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1.
Rev. neurol. (Ed. impr.) ; 77(4): 87-93, Agos 16, 2023. tab
Artículo en Inglés, Español | IBECS | ID: ibc-224060

RESUMEN

Introducción: La meningoencefalitis infecciosa (MEI) es una emergencia neurológica con importante morbimortalidad. El panel Biofire FilmArray? para meningitis/encefalitis (FAME) en el líquido cefalorraquídeo (LCR) ha demostrado ser una valiosa herramienta para el diagnóstico etiológico de la MEI, facilitando una terapia antimicrobiana dirigida. El objetivo es determinar el impacto del panel FAME en las decisiones terapéuticas antimicrobianas en pacientes con sospecha de MEI en las primeras 24 horas de la valoración clínica. Pacientes y métodos: Estudio observacional descriptivo que comenta las manifestaciones cínicas, los resultados de neuroimágenes y paraclínicos, y la antibioticoterapia de pacientes con sospecha de MEI. Se realizó un análisis del impacto que tiene el FAME en la terapia antimicrobiana en las primeras 24 horas de la valoración clínica de los pacientes. Resultados: Se incluyó a 44 pacientes. El tiempo promedio para obtener el resultado del panel FAME en el LCR fue de nueve horas, con un 20,4% (9/44) de pruebas positivas. En las primeras 24 horas de la valoración clínica, su resultado tuvo impacto en las decisiones terapéuticas antimicrobianas en el 75% (33/44) de los casos. En pacientes con alta sospecha clínica de MEI, el resultado del FAME permitió cambiar la terapia empírica inicial a una dirigida en el 15% (3/20) y suspender la terapia empírica inicial en el 35% (7/20) de los sujetos. En pacientes con baja sospecha clínica de MEI, su resultado permitió que al 25% (6/24) se le confirmara la sospecha y se le iniciara antibioticoterapia dirigida; y que al 70,8% (17/24) se le descartara el diagnóstico y no se le iniciara tratamiento. Conclusiones: El resultado del panel FAME en el LCR tiene alto impacto en la toma de decisiones terapéuticas antimicrobianas en las primeras 24 horas de la valoración clínica. Sin embargo, su interpretación debe hacerse con el contexto clínico, la epidemiología local y otros estudios diagnósticos.(AU)


Introduction: Infectious meningoencephalitis (IME) is a neurological emergency with a significant rate of morbidity and mortality. The Biofire FilmArray® meningitis/encephalitis (FAME) panel for testing in cerebrospinal fluid (CSF) has proven to be a valuable tool for the aetiological diagnosis of IME, facilitating targeted antimicrobial therapy. The aim is to determine the impact of the FAME panel on antimicrobial therapeutic decisions in patients with suspected IME in the first 24 hours of clinical assessment. Patients and methods: This is a descriptive observational study that comments on the clinical manifestations, the neuroimaging and paraclinical findings, and the antibiotic therapy of patients with suspected IME. An analysis was performed to determine the impact of FAME on antimicrobial therapy in the first 24 hours of the clinical assessment of patients. Results: Altogether 44 patients were included. The average time required to obtain the result of the FAME panel for testing in CSF was nine hours, with 20.4% (9/44) of tests yielding positive results. Within 24 hours of clinical assessment, their outcome had an impact on antimicrobial treatment decisions in 75% (33/44) of cases. In patients with a high clinical suspicion of IME, the result of FAME made it possible to change the initial empirical therapy to a targeted therapy in 15% (3/20) of cases and to discontinue the initial empirical therapy in 35% (7/20) of the subjects. In patients with low clinical suspicion of IME, their result allowed 25% (6/24) to have their suspicion confirmed and they were started on targeted antibiotic therapy; in contrast, 70.8% (17/24) had their diagnosis ruled out and were not started on treatment. Conclusions: The result of the FAME panel for testing in CSF has a high impact on antimicrobial therapeutic decisions within 24 hours of clinical assessment. However, it must be interpreted with the clinical context, local epidemiology and other diagnostic studies.(AU)


