• Center on Health Equity and Access
  • Clinical
  • Health Care Cost
  • Health Care Delivery
  • Insurance
  • Policy
  • Technology
  • Value-Based Care

The Burden of Hyperkalemia in Patients With Cardiovascular and Renal Disease

Publication
Article
Supplements and Featured PublicationsThe Burden of Hyperkalemia in Patients With Cardiovascular and Renal Disease
Volume 21
Issue 15 Suppl

Hyperkalemia is a potentially serious condition that can result in life-threatening cardiac arrhythmias and is associated with an increased mortality risk. Patients older than 65 years who have an advanced stage of chronic kidney disease (stage 3 or higher), diabetes, and/or chronic heart failure are at higher risk for hyperkalemia. To reduce disease progression and improve outcomes in these groups of patients, modulation of the renin-angiotensinaldosterone system (RAAS) is recommended by guidelines. One limiting factor of RAAS inhibitors at proven doses is the increased risk for hyperkalemia associated with their use. Although there are effective therapeutic options for the short-term, acute management of hyperkalemia, the available strategies for chronic control of high potassium levels have limited effectiveness. The management of high potassium in the long term often requires withdrawing or reducing the doses of drugs proven to reduce cardiovascular and renal outcomes (eg, RAAS inhibitors) or implementing excessive and often intolerable dietary restrictions. Furthermore, withholding RAAS inhibitors may lead to incremental healthcare costs associated with poor outcomes, such as end-stage renal disease, hospitalizations due to cardiovascular causes, and cardiovascular mortality. As such, there is an important unmet need for novel therapeutic options for the chronic management of patients at risk for hyperkalemia. Potential therapies in development may change the treatment landscape in the near future.

Am J Manag Care. 2015;21:S307-S315

For author information and disclosures, see end of text.

Hyperkalemia: Mechanisms, Patient Populations at Risk, and Prevalence

Potassium is an essential dietary mineral that is the main intracellular cation required for the maintenance of cell membrane potential, ion and solute transport, and the regulation of cell volume. Hyperkalemia is a potentially life-threatening condition that is defined as a serum potassium level above a reference range, usually greater than 5.0 mEq/L; severe hyperkalemia is often defined as a level greater than 6.0 mEq/L.1 Elevation of plasma potassium concentration decreases the ratio of intracellular to extracellular potassium, leading to partial depolarization of the cell membrane. These physiologic effects of hyperkalemia can result in muscle weakness, paralysis, life-threatening effects on cardiac conduction (eg, QRS widening), arrhythmias such as ventricular fibrillation, and sudden death.2,3

Hyperkalemia can be caused by an abnormal net release of potassium from cells, often due to trauma, metabolic acidosis, hemolytic states, or other cell degradations, usually in the setting of suboptimal kidney function. If not treated rapidly, the mortality rate for patients with severe hyperkalemia can be over 30%.4 Hyperkalemia may also result from impaired distribution between the intracellular and extracellular spaces due to other causes, as well as increased potassium intake, reduced renal excretion, or a combination of several of these factors.5

Those at greatest risk for hyperkalemia are persons older than 65 years who have an advanced stage of chronic kidney disease (CKD) (ie, stage 3-5), chronic heart failure (CHF), and/or diabetes and/or are taking medications known to increase serum potassium levels, notably inhibitors of the renin-angiotensin-aldosterone system (RAAS).1,5-9 In patients with diabetes, the presence of a constellation of multiple risk factors that interfere with potassium excretion—including hyporeninemic hypoaldosteronism, and renal tubular acidosis type IV—explains why the incidence of hyperkalemia is higher than in the general population.10

CKD is the most common risk factor for hyperkalemia due to the intrinsic pathophysiological effects of kidney dysfunction on potassium homeostasis and the superimposing cluster of cardiometabolic comorbidities—and their associated treatments—that frequently are present in patients with CKD.5 As the number and severity of comorbidities increase and further decline in renal function ensues, the prevalence of hyperkalemia and the number of recurrent episodes increases.

