Management of Hyperkalemia in a Patient with Improving Hyponatremia
Start Lokelma (sodium zirconium cyclosilicate) 10g three times daily for 48 hours, then transition to 5-10g once daily for maintenance, while closely monitoring both potassium and sodium levels within 24-48 hours and again at 7 days. 1
Immediate Assessment Priorities
Your patient's potassium of 5.9 mEq/L represents moderate hyperkalemia that requires prompt treatment, but this is not an emergency requiring acute interventions like calcium or insulin unless ECG changes are present 1. Before initiating Lokelma:
- Obtain an ECG immediately to assess for peaked T waves, flattened P waves, prolonged PR interval, or widened QRS complexes—these findings would escalate urgency regardless of the absolute potassium value 1
- Verify this is not pseudohyperkalemia from hemolysis, repeated fist clenching, or poor phlebotomy technique by repeating the measurement with proper technique 1
- Check renal function (eGFR) and assess urine output to determine if the patient has adequate kidney function for potassium excretion 1
Critical Consideration: Sodium Status
Your patient's sodium improved from 125 to 130 mEq/L, which is appropriate correction (not exceeding 8-10 mEq/L per 24 hours to avoid osmotic demyelination). However, sodium is still low at 130 mEq/L 1. This creates a unique challenge:
- Lokelma exchanges sodium for potassium in the GI tract, meaning it will deliver additional sodium to the patient 2, 3
- In your patient with recent severe hyponatremia, this sodium load could theoretically cause overly rapid correction if given at high doses
- Monitor sodium levels closely (within 24-48 hours) after starting Lokelma to ensure correction doesn't exceed safe rates 1
Lokelma Dosing Protocol
For acute correction (K+ 5.9 mEq/L):
- Start with 10g three times daily for 48 hours to rapidly lower potassium into the normal range (3.5-5.0 mEq/L) 1, 3
- This regimen achieves normokalaemia in 84% of patients within 24 hours and 98% within 48 hours 3
- Median time to normalization is 2.2 hours 3
For maintenance therapy:
- Transition to 5-10g once daily after achieving normokalaemia 1, 3
- The 5g dose maintains normokalaemia in 80% of patients, while 10g maintains it in 90% 3
- Titrate based on potassium levels checked at 7-10 days, then monthly for 3 months, then every 6 months 1
Medication Review and Adjustments
Identify and address contributing medications:
- Review for RAAS inhibitors (ACE inhibitors, ARBs, mineralocorticoid antagonists)—do NOT discontinue these life-saving medications at K+ 5.9 mEq/L; instead, use Lokelma to maintain them 1
- Eliminate or reduce: NSAIDs, trimethoprim, heparin, beta-blockers, potassium supplements, salt substitutes 1
- Optimize diuretic therapy with loop or thiazide diuretics (furosemide 40-80 mg daily) if adequate renal function present 1
Monitoring Protocol
Critical timepoints:
- 24-48 hours: Recheck potassium AND sodium to assess response and ensure sodium isn't correcting too rapidly 1, 3
- 7-10 days: Recheck potassium, sodium, and renal function after transitioning to maintenance dosing 1
- Monthly for 3 months, then every 6 months thereafter 1
Watch for hypokalemia: The 10g dose carries a 10% risk of hypokalemia, which may be even more dangerous than hyperkalemia 3, 1
Special Considerations for Your Patient
Advantages of Lokelma in this scenario:
- Rapid onset of action (~1 hour) makes it ideal for moderate hyperkalemia 1
- Effective across all CKD stages, including patients with eGFR <30 mL/min/1.73 m² 4
- Well-tolerated with low rates of serious adverse effects 2, 3
- Allows continuation of RAAS inhibitors if patient is on them for cardio/renoprotection 1, 5
Potential concern with sodium delivery:
- Edema is more common at higher doses (14% at 15g dose vs 2% at placebo) 3
- Given your patient's recent hyponatremia, monitor for signs of volume overload
- The sodium load from Lokelma is generally well-tolerated but requires monitoring in your specific case 2
Common Pitfalls to Avoid
- Don't use sodium bicarbonate unless metabolic acidosis is present (pH <7.35, bicarbonate <22 mEq/L)—it's not indicated for hyperkalemia alone 1
- Don't discontinue RAAS inhibitors at K+ 5.9 mEq/L—only consider temporary reduction if K+ >6.5 mEq/L 1
- Don't rely solely on dietary restriction—it's insufficient for managing K+ 5.9 mEq/L 1
- Don't forget to monitor sodium closely given your patient's recent severe hyponatremia 1
- Don't use older agents like sodium polystyrene sulfonate (Kayexalate)—it has delayed onset, limited efficacy, and risk of bowel necrosis 1