Toltzis Philip, Dul Michael, O'Riordan Mary Ann, Salvator Ann, Rosolowski Bonnie, Toltzis Hasida, Blumer Jeffrey L
Department of Pediatrics, Rainbow Babies and Children's Hospital, Case Western Reserve University, Cleveland, Ohio, USA.
Pediatr Infect Dis J. 2003 Feb;22(2):109-14. doi: 10.1097/01.inf.0000050241.65703.2e.
Cefepime has activity against many hospital-acquired Gram-negative pathogens resistant to earlier beta-lactam antibiotics. This study was designed to test whether preferential use of cefepime in a pediatric intensive care unit could reduce enteric colonization with antibiotic-resistant Gram-negative rods.
After a 6-month period of uncontrolled antibiotic use, cefepime was preferentially used during 2 years as treatment for nosocomial or serious community-acquired infection. Rectal swab specimens were obtained daily on every patient regardless of antibiotic exposure during the 6 months of uncontrolled antibiotic use and during the first and last 6 months of the 2 years of cefepime preference. The study outcome was rectal colonization with a facultative Gram-negative rod resistant to at least one of four antibiotics: cefepime; ceftazidime; gentamicin; or piperacillin-tazobactam.
The incidence of colonization by a resistant organism decreased only slightly during the first 6 months of cefepime use. By contrast, the number of antibiotic-resistant bacilli isolated from rectal swab specimens diminished from 27.6/100 patients during the baseline period to 12.9/100 patients by the last 6 months of the 2 years of cefepime preference (P < 0.01). The proportion of patients harboring at least one resistant organism decreased from 11.6% to 7.4% during the same time period (P < 0.01). A decrease in colonization with resistant organisms occurred for all the tested resistance phenotypes, including cefepime.
Cefepime may possess a low potential for promoting bacillary resistance in critically ill patients, suggesting that its preferential use might be a key element in limiting the presence of antibiotic resistance in the intensive care unit.
头孢吡肟对许多耐早期β-内酰胺类抗生素的医院获得性革兰氏阴性病原体具有活性。本研究旨在测试在儿科重症监护病房优先使用头孢吡肟是否能减少耐抗生素革兰氏阴性杆菌的肠道定植。
在6个月不受控制的抗生素使用期后,头孢吡肟在2年期间被优先用于治疗医院获得性或严重社区获得性感染。在不受控制的抗生素使用的6个月期间以及头孢吡肟优先使用的2年的前6个月和最后6个月期间,每天对每位患者采集直肠拭子标本。研究结果是直肠定植一种对四种抗生素中的至少一种耐药的兼性革兰氏阴性杆菌:头孢吡肟;头孢他啶;庆大霉素;或哌拉西林-他唑巴坦。
在使用头孢吡肟的前6个月,耐药菌定植的发生率仅略有下降。相比之下,从直肠拭子标本中分离出的耐抗生素杆菌数量从基线期的27.6/100患者减少到头孢吡肟优先使用2年的最后6个月时的12.9/100患者(P<0.01)。在同一时期,携带至少一种耐药菌的患者比例从11.6%降至7.4%(P<0.01)。所有测试的耐药表型,包括对头孢吡肟耐药的表型,耐药菌的定植均有所减少。
头孢吡肟在重症患者中促进细菌耐药的可能性可能较低,这表明优先使用该药可能是限制重症监护病房抗生素耐药性存在的关键因素。