Although the incidence and prevalence of hyperkalemia in the general population is unknown, some studies in hospitalized patients have reported incidence rates between 1 and 10 per 100 patients.11 In a Canadian retrospective population-based study, 2.6% of patients 66 years and older who presented to the emergency department were hyperkalemic, defined as a serum potassium level greater than 5.5mEq/L.12 Some retrospective US analyses have reported incidences between 2.5% and 3.2% in populations with diverse risk factors.9,13 Among those risk factors, the presence of CKD is significantly associated with higher frequencies of hyperkalemia, depending on the studied population and on the definition of hyperkalemia.9

Among the medications that can cause hyperkalemia, the most relevant in clinical practice are RAAS inhibitors because while they have been shown to confer mortality and morbidity benefits in patients with CKD, diabetes, and cardiovascular disease (CVD),14-17 the development of hyperkalemia frequently hinders their utilization at optimal doses for chronic cardiorenal protection.18 The interaction between the presence of CKD and the administration of RAAS inhibitors is highlighted by data from clinical trials showing how the incidence of hyperkalemia associated with RAAS inhibitors increases from less than 2% in patients without CKD to between 5% and 10% with dual inhibition of the RAAS in patients with CKD.19

Because randomized clinical trials typically exclude individuals with advanced cardiorenal comorbidities and the patients included in these trials are carefully monitored, reports from randomized clinical trials may underestimate the true burden of hyperkalemia, which is probably much higher in routine clinical practice. For instance, a study at a Veterans Administration clinic revealed that 11% of outpatients prescribed angiotensinconverting enzyme (ACE) inhibitors developed hyperkalemia over the 2-year study period.20 In addition, whereas the Randomized Aldactone Evaluation (RALES) study17 in patients with heart failure (HF) and serum creatinine less than 2.5 mg/dL reported only a 2% rate of hyperkalemia, subsequent analyses in unselected patients treated with ACE inhibitors who had recently been hospitalized for HF showed a significant increase in hyperkalemiarelated hospitalizations and deaths.21 This correlated with an increase in the prescription rate for spironolactone used in addition to ACE inhibitors following the publication of the RALES study.21 Bozkurt et al documented that 24% of patients with HF treated with spironolactone in clinical practice developed a serum potassium level greater than 5.2 mEq/L; of these, 12% had a serum potassium level greater than 6.0 mEq/L.22 Shah et al reported that hyperkalemia developed in 35% of patients with HF also treated with spironolactone and who had a baseline creatinine of 1.5 mg/dL or greater; and in 63% with a baseline creatinine of 2.5 mg/dL or greater, punctuating the clear trend toward increased hyperkalemia risk with declining kidney function.23

Consequences of Hyperkalemia

Hyperkalemia is often a silent condition that goes undetected until a patient exhibits serious consequences, such as ventricular arrhythmias, or may be detected incidentally upon laboratory testing. In patients with cardiorenal comorbidities, the risk for developing hyperkalemia is an ongoing concern. Hyperkalemia is associated with both clinical and economic consequences, including increased emergency department (ED) visits, hospitalizations, and mortality. These have a direct bearing on the overall cost of managing patients, especially in a managed care setting.

In 2011, approximately 67,000 visits to the ED were a direct result of elevated potassium levels.24 Of patients who visited the ED, 50% were admitted to the hospital, with an average length of stay of 3.2 days and mean inhospital charges of $24,178 per stay. A total of 84% of individuals hospitalized were older than 45 years. Thus, persons older than 45 years who are at risk for hyperkalemia should be monitored closely. The estimated total annual hospital charges for Medicare admissions with hyperkalemia as the primary diagnosis were approximately $697 million (US) in 2011.24

