Lançado
um registro global , disponível abaixo, para mulheres
expostas ao Zika durante a gravidez.
Os
detalhes do registro foram anunciados na edição de setembro do
periódico The Lancet Infectious Diseases. Os autores
afirmam que a esperança é que os dados coletados permitam aos pesquisadores
“fazer uma estimativa quantitativa dos riscos, identificar fatores de risco
específicos, caracterizar melhor o espectro da doença, investigar o efeito do
modo de transmissão no objetivo futuro para definir estratégias de triagem em
gestantes e mulheres férteis, bem como propor medidas preventivas e estratégias
de tratamento clínico adequadas para gestações expostas e neonatos infectados.”
Eles
acrescentaram que qualquer profissional da saúde que ofereça suporte ao
registro fornecendo casos bem-documentados será considerado um colaborador do
registro em qualquer publicação científica futura revisada por pares.
Registry for women exposed
to Zika virus during pregnancy
Studies are urgently needed
to answer the questions surrounding the ZIKA virus and its relation to the
congenital neurological conditions. The purpose of this registry is to
launch a prospective structured data collection to allow future
research projects leading to a better characterization of the risks
associated to ZIKA virus infection during pregnancy (e.g. to
characterize the spectrum of disease, to quantitatively estimate the risk of
microcephaly and other ZIKA virus associated birth defects, to identify
gestational ages with the highest transmission rate or risk factors such as
co-infections).
Inclusion criteria: Any pregnant
patient exposed to ZIKV during pregnancy (i.e. through mosquito bite,
unprotected sexual intercourse or other).
Exclusion criteria: patients considered
as minor in their jurisdiction and patients who have not given their informed
consent or are not able to consent for themselves will not be considerate
eligible in the registry.
The data collected
anonymously will be made available to any research group in the world following the
data-sharing agreement initiative (http://www.wellcome.ac.uk/News/Media-office/Press-releases/2016/WTP060169.htm), provided that they have
a clear, non-redundant research question and a biomedical research Ethics
committee approval (a list of on-going research projects will be kept
available).
Anyone supporting the registry by providing well-documented cases will be listed as a collaborator of the Zika in pregnancy registry in any future peer reviewed scientific publication having used data from the registry.
If you are willing to
collaborate, please fill in the information required to get an access to the
registry below:
Parte
superior do formulário
First
name *
Last name *
Email address *
Profession
Country of
residence *
Should be the country where
the health care provider works.
Hospital/facility *
Should be the
hospital/facility for which the health care provider works
Have the case(s) you
are going to report been reported elsewhere or published ? *
Yes No
Yes No
Have the patient from
whom you are about to share anonymous medical data given an informed consent to
do so ? *
Yes No
Yes No
Do you agree that a
member of the registry team contact you later to gather the follow-up
information about your patient(s) ? *
Yes No
Yes No
* Some fields have to
be filled.
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