Abstract
BackgroundMedication decision-making poses a challenge for a significant proportion of patients. This is an even more challenging for patients who have complex, rare, immune conditions that affect them at a young age and are associated with the use of life-long treatment, perceived by some as having significant risk of side effects and toxicity.IntroductionThe aim of our study was to examine the perspectives of women with lupus nephritis on facilitators to medication decision-making.MethodsWe used the nominal group technique (NGT), a structured formative process to elicit patient perspectives. An NGT expert moderated eight patient group meetings. Participants (n = 52) responded to the question “What sorts of things make it easier for people to decide to take the medicines that doctors prescribe for treating their lupus kidney disease?” Patients nominated, discussed, and prioritized facilitators to medication decisional processes.ResultsFifty-two women with lupus nephritis participated in eight NGT meetings (27 African-American, 13 Hispanic, and 12 Caucasian). Average age was 40.6 years (standard deviation (SD) = 13.3), and disease duration was 11.8 years (SD = 8.3); 36.5 % obtained at least a college education, and 55.8 % had difficulty in reading health materials. Patients generated 280 decision-making facilitators (range of 26 to 42 per panel). Of these, 102 (36 %) facilitators were perceived by patients as having relatively more influence in decision-making processes than others. Prioritized facilitators included effective patient-physician communication regarding benefits/harms, patient desire to live a normal life and improve quality of life, concern for their dependents, experiencing benefits and few/infrequent/no harms with lupus medications, and their affordability. Relative to African-Americans, Caucasian and Hispanic patients endorsed a smaller percentage of facilitators as influential. Level of agreement with which patients within panels independently agreed in their selections of the three most influential facilitators ranged from 33 % to 60 %.ConclusionsWe identified facilitators to lupus medication decision-making. This information will be used to populate a decision aid for lupus nephritis.Electronic supplementary materialThe online version of this article (doi:10.1186/s13075-015-0883-z) contains supplementary material, which is available to authorized users.
Highlights
The aim of our study was to examine the perspectives of women with lupus nephritis on facilitators to medication decision-making
Fifty-two women with lupus nephritis participated in eight nominal group technique (NGT) meetings (27 African-American, 13 Hispanic, and 12 Caucasian)
Relative to African-Americans, Caucasian and Hispanic patients endorsed a smaller percentage of facilitators as influential
Summary
The aim of our study was to examine the perspectives of women with lupus nephritis on facilitators to medication decision-making. It is not known what factors help patients in making a decision to start taking their lupus medications. This is a large gap in the literature. Our research was guided by a single question aimed at identifying factors that facilitated decisional processes involving medications for treating lupus nephritis: “What sorts of things make it easier for people to decide to take the medicines that doctors prescribe for treating their lupus kidney disease?”
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