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1.
QJM ; 112(3): 171-182, 2019 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-30247655

RESUMO

BACKGROUND: The severity of Tuberous Sclerosis Complex (TSC) can vary among affected individuals. Complications of TSC can be life threatening, with significant impact on patients' quality of life. Management may vary dependent on treating physician, local and national policies, and funding. There are no current UK guidelines. We conducted a Delphi consensus process to reach agreed guidance for the management of patients with TSC in the UK. METHODS: We performed a literature search and reviewed the 2012/13 international guideline for TSC management. Based on these, a Delphi questionnaire was formed. We invited 86 clinicians and medical researchers to complete an online survey in two rounds. All the people surveyed were based in the UK. Clinicians were identified through the regional TSC clinics, and researchers were identified through publications. In round one, 55 questions were asked. In round two, 18 questions were asked in order to obtain consensus on the outstanding points that had been contentious in round one. The data was analysed by a core committee and subcommittees, which consisted of UK experts in different aspects of TSC. The Tuberous Sclerosis Association was consulted. RESULTS: About 51 TSC experts took part in this survey. Two rounds were required to achieve consensus. The responders were neurologists, nephrologists, psychiatrist, psychologists, oncologists, general paediatricians, dermatologist, urologists, radiologists, clinical geneticists, neurosurgeons, respiratory and neurodisability clinicians. CONCLUSIONS: These new UK guidelines for the management and surveillance of TSC patients provide consensus guidance for delivery of best clinical care to individuals with TSC in the UK.


Assuntos
Esclerose Tuberosa/epidemiologia , Esclerose Tuberosa/terapia , Humanos , Vigilância da População , Qualidade de Vida , Inquéritos e Questionários , Reino Unido/epidemiologia
2.
Int Sch Res Notices ; 2017: 8404378, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29270462

RESUMO

Background. Facial angiofibromas affect most patients with tuberous sclerosis complex. They tend to progress, can cause recurrent bleeding and facial disfigurement, and have significant psychological effects. We reviewed the effectiveness and safety of topical sirolimus ointment 0.1%. We also assessed the effect of treatment on quality of life. Methods. We report our experience in using sirolimus ointment in 14 patients with TSC (9 children and 5 adults). The impact of sirolimus ointment was monitored with digital photography, dermatological review using a validated Facial Angiofibroma Severity Index (FASI), and quality of life assessments using the questionnaires PedsQL for children and SF36 for adults. Results. The FASI scores were improved in 12/14 cases after six months' treatment, and improvement was more likely in children (median FASI scores of improvement after treatment were 3 points for children and 1 for adults). Proxy-reported PedsQL scores for the total psychosocial domain improved significantly in the children in the cohort with treatment. Conclusions. Sirolimus ointment 0.1% administered once a day was effective in treating facial angiofibromas. It appears to be safe and well tolerated and to have a positive impact on patients' quality of life. It appeared to be most beneficial when started in childhood.

3.
J Biomech ; 55: 64-70, 2017 04 11.
Artigo em Inglês | MEDLINE | ID: mdl-28262284

RESUMO

Peripheral veno-arterial extra-corporeal membrane oxygenation (ECMO) is an artificial circulation that supports patients with severe cardiac and respiratory failure. Differential hypoxia during ECMO support has been reported, and it has been suggested that it is due to the mixing of well-perfused retrograde ECMO flow and poorly-perfused antegrade left ventricle (LV) flow in the aorta. This study aims to quantify the relationship between ECMO support level and location of the mixing zone (MZ) of the ECMO and LV flows. Steady-state and transient computational fluid dynamics (CFD) simulations were performed using a patient-specific geometrical model of the aorta. A range of ECMO support levels (from 5% to 95% of total cardiac output) were evaluated. For ECMO support levels above 70%, the MZ was located in the aortic arch, resulting in perfusion of the arch branches with poorly perfused LV flow. The MZ location was stable over the cardiac cycle for high ECMO flows (>70%), but moved 5cm between systole and diastole for ECMO support level of 60%. This CFD approach has potential to improve individual patient care and ECMO design.


