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Small Intestinal Bacterial Overgrowth 小肠细菌过度生长
IF 3.1 4区 医学 Q2 INFECTIOUS DISEASES Pub Date : 2024-08-22 DOI: 10.1007/s11908-024-00847-7
Eden Sharabi, Ali Rezaie

Purpose of review

Small intestinal bacterial overgrowth (SIBO) is a chronic gastrointestinal disorder wherein excessive and abnormal growth of bacteria in the small bowel generally causes abdominal pain, bloating, and change in bowel habits. Our understanding of the underlying pathology and microbiome changes in SIBO has advanced greatly in the last 20 years in parallel with advances in treatment methods and diagnostics. Here, we review many of the latest findings that describe the pathophysiology of SIBO as well as its risk factors, clinical behavior, diagnosis, and management.

Recent findings

Studies have begun to employ advanced molecular assays to sequence the small bowel microbiome to reveal the changes evident in SIBO. An increase in the abundance of members of the Enterobacteriaceae is the main alteration to the gut microbiome that correlates with SIBO diagnosis and symptom severity, and enhancement of specific gas-producing pathways has been demonstrated in SIBO. Diagnostic methods continue to evolve with novel methods of small bowel aspiration and changes to interpretation of hydrogen breath tests. Elemental diets are the newest treatment modality that offer an exciting alternative to antibiotic therapy.

Summary

The study of SIBO provides valuable insights into the small bowel microbiome, particularly using molecular testing. Exciting changes to our understanding and treatment of SIBO are already in progress. Future work will be able to better elucidate not only the altered microbiology, but also its gold standard of diagnosis, treatment modalities, and secondary prevention.

综述目的小肠细菌过度生长(SIBO)是一种慢性胃肠道疾病,小肠内细菌过度和异常生长通常会导致腹痛、腹胀和排便习惯改变。在过去 20 年中,随着治疗方法和诊断技术的进步,我们对 SIBO 潜在病理和微生物组变化的认识也有了很大提高。在此,我们回顾了许多描述 SIBO 的病理生理学及其风险因素、临床表现、诊断和管理的最新研究成果。最近的研究成果研究人员已开始采用先进的分子检测方法对小肠微生物组进行测序,以揭示 SIBO 的明显变化。肠杆菌科成员数量的增加是肠道微生物组的主要变化,与 SIBO 诊断和症状严重程度相关,而且已证实 SIBO 会增强特定的产气途径。随着小肠抽吸法的创新和氢气呼气试验解释的改变,诊断方法也在不断发展。元素膳食是最新的治疗方式,为抗生素治疗提供了令人兴奋的替代方案。摘要SIBO 的研究为我们了解小肠微生物组提供了宝贵的资料,特别是通过分子检测。我们对 SIBO 的理解和治疗正在发生令人兴奋的变化。未来的工作将不仅能更好地阐明微生物的变化,还能更好地阐明其诊断的金标准、治疗方法和二级预防。
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引用次数: 0
Nontuberculous Mycobacteria Pulmonary Infection in Children with Cystic Fibrosis 囊性纤维化儿童的非结核分枝杆菌肺部感染
IF 3.1 4区 医学 Q2 INFECTIOUS DISEASES Pub Date : 2024-08-02 DOI: 10.1007/s11908-024-00846-8
Sabiha R. Hussain, Amira M. Said, Jeffrey R. Starke

Purpose of Review

As children and adolescents with cystic fibrosis (CF) have lived longer, they have become more susceptible to pulmonary infection with nontuberculous mycobacteria (NTM). Most NTM infections are caused by the Mycobacterium avium complex (MAC) or Mycobacterium abscessus. We review what is currently known and recommended for treatment of these infections.

Recent Findings

Treatment of MAC infection is standardized and evidence-based, involving a combination of three oral drugs for 12 months. Treatment of M. abscessus infections is more difficult and not standardized owing to the: lack of bactericidal drugs; variability of drug susceptibilities; inability of in vitro antibiotic susceptibility testing to predict clinical success; lack of randomized trial data to guide therapy; need for initial parenteral therapy; higher rate of adverse reactions to the necessary medications; and high cost and limited availability of some of the drugs. Treatment involves an initial several month period including one or more parenteral antibiotics followed by a prolonged continuation phase using several of the best available oral antibiotics. Dual beta-lactam antibiotic and phage therapies offer some hope for improved outcomes in refractory cases.

