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1.
Bratisl Lek Listy ; 122(12): 912-917, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-34904854

RESUMO

OBJECTIVES: This study aimed to investigate the wound healing activity of liposomal Carpobrotus edulis powder extract (CEPE) formulation on incisional and excisional wounds in rat. BACKGROUND: In the event of any damage, the damaged tissue undergoes a process of regenerating itself, which is called wound healing. METHODS: Centella asiatica extract (CAE) was used as the reference molecule in the study. The wound healing process was tested by using the excisional and incisional wound model. On the 12th day of the study, maximum stress, stress, % of elongation values were evaluated in the incisional wound. Also; histological parameters and macroscopic photographic analyses were evaluated in the excisional wound. RESULTS: In the photo evaluations, the improvement was more prominent in both CAE and CEPE groups than in the control group. Histological evaluation showed that CEPE group had significant wound healing activity compared to the control and CAE groups. Axial tensile-elongation experiments in incisional wound tissue show that there was no significant difference between CAE and CEPE groups. CONCLUSION: Liposomal formulations of C.edulis extract were found to have positive effects on the healing process, both on excisional and incisional wound tissues (Tab. 2, Fig. 3, Ref. 30).


Assuntos
Pele , Cicatrização , Animais , Extratos Vegetais/farmacologia , Ratos
3.
J Reprod Immunol ; 141: 103172, 2020 09.
Artigo em Inglês | MEDLINE | ID: mdl-32634649

RESUMO

OBJECTIVE: Recurrent pregnancy loss (RPL) has been associated with thrombophilia. The use of prophylactic treatments against thrombophilia becomes necessary in order to increase the live birth rates in women with RPL. The aim of this study was to genotype thrombophilia associated polymorphisms and investigates the benefit of prophylactic treatment on the clinical pregnancy outcomes of women with specific genotypes of these polymorphisms. MATERIALS AND METHODS: A total of 62 women were included in this study. The polymorphisms associated with thrombophilia, including methyltetrahydrofolate reductase (MTHFR) 1298 and 677, Factor V Leiden (FVL) 1691, plasminogen activator inhibitor-1 (PA1-1) G/G and Factor II prothrombin 20,210, were genotyped using the real time PCR. The effect of prophylactic treatment using anti-coagulants of 0.4 mL dose of enoxaparin (3000-6000IU) and 75 mg dose of aspirin, 81 mg dose of aspirin, mineral of 15 mg dose of zinco c or10 mg dose of folic acid, was correlated with the genotypes of polymorphisms. RESULTS AND CONCLUSION: The clinical pregnancy outcomes were significantly improved in patients with MTHFR 677CC genotype when treated with zinco c. Furthermore, treatment with 75 mg of aspirin resulted in higher negative pregnancy rates in patients with MTHFR A1298C genotypes. Therefore, the results of this study should be used to re-evaluate the clinical applications in women with miscarriages.


Assuntos
Aborto Habitual/genética , Anticoagulantes/administração & dosagem , Metilenotetra-Hidrofolato Redutase (NADPH2)/genética , Trombofilia/genética , Aborto Habitual/prevenção & controle , Adulto , Anticoagulantes/efeitos adversos , Aspirina/administração & dosagem , Aspirina/efeitos adversos , Suplementos Nutricionais , Feminino , Ácido Fólico/administração & dosagem , Ácido Fólico/efeitos adversos , Humanos , Polimorfismo de Nucleotídeo Único , Gravidez , Taxa de Gravidez , Trombofilia/complicações , Trombofilia/tratamento farmacológico , Zinco/administração & dosagem
4.
Neuroscience ; 357: 12-19, 2017 08 15.
Artigo em Inglês | MEDLINE | ID: mdl-28577913

