Abdelaal Neveen Hassan, Aziz Nafisa Hassan Rifaat Abdel, Abdelaziz Asmaa Mohamed, Khalil Sahar Badr Hassan, Abdel-Latif Mohamed Mahmoud Mohamed
Clinical Pharmacy Unit, Department of Pharmacy and Medical Supplies, Assiut University Children's Hospital, Assiut, Egypt.
Department of Pediatrics, Faculty of Medicine, Assiut University, Assiut, Egypt.
J Pharm Health Care Sci. 2025 Sep 23;11(1):81. doi: 10.1186/s40780-024-00404-3.
Antimicrobial resistance represents a great global concern and initiating an antimicrobial stewardship program is one of the main efforts to control antimicrobial resistance through optimizing antimicrobial utilization. Antibiotics are used extensively and inappropriately in neonatal intensive care units (NICUs). The present study aimed to assess the clinical impact of the antibiotics stewardship program (ASP) in the NICU.
The study was conducted in two phases at the NICU, Assiut University Children’s Hospital, where 1200 patients were enrolled from January 2019 to June 2020. The pre-ASP phase included making NICU-specific antibiograms, choosing the antibiotic use evaluation measures, conducting antibiotic use evaluations, and designing the ASP. The ASP intervention phase included the implementation of ASP, which involved modifying the neonatal sepsis treatment protocol according to the local antibiotic susceptibility patterns and measuring its clinical outcomes. Categorical data were tested with Pearson’s chi-squared test and Fisher’s exact test. Numerical data were tested with the Wilcoxon rank sum test.
A total of 603 and 597 patients were enrolled in the pre-ASP and intervention-ASP phases, respectively. The ASP intervention phase showed a significant increase in the number of C-reactive protein tests [1(1–2)vs 2(1–3), = 0.001], microbiological cultures per patient [0(0–1) vs. 1(0–1), = 0.001], the number of patients taking definitive therapy [15.1% vs. 20.1%, = 0.023], and the number of pharmacist interventions per patient [1(1–1) vs. 1(1–2), = 0.001]. The duration of the antibiotic course [9(5–16) vs. 8(4–15), = 0.04] and the number of patients taking empirical therapy [38.6% vs. 30.7%, = 0.004] were significantly decreased in the ASP intervention phase. The prescribing rates of antibiotics and their consumption in terms of length of therapy were changed according to the NICU-specific antibiogram; however, days of therapy were unchanged in the ASP intervention phase. There was a significant reduction in the 14-day [46% vs. 28%, = 0.03] and 28-day [64% vs. 43%, = 0.022] mortality of patients with late-onset sepsis after modifying the neonatal sepsis treatment protocol according to the local antibiotic susceptibility patterns in the ASP intervention phase.
ASP implementation was successful in improving antibiotic prescribing and modifying the neonatal sepsis treatment protocol according to the local antibiotic susceptibility patterns, which resulted in reduced 14- and 28-day mortality.
Clinical Impact of an Antibiotic Stewardship Program in a Neonatal Intensive Care Unit, Registration number NCT04039152. Registered 31 July 2019 - Retrospectively registered. https://classic.clinicaltrials.gov/ct2/show/NCT04039152.
抗菌药物耐药性是全球广泛关注的问题,启动抗菌药物管理计划是通过优化抗菌药物使用来控制抗菌药物耐药性的主要措施之一。抗生素在新生儿重症监护病房(NICU)中被广泛且不恰当地使用。本研究旨在评估抗生素管理计划(ASP)在NICU中的临床影响。
该研究在阿斯尤特大学儿童医院的NICU分两个阶段进行,2019年1月至2020年6月期间共纳入1200例患者。ASP实施前阶段包括制定NICU特定的抗菌谱、选择抗生素使用评估措施、进行抗生素使用评估以及设计ASP。ASP干预阶段包括实施ASP,即根据当地抗生素敏感性模式修改新生儿败血症治疗方案并评估其临床结果。分类数据采用Pearson卡方检验和Fisher精确检验。数值数据采用Wilcoxon秩和检验。
ASP实施前阶段和干预阶段分别纳入603例和597例患者。ASP干预阶段C反应蛋白检测次数显著增加[1(1 - 2)对2(1 - 3),P = 0.001],每位患者的微生物培养次数[0(0 - 1)对1(0 - 1),P = 0.001],接受确定性治疗的患者人数[15.1%对20.1%,P = 0.023],以及每位患者的药师干预次数[1(1 - 1)对1(1 - 2),P = 0.001]。抗生素疗程时长[9(5 - 16)对8(4 - 15),P = 0.04]和接受经验性治疗的患者人数[38.6%对30.7%,P = 0.004]在ASP干预阶段显著减少。根据NICU特定抗菌谱,抗生素的处方率及其治疗时长方面的消耗量有所变化;然而,ASP干预阶段的治疗天数未变。在ASP干预阶段,根据当地抗生素敏感性模式修改新生儿败血症治疗方案后,迟发性败血症患者的14天死亡率[46%对28%,P = 0.03]和28天死亡率[64%对43%,P = 0.022]显著降低。
ASP的实施成功改善了抗生素处方,并根据当地抗生素敏感性模式修改了新生儿败血症治疗方案,从而降低了14天和28天死亡率。
新生儿重症监护病房抗生素管理计划的临床影响,注册号NCT04039152。2019年7月31日注册 - 回顾性注册。https://classic.clinicaltrials.gov/ct2/show/NCT04039152