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Chronic Kidney Disease:
Proposed Revisions to the
ICD-9-CM Classification
Lesley Stevens MD
Tufts-New England Medical Center
National Kidney Foundation
Objectives
• Kidney Failure
• Stages of Chronic Kidney Disease
• Definition and Classification of CKD
• GFR
• Proteinuria
• Etiology
• Current use of ICD-9-CM codes for CKD
• Proposed changes to ICD-9-CM
Incidence and Prevalence of End-Stage
Renal Disease in the US
Cardiovascular Mortality in the General
Population and in ESRD Treated by Dialysis
0.01
100
10
1
0.1
Annual mortality (%)
25–34 45–54 65–74 85
35–44 55–64 75–84
Male
Female
Black
White
Dialysis
General population
Age (years)
Costs of Associated with Initiation of
Dialysis
Figure 2a: All Patients
$-
$2,000
$4,000
$6,000
$8,000
$10,000
$12,000
$14,000
$16,000
-24 -22 -20 -18 -16 -14 -12 -10 -8 -6 -4 -2 1 3 5
Month
PMPM,
allowable
Inpatient Outpatient Other Part A Part B
St Peters, Khan, Ebben. Li, Xue, Pereira, Collins. Kidney Int. 200.
CKD
death
Stages in Progression of Chronic Kidney
Disease and Therapeutic Strategies
Complications
Screening
for CKD
risk factors
CKD risk
reduction;
Screening for
CKD
Diagnosis
& treatment;
Treat
comorbid
conditions;
Slow
progression
Estimate
progression;
Treat
complications;
Prepare for
replacement
Replacement
by dialysis
& transplant
Normal
Increased
risk
Kidney
failure
Damage  GFR
Definition of CKD
Structural or functional abnormalities of
the kidneys for >3 months, as
manifested by either:
1. Kidney damage, with or without decreased
GFR, as defined by
• pathologic abnormalities
• markers of kidney damage, including
abnormalities in the composition of the blood or
urine or abnormalities in imaging tests
2. GFR <60 ml/min/1.73 m2, with or without
kidney damage
Prevalence of CKD and Estimated Number
of Adults with CKD in the US (NHANES 88-94)
Stage Description
GFR
(ml/min/1.73 m2)
Prevalence*
N
(1000s)
%
1
Kidney Damage with
Normal or  GFR
 90 5,900 3.3
2
Kidney Damage with
Mild  GFR
60-89 5,300 3.0
3 Moderate  GFR 30-59 7,600 4.3
4 Severe  GFR 15-29 400 0.2
5 Kidney Failure < 15 or Dialysis 300 0.1
*Stages 1-4 from NHANES III (1988-1994). Population of 177 million with age 20. Stage 5 from USRDS (1998), includes
approximately 230,000 patients treated by dialysis, and assuming 70,000 additional patients not on dialysis. GFR estimated
from serum creatinine using MDRD Study equation based on age, gender, race and calibration for serum creatinine. For
Stage 1 and 2, kidney damage estimated by spot albumin-to-creatinine ratio 17 mg/g in men or 25 mg/g in women in two
measurements.
Prevalence of Abnormalities at each level of GFR
0
10
20
30
40
50
60
70
80
90
15-29 30-59 60-89 90+
Estimated GFR (ml/min/1.73 m2
)
Proportion
of
population
(%)
Hypertension* Hemoglobin < 12.0 g/dL
Unable to walk 1/4 mile Serum albumin < 3.5 g/dL
Serum calcium < 8.5 mg/dL Serum phosphorus > 4.5 mg/dL
*>140/90 or antihypertensive medication p-trend < 0.001 for each abnormality
Age-Standardized Rates of Death from Any Cause
(Panel A) and Cardiovascular Events (Panel B),
According to the Estimated GFR among 1,120,295
Ambulatory Adults
Go, A, et al. NEJM 351: 1296
Clinical Practice Guidelines for the Detection,
Evaluation and Management of CKD
Stage Description GFR Evaluation Management
At increased
risk
Test for CKD Risk factor management
1
Kidney
damage with
normal or 
GFR
>90
Diagnosis
Comorbid
conditions
CVD and CVD
risk factors
Specific therapy, based on diagnosis
Management of comorbid conditions
Treatment of CVD and CVD risk factors
2
Kidney
damage with
mild  GFR
60-89
Rate of
progression
Slowing rate of loss of kidney function 1
3
Moderate 
GFR
30-59 Complications Prevention and treatment of complications
4 Severe  GFR 15-29
Preparation for kidney replacement therapy
Referral to Nephrologist
5 Kidney Failure <15 Kidney replacement therapy
1
Target blood pressure less than 130/80 mm Hg. Angiotension converting enzyme inhibitors
(ACEI) or angiotension receptor blocker (ARB) for diabetic or non-diabetic kidney disease with spot
urine total protein-to-creatinine ratio of greater than 200 mg/g.
