The efficacy and safety of meropenem and tobramycin vs ceftazidime and tobramycin in the treatment of acute pulmonary exacerbations in patients with cystic fibrosis

被引:63
作者
Blumer, JL
Saiman, L
Konstan, MW
Melnick, D
机构
[1] Case Western Reserve Univ, Rainbow Babies & Childrens Hosp, Sch Med, Cleveland, OH 44106 USA
[2] Columbia Univ, New York, NY 10027 USA
[3] AstraZeneca, Wilmington, DE USA
关键词
acute pulmonary exacerbation; ceftazidime; cystic fibrosis; meropenem;
D O I
10.1378/chest.128.4.2336
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: Cystic fibrosis (CF) is characterized by chronic pulmonary infection with acute pulmonary exacerbations (APEs) requiring IV antibiotic treatment. We report on a blinded comparative trial of IV meropenem (40 mg/kg to 2 g q8h) or ceftazidime (5 mg/kg to 2 g q8h), each of which was administered with IV tobramycin (at a serum peak of >= 8 mu g/mL and a trough of < 2 mu g/mL), as treatment for CF patients with APEs. Methods: Patients who were : 5 years of age who were infected with ceftazidime-susceptible Pseudomonas aeruginosa were stratified by lung function and randomized to treatment with meropenem/tobramycin or ceftazidime/tobramycin. Patients infected with Burkholderia cepacia complex or ceftazidime-resistant P aeruginosa were assigned to receive open-label meropenem/tobramycin. Clinical response was assessed by spirometry to determine the change in percent predicted FEV1 and by a clinical acute change score (ACS). Results: One hundred two patients were randomized to meropenem/tobramycin (n = 50) or ceftazidime/tobramycin (n = 52). Nineteen patients received open-label meropenem/tobramycin. FEV1 was improvea at the end of treatment (EOT) with meropenem/tobramycin (mean [+/- SD] increase, 38.8 +/- 52.3%) and with ceftazidime/tobramycin (mean increase, 29.4 +/- 35.1%; p < 0.0001 vs baseline values). The proportion of patients with >= 15% relative increase from baseline FEV1 (satisfactory response) at day 7 was 62% for the meropenem/tobramycin group and 44% for the ceftazidime/tobramycin group (p = 0.04). The median time to FEV1 response was 4 days for meropenem/tobramycin therapy vs 6 days for ceftazidime/tobramycin therapy. Similarly, FEV1 improved in the open-label group (mean increase, 12.5 +/- 25.7%; p = 0.05). ACS improved in all three groups at EOT (p < 0.0001 vs baseline values). Conclusions: Therapy with both meropenem/tobramycin and ceftazidime/tobramycin improved pulmonary and clinical status and reduced sputum bacterial burden in CF patients with APEs. A larger proportion of patients receiving meropenem/tobramycin therapy demonstrated a satisfactory FEV1 response at day 7. Resistant P aeruginosa emerged infrequently during treatment with both regimens.
引用
收藏
页码:2336 / 2346
页数:11
相关论文
共 29 条
[1]  
[Anonymous], 2000, M7A5 NAT COMM CLIN L, pM7
[2]   The treatment of respiratory pseudomonas infection in cystic fibrosis - What drug and which way? [J].
Banerjee, D ;
Stableforth, D .
DRUGS, 2000, 60 (05) :1053-1064
[3]   CLINICAL-EVALUATION OF MEROPENEM VERSUS CEFTAZIDIME FOR THE TREATMENT OF PSEUDOMONAS SPP INFECTIONS IN CYSTIC-FIBROSIS PATIENTS [J].
BYRNE, S ;
MADDISON, J ;
CONNOR, P ;
DOUGHTY, I ;
DODD, M ;
JENNEY, M ;
WEBB, AK ;
DAVID, TJ .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1995, 36 :135-143
[4]   DEVELOPMENT OF ANTIBIOTIC-RESISTANCE IN PSEUDOMONAS-AERUGINOSA DURING 2 DECADES OF ANTIPSEUDOMONAL TREATMENT AT THE DANISH-CF-CENTER [J].
CIOFU, O ;
GIWERCMAN, B ;
PEDERSEN, SS ;
HOIBY, N .
APMIS, 1994, 102 (09) :674-680
[5]   VARIABILITY OF PULMONARY-FUNCTION TESTS IN CYSTIC-FIBROSIS [J].
COOPER, PJ ;
ROBERTSON, CF ;
HUDSON, IL ;
PHELAN, PD .
PEDIATRIC PULMONOLOGY, 1990, 8 (01) :16-22
[6]  
*CYST FIBR FDN, 2003, PAT REG 2002 ANN REP
[7]   Antibiotic therapy against Pseudomonas aeruginosa in cystic fibrosis:: a European consensus [J].
Döring, G ;
Conway, SP ;
Heijerman, HGM ;
Hodson, ME ;
Hoiby, N ;
Smyth, A ;
Touw, DJ .
EUROPEAN RESPIRATORY JOURNAL, 2000, 16 (04) :749-767
[8]   Prevention of resistance: A goal for dose selection for antimicrobial agents [J].
Drusano, GL .
CLINICAL INFECTIOUS DISEASES, 2003, 36 :S42-S50
[9]   Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis [J].
Emerson, J ;
Rosenfeld, M ;
McNamara, S ;
Ramsey, B ;
Gibson, RL .
PEDIATRIC PULMONOLOGY, 2002, 34 (02) :91-100
[10]  
HOIBY N, 1996, DANISH CYSTIC FIBROS