1142 infection control & hospital epidemiology october 2017, vol. 38, no. 10
reduced the proportion of newborns undergoing invasive evaluation and antibiotic treatment without any apparent adverse effects.33 Continued efforts such as these are a key component in further reducing unnecessary antimicrobial prescription in the NICU. Baseline antibiotic utilization in our NICU was low com-
pared to peer NICUs, yet we still demonstrated a statistically significant reduction in ampicillin utilization (the most fre- quently prescribed antibiotic in our NICU) in the stewardship period. This finding is likely the result of implementation of several aspects of our clinical guidelines which incorporate ampicillin use, including limiting the duration of postoperative antibiotic prophylaxis, eliminating the need for antibiotic prophylaxis after a single, uncomplicated urinary tract infection, and setting limitations for duration of treatment for NEC and early-onset clinical sepsis. No statistically significant changes in utilization of other commonly prescribed antibiotics, however, were
observed.Alowrate of tobramycin use was observed in the preintervention period that correlated with a gentamicin shortage, but not with changes in demographics or the burden of infection or NEC. The shortage may therefore have led to more judicious prescription practices. Clindamycin utilization remained unchanged over the study period. In our NICU, clindamycin is utilized as treatment for NEC. No significant changes in NEC rates observed over the study period may partly explain this finding. Vancomycin and cefotaxime utilization appeared to decline prior to ASP implementation. We experi- enced a substantial reduction in NICU-acquired infections from 2008 to 2010 after implementing an initiative to improve central-line–associated bloodstream infections,34 which may partially explain this observation. Our study has several limitations. DOT per 1,000 PD was used
as our main outcome measure, but the optimal metric for antibiotic stewardship has not been defined.4,35 Our primary focus was on improving antibiotic prescription, but we did not delve deeper into whether antimicrobial prescription practices are affected by specific conditions. We cannot prove that ASP implementation was directly responsible for any of the changes observed. Lastly, we were not powered to show differences in other outcome measures such as antimicrobial resistance between periods, so the impact of our programon this important metric remains undetermined. In summary, we demonstrated the successful design and
implementation of a multidisciplinary ASP in a level IV NICU, with improvements noted in antibiotic prescription practices. Our success is likely multifactorial, but we believe a key component was prospective audit and feedback to (and from) the prescriber. There has recently been a great deal of increased attention and resources allocated to the reduction of inappropriate antibiotic use on a national level, including international collaborative efforts among NICUs.36 Our efforts, as well as the overall reduction in antimicrobial utilization observed among NICUs in the Pediatric Health Information System, may exemplify a growing awareness that ASPs have the potential to not only reduce antibiotic overuse and misuse but
also to impact common neonatal morbidities and mortality faced by these extremely vulnerable infants.
acknowledgments
We would like to thank the NICU staff at YNHCH, and in the Division of Pediatric Surgery for their dedication, support, and diligence in improving antibiotic utilization. Financial support: No financial support was provided relevant to this article. Potential conflicts of interest: All authors report no conflicts of interest
relevant to this article. Address correspondence to Matthew J. Bizzarro, MD, Department of
Pediatrics, Division of Neonatal-Perinatal Medicine, PO Box 208064, New Haven, CT 06520-8064 (
matthew.bizzarro@
yale.edu).
references
1. Clark RH, Bloom BT, Spitzer AR, Gerstmann DR. Reported medication use in the neonatal intensive care unit: data from a large national data set. Pediatrics 2006;117:1979–1987.
2. Fonseca SN, Ehrenkranz RA, Baltimore RS. Epidemiology of antibiotic use in a neonatal intensive care unit. Infect Control Hosp Epidemiol 1994;15:156–162.
3. Wirtschafter DD, Padilla G, Suh O, Wan K, Trupp D, Fayard EE. Antibiotic use for presumed neonatally acquired infections far exceeds that for central line-associated blood stream infections: an exploratory critique. J Perinatol 2011;31:514–518.
4. Cantey JB, Wozniak PS, Sanchez PJ. Prospective surveillance of antibiotic use in the neonatal intensive care unit: results from the SCOUT study. Pediatr Infect Dis J 2015;34:267–272.