Clinical evidence shows that increases in serum potassium above the normal range are associated with higher mortality rate, especially as an individual ages and in patients with comorbidities (Figure 18).7,8 Other studies have noted that hyperkalemia is one of the greatest risk factors associated with all-cause mortality in patients with pre-existing CVD, advanced CKD,6 patients without CKD,9 and patients undergoing dialysis (Figure 226).25,26 A retrospective analysis of 15,803 patients with CKD and CVD treated with antihypertensive drugs revealed that patients with hyperkalemia had higher rates of hospital admissions and mortality compared with normokalemic patients.6 The association of mortality risk with hyperkalemia was also studied in a retrospective analysis conducted in a large national cohort including more than 240,000 US Veterans with at least 1 hospitalization and at least 1 serum potassium measurement during a year.9 The authors determined the risk of death (odds ratio) within 1 day of a hyperkalemic event in patients with CKD compared with normokalemic non-CKD patients. This study showed that patients with CKD were significantly more likely to experience a hyperkalemic event than those without CKD, but also that hyperkalemia increased the odds of death within 1 day regardless of kidney function. The risk of death correlated incrementally with severity of hyperkalemia (moderate hyperkalemia defined as serum potassium level ≥5.5 mg/dL and <6.0 mg/dL and severe hyperkalemia defined as ≥6.0 mg/dL).9

Current Management of Hyperkalemia

Both acute and chronic treatment strategies are critical for the management of patients at risk of hyperkalemia. The currently available treatment strategies mainly focus on emergency and intermediate care, and limited options are available for chronic management of patients at risk of recurrent hyperkalemia. Interventions for chronic management are limited to reducing or eliminating exacerbating factors, including RAAS inhibitors. Table 13,5,18,19,48,50,51 shows the list of interventions commonly used for the management of hyperkalemia.3,5,19

Acute Management

The options for the acute management of hyperkalemia may be further divided into those that start acting within minutes and are more appropriate for emergency management and those that require a few hours to exert therapeutic effects and are suitable for intermediate or subacute care. Included among the former are nebulized or inhaled beta-2—receptor agonists (eg, albuterol, salbutamol); intravenous insulin-and-glucose, which stimulates intracellular potassium uptake; and calcium gluconate salt for membrane stabilization. The goals of immediate management are to induce potassium transport into the intracellular space and remove potassium from the body to quickly restore the normal electrophysiology of the cell membrane and prevent cardiac arrhythmias.3 Sodium bicarbonate, loop diuretics, dialysis, and the potassium-binding resin sodium polystyrene sulfonate (SPS) have played a role in subacute management of hyperkalemia, with dialysis and loop diuretics also having a role in its chronic management.

Beta-2 Receptor Agonists

Beta-2 receptor agonists lower serum potassium by promoting its redistribution to the intracellular space. The effect of these agents is mediated independently of insulin and aldosterone. Their onset of action is 30 minutes and duration of effect is 2 to 4 hours.19 As is expected by their mechanism of action, these agents do not affect total body potassium levels.19

Insulin-Glucose

A commonly used regimen to acutely treat hyperkalemia is the intravenous administration of 10 units of regular insulin along with 25 g of glucose.27 Insulin works by redistributing potassium into the cells. Despite the concomitant administration of glucose with insulin, hypoglycemia is a recognized complication of this treatment.28 Insulin works within 30 minutes and its effect lasts 4 to 6 hours.19

Calcium Gluconate

Intravenously administered calcium gluconate can begin to stabilize membrane potential in 1 to 3 minutes, as indicated by normalization of electrocardiographic changes. The duration of the effect is 30 to 60 minutes and doses can be repeated if no adverse effects are observed.19 As with several of the other acute treatment options, serum potassium level is unaffected.

Sodium Bicarbonate

The use of intravenous bicarbonate is recommended when metabolic acidosis is the cause of hyperkalemia. The hypokalemic effect of bicarbonate infusion may require many hours of administration (4-6 hours).29 Thus, no immediate reduction in serum potassium levels should be expected. Metabolic alkalosis can develop from the use of higher doses.