Asunto(s)
Humanos , Masculino , Femenino , Adulto Joven , Adulto , Persona de Mediana Edad , Anciano , Meningitis/congénito , Encefalitis Infecciosa/tratamiento farmacológico , Encefalitis Infecciosa/diagnóstico , Meningoencefalitis/diagnóstico , Antibacterianos , Toma de Decisiones Clínicas , Colombia , Epidemiología Descriptiva , Neurología , Enfermedades del Sistema Nervioso
2.
Curr Opin Infect Dis ; 36(3): 186-191, 2023 06 01.
Artículo en Inglés | MEDLINE | ID: mdl-37093056

RESUMEN

PURPOSE OF REVIEW: Free-living amebae (FLA) including Naegleria fowleri , Balamuthia mandrillaris , and Acanthamoeba species can cause rare, yet severe infections that are nearly always fatal. This review describes recent developments in epidemiology, diagnosis, and treatment of amebic meningoencephalitis. RECENT FINDINGS: Despite similarities among the three pathogenic FLA, there are notable variations in disease presentations, routes of transmission, populations at risk, and outcomes for each. Recently, molecular diagnostic tools have been used to diagnose a greater number of FLA infections. Treatment regimens for FLA have historically relied on survivor reports; more data is needed about novel treatments, including nitroxoline. SUMMARY: Research to identify new drugs and guide treatment regimens for amebic meningoencephalitis is lacking. However, improved diagnostic capabilities may lead to earlier diagnoses, allowing earlier treatment initiation and improved outcomes. Public health practitioners should continue to prioritize increasing awareness and providing education to clinicians, laboratorians, and the public about amebic infections.


Asunto(s)
Acanthamoeba , Amebiasis , Infecciones Protozoarias del Sistema Nervioso Central , Encefalitis Infecciosa , Meningoencefalitis , Humanos , Infecciones Protozoarias del Sistema Nervioso Central/diagnóstico , Infecciones Protozoarias del Sistema Nervioso Central/tratamiento farmacológico , Infecciones Protozoarias del Sistema Nervioso Central/epidemiología , Amebiasis/diagnóstico , Amebiasis/tratamiento farmacológico , Amebiasis/epidemiología , Meningoencefalitis/diagnóstico , Meningoencefalitis/tratamiento farmacológico , Meningoencefalitis/epidemiología , Encefalitis Infecciosa/diagnóstico , Encefalitis Infecciosa/tratamiento farmacológico , Encefalitis Infecciosa/epidemiología
3.
Infection ; 51(4): 859-867, 2023 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-36152225

RESUMEN

PURPOSE: Data on encephalitis in elderly patients are scarce. We aimed to describe the characteristics, aetiologies, management, and outcome of encephalitis in patients older than 65 years. METHODS: We performed an ancillary study of ENCEIF, a prospective cohort that enrolled all cases of encephalitis managed in 46 clinical sites in France during years 2016-2019. Cases were categorized in three age groups: (1) 18-64; (2) 65-79; (3) ≥ 80 years. RESULTS: Of the 494 adults with encephalitis enrolled, 258 (52%) were ≥ 65 years, including 74 (15%) ≥ 80 years. Patients ≥ 65 years were more likely to present with coma, impaired consciousness, confusion, aphasia, and rash, but less likely to present with fever, and headache (P < 0.05 for each). Median cerebrospinal fluid (CSF) white cells count was 61/mm3[13-220] in 65-79 years, 62 [17-180] in ≥ 80 years, vs. 114 [34-302] in < 65 years (P = 0.01). The proportion of cases due to Listeria monocytogenes and VZV increased after 65 years (P < 0.001), while the proportion of tick-borne encephalitis and Mycobacterium tuberculosis decreased with age (P < 0.05 for each). In-hospital mortality was 6/234 (3%) in < 65 years, 18/183 (10%) in 65-79 years, and 13/73 (18%) in ≥ 80 years (P < 0.001). Age ≥ 80 years, coma on admission, CSF protein ≥ 0.8 g/L and viral encephalitis were independently predictive of 6 month mortality. CONCLUSION: Elderly patients represent > 50% of adults with encephalitis in France, with higher proportion of L. monocytogenes and VZV encephalitis, increased risk of death, and sequels. The empirical treatment currently recommended, aciclovir and amoxicillin, is appropriate for this age group.