Summary

The goals for therapy of M. abscessus infections should be considered prior to the onset of treatment, and often are aimed toward improvement in symptoms and quality of life rather that eradication of the organism.

综述目的 随着囊性纤维化(CF)儿童和青少年寿命的延长,他们更容易受到非结核分枝杆菌(NTM)的肺部感染。大多数非结核分枝杆菌感染是由鸟分枝杆菌复合体(MAC)或脓肿分枝杆菌引起的。我们回顾了目前已知的治疗这些感染的方法和建议。最新研究结果MAC感染的治疗是标准化的循证治疗,包括三种口服药物的联合治疗,疗程为12个月。脓毒症鹅口疮感染的治疗更加困难,而且没有标准化,原因包括:缺乏杀菌药物;药物敏感性多变;体外抗生素敏感性测试无法预测临床成功率;缺乏随机试验数据指导治疗;需要进行初始肠外治疗;必要药物的不良反应率较高;部分药物成本高昂且供应有限。治疗包括最初的几个月,使用一种或多种肠外抗生素,然后使用几种最好的口服抗生素进行长期的持续治疗。小结脓毒症荚膜杆菌感染的治疗目标应在治疗开始前考虑,其目的通常是改善症状和生活质量,而不是根除病原体。
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引用次数: 0
Gastrointestinal Manifestation of MPox MPox 的胃肠道表现
IF 3.1 4区 医学 Q2 INFECTIOUS DISEASES Pub Date : 2024-07-11 DOI: 10.1007/s11908-024-00845-9
Timothy Trestrail, Karishma Kodia, Vanessa W. Hui

Purpose of Review

Mpox, formerly known as monkeypox, is a zoonotic illness caused by a virus that is part of the Orthopoxvirus family. Originally identified in humans in the Democratic Republic of Congo in 1970, the disease has been endemic in central African nations. In 2022, an outbreak of Monkeypox warranted a declaration by the World Health Organization (WHO) that the virus was a Public Health Emergency of International Concern. Prior literature documented the dermatological manifestations of the disease, but fewer papers have described and navigated the complexities of mpox gastrointestinal manifestations. We aim to update the current literature on the gastrointestinal (GI) manifestations of mpox, through a review of the literature via PubMed search for English language papers reporting GI manifestations of the virus.

Recent Findings

Individual reports of symptomatic manifestations of mpox have been reported. Upper and lower GI symptoms have been described and, in multiple cases, required multidisciplinary team care to successfully treat the patients.

Summary

GI manifestations of mpox disease are reported in a variety of severities and, in some instances, may require multidisciplinary management.

审查目的天花,原名猴痘,是由一种属于正痘病毒科的病毒引起的人畜共患疾病。该病最初于 1970 年在刚果民主共和国的人类身上发现,之后一直在非洲中部国家流行。2022 年,猴痘疫情爆发,世界卫生组织(WHO)宣布该病毒为国际关注的突发公共卫生事件。以前的文献记录了该疾病的皮肤病表现,但较少文献描述和介绍猴痘胃肠道表现的复杂性。我们旨在通过在 PubMed 上检索报告该病毒胃肠道表现的英文文献,对当前有关水痘胃肠道表现的文献进行更新。上消化道和下消化道症状均有描述,在多个病例中,需要多学科团队护理才能成功治疗患者。总结据报道,水痘疾病的消化道表现有多种严重程度,在某些情况下可能需要多学科管理。
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引用次数: 0
Contemporary Management of Pediatric Invasive Fungal Rhinosinusitis 小儿侵袭性真菌性鼻炎的现代治疗方法
IF 3.1 4区 医学 Q2 INFECTIOUS DISEASES Pub Date : 2024-06-08 DOI: 10.1007/s11908-024-00844-w
Sheng Zhou, Alison Yu, Ethan Frank, Bastien A. Valencia-Sanchez, Sonja Chen, Sean P Polster, Vijay A Patel
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引用次数: 0
Climate Change and Meningoencephalitis in the Americas: A Brewing Storm 气候变化与美洲脑膜脑炎:酝酿中的风暴
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-05-29 DOI: 10.1007/s11908-024-00843-x
Elyssa Dionne, Francisco Machiavello Roman, Shelli Farhadian

