Knowing Patients

Jeannette Pols

Science Technology & Human Values · 2013 · 236 citations · 55 references

Concepts

TL;DR

Science and technology studies examine how lay influence shapes science, often focusing on political or epistemological effects, while the category of experiential knowledge remains vague and is sometimes equated with expert patient knowledge. The study aims to articulate how patients generate and use knowledge in daily life and to determine how that knowledge can be transferred into scientific discourse. It proposes two approaches—ethnographic studies of patients’ knowledge practices and systematic collection of patient-generated techniques—to convert patient knowledge into science. A case study of severe lung disease patients demonstrates that patient knowledge functions as practical knowledge translating medical information into daily life, combining homegrown know-how and peer advice, and producing techniques that can be shared with others.

Abstract

Science and technology studies concerned with the study of lay influence on the sciences usually analyze either the political or the normative epistemological consequences of lay interference. Here I frame the relation between patients, knowledge, and the sciences by opening up the question: How can we articulate the knowledge that patients develop and use in their daily lives (patient knowledge) and make it transferable and useful to others, or, `turn it into science’? Elsewhere, patient knowledge is analyzed either as essentially different from or similar to medical knowledge. The category of experiential knowledge is vague and is used to encompass many types of experience, whereas the knowledge of the `expert patient’ may be assumed to have the shape of up-to-date medical information. This paper shows through a case study of people with severe lung disease that patient knowledge can be understood as a form of practical knowledge that patients use to translate medical and technical knowledge into something useful to their daily life with disease. Patients coordinate this with homegrown know-how and advice from fellow patients, weighing different values - of which `taking good care of one’s body’ is but one - that may conflict in a specific situation. These practices result in sets of techniques that may be made useful to others. The paper argues for two alternatives to state-of-the-art medical research to turn patient knowledge into science: ethnographies of knowledge practices (how patients know) and the collection and making accessible of techniques (what patients know).

References

55