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1.
Bioresour Technol ; 372: 128659, 2023 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-36690219

RESUMO

Optimizing bioreactor performance for organic matter removal can achieve sustainable and energy-efficient micropollutant removal in subsequent tertiary treatment. Bioreactor performance heavily depends on its resident microbial community; hence, a deeper understanding of community dynamics is essential. The microbial communities of three different bioreactors (biological activated carbon, moving bed biofilm reactor, sand filter), used for organic matter removal from wastewater treatment effluent, were characterized by 16S rRNA gene amplicon sequence analysis. An interdependency between bioreactor performance and microbial community profile was observed. Overall, Proteobacteria was the most predominant phylum, and Comamonadaceae was the most predominant family in all bioreactors. The relative abundance of the genus Roseococcus was positively correlated with organic matter removal. A generalized Lotka-Volterra (gLV) model was established to understand the interactions in the microbial community. By identifying microbial dynamics and their role in bioreactors, a strategy can be developed to improve bioreactor performance.


Assuntos
Águas Residuárias , Purificação da Água , Eliminação de Resíduos Líquidos , RNA Ribossômico 16S/genética , Reatores Biológicos/microbiologia
2.
Allergy ; 73(3): 705-712, 2018 03.
Artigo em Inglês | MEDLINE | ID: mdl-29083482

RESUMO

BACKGROUND: Omalizumab is an effective and well-tolerated treatment for chronic spontaneous urticaria (CSU). Markers and predictors of response are largely unknown, but needed to optimize omalizumab treatment. Omalizumab targets IgE, and IgE levels may be linked to the effects of treatment. We evaluated whether response rates to treatment with omalizumab in patients with CSU are linked to their baseline IgE levels, their IgE levels after omalizumab treatment, and the ratio of on treatment IgE and baseline IgE levels. METHODS: Chronic spontaneous urticaria (CSU) patients (n = 113) were treated with omalizumab 300 mg/4 weeks for 12 weeks, when their treatment responses, that is, no, partial, or complete response, were assessed by use of the urticaria activity score, physician and patient visual analog scale, and treatment effectiveness score. Total IgE levels were measured before treatment (bIgE) with omalizumab and 4 weeks thereafter (w4IgE). RESULTS: Nonresponders to omalizumab had significantly lower bIgE levels (17.9, 17.0-55.0 IU/mL) than partial responders (82.0, 46.2-126.5 IU/mL, P = .008) and complete responders (73.7, 19.45-153.8 IU/mL, P = .032). Nonresponders also had lower w4IgE levels and lower ratios of w4IgE/bIgE levels than partial and complete responders (P < .001). Nonresponse to omalizumab was best predicted by patients' w4IgE/bIgE ratios, significantly better than by bIgE levels (P = .016). CONCLUSIONS: In CSU, total IgE levels and their change predict the response to treatment with omalizumab. The assessment of pre- and post-treatment IgE levels and their ratio may help to improve the management of CSU in patients who require omalizumab treatment.


Assuntos
Antialérgicos/uso terapêutico , Imunoglobulina E/imunologia , Omalizumab/uso terapêutico , Urticária/tratamento farmacológico , Urticária/imunologia , Adulto , Feminino , Humanos , Imunoglobulina E/sangue , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Resultado do Tratamento , Urticária/sangue
4.
Clin Radiol ; 70(1): 48-53, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25446324

RESUMO

AIM: To define and assess the short-term clinical feasibility of fill and aspirate foam sclerotherapy (FAFS) for treating large superficial varicose veins concomitant to endovenous laser ablation (EVLA). MATERIALS AND METHODS: Twenty-seven patients who refused to have phlebectomies with great saphenous vein reflux and large superficial varicosities were included in the study. Both EVLA and FAFS were performed concomitantly. FAFS is a technique in which all or most of the bubbles and blood-foam mixture are removed from the targeted large varicose veins immediately after the foam has caused sufficient damage to the endothelial cells. Patients were reviewed 1 month and 6 months after the treatment. Improvement in the clinical, aetiological, anatomical, and pathological classification (CEAP), and clinical severity was graded using the revised venous clinical severity score (rVCSS) and cosmetic results were investigated at the 6 month visit. RESULTS: Ablation of GSV was performed in 27 limbs in 27 patients (19 males, 70.3%; mean age 44 years; range 21-69 years). All patients had a technically successful FAFS treatment. The CEAP classification score, the rVCSS values, and the cosmetic results showed prominent improvement 6 months after the treatment. There were no significant complications, such as stroke, skin burns, necrosis, paresthesia, deep-vein thrombosis, or allergic reaction. None of the patients experienced neurological events. CONCLUSION: FAFS is a promising safe and effective technique for treating large superficial varicosities concomitant to EVLA of the truncal veins with excellent clinical results. Randomized prospective studies with larger series are required to compare the FAFS with ambulatory phlebectomy and standard foam sclerotherapy.