Asunto(s)
Encefalitis , Encefalitis Infecciosa , Adulto , Humanos , Anciano , Anciano de 80 o más Años , Estudios Prospectivos , Coma/complicaciones , Encefalitis Infecciosa/tratamiento farmacológico , Encefalitis Infecciosa/epidemiología , Encefalitis Infecciosa/complicaciones , Encefalitis/tratamiento farmacológico , Encefalitis/epidemiología , Aciclovir , Francia/epidemiología , Herpesvirus Humano 3
4.
J Pediatric Infect Dis Soc ; 11(12): 578-581, 2022 Dec 28.
Artículo en Inglés | MEDLINE | ID: mdl-36041049

RESUMEN

We report the first case of Balamuthia mandrillaris granulomatous amoebic encephalitis definitively acquired in Africa. Our case emphasizes initial nonspecific dermatological features, delays in confirmation of the diagnosis, difficulties accessing recommended medication, and uncertainty about optimal treatment of a disease with a frequently fatal outcome.


Asunto(s)
Amebiasis , Balamuthia mandrillaris , Encefalitis , Encefalitis Infecciosa , Humanos , Pueblo Africano , Amebiasis/diagnóstico , Amebiasis/tratamiento farmacológico , Encéfalo , Encefalitis/diagnóstico , Encefalitis/tratamiento farmacológico , Resultado Fatal , Granuloma , Encefalitis Infecciosa/diagnóstico , Encefalitis Infecciosa/tratamiento farmacológico , Preescolar
6.
Pediatr Infect Dis J ; 40(6): 513-517, 2021 06 01.
Artículo en Inglés | MEDLINE | ID: mdl-33902074

RESUMEN

BACKGROUND: Infectious encephalitis represents a rare but potentially severe clinical condition. However, limited international data are available in pediatric age. METHODS: We conducted a retrospective study to review (a) the clinical presentation; (b) laboratory, radiology, and neurophysiology findings; (c) the correlations between these exams and outcome; and (d) the therapy performed. RESULTS: Fifty-six patients were enrolled [22 female (39.6%), mean age 4.7 years, IQR 0.7-8.7 years], 19.6% presented neurologic sequelae. HSV was the single most frequently isolated pathogen (19.6%), although in most cases, the etiology remained undefined. 41.1% children presented prodromal before the development of neurologic signs. Fever was the most frequent constitutional symptom (83.9% of cases). Cerebrospinal fluid was normal in 48.5% of cases and electroencephalograpy in 24.5% cases. Brain computed tomography scans was normal in 33 (91.7%) cases, while cerebral magnetic resonance imaging (MRI) showed pathologic findings in 62.5% of cases. MRI was the only parameter associated with neurologic sequalae [P = 0.01; OR, 8.1 (95% CI: 1.52-42.84)]. CONCLUSIONS: Pediatric encephalitis is a heterogeneous entity with nonspecific clinical and laboratory findings, with undefined etiologies in most times. MRI can play a primary role, both on a diagnostic and prognostic point-of-view, and its role should be implemented and made more accessible. Further studies are needed to define the exact role and timing of steroids.


Asunto(s)
Encéfalo/efectos de los fármacos , Encefalitis Infecciosa/diagnóstico por imagen , Encefalitis Infecciosa/tratamiento farmacológico , Encéfalo/patología , Encéfalo/virología , Niño , Preescolar , Encefalitis por Herpes Simple/líquido cefalorraquídeo , Encefalitis por Herpes Simple/diagnóstico por imagen , Femenino , Fiebre/virología , Humanos , Lactante , Encefalitis Infecciosa/líquido cefalorraquídeo , Imagen por Resonancia Magnética , Masculino , Estudios Retrospectivos
7.
Am J Trop Med Hyg ; 104(4): 1260-1264, 2021 01 11.
Artículo en Inglés | MEDLINE | ID: mdl-33432905