Loop Diuretics

Diuretics, especially loop diuretics, are commonly used to prevent a rise in serum potassium and to control volume overload in patients with CKD. In the African American Study of Kidney Disease and Hypertension (AASK), the use of diuretics was associated with a 59% decrease in the risk of hyperkalemia.30 Some diuretics, however, can increase the risk for gout, diabetes, and volume depletion and precipitate a worsening of kidney function; therefore, they may not be ideal agents for lowering serum potassium levels in the long term.

Dialysis

Although hemodialysis is effective in reducing serum potassium levels, ironically, the concentration of potassium in the dialysate can contribute to hyperkalemia. The results of 1 study revealed potassium-free dialysate was 24% more effective than 1-K (ie, 1 mEq/L concentration) dialysate and 50% more effective than 2-K dialysate in removing body potassium; new ectopy was recorded in only 1 patient studied.31 In a large observational study, a pre-dialysis serum potassium level of 4.6 mEq/L to 5.3 mEq/L was associated with the greatest survival in patients undergoing maintenance hemodialysis.25

Sodium Polystyrene Sulfonate

Until recently, SPS was the only drug indicated for the treatment of hyperkalemia. SPS was approved more than 50 years ago, before the modern regulatory standards for demonstrating efficacy were employed. The approval of SPS was based on less stringent evidence from clinical studies that would not likely pass the scrutiny of the US Food and Drug Administration (FDA) today. The drug is typically used in hospitals32,33 and less frequently in the outpatient setting due to issues with tolerability.34 Recently, the FDA requested that the manufacturer of Kayexalate (Concordia, Ontario, Canada) conduct drug—drug interaction studies.35 A small retrospective analysis showed that mean serum potassium concentrations were within the normal range in 94% of patients after a single dose of SPS32; however, a comprehensive data review suggested there was no consistent evidence of efficacy.36 Clinicians must be cognizant of this and other risks associated with SPS therapy. For example, caution is advised for patients who cannot tolerate even a small increase in sodium loads, such as those with severe CHF, severe hypertension, or marked edema. Although sodium should be restricted in these individuals to less than 2000 mg per day, the average daily dose of SPS is 15 to 60 g, with each gram of SPS containing 100 mg of sodium; thus, the patient receives 1.5 to 6.0 g of extra sodium load with daily SPS treatment.37 The results of an analysis of 30 articles detailing 58 adverse events reported with SPS38 showed that 76% involved the colon and that the overall mortality rate for patients with gastrointestinal (GI) injury associated with SPS use was 33%. In 2009, the FDA issued a warning to healthcare practitioners regarding reports of intestinal necrosis, which can be fatal, and other serious GI adverse events such as bleeding, ischemic colitis, and perforation associated with administration of SPS; this report was further refined 2 years later.39 Although rare, cases of necrosis can be associated with death. In the Harel systematic review, 94% of patients who died from GI injury had colonic necrosis on biopsy.38

Chronic Management

Although the short-term, acute management of hyperkalemia is effective and can stabilize serum potassium, these treatments do not address chronic risk. It is important to identify the underlying causes (ancillary factors) that contributed to an acute hyperkalemic event and manage these causes/factors on an ongoing basis, if needed. As previously discussed, several factors increase the likelihood of chronic hyperkalemia, including high potassium intake and the use of RAAS inhibitors and other drugs that cause increases in serum potassium.40-44 However, current options to manage hyperkalemia on a long-term basis are limited and robust data on their efficacy and safety in the outpatient setting are lacking.

