, V275, P408
  • [10] BODEY GP, 1976, CHEMOTHERAPY, V1, P69