Key result
QT-prolonging medications are used in ~76% of predialysis CKD visits and linked to QTc prolongation.
Why the study?
Several drugs used in predialysis CKD can prolong electrocardiographic conduction, but their association with QT duration was not well characterized.
Are QT-prolonging medications associated with increased QT duration in patients with predialysis CKD?
Observational (n=16,451)
Are QT-prolonging medications associated with increased QT duration in patients with predialysis CKD?
The use of QT-prolonging medications is highly prevalent in predialysis CKD patients and is associated with significant QTc prolongation, highlighting potential safety concerns in this high-risk population.
BACKGROUND AND OBJECTIVES: Several drugs used in CKD can prolong electrocardiographic conduction. We examined the use of electrocardiogram QT-prolonging medications in predialysis CKD and their association with QT duration. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: =16,451 visits) along with diuretics and proton pump inhibitors, given their potential for electrolyte disturbances, were examined for QT interval prolongation. RESULTS: Mean QT interval corrected for heart rate was at 414±21 (±SD) milliseconds and prolonged (≥450 milliseconds) in 4.6% of electrocardiograms. QT interval corrected for heart rate was inversely related to serum potassium and calcium. Medications classified as QT prolonging were taken at 76% of visits, with two or more of these taken at 33% of visits. Of 30 medications examined, eight were associated with statistically significant QT interval corrected for heart rate prolongation after adjustment for comorbidities, potassium, and calcium, including amiodarone (+10±2 milliseconds), metolazone (+7±2 milliseconds), fluoxetine (+4±1 milliseconds), citalopram (+4±1 milliseconds), hydroxyzine (+4±1 milliseconds), escitalopram (+3±2 milliseconds), venlafaxine (+3±1 milliseconds), and furosemide (+3±0 milliseconds). Potassium-depleting diuretics were associated with minimal decrements in potassium (between 0.1 and 0.3 mEq/L) and smaller changes in calcium. Diuretics associated with a change in QT interval corrected for heart rate before adjustment for potassium and calcium were metolazone (+8±3 milliseconds), furosemide (+4±1 milliseconds), and spironolactone (-3±3 milliseconds). Most of the QT prolongation associated with metolazone and furosemide, but not spironolactone, remained after adjustment for potassium and calcium. Proton pump inhibitors were not associated with QT prolongation. CONCLUSIONS: Use of medications associated with QT prolongation is common in CKD; the safety implications of these findings should be considered in these high-risk patients. PODCAST: This article contains a podcast at https://www.asn-online.org/media/podcast/CJASN/2017_08_09_CJASNPodcast_17_09_b.mp3.
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Snitker et al. (2017) conducted an observational in Predialysis chronic kidney disease (CKD) (n=16,451). QT-prolonging medications vs. Non-use of specific QT-prolonging medications was evaluated on QT interval corrected for heart rate (QTc) prolongation. In patients with predialysis CKD, QT-prolonging medications were taken at 76% of visits, with 8 medications including amiodarone significantly associated with QTc prolongation.
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