Acute renal failure(ARF)
? Is the clinical syndrome in which sudden decreasing in renal function result in inability of kidney to maintain fluid and electrolyte homeostasis, 2-3% in children, 8% in neonatal ICU.
? Causes
? A-prerenal causes
1- dehydration
? 2- hemorrhage
? 3- hypoalbunimia
? 4- heart failure
?
B- intrinsic causes , glomeruler diseases 1- post infectious GN
? 2- lupus GN, HSP,
? 3- HUS
? 4- acute tubuler necrosis
? 5- RVT
?
C- post renal 1- posterior urethral valve
? 2- uretro-pelvic junction obstruction
? 3- stone, neurogenic bladder
C/F
? - vomiting, diarrhea 3 days prerenal
? - 6 years child with recent pharangitis+edema+HT=PSGN
? - critical ill child with protracted HT and HX of exposure to nephrotoxin ATN
? - neonate with hydronephrosis in prenatal U/S congenital P UJ obstruction.
?
Physical examination
? - volume status, tachycardia, dry mouth, poor peripheral circulation, prerenal cause
? - peripheral edema, basal creptation, gallop rythem, suggest GN, ATN
? - rash +nephritis=SLE, HSP
Laboratory finding
? anemia due to 1- hemolytic(SLE, RVT, HUS)
? 2- delutional
?
leucopenia(SLE)
? - thrombocytopenia((SLE, RVT, HUS)
? - hyponatremia(delutional)
? -metabolic acidosis
? -BUN, S.Cre increase
? -uric acid , K+, Ph++, increase
? - CA++ low
? - C3 level low in(SLE, PSGN, radiation GN, membarenoprolefrative)
? - Abs in PSGN
? -GUA 1- RBC, protienurea, granuler cast, internsic cause
? 2- WBC, WBC cast, low grade protienurea, RBC, tubulointerstesial disease
urinary indices may be useful in differentiation of pre renal and internsic ARF
? Intrinsic Indices Pre renal
? Sp.gravity >1.020 <1.010
? Ur.osmolality >500 <350
? Ur.NA+(Mag/L) <20 >40
? FENA+ <1 >2
? BUN/S.cre >20 <20
? FENA+=Una X Pcre/P na X Ucre
?
CXR cardiomegaly, pulmonary edema.
? - Renal U/S hydronephrosis, hydroureter, obstruction
? - Renal biopsy may needed
.
Treatment
?
1- infant and children with obstruction or non ambulatory child bladder catheter, to collect UOP
?
- fluid therapy according to volume status
? A- in case of Hypovolemia, N/S 20 CC/kg within 30 min may be repeted 2 or 3 times and watch the UOP in 2 hour , if no possible of internsic or post renal.
? Diuretics indicated provided that good volume status Frusamide 2-4 mg/kg+MANITOL 0.5g/kg , if no UOP within 30 min , consider diuretic infution , if no UOP, consider Dopamin 2-3Mig/kg/min with diuretic , if no UOP, stop diuretic and fluid should be restricted.
?
B-in case of normal volemia consider(insensible water loss) 400 cc/m2 /day + the fluid equal to the UOP.
? C- in case of Hypervolemia insensible water loss and UOP should be omitted.
? Type of the fluid is glucose-containing solution 10-30% as maintaince .
? Input, output, UOP, chemistry sh be checked daily.
? 3- Hyperkalemia >6mg/dl may lead to cardiac arrythemia (ECG=tent T wave , widing QRS, ST depression, and arrest).
? Indication of withholding of K+(fluid, diet)+Resin 1g/kg orally or rectally by enema every 2-4 hour.
? If >7mg/dl give the flowing
? 1- Ca.gluconate 10% 1cc/kg within 3-5min
? 2- NACO3 1-2cc/kg over 5-10min
? 3- Reguler insulin 0.1U/kg with glucose 50% 1cc/kg over 1hour.
? If inspite of all these measure , still persistent hyperkalemia consider dialysis
.
