Informed consent: what is it? Who can give it? How do we improve it?
The freedom to choose is integral to our daily lives, directs our interactions with patients, and is a key component of our conduct of human-subjects research. Most of the historical errors and atrocities in human experimentation had at their core a failure of consent. In response to those events, n...
| Published in: | Respiratory Care Vol. 53; no. 10; pp. 1337 - 1342 |
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| Format: | tables/charts Journal Article |
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Mary Ann Liebert, Inc.
Oct2008
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| Online Access: | View this record in EBSCOhost |
| fields | @attributes: recordID: 1 pdfLink: plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=105568231&site=ehost-live header: @attributes: shortDbName: ccm uiTerm: 105568231 longDbName: CINAHL Complete uiTag: AN controlInfo: bkinfo: dissinfo: jinfo: jid: 00201324 4GG jtl: Respiratory Care issn: 00201324 maglogo: N pubinfo: dt: Oct2008 vid: 53 iid: 10 pid: 1365 pub: Mary Ann Liebert, Inc. place: New Rochelle, New York artinfo: ui: 105568231 105568231 2010090607 NLM18811997 105568231 ppf: 1337 ppct: 5 formats: fmt: @attributes: type: P tig: atl: Informed consent: what is it? Who can give it? How do we improve it? aug: au: Neff MJ affil: Division of Pulmonary and Critical Care Medicine, Department of Medicine, University of Washington, Seattle, Washington sug: subj: Consent (Research) Research Subjects Consent Classification Durable Power of Attorney Government Regulations United States Institutional Review United States ab: The freedom to choose is integral to our daily lives, directs our interactions with patients, and is a key component of our conduct of human-subjects research. Most of the historical errors and atrocities in human experimentation had at their core a failure of consent. In response to those events, national and international law developed to direct researchers to a process of informed consent to participate in research. The application of this process, though, can be challenging. What does this process look like? does it require written documentation, and if so what type? Who can give informed consent? Though researchers worldwide would agree on the concept of informed consent, the nuts and bolts of applying this ideal can create obstacles to researchers, confusion to subjects, and increasing regulations that may or may not help achieve the goal. I will review the current regulatory guidelines, summarize the types of consent, and consider options for improving the informed-consent process. pubtype: Academic Journal doctype: tables/charts Journal Article ougenre: Article language: English refInfo: holdings: @attributes: islocal: N |
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