Key result
Extended-release niacin was discontinued by 43.5% of participants by month 13, with 82% of those who discontinued reporting moderate to extreme flushing symptoms.
Why the study?
What is the severity and impact of niacin-induced flushing on treatment satisfaction and discontinuation in patients newly prescribed extended-release niacin?
Observational (n=306)
What is the severity and impact of niacin-induced flushing on treatment satisfaction and discontinuation in patients newly prescribed extended-release niacin?
In a real-world setting, niacin-induced flushing is highly bothersome and significantly impacts treatment continuation, with 43.5% of patients discontinuing therapy by 13 months.
Answers are grounded in this paper and cite their sources.
High discontinuation from flushing may limit extended-release niacin use; leaves open need for mitigation strategies in future studies.
BACKGROUND: Niacin has lipid-modifying efficacy and cardiovascular benefit, but is underutilised because of niacin-induced flushing (NIF). This real-world, prospective, observational study characterised the severity and impact of NIF symptoms among participants who were newly prescribed extended-release (ER) niacin. METHODS: Participants were surveyed daily during week 1 of therapy, at weeks 5, 9, 13, and at months 7, 10 and 13. Surveys included the Flushing Symptom Questionnaire (FSQ), which includes the Global Flushing Severity Score (GFSS) question, the Flushing Impact Questionnaire (FIQ) and the Treatment Satisfaction Questionnaire for Medication (TSQM). RESULTS: Overall, 306 participants were enrolled. During week 1, 30.0% of participants reported a maximum GFSS ≥ 4 (moderate or greater). Mean FIQ domain scores increased with increasing flushing severity, primarily driven by the Irritation/Frustration domain. By week 13, only 2.5% of participants had attained a 2 g ER niacin dose. By month 13, 43.5% (n = 133) had discontinued ER niacin. At discontinuation, only 3.1% of participants had attained the 2 g dose. Over half of the participants who discontinued experienced flushing symptoms: 82% reported moderate to extreme flushing (GFSS ≥ 4), and 68% reported severe to extreme flushing (GFSS ≥ 7). Participants who discontinued and had flushing side effects reported high degrees of impact in the FIQ Irritation/Frustration domain, and high dissatisfaction as a result of side effects, as measured by the TSQM. CONCLUSION: In a real-world setting, NIF side effects were bothersome and had an impact on the continuation of therapy.
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Rhodes et al. (2013) conducted an observational in Newly prescribed extended-release niacin (n=306). Extended-release (ER) niacin was evaluated on Discontinuation of ER niacin by month 13. Extended-release niacin was discontinued by 43.5% of participants by month 13, with 82% of those who discontinued reporting moderate to extreme flushing symptoms.
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