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1.
Phlebology ; 33(6): 397-406, 2018 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-28583026

RESUMEN

Objective Chronic cerebrospinal venous insufficiency (CCSVI) is a condition associated with multiple sclerosis (MS). One mechanism that has been proposed is that the venous obstructions found in MS are due to a chronic persistent venulitis caused by the intra-cellular bacterial parasite, Chlamydophila pneumoniae (Cpn). The objective of the current study is to determine the effect of a combined antibiotic protocol (CAP) on the venous flow in MS patients as measured by a quantitative duplex ultrasound examination (QDUS). Method A non-randomised before-after cohort study was conducted to investigate differences in blood flow volumes pre and 6-months post antibiotic treatment for Cpn infection. Flow volume data were measured by QDUS across affected and unaffected sides from multiple veins segments, including internal jugular vein (IJV) segments J2 and J3, and vertebral vein (VV), as well as global arterial blood flow (GABF). Results 91 patients were included in the study. 64 (70%) were found to have positive Cpn serology. There was a statistically significant post-treatment difference seen for the affected side of Cpn infected patients (mean difference = 56 mL/min, p = 0.02). There was a non-significant increase seen for the affected side of uninfected patients (mean difference = 23 mL/min, p = 0.2). The difference in these effects (34 mL/min) was not statistically significant ( p = 0.3). The mean flow rate decreased in the unaffected side for both infected (-27 mL/min, p = 0.5) and uninfected patients (-69 mL/min, p = 0.01). There was a statistically significant post-treatment increase in GABF for the infected patients (mean difference = 90 mL/min, p = 0.02) and a difference of 76 mL/min for non-infected patients ( p = 0.01). Conclusion A CAP appears to improve the extra-cranial circulation in patients diagnosed with MS. This effect is statistically significant in patients with positive Cpn serology, although patients with negative Cpn serology also show some benefit, betraying a lack of specificity of this effect.


Asunto(s)
Antibacterianos/administración & dosificación , Infecciones por Chlamydophila/tratamiento farmacológico , Chlamydophila pneumoniae , Esclerosis Múltiple/tratamiento farmacológico , Flujo Sanguíneo Regional/efectos de los fármacos , Insuficiencia Venosa/tratamiento farmacológico , Adulto , Anciano , Infecciones por Chlamydophila/diagnóstico por imagen , Estudios de Cohortes , Femenino , Humanos , Venas Yugulares/diagnóstico por imagen , Masculino , Persona de Mediana Edad , Esclerosis Múltiple/diagnóstico , Esclerosis Múltiple/microbiología , Factores de Tiempo , Insuficiencia Venosa/diagnóstico por imagen , Insuficiencia Venosa/microbiología
2.
J Dtsch Dermatol Ges ; 12(3): 188-209; quiz 210, 188-211; quiz 212, 2014 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-24533779

RESUMEN

Dermatomycoses are caused most commonly by dermatophytes. The anthropophilic dermatophyte Trichophyton rubrum is still the most frequent causative agent worldwide. Keratinolytic enzymes, e.g. hydrolases and keratinases, are important virulence factors of T. rubrum. Recently, the cysteine dioxygenase was found as new virulence factor. Predisposing host factors play a similarly important role for the development of dermatophytosis of the skin and nails. Chronic venous insufficiency, diabetes mellitus, disorders of cellular immunity, and genetic predisposition should be considered as risk factors for onychomycosis. A new alarming trend is the increasing number of cases of onychomycosis - mostly due to T. rubrum - in infancy. In Germany, tinea capitis is mostly caused by zoophilic dermatophytes, in particular Microsporum canis. New zoophilic fungi, primarily Trichophyton species of Arthroderma benhamiae, should be taken into differential diagnostic considerations of tinea capitis, tinea faciei, and tinea corporis. Source of infection are small household pets, particularly rodents, like guinea pigs. Anthropophilic dermatophytes may be introduced by families which immigrate from Africa or Asia to Europe. The anthropophilic dermatophytes T. violaceum, T. tonsurans (infections occurring in fighting sports clubs as "tinea gladiatorum capitis et corporis") and M. audouinii are causing outbreaks of small epidemics of tinea corporis and tinea capitis in kindergartens and schools. Superficial infections of the skin and mucous membranes due to yeasts are caused by Candida species. Also common are infections due to the lipophilic yeast fungus Malassezia. Today, within the genus Malassezia more than 10 different species are known. Malassezia globosa seems to play the crucial role in pityriasis versicolor. Molds (also designated non-dermatophyte molds, NDM) are increasingly found as causative agents in onychomycosis. Besides Scopulariopsis brevicaulis, several species of Fusarium and Aspergillus are found.