Assuntos
Terapia a Laser/métodos , Veia Safena/cirurgia , Escleroterapia/métodos , Varizes/terapia , Adulto , Idoso , Estudos de Viabilidade , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Resultado do Tratamento , Adulto Jovem
5.
Acta Radiol ; 55(6): 676-81, 2014 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-24052362

RESUMO

BACKGROUND: In patients with contraindication for beta-blockers who are also under long-term calcium channel-blocker therapy for any reason, ivabradine may be used as an alternative treatment to achieve the target heart rate. PURPOSE: To assess whether single dose oral ivabradine in patients referred for coronary computed tomography angiography (CCTA) is safe and can significantly decrease heart rate compared to intravenous (i.v.) metoprolol in patients receiving long-term calcium channel-blocker therapy. MATERIAL AND METHODS: One-hundred and twenty patients who were under calcium channel-blocker therapy referred for CCTA were randomized to premedication with single dose (15 mg) ivabradine (n = 63) or i.v. metoprolol (5-10 mg) (n = 62). Hearth rate (HR) was assessed at admission (HR1), prescan (HR2), and during CCTA scan (HR3) for all patients. Blood pressure (BP) was measured before medication (BP1) and immediately before CCTA scan (BP2). RESULTS: Although the HR averages of two groups were not significantly different before medication (HRIv1 = 80 ± 7 bpm vs. HRß1 = 81 ± 7 bpm; P = 0.42), significant HR reduction was observed in the ivabradine group (HRIv3 = 62 ± 7 bpm) when compared to the metoprolol group (HRß3 = 66 ± 6 bpm; P = 0.001). Decreases in HR forivabradine (18 ± 6 bpm) was significantly higher than for metoprolol (15 ± 4 bpm; P = 0.003) without relevant side-effects. Ivabradine showed no significant effect on either systolic BP or diastolic BP (siBPIv1, 139 ± 10; siBPIv2, 138 ± 10; P = 0.260; diBPIv1, 81 ± 7; diBPIv2, 81 ± 6; P = 0.59). Nevertheless, metoprolol group demonstrated significant reduction in both SiBP and DiBP (siBPß1, 136 ± 11; siBPß2 130 ± 11; P < 0.001; diBPß1, 81 ± 6; diBPß2, 78 ± 6; P < 0.001). CONCLUSION: Single dose ivabradine is safe and significantly more effective than i.v. metoprolol in decreasing HR in patients under calcium channel-blocker therapy.


Assuntos
Benzazepinas/administração & dosagem , Bloqueadores dos Canais de Cálcio/administração & dosagem , Angiografia Coronária/métodos , Frequência Cardíaca/efeitos dos fármacos , Metoprolol/administração & dosagem , Pré-Medicação/métodos , Administração Oral , Antiarrítmicos/administração & dosagem , Pressão Sanguínea/efeitos dos fármacos , Doença da Artéria Coronariana/diagnóstico por imagem , Relação Dose-Resposta a Droga , Feminino , Humanos , Injeções Intravenosas , Ivabradina , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Tempo
9.
Environ Monit Assess ; 156(1-4): 241-55, 2009 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18780152

RESUMO

Various natural hazards such as landslides, avalanches, floods and debris flows can result in enormous property damages and human casualties in Eastern Black Sea region of Turkey. Mountainous topographic character and high frequency of heavy rain are the main factors for landslide occurrence in Ardesen, Rize. For this reason, the main target of the present study is to evaluate the landslide hazards using a sequence of historical aerial photographs in Ardesen (Rize), Turkey, by Photogrammetry and Geographical Information System (GIS). Landslide locations in the study area were identified by interpretation of aerial photographs dated in 1973 and 2002, and by field surveys. In the study, the selected factors conditioning landslides are lithology, slope gradient, slope aspect, vegetation cover, land class, climate, rainfall and proximity to roads. These factors were considered as effective on the occurrence of landslides. The areas under landslide threat were analyzed and mapped considering the landslide conditioning factors. Some of the conditioning factors were investigated and estimated by employing visual interpretation of aerial photos and topographic data. The results showed that the slope, lithology, terrain roughness, proximity to roads, and the cover type played important roles on landslide occurrence. The results also showed that degree of landslides was affected by the number of houses constructed in the region. As a consequence, the method employed in the study provides important benefits for landslide hazard mitigation efforts, because a combination of both photogrammetric techniques and GIS is presented.