Purpose of Review

Climate change has significantly impacted the ecological interactions between pathogens, vectors and human populations. Regional variations in temperature and precipitation patterns have shifted the geographic spread and seasonality of infectious diseases. Cases of meningoencephalitis, in particular those caused by vector-borne infections, are likewise expected to display changes in seasonality and geographic distribution. We review the current evidence on the impact of climate change on the epidemiology of vector-borne meningoencephalitis in the Americas.

Recent Findings

Epidemiologic data and climate models have shown a northward expansion of Lyme disease, West Nile virus, La Crosse virus and Eastern Equine virus infections. Similar geographic shifts are expected to occur with St Louis virus, Everglades virus and Powassan virus infections. These increased incidence is deemed to be the result of warmer winters and heavier precipitation seasons.

Summary

Climate change has led to epidemiologic changes of vector-borne meningoencephalitis in the Americas, and further changes are expected to occur. The impact of climate change on the incidence, seasonality and geographic distribution of vectors and pathogens should be monitored closely.

综述目的气候变化对病原体、病媒和人类之间的生态相互作用产生了重大影响。气温和降水模式的区域性变化改变了传染病的地理分布和季节性。脑膜脑炎病例,尤其是由病媒传染引起的脑膜脑炎病例,预计在季节性和地理分布上也会发生变化。最近的研究结果流行病学数据和气候模型显示,莱姆病、西尼罗河病毒、拉克罗斯病毒和东马病毒感染病例向北扩展。预计圣路易斯病毒、大沼泽地病毒和波瓦桑病毒感染也会发生类似的地理转移。气候变化已导致美洲病媒传播脑膜脑炎的流行病学发生变化,预计还会发生进一步的变化。应密切监测气候变化对病媒和病原体的发病率、季节性和地理分布的影响。
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引用次数: 0
Norovirus Infection in Transplant Recipients 移植受者感染诺如病毒
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-05-18 DOI: 10.1007/s11908-024-00842-y
Matthew Ringer, Maricar Malinis

Purpose of Review

Norovirus is a leading cause of diarrhea in transplant recipients. Norovirus can cause a severe acute syndrome in this patient population. Transplant recipients can also develop a chronic diarrheal syndrome with associated frailty, prolonged viral shedding, hospitalizations, and rejection, with associated mortality. Despite the significant burden of disease and improved diagnostics, there are no specific treatments to target norovirus. We aim to review the virology, epidemiology, diagnosis, clinical presentation, management, and prevention of norovirus.

Recent Findings

A recent retrospective observational study included nine solid organ transplant recipients (5 kidneys, 2 kidney-pancreas, 1 heart, and 1 lung) with chronic norovirus (median duration of diarrhea 12 weeks). Six of these nine patients demonstrated resolution of diarrhea at hospital discharge after oral human immune globulin. A recent phase II randomized controlled trial including solid organ transplant and bone marrow transplant recipients with norovirus compared nitazoxanide with placebo. Nitazoxanide did not demonstrate improved time to resolution of symptoms or duration of viral shedding but may have resulted in transient symptom improvement.

Summary

Norovirus causes significant morbidity and mortality in transplant recipients. Although there are no approved treatment options, there are multiple strategies available, including supportive care, reduction in immunosuppression, intravenous immunoglobulin (IVIG), oral human immune globulin (OHIG), vitamin A, ribavirin, nitazoxanide, and the use of mammalian target of rapamycin (mTOR) inhibitors. Randomized controlled trials are needed to better study these strategies and prevention through the development of a universally available vaccine.