Definition of ESRD vs Kidney Failure
• ESRD is a federal government defined
term that indicates chronic treatment by
dialysis or transplantation
• Kidney Failure: GFR < 15 ml/min/1.73
m2 or on dialysis.
Importance of Proteinuria in CKD
Interpretation Explanation
Marker of kidney
damage
Spot urine albumin-to-creatinine ratio >30 mg/g or
spot urine total protein-to-creatinine ratio >200 mg/g
for >3 months defines CKD
Clue to the type
(diagnosis) of CKD
Spot urine total protein-to-creatinine ratio >500-
1000 mg/g suggests diabetic kidney disease,
glomerular diseases, or transplant glomerulopathy.
Risk factor for adverse
outcomes
Higher proteinuria predicts faster progression of
kidney disease and increased risk of CVD.
Effect modifier for
interventions
Strict blood pressure control and ACE inhibitors are
more effective in slowing kidney disease
progression in patients with higher baseline
proteinuria.
Hypothesized
surrogate outcomes
and target for
interventions
If validated, then lowering proteinuria would be a
goal of therapy.
Albuminuria as a Risk Factor for CVD in
PREVEND
Hillege HL et al. Circulation 2002: 106: 1777-1782
Progression of Kidney Disease related to
level of proteinuria and blood pressure
lowering in MDRD Study
Petersen. Annals of Internal Medicine. 1995
Clinical Practice Guidelines for
Management of Hypertension in CKD
Type of Kidney Disease Blood Pressure
Target
(mm Hg)
Preferred Agents
for CKD, with or
without
Hypertension
Other Agents
to Reduce CVD Risk
and Reach Blood
Pressure Target
Diabetic Kidney Disease
<130/80
ACE inhibitor
or ARB
Diuretic preferred,
then BB or CCB
Nondiabetic Kidney
Disease with Urine Total
Protein-to-Creatinine
Ratio 200 mg/g
Nondiabetic Kidney
Disease with Spot Urine
Total Protein-to-Creatinine
ratio <200 mg/g None preferred
Diuretic preferred,
then ACE inhibitor,
ARB, BB or CCB
Kidney Disease in Kidney
Transplant Recipient
CCB, diuretic, BB,
ACE inhibitor, ARB
Classification of CKD by Diagnosis
• Diabetic Kidney Disease
• Glomerular diseases (autoimmune diseases,
systemic infections, drugs, neoplasia)
• Vascular diseases (renal artery disease,
hypertension, microangiopathy)
• Tubulointerstitial diseases (urinary tract infection,
stones, obstruction, drug toxicity)
• Cystic diseases (polycystic kidney disease)
• Diseases in the transplant (Allograft nephropathy,
drug toxicity, recurrent diseases, transplant
glomerulopathy)
Current use of ICD-9-CM codes for
Kidney Disease
• ICD-9-CM codes for kidney disease were
used in 1% of all patients.
