AIM To ascertain the impact of routine application of the informed consent form at the primary dental care units of the Galician Health Service. STUDY DESIGN Non random selection of consecutive patients seeking tooth extraction between 9 January and 7 March 2007 at the dental care units of Burela, Praza do Ferrol and Viveiro (Lugo). The study included sociodemographic, clinical, utilization, ...

Consenting to participate in a clinical research study after being properly and correctly informed upholds the basic ethical principle of "autonomy" in human research. The informed consent is a process by which the physician sensitizes the patient about the nature, procedures, risks benefits, treatment schedules, etc of the study in a language that is non-technical and understandable by the stu...

The notion of patient’s consent plays a major role in granting access to medical data. In typical healthcare systems, consent is captured by a form that the patient has to fill in and sign. In e-Health systems, the paper-form consent is being replaced by access control mechanisms that regulate access to medical data while taking into account electronic content. This helps in empowering the pati...

Informed consent is a communication process of providing the patient/parents/guardians with relevant information regarding the treatment and the diagnosis, so that they can make informed decisions. The process of informed consent in pediatric patients is not well understood. The amount of information to be disclosed in an informed consent is a matter of debate. There are four basic elements to ...

Informed consent is the cornerstone of human research subject protection. Many subjects sign consent documents without understanding the study purpose, procedures, risks, benefits, and their rights. Proof of comprehension is not required and rarely obtained. Understanding might improve by using an interactive system with multiple options for hearing, viewing and reading about the study and the ...

Paediatric haematology, oncology and bone marrow transplant (BMT) patients frequently require transfusion of blood products. Our institution required a new transfusion consent be obtained every admission. The objectives of this project were to: revise inpatient blood products consent form to be valid for 1 year, decrease provider time spent consenting from 15 to <5 min per admission, and improv...

Improving the informed consent process in clinical research is of constant concern to regulatory authorities in the field and presents a challenge for both the specialists and patients involved. Informed consent is a process that should adequately match the complexity of clinical research. In analyzing the behaviour of 68 patients during the informed consent process related to the clinical rese...

The particular characteristics associated with qualitative longitudinal research in the disciplines of psychology and social science have prompted the development of informed consent. There are analogies between these characteristics and the collection and analysis of data in online settings. How and why informed consent has developed in qualitative longitudinal research, both theoretically and...

Abstract Consent expresses a voluntary decision, taken after disclosure of information, to accept treatment considering risks, benefits, and possible consequences. This study analyzed the role consent forms in decisions by São Paulo State Court Justice. Bibliographic search was conducted using keywords “consent form” “medical error.” The 65 rulings identified were Excel. Of 15 cases which patie...