RESUMO

Resveratrol (3,5,4'-stilbenetriol), a natural polyphenol produced by various plants, has attracted attention over the past decade because of its multiple beneficial properties, including anti-inflammatory, anti-oxidant and chemopreventive, yet, there is limited information about its antiepileptic effects. Moreover, its poor solubility in water and low bioavailability are the challenging issues. In the present study, we aimed to investigate effects of free resveratrol and resveratrol delivered in amphipathic liposomal delivery system, which has a high blood-brain barrier crossing potential, on penicillin-induced epileptic seizure model. For this purpose, adult male Sprague-Dawley rats were divided into four groups as saline (Control), liposome (LIP), free resveratrol (RES) and resveratrol+liposome (RES+LIP). Penicillin-induced epileptic activity was recorded for 120 min by electrocorticography. Glutathione S-transferase (GST), Glutathione (GSH), Superoxide dismutase (SOD) and Malondialdehyde (MDA) assays were performed in brain tissues collected. Our results showed that RES+LIP was the most effective anticonvulsant treatment on penicillin-induced epileptic seizures when compared to control, as RES+LIP immediately decreased the number of spikes per minute. GST and SOD activity, as well as the GSH levels, were significantly increased in the RES+LIP group as compared with the control group. Also, the MDA levels were significantly higher in the RES+LIP compared to RES and control groups. In conclusion, RES+LIP treatment was more effective on the decrease in spike frequency and spike amplitudes than other treatments. Our results suggest that the RES+LIP is more effective than RES on penicillin-induced epileptiform activity.


Assuntos
Anticonvulsivantes/administração & dosagem , Portadores de Fármacos , Epilepsia/tratamento farmacológico , Lipossomos , Estilbenos/administração & dosagem , Animais , Antioxidantes/administração & dosagem , Encéfalo/efeitos dos fármacos , Encéfalo/metabolismo , Eletrocorticografia , Epilepsia/metabolismo , Glutationa/metabolismo , Glutationa Transferase/metabolismo , Masculino , Malondialdeído/metabolismo , Penicilinas , Distribuição Aleatória , Ratos Sprague-Dawley , Resveratrol , Superóxido Dismutase/metabolismo
5.
Acta Otorhinolaryngol Ital ; 34(5): 310-6, 2014 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-25709146

RESUMO

The aim of this study was to describe our experience with benign parapharyngeal space tumours resected via a transcervical route without mandibulotomy and to investigate associated postoperative sequelae and complications. The study investigated and analysed the retrospective charts of 44 patients who underwent surgery for benign parapharyngeal space tumours over a 10-year period. The diagnosis was reached in all patients with clinical and radiologic findings; preoperative fine-needle aspiration biopsy was not performed in any case. The preferred means of accessing the parapharyngeal space in all patients was a transcervical route. In 5 of these patients, transparotid extension was performed due to the position of the tumour. Tumours were classified radiologically as poststyloid in 27 cases and prestyloid in 17 cases. The final histopathologic diagnosis was vagal paraganglioma in 16 cases, pleomorphic adenoma in 13 cases, schwannoma in 10 cases and comparatively rarer tumours in the remaining 5 cases. In three patients, cranial nerve paralysis was observed during preoperative evaluation. Permanent cranial nerve paralysis occurred in 19 cases (43.2%) in the postoperative period, the majority of which were neurogenic tumours such as vagal paraganglioma (n = 16) and schwannoma (n = 2), and one case of non-neurogenic parapharyngeal tumour. The median duration of follow-up was 61 ± 33 months. There was no local recurrence in any patient during the follow-up period. A transcervical approach should be the first choice for excision of parapharyngeal space tumours, except for recurrent or malignant tumours, considering its advantages of providing direct access to the neoplasm, adequate control of neurovascular structures from the neck and optimal aesthetic outcomes due to preservation of mandibular continuity with minimal morbidity and hospitalisation time.


