“揭开不寻常的面纱”:一系列多药耐药的伊丽莎白氏脑膜炎败血症导致早产儿迟发性败血症和脑膜炎的病例。

Q2 Pharmacology, Toxicology and Pharmaceutics
F1000Research Pub Date : 2025-02-06 eCollection Date: 2024-01-01 DOI:10.12688/f1000research.158137.2
Prajnha U P, Anisha Maria Fernandes, Suchitra Shenoy M, Sinchana Bhat
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引用次数: 0

摘要

伊莉莎白菌脑膜炎败血症是一种罕见的院内病原体,可引起新生儿和免疫功能低下个体的脑膜炎、肺炎和败血症。它对许多常用的用于治疗革兰氏阴性病原体的一线抗生素具有耐药性。在此,我们提出三例迟发性脓毒症与多药耐药(MDR)伊丽莎白脑膜炎败血症高危新生儿。病例1是1天大的早产低体重婴儿,表现为呼吸窘迫综合征和感染性休克。患者插管并给予经验性广谱抗生素和抗真菌药物。血培养培养出克鲁氏念珠菌,因此开始使用两性霉素B。第27天重复血培养显示革兰氏阴性杆菌,经MALDI-TOF鉴定为伊丽莎白氏脑膜炎败血症。抗生素药敏试验(AST)显示对哌拉西林/他唑巴坦耐药,但对万古霉素、左氧氟沙星和米诺环素敏感。静脉注射万古霉素,临床改善,血培养阴性。病例2是一个11天大的早产,低出生体重婴儿,表现为发烧。初步调查显示全血细胞计数(CBC)参数正常,CRP水平升高。血液和脑脊液培养分离出具有类似AST模式的伊丽莎白氏脑膜炎败血症。临床好转且随访血培养阴性后开始静脉注射环丙沙星。病例3为1日龄早产儿,与胎龄相符,表现为呼吸窘迫综合征。婴儿插管并开始肌力支持和静脉注射抗生素。第4天血培养显示脑膜炎败血症,开始使用万古霉素。第6天和第14天的后续培养培养出鲍曼不动杆菌。给予左氧氟沙星联合粘菌素治疗,7天后血培养为阴性,临床改善。伊丽莎白氏脑膜炎败血症是医院获得性感染的一个重要原因,特别是在新生儿重症监护病房(NICU),导致暴发。临床医生必须高度怀疑在高危患者中引起败血症和脑膜炎的革兰氏阴性杆菌脑膜炎脓毒杆菌。最近的技术进步使准确的物种形成能够指导治疗并降低发病率和死亡率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
"Unmasking the Uncommon": A case series of multi-drug resistant Elizabethkingia meningoseptica causing late-onset sepsis and meningitis in preterm neonates.

Elizabethkingia meningoseptica is an uncommon nosocomial pathogen that causes meningitis, pneumonia, and sepsis in neonates and in immunocompromised individuals. It exhibits resistance to many commonly employed first-line antibiotics used to treat gram-negative pathogens. Herein, we present three cases of late-onset sepsis with multi-drug resistant (MDR) Elizabethkingia meningoseptica in high-risk neonates. Case 1 was a one-day-old preterm low-birth-weight infant who presented with respiratory distress syndrome and septic shock. The patient was intubated and administered empirical broad-spectrum antibiotics and antifungal agents. Blood culture grew Candida krusei, hence Amphotericin B was initiated. Repeat blood culture on day 27 showed gram-negative bacilli, identified as Elizabethkingia meningoseptica by MALDI-TOF . Antibiotic susceptibility testing (AST) revealed resistance to Piperacillin/Tazobactam, but sensitivity to Vancomycin, Levofloxacin, and Minocycline. IV Vancomycin was administered, which resulted in clinical improvement and negative blood culture results. Case 2 was an eleven-day-old preterm, low-birth-weight baby who presented with fever. Initial investigations revealed normal complete blood counts (CBC) parameters and elevated CRP levels. Blood and CSF cultures isolated Elizabethkingia meningoseptica with a similar AST pattern. Intravenous Ciprofloxacin was initiated with clinical improvement and negative follow-up blood cultures. Case 3 was a one-day-old preterm baby, appropriate-to-gestational age, presenting with respiratory distress syndrome. The infant was intubated and started on inotropic support and intravenous antibiotics. Blood cultures on day 4 showed Elizabethkingia meningoseptica and Vancomycin was started. Follow-up cultures on days 6 and 14 grew Acinetobacter baumannii. A combination of Levofloxacin and Colistin was added, and blood cultures were negative after seven days, with clinical improvement. Elizabethkingia meningoseptica is a significant cause of hospital-acquired infections, especially in Neonatal Intensive Care Unit (NICU), leading to outbreaks. Clinicians must have a high degree of suspicion of E. meningoseptica for gram-negative bacilli causing sepsis and meningitis in high-risk patients. Recent technological advances have enabled accurate speciation to guide therapy and reduce morbidity and mortality rates.

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来源期刊
F1000Research
F1000Research Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
5.00
自引率
0.00%
发文量
1646
审稿时长
1 weeks
期刊介绍: F1000Research publishes articles and other research outputs reporting basic scientific, scholarly, translational and clinical research across the physical and life sciences, engineering, medicine, social sciences and humanities. F1000Research is a scholarly publication platform set up for the scientific, scholarly and medical research community; each article has at least one author who is a qualified researcher, scholar or clinician actively working in their speciality and who has made a key contribution to the article. Articles must be original (not duplications). All research is suitable irrespective of the perceived level of interest or novelty; we welcome confirmatory and negative results, as well as null studies. F1000Research publishes different type of research, including clinical trials, systematic reviews, software tools, method articles, and many others. Reviews and Opinion articles providing a balanced and comprehensive overview of the latest discoveries in a particular field, or presenting a personal perspective on recent developments, are also welcome. See the full list of article types we accept for more information.
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