Assuntos
Aorta/fisiopatologia , Simulação por Computador , Oxigenação por Membrana Extracorpórea , Hidrodinâmica , Veias/fisiopatologia , Adulto , Débito Cardíaco , Ventrículos do Coração/fisiopatologia , Humanos , Masculino , Modelos Biológicos , Insuficiência Respiratória/fisiopatologia , Insuficiência Respiratória/terapia
5.
Appl Clin Inform ; 4(2): 170-84, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23874356

RESUMO

BACKGROUND: Increased usage of MedlinePlus by Spanish-speakers was observed after introduction of MedlinePlus in Spanish. This probably reflects increased usage of MEDLINE and PubMed by those with greater fluency in the language in which it is presented; but this has never been demonstrated in English speakers. Evidence that lack of English fluency deters international healthcare personnel from using PubMed could support the use of multi-language search tools like Babel-MeSH. OBJECTIVES: This study aims to measure the effects of language fluency and other socioeconomic factors on PubMed MEDLINE and MedlinePlus access by international users. METHODS: We retrospectively reviewed server pageviews of PubMed and MedlinePlus from various periods of time, and analyzed them against country statistics on language fluency, GDP, literacy rate, Internet usage, medical schools, and physicians per capita, to determine whether they were associated. RESULTS: We found fluency in English to be positively associated with pageviews of PubMed and MedlinePlus in countries with high literacy rates. Spanish was generally found to be positively associated with pageviews of MedlinePlus en Español. The other parameters also showed varying degrees of association with pageviews. CONCLUSIONS: After adjusting for the other factors investigated in this study, language fluency was a consistently significant predictor of the use of PubMed, MedlinePlus English and MedlinePlus en Español. This study may support the need for multi-language search tools and may increase access of health information resources from non-English speaking countries.


Assuntos
Barreiras de Comunicação , Idioma , MedlinePlus/estatística & dados numéricos , PubMed/estatística & dados numéricos , Produto Interno Bruto/estatística & dados numéricos , Humanos , Internacionalidade , Internet/estatística & dados numéricos , Médicos/provisão & distribuição , Faculdades de Medicina/provisão & distribuição , Fatores Socioeconômicos
6.
Arch Dis Child ; 97(4): 316-9, 2012 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-21459880

RESUMO

BACKGROUND: The isolated finding of an unexplained chronic subdural haematoma in an infant may suggest non-accidental head injury (NAHI). The authors report a previously undescribed cause of multifocal chronic subdural haematoma in infancy which could result in a misdiagnosis of previous NAHI. METHODS: Two infants, aged 3 and 4 months of age, presented with progressively increasing head circumference measurements from birth. There was no history of encephalopathy. Retinal haemorrhages were not present. CT and MRI demonstrated bilateral subdural fluid collections over the frontal regions that were consistent with either chronic subdural haematomas or haemorrhagic subdural effusions. In view of the possibility of NAHI, child protection investigations were initiated. FINDINGS: In neither case did the child protection investigations raise concerns. Comprehensive investigations for known haematological and metabolic disorders associated with subdural haematomas or effusions in infants were all normal. In both cases the infant's mother had a history of Sjögren's syndrome and both infants had positive anti-Ro antibody at presentation. CONCLUSIONS: Transplacental acquisition of anti-Ro antibodies has been associated with external hydrocephalus. External hydrocephalus has been recognised as a predisposing factor for subdural haemorrhage. These are the first reported cases linking the presence of anti-Ro antibodies and external hydrocephalus with subdural fluid collections in infancy.


Assuntos
Anticorpos Antinucleares/sangue , Hematoma Subdural Crônico/imunologia , Hidrocefalia/imunologia , Maus-Tratos Infantis/diagnóstico , Traumatismos Craniocerebrais/diagnóstico , Diagnóstico Diferencial , Feminino , Hematoma Subdural Crônico/diagnóstico , Humanos , Hidrocefalia/diagnóstico , Lactente , Imageamento por Ressonância Magnética , Troca Materno-Fetal/imunologia , Gravidez , Complicações na Gravidez/imunologia , Síndrome de Sjogren/imunologia , Tomografia Computadorizada por Raios X
7.
Appl Clin Inform ; 3(3): 326-33, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23646080