Assuntos
Adenoma Pleomorfo/cirurgia , Neoplasias de Cabeça e Pescoço/cirurgia , Neurilemoma/cirurgia , Paraganglioma/cirurgia , Adulto , Idoso , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Faringe , Estudos Retrospectivos , Procedimentos Cirúrgicos Operatórios/métodos
6.
Int J Obes (Lond) ; 38(1): 148-51, 2014 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23649472

RESUMO

The central melanocortin system is essential for the regulation of long-term energy homeostasis in humans. Rodent experiments suggest that this system also affects glucose metabolism, in particular by modulating peripheral insulin sensitivity independently of its effect on adiposity. Rare patients with complete genetic defects in the central melanocortin system can provide insight into the role of this system in glucose homeostasis in humans. We here describe the eighth individual with complete proopiomelanocortin (POMC) deficiency and the first with coincidental concomitant type 1 diabetes, which provides a unique opportunity to determine the role of melanocortins in glucose homeostasis in human. Direct sequencing of the POMC gene in this severely obese patient with isolated adrenocorticotropic hormone deficiency identified a homozygous 5' untranslated region mutation -11C>A, which we find to abolish normal POMC protein synthesis, as assessed in vitro. The patient's insulin requirements were as expected for his age and pubertal development. This unique patient suggests that in humans the central melanocortin system does not seem to affect peripheral insulin sensitivity, independently of its effect on adiposity.


Assuntos
Insuficiência Adrenal/genética , Diabetes Mellitus Tipo 1/genética , Resistência à Insulina/genética , Melanocortinas/metabolismo , Obesidade/genética , Obesidade Infantil/genética , Pró-Opiomelanocortina/deficiência , Insuficiência Adrenal/complicações , Criança , Metabolismo Energético , Comportamento Alimentar , Genótipo , Homeostase , Humanos , Masculino , Melanocortinas/genética , Obesidade/complicações , Obesidade Infantil/etiologia , Pró-Opiomelanocortina/genética , Análise de Sequência de DNA , Aumento de Peso/genética
7.
Int J Obes (Lond) ; 35(3): 457-61, 2011 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-20733581

RESUMO

Bariatric surgery is often successful for treatment of severe obesity. The mechanisms of weight loss after bariatric surgery and the role of central energy homeostatic pathways in this weight loss process are not well understood. The study of individuals with complete loss of function of genes important in the leptin-melanocortin system may help establish the significance of these pathways for weight loss after bariatric surgery. We describe the outcome of bariatric surgery in an adolescent with compound heterozygosity and complete functional loss of both alleles of the melanocortin 4 receptor (MC4R). The patient underwent laparoscopic adjustable gastric banding and truncal vagotomy at years of age, which resulted in initial, but not long-term weight loss. Our experience with this patient suggests that complete MC4R deficiency impairs response to gastric banding and results in poor weight loss after this surgery.


Assuntos
Cirurgia Bariátrica/métodos , Obesidade Mórbida/cirurgia , Receptor Tipo 4 de Melanocortina/deficiência , Redução de Peso/fisiologia , Adolescente , Humanos , Masculino , Obesidade Mórbida/genética , Resultado do Tratamento , Redução de Peso/genética
8.
Folia Microbiol (Praha) ; 55(1): 35-8, 2010 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-20336502

RESUMO

Some bacteria were isolated from Dendroctonus micans and its specific predator, Rhizophagus grandis. Six bacteria from D. micans were identified as Bacillus pumilus, Enterobacter intermedius, Citrobacter freundii, Cellulomonas flavigena, Microbacterium liquefaciens and Enterobacter amnigenus, three bacteria from R. grandis as Klebsiella pneumoniae, Pantoea agglomerans and Serratia grimesii, on the basis of fatty acid methyl ester analysis and carbon utilization profile by using Microbial Identification and Biolog Microplate Systems. Their insecticidal effects were tested on larvae and adults of D. micans.