Assuntos
Monitoramento Ambiental/métodos , Deslizamentos de Terra , Sistemas de Informação Geográfica , Geografia , Chuva , Medição de Risco , Turquia
11.
Zentralbl Neurochir ; 69(1): 47-50, 2008 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-18393166

RESUMO

A 17-year-old boy was referred with a 2-month history of low back pain and bilateral sciatica and difficulty in ambulation. Neurological examination found mild muscle weakness and diminished deep tendon reflexes in his right leg. Lumbar magnetic resonance imaging revealed an intradural-extramedullary tumor at the level of the L4, exiting through the right L4-L5 intervertebral foramen into the right psoas muscle. After total resection of the tumor, histopathological diagnosis revealed a gangliocytic paraganglioma. There are 184 paraganglioma cases reported at the lumbar region to date, and only 4 of them were in the pediatric age group. This report is the fifth paraganglioma case in the lumbar region and the first gangliocytic paraganglioma case in the pediatric age population.


Assuntos
Cauda Equina/patologia , Paraganglioma/patologia , Neoplasias do Sistema Nervoso Periférico/patologia , Adolescente , Dor nas Costas/etiologia , Cauda Equina/cirurgia , Humanos , Imuno-Histoquímica , Laminectomia , Imageamento por Ressonância Magnética , Masculino , Cãibra Muscular/etiologia , Procedimentos Neurocirúrgicos , Paraganglioma/cirurgia , Neoplasias do Sistema Nervoso Periférico/cirurgia , Proteínas S100/metabolismo , Tomografia Computadorizada por Raios X
13.
J Eur Acad Dermatol Venereol ; 20(3): 337-40, 2006 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-16503901

RESUMO

Linear atrophoderma of Moulin has a distinctive disease pattern characterized by hyperpigmented atrophoderma and was described originally in 1992. It follows the line of Blaschko, and occurs without preceding inflammation, subsequent induration or scleroderma. The lesions usually develop during childhood or adolescence, and the prognosis is good. The diagnosis is made clinically and histopathologically. In our 18-year-old male patient, there were atrophic plaques unilaterally located on the trunk and arm, and white discoloration on all finger nails. Histopathological examination revealed epidermal atrophy together with disruption of collagen fibres.


Assuntos
Hiperpigmentação/diagnóstico , Doenças da Unha/diagnóstico , Adolescente , Atrofia/complicações , Atrofia/diagnóstico , Atrofia/patologia , Diagnóstico Diferencial , Humanos , Hiperpigmentação/complicações , Hiperpigmentação/patologia , Masculino , Doenças da Unha/complicações , Doenças da Unha/patologia , Unhas/patologia
14.
J Eur Acad Dermatol Venereol ; 20(2): 149-52, 2006 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-16441621

RESUMO

BACKGROUND: The analysis of sister chromatid exchange (SCE) is a cytogenetic technique used to show DNA damage as a result of an exchange of DNA fragments between sister chromatids. It is known that there is an increased SCE frequency in Behçet's disease (BD). OBJECTIVE: To investigate whether human leucocyte antigen (HLA)-B51-positive patients with Behçet's disease exhibit higher SCE frequencies than those without HLA-B51. METHODS: Lymphocytes from 75 patients (38 women, 37 men) and from 50 controls (28 women, 22 men) were cultured in darkness for 72 h in the presence of bromodeoxyuridine. Metaphase chromosomes were stained with a fluorescence plus Giemsa technique after a standard harvest procedure. For HLA-B51 typing, DNA was extracted from ethylenediaminetetraacetic acid blood samples and HLA-B5 allele genotyping was performed by the polymerase chain reaction (PCR)-sequence specific primer method. RESULTS: Thirty-nine of 75 patients with BD (52%) and 15 of 50 controls (30%) were found HLA-B51-positive. The SCE frequencies in HLA-B51-positive patients were higher than in HLA-B51-negative ones (P < 0.001), whereas no difference was detected in the control group. CONCLUSION: This study revealed that there was a significant association between elevated SCE frequencies and existence of HLA-B51 patients with BD.


Assuntos
Síndrome de Behçet/genética , Predisposição Genética para Doença , Antígenos HLA-B/genética , Adulto , Idoso , Síndrome de Behçet/epidemiologia , Estudos de Casos e Controles , Feminino , Marcadores Genéticos , Antígenos HLA-B/sangue , Humanos , Masculino , Pessoa de Meia-Idade , Reação em Cadeia da Polimerase , Troca de Cromátide Irmã , Turquia/epidemiologia , População Branca/genética
15.
Acta Neurol Scand ; 112(5): 343-6, 2005 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-16218919

RESUMO

Spinal subdural abscesses (SSA) are rare and to date only 57 cases have been reported. The exact incidence of the SSA is unknown. The most affected region is the thoraco-lumbar spine and the most common bacterial source is Staphylococcus aureus. The timing for magnetic resonance imaging is very important in these patients. Because early diagnosis and emergent treatment is vital to prevent the formation or progression of neurologic deficits.


