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Red Flags in Renal Disease
Glomerular Diseases
(Nephritic/ Nephrotic Syndrome)
UTI
Acute VS Chronic Kidney Disease
Pediatric Nephrology 101
What Every Medical Student
Should Know
• Recognize Red Flags in Renal
Disease
• Understand the pahophysiology
of common pediatric renal
diseases
• Correlate and interpret the clinical
and laboratory findings
• Formulate a differential diagnosis
• Plan the appropriate management
• Recognize complications
associated with pediatric renal
disease as well as its prognosis
Red Flags in Renal Disease
Pediatric Nephrology 101
• - the passage of a larger
amount of urine than
normal
• daily urine output
exceeding 2L
in school-aged children
is unusual
• indicates decrease in
concentrating ability
• important to distinguish
polyuria from frequency
of micturition
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Pediatric Nephrology 101
Red Flags in Renal Disease
POLYURIA
• healthy neonate Is
oliguric for the first
2–3 days of life until
the onset of the
postnatal diuresis
• 92% - 1st 24 h of life
• Almost ALL in the
first 48 h
• Oliguria is defined a
urine output of less
than 500 ml/24 h/ 1.73
m2
• The most common
cause - intra- vascular
volume depletion
• Other Causes
• intrinsic
• obstructive
Red Flags in Renal Disease
Pediatric Nephrology 101
OLIGO/ANURIA
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DYSURIA
• Symptoms specific to
the urinary tract
• hematuria
• discharge
• malodorous urine
• frequency
• urgency
• refusal to void
• new-onset
nocturnal enuresis
• daytime
incontinence
• pain on urination
• inflammation, irritation,
or obstruction of the
urinary tract
• Associated with
• UTIs
• urethritis
• chemical or
traumatic irritation
• Possible Causes
• exposure to irritants
to the mucosal lining
of the urethra/bladder
• bladder bowel
dysfunction
• trauma
• sexually transmitted
infection
• A family history of
nephrolithiasis
Red Flags in Renal Disease
Pediatric Nephrology 101
HYPERTENSION
Flynn JT, Kaelber DC, Baker-Smith CM, et al.
Clinical practice guideline for screening and management of high blood pressure i
n children and adolescents. Pediatrics.
Red Flags in Renal Disease
Pediatric Nephrology 101
HYPERTENSION
Flynn JT, Kaelber DC, Baker-Smith CM, et al.
Clinical practice guideline for screening and management of high blood pressure i
n children and adolescents. Pediatrics.
Red Flags in Renal Disease
Pediatric Nephrology 101
• 1-5% prevalence in
children
• secondary to renal,
cardiovascular,
endocrine
• part of spectrum of
essential
hypertension
• 3 most common
symptoms
• headache, difficulty
sleeping and
tiredness
• routine BP screening
starting age 3 years
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+ Free plan
EDEMA
• a major clinical
manifestation of ECF
volume expansion
• Nephrotic Syndrome
• proteinuria
• hypoalbuminemia
• hyperlipidemia
• edema
first evident as swelling
of the periorbital region
more generalized
edema develops in a
gravity dependent
distribution
• Acute Nephritic
Syndrome / acute renal
impairment as a result
of failure of salt and
water excretion
• peripheral edema
• intravascular volume
expansion
• hypertension
• pulmonary edema
Red Flags in Renal Disease
Pediatric Nephrology 101
PALLOR
• Anemia is one of the most
common complications of
CKD during childhood
• K/DOQI Anemia
Management guidelines
defined anemia as a
hemoglobin value less than
11 gm/dl in pre-pubertal
patients with CKD
Red Flags in Renal Disease
Pediatric Nephrology 101
PROTEINURIA
Significant quantities of protein in the
urine will result in it becoming frothy.