Assuntos
Bactérias/classificação , Bactérias/isolamento & purificação , Besouros/microbiologia , Gorgulhos/microbiologia , Animais , Bactérias/química , Bactérias/patogenicidade , Técnicas de Tipagem Bacteriana , Ácidos Graxos/análise , Larva/microbiologia , Análise de Sobrevida , Virulência
9.
J Laryngol Otol ; 124(6): 646-9, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20163749

RESUMO

BACKGROUND: This study sought to evaluate the incidence, aetiology, clinical features and treatment modalities for laryngocoele formation after supracricoid partial laryngectomy. METHODS: The medical charts of 62 patients who had undergone supracricoid partial laryngectomy were reviewed. RESULTS: Three patients developed laryngocoele, giving an incidence of 4.8 per cent. Two of these patients presented with a cervical mass, dyspnoea and fever. The mobility of the arytenoids was disturbed on the involved side. The third patient was admitted complaining only of a compressible cervical mass. In all patients, diagnosis was made by computed tomography scan. The transcervical surgical approach was preferred for resection. CONCLUSION: Laryngocoele can occur as a late complication of supracricoid partial laryngectomy. Remnants of the laryngeal ventricle may be the cause of laryngocoele formation. The integrity of the laryngeal ventricle in the resected specimen should be routinely checked in order to avoid this rare complication. Clinicians should be aware that, following supracricoid partial laryngectomy, a cervical mass presenting with dyspnoea and disturbance of arytenoid mobility does not always indicate tumour recurrence.


Assuntos
Carcinoma de Células Escamosas/complicações , Doenças da Laringe/etiologia , Laringectomia/efeitos adversos , Adulto , Idoso , Carcinoma de Células Escamosas/cirurgia , Dilatação Patológica/etiologia , Feminino , Humanos , Incidência , Doenças da Laringe/epidemiologia , Doenças da Laringe/terapia , Neoplasias Laríngeas/complicações , Neoplasias Laríngeas/cirurgia , Laringectomia/métodos , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Tomografia Computadorizada por Raios X , Resultado do Tratamento
10.
J Asthma ; 46(10): 1037-41, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19995143

RESUMO

Nasal polyposis (NP) is considered a subgroup of chronic rhinosinusitis and is commonly associated with asthma, bronchiectasis, and cystic fibrosis. A certain subgroup of nasal polyposis is known as Aspirin Exacerbated Respiratory Disease (AERD), previously called Samter's Triad or aspirin triad, comprising polyposis, asthma, and aspirin hypersensitivity and makes up almost 10% of cases of NP. Therapy of NP involves a combination of medical and surgical treatments. However, recurrences are common, particularly in patients with asthma and aspirin hypersensitivity. Both topical and systemic corticosteroids form the mainstay of conservative therapy for NP as well as a primary treatment and prevention for recurrences. They have been shown to improve nasal breathing, rhinitis symptoms, and reduce the size of NP, along with the rate of recurrence. There is great concern about the adverse effects of systemic steroids, especially when long-term usage is necessary to maintain improvement. So far, no knowledge exists about the effects of methotrexate (MTX) on NP of the patients with asthma. We report two patients whose NP dramatically reduced in size after a course of MTX therapy administered as an additional treatment for their steroid- dependent asthma.


Assuntos
Aspirina/imunologia , Asma/tratamento farmacológico , Hipersensibilidade a Drogas/complicações , Metotrexato/uso terapêutico , Pólipos Nasais/tratamento farmacológico , Corticosteroides/uso terapêutico , Idoso , Asma/complicações , Asma/fisiopatologia , Endoscopia , Feminino , Volume Expiratório Forçado/efeitos dos fármacos , Volume Expiratório Forçado/fisiologia , Humanos , Metotrexato/farmacologia , Metilprednisolona/uso terapêutico , Pessoa de Meia-Idade , Cavidade Nasal/efeitos dos fármacos , Cavidade Nasal/patologia , Pólipos Nasais/complicações , Pólipos Nasais/diagnóstico por imagem , Pólipos Nasais/patologia , Seios Paranasais/diagnóstico por imagem , Seios Paranasais/efeitos dos fármacos , Tomografia Computadorizada por Raios X
11.
Ideggyogy Sz ; 61(7-8): 250-4, 2008 Jul 30.
Artigo em Inglês | MEDLINE | ID: mdl-18763481

