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Graduate Studies

Seeing Biomedically: the Routine Grounds of Translation in Patient Oriented Research

Abstract

dc:description.abstract

In this dissertation, I show how two doctors perpetuate social divisions and reproduce biomedicine as an institution of social control when taking a patient oriented approach to translational research. The two doctors collected data directly from patients and privileged patients’ personal experience of disease. One doctor presented the patient’s authentic voice of experience at an international medical conference. The doctors considered themselves dedicated to normalizing patients and preventing the difficulties and challenges of social exclusion. Yet, an ethnomethodological analysis of transcripts of conversations between the two doctors and between one of the doctors and a patient reveal that the two doctors normalize and marginalize patients they recognize as “disease damaged”, concealing patients’ lived experiences of social inequality. The doctors’ research protocol encourages and facilitates collaboration between patients, their attending doctors and the research team. A patient, who was a practicing physician before she had the disease, is the Principal Investigator’s Research Assistant. The Principal Investigator treats his Research Assistant as an expert patient and as a physician colleague. The PI takes a patient oriented approach when collecting and analyzing the patient’s descriptions of her disease experience. The patient speaks for herself as the voice of experience at an international medical conference. A close analysis of the transcripts reveals, however, that given their accountabilities as translational researchers to the scientific community, the doctors exclude permanent disease damage as a researchable topic. The doctors sympathetically acknowledge the consequences of disease damage, express empathy toward, patients they regard as a “disease-damaged”. Yet, by viewing these patients’ experiences through the translational research lens, they also produce social inequality. Patient oriented translational research reproduces cultural knowledge about biomedicine as an institution of social control and perpetuates social divisions.

Degree

thesis:*
Name thesis:degree_name
Doctor of Philosophy (PhD)
Discipline thesis:degree_discipline
Educational Research
Grantor dc:publisher.institution
Graduate Studies
Year dc:date.issued
2014

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Harasym, Patricia Marie
Advisors dc:contributor.advisor
  • Heyman, Richard David
  • Schneider, Barbara

Subjects

dc:subject × 1

Rights

dc:rights
Statement dc:rights
  • University of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.
Language dc:language.iso
eng

Identifiers

dc:identifier.*
OAI identifier oai:identifier
oai:ucalgary.scholaris.ca:11023/1248

Chain of custody

source
Harvested from
University of Calgary
Base URL
ucalgary.scholaris.ca/server/oai/request
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Harasym, Patricia Marie. Seeing Biomedically: the Routine Grounds of Translation in Patient Oriented Research. Graduate Studies, 2014. http://hdl.handle.net/11023/1248