Asunto(s)
Arthrodermataceae/aislamiento & purificación , Dermatomicosis/epidemiología , Dermatomicosis/microbiología , Diabetes Mellitus/epidemiología , Enfermedades del Sistema Inmune/epidemiología , Insuficiencia Venosa/epidemiología , Causalidad , Comorbilidad , Dermatomicosis/genética , Diabetes Mellitus/genética , Diabetes Mellitus/microbiología , Medicina Basada en la Evidencia , Predisposición Genética a la Enfermedad/genética , Humanos , Enfermedades del Sistema Inmune/genética , Enfermedades del Sistema Inmune/microbiología , Prevalencia , Factores de Riesgo , Tasa de Supervivencia , Insuficiencia Venosa/genética , Insuficiencia Venosa/microbiología
3.
Phlebology ; 27(5): 207-18, 2012 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-22240624

RESUMEN

The aetiology proposed for the development of chronic cerebrospinal venous insufficiency (CCSVI) associated with multiple sclerosis (MS) has been the presence of congenital truncular venous malformations. However, this hypothesis is not consistent with the epidemiology or geographical incidence of MS and is not consistent with many of the ultrasonographic or radiographical findings of the venous disturbances found in MS patients. However, the probability of a venous aetiology of MS remains strong based on evidence accumulated from the time the disorder was first described. The method used in this review was to search PubMed for all past medical publications related to vascular, venous, haematological, epidemiological, biochemical, and genetic investigations and treatments of MS. Epidemiological and geographical findings of prevalence of MS indicate the involvement of an infective agent. This review of the venous pathology associated with MS describes a hypothesis that the pathogenesis of the venous disease could be initiated by a respiratory infective agent such as Chlamydophila pneumonia, which causes a specific chronic persistent venulitis affecting the cerebrospinal venous system. Secondary spread of the agent would initially be via the lymphatic system to specifically involve the azygos, internal jugular and vertebral veins. The hypothesis proposes mechanisms by which an infective venous vasculitis could result in the specific neural damage, metabolic, immunological and vascular effects observed in MS. The hypothesis described is consistent with many of the known facts of MS pathogenesis and therefore provides a framework for further research into a venous aetiology for the disease. If MS does result from a chronic infective venulitis rather than a syndrome involving congenital truncular venous malformations, then additional therapies to the currently used angioplasties will be required to optimize results.


Asunto(s)
Infecciones por Chlamydophila , Chlamydophila pneumoniae , Esclerosis Múltiple , Enfermedades Vasculares de la Médula Espinal , Vasculitis , Insuficiencia Venosa , Infecciones por Chlamydophila/epidemiología , Infecciones por Chlamydophila/terapia , Humanos , Esclerosis Múltiple/epidemiología , Esclerosis Múltiple/microbiología , Esclerosis Múltiple/terapia , Vasculitis/epidemiología , Vasculitis/microbiología , Vasculitis/terapia , Insuficiencia Venosa/epidemiología , Insuficiencia Venosa/microbiología , Insuficiencia Venosa/terapia
4.
Am J Med ; 86(6 Pt 2): 801-8, 1989 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-2658581

RESUMEN

PURPOSE: Lower extremity infections in the presence vascular insufficiency are difficult and costly to treat. Few well-controlled clinical trials evaluating the management of these infections exist. We decided to investigate the ability of a new fluoroquinolone, ciprofloxacin, to reduce the morbidity associated with these infections and the amount of in-hospital time required for the administration of antibiotic therapy. PATIENTS AND METHODS: Forty-eight patients with peripheral vascular disease (46 with diabetes mellitus) who presented to the hospital for treatment of lower extremity infections were randomized in a blinded fashion to receive oral ciprofloxacin at a dosage of either 750 mg or 1,000 mg twice daily. Patients with osteomyelitis received three months of therapy and those with infections limited to soft tissues, three weeks of ciprofloxacin treatment. All subjects were followed for one year. RESULTS: One patient received an amputation 24 hours after enrollment, and two patients discontinued therapy after 20 and 34 days because of adverse effects and were not evaluable. At the one-year follow-up, 27 of the 45 (60 percent) evaluable patients had a fully successful outcome defined as not requiring either repeat antimicrobial therapy for their initial infection or amputation of the involved extremity. In the group of 18 patients in whom therapy failed, a total of only nine amputations were required. In the 15 patients whose lesion closed during therapy, 93% (14 patients) experienced a long-term successful outcome. CONCLUSION: Treatment with this new fluoroquinolone offers promise for the improved outcome of patients with the serious infectious complication of infected lower extremity ulcerations in peripheral vascular disease, diabetes mellitus, or both.


Asunto(s)
Infecciones Bacterianas/tratamiento farmacológico , Ciprofloxacina/administración & dosificación , Complicaciones de la Diabetes , Angiopatías Diabéticas/complicaciones , Úlcera de la Pierna/complicaciones , Insuficiencia Venosa/complicaciones , Adulto , Bacterias/efectos de los fármacos , Bacterias/aislamiento & purificación , Infecciones Bacterianas/etiología , Infecciones Bacterianas/microbiología , Ciprofloxacina/efectos adversos , Ciprofloxacina/farmacocinética , Ciprofloxacina/farmacología , Ensayos Clínicos como Asunto , Diabetes Mellitus/microbiología , Angiopatías Diabéticas/microbiología , Método Doble Ciego , Femenino , Humanos , Úlcera de la Pierna/tratamiento farmacológico , Úlcera de la Pierna/microbiología , Masculino , Pruebas de Sensibilidad Microbiana , Distribución Aleatoria , Insuficiencia Venosa/microbiología
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