RESUMO

Idiopathic Tolosa-Hunt syndrome (ITHS) is a very rare cause of painful ophthalmoplegia characterized by unilateral orbital pain, ipsilateral oculomotor paralysis and prompt response to steroids. In this paper we report 4 additional cases of ITHS. This rare cause of painful ophthalmoplegia effects the cranial nerves due to a granulomatous lesion of unknown etiology in the cavernous sinus or superior orbital fissure. The International Headache Society redefined the diagnostic criteria for ITHS but it is still mostly a diagnosis of exclusion. Careful evaluation and follow-up is essential for diagnosis. Optimal therapy duration and dosage and prophylactic treatment in recurrent cases needs further research.


Assuntos
Oftalmoplegia/etiologia , Síndrome de Tolosa-Hunt/complicações , Síndrome de Tolosa-Hunt/diagnóstico , Adulto , Idoso , Diagnóstico Diferencial , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Dor/etiologia , Síndrome de Tolosa-Hunt/patologia
12.
Psychosom Med ; 69(4): 344-7, 2007 May.
Artigo em Inglês | MEDLINE | ID: mdl-17510287

RESUMO

BACKGROUND: P-wave dispersion (PWD) is defined as the difference between the maximum and the minimum P-wave (Pmax and Pmin, respectively) duration. Significant variation in cardiac atrial PWD has been correlated with changes in systemic autonomic tone such as during periods of anxiety. It is also known that the degree of PWD seen on 12-lead electrocardiogram (ECG) may be a predictor of susceptibility of the atrial myocardium to future atrial fibrillation (AF). Therefore, we firstly aimed to show an association between PWD and panic disorder, a state of high sympathetic tone. METHODS: PWD was measured in 40 outpatients with panic disorder and in 40 physically and mentally healthy age- and gender-matched controls. In addition, the Panic Agoraphobia Scale (PAS) and the Hamilton Depression Rating Scale (HDRS) were scored concomitantly. RESULTS: Both Pmax and Pmin were significantly higher than those of healthy controls. PWD was significantly greater in the panic disorder group than in the controls. As expected, the mean score on PAS was significantly higher for the panic disorder group than for the controls and correlated significantly with PWD. Heart rate (measured as RR intervals in milliseconds on electrocardiogram) did not differ significantly between the groups. CONCLUSIONS: The findings of the present study suggest that the disorder may be associated with an increase in PWD. This association may result from prolonged anxiety and increase in sympathetic modulation, which are main characteristics of panic disorder.


Assuntos
Frequência Cardíaca/fisiologia , Transtorno de Pânico/fisiopatologia , Adulto , Arritmias Cardíacas/psicologia , Estudos de Casos e Controles , Eletrocardiografia , Feminino , Humanos , Masculino
13.
Med Vet Entomol ; 18(3): 306-7, 2004 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-15347400

RESUMO

Specimens of the millipede, Nopoiulus kochii (Gervais) were seen in faeces and vomit of a 14-year-old boy residing in Oltu, Erzurum, Turkey. The patient complained of a burning sensation in his throat and stomach-ache. Physical examination revealed no pathological findings, and how the patient became infected was unknown. Anti-parasitic drugs (niclosamide, albendazole), which he had been taking intermittently for 2 years by the prescription of a physician, had not resolved the problem.


