Improving the Detection of Chronic Kidney Disease Ayub Akbari, Heather D Clark, Peter J Swedko, Pete - PowerPoint PPT Presentation

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Improving the Detection of Chronic Kidney Disease Ayub Akbari, Heather D Clark, Peter J Swedko, Pete

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Title: Improving the Detection of Chronic Kidney Disease Ayub Akbari, Heather D Clark, Peter J Swedko, Pete


1
Improving the Detection of Chronic Kidney
DiseaseAyub Akbari, Heather D Clark, Peter J
Swedko, Peter O Magner, Daylily Ooi, Lisa J
Moore, William E Hogg Jacques Lemelin

2
ESRD is Increasing
3
(No Transcript)
4
Cost to Health Care
  • In 1999 about 2 billion was spent in Canada on
    caring for patients with ESRD.

5
How can we delay progression to ESRD and Improve
care?
  • Management of Hypertension
  • Use of ACE inhibitors and ARBS
  • Management of Anemia
  • Management of electrolyte imbalance
  • Management of malnutrition

6
Early Detection of Kidney Disease is the KEY
7
Serum Creatinine is NOT GFR!
GFR ml/min
Creatinine Clearance ml/min
Serum Creatinine umol/L
8
Determinants of Serum Creatinine
Muscle mass Rate of turnover
Serum Creatinine
Filtration Tubular Secretion
9
The Solution
  • GFR should be calculated from prediction
    equations and reported directly to the physician
    with a multi faceted educational intervention

10
Intervention
  • Laboratory reporting of GFR
  • Automatic reporting of the CG GFR by the Ottawa
    Hospital laboratory whenever the primary care
    physician requested a serum creatinine test
  • On-site phlebotomist at the family practice
    clinic submitted patients weight on the lab
    requisition whenever serum creatinine was ordered

11
Methods
  • Subjects
  • all patients in an academic family practice
    associated with the Ottawa Hospital who
  • were aged 65 or greater (elderly)
  • could have a Cockcroft-Gault GFR (CG GFR)
    calculated from their medical record between
    August 1997 and August 2000

12
Methods (2)
  • Exclusion Criteria
  • they were undergoing dialysis
  • they did not return for a follow-up appointment
    with their physician during the intervention
    period
  • their CG GFR was less than 0.5 ml/sec
  • we deemed it unethical not to inform the primary
    care physicians of these patients severely
    impaired kidney function

13
Methods (3)
  • Primary outcome
  • Detection of CKD (CG GFR lt 1.3 ml/sec) by the
    family physician, both before and after the
    intervention
  • Detection of CKD was defined as any evidence in
    the medical record that the physician had
    recognized impaired kidney function

14
Results
  • 700 patients aged ? 65 in whom CG GFR could be
    calculated
  • Excluded
  • 39 with CG GFR lt 0.5 ml/sec
  • 322 had no CG GFR at OH lab
  • 15 did not see their physician in follow-up after
    the CG GFR

N 324
15
Table 1 Characteristics of Study Patients
CG GFR Cockcroft-Gault calculated glomerular
filtration rate. Values are means ? standard
deviation
16
Figure 1 Detection Rate of Chronic Kidney Disease
Relative Increase 496.4
69
14
Pre-Intervention
Post-Intervention
17
Women Have Lower Serum Creatinine
Even Though Their CrCl is the Same as Men
18
Conclusions
  • Laboratory reporting of estimated GFR, along with
    an educational intervention, resulted in a
    dramatic increase in the detection of CKD by
    primary care physicians.
  • The use of laboratory-reported GFR can eliminate
    bias towards the detection of CKD in men and
    diabetics.

19
Limitations
  • Before and after study (not randomized)
  • Single centre
  • Tertiary care centre
  • Residents
  • Very intensive educational intervention
  • GFR lt 30 ml/min excluded
  • Only elderly studied

20
Next Steps
  • Randomized controlled trial
  • Intervention at community level
  • Include patients with severe CKD
  • Measure impact on nephrology services
  • Does early detection matter for mild renal
    failure?
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