Diet

Management of hyperkalemia from a dietary perspective includes reducing potassium intake and discontinuing potassium supplements. It is recommended that those at risk for hyperkalemia avoid or limit the intake of foods that are high in potassium, such as oranges and orange juice, nectarines, kiwis, raisins or other dried fruit, bananas, cantaloupe, honeydew, prunes, and salt substitutes. Patients should be aware that limiting these foods can cause constipation or other GI side effects.45,46 Restricting dietary potassium intake also contradicts healthy dietary recommendations to prevent kidney disease, stroke, and CVD (the so-called DASH [Dietary Approaches to Stop Hypertension] diet); however, this is considered a trade-off that patients need to make to reduce the risks of chronic hyperkalemia.47,48 Discontinuation/Dose-Reduction of RAAS Inhibitors Identification and interruption of hyperkalemia-inducing medications is one of the guideline-recommended strategies for preventing recurrent episodes of elevated serum potassium. Drug-induced hyperkalemia, one of the most frequent causes of hyperkalemia, is triggered either by inhibiting renal potassium excretion or by blocking extrarenal removal. Thus, it is essential that when clinicians reconcile a patient’s medication profile, dosage(s) of drugs needed to treat their disease(s) may need to be reduced or it may be necessary to avoid and/or discontinue any medications associated with hyperkalemia (Table 244,49). This is especially true for RAAS inhibitors. In an observational retrospective study of patients not undergoing dialysis and who had serum potassium of 6.5 mEq/L or greater on admission or during the hospital stay, more than 60% were taking at least one drug known to cause or worsen hyperkalemia.43 Unfortunately, these therapies may be discontinued in patients who would most benefit from these medications. In a study of 279 patients with CKD, hyperkalemia was the most common reason (66.6%) why clinicians discontinued RAAS inhibitors and was the reason for not starting RAAS inhibitor therapy in 13.8% of individuals.42 In a comprehensive analysis of a large database of electronic medical records from Humedica, Epstein et al observed that after an event of moderate to severe hyperkalemia, almost half of the patients previously on a maximum dose of RAAS inhibitors reduced the dose or discontinued their RAAS inhibitor therapy.18 It is important to point out that in those patients in whom the RAAS inhibitors were discontinued or given at suboptimal dosage, a higher percentage of adverse outcomes or mortality was observed. Mortality was observed twice as frequently in patients who were discontinued from RAAS inhibitors or were receiving a suboptimal dose irrespective of comorbidity status.18

Conclusions

Hyperkalemia is a common and clinically relevant problem in patents with cardiovascular and renal diseases, and although it can be asymptomatic in many cases, it has potentially serious consequences that can lead to significant morbidity and mortality. The treatment paradigm for hyperkalemia has remained without major advances for the past 50 years. Discontinuation of life-saving, evidence-based, recommended medications remains the main strategy to prevent the recurrence of chronic hyperkalemia. This has negative consequences in our healthcare systems as a result of adverse renal and cardiovascular events. As such, there is an important unmet need for novel therapeutic options for the chronic management of patients with, and at risk for, hyperkalemia. The potential availability of new therapies may change the treatment landscape in the near future.

Editor’s Note: In October 2015, after this manuscript was completed, the FDA approved an additional product for the treatment of hyperkalemia. Acknowledgements: Medical writing support was provided by Robert Lamb, PharmD; critical review of the manuscript was provided by Julie Obeid; and editorial support was provided by Eugene Gillespie, PhD.

Author affiliations: Barnabas Health, West Orange, NJ (RTA); Medical Affairs, Relypsa, Inc, Redwood City, CA (WWB); VRx Pharmacy Services, LLC, Salt Lake City, UT (JDD); Medical Content and Strategy, Insyght Interactive, Los Angeles, CA (EO-T).

Funding source: This publication was sponsored by Relypsa, Inc.

Author disclosures: Dr Adamson reports serving as consultant or paid advisory board member for Relypsa, Inc. Dr Benton reports employment and stock ownership with Relypsa, Inc. Dr Dunn reports receipt of honoraria from Relypsa, Inc. Dr Orozco-Torrentera reports employment with Insyght Interactive (Insyght Interactive was paid by Relypsa, Inc for involvement in preparation of manuscript).