Assuntos
Empiema Subdural/diagnóstico , Doenças da Coluna Vertebral/diagnóstico , Infecções Estafilocócicas/diagnóstico , Adulto , Vértebras Cervicais/patologia , Vértebras Cervicais/cirurgia , Descompressão Cirúrgica , Diagnóstico Diferencial , Empiema Subdural/patologia , Feminino , Humanos , Laminectomia , Imageamento por Ressonância Magnética , Exame Neurológico , Cuidados Pós-Operatórios , Medula Espinal/patologia , Medula Espinal/cirurgia , Compressão da Medula Espinal/diagnóstico , Doenças da Coluna Vertebral/cirurgia , Infecções Estafilocócicas/cirurgia , Vértebras Torácicas/patologia , Vértebras Torácicas/cirurgia , Vancomicina/administração & dosagem
16.
Ann Acad Med Singap ; 33(5): 596-9, 2004 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-15531955

RESUMO

INTRODUCTION: Behcet's disease (BD) is a chronic systemic disorder characterised by oral and genital ulcerative lesions, ocular and cutaneous manifestations. Cytokines are the major mediators of immunologic and inflammatory reactions. Nitric oxide is reactive nitrogen intermediate which plays a key role in pathogenesis of many inflammatory and autoimmune skin diseases. The study was conducted to determine serum interleukin-2 (IL-2), interleukin-6 (IL-6), tumour necrosis factor (TNF)-alpha and nitric oxide levels in relation to the pathogenesis of Behcet's disease. MATERIALS AND METHODS: Serum IL-2, IL-6, and TNF-alpha levels were measured with test kits by enzyme-linked immunosorbent assay (ELISA) method, while serum nitric oxide levels were determined with a test kit by colorimetric method. Serum IL-2, IL-6, TNF-alpha and nitric oxide concentrations in 27 patients with Behcet's disease and in 16 healthy controls were determined by extrapolation from their standard curves. The significance of the mean differences between the 2 groups was assessed by the Mann-Whitney U test. RESULTS: The serum levels of IL-2, IL-6, TNF-alpha, and nitric oxide concentrations in patients with BD were significantly higher than those of the controls (P <0.001). CONCLUSION: Our results suggest that elevated levels of IL-2, IL-6, TNF-alpha, and nitric oxide in Behcet's disease appear to be related to the disease.


Assuntos
Síndrome de Behçet/diagnóstico , Interleucina-2/sangue , Interleucina-6/sangue , Óxido Nítrico/sangue , Fator de Necrose Tumoral alfa/análise , Adolescente , Adulto , Síndrome de Behçet/sangue , Biomarcadores/sangue , Estudos de Casos e Controles , Ensaio de Imunoadsorção Enzimática , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Probabilidade , Prognóstico , Valores de Referência , Medição de Risco , Sensibilidade e Especificidade , Índice de Gravidade de Doença
17.
Tissue Antigens ; 64(3): 293-7, 2004 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-15304011

RESUMO

Class I human leucocyte antigen (HLA)-B51 is well known to be associated with Behcet's disease in many ethnic groups. However, there has been no published paper with respect to its association with HLA class I and class II among the Turkish people who live in the eastern region of Turkey. Moreover, as it is known that B51 antigen is encoded by 21 alleles, B*5101-5121, HLA-B51 allele typing was performed, as well as HLA class I and class II genotyping of 75 patients with the disease and the 54 individuals in the matched control group. The result shows that the HLA-B51 frequency was significantly higher (58.66%) in the patient group, compared to that in the control group (18.51%) (OR = 6.245). In the subtyping of B51 alleles, 44 B51-positive patients possessed B*5101 (45.5%), B*5108 (25%), B*5105 (9.1%) and B*5104 (4.5%). There was no significant difference in the HLA-B51 allelic distribution between the patient group and the control group. However, homozygous carriers of HLA-B51 showed considerably high risk (OR = 2.647) in the patient group, compared to that in the control group. In the genotyping of class II HLA alleles, while HLA-DRB1*04 (45.3%) and HLA-DRB1*07 (24%) were the predominant alleles in the patient group, DRB1*11 (50%) appeared to be more common in the control group.