GFR Sensitivity Specificity
30-59 6 97
< 30 39 96
* GFR in ml/min/1.72 m2
Current use of ‘585’ (chronic renal
failure) in 277, 262 adults visiting an
outpatient commercial clinical
laboratory
GFR (ml/min/1.73 m2)*
>90 60-89 30-59 15-29 <15
No 585 code** 13 60 27 3 <1
585 code 10 62 23 2 <1
* GFR in ml/min/1.72 m2
**Row Percentages
Proposed Classification: ESRD code
585 End Stage Renal Disease;
on dialysis
585.1 End Stage Renal Disease;
transplanted
Use additional code to identify
chronic kidney disease (586.1-586.9)
Proposed Classification: CKD code
586.1 Stage I CKD: Kidney damage with normal or
increased glomerular filtration rate (GFR), greater than
or equal to 90 ml/min/1.73m2
586.2 Stage II CKD: Kidney damage with mild decrease in
GFR 60-89 ml/min/1.73m2
586.3 Stage III CKD: Kidney damage with moderate
decrease in GFR 30-59 ml/min/1.73m2
586.4 Stage IV CKD: Kidney damage with severe decrease
in GFR 15-29 ml/min/1.73m2
586.5 Stage V CKD: Kidney damage with GFR of less than
15 ml/min/1.73m2 Kidney failure with GFR less than 15
ml/min/1.73m2 and not on dialysis
Note: Codes apply only to patients diagnosed kidney disease > 3 mo
Proposed Classification:
CKD code 5th digit
• Each 586 (CKD) code requires a 5th
digit to indicate evidence of proteinuria
or albuminuria
– 586.X0 for those without evidence of proteinuria or
albuminuria
– 586.X1 for those with evidence of proteinuria or
albuminuria
Proposed Classification: Etiology
• Instructions to code for CKD stage
along with disease specific codes
250.4 Diabetes with renal manifestations
Use additional code to identify manifestation, as:
Add chronic kidney disease (585.1-585.9)
582.81 Chronic glomerulonephritis in diseases
classified elsewhere: amyloidosis, SLE
Use additional code to identify manifestation, as:
Add chronic kidney disease (585.1-585.9)
Benefits of Revised ICD-9-CM codes
1. Distinguish between ESRD and CKD; between dialysis
and transplantation
2. Assess risk for adverse outcomes, expected
complications and comorbid disease by the combination
of severity of CKD (stages), proteinuria and diagnosis
3. Determine which patients require specific treatments
based on severity of CKD, and in particular proteinuria
4. Examine of health care utilization and costs. Assess
rural and urban settings and racial disparities
5. Assess quality of care delivered
6. Progress toward achievement of Healthy People 2010
goals
7. Allow CMS and USRDS to develop specific research
files to investigators to enhance our knowledge of CKD
by the major risk groups

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att_CKD_oct04.power point presentation ppt

  • 1. Chronic Kidney Disease: Proposed Revisions to the ICD-9-CM Classification Lesley Stevens MD Tufts-New England Medical Center National Kidney Foundation
  • 2. Objectives • Kidney Failure • Stages of Chronic Kidney Disease • Definition and Classification of CKD • GFR • Proteinuria • Etiology • Current use of ICD-9-CM codes for CKD • Proposed changes to ICD-9-CM
  • 3. Incidence and Prevalence of End-Stage Renal Disease in the US
  • 4. Cardiovascular Mortality in the General Population and in ESRD Treated by Dialysis 0.01 100 10 1 0.1 Annual mortality (%) 25–34 45–54 65–74 85 35–44 55–64 75–84 Male Female Black White Dialysis General population Age (years)
  • 5. Costs of Associated with Initiation of Dialysis Figure 2a: All Patients $- $2,000 $4,000 $6,000 $8,000 $10,000 $12,000 $14,000 $16,000 -24 -22 -20 -18 -16 -14 -12 -10 -8 -6 -4 -2 1 3 5 Month PMPM, allowable Inpatient Outpatient Other Part A Part B St Peters, Khan, Ebben. Li, Xue, Pereira, Collins. Kidney Int. 200.