• represents significant
renal disorder
• Dipstick analysis
followed by formal
quantification of
protein content
Red Flags in Renal Disease
Pediatric Nephrology 101
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HEMATURIA
• presence of RBCs in
urine
• Microscopic Hematuria
5 red blood cells
(RBCs)/mL of urine in a
counting chamber
or 2 RBCs/high-power
field (hpf) of urinary
sediment
• Chronic medical
problems,
multisystemic disease -
SLE, Wegener’s
granulomatosis,
Goodpasture syndrome
• History of trauma -
Bleeding in the Urinary
Tract
• Recent Throat/Skin
Infection - PSGN
• Presence/Family
history of hearing loss
- Alport’s Syndrome
• Presence of purpuric
rashes over the lower
extremities - HSP
• Hypertension - Acute
Nephritis
• History of fever, flank
pain, dysuria - UTI
Red Flags in Renal Disease
Pediatric Nephrology 101
Any symptom can be a presentation of
kidney disease
Complete History and PE is key
One should be familiar with the modes of
presentation of different renal conditions and
should have a high index of suspicion of renal
disease
Pediatric Nephrology 101
Red Flags in Renal Disease
Pediatric Nephrology
Lecture Series
Maria Dalla J. Dosado, MD
Bedside ROUNDS
BED1
4 year
old male
edema for 2
weeks frothy
urine
cough 1 week duration
Laboratorie
s Normal
CBC
Serum albumin 20mg/dL
Urinalysis protein +3, RBC3-5, WBC
4-5, bacteria few
Normal Protein Excretion
Avner, et al, Pediatric Nephrology 2007
DOI 10.1007/978-3-662-43596-0
Protein in Urinalysis
Urinalysis Protein
Trace <0.3g/dL
+1 <1g/dL
+2 1g-3g/dL
+3 3-20g/dL
+4 >20g/dL Avner, et al, Pediatric Nephrology 2007
DOI 10.1007/978-3-662-43596-0
T
ypes of Proteinuria
Glomerular proteinuria
increased filtration of protein across
the glomerular membrane
most commoncause of proteinuria in children
~glomerular disease
~other non-pathologic conditions such as
orthostatic proteinuria, fever, and excessive
exercise
Avner, et al, Pediatric Nephrology 2007
DOI 10.1007/978-3-662-43596-0
T
ypes of Proteinuria
T
ubular proteinuria
reduced reabsorption of freely filtered LMWProteins
Overflow proteinuria
due to increased levels of low molecular weight
proteins in the plasma
~ overwhelm tubular reabsorptive capacity
Avner, et al, Pediatric Nephrology 2007
DOI 10.1007/978-3-662-43596-0
Conditions with Proteinuria
Exercise
Fever
Orthostatic
Dehydration
Drugs
Chemotherap
y Heavy
metals
Antibiotics
Medical conditions
Hemolysis
Rhabdomyolysis
Multiple
myeloma
Amyloidosis
Kidney diseases
Glomerulonephritis
T
ubular diseases
Reflux
nephropathy
Diabetes Mellitus
Avner, et al, Pediatric Nephrology 2007
DOI 10.1007/978-3-662-43596-0
Patient A
DIAGNOSIS
UnderlyingAbnormality
in NEPHROTIC
SYNDROME
Increased permeability of the
glomerular capillary wall
• massive proteinuria
• hypoalbuminemia
UnderlyingAbnormality
in NEPHROTIC
SYNDROME
Podocyte
- epithelial cell
- foot processes
- slit diaphragms
- nephrin
- podocin
- CD2AP
- α-actinin 4
Podocyte Functions
• structural support of the
capillary loop
• major component of the
glomerular filltration
barrier to proteins
• involved in synthesis and
repair of the glomerular
basement membrane
UnderlyingAbnormality
in NEPHROTIC
SYNDROME Podocyte injury or genetic
mutations of genes produc-
ing podocyte proteins may
cause nephrotic-range
proteinuria
• foot process effacement of
the podocyte
• decrease in number of
functional podocytes
• altered slit diaphragm
integrity
increased protein “leakiness” across the glomerular capillary wall into the urinary space
Immune System
? contributes to the overall
pathogenesis of the nephrotic
syndrome
*MCNS occur after viral infections
*MCNS in children with HL and T cell lymphoma
*use of immunosupressive agents in cases of SRNS
Causes of Nephrotic Syndrome
Avner, et al, Pediatric Nephrology 2007
DOI 10.1007/978-3-662-43596-0
Nephrotic Syndrome