Assuntos
Síndrome de Behçet/genética , Antígenos de Histocompatibilidade Classe II/genética , Antígenos de Histocompatibilidade Classe I/genética , Síndrome de Behçet/epidemiologia , Frequência do Gene , Genótipo , Humanos , Fenótipo , Fatores de Risco , Turquia/epidemiologia
18.
Neurol India ; 50(4): 459-61, 2002 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-12577095

RESUMO

The frequency of complications resulting from angiograms reported in the literature vary between 0.2-5 percent. This study was planned to determine the changes in cerebral blood flow velocity before and after angiography, using transcranial doppler in patients of subarachnoid hemorrhage (SAH) undergoing angiographies. Thirty patients with subarachnoid hemorrhage underwent transcranial doppler ultrasonography immediately before and after angiography. Nonionic water-soluble agents were used during the angiograms. The mean flow velocity (MFV) and pulsatility index (PI) at the M1 segment of both middle cerebral arteries was simultaneously measured. When the patients (11 male, 19 female, mean age+SD; 52.45+12.06) were compared according to changes in MFV and PI, pre and post-angiography, there was no statistical difference in MFV (p=0.51 and p=0.99, left and right side respectively), and in PI (p=0.48 and p=0.66) pre and post angiography. Although angiogram can be used to detect vasospasm in SAH, it can also be cause of vasospasm, partially due to the effect of the contrast agent on the cerebral arteries. This study proposes that the angiographic method is still safe and TCD can be used to follow up any possible changes in diameter of cerebral arteries before and after angiography.


Assuntos
Angiografia Cerebral , Circulação Cerebrovascular , Hemorragia Subaracnóidea/diagnóstico , Hemorragia Subaracnóidea/fisiopatologia , Ultrassonografia Doppler Transcraniana , Adulto , Velocidade do Fluxo Sanguíneo , Feminino , Humanos , Masculino , Pessoa de Meia-Idade
19.
Spine (Phila Pa 1976) ; 26(15): 1726-8, 2001 Aug 01.
Artigo em Inglês | MEDLINE | ID: mdl-11474362

RESUMO

STUDY DESIGN: An extremely rare presentation of an isolated spinal toxoplasmic arachnoiditis is described. OBJECTIVE: To draw attention to the fact that spinal arachnoid membranes may be a potential reservoir for Toxoplasma gondii. SUMMARY OF BACKGROUND DATA: Central nervous system toxoplasmosis is a common manifestation in patients who are immunodeficient. Reports on the spinal toxoplasmosis are rare and focused on spinal cord involvement. METHODS: An adult patient presented with symptoms of spastic paraparesis that had begun 13 years before admission. Thoracic spinal magnetic resonance imaging showed small lesions in posterior subarachnoid space at Th7-Th8. A Th7-Th8 laminectomy was performed. Intradural-extramedullary lesions were excised. RESULTS: Clinical, immunologic, and pathologic examinations showed adhesive spinal arachnoiditis associated with osteoid formation caused by past toxoplasmic infection. There was no impairment of the immunologic defense system. CONCLUSION: Where no causative factor is found in serious spinal adhesive arachnoiditis, the possibility of spinal toxoplasmosis should also be investigated.


Assuntos
Aracnoidite/diagnóstico , Ossificação Heterotópica/diagnóstico , Doenças da Medula Espinal/diagnóstico , Toxoplasmose/diagnóstico , Adulto , Animais , Aracnoidite/complicações , Aracnoidite/parasitologia , Calcinose/etiologia , Calcinose/parasitologia , Calcinose/patologia , Feminino , Humanos , Imageamento por Ressonância Magnética , Ossificação Heterotópica/complicações , Ossificação Heterotópica/parasitologia , Doenças da Medula Espinal/complicações , Doenças da Medula Espinal/parasitologia , Toxoplasma/crescimento & desenvolvimento , Toxoplasma/isolamento & purificação , Toxoplasmose/complicações
20.
J Dermatol ; 28(6): 329-31, 2001 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-11476113

RESUMO

Folliculitis decalvans is a rare and chronic progressive hair disorder leading to scarring alopecia and atrophy. Its etiology is still unclear. It starts with areas of perifollicular erythema, and follicular papules and pustules spread peripherally, leaving central scarred patches of alopecia. We report a 27-year-old man who presented with folliculitis decalvans involving the scalp, face, nape, and beard. There were pustules, crusts, and scarring alopecia on the scalp and beard.


Assuntos
Foliculite/diagnóstico , Adulto , Diagnóstico Diferencial , Face , Foliculite/patologia , Humanos , Masculino , Pescoço , Couro Cabeludo
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