1. Managing Chronic Kidney Disease in the Elderly Veteran Ann M. O’Hare, MA MD Staff Physician, VAPSHCS Assistant Professor of Medicine University of Washington

2. For Ann O’Hare’s financial disclosure statement: http://depts.washington.edu/greccva/OHare_Disclosure.doc http://depts.washington.edu/greccva/OHare_Disclosure.doc

3. Gross, C. P. et. al. Ann Intern Med 2002;137:10-16 Generalizability of RCTs

4. RCTs in high impact medical journals Van Spall, JAMA 2007

5. Mean age of participants in heart failure trials Heiat et al, Archives of Internal Medicine, 2002

6. Exclusion criteria of heart failure trials

7. Acute MI A total of 214 trials met inclusion criteria, involving 150,920 study subjects. Over 60% of trials excluded persons over the age of 75 years. Studies published after 1980 were more likely to have age-based exclusions compared with studies published before 1980 Gurwitz, JAMA, 1992

8. Cancer treatment trials Hutchins, NEJM 1999

9. Exclusion of elderly in clinical trials National Institutes of Health Revitalization Act of 1993 (Public Law 103-143) –Requirements for the inclusion of women and minorities in clinical trials but not the elderly

10. Randomized Aldactone Evaluation Study (RALES) Pitt B, Zannad F, Remme WJ, et al. The effect of spironolactone on morbidity and mortality in patients with severe heart failure. N Engl J Med 1999;341:709-717. [[

11. Rates of spironolactone prescription Juurlink et al. Rates of hyperkalemia after publication of the Randomized Aldactone Evaluation Study. N Engl J Med. 2004 Aug 5;351(6):543-51.

12. Rates admission for hyperkalemia

13. Rates of death

15. Action to Control Cardiovascular Risk in Diabetes (ACCORD) 10,251 adults with established type 2 diabetes Aged 40 to 82 (average age 62) had diabetes for an average of 10 years either already had diagnosed CVD or they had at least two CVD risk factors.

16. Chronic kidney disease Levey et al, Annals of Internal Medicine, 2003

17. Copyright restrictions may apply. Coresh, J. et al. JAMA 2007;298:2038-2047. Prevalence of Chronic Kidney Disease (CKD) Stages by Age Group in NHANES 1988-1994 and 1999-2004

18. CKD is common in the elderly.

19. In VA 75-85 group is largest Adapted from O’Hare et al JASN 2007

20. High prevalence of co- morbidities

21. Practice guidelines

22. Framework Can existing guidelines for the management of CKD be generalized to these older patients? –What is the strength of evidence? –Does the evidence pertain specifically to older patients with CKD? What are the characteristics of patients enrolled in clinical trails? –If not, can the available evidence reasonably be extrapolated to older patients? Is there any reason to expect that real and perceived benefits of an intervention might differ by age? –Does CKD have similar features in older and younger patients? –Does CKD have similar clinical implications in older and younger patients? Are the risks of the intervention comparable in older and younger patients? –Do the adverse effects of the intervention differ by age? –Do similar adverse effects have different implications for older and younger patients?

23. What is the quality of the evidence?

25. Early treatment can make a difference 100 10 0 No Treatment Current Treatment Early Treatment 47911 Time (years) Kidney Failure GFR (mL/min/1.73 2 )

26. “Strong” evidence: the example of ACE inhibitors Patients with diabetic kidney disease, with or without hypertension, should be treated with an ACE inhibitor or an ARB ACE inhibitors and ARBs are effective in slowing the progression of kidney disease with microalbuminuria due to type 1 and type 2 diabetes (Strong). ACE inhibitors, ARBs, and nondihydropyridine calcium-channel blockers have a greater antiproteinuric effect than other antihypertensive classes in diabetic kidney disease (Strong). Patients with nondiabetic kidney disease and spot urine total protein to creatinine ratio ≥200 mg/g, with or without hypertension, should be treated with an ACE inhibitor or ARB. ACE inhibitors are more effective than other antihypertensive agents in slowing the progression of most nondiabetic kidney diseases (Strong). The beneficial effect is greater in patients with higher levels of proteinuria (Strong).

27. Recommendations for clinical performance measures GUIDELINE 8 All patients with diabetic kidney disease should be treated with either an ACE inhibitor or an ARB (Guideline 8.2), unless there is a documented contraindication in the medical record (such as pregnancy or a history of allergy; see Table 124).Table 124 GUIDELINE 9 All patients with nondiabetic kidney disease and spot urine total protein-to-creatinine ratio ≥200 mg/g) should be treated with either an ACE inhibitor or an ARB (Guideline 9.2), unless there is a documented contraindication in the medical record (such as pregnancy or a history of allergy; see Table 124).Table 124

28. Adherence to treatment guidelines – room for improvement The percentage of diabetic CKD patients receiving ACE-Is/ARBs has been slow to improve Percent of patients USRDS ADR, 2007