RESUMO

BACKGROUND: Smartphones are increasingly important for clinical decision support, but smartphone and Internet use are limited by cost or coverage in many settings. txt2MEDLINE provides access to published medical evidence by text messaging. Previous studies have evaluated this approach, but we found no comparisons with other tools in this format. OBJECTIVES: To compare txt2MEDLINE with other databases for answering clinical queries by text messaging in low-resource settings. METHODS: Using varied formats, we searched txt2MEDLINE and five other search portals (askMEDLINE, Cochrane, DynaMed, PubMed PICO, and UpToDate) to develop optimal strategies for each. We then searched each database again with five benchmark queries, using the customized search-optimization formats. We truncated the results to less than 480 characters each to simulate delivering them to a maximum of three text messages. Clinicians with practice experience in low-resource areas scored the results on a 5-point Likert scale. RESULTS: Median scores and standard deviations from 17 reviewers were: txt2M2MEDLINE, 3.2±0.82 (control); askMEDLINE, 3.2±0.90 (p = 0.918); Cochrane, 3.8±0.58 (p = 0.073); DynaMed, 3.6±0.65 (p = 0.105); PubMed PICO, 3.6±0.82 (p = 0.005); and UpToDate, 4.0±0.52 (p = 0.002). Our sample size was sufficiently powered to find differences of 1.0 point. CONCLUSIONS: Comparing several possible sources for texting-based clinical-decision-support information, our results did not demonstrate one-point differences in usefulness on a scale of 1 to 5. PubMed PICO and UpToDate were significantly better than txt2MEDLINE, but with relatively small improvements in Likert score (0.4 and 0.8, respectively). In a texting-only setting, txt2MEDLINE is comparable to simulated alternatives based on established reference sources.


Assuntos
Telefone Celular , Sistemas de Apoio a Decisões Clínicas/normas , MEDLINE , Informática Médica/métodos , PubMed , Envio de Mensagens de Texto , Informática Médica/normas , Ferramenta de Busca/métodos , Ferramenta de Busca/estatística & dados numéricos
8.
Arch Dis Child ; 95(1): 12-9, 2010 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-19951935

RESUMO

OBJECTIVE: Stroke is an important but under-recognised cause of childhood mortality. The authors aimed to describe the trends in mortality from childhood stroke in England and Wales between 1921 and 2000. DESIGN: The study searched the Office for National Statistics mortality database for the years 1921-2000 using appropriate, previously validated International Classification of Diseases codes. Mortality rates were analysed by period of death, gender, age at death, birth cohort and stroke subtype. RESULTS: 6029 deaths from childhood stroke were found between 1921 and 2000. Analysis by period of death demonstrated an initial decline in mortality followed by a steep rise in the 1940s. Subsequently, rates declined from the late 1960s onwards. At all time points males had a higher mortality rate than females. Infants had a relatively high mortality rate (24.5 per million person years) but rates fell steeply in early childhood (2.5 per million person years at age 5-9 years) before rising again in late adolescence (7.5 per million person years at age 15-19 years). An increased rate was found for males at all ages (RR = 1.24, p<0.0001) but was greatest in infancy (RR = 1.45, p<0.0001). Haemorrhagic stroke accounted for 71% of stroke deaths. Birth cohort analysis showed a trend of declining mortality with each successive generation since the 1950s. CONCLUSIONS: This study describes characteristics and temporal changes in childhood stroke mortality in the 20(th) century. In particular, the higher mortality rates in males and infants, the importance of deaths from haemorrhagic stroke and the finding of a decline in birth cohort mortality since the 1950s provide aetiological insights.


Assuntos
Acidente Vascular Cerebral/mortalidade , Adolescente , Distribuição por Idade , Criança , Pré-Escolar , Bases de Dados Factuais , Inglaterra/epidemiologia , Feminino , Humanos , Lactente , Recém-Nascido , Classificação Internacional de Doenças , Masculino , Mortalidade/tendências , Distribuição por Sexo , País de Gales/epidemiologia , Adulto Jovem
9.
Arch Dis Child ; 94(9): 729-33, 2009 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-19700427

RESUMO

The current regulations for conducting non-commercial clinical trials in Europe are many and complex. These are explored from the perspective of a UK based non-commercial international clinical trial. The reasons for the difficulties encountered are discussed and suggestions made as to how best to overcome them. Improvements are suggested for our law makers and competent authorities. It is argued that the current regulatory environment could be considered unethical as it inhibits and delays research.