RESUMEN

Organisms penetrate the central nervous system (CNS) via three routes. The commonest is the hematogenous route, and other routes include contiguous or penetrating injury or rarely via retrograde axoplasmic route. Although the axoplasmic highway is often used by viruses, only a few bacteria are known to penetrate the CNS via this route. We present a 57-year-old man who developed a penetrating injury while working in a field. Over the next 4 months, he developed pain at the site of the poorly healing wound, which ascended up the right leg and presented as a conus-cauda syndrome. Magnetic resonance imaging (MRI) showed an enhancing intradural intramedullary enhancing lesion in the conus on the right side with cord edema from D11 to L1 level. Extensive evaluation was negative, and he continued to progress to holocord myelitis and developed bilateral corticospinal tract lesions ("tractopathy") in the brain stem and internal capsule. He died after developing a right-sided cerebritis with mass effect. Tissue biopsy from the brain at the time of decompressive craniectomy grew Burkholderia pseudomallei and confirmed a diagnosis of neuromelioidosis (NM). We reviewed the literature for NM, its variable presentations, and the concept of an "infectious tractopathy" and imaging findings which could generate suspicion of this entity.


Asunto(s)
Traumatismos de los Pies/complicaciones , Pie/microbiología , Encefalitis Infecciosa/diagnóstico por imagen , Encefalitis Infecciosa/microbiología , Melioidosis/complicaciones , Mielitis/complicaciones , Antibacterianos/uso terapéutico , Encéfalo/diagnóstico por imagen , Encéfalo/microbiología , Burkholderia pseudomallei/patogenicidad , Resultado Fatal , Pie/patología , Traumatismos de los Pies/microbiología , Humanos , Encefalitis Infecciosa/tratamiento farmacológico , Encefalitis Infecciosa/etiología , Imagen por Resonancia Magnética , Masculino , Melioidosis/diagnóstico por imagen , Melioidosis/tratamiento farmacológico , Persona de Mediana Edad , Médula Espinal/patología
8.
Artículo en Inglés | MEDLINE | ID: mdl-33238854

RESUMEN

BACKGROUND: Infectious encephalitis is a serious and challenging condition to manage. This overview summarizes the current literature regarding the etiology, clinical manifestations, diagnosis, management, and recent patents of acute childhood infectious encephalitis. METHODS: We used PubMed Clinical Queries as a search engine and used keywords of "encephalitis" AND "childhood" Patents were searched using the key term "encephalitis" in google.patents.- com and patentsonline.com. RESULTS: Viral encephalitis is the most common cause of acute infectious encephalitis in children. In young children, the clinical manifestations can be non-specific. Provision of empiric antimicrobial therapy until a specific infectious organism has been identified, which in most cases includes acyclovir, is the cornerstone of therapy. Advanced investigation tools, including nucleic acid-based test panel and metagenomic next-generation sequencing, improve the diagnostic yield of identifying an infectious organism. Supportive therapy includes adequate airway and oxygenation, fluid and electrolyte balance, cerebral perfusion pressure support, and seizure control. Recent patents are related to the diagnosis, treatment, and prevention of acute infectious encephalitis. CONCLUSION: Viral encephalitis is the most common cause of acute infectious encephalitis in children and is associated with significant morbidity. Recent advances in understanding the genetic basis and immunological correlation of infectious encephalitis may improve treatment. Third-tier diagnostic tests may be incorporated into clinical practice. Treatment is targeted at the infectious process but remains mostly supportive. However, specific antimicrobial agents and vaccines development is ongoing.


Asunto(s)
Encefalitis Infecciosa/diagnóstico , Encefalitis Infecciosa/tratamiento farmacológico , Niño , Encefalitis Viral , Humanos , Patentes como Asunto
11.
Exp Parasitol ; 218: 108008, 2020 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-32979343

RESUMEN

Acanthamoeba sp. is a free living amoeba that causes severe, painful and fatal infections, viz. Acanthamoeba keratitis and granulomatous amoebic encephalitis among humans. Antimicrobial chemotherapy used against Acanthamoeba is toxic to human cells and show side effects as well. Infections due to Acanthamoeba also pose challenges towards currently used antimicrobial treatment including resistance and transformation of trophozoites to resistant cyst forms that can lead to recurrence of infection. Therapeutic agents targeting central nervous system infections caused by Acanthamoeba should be able to cross blood-brain barrier. Nanoparticles based drug delivery put forth an effective therapeutic method to overcome the limitations of currently used antimicrobial chemotherapy. In recent years, various researchers investigated the effectiveness of nanoparticles conjugated drug and/or naturally occurring plant compounds against both trophozoites and cyst form of Acanthamoeba. In the current review, a reasonable effort has been made to provide a comprehensive overview of various nanoparticles tested for their efficacy against Acanthamoeba. This review summarizes the noteworthy details of research performed to elucidate the effect of nanoparticles conjugated drugs against Acanthamoeba.


