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- Medical: Health Care
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- Informirani pristanak je izjava pacijenta ili ispitanika nekog znanstvenog istrazivanja koja lijecnika ili medicinskog istrazivaca opunomocuje da provede odredjene mjere, terapiju, ili da ukljuci ispitanika u istrazivacki protokol. Croatian Scientific Bibliography - by Dubravka Hrastovec
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- Informirani pristanak promice individualnu autonomiju pacijenta i ispitanika, potice racionalno donosenje odluka, osujecuje uplitanje javnosti, upucuje lijecnike i istrazivace na eticku samokontrolu, smanjuje opasnost od gradjanske i krivicne odgovornosti lijecnika, istrazivaca i njihovih ustanova. - Croatian Scientific Bibliography by Dubravka Hrastovec
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Compare [close] Compare [close] - Catalan
- Medical: Health Care
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- Assentiment que dóna una persona a una intervenció terapèutica o exploratòria o bé a la participació en un estudi un cop ha estat informada de les característiques que té i de les conseqüències previsibles que se'n poden derivar. TERMCAT - by Gemma Sanza Porcar
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- Des de fa temps, tots els centres assistencials de Catalunya han treballat per implantar
decididament l'anomenat consentiment informat (CI) i en molts d'ells s'ha impulsat un debat
i una reflexió dels professionals sanitaris en la introducció d'una pràctica no solament
formal, sinó també real que contribueixi decididament al canvi d'hàbits i actituds - GENCAT by Gemma Sanza Porcar
- El consentiment informat s'ha d'entendre com l'acceptació per part d'un malalt competent d'un procediment diagnòstic o terapèutic després de tenir la informació adequada per implicar-se lliurement en la decisió - Servei Català de la Salut by Gemma Sanza Porcar
- Pel que fa a l’especialitat d’Anestesiologia, Reanimació i Terapèutica del Dolor, tenim
en la entrevista preoperatòria una de les ocasions on es fa més necessària, ja que, a
més dels objectius “mèdics” de la visita tals com valorar la història clínica, els riscs, etc.
està el de donar informació, arribar a un acord sobre la tècnica a emprar i sol·licitar el
consentiment informat - SCARTD by Gemma Sanza Porcar
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Compare [close] - English
- Medical: Health Care
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- The process of obtaining a patient's permission for a procedure after the patient and doctor have discussed the risks, benefits, and alternatives of the procedure and the patient understands them. US Food and Drug Administration
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- As long as the patient is mentally and physically able to make his or her own decisions, medical care cannot begin unless the patient gives informed consent. - American Cancer Society
- Prior to surgery, your child's physician will give you a careful explanation of what procedure will be performed and the risks involved. You will be asked to sign an informed consent form which states in detail that you understand the risks and benefits of your child's surgery. - Morgan Stanley Children's Hospital of New York
- To give informed consent to all procedures and treatment to be rendered, and to have questions answered; and to refuse and/or to discontinue procedures and treatment and to be informed of the consequences of such a decision. - Washington Adventist Hospital
Compare [close] Compare [close] - Dutch
- Medical: Health Care
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- geïnformeerde toestemming
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- Goede voorlichting houdt o.a. in dat patiënten worden geïnformeerd over de mogelijke nadelen van bepaalde ingrepen, eventuele alternatieven, te verwachten resultaten, enz. Ze moeten op grond van juiste informatie kunnen kiezen of ze een onderzoek of behandeling willen ondergaan. Dat heet “geïnformeerde toestemming” of “informed consent”. Test-Aankoop - by Katrien De Clercq
- Example sentence(s)
- Tijdens het vooronderzoek zal men u vragen een formulier van “geïnformeerde toestemming” te ondertekenen. Wanneer u tekent, bevestigt u dat u de nodige informatie heeft ontvangen, dat u ze heeft begrepen en dat u uit vrije wil aan de studie wenst deel te nemen. Ook de persoon die de studie toelicht, ondertekent dit document. De geïnformeerde toestemming is geen bindend contract. U bent op elk moment vrij om uit de studie te stappen.
- SGS by Katrien De Clercq
- Een geïnformeerde toestemming betekent dat u toestemt deel te nemen aan een klinisch onderzoek nadat u schriftelijk en mondeling bent geïnformeerd door een arts en/of studieverpleegkundige over de klinische studie. - Amgen by Katrien De Clercq
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