Assuntos
Ensaios Clínicos como Assunto/métodos , Cooperação Internacional , Pediatria , Criança , Ensaios Clínicos como Assunto/economia , Ensaios Clínicos como Assunto/ética , Humanos
10.
Arch Dis Child ; 94(10): 790-4, 2009 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-19556220

RESUMO

BACKGROUND: Cerebral venous sinus thrombosis (CVST) in children is associated with a high incidence of serious morbidity and mortality. The presenting features are variable. It can be diagnostically challenging and the optimal treatment is uncertain. AIM: To describe the features of a series of children with CVST treated in a single paediatric neurology centre and to discuss the role of local thrombolysis. METHODS: Electronic databases were searched using diagnostic labels and International Classification of Diseases (ICD) codes to identify children aged 1 month to under 17 years with CVST. Their records were reviewed. RESULTS: 21 children were identified over a period of 8.25 years with a median age of 7.1 years. The presenting symptoms included headache (15 children), vomiting (14 children) and visual disturbance (eight children). Signs found included papilloedema (16 children), fever (six children) and sixth nerve palsy (six children). The most common underlying condition was middle ear infection (13 children). All cases received unfractionated heparin and four severe cases received local pharmacological thrombolysis. 48% of cases had an adverse outcome (death, chronic intracranial hypertension, residual hemiparesis or sixth nerve palsy). DISCUSSION: CVST has non-specific presenting features and a high risk of significant morbidity. CVST is typically found in association with a predisposing condition. Although heparin is the mainstay of treatment, thrombolysis may reverse deterioration as seen in three cases in this series. However, there is insufficient evidence to recommend the routine use of thrombolysis at present.


Assuntos
Trombose dos Seios Intracranianos/diagnóstico , Trombose dos Seios Intracranianos/tratamento farmacológico , Terapia Trombolítica/métodos , Adolescente , Anticoagulantes/uso terapêutico , Criança , Pré-Escolar , Feminino , Fibrinolíticos/uso terapêutico , Seguimentos , Transtornos da Cefaleia Secundários/etiologia , Heparina/uso terapêutico , Humanos , Lactente , Masculino , Fatores de Risco , Trombose dos Seios Intracranianos/complicações , Trombofilia/complicações , Trombofilia/diagnóstico , Fatores de Tempo , Ativador de Plasminogênio Tecidual/uso terapêutico , Resultado do Tratamento , Transtornos da Visão/etiologia , Vômito/etiologia
11.
J Biomech ; 42(6): 755-61, 2009 Apr 16.
Artigo em Inglês | MEDLINE | ID: mdl-19281988

RESUMO

Spontaneous dissection of the cervical internal carotid artery (sICAD) is a major cause of stroke in young adults. A tear in the inner part of the vessel wall triggers sICAD as it allows the blood to enter the wall and develop a transmural hematoma. The etiology of the tear is unknown but many patients with sICAD report an initiating trivial trauma. We thus hypothesised that the site of the tear might correspond with the location of maximal stress in the carotid wall. Carotid artery geometries segmented from magnetic resonance images of a healthy subject at different static head positions were used to define a path of motion and deformation of the right cervical internal carotid artery (ICA). Maximum head rotation to the left and rotation to the left combined with hyperextension of the neck were investigated using a structural finite element model. A role of the carotid sinus as a geometrically compliant feature accommodating extension of the artery is shown. At the extreme range of the movements, the geometrical compliance of the carotid sinus is limited and significant stress concentrations appear just distal to the sinus with peak stresses at the internal wall on the posterior side of the vessel following maximum head rotation and on the anteromedial portion of the vessel wall following rotation and hyperextension. Clinically, the location of sICAD initiation is 10-30 mm distal to the origin of the cervical ICA, which corresponds with the peak stress locations observed in the model, thus supporting trivial trauma from natural head movements as a possible initiating factor in sICAD.