5. Almuneef MA, Baltimore RS, Farrel PA, Reagan-Cirincione P, Dembry LM. Molecular typing demonstrating transmission of gram-negative rods in a neonatal intensive care unit in the absence of a recognized epidemic. Clin Infect Dis 2001;32: 220–227.
6. Bizzarro MJ, Gallagher PG. Antibiotic-resistant organisms in the neonatal intensive care unit. Semin Perinatol 2007;31:26–32.
7. Patel SJ, Saiman L. Antibiotic resistance in neonatal intensive care unit pathogens: mechanisms, clinical impact, and prevention including antibiotic stewardship. Clin Perinatol 2010;37: 547–563.
8. Shane AL, Stoll BJ. Recent developments and current issues in the epidemiology, diagnosis, and management of bacterial and fungal neonatal sepsis. Am J Perinatol 2013;30:131–141.
9. Aliaga S, Clark RH, Laughon M, et al. Changes in the incidence of candidiasis in neonatal intensive care units. Pediatrics 2014;133:236–242.
10. Tripathi N, Cotten CM, Smith PB. Antibiotic use and misuse in the neonatal intensive care unit. Clin Perinatol 2012;39:61–68.
11. Alexander VN, Northrup V, Bizzarro MJ. Antibiotic exposure in the newborn intensive care unit and the risk of necrotizing enterocolitis. J Pediatr 2011;159:392–397.
12. Cotten CM, Taylor S, Stoll B, et al. Prolonged duration of initial empirical antibiotic treatment is associated with increased rates of necrotizing enterocolitis and death for extremely low birth weight infants. Pediatrics 2009;123:58–66.
13. Kuppala VS, Meinzen-Derr J, Morrow AL, Schibler KR. Prolonged initial empirical antibiotic treatment is associated with adverse outcomes in premature infants. JPediatr 2011;159:720–725.
Page 1 |
Page 2 |
Page 3 |
Page 4 |
Page 5 |
Page 6 |
Page 7 |
Page 8 |
Page 9 |
Page 10 |
Page 11 |
Page 12 |
Page 13 |
Page 14 |
Page 15 |
Page 16 |
Page 17 |
Page 18 |
Page 19 |
Page 20 |
Page 21 |
Page 22 |
Page 23 |
Page 24 |
Page 25 |
Page 26 |
Page 27 |
Page 28 |
Page 29 |
Page 30 |
Page 31 |
Page 32 |
Page 33 |
Page 34 |
Page 35 |
Page 36 |
Page 37 |
Page 38 |
Page 39 |
Page 40 |
Page 41 |
Page 42 |
Page 43 |
Page 44 |
Page 45 |
Page 46 |
Page 47 |
Page 48 |
Page 49 |
Page 50 |
Page 51 |
Page 52 |
Page 53 |
Page 54 |
Page 55 |
Page 56 |
Page 57 |
Page 58 |
Page 59 |
Page 60 |
Page 61 |
Page 62 |
Page 63 |
Page 64 |
Page 65 |
Page 66 |
Page 67 |
Page 68 |
Page 69 |
Page 70 |
Page 71 |
Page 72 |
Page 73 |
Page 74 |
Page 75 |
Page 76 |
Page 77 |
Page 78 |
Page 79 |
Page 80 |
Page 81 |
Page 82 |
Page 83 |
Page 84 |
Page 85 |
Page 86 |
Page 87 |
Page 88 |
Page 89 |
Page 90 |
Page 91 |
Page 92 |
Page 93 |
Page 94 |
Page 95 |
Page 96 |
Page 97 |
Page 98 |
Page 99 |
Page 100 |
Page 101 |
Page 102 |
Page 103 |
Page 104 |
Page 105 |
Page 106 |
Page 107 |
Page 108 |
Page 109 |
Page 110 |
Page 111 |
Page 112 |
Page 113 |
Page 114 |
Page 115 |
Page 116 |
Page 117 |
Page 118 |
Page 119 |
Page 120 |
Page 121 |
Page 122 |
Page 123 |
Page 124 |
Page 125 |
Page 126 |
Page 127 |
Page 128 |
Page 129 |
Page 130 |
Page 131 |
Page 132 |
Page 133 |
Page 134 |
Page 135 |
Page 136 |
Page 137 |
Page 138 |
Page 139 |
Page 140 |
Page 141 |
Page 142 |
Page 143 |
Page 144