Asunto(s)
Acanthamoeba/efectos de los fármacos , Amebicidas/administración & dosificación , Nanopartículas/administración & dosificación , Acanthamoeba/crecimiento & desarrollo , Queratitis por Acanthamoeba/tratamiento farmacológico , Queratitis por Acanthamoeba/parasitología , Amebiasis/tratamiento farmacológico , Amebiasis/mortalidad , Amebiasis/parasitología , Amebicidas/farmacología , Amebicidas/uso terapéutico , Biguanidas/administración & dosificación , Biguanidas/farmacología , Biguanidas/uso terapéutico , Infecciones Protozoarias del Sistema Nervioso Central/tratamiento farmacológico , Infecciones Protozoarias del Sistema Nervioso Central/mortalidad , Infecciones Protozoarias del Sistema Nervioso Central/parasitología , Clorhexidina/administración & dosificación , Clorhexidina/farmacología , Clorhexidina/uso terapéutico , Sistemas de Liberación de Medicamentos , Inmunocompetencia , Huésped Inmunocomprometido , Encefalitis Infecciosa/tratamiento farmacológico , Encefalitis Infecciosa/mortalidad , Encefalitis Infecciosa/parasitología , Nanopartículas/clasificación , Nanopartículas/uso terapéutico , Trofozoítos/efectos de los fármacos
12.
Am J Case Rep ; 21: e923219, 2020 Jun 30.
Artículo en Inglés | MEDLINE | ID: mdl-32603318

RESUMEN

BACKGROUND Acanthamoeba are free-living amoebae with potential to infect immunocompromised hosts. The mortality rate of granulomatous amebic encephalitis (GAE) due to Acanthamoeba exceeds 90% and there are currently no reports of survival of this infection in recipients of hematopoietic stem cell transplant. CASE REPORT We report herein the case of a 32-year-old man presenting to our service with abrupt neurological deterioration and seizures 5 months after allogeneic stem cell transplantation for Hodgkin lymphoma. Clinical and imaging findings were non-specific at presentation. Multiple circumscribed, heterogenous, mass-like lesions were identified on MRI. Brain biopsy was performed and revealed multiple cysts and trophozoites suggesting a diagnosis of granulomatous amebic encephalitis. PCR testing confirmed Acanthamoeba. Treatment with miltefosine, metronidazole, azithromycin, fluconazole, pentamidine isethionate, and co-trimoxazole was instituted and the patient survived and shows continued improvement with intensive rehabilitation. CONCLUSIONS We report the first successful outcome in this setting. The diagnosis would have been missed on cerebrospinal fluid analysis alone, but was rapidly made by histological analysis of brain biopsy. This diagnostically challenging infection is likely under-recognized. Early brain biopsy and commencement of a prolonged miltefosine-containing anti-ameba regimen can be curative.


Asunto(s)
Amebiasis/diagnóstico , Granuloma/parasitología , Trasplante de Células Madre Hematopoyéticas , Encefalitis Infecciosa/diagnóstico , Receptores de Trasplantes , Adulto , Amebiasis/tratamiento farmacológico , Antiprotozoarios/uso terapéutico , Encéfalo/diagnóstico por imagen , Encéfalo/parasitología , Quimioterapia Combinada , Granuloma/tratamiento farmacológico , Humanos , Huésped Inmunocomprometido , Encefalitis Infecciosa/tratamiento farmacológico , Imagen por Resonancia Magnética , Masculino
13.
Exp Parasitol ; 215: 107915, 2020 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-32461112