History
insidious onset of edema
progressing to frank anasarca
Decreased urine output
OtherSymptoms-diarrhea,abdominal
pain,poorappetite and irritability
Avner, et al, Pediatric Nephrology 2007
DOI 10.1007/978-3-662-43596-0
Nephrotic Syndrome
Clinical Consequences
• Edema
• Hyperlipidemia
• Increased susceptibility
to infections
• Hypercoagulability
Volume Expanded (Overfill)
( FeNa >0.2 , Urine K index >0.6 )
Volume Contracted (Underfill)
(FeNa<0.2, Urine K index
<0.6)
Avner, et al, Pediatric Nephrology 2007
DOI 10.1007/978-3-662-43596-0
Nephrotic Syndrome:Work Up
Low Serumalbumin
HighSerumCholesterol
CBC- Hemoconcentrated
KUBUTZ
- normalorenlargedkidneys
Urinalysis
- 3+ urineproteindipstick
- MicroscopicHematuria
Randomspoturine protein
- >2000 mg/g
(200mg/mmol)
24 hourtotal protein excretion
->40mg/m2/hr
Renal Biopsy
Avner et al, Pediatric Nephrology 2007
Management
cause
Anti-proteinuric agents
ImmunosuppreS
u
sp
sp
o
ir
ot
i
v
neTreatment
Antibiotics
prednisone or prednisolD
on
iue
retics
Dependass
o
i
n
n
g
u
l
n
e
d
d
e
a
r
l
i
y
l
y
i
n
d
g
o
s
eof 60 m
A
g
l
b
/
m
u
m
2
i
/
n
d
i
n
a
f
y
u
s
o
i
o
r
n
2 mg/kg/da
(A
yCE inhibitors, ARBs)
maximum of 60 mg daily for 4-6
wk Withdrawal of offending
agf
e
o
n
llt
o
s
wed by alternate-day prednisone
(starting at 40 mg/m2 qod or 1.5 mg/kg qod) for a period
ranging from 8 wk to 5 mo,with tapering of the dose
Avner et al, Pediatric Nephrology 2007
Management
Depends on underlying
cause
Antibiotics
A
lbum in infusion
Anti-proteinuric agents
ResponseSupportiveT
reatment
the attainment of remission withD
i
iu
nr
e
t
ti
c
hs
einitial 4
wk of corticosteroid therapy
Remissio
(
n
ACE inhibitors, ARBs)
Witu
hd
ri
rn
aw
ea
p
lr
o
o
fto
e
fi
fn
en:
dc
in
r
g
eatinine ratio of <0.2 or
<1+ p
r
o
a
t
e
g
i
e
n
n
t
o
s
n urine dipstick for 3 consecutive
days
Management
Referral to Nephrology
Frequent Relapsers
Steroid
Dependent
Steroid Resistant
Avner et al, Pediatric Nephrology 2007
Avner et al, Pediatric Nephrology 2007
Management
cause
agents
Antibiotics
Diuretics
Albumin infusion
Anti-proteinuric agents
(ACE inhibitors, ARBs)
Alternative Therapies to Corticosteroids in the Treatment of
Nephrotic Syndro
S
m
up
e
portiveTreatment
• C
D
y
e
c
p
l
e
o
n
p
d
h
o
s
s
o
p
n
h
a
u
m
n
d
i
d
e
e
r
l
y
i
n
g
• Calcineurin Inhibitors
•W
M
it
y
h
cd
or
p
a
h
w
en
a
o
llo
at
feoffending
• Rituximab
Bed 2
6yo
Male URTI 2 weeks prior to
consult
facial edema and dark colored urine
blood pressure = 120/80mm/Hg
Urinalysis = RBCTNTC/WBC8-10/ Protein +4
80% dysmorphic RBCon phase constrast microscopy
Diagnosis?
A.Acute Hemorrhagic Cystitis
B.Minimal Change Nephrotic Syndrome
C.Post Infectious Glomerulonephritis
D.UricAcid Urolithiasis
Clinical Approach to a
child with
Hematuria
Confirm the presence of hematuria
Differentiate glomerular from non-glomerular
causes
Detailed history and physical examination to
determine the underlying cause
Assess severity and associated complications
of the hematuria
HEMA
TURIA
Hematuria
presence of RBCs in urine
Microscopic Hematuria
5 red blood cells (RBCs)/mL of urine in a counting
chamber
or
2 RBCs/high-power field (hpf) of urinary sediment
Dela Cena, 2017 NKTI PNAA 5th Symposium
HISTORY & PE PROBABLE DISEASES
Recent throat infection,
skin infection
Post -Infectious Glomerulonephritis
Presence/Family history of hearing
loss
Presence of purpuric rashes over
the lower extremities
Hypertension
History of fever, flank pain, dysuria
Chronic medical problems,
multisystemic disease
History of trauma
Alport’s Syndrome
Henoch-Schonlein Purpura
Acute nephritis/ nephritic syndrome
UTI
SLE, Wegener’s granulomatosis,
Goodpasture syndrome
Bleeding in urinary tract
Causes of Hematuria
Dela Cena, 2017 NKTI PNAA 5th Symposium
Glomerular vs Non-
glomerular
Hematuria
•
•
Evaluation of hematuria in children.