Authorship information: Concept and design (RTA, WWB, JDD, EO-T); analysis and interpretation of data (JDD); drafting of the manuscript (RTA, WWB, JDD, EO-T); critical revision of the manuscript for important intellectual content (RTA, WWB, JDD, EO-T); and supervision (EO-T).

Address correspondence to: Jeffrey D. Dunn, PharmD, MBA, VRx Pharmacy Services, LLC, 19 E 200 S, Floor 10, Salt Lake City, UT 84111; jdunn@myvrx.com.

  1. Kidney Disease Outcomes Quality Initiative. K/DOQI clinical practice guidelines on hypertension and antihypertensive agents in chronic kidney disease. Am J Kidney Dis. 2004;43(5 [suppl 1]): S1-S290.
  2. Ahmed J, Weisberg LS. Hyperkalemia in dialysis patients. Semin Dial. 2001;14(5):348-356.
  3. Weisberg LS. Management of severe hyperkalemia. Crit Care Med. 2008;36(12):3246-3251.
  4. An JN, Lee JP, Jeon HJ, et al. Severe hyperkalemia requiring hospitalization: predictors of mortality. Crit Care. 2012; 16(6):R225.
  5. Kovesdy CP. Management of hyperkalemia: an update for the internist [published online June 18, 2015]. Am J Med. doi: 10.1016/j.amjmed.2015.05.040.
  6. Jain N, Kotla S, Little BB, et al. Predictors of hyperkalemia and death in patients with cardiac and renal disease. Am J Cardiol. 2012;109(10):1510-1513.
  7. Pitt B, Collins A, Reaven N, et al. Effect of cardiovascular comorbidities on the mortality risk associated with serum potassium. Poster presented at: American Heart Association 2014 Scientific Sessions; November 15-19, 2014; Chicago, IL.
  8. Hayes J, Kalantar-Zadeh K, Lu JL, Turban S, Anderson JE, Kovesdy CP. Association of hypo- and hyperkalemia with disease progression and mortality in males with chronic kidney disease: the role of race. Nephron Clin Pract. 2012;120(1):c8-c16.
  9. Einhorn LM, Zhan M, Hsu VD, et al. The frequency of hyperkalemia and its significance in chronic kidney disease. Arch Intern Med. 2009;169(12):1156-1162.
  10. Liamis G, Liberopoulos E, Barkas F, Elisaf M. Diabetes mellitus and electrolyte disorders. World J Clin Cases. 2014;2(10): 488-496.
  11. Hollander-Rodriguez JC, Calvert JF Jr. Hyperkalemia. Am Fam Phys. 2006;73(2):283-290.
  12. Fleet JL, Shariff SZ, Gandhi S, Weir MA, Jain AK, Garg AX. Validity of the International Classification of Diseases 10th revision code for hyperkalaemia in elderly patients at presentation to an emergency department and at hospital admission. BMJ Open. 2012;2(6):e002011.
  13. Drawz PE, Babineau DC, Rahman M. Metabolic complications in elderly adults with chronic kidney disease. J Am Geriatr Soc. 2012;60(2):310-315.
  14. Brenner BM, Cooper ME, de Zeeuw D, et al; RENAAL Study Investigators. Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy. N Engl J Med. 2001;345(12):861-869.
  15. Lewis EJ, Hunsicker LG, Clarke WR, et al; Collaborative Study Group. Renoprotective effect of the angiotensin-receptor antagonist irbesartan in patients with nephropathy due to type 2 diabetes. N Engl J Med. 2001;345(12):851-860.
  16. Yusuf S, Sleight P, Pogue J, Bosch J, Davies R, Dagenais G; The Heart Outcomes Prevention Evaluation Study Investigators. Effects of an angiotensin-converting-enzyme inhibitor, ramipril, on cardiovascular events in high-risk patients. N Engl J Med. 2000; 342(3):145-153.