? 4- Acidosis if mild rarely need treatment , if sever PH <7.15 NAHCO3 <8 with hyperkalemia need NAHCO3 infusion (desire PH 7.2, NAHCO3 12)
.
? 5- Hypocalcemia primarily treated by lowering S.PH++ , and Ca++ sh be not given I-V unless with tetany to ovoid Ca . deposition in tissue, use Ca. carbonate 1-3 tab with meal
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? 6- Hyponatremia delutional need fluid restriction , if <120 or symptomatic(seizure, lethargy )need 3%NACL .
? NACL in m.ag required=0.6XBwt X (125- s.NA)
? 7- Bleeding due to platelet dysfunction, stress, heparin(dialysis), need oral or I.V H2 blocker ranitidine
? 8- HT in GN, HUS, need salt and water restriction, Nefidipine 0,25-0,5mg/kg every 2-6hour(max 10mg), B.blocker,long acting Ca.cannel blocker., if sever crisis need NA nitropruside or Labetalol infusion
.
? 9- Anemia mild, delutional , packed RBC, 10 cc/kg within 4-6hour if Hb <7g/dl(better fresh)
? 10- nutrition NA, PH, K, should be restricted in most cases, protein should be moderately decrease, increase calorie intake
.
11- Dialysis indicated in
? a-volume over load +evidence of HT, and /or pulmonary edema refractory to treatment
? b- persistent hyperkalemia
? c- sever acidosis unresponsive to treatment
? d- neurological symptoms(alter mental state , seizure)
? e- BUN >100-150mg/dl or lower if rapidly rising.
? f- Ca/Ph imbalance with hypocalcemia tetany .
? g- inability to provide adequate nutritional intake because of need for sever fluid restriction.
Chronic kidney disease(CKD)
? is defined as either renal injury (proteinuria) and/or a glomerular filtration rate <60 mL/min/1.73 m2 for <3 mo..
? GFR (ml/min/1.73m²)= K x height(cm)/S.Cre(mg/dl)
? K =0.33 for LBW infant<1year
? K =0.45 for infant <1year
? K =0.55 for child and adolescent female
? K =0.7 for adolescent male
? Mild CRF= GFR 50-75 ml/min/1.73m²
? Moderate GRF= GFR 25-50 ml/min/1.73m²
? Severe GRF= GFR 10-25 ml/min/1.73m²
? End stage renal disease (ESRD)= <10 ml/min/1.73m²
- Standardized Terminology for Stages of Chronic Kidney Disease
? -STAGE DESCRIPTION GFR (mL/min/1.73 m2) Stage 1 Kidney damage with normal or increased GFR >90
? Stage 2 Kidney damage with mild decrease in GFR 60–89
? Stage 3 Moderate decrease in GFR 30–59
? Stage 4 Severe decrease in GFR 5–29
? Stage 5 Kidney failure <15 or on dialysis
? End-stage renal disease (ESRD) is an administrative term in the USA, defining all patients treated with dialysis or kidney transplantation. Patients with ESRD are a subset of the patients with Stage 5 CKD
Etiology
? 1- congenital most common in <5 year of age (renal dysplesia, obstreuctive uropathy)
? 2- acquired various glomeruler disease
? 3- inherited Alpert syndrome , both are more common >than 5year of age
? 4- metabolic cystenosis
Pathogenesis
? Many factors play role
? 1- hyperfilteration theory
? 2- persistent proteiurea
? 3- systemic arterial renal hypertention
? 4- renal calcium-phosphrous deposition
? 5- hyperlipidemia
C/F mechanism
? -acidosis 1- impair HCO3 absorption
? 2- ?net acid excretion
? - ? nitrogeniuos products ?? GFR
? - NA+ retention 1- ? rennin
? 2- oliqurea
? - NA+ wasting 1- solute diuresis
? 2- tubuler damage
? - Hyperkalemia 1- ? GFR
? 2- acidosis
? 3- ? K intake
? - Renal osteodystrophy 1- impair renal production of active D3
? 2- hyper ph++
? 3- secondary hyperparathyroidism
? 4- inadequate caloric intake --
? - Growth retardation 1- renal ostiodystrophy
? 2- metabolic acidosis
? 3- anemia,
? 4- growth H resistence
? - Anemia 1- ? erythropioten production
? 2- iron, folate, B12 ??