综述目的 诺如病毒是导致移植受者腹泻的主要原因。诺罗病毒可在这一患者群体中引发严重的急性综合征。移植受者也可能患上慢性腹泻综合征,并伴有虚弱、病毒长期脱落、住院和排斥反应以及相关的死亡率。尽管疾病负担沉重,诊断方法也有所改进,但目前还没有针对诺如病毒的特殊治疗方法。我们旨在回顾诺如病毒的病毒学、流行病学、诊断、临床表现、管理和预防。最近的研究结果 最近的一项回顾性观察研究纳入了 9 名患有慢性诺如病毒的实体器官移植受者(5 名肾脏、2 名肾胰脏、1 名心脏和 1 名肺)(中位腹泻持续时间为 12 周)。这九名患者中有六名在口服人免疫球蛋白后,出院时腹泻症状得到缓解。最近进行的一项 II 期随机对照试验比较了硝唑沙尼和安慰剂的疗效,试验对象包括患有诺如病毒的实体器官移植和骨髓移植受者。尼他唑嗪类药物并没有改善症状缓解的时间或病毒脱落的持续时间,但可能会导致短暂的症状改善。虽然目前还没有获得批准的治疗方案,但有多种策略可供选择,包括支持性护理、减少免疫抑制、静脉注射免疫球蛋白 (IVIG)、口服人免疫球蛋白 (OHIG)、维生素 A、利巴韦林、硝氮杂酰胺以及使用哺乳动物雷帕霉素靶点 (mTOR) 抑制剂。需要进行随机对照试验,以更好地研究这些策略和通过开发普遍可用的疫苗进行预防。
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引用次数: 0
Role of Povidone-Iodine in Reducing Surgical Site Infection 聚维酮碘在减少手术部位感染中的作用
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-04-11 DOI: 10.1007/s11908-024-00841-z
A. Haleem, C. L. Abad

Purpose of Review

Surgical site infections (SSIs) are associated with significant morbidity and mortality. Given the role of endogenous carriage of Staphylococcus aureus, current patient decolonization strategies revolve around the application of topical antiseptic agents prior to and at the time of surgery.

Recent Findings

Intranasal single-application povidone-iodine (PVP-I) on the day of surgery is an emerging, attractive alternative to the established approach of a 5-day course of intranasal mupirocin for preoperative decolonization.

Summary

PVP-I appears more convenient and cost-effective for both patients and healthcare systems, and its role in reducing SSI is under investigation. However, most published literature consists of retrospective, single-center studies primarily done in orthopedic surgical populations. Based on current data, PVP-I appears to be as equally effective in SSI reduction as mupirocin, but larger and better-quality studies are needed to implement a change from currently established preoperative decontamination practices.

综述目的手术部位感染(SSI)与严重的发病率和死亡率有关。鉴于金黄色葡萄球菌的内源性携带作用,目前的患者去菌策略主要是在手术前和手术时使用局部消毒剂。近期发现在手术当天鼻内单次使用聚维酮碘(PVP-I)是一种新兴的、有吸引力的方法,可替代术前使用莫匹罗星进行 5 天疗程的既定方法。然而,大多数已发表的文献都是主要针对骨科手术人群进行的回顾性单中心研究。根据目前的数据,PVP-I 在减少 SSI 方面似乎与莫匹罗星同样有效,但要改变目前既定的术前消毒做法,还需要进行更大规模和质量更高的研究。
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引用次数: 0
Correction to: Long Story Short: Establishing Breakpoints for Antimicrobials and 2023 Updates 更正:长话短说:确定抗菌药物的断点和 2023 年更新
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-03-21 DOI: 10.1007/s11908-024-00840-0
M. Bixby, Dina Zheng, Elizabeth B. Hirsch
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引用次数: 0
Care Bundles in Surgical Site Infection Prevention: A Narrative Review 手术部位感染预防中的护理捆绑:叙述性综述
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-03-01 DOI: 10.1007/s11908-024-00837-9
Patrick R. Ching

Purpose of Review

Surgical site infections are healthcare-associated infections that cause significant morbidity and mortality. Best practices in prevention of these infections are combined in care bundles for consistent implementation.

