cv risk factors, bp control and progression of renal function in our ckd outpatient population

15
CARDIOVASCULAR RISK FACTORS, BLOOD PRESSURE CONTROL, AND KIDNEY FUNCTION PROGRESSION AMONG CHRONIC KIDNEY DISEASE POPULATION. Jafar Al-Said, M.B. CHb. MD. FASN, FACP. Teerath Kumar MBBS. FCPS. Soni Murdeshwar. Bahrain Specialist Hospital Introduction: Patients with HTN and CKD has increased CV risk factors. CKD OPD population at Bahrain Specialist Hospital were analyzed. Aim: study our CKD population regarding: CV risk profile. HTN prevalence & treatment. Kidney function progression. Methodology: * Retrospective. * OPD population with CKD. * 102 months. Oct. 2003 – April 2012. Data: Demographic, CV risk & medications. Estimate eGFR by CKD EPI. Exclude: Transplant, Pregnant, Primary GN. Results: * Mean age 58.7 y (SE 0.9). * Males 61% Kidney function outcome Final BP control: Type of medications used Number of medication needed to keep BP <140/90 Prevalence of CV Risks among CKD Relation of the number of CV risk & CKD stage Cumulative numbers of CV risk factors in CKD Conclusion: Among our CKD patients: - HTN is the most Common CV risk factors. - CV risk factors increase with CKD stage. - 58% needed combination antiHTN Medications. - CKD progression was stable over 108 months. - Final eGFR was correlated with: Gender, DM, systolic BP, Albumin, Ca blocker, Vasodil. & NTG. Univariat correlation with eGFR progression Uncontrolled Controlled 43 % 57 % 1 2 3 4 5 6 7 8 0% 10% 20% 30% 5% 11% 18% 24% 17%18% 6% 1% Mean = 4 HTN Hyperlipi. DM Hyp eru ric. IHD PVD Stroke 0% 40% 80% 91% 72% 60% 43% 20% 9% 6% I II III IV V 1 2 3 4 2.5 2.4 3.1 3.2 3.5 P = 0.001 0 1 2 3 4 5 6 0% 10% 20% 30% 40% 12% 30% 36% 12% 7% 2% 1% 0% 15% 30% 45% 60% 61% 29% 38% 14% 41% 3% 10% 14%

Upload: jafaralsaid

Post on 20-Nov-2014

182 views

Category:

Education


0 download

DESCRIPTION

Progression of Renal function and BP control in CKD patients followed in the OPD at Bahrain Specialist Hospital

TRANSCRIPT

Page 1: CV risk factors, BP control and progression of Renal Function in our CKD outpatient population

CARDIOVASCULAR RISK FACTORS, BLOOD PRESSURE CONTROL, AND KIDNEY FUNCTION PROGRESSION AMONG CHRONIC KIDNEY DISEASE POPULATION.

Jafar Al-Said, M.B. CHb. MD. FASN, FACP. Teerath Kumar MBBS. FCPS. Soni Murdeshwar.Bahrain Specialist Hospital

Introduction:Patients with HTN and CKD has increased CV risk factors. CKD OPD population at Bahrain Specialist Hospital were analyzed.

Aim: study our CKD population regarding: • CV risk profile.• HTN prevalence & treatment.• Kidney function progression.Methodology: * Retrospective. * OPD population with CKD. * 102 months. Oct. 2003 – April 2012.

Data: Demographic, CV risk & medications.Estimate eGFR by CKD EPI.

Exclude: Transplant, Pregnant, Primary GN.

Results: * Mean age 58.7 y (SE 0.9). * Males 61%

Kidney function outcome

Final BP control:

Type of medications used

Number of medication needed to keep BP <140/90

Prevalence of CV Risks among CKD

Relation of the number of CV risk & CKD stage

Cumulative numbers of CV risk factors in CKD

Conclusion: Among our CKD patients:- HTN is the most Common CV risk factors.- CV risk factors increase with CKD stage.- 58% needed combination antiHTN Medications.- CKD progression was stable over 108 months.- Final eGFR was correlated with: Gender, DM, systolic BP, Albumin, Ca blocker, Vasodil. & NTG.

Univariat correlation with eGFR progression

Uncontrolled

Controlled

43%

57%

1 2 3 4 5 6 7 80%5%

10%15%20%25%30%

5%

11%

18%

24%

17% 18%

6%1%

Mean = 4

HTN

Hyperlipi.

DM

Hyperu

ric.

IHD

PVDStr

oke0%

20%40%60%80%

100%

91%72%

60%

43%20% 9% 6%

I II III IV V1

2

3

4

2.5 2.4

3.1 3.23.5

P = 0.001

0 1 2 3 4 5 60%

10%

20%

30%

40%

12%

30% 36%

12% 7%2% 1%

RAAS

Diuretics

B-Blocker

Alpha/Beta

blo.