29. ACE DM 1 ACE DM 2ARB DM II ACE or ARB non-diabetic CKD All Number of studies6115931 Number of patients7754,9414,2676,45116,434 Explicit upper age exclusion, %3 (49-57)5 (50-80)3 (70-80)7 (65-70)18 (58%) Maximum age of participants <70*4 (67%)3 (27%)3 (60%)7 (78%)17 (55%) Comorbidity exclusion, %3 (50%)9(82%)4 (80%)8 (89%)24 (77%) Weighted mean age, range33.7 (28.9-39) 63.7 (44- 70.2) 59.4 (58.6-60) 63.3 (45.3- 70.2) 60.8 Enrollment characteristics of trials of ACE or ARB to slow progression of CKD 2004 KDOQI guidelines on Hypertension and Anti-hypertensive agents in CKD; 2007 KDOQI guideline on Diabetes and Chronic Kidney Disease

30. Scatter plot of mean age by number of participants Mean weighted age 60.8 yr

31. ALLHAT ALLHAT differs in some important ways from other studies of antihypertensive agents in CKD. –First, the ACE inhibitor and dihydropyridine calcium-channel blocker were prescribed without a diuretic. By contrast, other studies in CKD have compared classes of antihypertensive agents usually prescribed in combination with a diuretic. –Second, the risk of kidney failure was lower than observed in other studies in CKD. –Third, proteinuria was not measured in ALLHAT, either in baseline or in follow-up. By contrast, most studies in CKD have included patients with proteinuria. –Thus, differences between ALLHAT and other studies in CKD may be due to the study design and the type of patient enrolled, rather than true differences in efficacy of combinations of antihypertensive agents used in CKD in slowing progression of kidney disease.

32. Jafar, T. H. et. al. Ann Intern Med 2001;135:73-87 Risk for end-stage renal disease (ESRD) (A), combined outcome of doubling of serum creatinine or ESRD (B), or relative risk for these outcomes (CandD) in patients taking angiotensin-converting enzyme inhibitors (squares) and controls (circles), according to baseline urinary protein excretion

33. It is the opinion of the Work Group that the ALLHAT results do not rule out a beneficial effect of ACE inhibitors in nondiabetic kidney disease, particularly in patients with proteinuria. Instead, the Work Group concluded that ACE inhibitors should be used to delay the progression of most nondiabetic kidney diseases.

34. Copyright restrictions may apply. Coresh, J. et al. JAMA 2007;298:2038-2047. Prevalence of Chronic Kidney Disease (CKD) Stages by Age Group in NHANES 1988-1994 and 1999-2004

35. CKD “phenotype” in older patients NHANES 99-04: inclusive of patients 20 and older with a measured serum creatinine and single spot urine albumin and creatinine measurement (n=13,011) CKD (n=1,525): –eGFR<60 –eGFR>=60 with ACR>=200 mg/g

36. O’Hare et al, unpublished work

37. 70.2 yr 59.7 yr 52.4 yr O’Hare et al, unpublished work

38. Burden of co-morbidity O’Hare et al, unpublished work

39. 162,277 veterans with an eGFR =200mg/g

40. Summary patients The vast majority of older individuals with CKD do not have proteinuria and do not have diabetes. More than half of all non-proteinuric diabetic and non-diabetic CKD occurs in those 70 or older. Older patients with CKD have a higher prevalence of co-existing cardiovascular disease compared with their younger counterparts.

41. Summary trials Most trials of ACE/ARB conducted among populations with diabetes Most have an upper age exclusion Most have not enrolled participants older than 70 ALLHAT included the largest number of participants (with and without diabetes) and had the highest mean age and was a negative trial ALLHAT participants accounted for 58% of all participants in trials of non-diabetic CKD

42. Background considerations in evaluating benefits of ACE/ARB in elderly We know very little about how the course of CKD varies with age. CKD progression may be slower in the elderly though this may reflect the higher prevalence of non- proteinuric CKD. It is unclear that the same proxy outcomes are appropriate in elders (e.g. development of albuminuria in patients with diabetes). Limited life expectancy. Competing risk of death is much higher in older compared with younger adults with CKD. Higher prevalence of competing co-morbid conditions and polypharmacy in older patients with CKD may modify the benefits of ACE or ARB.

43. Rate of change in eGFR Hemmelgarn et al, Kidney International Kidney Int. 2006 Jun;69(12):2155-61.

44. Absolute risk of ESRD decreases with age among patients with similar level of eGFR

45. Do the real and perceived risks of treatment differ by age? Side effect profile of ace inhibitors in older patients is largely unstudied. Burden of a given side-effect may differ by age (e.g. hyperkalemia may prompt hospital admission vs. outpatient treatment in a frail older patient). Multiple comorbidities and polypharmacy so common in the elderly may complicate the burden and risks of any intervention.

46. What can primary care providers do?