Assuntos
Dissecação da Artéria Carótida Interna/fisiopatologia , Dissecação da Artéria Carótida Interna/cirurgia , Análise de Elementos Finitos , Humanos , Pescoço , Estresse Fisiológico
12.
Arch Dis Child ; 93(9): 751-4, 2008 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-18456692

RESUMO

OBJECTIVES: (1) In a population-based study of tuberous sclerosis (TSC), to identify the number of patients presenting with symptomatic giant cell astrocytomas (GCAs); (2) within a subset of this population, to identify the number who would be diagnosed with GCAs on predetermined radiological criteria. METHODS: Patients with TSC in Wessex (a geographical region of England) were identified, and their medical history determined. A subset were invited to have a cranial MRI if they did not have a history of a symptomatic GCA and if they were likely to tolerate cranial imaging without a general anaesthetic. Scans were performed according to a standard protocol on a single scanner and were reported blindly by a neuroradiologist. RESULTS: 179 people were identified with TSC. Ten of these had a history of treatment for a symptomatic GCA. Forty-one of the remainder had a cranial MRI. Thirty-nine of these had subependymal nodules, of whom 24 (59%) had at least one (maximum 11) that showed enhancement with gadolinium. In seven (17%), the lesion was >1 cm, and all of these lesions showed gadolinium enhancement. CONCLUSIONS: In this study, the proportion of patients with TSC who had a history of symptomatic GCA was 5.6%. In the subset without such a history, who underwent imaging, the number diagnosed as having a GCA on radiological criteria was much higher (59% gadolinium enhancement and 17% >1 cm in size). Screening for GCAs (performing scans on asymptomatic patients with TSC) would therefore identify large numbers of patients who had not presented with symptoms. This finding leads us to recommend that screening should not be undertaken.


Assuntos
Astrocitoma/epidemiologia , Neoplasias Encefálicas/epidemiologia , Esclerose Tuberosa/epidemiologia , Adolescente , Adulto , Astrocitoma/diagnóstico , Neoplasias Encefálicas/diagnóstico , Criança , Estudos Transversais , Feminino , Humanos , Hipertensão Intracraniana/etiologia , Hipertensão Intracraniana/cirurgia , Imageamento por Ressonância Magnética , Masculino , Transtornos Mentais/etiologia , Tomografia Computadorizada por Raios X , Esclerose Tuberosa/diagnóstico , Proteínas Supressoras de Tumor/metabolismo
13.
J Child Psychol Psychiatry ; 49(10): 1061-8, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-18422546

RESUMO

BACKGROUND: Long-chain omega-3 polyunsaturated fatty acids are thought to be important for fetal neurodevelopment. Animal studies suggest that a deficiency of omega-3 fatty acids may lead to behavioural or cognitive deficits. As oily fish is a major dietary source of omega-3 fatty acids, it is possible that low intake of fish during pregnancy may have adverse effects on the developing fetal brain. METHODS: We used the Strengths and Difficulties Questionnaire and the Wechsler Abbreviated Scale of Intelligence to assess behavioural problems and intelligence in 217 nine-year-old children. The mothers of these children had participated in a study of nutrition during pregnancy during which fish intake was assessed in early and late gestation. RESULTS: Children whose mothers had eaten oily fish in early pregnancy had a reduced risk of hyperactivity compared to those whose mothers did not eat oily fish: OR .34, 95% CI .15 to .78, after adjustment for potential confounding factors. Children whose mothers had eaten fish (whether oily or non-oily) in late pregnancy had a verbal IQ that was 7.55 points higher (95% CI .75 to 14.4) than those whose mothers did not eat fish. There were, however, no significant associations between fish intake in pregnancy and other behavioural problems or full-scale and performance intelligence, after adjustment for potential confounding factors. CONCLUSIONS: Although maternal fish intake in pregnancy was associated with hyperactivity scores and verbal IQ in children, in general, how much fish women ate during pregnancy appeared to have little long-term relation with neurodevelopmental outcomes in their child.