  17. Pitt B, Zannad F, Remme WJ, et al; Randomized Aldactone Evaluation Study Investigators. The effect of spironolactone on morbidity and mortality in patients with severe heart failure. N Engl J Med. 1999;341(10):709-717.
  18. Epstein M, Reaven NL, Funk SE, McGaughey KJ, Oestreicher N, Knispel J. Evaluation of the treatment gap between clinical guidelines and the utilization of renin-angiotensin-aldosterone system inhibitors. Am J Manag Care. 2015;21(suppl 11):S212-S220.
  19. Kovesdy CP. Management of hyperkalaemia in chronic kidney disease. Nat Rev Nephrol. 2014;10(11):653-662.
  20. Reardon LC, Macpherson DS. Hyperkalemia in outpatients using angiotensin-converting enzyme inhibitors. How much should we worry? Arch Intern Med. 1998;158(1):26-32.
  21. Juurlink DN, Mamdani MM, Lee DS, et al. Rates of hyperkalemia after publication of the Randomized Aldactone Evaluation Study. N Engl J Med. 2004;351(6):543-551.
  22. Bozkurt B, Agoston I, Knowlton AA. Complications of inappropriate use of spironolactone in heart failure: when an old medicine spirals out of new guidelines. J Am Coll Cardiol. 2003;41(2):211-214.
  23. Shah KB, Rao K, Sawyer R, Gottlieb SS. The adequacy of laboratory monitoring in patients treated with spironolactone for congestive heart failure. J Am Coll Cardiol. 2005;46(5):845-849.
  24. Healthcare Cost and Utilization Project. http://hcupnet.ahrq.gov/HCUPnet.jsp. Accessed August 5, 2015.
  25. Kovesdy CP, Regidor DL, Mehrotra R, et al. Serum and dialysate potassium concentrations and survival in hemodialysis patients. Clin J Am Soc Nephrol. 2007;2(5):999-1007.
  26. Torlén K, Kalantar-Zadeh K, Molnar MZ, Vashistha T, Mehrotra R. Serum potassium and cause-specific mortality in a large peritoneal dialysis cohort. Clin J Am Soc Nephrol. 2012;7(8):1272-1284.
  27. American Heart Association. Guidelines for cardiopulmonary resuscitation and emergency cardiovascular care. Part 10.1: lifethreatening electrolyte abnormalities. Circulation. 2005;112:IV-121—IV-125.
  28. Apel J, Reutrakul S, Baldwin D. Hypoglycemia in the treatment of hyperkalemia with insulin in patients with end-stage renal disease. Clin Kidney J. 2014;7(3):248-250.
  29. Fraley DS, Adler S. Correction of hyperkalemia by bicarbonate despite constant blood pH. Kidney Int. 1977;12(5):354-360.
  30. Weinberg JM, Appel LJ, Bakris G, et al; African American Study of Hypertension and Kidney Disease Collaborative Research Group. Risk of hyperkalemia in nondiabetic patients with chronic kidney disease receiving antihypertensive therapy. Arch Intern Med. 2009;169(17):1587-1594.
  31. Hou S, McElroy PA, Nootens J, Beach M. Safety and efficacy of low-potassium dialysate. Am J Kidney Dis. 1989;13(2):137-143.
  32. Kessler C, Ng J, Valdez K, Xie H, Geiger B. The use of sodium polystyrene sulfonate in the inpatient management of hyperkalemia. J Hosp Med. 2011;6(3):136-140.
  33. Watson MA, Baker TP, Nguyen A, et al. Association of prescription of oral sodium polystyrene sulfonate with sorbitol in an inpatient setting with colonic necrosis: a retrospective cohort study. Am J Kidney Dis. 2012;60(3):409-416.
  34. Lazich I, Bakris GL. Predication and management of hyperkalemia across the spectrum of kidney disease. Semin Nephrol. 2014;34(3):333-339.