Kevin E. C. MeyersPublished 2004 in
The Urologic clinics of North America
Acute Nephritic Syndrome
• glomerular hematuria
• hypertension
• edema
• moderate proteinuria
Hematuria &Acute
Nephritic
Syndrome
History
acute onset of edema and dark colored urine
*oliguria
Physical Examination
Hypertension due to fluid overload
Localized periorbital /facial edema
Hematuria &Acute
Nephritic
Syndrome
Pertinent Laboratory
• ** 5RBCs/HPF in the urine w/ CG casts
• Dysmorphic RBCs in phase contrast microscopy
• Non-Nephrotic Range Proteinuria
Hematuria &Acute
Nephritic
Syndrome
Complications
• Hypertensive Encephalopathy
• Congestive Heart Failure
• Acute Kidney Injury
• Rapidly Progressive Glomerulonephritis
Hematuria &Acute
Nephritic
Syndrome
-Differential Diagnosis-
Post Streptococcal Glomerulonephritis
IgA nephropathy
HSP Nephritis
Hematuria &Acute
Nephritic
Syndrome
Post Streptococcal Glomerulonephritis
immune complex mediated process for Group A Beta
Hemolytic Streptococcus
*gross hematuria ~2-4 weeks post respiratory or skin
infection
*low C3
*+ /-ASO/ Anti DNAse
Hematuria &Acute
Nephritic
Syndrome
Ig A Nephropathy
recurrent episodes of gross hematuria 1-2 days after a viral
respiratory infection or GI infection
*absent latent phase
*mesangial IgA deposits on renal biopsy
initially considered a benign condition
spontaneous remission in IgAN patients with minor glomerular abnormalities or focal mesangial
proliferation
20–50 % of adults would ultimately progress to end-stage
renal failure
Hematuria &Acute
Nephritic
Syndrome
Henoch Schonlein Purpura Nephritis
within 3 months of onset of a palpable rash, joint pains and
GI complaints
*Hallmark - HEMATURIA
** 8 0 % will manifest in 4 weeks
*** 9 5 % within 3 months
Management
Depends on underlying cause
Supportive (PSGN)
Fluid and salt limitation
Diuretics
Anti-hypertensive drugs
Immunosuppression
Nephrology Referral
Hematuria &Acute Nephritic
Syndrome:PSGN- Patient Follow Up
Gross Hematuria - 3 weeks
C3 - 2-3 months
Proteinuria - 3-6 months
Microscopic Hematuria - 1 year
Diagnosis
Post Infectious Glomerulonephritis
Glomerular Diseases in Childhood

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5: NEPHROLOGY-1.pdf

  • 1.
  • 2. Red Flags in Renal Disease Glomerular Diseases (Nephritic/ Nephrotic Syndrome) UTI Acute VS Chronic Kidney Disease Pediatric Nephrology 101 What Every Medical Student Should Know • Recognize Red Flags in Renal Disease • Understand the pahophysiology of common pediatric renal diseases • Correlate and interpret the clinical and laboratory findings • Formulate a differential diagnosis • Plan the appropriate management • Recognize complications associated with pediatric renal disease as well as its prognosis
  • 3. Red Flags in Renal Disease Pediatric Nephrology 101
  • 4. • - the passage of a larger amount of urine than normal • daily urine output exceeding 2L in school-aged children is unusual • indicates decrease in concentrating ability • important to distinguish polyuria from frequency of micturition Lorem ipsum dolor sit Dolor sit amet conscter pod Consectetur adipiscing Pediatric Nephrology 101 Red Flags in Renal Disease POLYURIA
  • 5. • healthy neonate Is oliguric for the first 2–3 days of life until the onset of the postnatal diuresis • 92% - 1st 24 h of life • Almost ALL in the first 48 h • Oliguria is defined a urine output of less than 500 ml/24 h/ 1.73 m2 • The most common cause - intra- vascular volume depletion • Other Causes • intrinsic • obstructive Red Flags in Renal Disease Pediatric Nephrology 101 OLIGO/ANURIA
  • 6. Lorem ipsum dolor sit Dol r pod Con or sit amet conscte sectetur adipiscing DYSURIA • Symptoms specific to the urinary tract • hematuria • discharge • malodorous urine • frequency • urgency • refusal to void • new-onset nocturnal enuresis • daytime incontinence • pain on urination • inflammation, irritation, or obstruction of the urinary tract • Associated with • UTIs • urethritis • chemical or traumatic irritation • Possible Causes • exposure to irritants to the mucosal lining of the urethra/bladder • bladder bowel dysfunction • trauma • sexually transmitted infection • A family history of nephrolithiasis Red Flags in Renal Disease Pediatric Nephrology 101