RESUMEN

Acanthamoeba castellanii is an opportunistic protozoan responsible for serious human infections including Acanthamoeba keratitis and granulomatous amoebic encephalitis. Despite advances in antimicrobial therapy and supportive care, infections due to Acanthamoeba are a major public concern. Current methods of treatment are not fully effective against both the trophozoite and cyst forms of A. castellanii and are often associated with severe adverse effects, host cell cytotoxicity and recurrence of infection. Therefore, there is an urgent need to develop new therapeutic approaches for the treatment and management of Acanthamoebic infections. Repurposing of clinically approved drugs is a viable avenue for exploration and is particularly useful for neglected and rare diseases where there is limited interest by pharmaceutical companies. Nanotechnology-based drug delivery systems offer promising approaches in the biomedical field, particularly in diagnosis and drug delivery. Herein, we conjugated an antihyperglycemic drug, metformin with silver nanoparticles and assessed its anti-acanthamoebic properties. Characterization by ultraviolet-visible spectrophotometry and atomic force microscopy showed successful formation of metformin-coated silver nanoparticles. Amoebicidal and amoebistatic assays revealed that metformin-coated silver nanoparticles reduced the viability and inhibited the growth of A. castellanii significantly more than metformin and silver nanoparticles alone at both 5 and 10 µM after 24 h incubation. Metformin-coated silver nanoparticles also blocked encystation and inhibited the excystation in Acanthamoeba after 72 h incubation. Overall, the conjugation of metformin with silver nanoparticles was found to enhance its antiamoebic effects against A. castellanii. Furthermore, the pretreatment of A. castellanii with metformin and metformin-coated silver nanoparticles for 2 h also reduced the amoebae-mediated host cell cytotoxicity after 24 h incubation from 73% to 10% at 10 µM, indicating that the drug-conjugated silver nanoparticles confer protection to human cells. These findings suggest that metformin-coated silver nanoparticles hold promise in the improved treatment and management of Acanthamoeba infections.


Asunto(s)
Acanthamoeba castellanii/efectos de los fármacos , Metformina/administración & dosificación , Queratitis por Acanthamoeba/tratamiento farmacológico , Queratitis por Acanthamoeba/parasitología , Antiinfecciosos Locales/farmacología , Infecciones Protozoarias del Sistema Nervioso Central/tratamiento farmacológico , Infecciones Protozoarias del Sistema Nervioso Central/parasitología , Clorhexidina/farmacología , Células HeLa , Humanos , Encefalitis Infecciosa/tratamiento farmacológico , Encefalitis Infecciosa/parasitología , Nanopartículas del Metal/administración & dosificación , Nanopartículas del Metal/uso terapéutico , Metformina/farmacología , Metformina/uso terapéutico , Microscopía de Fuerza Atómica , Enquistamiento de Parásito/efectos de los fármacos , Plata , Espectrofotometría Ultravioleta , Trofozoítos/efectos de los fármacos
16.
J Infect Chemother ; 26(1): 101-106, 2020 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-31445817

RESUMEN

OBJECTIVES: This is a retrospective observational study conducted in one of the largest clinical center of neurosurgery in China. Our aim was to determine the epidemiological characteristics of carbapenem-resistant Enterobacteriaceae (CRE) related meningitis/encephalitis and to elucidate the risk factors for CRE neurosurgical infections. PATIENTS AND METHODS: We performed a retrospective study between January 2012 and December 2017 of patients who underwent neurosurgery. The medical records of each patient were reviewed, and 20 clinical variables on risk factors were extracted and evaluated by Multivariate logistic analysis for CRE-meningitis/encephalitis. RESULTS: In 2012-2017, the positive rate of neurosurgical meningitis/encephalitis was 7.9% (2947/29605), Enterobacteriaceae accounted for 6.3% (185/2947) of all bacterial infections. Totally, 133 Enterobacteriaceae include 26 CRE isolates were available in this study. Of them, Univariate analysis showed that the risk factors of CRE meningitis were ventilator, bacteremia, Intensive Care Unit (ICU) admission, hospital acquired pneumonia and mortality attribute to infection. Multivariate logistic analysis showed that hospital acquired pneumonia and mortality attribute to infection were independent risk factors for CRE meningitis. CONCLUSION: CRE is one of the most serious drug-resistant bacteria published by World Health Organization (WHO) in 2016, and meningitis/encephalitis caused by CRE is an important sign of the failure of the neurosurgery, which demands the physician's immediate attention.


