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1.
Eur J Cardiovasc Nurs ; 22(5): 472-481, 2023 07 19.
Artigo em Inglês | MEDLINE | ID: mdl-36190843

RESUMO

AIMS: Electronic health (eHealth) sources have great potential to improve patients' access to health information for self-management of secondary prevention after percutaneous coronary intervention (PCI). It remains unclear, however, whether patients are health-related digitally active and whether they have sufficient eHealth literacy. This study aimed to determine the extent to which patients after PCI are health-related digitally active at baseline, 2 and 6 months after PCI, and to determine the association between patients' eHealth literacy and their health-related digital activity. METHODS AND RESULTS: This multicentre cohort study included patients at three large referral PCI centres in Norway (n = 1970). Data were collected from medical records, national registries, and patients' self-reports. The eHealth Literacy Scale (eHEALS) assessed patients' eHealth literacy. At baseline, 67% had used the internet to find health information. The mean eHEALS score was 25.71 (standard deviation 6.22), illustrating a lower level of eHealth literacy. There were substantial associations between eHealth literacy and use of the internet to find health information [coefficient 10.90, 95% confidence interval (CI) 8.05-14.57]. At the 2-month follow-up, there were substantial associations between baseline eHealth literacy and use of the internet to find information about health, prevention, illness, or treatment [odds ratio (OR) 1.19, 95% CI 1.14-1.24] and use of health applications (OR 1.15, 95% CI 1.08-1.22). CONCLUSION: This study provides evidence that patients' level of eHealth literacy after PCI is associated to how patients use, and can make use of, eHealth technology for health information. REGISTRATION: ClinicalTrials.gov (NCT03810612).


Assuntos
Letramento em Saúde , Intervenção Coronária Percutânea , Telemedicina , Humanos , Estudos de Coortes , Inquéritos e Questionários , Telemedicina/métodos , Estudos Transversais , Eletrônica , Tecnologia
2.
Child Care Health Dev ; 42(5): 735-41, 2016 09.
Artigo em Inglês | MEDLINE | ID: mdl-27283955

RESUMO

BACKGROUND: Musculoskeletal pain in cerebral palsy (CP) is common, but probably undertreated. The aim of the study was to explore if recurrent musculoskeletal pain (RMP) related to the CP condition was associated with visits to the family doctor [general practitioner (GP)] and specialist habilitation centre in youth with CP. METHODS: Seventy-four youth with CP (mean age 16.5 years, 40 boys) from the same geographical area were assessed by clinical examination, semi-structured interview on pain (adolescent and parent together), the two questions on pain from the Child Health Questionnaire (parents only) and a structured interview on health care services. Gross Motor Function Classification System was level I 39%, level II 23%, level III 8% and levels IV and V 30%. RESULTS: Thirty-five participants (47%) had visited their GP last year, and 49 (66%) had visited the specialist habilitation centre. The presence of RMP (n = 58; 78%) was not significantly associated with having visited the GP or the specialist habilitation centre. Still, in participants with RMP, increasing pain severity was associated with having visited the GP. Rest, massage, change of position and oral drugs were the most common measures taken to relieve RMP. Three adolescents with RMP did not take any measures to relieve pain. CONCLUSION: Youth with RMP do take measures to relieve pain, but usually not in the direction of consulting the health care services available unless the pain is severe. Both youth with CP and their caregivers should be encouraged to discuss RMP with their professional network of care.


Assuntos
Paralisia Cerebral/complicações , Medicina de Família e Comunidade/estatística & dados numéricos , Dor Musculoesquelética/etiologia , Aceitação pelo Paciente de Cuidados de Saúde/estatística & dados numéricos , Adolescente , Paralisia Cerebral/terapia , Feminino , Humanos , Masculino , Dor Musculoesquelética/terapia , Noruega , Medição da Dor/métodos , Recidiva , Centros de Reabilitação/estatística & dados numéricos
3.
Acta Paediatr ; 99(11): 1661-5, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-19912148

RESUMO

AIM: The aim of the study was to explore the timing of effects of intrathecal baclofen therapy in children with cerebral palsy. METHODS: Thirty five children with severe disabilities with cerebral palsy who started continuous intrathecal baclofen therapy (CITB) were followed for 18 months. Pain, number of awakenings during night, spasticity, GMFM-66 scores and PEDI scores were recorded the day before pump implantation and after 6 and 18 months of treatment respectively. RESULTS: Introduction of CITB was associated with changes across all ICF dimensions. Reduced pain and improved sleep occurred within 6 months of treatment. Social function improved within 6 months and continued to improve until 18 months of CITB. Mobility also improved, but with a latency. CONCLUSION: There seems to be a sequence of changes after introduction of continuous intrathecal baclofen in a child with cerebral palsy that may guide the multidisciplinary team in their timing of therapy during post-surgical follow-up.


