Background
Guideline-recommended hyperkalemia management includes dietary potassium (K+) restriction, bicarbonate correction, diuretics, and K+ binders with dose reduction of renin-angiotensin-aldosterone system inhibitors as a last resort. The extent to which these recommendations are implemented is uncertain as real-world data on hyperkalaemia management are limited. The Tracking Treatment Pathways in Adult Patients With Hyperkalemia (TRACK) study is a multinational, prospective, longitudinal study that is being conducted to address this knowledge gap. We report the design and baseline cohort characteristics of this real-world study of hyperkalaemia management decision-making.
Methods
This study enrolled participants within 21 days of an episode of hyperkalaemia in 4 European countries (United Kingdom, Spain, Germany, Italy) and the United States. During 12-month follow up, data collected will include participant and healthcare provider characteristics (specialty and practice setting), hyperkalaemia treatment objectives and strategies, rationale for management decisions and indicators of response, and patient-reported perceptions of their hyperkalaemia treatment.
Results
The enrolled cohort includes 1330 participants, mean age 68 years, of whom 31% were women. At baseline, 6% reported heart failure, 55% chronic kidney disease, 29% both and 9% neither. Most participants (57%) were taking an angiotensin converting enzyme inhibitor, angiotensin receptor blocker or angiotensin receptor/neprilysin inhibitor at baseline. Mineralocorticoid receptor antagonist use was lower (14%).
Conclusions
The prospective TRACK study will shed light on practitioners’ hyperkalaemia management decision-making and assess the impact of their decisions on hyperkalaemia recurrence. Understanding practitioners’ underlying thought processes will facilitate efforts to improve hyperkalaemia management.
Clinicaltrials.gov NCT05408039