Asunto(s)
Enterobacteriaceae Resistentes a los Carbapenémicos , Infecciones por Enterobacteriaceae/epidemiología , Encefalitis Infecciosa/epidemiología , Meningitis Bacterianas/epidemiología , Complicaciones Posoperatorias/epidemiología , Adulto , Antibacterianos/farmacología , Antibacterianos/uso terapéutico , Enterobacteriaceae Resistentes a los Carbapenémicos/efectos de los fármacos , Enterobacteriaceae Resistentes a los Carbapenémicos/aislamiento & purificación , Infecciones por Enterobacteriaceae/tratamiento farmacológico , Infecciones por Enterobacteriaceae/microbiología , Femenino , Humanos , Encefalitis Infecciosa/tratamiento farmacológico , Encefalitis Infecciosa/microbiología , Masculino , Meningitis Bacterianas/tratamiento farmacológico , Meningitis Bacterianas/microbiología , Pruebas de Sensibilidad Microbiana , Persona de Mediana Edad , Procedimientos Neuroquirúrgicos/efectos adversos , Complicaciones Posoperatorias/tratamiento farmacológico , Complicaciones Posoperatorias/microbiología , Estudios Retrospectivos , Factores de Riesgo , Resultado del Tratamiento
17.
Mol Pharm ; 17(1): 145-154, 2020 01 06.
Artículo en Inglés | MEDLINE | ID: mdl-31800255

RESUMEN

Cryptococcus neoformans (C. neoformans) is one of the most well-known zoonotic fungal pathogens. Cryptococcal encephalitis remains a major cause of morbidity and mortality in immunocompromised hosts. Effective and targeting killing of C. neoformans in the brain is an essential approach to prevent and treat cryptococcal encephalitis. In this study, a fluorescent polypyridyl ruthenium complex RC-7, {[phen2Ru(bpy-dinonyl)](PF6)2 (phen = 1,10-phenanthroline, bpy-dinonyl = 4,4'-dinonyl-2,2'-bipyridine)}, was screened out, which showed a highly fungicidal effect on C. neoformans. The values of minimum inhibitory concentration (MIC) and minimum fungicidal concentration (MFC) in antifungal activities were significantly lower than fluconazole as the control. Moreover, RC-7 was prepared as a brain-targeting nanoliposome (RDP-liposome; RDP is a peptide derived from rabies virus glycoprotein) for in vivo application. The results revealed that the liposomes could accumulate in the encephalitis brain and play an antifungal role. Compared with the cryptococcal encephalitis model mice, the RDP-liposomes remarkably prolonged the survival days of the encephalitis-bearing mice from 10 days to 24 days. Here, we introduce a polypyridyl ruthenium complex that could be used as a novel antifungal agent, and this study may have a broad impact on the development of targeted delivery based on ruthenium complex-loaded liposomes for theranostics of cryptococcal encephalitis.


Asunto(s)
Antifúngicos/administración & dosificación , Encéfalo/efectos de los fármacos , Criptococosis/tratamiento farmacológico , Cryptococcus neoformans/efectos de los fármacos , Encefalitis Infecciosa/tratamiento farmacológico , Liposomas/administración & dosificación , Nanocápsulas/administración & dosificación , Compuestos de Rutenio/administración & dosificación , Animales , Antifúngicos/síntesis química , Antifúngicos/química , Antifúngicos/uso terapéutico , Encéfalo/microbiología , Encéfalo/patología , Células Cultivadas , Criptococosis/microbiología , Criptococosis/mortalidad , Cryptococcus neoformans/metabolismo , Fluconazol/administración & dosificación , Fluconazol/uso terapéutico , Glicoproteínas/química , Encefalitis Infecciosa/microbiología , Encefalitis Infecciosa/mortalidad , Liposomas/síntesis química , Liposomas/química , Liposomas/ultraestructura , Ratones , Ratones Endogámicos BALB C , Pruebas de Sensibilidad Microbiana , Microscopía Electrónica de Transmisión , Nanocápsulas/química , Nanocápsulas/uso terapéutico , Neuronas/efectos de los fármacos , Fragmentos de Péptidos/química , Compuestos de Rutenio/química , Compuestos de Rutenio/uso terapéutico , Nanomedicina Teranóstica , Distribución Tisular , Proteínas Virales/química
18.
Medicine (Baltimore) ; 98(50): e18289, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-31852106

