1 / 29

Cardiovascular Hot topics ‘CKD’

Cardiovascular Hot topics ‘CKD’. Dr Saqib Mahmud MBBS, MD, MRCP(UK), MRCPS(Glasg), MRCGP. CKD. The introduction of routine reporting of eGFR has led to 3 outcomes in primary care; ‘Worried patients, Increased workload & confused clinicians’.BMJ2006

cree
Download Presentation

Cardiovascular Hot topics ‘CKD’

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Cardiovascular Hot topics‘CKD’ Dr Saqib Mahmud MBBS, MD,MRCP(UK), MRCPS(Glasg), MRCGP

  2. CKD • The introduction of routine reporting of eGFR has led to 3 outcomes in primary care; • ‘Worried patients, Increased workload & confused clinicians’.BMJ2006 (Referral rates remain high due to uncertainty how to manage newly diagnosed CKD cases)

  3. Why has CKD been selected as a quality indicator?QOF2 2006 • Patients with CKD have very high rates of vascular disease & require aggressive management of vascular risk factors. (early CKD risk of death from CVD>ESRF)-low GFR predicts CV disease • Its incidence is rising dramatically. (doubled in last 10yrs,5% adult population) • S Cr does not rise until GFR has fallen by 50-70% • Early interventions in CKD improve cardiac & renal outcomes

  4. eGFR-bestestimate of renal function • Based on S Cr, age, sex & ethnic origin. • Does not apply to children, ARF, pregnant women, oedematous & malnourished. • eGFR falls after eating meat, ideally fasting sample or avoid eating cooked meat day before. • CKD-diagnosed 2 eGFRs 3/12 apart, not on the basis of single eGFR

  5. CKD-classification

  6. Clinical Signs & Symptoms • Tiredness • Anorexia, nausea, vomiting • Generalized pruritis • Nocturia, frequency, oliguria, haematuria • Frothy urine • Loin pain • Pallor, peripheral & pulmonary oedema • Pleural effusion & SOB • leuconychia

  7. QOF 2006 – CKD register • CKD1- register of pts>18 with CKD3-5 • CKD2-(90%) on register with record of BP in last 15/12 • CKD3-(70%) on register with BP<140/85 • CKD4-(80%) patients on ACEI/A2RB-or CI • Worth 27pts=£3,364/-

  8. Conditions with risk of developing CKD • Hypertension • Diabetes • Heart failure • Vascular disease • Urinary outflow obstruction • Multi-system diseases eg;RA, SLE,vasculitis • APKD or reflux nephropathy • Long term Drugs-lithium, cyclosporin,NSAIDs,mesalazine

  9. Monitoring renal function • Stage 1 & 2 requires evidence of renal damage eg; Proteinuria, microalbuminuria, haematuria without urological cause or known polycystic kidney disease or GN. (Annual U & Es) • Stage 3  6/12 • Stages 4 & 53/12

  10. Urine tests • Dipstick urinalysis for protein, • If +ve  msu to exclude infection & EMU for ACR(+>30mg/mmol) or PCR(+>45) • In diabetics, dipstick negativeACR for microalbuminuria (+>2.5mg/mmol-males,>3.5 in women)

  11. Management – is easy • ‘CKD rarely means dialysis’ • Monitor renal function closely- assess rate of change • Tight BP control with preferential use of ACEI or A2RB • Pay close attention to CV risk

  12. New patient with eGFR<60 • Review previous results ?rate of deterioration • Review medication ?nephrotoxicity • Check BP, urine, full clinical assessment eg ?palpable bladder • Repeat U&E within 5/7 (?rapid progression) • Referral criteria- renal function stable monitor • Stage 4(if stable, monitor) & 5 should be referred • Stage 3 if deteriorating function

  13. Long term management to delay progression and reduce CV events • Life style advise smoking cessation, wt reduction, exercise, low protein diet • Aspirins & statins if CVD risk 15-20% • (evidence is that all CKD patients are high risk) • Strict BP control-QOF2 target <140/85, but renal guidelines best practice target is 130/80 -UK CKD&JBS2 guidelines. • Check U&Es before starting, 2/52 after & also 2/52 every dose change of ACEI or A2RBs • Aspirin->BP<150/90, target TC<4,LDL<2

  14. Additional management-CKD3 Renal USS if LUTS, refractory HTN, unexpected fall in GFR Immunise-influenza, pneumococcus, Hep B in CKD4&5 If HB<11-exclude other causes, refer for ESA, iv Fe

  15. Renal osteodystrophy • Renal failure failure of Vit D hydroxylation secondary hyperparathyroidism • increased # risk due to faulty bone remodelling & lowered BMD. • Check PTH levels, if low check 25-hydroxy Vit D levels • Rx- ergo or colecalciferol with calcium/bisphosphonates

  16. Bone disease in CKD • Recent Irish study found 76% of osteoporosis cases in CKD patients • Patients with CKD 4&5 had significantly lower BMD at hip & spine + high bone turnover • 2 fold increased risk of vertebral fractures • Statins - known to have beneficial effect in prevention of osteoporosis as well as decreased incidence of sepsis in CKD!

  17. ACEI / A2RB-Rxor the cause • ACEI/A2RBs improve outcomes but in some patients can be nephrotoxic • A slight reduction in GFR (<15%) or increase in creatinine is a normal haemodynamic response to ACE inhibition & is normally not an indication to stop Rx unless creatinine rises by >30% • Heart failure-rise in CR upto 50% baseline or 200umol/l is acceptable-(NICE)

  18. Renal artery stenosis • GFR- difference b/w flow of blood into glomeruli via afferent arteriole & flow out via efferent arteriole • This is not dependent on AT II normally but kidneys can increase GFR by local production of AT II which vasoconstricts efferent arteriole • In RAS-GFR is dependent on AT II mediated efferent arteriole vasoconstriction

  19. Renin- Angiotensin system

  20. RAS-cont • RAS is likely if rise in S Cr in absence of significant drop in BP • ‘Flash pulmonary oedema’-bilateral RAS predisposes to episodic catastrophic pulmonary oedema-often misdiagnosed as LVF until ACEI Rx causes rapid rise in S Cr • Renal function usually reverts to baseline on stopping ACEI • Small kidneys in Renal USS-strong indicator

  21. RAS-cont

  22. Rx in RAS • Ca channel blockers (dihydropyridines)-Rx of choice in RAS • Also indicated when ACE Is are not tolerated • Targeting BP lowering aggressive is more important than choice of Rx- ALHAT study

  23. Prescribing in CKD • Avoid NSAIDs, codeine • Withold ACEIs in hypovolaemic states-gastroenteritis etc • Antibiotics, digoxin, metformin etc – • ‘use with caution’ • (reduce dose or frequency)

  24. What about elderly patients with low eGFR- how should we manage them? • The guideline makes no age distinctions • BMJ2006;it is ageist not to Rx CKD just because someone is elderly. • BJGP editorial Dec2006;elderly with CKD still benefit from CV risk factor intervention and strict BP control in elderly slows rate of renal decline • Use clinical judgement & patient circumstances

  25. Key points….. • CKD patients have high risks of CV events & so CVD prevention should be fundamental to the management of CKD • Risk of ESRF is very low(ckd3-1.1%:24.3% CV death-5yr) • Best practice target BP is 130/80 with preferential use of ACEI / A2RB • Consider aspirin and statins • Life style advise & low protein diet • Consider Bisphosphonates & Ca for CKD assoc bone disease • ACEIs not necessary for all CKD pts

  26. Thank you-questions??? ‘The enemy of good is better’

More Related