  • 6. CKD death Stages in Progression of Chronic Kidney Disease and Therapeutic Strategies Complications Screening for CKD risk factors CKD risk reduction; Screening for CKD Diagnosis & treatment; Treat comorbid conditions; Slow progression Estimate progression; Treat complications; Prepare for replacement Replacement by dialysis & transplant Normal Increased risk Kidney failure Damage  GFR
  • 7. Definition of CKD Structural or functional abnormalities of the kidneys for >3 months, as manifested by either: 1. Kidney damage, with or without decreased GFR, as defined by • pathologic abnormalities • markers of kidney damage, including abnormalities in the composition of the blood or urine or abnormalities in imaging tests 2. GFR <60 ml/min/1.73 m2, with or without kidney damage
  • 8. Prevalence of CKD and Estimated Number of Adults with CKD in the US (NHANES 88-94) Stage Description GFR (ml/min/1.73 m2) Prevalence* N (1000s) % 1 Kidney Damage with Normal or  GFR  90 5,900 3.3 2 Kidney Damage with Mild  GFR 60-89 5,300 3.0 3 Moderate  GFR 30-59 7,600 4.3 4 Severe  GFR 15-29 400 0.2 5 Kidney Failure < 15 or Dialysis 300 0.1 *Stages 1-4 from NHANES III (1988-1994). Population of 177 million with age 20. Stage 5 from USRDS (1998), includes approximately 230,000 patients treated by dialysis, and assuming 70,000 additional patients not on dialysis. GFR estimated from serum creatinine using MDRD Study equation based on age, gender, race and calibration for serum creatinine. For Stage 1 and 2, kidney damage estimated by spot albumin-to-creatinine ratio 17 mg/g in men or 25 mg/g in women in two measurements.
  • 9. Prevalence of Abnormalities at each level of GFR 0 10 20 30 40 50 60 70 80 90 15-29 30-59 60-89 90+ Estimated GFR (ml/min/1.73 m2 ) Proportion of population (%) Hypertension* Hemoglobin < 12.0 g/dL Unable to walk 1/4 mile Serum albumin < 3.5 g/dL Serum calcium < 8.5 mg/dL Serum phosphorus > 4.5 mg/dL *>140/90 or antihypertensive medication p-trend < 0.001 for each abnormality
  • 10. Age-Standardized Rates of Death from Any Cause (Panel A) and Cardiovascular Events (Panel B), According to the Estimated GFR among 1,120,295 Ambulatory Adults Go, A, et al. NEJM 351: 1296
  • 11. Clinical Practice Guidelines for the Detection, Evaluation and Management of CKD Stage Description GFR Evaluation Management At increased risk Test for CKD Risk factor management 1 Kidney damage with normal or  GFR >90 Diagnosis Comorbid conditions CVD and CVD risk factors Specific therapy, based on diagnosis Management of comorbid conditions Treatment of CVD and CVD risk factors 2 Kidney damage with mild  GFR 60-89 Rate of progression Slowing rate of loss of kidney function 1 3 Moderate  GFR 30-59 Complications Prevention and treatment of complications 4 Severe  GFR 15-29 Preparation for kidney replacement therapy Referral to Nephrologist 5 Kidney Failure <15 Kidney replacement therapy 1 Target blood pressure less than 130/80 mm Hg. Angiotension converting enzyme inhibitors (ACEI) or angiotension receptor blocker (ARB) for diabetic or non-diabetic kidney disease with spot urine total protein-to-creatinine ratio of greater than 200 mg/g.
  • 12. Definition of ESRD vs Kidney Failure • ESRD is a federal government defined term that indicates chronic treatment by dialysis or transplantation • Kidney Failure: GFR < 15 ml/min/1.73 m2 or on dialysis.
  • 13. Importance of Proteinuria in CKD Interpretation Explanation Marker of kidney damage Spot urine albumin-to-creatinine ratio >30 mg/g or spot urine total protein-to-creatinine ratio >200 mg/g for >3 months defines CKD Clue to the type (diagnosis) of CKD Spot urine total protein-to-creatinine ratio >500- 1000 mg/g suggests diabetic kidney disease, glomerular diseases, or transplant glomerulopathy. Risk factor for adverse outcomes Higher proteinuria predicts faster progression of kidney disease and increased risk of CVD. Effect modifier for interventions Strict blood pressure control and ACE inhibitors are more effective in slowing kidney disease progression in patients with higher baseline proteinuria. Hypothesized surrogate outcomes and target for interventions If validated, then lowering proteinuria would be a goal of therapy.