  35. Food and Drug Administration. FDA drug safety communication: FDA requires drug interaction studies with potassium-lowering drug Kayexalate (sodium polystyrene sulfonate). http://www.fda.gov/Drugs/DrugSafety/ucm468035.htm. Published October 22, 2015. Accessed October 23, 2015.
  36. Sterns RH, Rojas M, Bernstein P, Chennupati S. Ion-exchange resins for the treatment of hyperkalemia: are they safe and effective? J Am Soc Nephrol. 2010;21(5):733-735.
  37. Kayexalate [prescribing information]. Bridgewater, NJ: sanofiaventis US LLC; 2010.
  38. Harel Z, Harel S, Shah PS, Wald R, Perl J, Bell CM. Gastrointestinal adverse events with sodium polystyrene sulfonate (Kayexalate) use: a systematic review. Am J Med. 2013;126(3):264, e9-e24.
  39. Food and Drug Administration. Safety: Kayexalate (sodium polystyrene sulfonate) powder. http://www.fda.gov/Safety/MedWatch/SafetyInformation/ucm186845.htm. Published January 2011. Accessed August 12, 2015.
  40. Albert NM, Yancy CW, Liang L, et al. Use of aldosterone antagonists in heart failure. JAMA. 2009;302(15):1658-1665.
  41. Pappoe LS, Winkelmayer WC. ACE inhibitor and angiotensin II type 1 receptor antagonist therapies in elderly patients with diabetes mellitus: are they underutilized? Drugs Aging. 2010;27(2):87-94.
  42. Yildirim T, Arici M, Piskinpasa S, et al. Major barriers against renin-angiotensin-aldosterone system blocker use in chronic kidney disease stages 3-5 in clinical practice: a safety concern? Ren Fail. 2012;34(9):1095-1099.
  43. Noize P, Bagheri H, Durrieu G, et al. Life-threatening drugassociated hyperkalemia: a retrospective study from laboratory signals. Pharmacoepidemiol Drug Saf. 2011;20(7):747-753.
  44. Ben Salem C, Badreddine A, Fathallah N, Slim R, Hmouda H. Drug-induced hyperkalemia. Drug Saf. 2014;37(9):677-692.
  45. Potassium and your CKD diet. National Kidney Foundation website. https://www.kidney.org/atoz/content/potassium. Accessed October 7, 2015.
  46. National Kidney Disease Education Program. Chronic kidney disease (CKD) and diet: assessment, management, and treatment. National Institute of Diabetes and Digestive and Kidney Diseases website. http://www.niddk.nih.gov/health-information/health-communication-programs/nkdep/a-z/Documents/ckd-dietassess-manage-treat-508.pdf. Updated April 2015. Accessed October 7, 2015.
  47. National Heart, Lung, and Blood Institute. Description of the DASH eating plan. https://www.nhlbi.nih.gov/health/health-topics/topics/dash. Updated September 16, 2015. Accessed October 7, 2015.
  48. Kalantar-Zadeh K, Tortorici AR, Chen JL, et al. Dietary restrictions in dialysis patients: is there anything left to eat? Semin Dial. 2015;28(2):159-168.
  49. Palmer BF. Managing hyperkalemia caused by inhibitors of the renin-angiotensin-aldosterone system. N Engl J Med. 2004;351(6):585-592.
  50. Maher T, Schambelan M, Kurtz I, Hulter HN, Jones JW, Sebastian A. Amelioration of metabolic acidosis by dietary potassium restriction in hyperkalemic patients with chronic renal insufficiency. J Lab Clin Med. 1984;103(3):432-445.
  51. Heiden S, Buus AA, Jensen MH, Hejlesen OK. A diet management information and communication system to help chronic kidney patients cope with diet restrictions. Stud Health Technol Inform. 2013;192:543-547.
© 2024 MJH Life Sciences
AJMC®
All rights reserved.