Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros










Intervalo de ano de publicação
1.
Med Devices (Auckl) ; 6: 141-6, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24039458

RESUMO

Close adherence to the recommended treatment regimen is important for the success of recombinant human growth hormone therapy, although nonadherence can be common. Ease of use and safety during use/storage are among several important factors in the design of a growth hormone injection device intended for long-term use. This study was performed to validate the usability and assess the ease of use of a new pen device (SurePal™) that has been developed to support daily administration of the recombinant human growth hormone product, Omnitrope® (somatropin). The primary objectives of the study were to assess if study participants, representing intended users of the pen in clinical practice, were able to perform an injection procedure into an injection pad effectively and safely and disassemble the pen without receiving a needlestick injury. A total of 106 participants (61 adults and 45 children/adolescents) were enrolled at two study centers (one in the US, one in Germany). Results for both primary usability tasks met the predefined acceptance criteria, with >85% of participants successfully performing each task. All of the other tasks/handling steps assessed were also successfully performed by most participants, with high success rates reflected in the high proportion of participants who classified each task as "very easy" or "easy". After a second use of the device, 87%-97% of participants rated it as "very easy" or "easy" to use. In summary, the new pen device is safe and easy to use for both adults and children, and will help to support effective, long-term daily administration of the recombinant human growth hormone product, Omnitrope®.

2.
Rev. AMRIGS ; 42(4): 226-31, out.-dez. 1998.
Artigo em Português | LILACS | ID: lil-257166

RESUMO

A síndrome do X frágil é caracterizada por retardo mental, alterações do comportamento, orelhas grandes, face alongada, macroorquidismo, displasia leve do tecido conjuntivo e detecção do sítio frágil Xq27.3 em meio deficiente em folato. Esta síndrome é causada po uma repetição da expansão do trinucleotídeo CGG no gen FMR1...


Assuntos
Humanos , Criança , Síndrome do Cromossomo X Frágil/fisiopatologia , Doenças Genéticas Inatas , Deficiência Intelectual/etiologia
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...