Assuntos
Baclofeno/administração & dosagem , Paralisia Cerebral/tratamento farmacológico , Crianças com Deficiência/reabilitação , Relaxantes Musculares Centrais/administração & dosagem , Adolescente , Criança , Pré-Escolar , Avaliação da Deficiência , Esquema de Medicação , Feminino , Seguimentos , Humanos , Bombas de Infusão Implantáveis , Masculino , Atividade Motora , Espasticidade Muscular/tratamento farmacológico , Medição da Dor , Distúrbios do Início e da Manutenção do Sono , Fatores de Tempo , Resultado do Tratamento
4.
Mol Ecol ; 13(2): 277-90, 2004 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-14717887

RESUMO

Bottlenecks can have lasting effects on genetic population structure that obscure patterns of contemporary gene flow and drift. Sockeye salmon are vulnerable to bottleneck effects because they are a highly structured species with excellent colonizing abilities and often occupy geologically young habitats. We describe genetic divergence among and genetic variation within spawning populations of sockeye salmon throughout the Lake Clark area of Alaska. Fin tissue was collected from sockeye salmon representing 15 spawning populations of Lake Clark, Six-mile Lake, and Lake Iliamna. Allele frequencies differed significantly at 11 microsatellite loci in 96 of 105 pairwise population comparisons. Pairwise estimates of FST ranged from zero to 0.089. Six-mile Lake and Lake Clark populations have historically been grouped together for management purposes and are geographically proximate. However, Six-mile Lake populations are genetically similar to Lake Iliamna populations and are divergent from Lake Clark populations. The reduced allelic diversity and strong divergence of Lake Clark populations relative to Six-mile Lake and Lake Iliamna populations suggest a bottleneck associated with the colonization of Lake Clark by sockeye salmon. Geographic distance and spawning habitat differences apparently do not contribute to isolation and divergence among populations. However, temporal isolation based on spawning time and founder effects associated with ongoing glacial retreat and colonization of new spawning habitats contribute to the genetic population structure of Lake Clark sockeye salmon. Nonequilibrium conditions and the strong influence of genetic drift caution against using estimates of divergence to estimate gene flow among populations of Lake Clark sockeye salmon.


Assuntos
Efeito Fundador , Variação Genética , Genética Populacional , Reprodução/fisiologia , Salmão/genética , Alaska , Animais , Água Doce , Frequência do Gene , Geografia , Comportamento de Retorno ao Território Vital/fisiologia , Repetições de Microssatélites/genética , Dinâmica Populacional , Análise de Componente Principal , Salmão/fisiologia
5.
Tidsskr Nor Laegeforen ; 118(24): 3769-72, 1998 Oct 10.
Artigo em Norueguês | MEDLINE | ID: mdl-9816946

RESUMO

In this article we present a Norwegian family with hereditary multiple exostoses and a review of relevant literature. 21 family members were examined; ten males and six females had multiple exostoses, the youngest from six months of age. The exostoses had led to compression of nerves, disturbance of bone growth with shortening and bowing of the forearm bones, and valgus deformity of the knee and ankle. Physical function and quality of life was generally well preserved. Contrary to most reports, nearly half of the patients had allegedly noticed growth or debut of exostoses in adulthood. Almost half of the patients had had the exostoses removed surgically twice, (median value). Malignant transformation of exostoses has not been observed in the family.


Assuntos
Exostose Múltipla Hereditária/diagnóstico , Adolescente , Adulto , Criança , Pré-Escolar , Exostose Múltipla Hereditária/complicações , Exostose Múltipla Hereditária/genética , Exostose Múltipla Hereditária/psicologia , Feminino , Humanos , Lactente , Masculino , Noruega , Linhagem , Qualidade de Vida
6.
Tidsskr Nor Laegeforen ; 118(14): 2153-4, 1998 May 30.
Artigo em Norueguês | MEDLINE | ID: mdl-9656809

RESUMO

Emotional and behavioural disorders are frequent complications of mental retardation that often go unrecognised or untreated. We describe a 13-year old girl with Down's syndrome and depressive illness who responded well to paroxetin. The importance of organizing comprehensive health provision for children with mental retardation in a way that focuses both psychiatric and physical illness is emphasised.


