Seliem W A, Sultan A M
Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Department of Pediatrics, Mansoura University, Mansoura, Egypt.
J Neonatal Perinatal Med. 2018;11(3):323-330. doi: 10.3233/NPM-17128.
This study was conducted to find out the bacterial causes of early onset neonatal sepsis and their susceptibility pattern for different classes of antibiotics in neonates admitted to neonatal intensive care unit (NICU) of Mansoura-Egypt.
A descriptive cross-sectional study was conducted. All admitted newborns to our study were infants at <72 hours of age with clinical features of sepsis or product of an in-house delivery at Mansoura University Hospital with risk factors for neonatal sepsis. Identification of Gram-negative isolates was confirmed by API 20E kits (bioMerieux). Antibiotic susceptibility was performed by Kirby-Bauer disc diffusion method. Bacteria resistant to ≥3 antimicrobial classes were counted as multidrug resistant.
One hundred eighty eight babies were admitted to our study. Positive blood culture was reported in 34.6% of newborn infants with prevalence of 4.02/1,000 live births. The most common isolated bacteria in early onset neonatal sepsis were coagulase negative staphylococci followed by Klebsiella pneumoniae and Serratia marcescens. The Gram-positive bacteria showed high resistance to ampicillin 93.9% while all the isolates were susceptible to vancomycin. The isolated Gram-negative bacteria were highly resistant to ampicillin [96.9%], amoxicillin-clavulanic acid [90.6%], cefotaxime [84.4%] and ceftazidime [84.4%]. Best sensitivity among all isolates was observed to imipenem. Multidrug resistance was observed among 45.5% of the Gram-positive and 68.8% of Gram-negative isolates.
Appropriate identification of the source of infection and initiation of an effective management can reduce both mortality and morbidity associated with neonatal sepsis. The challenge is to initiate immediate empirical antibiotic therapy according to a strictly implemented updated antibiotic policy based on an individualized community established antimicrobial sensitivity pattern of microorganisms causing early onset neonatal sepsis.
本研究旨在查明埃及曼苏拉新生儿重症监护病房(NICU)收治的新生儿早发型败血症的细菌病因及其对不同种类抗生素的药敏模式。
开展了一项描述性横断面研究。纳入本研究的所有新生儿均为年龄小于72小时、具有败血症临床特征的婴儿,或在曼苏拉大学医院经院内分娩且具有新生儿败血症危险因素的婴儿。革兰氏阴性菌分离株通过API 20E试剂盒(生物梅里埃公司)进行鉴定。采用 Kirby-Bauer 纸片扩散法进行抗生素敏感性检测。对≥3类抗菌药物耐药的细菌被视为多重耐药菌。
188名婴儿纳入本研究。34.6%的新生儿血培养呈阳性,患病率为4.02/1000活产儿。早发型新生儿败血症中最常见的分离细菌是凝固酶阴性葡萄球菌,其次是肺炎克雷伯菌和粘质沙雷氏菌。革兰氏阳性菌对氨苄西林的耐药率高达93.9%,而所有分离株对万古霉素均敏感。分离出的革兰氏阴性菌对氨苄西林[96.9%]、阿莫西林-克拉维酸[90.6%]、头孢噻肟[84.4%]和头孢他啶[84.4%]高度耐药。所有分离株中对亚胺培南的敏感性最佳。45.5%的革兰氏阳性菌和68.8%的革兰氏阴性菌分离株存在多重耐药。
正确识别感染源并启动有效的管理措施可降低新生儿败血症相关的死亡率和发病率。面临的挑战是根据严格执行的最新抗生素政策,依据引起早发型新生儿败血症的微生物的个体化社区确定的抗菌药敏模式,立即开始经验性抗生素治疗。