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Pediatric Chronic kidney disease

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Page 1: Pediatric Chronic kidney disease

DEEPSHIKHA

2ND YR PGT

ICH, KOLKATA

CHRONIC KIDNEY DISEASE

Page 2: Pediatric Chronic kidney disease

DEFINITIONStructural 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

Page 3: Pediatric Chronic kidney disease

CLASSIFICATION (KDIGO 2012)

CGA Classification:

1. CAUSE

2. GFR

3. ALBUMINURIA

Page 4: Pediatric Chronic kidney disease

CLASSIFICATION (KDIGO

2012)

Page 5: Pediatric Chronic kidney disease

CAUSES < 5 year old

1. CONGENITAL ANOMALIES- Renal hypoplasia, dysplasia, congenital nephrotic syndrome, prune belly syndrome, PCKD, RVT, cortical necrosis

2. OBSTRUCTIVE UROPATHY- PUV, PUJ obstruction3. HUS

> 5 year old1. Acquired- GLOMERULONEPHRITIS2. Inherited- Juvenile nephronophthisis, Alport syndrome

All age groups1. METABOLIC DISORDERS- cystinosis, hyperoxaluria2. Inherited- Polycystic kidney disease

Page 6: Pediatric Chronic kidney disease

PATHOGENESIS

HYPERFILTRATION INJURY

PROTEINURIA

HYPERTENSION

HYPERPHOSPHATEMIA

Page 7: Pediatric Chronic kidney disease

COMPLICATIONS

GROWTH RETARDATION

a. Malnutrition, anemia

b. Metabolic acidosis

c. Bone disease

d. Resistance to growth hormone

e. Reduced levels of sex hormones

ANEMIA

a. Lack of erythropoietin

b. Uremia

c. Iron and folate deficiency

d. Hyperparathyroidism causing myelofibrosis

Page 8: Pediatric Chronic kidney disease

COMPLICATIONS

MINERAL & BONE DISORDER (CKD-MBD)

a. Decreased production of 1,25 DHD3

b. Reduced excretion of Phosphorus

c. Stimulation of PTH

d. Adynamic lesions

e. Metabolic acidosis

METABOLIC ACIDOSIS

HYPERKALEMIA

NEUROLOGICAL ABNORMALITIES-

Encephalopathy, hypotonia, truncal ataxia,

peripheral neuropathy

Page 9: Pediatric Chronic kidney disease

COMPLICATIONS

HYPERTENSION

HYPERLIPIDEMIA

INFECTIONS

BLEEDING TENDENCY

GLUCOSE INTOLERANCE

PERICARDITIS, LEFT VENTRICULAR

DYSFUNCTION

Page 10: Pediatric Chronic kidney disease

PRESENTATION

7yr old, female

Wt- 12 kgs, Ht- 94 cm

H/O intermittent fever - 1 & ½ months

Progressive respiratory distress - 5 days

Irritability with episodes of drowsiness - 1 day

No past h/o polyuria, oliguria, reddish urine, swelling of

body

O/E: Drowsy, Pallor ++, Oedema-nil

HR- 120/min, BP- 143/92, S1S2-N, No murmur

RR- 62/min, shallow breaths, B/L air entry-N

P/A- Hepatosplenomegaly, no renal mass, no fluid

Page 11: Pediatric Chronic kidney disease

PRESENTATION

TLC- 26000, HB- 3.8 g/dl, Platelet- 1.91 lacs

U- 329 mg/dl, Cr- 6.65 mg/dl

Na- 126, K- 3.7, Ca- 6.1, P- 9.6, ALP- 98, CRP- 2.7

Venous blood gas:

pH = 7.04

HCO3= 2.2

PCO2 = 8.4

BE = -26

Urine- 6-8 pus cells, 10-12 RBCs, 1+ albuminuria

PTH- 1074 pg, Vit D- 8.86 ng/ml

Page 12: Pediatric Chronic kidney disease

DIAGNOSIS INITIAL TESTS

CAUSE?Ultrasonography, MRIRadionuclide studiesRenal biopsy- histological study

GFR?Modified Schwartz formula:

ALBUMINURIA?PCR, ACR24 Hr urinary protein

GFR = K * Height (in cm)

Serum creatinine (mg/dl)

K= 0.413

Page 13: Pediatric Chronic kidney disease

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

NormalIncreased

risk

Kidney

failureDamage GFR

Page 14: Pediatric Chronic kidney disease

RISK FACTORS FOR CKD

VUR with recurrent UTI and renal scarring

Obstructive uropathy

Past H/O acute nephritis, nephrotic syndrome, HSP

H/O renal failure in perinatal period

Family H/O kidney disease

Renal dysplasia or hypoplasia

Low birth weight infants

Diabetes, hypertension

SLE, vasculitis

Page 15: Pediatric Chronic kidney disease

SLOWING PROGRESSION OF

CKD Risk factors for progression of CKD:

1. HYPERTENSION

2. PROTEINURIA

Target BP to be kept below 50th percentile, both systolic and diastolic.