  • 14. Albuminuria as a Risk Factor for CVD in PREVEND Hillege HL et al. Circulation 2002: 106: 1777-1782
  • 15. Progression of Kidney Disease related to level of proteinuria and blood pressure lowering in MDRD Study Petersen. Annals of Internal Medicine. 1995
  • 16. Clinical Practice Guidelines for Management of Hypertension in CKD Type of Kidney Disease Blood Pressure Target (mm Hg) Preferred Agents for CKD, with or without Hypertension Other Agents to Reduce CVD Risk and Reach Blood Pressure Target Diabetic Kidney Disease <130/80 ACE inhibitor or ARB Diuretic preferred, then BB or CCB Nondiabetic Kidney Disease with Urine Total Protein-to-Creatinine Ratio 200 mg/g Nondiabetic Kidney Disease with Spot Urine Total Protein-to-Creatinine ratio <200 mg/g None preferred Diuretic preferred, then ACE inhibitor, ARB, BB or CCB Kidney Disease in Kidney Transplant Recipient CCB, diuretic, BB, ACE inhibitor, ARB
  • 17. Classification of CKD by Diagnosis • Diabetic Kidney Disease • Glomerular diseases (autoimmune diseases, systemic infections, drugs, neoplasia) • Vascular diseases (renal artery disease, hypertension, microangiopathy) • Tubulointerstitial diseases (urinary tract infection, stones, obstruction, drug toxicity) • Cystic diseases (polycystic kidney disease) • Diseases in the transplant (Allograft nephropathy, drug toxicity, recurrent diseases, transplant glomerulopathy)
  • 18. Current use of ICD-9-CM codes for Kidney Disease • ICD-9-CM codes for kidney disease were used in 1% of all patients. GFR Sensitivity Specificity 30-59 6 97 < 30 39 96 * GFR in ml/min/1.72 m2
  • 19. Current use of ‘585’ (chronic renal failure) in 277, 262 adults visiting an outpatient commercial clinical laboratory GFR (ml/min/1.73 m2)* >90 60-89 30-59 15-29 <15 No 585 code** 13 60 27 3 <1 585 code 10 62 23 2 <1 * GFR in ml/min/1.72 m2 **Row Percentages
  • 20. Proposed Classification: ESRD code 585 End Stage Renal Disease; on dialysis 585.1 End Stage Renal Disease; transplanted Use additional code to identify chronic kidney disease (586.1-586.9)
  • 21. Proposed Classification: CKD code 586.1 Stage I CKD: Kidney damage with normal or increased glomerular filtration rate (GFR), greater than or equal to 90 ml/min/1.73m2 586.2 Stage II CKD: Kidney damage with mild decrease in GFR 60-89 ml/min/1.73m2 586.3 Stage III CKD: Kidney damage with moderate decrease in GFR 30-59 ml/min/1.73m2 586.4 Stage IV CKD: Kidney damage with severe decrease in GFR 15-29 ml/min/1.73m2 586.5 Stage V CKD: Kidney damage with GFR of less than 15 ml/min/1.73m2 Kidney failure with GFR less than 15 ml/min/1.73m2 and not on dialysis Note: Codes apply only to patients diagnosed kidney disease > 3 mo
  • 22. Proposed Classification: CKD code 5th digit • Each 586 (CKD) code requires a 5th digit to indicate evidence of proteinuria or albuminuria – 586.X0 for those without evidence of proteinuria or albuminuria – 586.X1 for those with evidence of proteinuria or albuminuria
  • 23. Proposed Classification: Etiology • Instructions to code for CKD stage along with disease specific codes 250.4 Diabetes with renal manifestations Use additional code to identify manifestation, as: Add chronic kidney disease (585.1-585.9) 582.81 Chronic glomerulonephritis in diseases classified elsewhere: amyloidosis, SLE Use additional code to identify manifestation, as: Add chronic kidney disease (585.1-585.9)
  • 24. Benefits of Revised ICD-9-CM codes 1. Distinguish between ESRD and CKD; between dialysis and transplantation 2. Assess risk for adverse outcomes, expected complications and comorbid disease by the combination of severity of CKD (stages), proteinuria and diagnosis 3. Determine which patients require specific treatments based on severity of CKD, and in particular proteinuria 4. Examine of health care utilization and costs. Assess rural and urban settings and racial disparities 5. Assess quality of care delivered 6. Progress toward achievement of Healthy People 2010 goals 7. Allow CMS and USRDS to develop specific research files to investigators to enhance our knowledge of CKD by the major risk groups