RESUMEN

INTRODUCTION: More than 1200 different types of microbes were found in the human mouth, only some of these microorganisms were associated with intracranial bacterial infection. However, there are limited data available about the Pseudoramibacter alactolyticus (P alactolyticus) or Mycobacterium tuberculosis (MTB) intracranial infections oral origin. PATIENT CONCERNS: Here, we reported a rarely case with P alactolyticus and MTB coinfection in central nervous after dental extraction. The 44-year-old man presented with progressive headache over the last 2 weeks and a sustained fever >39°C, with a dental extraction performed 2 days before the onset of headache. DIAGNOSIS: P alactolyticus and MTB were confirmed by real-time polymerase chain reaction targeting the16S ribosomal RNA gene. The presence of MTB was also demonstrated by positive acid-fast staining of the purulent discharge. INTERVENTIONS: The patient was treated by metronidazole and anti-TB treatment OUTCOMES:: The patient fully recovered without sequela. CONCLUSION: In conclusion there should be awareness of the possibility of P alactolyticus or MTB intracranial infections following tooth extraction.


Asunto(s)
Clostridiales/aislamiento & purificación , Coinfección/etiología , Encefalitis Infecciosa/etnología , Mycobacterium tuberculosis/aislamiento & purificación , Extracción Dental/efectos adversos , Tuberculosis del Sistema Nervioso Central/etiología , Adulto , Antibacterianos/uso terapéutico , Clostridiales/genética , Coinfección/tratamiento farmacológico , Coinfección/microbiología , Humanos , Encefalitis Infecciosa/tratamiento farmacológico , Encefalitis Infecciosa/microbiología , Imagen por Resonancia Magnética , Masculino , Mycobacterium tuberculosis/genética , ARN Bacteriano/análisis , Tuberculosis del Sistema Nervioso Central/tratamiento farmacológico , Tuberculosis del Sistema Nervioso Central/microbiología
20.
Artículo en Inglés | MEDLINE | ID: mdl-31685474

RESUMEN

Miltefosine is an alkylphosphocholine compound that is used primarily for treatment of leishmaniasis and demonstrates in vitro and in vivo antiamebic activity against Acanthamoeba species. Recommendations for treatment of amebic encephalitis generally include miltefosine therapy. Data indicate that treatment with an amebicidal concentration of at least 16 µg/ml of miltefosine is required for most Acanthamoeba species. Although there is a high level of mortality associated with amebic encephalitis, a paucity of data regarding miltefosine levels in plasma and cerebrospinal fluid in vivo exists in the literature. We found that despite aggressive dosing (oral miltefosine 50 mg every 6 h) and therapeutic plasma levels, the miltefosine concentration in cerebrospinal fluid was negligible in a patient with AIDS and Acanthamoeba encephalitis.


Asunto(s)
Infecciones Oportunistas Relacionadas con el SIDA/tratamiento farmacológico , Amebiasis/tratamiento farmacológico , Amebicidas/sangre , Amebicidas/líquido cefalorraquídeo , Infecciones Protozoarias del Sistema Nervioso Central/tratamiento farmacológico , Encefalitis Infecciosa/tratamiento farmacológico , Fosforilcolina/análogos & derivados , Infecciones Oportunistas Relacionadas con el SIDA/sangre , Infecciones Oportunistas Relacionadas con el SIDA/líquido cefalorraquídeo , Acanthamoeba/efectos de los fármacos , Acanthamoeba/aislamiento & purificación , Adulto , Amebiasis/sangre , Amebiasis/líquido cefalorraquídeo , Amebicidas/administración & dosificación , Encéfalo/parasitología , Infecciones Protozoarias del Sistema Nervioso Central/sangre , Infecciones Protozoarias del Sistema Nervioso Central/líquido cefalorraquídeo , Humanos , Encefalitis Infecciosa/sangre , Encefalitis Infecciosa/líquido cefalorraquídeo , Masculino , Fosforilcolina/administración & dosificación , Fosforilcolina/sangre , Fosforilcolina/líquido cefalorraquídeo
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