Treatment to be started when BP is consistently> 90th

centile

Target proteinuria <300 mg/ m2 /day @ at least 1g/day

Drug of choice: ACE inhibitors or ARBs

Dietary protein restriction- not recommended in children

Control of hyperlipidemia (no data in children)

Vitamin D analogs, Erythropoietin

Page 16: Pediatric Chronic kidney disease

LONG TERM MANAGEMENT NUTRITIONAL MODIFICATIONS:

1. Supply RDA in normal children, 125% RDA in malnourished

2. 55-60% carbohydrates, 30% fat, 10% proteins

3. In top fed infants, use special formulae with high calorie, low

Sodium and Phosphorus

4. Use high biological value proteins, supplement extra

0.4g/kg/day children on haemodialysis and 0.8 on peritoneal

dialysis

5. If dyslipidemia present, restrict fats to <10%

6. Supplement vitamins to maintain RDA, extra if on dialysis

7. Restrict dietary phosphorus to 80-100% RDA

8. Restrict salt intake to 0.8-1g/day in hypertensive

Page 17: Pediatric Chronic kidney disease

LONG TERM MANAGEMENT

TREATMENT FOR GROWTH FAILURE:

Assesment of growth every 6 months in CKD children,

1-3 monthly in children with polyuria, severe

malnutrition, growth failure and on dialysis

Recombinant Human Growth Hormone therapy

0.05mg/kg/day (30IU/ m2 /week) S/C daily

Look for side effects- hyperglycemia, worsened MBD,

Pseudotumor cerebri

TREATMENT OF ACIDOSIS

Maintain serum HCO3 level of 20-22meq/l

Oral bicarbonate supplement @ 2-3meq/kg if level

falls below15meq/l

Page 18: Pediatric Chronic kidney disease

LONG TERM MANAGEMENT

MANAGING MINERAL BONE DISEASE:

Annual monitoring of serum Ca, P, and PTH in CKD stage2

onwards, 3-6 monthly in advanced disease

Step 1- normalise Phosphate level by dietary restriction (800-

1000mmg/day), Calcium carbonate or acetate (P binder) 30-

60mg/day

In case of hypercalcemia, Aluminium hydroxide or Sevelamer

hydrochloride to be used as binder

Document Vitamin D deficiency, and then give therapeutic dose

plus maintenance

Vitamin D analogs to be used in stage 5 CKD, persistent high

PTH with normal Ca and Phosphorus

Orthopaedic interventions

Page 19: Pediatric Chronic kidney disease

LONG TERM MANAGEMENT

EVALUATION & TREATMENT OF ANEMIA:

Check Hb% when clinically indicated in early CKD,

annuallly in stage G3, semiannually in GFR<30 patients

Above stage 3, routine supplementation of Iron & Folic

Acid

Evaluate for iron deficiency if anemic, start oral iron 2-6

mg/kg/day

Patient on haemodialysis- IV iron 1-2mg/kg/week

In refractory cases, start Erythropoietin @30-

300U/kg/week followed by 60-600U/kg/week maintenance

Do not exceed Hb > 13g/dl

Page 20: Pediatric Chronic kidney disease

LONG TERM MANAGEMENT

Treat AKI precipitating factors urgently

Treat intercurrent infections promptly using

antibiotics in renal doses, avoiding nephrotoxic

drugs

Immunisation- HepB, pneumococcal vaccines,

annual influenza vaccines. *Live vaccines

contraindicated after transplant

Renal replacement therapy- Peritoneal dialysis or

haemodialysis

Renal transplant

Page 21: Pediatric Chronic kidney disease

…Back to case GFR= 0.413* 94cm / 6.6 = 5.88ml/min/1.73 m2

USG – B/L bright heterogenous kidney

TREATMENT:

IVF adjusted to urine output

Calcium correction

Acidosis correction with Bicarbonate

PRBC transfusion

Antihypertensive- amlodipine

Haemodialysis- 5 cycles

Advised for renal transplant

Renal biopsy done- report pending

Discharged with oral Calcium, Vit D, Stamlo, Iron, Multivitamin, advice of intermittent haemodialysis and later renal transplant

Page 22: Pediatric Chronic kidney disease

THANKYOU