Assuntos
Transtornos de Deficit da Atenção e do Comportamento Disruptivo/fisiopatologia , Dieta , Ácidos Graxos Ômega-3 , Peixes , Inteligência/fisiologia , Fenômenos Fisiológicos da Nutrição Materna , Adulto , Animais , Encéfalo/embriologia , Criança , Feminino , Seguimentos , Humanos , Masculino , Gravidez , Análise de Regressão , Reino Unido
14.
J Intellect Disabil Res ; 50(Pt 8): 561-9, 2006 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-16867063

RESUMO

BACKGROUND: Tuberous sclerosis (TS) is a multi- system disorder with complex genetics. The neurodevelopmental manifestations of TS are responsible for considerable morbidity. The prevalence of epilepsy and intellectual disabilities among individuals with TS have been well described. Ours is the first study that explores the prevalence and pattern of psychopathology in a population-based sample of adults with TS. METHODS: Sixty subjects were identified through a capture-recapture analysis of TS. Information was gathered as to seizure history, cognitive functioning (WISC-III) and psychopathology (SADS-L, SAPPA). Lifetime psychopathology was categorized according to Research Diagnostic Criteria. The overall pattern of mental illness (MI) was examined as well as how this varied with IQ and seizure history. RESULTS: Twenty-four (40.0%) subjects had a history of MI. The most common diagnosis was that of an affective disorder [18 (30.0%)], the majority of which were major depressive episodes. Alcoholism [4 (6.7%)] and anxiety disorders [3 (5.0%)] were the next most common diagnoses. Two (3.3%) subjects had had a tic disorder. Only one individual had a diagnosis of schizophrenia. MI was found in 75.0% of those with a history of epilepsy and 37.5% of those without epilepsy. MI was significantly more prevalent in those with a full-scale IQ above 70. CONCLUSIONS: A significant proportion of adult with TS experience MI. MI was significantly more [corrected] prevalent in subjects with a full-scale IQ above 70. Reasons for such a finding are explored, and related methodological considerations for future research outlined.


Assuntos
Epilepsia/psicologia , Deficiência Intelectual/psicologia , Transtornos Mentais/psicologia , Esclerose Tuberosa/psicologia , Adulto , Alcoolismo/epidemiologia , Alcoolismo/genética , Alcoolismo/psicologia , Transtornos de Ansiedade/epidemiologia , Transtornos de Ansiedade/genética , Transtornos de Ansiedade/psicologia , Comorbidade , Estudos Transversais , Transtorno Depressivo Maior/epidemiologia , Transtorno Depressivo Maior/genética , Transtorno Depressivo Maior/psicologia , Epilepsia/epidemiologia , Epilepsia/genética , Feminino , Humanos , Deficiência Intelectual/epidemiologia , Deficiência Intelectual/genética , Inteligência , Masculino , Transtornos Mentais/epidemiologia , Transtornos Mentais/genética , Pessoa de Meia-Idade , Esquizofrenia/epidemiologia , Esquizofrenia/genética , Estatística como Assunto , Transtornos de Tique/epidemiologia , Transtornos de Tique/genética , Transtornos de Tique/psicologia , Esclerose Tuberosa/epidemiologia , Esclerose Tuberosa/genética , Escalas de Wechsler
15.
J Med Genet ; 43(9): 729-34, 2006 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-16611748

RESUMO

OBJECTIVE: To determine the frequency of mutations in CDKL5 in both male and female patients with infantile spasms or early onset epilepsy of unknown cause, and to consider whether the breadth of the reported phenotype would be extended by studying a different patient group. METHODS: Two groups of patients were investigated for CDKL5 mutations. Group 1 comprised 73 patients (57 female, 16 male) referred to Cardiff for CDKL5 analysis, of whom 49 (42 female, 7 male) had epileptic seizure onset in the first six months of life. Group 2 comprised 26 patients (11 female, 15 male) with infantile spasms previously recruited to a clinical trial, the UK Infantile Spasms Study. Where a likely pathogenic mutation was identified, further clinical data were reviewed. RESULTS: Seven likely pathogenic mutations were found among female patients from group 1 with epileptic seizure onset in the first six months of life, accounting for seven of the 42 in this group (17%). No mutations other than the already published mutation were found in female patients from group 2, or in any male patient from either study group. All patients with mutations had early signs of developmental delay and most had made little developmental progress. Further clinical information was available for six patients: autistic features and tactile hypersensitivity were common but only one had suggestive Rett-like features. All had a severe epileptic seizure disorder, all but one of whom had myoclonic jerks. The EEG showed focal or generalised changes and in those with infantile spasms, hypsarrhythmia. Slow frequencies were seen frequently with a frontal or fronto-temporal predominance and high amplitudes. CONCLUSIONS: The spectrum of the epileptic seizure disorder, and associated EEG changes, in those with CDKL5 mutations is broader than previously reported. CDKL5 mutations are a significant cause of infantile spasms and early epileptic seizures in female patients, and of a later intractable seizure disorder, irrespective of whether they have suspected Rett syndrome. Analysis should be considered in these patients in the clinical setting.


