Introducing 

Prezi AI.

Your new presentation assistant.

Refine, enhance, and tailor your content, source relevant images, and edit visuals quicker than ever before.

Loading…
Transcript

CHRONIC KIDNEY DISEASE

CLINICAL PRACTICE GUIDELINES

PGI Horacio, Mel Patrick A.

Objectives

Topic

1. To define and classify Chronic Kidney disease

2. To identify and predict CKD progression

3. To discuss management of CKD based on CPG

Definition and Classification of CKD

topic

CKD is defined as abnormalities of kidney structure or function, present for >3 months, with implications for health

Criteria for CKD (either of the following present for >3 months)

criteria

Markers of kidney damage (one or more)

  • Albuminuria (AER >/=30mg/24hrs)
  • Urine sediment abnormalities
  • Electrolyte and other abnormalities due to tubular disorders
  • Pathologic abnormalities
  • Structural abnormalities detected by imaging
  • History of kidney transplant

Decreased GFR

  • GFR <60ml/min/1.73m2

Staging of CKD

  • Classified based on cause, GFR category, and albuminuria category (CGA)
  • Assign cause of CKD based on presence or absence of systemic disease and the location within the kidney
  • Assign

GFR categories

GFR categories

Albuminuria categories

Prognosis

Pathophysiology of CKD

Pathophysio

of CKD

Mechanisms of kidney damage:

1. Initiating mechanism specific to an underlying etiology

  • Abnormalities in kidney development
  • Immune complex deposition
  • Glomerulonephritis
  • Toxin exposure

2. Set of progressive mechanism

  • Hyperfiltration and hypertrophy of viable nephrons

Topic

Topic

Topic

Cockcroft-Gault Formula (Creatinine Clearance)

CrCl (male)= [(140-age) x weight in kg]/ (serum creatine x 72)

CrCl (female)= CrCl (male) x 0.85

Topic

Management of progression and complications of CKD

Topic

Prevention of CKD progression

  • BP and RAAS interruption
  • CKD and risk of AKI
  • Protein intake
  • Glycemic control
  • Salt intake
  • Hyperuricemea
  • lifestyle
  • diet

BP and RAAS interruption

Topic

1. Individualize BP targets and agents according to age, coexistent cardiovascular disease and other comorbidities,

risk of progression of CKD.

2. Inquire about postural dizziness and check for postural hypotension regularly when treating CKD patients with BP-lowering drugs.

3. Tailor BP treatment regimens in elderly patients with CKD by carefully considering age, comorbidities and

other therapies, with gradual escalation of treatment and close attention

  • electrolyte disorders,
  • acute deterioration in kidney function
  • orthostatic hypotension and
  • drug side effects.

4. both diabetic and non-diabetic adults with CKD and with urine albumin excretion of

>/=30 mg/24 hours whose BP is consistently

>140 mm Hg systolic or >90 mm Hg

  • maintain a BP that is consistently <140 mm Hg systolic and <90 mm Hg diastolic.

5. both diabetic and non-diabetic adults with CKD and with urine albumin excretion of

>/=30 mg/24 hours (or equivalent*) whose office BP is consistently

  • >130 mm Hg systolic or >80 mm Hg

diastolic maintain

  • <130 mm Hg systolic and <80 mm Hg diastolic.

6. ARB or ACE-I be used in diabetic adults with CKD and urine albumin excretion 30–300 mg/

24 hours.

7. recommended that an ARB or ACE-I be used in both diabetic and non-diabetic adults with CKD and urine

albumin excretion >/=300 mg/24 hours

8. There is insufficient evidence to recommend combining an ACE-I with ARBs to prevent progression of CKD.

Protein intake

Topic

1. lowering protein intake to 0.8 g/kg/day in adults with diabetes or without diabetes and

GFR <30 ml/min/1.73 m2 (G4-G5), with appropriate education.

