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Roger Clarke

Publications and source records attributed to Roger Clarke.

8 recordsLinked to original sources
PubMed2005

21st century challenges in radiation protection and shielding: draft 2005 recommendations of ICRP.

The International Commission on Radiological Protection regularly examines the status of its recommendations and reviews the increasing knowledge of the effects of exposure to ionising radiation in order to decide whether new recommendations are needed. The Commission strives to make its system more coherent and comprehensible, while recognising the need for stability in international and national regulations, many of which have, only fairly recently, implemented the 1990 Recommendations. However, new scientific data have been produced since 1990 and there have been societal developments in that more openness or transparency is expected in developing new recommendations and, in addition, there has been a move from the utilitarian approach of 'the greatest good for the greatest number', to one with more concern for the 'individual', all of which have inevitably led to some changes in the formulation of the recommendations. This paper outlines the proposals for the 2005 Recommendations.

Guidelines as Topic↗
PubMed2005

A history of the international commission on radiological protection.

Within twelve months of the discovery of x rays, papers appeared in the literature reporting adverse effects from high exposure. By the time of the First World War, several countries were proposing restrictions for the exposure of radiation workers. In 1925, the first International Congress of Radiology, held in London, considered the need for a protection committee, which it established at its second Congress in Stockholm in 1928. This paper traces the history of the development, by ICRP, of its policies and the personalities involved in their development from its inception up to the modern era. The paper follows the progress from the early controls on worker doses to avoid deterministic effects, through the identification of stochastic effects to the concerns about increasing public exposure. The key features of the Recommendations made by ICRP from 1928 up to the current 1990 version are identified.

Animals↗
PubMed2005

A history of the international commission on radiological protection.

Within twelve months of the discovery of x rays, papers appeared in the literature reporting adverse effects from high exposure. By the time of the First World War, several countries were proposing restrictions for the exposure of radiation workers. In 1925, the first International Congress of Radiology, held in London, considered the need for a protection committee, which it established at its second Congress in Stockholm in 1928. This paper traces the history of the development, by ICRP, of its policies and the personalities involved in their development from its inception up to the modern era. The paper follows the progress from the early controls on worker doses to avoid deterministic effects, through the identification of stochastic effects to the concerns about increasing public exposure. The key features of the Recommendations made by ICRP from 1928 up to the current 1990 version are identified.

Animals↗
PubMed2003

e-Consent: The design and implementation of consumer consent mechanisms in an electronic environment.

The effective coordination of health care relies on communication of confidential information about consumers between different health and community care services. However, consumers must be able to give or withhold "e-Consent" to those who wish to access their electronic health information. There are several possible forms for e-Consent. In the general consent model, a patient provides blanket consent for access to his or her information by an organization for all future information requests. Conversely, general denial explicitly denies consent for information to be used in future circumstances, and in each new episode of care, a new consent would be needed to obtain information. In the general consent with specific denial model, a patient attaches specific exclusion conditions to his or her general approval to future accesses. In contrast, in the general denial with explicit consent model, a patient issues a blanket block on all future accesses but allows the inclusion of future use under specified conditions. There also are several alternative functions for an e-Consent system. Consent could be captured as a matter of legal record. E-Consent systems could be more active by prompting clinicians to indicate that they have noted consent conditions before they access a record. Finally, the record of patient consent could be fully active and used as a gatekeeper in a distributed information environment. There probably will need to be some form of data object that is associated with patient information. This e-Consent object (or e-Co) will contain the specific conditions under which the data to which it is attached can be retrieved. Given the complexity of clinical work and the substantial variation we can expect in an individual's desire to make his or her personal medical details available, it is unlikely a "one size fits all" approach to e-Consent will work. Consequently, with a well-chosen consent design, it should be possible to balance the specific need for privacy of some of the population against the desire by others to err on the side of clinical safety, and clinicians desire to minimize the burden that an electronic consent mechanism would impose.

Access to Information↗