? 3- ?? RBC survival
? - Bleeding tendency 1- platelet dysfunction
? - Infection 1- granulocyte dysfunction
? 2- cellular immunity dysfunction
? - Neurological symptoms 1- uremic toxin
? 2- aluminum toxicity
? 3- HT
? - HT 1- volume overload
? 2- excess rennin
? - Pericarditis 1- HT
? 2- fluid over load
Lab Finding
? Hyper K+, hypoNA+, acidosis, hypoCA++, hyperph++, hyperurecimia.
? GUA protienurea
? CBC, normochromic normocytic anemia
Treatment
? 1- fluid therapy and electrolyte management
? Most patient have normal NA+ and water balance
? Renal dysplesia significant NA+ loss, so we give benefit of higher volume , low caloric density feedung with NA+ supplementation.
? In HT, NA+ resterction, +diuretic therapy
? Hyperkalemia, treated by Resin, alkanizing agent, and no K+ in diet
? 2- Acidosis
? either Bicitra((1 mq NA+ citrate or NA+ Bicorbonate9680 mq equal 8mq base to maintain S.HCO3 22mq/l
? 3- Nutrition
? PH++, K+, NA+, should be restricted according to patient lab finding and fluid balance, Similac formula can be used(low PH++)
? Calorie according to age recommendation
? Protein, should be 2.5g/kg/day , with high biological value(to soluble aminoacid rather than nitrogenious substance)(egg, milk, meat, and fish)
? Water soluble vitamin (Nephrocap), zinc and iron are needed, while fat soluble vitamin is not.
? 4- Growth
? Recombinant human GH, 0,05mg/kg/day s.c to achieve normal height velocity for age with periodic assessment give until
? A- reach 50th centile of midparental HT
? B- final adult HT
? C- undergo renal transplant
? 5- Renal ostiodystrophy
? Indicate spectrum of bone disorder seen in patient with CRF, , high bone turnover with secondary hyperparathyroidism and skeletal pathological finding is a Ostitis Fibrosa Cystica , occur when GFR <50% of normal,
? ?? active D3 ???? in intestinal CA++ absorption?hypoCA++???parath H?? bone resorption ??CA++ level
? When GFR < TO 20-25% of normal , PH++ excretion decrease ?hyperph++ and lead to hypoCA++ and ?parath H
? C/F
? Muscle weakness, bone pain, fracture with minor trauma
? Ricketic chnges
? Lab finding, ?S.Ca,?S.ph, ? AKP, normal or ?parath H
? X.rays widing of metaphyseal space , subperiostial resorption.
? Treatment 1- low ph diet(similac formula)
? 2-Ca.carbonate or acetate (ph. Binder agent), site effect is hypercalcemia, now we use non-ph. Binder agent
? 3- most important is Vit D indicated in
? A- renal ostiodystrophy with PTH >than 3 times its level
? B- persistent hypoCa , inspite of ??S.ph
? Dose is 0.01-0.05Mg/kg/day
? Calciterol (one ?.cap or drop)
? Many nephrologists recommends to maintain Ca/Ph, Ca x Po4 less than 55 to decrease the possibility of Ca.Ph salt deposition.
? 6- Anemia
? Desired Hb level is 11-12 g/dl
? Use of Erythropoietin 50-150mg/kg/dose s.c one to 3 times /week when Hb <10g/dl
? With use of Erythropoietin , give iron oral or i.v
? 7- HT
? Volume over load diuretics
? Excessive rennin ACE inhibitors , Angio II blocker (Lasartan) , effective in lowering of HT
? 8-Immunization
? MMR, Varecella , should be given before transplantation
? Influenza vaccine should be given annually.
? Flow up
? Hb, S.electrolyte, BUN, S.Cre, Ca, Ph, AKP, , PTH, X.rays of bo