Patel Payal D, Bhagat Palak, Bartlett Allison H, Bondi Deborah S
J Pediatr Pharmacol Ther. 2020;25(2):117-123. doi: 10.5863/1551-6776-25.2.117.
There is a national drug shortage of cefotaxime, and ceftazidime is recommended as an alternative to cefotaxime for neonates. This study evaluated culture-positive late-onset sepsis (LOS), multidrug resistant organisms (MDROs), and other neonatal outcomes with the use of ceftazidime compared with cefotaxime in neonates.
This was a single-center, retrospective cohort study of neonatal subjects who received at least 24 hours of ceftazidime or cefotaxime between April 1, 2015, and August 1, 2017. Subjects were excluded if they received the alternate antibiotic for more than 24 hours.
A total of 101 subjects were included (ceftazidime, n = 58; cefotaxime, n = 43). Median gestational ages were significantly different between groups (28.1 [IQR, 25.0-36.6] weeks versus 32.3 [IQR, 26.9-37.4] in the ceftazidime and cefotaxime groups, respectively, p < 0.05). Results showed a non-statistically significant increased incidence of culture-positive LOS (17.2% versus 2.3%, respectively, adjusted OR 6.51 [95% CI, 0.78-55.23], p = 0.09) and MDRO infections (5.2% versus 0%, respectively, p = 0.26) with the use of ceftazidime compared with cefotaxime. There was a statistically significant increased risk of stage II to III necrotizing enterocolitis (NEC) with the use of ceftazidime (22.4% versus 2.3%, respectively, adjusted OR 9.68 [95% CI, 1.18-79.45], p = 0.04).
This study found a statistically significant increase in stage II to III NEC with the use of ceftazidime compared with cefotaxime. There was a higher rate of culture-positive LOS and MDRO infections with ceftazidime, but this was not significant. Further research is warranted to assess the implications ceftazidime use in neonates.
头孢噻肟全国性短缺,头孢他啶被推荐作为新生儿头孢噻肟的替代药物。本研究评估了与头孢噻肟相比,使用头孢他啶治疗新生儿血培养阳性迟发性败血症(LOS)、多重耐药菌(MDROs)及其他新生儿结局的情况。
这是一项单中心回顾性队列研究,研究对象为2015年4月1日至2017年8月1日期间接受至少24小时头孢他啶或头孢噻肟治疗的新生儿。若接受替代抗生素治疗超过24小时,则将其排除。
共纳入101名受试者(头孢他啶组58例;头孢噻肟组43例)。两组的中位胎龄有显著差异(头孢他啶组为28.1[四分位间距,25.0 - 36.6]周,头孢噻肟组为32.3[四分位间距,26.9 - 37.4]周,p<0.05)。结果显示,与头孢噻肟相比,使用头孢他啶时血培养阳性LOS的发生率增加,但无统计学意义(分别为17.2%和2.3%,校正比值比6.51[95%置信区间,0.78 - 55.23],p = 0.09),MDRO感染率也增加(分别为5.2%和0%,p = 0.26)。使用头孢他啶时,II至III期坏死性小肠结肠炎(NEC)的风险有统计学意义的增加(分别为22.4%和2.3%,校正比值比9.68[95%置信区间,1.18 - 79.45],p = 0.04)。
本研究发现,与头孢噻肟相比,使用头孢他啶时II至III期NEC有统计学意义的增加。头孢他啶治疗血培养阳性LOS和MDRO感染的发生率较高,但无统计学意义。有必要进一步研究以评估在新生儿中使用头孢他啶的影响。