Assuntos
Artrópodes , Enteropatias Parasitárias/parasitologia , Adolescente , Animais , Fezes/parasitologia , Humanos , Masculino , Turquia , Vômito/parasitologia
14.
Int J Pediatr Otorhinolaryngol ; 61(2): 129-34, 2001 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-11589979

RESUMO

Refsum's disease is a disorder of lipid metabolism with pigmentary retinopathy, demyelinating neuropathy, ataxia, and hearing loss. Previous histological studies have located the site of hearing impairment in the inner ear, but it has never been confirmed audiologicaly in the literature. In this reported case of Refsum's disease, despite hearing loss and absence of response in ABR, robust otoacoustic emissions were measured. Together with these and other audiological findings, we conclude that our case might be the first reported case of Refsum's disease with auditory neuropathy. The site of the hearing abnormality in Refsum's disease may be 'post-outer hair cells' in some cases as in the current case. Because of their limited benefits and risk of noise-induced damage to outer hair cells, the use of hearing aids before otoacoustic emission measurements should be considered cautiously in Refsum's disease.


Assuntos
Audiometria/métodos , Potenciais Evocados Auditivos do Tronco Encefálico , Perda Auditiva Neurossensorial/diagnóstico , Emissões Otoacústicas Espontâneas , Doença de Refsum/complicações , Criança , Perda Auditiva Neurossensorial/etiologia , Humanos , Masculino , Doença de Refsum/diagnóstico , Sensibilidade e Especificidade
15.
J Laryngol Otol ; 115(7): 573-5, 2001 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-11485593

RESUMO

We report the clinical course in a 25-year-old male patient of neurofibromatosis with malignant triton tumour (MTT). Triton tumour is a peripheral nerve sheath tumour with rhabdomyoblastic differentiation. This is relatively rare tumour of head and neck region and only 26 cases have been reported to date. The present case is the first reported MTT of parapharyngeal space, one of the most aggressive course among all head and neck MTTs, resulting in the death of the patient within three months following surgical resection. The aggressive nature of this tumour necessitates adjuvant therapeutic measures in addition to radical surgery in order to obtain better survival rates.


Assuntos
Neurilemoma/diagnóstico , Neoplasias Faríngeas/diagnóstico , Adulto , Evolução Fatal , Seguimentos , Humanos , Masculino , Neurilemoma/cirurgia , Neurofibromatose 1/diagnóstico , Neoplasias Faríngeas/cirurgia
16.
Int J Pediatr Otorhinolaryngol ; 58(3): 215-21, 2001 May 11.
Artigo em Inglês | MEDLINE | ID: mdl-11335009

RESUMO

OBJECTIVE: (a) To report computed tomography findings of eight new cases with Waardenburg's syndrome (WS) type I and review reported temporal bone radiographic and histopathological findings in WS with hearing loss; (b) To determine the frequency of inner ear pathologies that may contraindicate cochlear implantation. METHODS: A review of 1166 pediatric patients with sensorineural hearing loss revealed 12 cases (1%) with WS, whose family screenings disclosed additional 12 subjects with the same disorder. Among these 24 cases, eight had WS type I and were subjected to computed tomography scanning of temporal bone. Imaging findings of 28 cases reported previously in English literature were evaluated together with our eight patients. RESULTS: Malformation of the inner ear was found in none of the nine WS type I cases evaluated here, while the frequency of internal acoustic canal malformation was 11%. Regardless of the subtypes of the syndrome, 6 of 36 cases (17%) had radiological abnormality of the inner ear. Malformation and/or absence of the semicircular canals were the most common congenital abnormality of the inner ear. Hypoplasia of the cochlea was present in 3 of 36 cases (8%). CONCLUSIONS: Abnormality of bony labyrinth in WS with congenital deafness is not a frequent finding, particularly in WS type I. Therefore, the otologist and audiologist must keep in mind that most of these cases are suitable for cochlear implantation regarding inner ear anatomy.