Recent Findings

Care bundles have been used in nearly all surgical specialties. While the composition and size of bundles vary, the effect of a bundle depends on the number of evidence-based interventions included and the consistency of implementation. Bundles work because of the cooperation and collaboration among members of a team. Bundles for prevention of surgical site infections should address the multiple risk factors for infection before, during, and after the surgery.

Summary

Bundles increase standardization of processes and decrease operative variance that both lead to reductions in surgical site infections.

综述目的 手术部位感染是与医疗保健相关的感染,会导致严重的发病率和死亡率。最近的研究结果几乎所有外科专科都采用了护理包。虽然护理包的组成和规模各不相同,但护理包的效果取决于所包含的循证干预措施的数量和实施的一致性。捆绑疗法之所以有效,是因为团队成员之间的合作与协作。预防手术部位感染的捆绑方案应针对术前、术中和术后感染的多种风险因素。摘要捆绑方案提高了流程的标准化程度,减少了手术中的差异,从而减少了手术部位感染。
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引用次数: 0
Exploring the Potential of Farnesol as a Novel Antifungal Drug and Related Challenges 探索法呢醇作为新型抗真菌药物的潜力及相关挑战
IF 3.1 4区 医学 Q1 Medicine Pub Date : 2024-02-26 DOI: 10.1007/s11908-024-00839-7

Abstract

Purpose of Review

Farnesol (FOH) is a quorum-sensing molecule with potential as an antifungal drug. Given the growing concern about fungal drug resistance, exploring new solutions is crucial. Therefore, summarizing the antifungal activity of FOH is expected to be the basis for further FOH research and application. Herein, we reviewed the in vitro and in vivo antifungal efficacy of FOH alone and in combination with conventional antifungal drugs, as well as its mechanisms of action. Furthermore, we discussed the prospects and challenges of the FOH application in detail.

Recent Findings

Recent studies have revealed that FOH can target various aspects, such as reactive oxygen species production, induction of apoptosis, and modulation of virulence factors, to inhibit fungal growth and reduce fungal pathogenicity, thereby exerting its antifungal activity. Furthermore, FOH can suppress resistance-associated genes, such as those of biofilm and ergosterol, so as to enhance the fungicidal effectiveness of conventional antifungal drugs. However, the action mechanism of FOH on drug efflux pumps remains unclear and warrants further investigation.

Summary

FOH can prevent and treat fungal infections. It exerts significant antimicrobial effects on fungal planktonic and biofilm cells, enhances the antimicrobial efficacy of conventional antifungal drugs, and reverses and reduces fungal drug resistance. However, further in vitro and in vivo studies are needed to assess the safety of FOH due to potential adverse effects on immune cells and other factors.

摘要 综述目的 法尼醇(FOH)是一种法定人数感应分子,具有作为抗真菌药物的潜力。鉴于真菌耐药性问题日益受到关注,探索新的解决方案至关重要。因此,总结 FOH 的抗真菌活性有望为 FOH 的进一步研究和应用奠定基础。在此,我们综述了 FOH 单独或与传统抗真菌药物联用的体外和体内抗真菌功效及其作用机制。此外,我们还详细讨论了 FOH 的应用前景和挑战。 最新研究结果 最新研究发现,FOH 可针对活性氧生成、诱导细胞凋亡和调节毒力因子等多个方面抑制真菌生长,降低真菌致病性,从而发挥其抗真菌活性。此外,FOH 还能抑制抗药性相关基因,如生物膜基因和麦角固醇基因,从而增强传统抗真菌药物的杀真菌效果。然而,FOH 对药物外流泵的作用机制仍不清楚,有待进一步研究。 总结 FOH 可以预防和治疗真菌感染。它对真菌浮游细胞和生物膜细胞有明显的抗菌作用,能增强常规抗真菌药物的抗菌效果,并能逆转和降低真菌耐药性。不过,由于 FOH 可能对免疫细胞和其他因素产生不利影响,因此还需要进一步的体外和体内研究来评估其安全性。
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引用次数: 0
期刊
Current Infectious Disease Reports
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