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1.
Hosp Pediatr ; 9(7): 501-507, 2019 07.
Artigo em Inglês | MEDLINE | ID: mdl-31160472

RESUMO

BACKGROUND AND OBJECTIVES: Pain management in children often is inadequate, and the single most common painful procedure in children who are hospitalized is needle procedures. Virtual reality (VR) is a promising and engaging intervention that may help to decrease anxiety and pain in children undergoing painful procedures. Our aim for this study is to investigate patient satisfaction and pain reduction by using a three-dimensional VR interactive game as a distraction. METHODS: In this randomized clinical trial, we enrolled 64 children aged 7 to 16 years who were scheduled for venous cannulation. Patients assigned to the control group were adherent to our standard of care, including topical numbing cream, positioning, and distraction by a specialized pain nurse. In the study group, children were adherent to the standard of care and were distracted by an interactive VR game. Primary outcomes were patient satisfaction and the procedural pain assessed by using a visual analog score; secondary outcomes were the procedural time and any adverse events. RESULTS: We found a high level of patient satisfaction with using the VR custom-made three-dimensional interactive game. All children (28 of 28 [100%]) in the VR group answered that they would prefer VR as a distraction for a later procedure, a borderline significant result compared with that of the control group (26 of 31 [84.9%]). No significant difference was found in pain scores and procedural times between the 2 groups. The number of adverse effects was low, with no significant difference between the 2 groups. CONCLUSIONS: We found no difference in pain scores but higher satisfaction when using VR versus standard care as part of a multimodal approach for management of procedural pain in children.


Assuntos
Manejo da Dor/instrumentação , Dor Processual/prevenção & controle , Satisfação do Paciente/estatística & dados numéricos , Interface Usuário-Computador , Realidade Virtual , Adolescente , Criança , Análise Custo-Benefício , Feminino , Hospitais Pediátricos , Humanos , Masculino , Manejo da Dor/psicologia , Medição da Dor , Dor Processual/psicologia
2.
Dan Med J ; 64(9)2017 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-28874241

RESUMO

INTRODUCTION: Infant botulism is a rare, probably underdiagnosed, life-threatening disease caused by the toxin-producing bacterium Clostridium botulinum. METHODS: We investigated reported cases of infant botulism in Denmark from 1995 to 2015, and compared the incidence with that of other western countries. RESULTS: We found nine cases of infant botulism in Denmark from 1995 to 2015. The incidence of infant botulism in Denmark was similar to that seen in other western countries, but likely underestimated. The source of infection was only confirmed in a single case. Four cases received botulism immune globulin, intravenous (BIG-IV), which was administered within 7-10 days from admission. CONCLUSIONS: Infant botulism is probably underdiagnosed. Increased awareness is crucial to be able to recognise the condition. The time delay from hospital admission to administration of BIG-IV is challenging. Studies have shown that BIG-IV reduces both mean duration of intensive care and mean length of hospital stay; however, this was not confirmed in our work due to the limited number of patients. FUNDING: none. TRIAL REGISTRATION: not relevant.


Assuntos
Botulismo/epidemiologia , Dinamarca/epidemiologia , Feminino , Hospitalização/estatística & dados numéricos , Humanos , Incidência , Lactente , Masculino
3.
Eur J Paediatr Neurol ; 19(6): 719-21, 2015 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-26278497

RESUMO

INTRODUCTION: DYT11 is an autosomal dominant inherited movement disorder characterized by myoclonus and dystonia. CLINICAL PRESENTATION: We present a case with atypical symptoms and with episodes of ataxia and myoclonus preceded by infections. Atypical presentation of opsoclonus myoclonus syndrome was suspected and treatment with bolus steroids and immunoglobulin were initiated with some response over 28 months. A re-evaluation gave suspicion of a dyskinetic disorder and whole exome-sequencing was performed but no causal variant was identified. OUTCOME: A specific analysis of the SGCE gene was subsequently initiated, which revealed a pathogenic aberration confirming the diagnosis of DYT11. CONCLUSION: A clinical DYT11 diagnosis can be difficult to establish in early childhood without a known family history.


Assuntos
Distúrbios Distônicos/diagnóstico , Síndrome de Opsoclonia-Mioclonia/diagnóstico , Anti-Inflamatórios/uso terapêutico , Dexametasona/uso terapêutico , Diagnóstico Diferencial , Erros de Diagnóstico , Distúrbios Distônicos/genética , Distúrbios Distônicos/terapia , Exoma , Feminino , Deleção de Genes , Humanos , Imunização Passiva , Lactente , Síndrome de Opsoclonia-Mioclonia/genética , Sarcoglicanas/genética , Esteroides/uso terapêutico
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