Assuntos
Surdez/diagnóstico por imagem , Orelha Interna/diagnóstico por imagem , Osso Temporal/diagnóstico por imagem , Síndrome de Waardenburg/diagnóstico por imagem , Criança , Surdez/complicações , Surdez/congênito , Orelha Interna/anormalidades , Humanos , Tomografia Computadorizada por Raios X , Síndrome de Waardenburg/complicações
17.
J Electrocardiol ; 34 Suppl: 93-6, 2001.
Artigo em Inglês | MEDLINE | ID: mdl-11781942

RESUMO

T-wave alternans (TWA) is a harbinger of ventricular vulnerability and an important prognostic indicator for torsade de pointes and likely sudden death in patients with LQTS. We analyzed the occurrence of TWA in 18 patients with LQTS (7 males, 11 females, ages ranging from 6 months to 32 years--median 8.4 years). Analysis was performed with software to investigate dynamics of cycle length mediated repolarization changes. Digital Holter ECG analysis revealed macroscopic, true TWA in 3 of 18 patients. TWA showed a variable morphological expression. One patient had continuous changes of T wave polarity, but not on a periodic beat-to-beat basis. Onsets of macroscopic TWA were preceded by long/short cycle length sequences and tachycardic rates above 130 to 140 bpm. Impact of ventricular premature beats on TWA onset was insignificant. Two of the identified patients with TWA had sudden cardiac death during follow-up (one refused PM therapy). At present, TWA cannot be detected automatically from Holter ECGs and therefore may be missed, despite the potential danger for the individuals. The observation that predominantly high beat rates and not beat rate changes, per se, triggered episodes of TWA renders difficult general therapeutic recommendations for the identified patients at risk.


Assuntos
Eletrocardiografia Ambulatorial , Síndrome do QT Longo/diagnóstico , Processamento de Sinais Assistido por Computador , Criança , Morte Súbita Cardíaca/epidemiologia , Feminino , Humanos , Síndrome do QT Longo/fisiopatologia , Masculino , Prognóstico , Torsades de Pointes/epidemiologia
18.
Turk J Haematol ; 17(3): 119-22, 2000 Sep 05.
Artigo em Inglês | MEDLINE | ID: mdl-27263501

RESUMO

Microvascular occlusion in sickle cell disease (SCD) is a multifactorial process. Disordered coagulation may play a role in the pathogenesis of vaso occlusive crisis (VOC). The aim of this study was to evaluate the patients and to investigate their Protein C (PC), Protein S (PS) and AT-III levels during normal and crisis periods. A total of 18 patients with SCD were included in this study at the Antalya State Hospital, Thalassemia Center. The mean number of VOC episodes of the patients per year was 4.1 - 3.2. Complications in patients included 4 cases of osteonecrosis (23.5%), 2 cases of holealithiasis (11.7%), 2 cases of leg ulcers (11.7%), and 3 splenectomies (17.6%). The patients during noncrisis periods have lower cholesterol and higher triglycerides levels than the controls (p< 0.001). Hepatic and renal functions were normal in all patients. The mean totals of the PS, PC and AT-III levels were statistically lower both in non crisis and in crisis periods than the control (p< 0.001), but there was no statistical difference between the levels durining noncrisis and crisis periods. In conclusion, PC, PS and AT-IIII deficiencies in patients with SCD are certain. However, these deficiencies do not change during noncrisis and crisis situations and does not play a role on the period of crisis. Abnormal lipid patterns may be a predisposing condition for a crisis.

19.
Int J Pediatr Otorhinolaryngol ; 45(2): 167-9, 1998 Oct 02.
Artigo em Inglês | MEDLINE | ID: mdl-9849685

RESUMO

Mumps is the most common cause of unilateral acquired sensorineural hearing loss in children. Although it usually affects the salivary glands. the inner ear may be involved. Deafness is usually unilateral, sudden in onset, profound and permanent. Bilateral total sensorineural hearing loss had been rarely reported in English literature. We present a case of total deafness due to asymptomatic mumps infection.


Assuntos
Surdez/etiologia , Perda Auditiva Súbita/etiologia , Caxumba/complicações , Pré-Escolar , Surdez/terapia , Feminino , Perda Auditiva Súbita/terapia , Humanos , Terapia de Imunossupressão , Falha de Tratamento
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