SUPERIORITY OF AZTREONAM CLINDAMYCIN COMPARED WITH GENTAMICIN CLINDAMYCIN IN PATIENTS WITH PENETRATING ABDOMINAL-TRAUMA

被引:22
作者
FABIAN, TC
HESS, MM
CROCE, MA
WILSON, RS
WILSON, SE
CHARLAND, SL
RODMAN, JH
BOUCHER, BA
机构
[1] UNIV TENNESSEE CTR HLTH SCI, DEPT SURG, MEMPHIS, TN 38163 USA
[2] UNIV TENNESSEE CTR HLTH SCI, DEPT CLIN PHARM, MEMPHIS, TN 38163 USA
[3] WAYNE STATE UNIV, DEPT SURG, DETROIT, MI 48202 USA
[4] UNIV CALIF IRVINE, DEPT SURG, IRVINE, CA 92717 USA
[5] PHILADELPHIA COLL PHARM & SCI, DEPT PHARM PRACTICE & PHARM ADM, PHILADELPHIA, PA 19104 USA
[6] ST JUDE CHILDRENS RES HOSP, MEMPHIS, TN 38101 USA
关键词
D O I
10.1016/0002-9610(94)90202-X
中图分类号
R61 [外科手术学];
学科分类号
摘要
There were 73 evaluable patients entered into a prospective, double-blinded trial comparing aztreonam/clindamycin (A/C) to gentamicin/clindamycin (G/C) for the prevention of infection after penetrating abdominal trauma. Aztreonam was administered at a dosage of 2 g every 8 hours and gentamicin at 5 mg/kg for the first 24 hours and then adjusted by serum monitoring to a peak of 6 to 8 mug/mL and a trough of less than 2 mug/mL; all patients received 900 mg of clindamycin every 8 hours. Patients with colon wounds received 4 days of antibiotics, and the remaining patients received a 24-hour course. Gunshot wounds occurred in 69% of patients: 74% of all patients had some hollow viscus injury, and 26% had only solid viscus injury. The groups were well matched according to abdominal trauma index, percentage with colon injury, and transfusion requirements. Failures occurred in eight patients (11%): two wound infections, five intra-abdominal infections, and one case of necrotizing fasciitis. Seven infections occurred in 36 (19%) G/C patients compared with 1 in 37 (3%) A/C patients (p < 0.03). The hospital stay was 12 +/- 11 days for G/C patients and 8 +/- 7 for A/C patients (p < 0.12). The superiority of the A/C regimen may be partially attributable to relative underdosing of gentamicin (approximately half of the patients had inadequate levels after 24 hours) combined with a favorable pharmacokinetic profile (significantly prolonged half-life) of aztreonam in this clinical setting.
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页码:291 / 296
页数:6
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