Assuntos
Deficiência Intelectual/genética , Mutação/genética , Proteínas Serina-Treonina Quinases/genética , Convulsões/epidemiologia , Convulsões/genética , Espasmos Infantis/genética , Adolescente , Adulto , Idade de Início , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Recém-Nascido , Masculino
16.
Phys Rev Lett ; 95(19): 197001, 2005 Nov 04.
Artigo em Inglês | MEDLINE | ID: mdl-16384012

RESUMO

The magnetic field dependence of the vortex core size in the multiband superconductor NbSe2 has been determined from muon spin rotation measurements. The spatially extended nature of the quasiparticle core states associated with the smaller gap leads to a rapid field-induced shrinkage of the core size at low fields, while the more tightly bound nature of the states associated with the larger gap leads to a field-independent core size for fields greater than 4 kOe. A simple model is proposed for the density of delocalized core states that establishes a direct relationship between the field-induced reduction of the vortex core size and the corresponding enhancement of the electronic thermal conductivity. We show that this model accurately describes both NbSe2 and the single-band superconductor V3Si.

19.
Arch Dis Child ; 89(6): 530-3, 2004 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15155396

RESUMO

BACKGROUND: The aetiology of the learning difficulty in tuberous sclerosis is debated. It may be related to the amount of tubers in the brain or caused by the infantile spasms that occur in early life. AIMS: To examine the relative contributions to final intelligence (IQ) made by both cerebral tubers and infantile spasms. METHODS: As part of an epidemiological study of tuberous sclerosis in the south of England, patients were recruited who were able to undergo magnetic resonance imaging (MRI) without the need for an anaesthetic. Epilepsy history was determined by interview and review of clinical records. IQ was assessed using either Wechsler intelligence scales or Raven's matrices. RESULTS: A total of 41 patients consented to have an MRI scan. IQ scores were normally distributed about a mean of 91. Twenty six patients had a positive history of epilepsy, and 11 had suffered from infantile spasms. There was a significant relation between the number of tubers and IQ. Infantile spasm status partly confounded the relation between tubers and IQ, but did not render the relation statistically insignificant. The relation between infantile spasms and learning difficulty remained strong even when controlling for the number of tubers.


Assuntos
Deficiências da Aprendizagem/etiologia , Espasmos Infantis/etiologia , Esclerose Tuberosa/complicações , Adolescente , Adulto , Idoso , Córtex Cerebral , Criança , Inglaterra/epidemiologia , Feminino , Humanos , Lactente , Inteligência , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Esclerose Tuberosa/patologia , Escalas de Wechsler/normas
20.
Complement Ther Med ; 11(1): 28-32, 2003 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-12667972

RESUMO

OBJECTIVES: To examine the relationship between postmodern values, demographic variables and people's attitudes towards and use of acupuncture, aromatherapy and naturopathy. DESIGN: One hundred and seventy-one adults completed a survey measuring postmodern values about health, attitudes towards and use of complementary and alternative medicine (CAM), age, gender, education, and current and recent health. SETTING: Griffith University, Gold Coast, Australia. MAIN OUTCOME MEASURES: Attitudes to CAM and use of CAM. RESULTS: Postmodern values significantly predicted attitudes to CAM and actual use of CAM. Age also significantly predicted attitudes to CAM. CONCLUSIONS: The results highlight the importance of patients' belief in natural remedies and in their active involvement in the healing process.


Assuntos
Atitude Frente a Saúde , Terapias Complementares/psicologia , Aceitação pelo Paciente de Cuidados de Saúde/psicologia , Valores Sociais , Adolescente , Adulto , Fatores Etários , Idoso , Austrália , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Inquéritos e Questionários
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