Ca Block

er

Alpha Blocker

Vasodila

tor

NTG

0%15%30%45%60% 61%

29%38%

14%

41%

3%10% 14%

Page 2: CV risk factors, BP control and progression of Renal Function in our CKD outpatient population

CARDIOVASCULAR RISK FACTORS, BLOOD PRESSURE CONTROL, AND KIDNEY FUNCTION PROGRESSION AMONG CKD POPULATION.

Jafar Al-Said, M.B. CHb. MD. FASN, FACP. Teerath Kumar MBBS. FCPS. Soni Murdeshwar

23rd Annual European Society of Hypertension meeting. Milan. 16. June. 2013

Page 3: CV risk factors, BP control and progression of Renal Function in our CKD outpatient population

Introduction• Patients with HTN and CKD have increased CV risk

factors.

• Different population have different CV risk profile.

• Determining the CV risk factors will help in planning a preventive protocol for these patients.

• We wanted to identify the CV risk for our CKD population at Bahrain Specialist Hospital.

Page 4: CV risk factors, BP control and progression of Renal Function in our CKD outpatient population

Aim• Determine the CV risk profile among our

CKD population.

• Identify HTN prevalence in that cohort. & their treatment.

• Determine the progression of CKD among these patients an their related factors.

Page 5: CV risk factors, BP control and progression of Renal Function in our CKD outpatient population

Methodology

Retrospective. • OPD population with CKD. • 102 months. Oct. 2003 – April 2012.

Data: Demographic, CV risk & medications.Estimate eGFR by CKD EPI.

Exclude: Transplant, Pregnant, Primary GN.

Page 6: CV risk factors, BP control and progression of Renal Function in our CKD outpatient population

Results

Total CKD population = 245 .

Total CKD and HTN = 223.

Mean age 58.7 y (SE 0.9).

Males 61%.

Page 7: CV risk factors, BP control and progression of Renal Function in our CKD outpatient population

Cardiovascular risk factors Total CKD population, n = 245

HTN Hyperlipi. DM Hyperuric. IHD PVD Stroke0%

10%

20%

30%

40%

50%

60%

70%

80%

90%

100%91%

72%

60%

43%

20%9%

6%

Type of CV disease

Page 8: CV risk factors, BP control and progression of Renal Function in our CKD outpatient population

Total CV risk including Age, Gender & BMI

1 2 3 4 5 6 7 80%

5%

10%

15%

20%

25%

30%

5%

11%

18%

24%

17% 18%

6%

1%

Mean = 4

Cumulative number of CV risks

Page 9: CV risk factors, BP control and progression of Renal Function in our CKD outpatient population

Mean number of CV risk factors according to CKD stage.Other than CKD.

I II III IV V1

1.5

2

2.5

3

3.5

4

2.5 2.4

3.1 3.2

3.5P = 0.001

Mea

n N

umbe

r of

CV

ri

sk fa

ctor

s

CKD staging

Page 10: CV risk factors, BP control and progression of Renal Function in our CKD outpatient population

Blood Pressure Control < 140/90mmHg

43%

57%Controlled

Uncontrolled

Page 11: CV risk factors, BP control and progression of Renal Function in our CKD outpatient population

Number of Anti HTN medications needed to control BP <140/90mmHg in CKD & HTN

0 1 2 3 4 5 60%

5%

10%

15%

20%

25%

30%

35%

40%

12%

30%

36%

12%

7%

2% 1%

Number of Anti HTN Medications

Page 12: CV risk factors, BP control and progression of Renal Function in our CKD outpatient population

RAAS

Diuretics

B-Blocker

Alpha/Betab

locker

Ca Blocke

r

Alpha Blocke

r

Vasodila

torNTG

0%

10%

20%

30%

40%

50%

60%

70%61%

29%

38%

14%

41%

3%10%

14%

Antihypertensive drugs used in the HTN group

Page 13: CV risk factors, BP control and progression of Renal Function in our CKD outpatient population

`Progression of kidney function among HTN CKD population

Page 14: CV risk factors, BP control and progression of Renal Function in our CKD outpatient population

Variables Correlation Coefficient PGender -0.29 <0.0001DM -0.19 0.006First Systolic -0.15 0.03First Hb 0.44 <0.0001First Albumin 0.27 0.003Final Albumin 0.21 0.04Ca Channel -0.16 0.023Vasodilator -0.23 0.001NTG -0.21 0.002

Independent Univariate Correlated Variables with final eGFR.

Page 15: CV risk factors, BP control and progression of Renal Function in our CKD outpatient population

Final Conclusion• CKD patient carry high CV risk factors.

• HTN is the most common CV risk factor among CKD population.

• 57 % of the HTN CKD were controlled after 2 years of follow up.

• 58% of the CKD and HTN patient needed > AntiHTN medication to control BP.

• Kidney function was stable over 2 years.