2. avoiding high protein intake (41.3 g/kg/day) in adults with CKD at risk of progression.

Topic

Glycemic control

1. a target hemoglobin A1c (HbA1c) of 7.0% (53 mmol/mol) to prevent or delay progression of the microvascular complications of diabetes, including diabetic kidney disease.

2. not to treat an HbA1c target of <7.0% (<53 mmol/mol) in patients at risk of hypoglycemia.

4. In people with CKD and diabetes, glycemic control should be part of a multifactorial intervention strategy

  • addressing blood pressure control
  • cardiovascular risk

promoting the use of ACEi or ARBs, statins, and antiplatelet therapy.

Salt intake

lowering salt intake to <90 mmol (<2 g) per day of sodium (corresponding to 5g of sodium chloride) in adults, unless contraindicated.

Topic

1. restriction of sodium intake for children with CKD who have hypertension or prehypertension

2. supplemental free water and sodium supplements for children with CKD and polyuria to avoid chronic intravascular depletion and to promote optimal growth.

Hyperuricemia

Topic

There is insufficient evidence to support or refute the use of agents to lower serum uric acid concentrations in people with CKD and either symptomatic or asymptomatic hyperuricemia in order to delay progression of CKD.

Lifestyle

Topic

people with CKD be encouraged to undertake physical activity compatible with cardiovascular health and tolerance (aiming for at least 30 minutes 5 times per week), achieve a healthy weight (BMI 20 to 25), and stop smoking.

Additional dietary advice

Topic

individuals with CKD

  • receive expert dietary advice
  • education program, tailored to severity of CKD
  • the need to intervene on salt, phosphate, potassium, and protein intake.

COMPLICATIONS ASSOCIATED WITH LOSS OF KIDNEY FUNCTION

  • Identification of anemia in CKD

  • Evaluation of anemia in people with CKD

Topic

Identification of anemia in CKD

Topic

1. Diagnose anemia in adults and children >15 years with CKD when the Hb concentration is <13.0 g/dl in males and <12.0 g/dl in females.

2. Diagnose anemia in children with CKD if Hb concentration is

  • <11.0 g/dl in children 0.5–5 years,
  • <11.5 g/dl in children 5–12 years,
  • <12.0 g/dl in children 12-15 years.

Evaluation of anemia in people with CKD

Topic

To identify anemia in people with CKD measure Hb concentration

  • when clinically indicated in people with GFR >/=60 (G1-G2)
  • at least annually in people with GFR 30–59 (G3a-G3b)
  • at least twice per year in people with GFR <30 (G4-G5).

CKD METABOLIC BONE DISEASE INCLUDING LABORATORY ABNORMALITIES

Topic

1. measure serum levels of calcium, phosphate, PTH, and alkaline phosphatase activity at least

once in adults with GFR <45 (G3b-G5) to determine

  • baseline values
  • inform prediction equations

2. not to perform bone mineral density testing routinely in those with eGFR <45

(G3b-G5), as information may be misleading or unhelpful.

3. In people with GFR <45 (G3b-G5), we suggest maintaining serum phosphate

concentrations in the normal range.

4. In people with GFR <45 (G3b-G5) the optimal PTH level is not known.

  • first evaluated for hyperphosphatemia, hypocalcemia, and vitamin D deficiency.

Topic

Vitamin D supplementation and bisphosphonates in people with CKD

1. not to routinely prescribe vitamin D supplements or vitamin D analogs, in the absence of suspected or

documented deficiency, to suppress elevated PTH concentrations in people with CKD not on dialysis.

2. not to prescribe bisphosphonate treatment in people with GFR <30 (G4-G5) without a strong clinical rationale.

ACIDOSIS

people with CKD and serum bicarbonate concentrations <22 mmol/l treatment with oral

bicarbonate supplementation be given to maintain within the normal range, unless contraindicated.

Topic

Learn more about creating dynamic, engaging presentations with Prezi