Assuntos
Depressão/complicações , Síndrome de Down/complicações , Adolescente , Antidepressivos de Segunda Geração/uso terapêutico , Depressão/diagnóstico , Depressão/tratamento farmacológico , Síndrome de Down/psicologia , Feminino , Humanos , Paroxetina/uso terapêutico
9.
J Craniofac Genet Dev Biol ; 16(2): 122-5, 1996.
Artigo em Inglês | MEDLINE | ID: mdl-8773903

RESUMO

We report on a mentally retarded boy with epileptic seizures, microcephaly, ataxia, and developmental delay. His clinical features were consistent with Angelman syndrome. Fluorescent in situ hybridization and DNA analysis showed a deletion of chromosome 15 q11-13 and thus confirmed the diagnosis. In addition, the patient had a unilateral, incomplete cleft lip, a feature which has not previously been reported in Angelman syndrome.


Assuntos
Síndrome de Angelman/genética , Cromossomos Humanos Par 15 , Fenda Labial/genética , Síndrome de Angelman/complicações , Pré-Escolar , Deleção Cromossômica , Fenda Labial/etiologia , Epilepsia/complicações , Epilepsia/tratamento farmacológico , Face/anormalidades , Feminino , Humanos , Hibridização in Situ Fluorescente , Recém-Nascido , Deficiência Intelectual/complicações , Deficiência Intelectual/genética , Masculino , Microcefalia/genética , Polimorfismo Genético , Gravidez
10.
Tidsskr Nor Laegeforen ; 116(1): 30-3, 1996 Jan 10.
Artigo em Norueguês | MEDLINE | ID: mdl-8553331

RESUMO

In spring 1992 a blood conservation programme was established at Nordland Central Hospital with emphasis on indications for blood transfusion and intraoperative blood salvage (cell-saver). Medical records from all patients who underwent hip arthroplasty during the period 1 June 1991 to 28 February 1994 were examined. Mean transfusion of homologous SAGMAN-blood (bank blood) was substantially reduced during the period: for total prosthesis (n = 192) from 2.6 to 1.1 units per operation (p < 0.0001) and for hemiprosthesis (n = 66) from 3.1 to 0.9 units per operation (p = 0.0202). The percentage of patients in each of these two groups who did not receive blood transfusion at all increased from 18 to 61 in the first group (p < 0.0001) and from 24 to 65 (p = 0.0202) in the second. The substantial reduction of bank blood transfusion in this material conforms with current international transfusion guidelines. A particular benefit, considering the risk of transfusing contagious blood, is the marked increase in the number of patients who did not receive any blood product at all.


Assuntos
Preservação de Sangue , Transfusão de Sangue/estatística & dados numéricos , Prótese de Quadril/métodos , Idoso , Transfusão de Sangue Autóloga/estatística & dados numéricos , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Noruega
11.
Tidsskr Nor Laegeforen ; 109(22): 2136-8, 1989 Aug 10.
Artigo em Norueguês | MEDLINE | ID: mdl-2772879

RESUMO

44 hips operated for insertion of the Christiansen hemiprosthesis at the County hospital of Nordland from 1968 to 1976 were evaluated in 1986. Seven hips had been reoperated because of loosening or mechanical failure of the prosthesis. Another four prostheses were found to have loosened at the time of follow-up, bringing the total loosening frequency up to 25 percent, 26 patients reported no pain from the hip, 20 of these were still in normal activity with no restriction in walking as a consequence of the defect hip. All the prostheses had been inserted in a varus position. Acetabular protrusion was found in 14 cases, indicating that there are frictional forces working at the hip joint, also with the trunnion bearing system. The average time from operation to verified loosening was nine years. The trunnion bearing may thus have spared the hip joint from stress during the first years of use.


Assuntos
Prótese de Quadril , Idoso , Estudos de Avaliação como Assunto , Feminino , Seguimentos , Articulação do Quadril/diagnóstico por imagem , Prótese de Quadril/efeitos adversos , Humanos , Masculino , Pessoa de Meia-Idade , Radiografia , Reoperação
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