  • 7. HYPERTENSION Flynn JT, Kaelber DC, Baker-Smith CM, et al. Clinical practice guideline for screening and management of high blood pressure i n children and adolescents. Pediatrics. Red Flags in Renal Disease Pediatric Nephrology 101
  • 8. HYPERTENSION Flynn JT, Kaelber DC, Baker-Smith CM, et al. Clinical practice guideline for screening and management of high blood pressure i n children and adolescents. Pediatrics. Red Flags in Renal Disease Pediatric Nephrology 101 • 1-5% prevalence in children • secondary to renal, cardiovascular, endocrine • part of spectrum of essential hypertension • 3 most common symptoms • headache, difficulty sleeping and tiredness • routine BP screening starting age 3 years
  • 9. Lorem ipsum dolor Dolor sit amet cons mecter Consectetur adipis + Free plan EDEMA • a major clinical manifestation of ECF volume expansion • Nephrotic Syndrome • proteinuria • hypoalbuminemia • hyperlipidemia • edema first evident as swelling of the periorbital region more generalized edema develops in a gravity dependent distribution • Acute Nephritic Syndrome / acute renal impairment as a result of failure of salt and water excretion • peripheral edema • intravascular volume expansion • hypertension • pulmonary edema Red Flags in Renal Disease Pediatric Nephrology 101
  • 10. PALLOR • Anemia is one of the most common complications of CKD during childhood • K/DOQI Anemia Management guidelines defined anemia as a hemoglobin value less than 11 gm/dl in pre-pubertal patients with CKD Red Flags in Renal Disease Pediatric Nephrology 101
  • 11. PROTEINURIA Significant quantities of protein in the urine will result in it becoming frothy. • represents significant renal disorder • Dipstick analysis followed by formal quantification of protein content Red Flags in Renal Disease Pediatric Nephrology 101
  • 12. Lorem ipsum dolor sit Dolor sit amet conscter pod Consectetur adipiscing HEMATURIA • presence of RBCs in urine • Microscopic Hematuria 5 red blood cells (RBCs)/mL of urine in a counting chamber or 2 RBCs/high-power field (hpf) of urinary sediment • Chronic medical problems, multisystemic disease - SLE, Wegener’s granulomatosis, Goodpasture syndrome • History of trauma - Bleeding in the Urinary Tract • Recent Throat/Skin Infection - PSGN • Presence/Family history of hearing loss - Alport’s Syndrome • Presence of purpuric rashes over the lower extremities - HSP • Hypertension - Acute Nephritis • History of fever, flank pain, dysuria - UTI Red Flags in Renal Disease Pediatric Nephrology 101
  • 13. Any symptom can be a presentation of kidney disease Complete History and PE is key One should be familiar with the modes of presentation of different renal conditions and should have a high index of suspicion of renal disease Pediatric Nephrology 101 Red Flags in Renal Disease
  • 16. BED1 4 year old male edema for 2 weeks frothy urine cough 1 week duration Laboratorie s Normal CBC Serum albumin 20mg/dL Urinalysis protein +3, RBC3-5, WBC 4-5, bacteria few
  • 17. Normal Protein Excretion Avner, et al, Pediatric Nephrology 2007 DOI 10.1007/978-3-662-43596-0
  • 18. Protein in Urinalysis Urinalysis Protein Trace <0.3g/dL +1 <1g/dL +2 1g-3g/dL +3 3-20g/dL +4 >20g/dL Avner, et al, Pediatric Nephrology 2007 DOI 10.1007/978-3-662-43596-0
  • 19. T ypes of Proteinuria Glomerular proteinuria increased filtration of protein across the glomerular membrane most commoncause of proteinuria in children ~glomerular disease ~other non-pathologic conditions such as orthostatic proteinuria, fever, and excessive exercise Avner, et al, Pediatric Nephrology 2007 DOI 10.1007/978-3-662-43596-0
  • 20. T ypes of Proteinuria T ubular proteinuria reduced reabsorption of freely filtered LMWProteins Overflow proteinuria due to increased levels of low molecular weight proteins in the plasma ~ overwhelm tubular reabsorptive capacity Avner, et al, Pediatric Nephrology 2007 DOI 10.1007/978-3-662-43596-0
  • 21. Conditions with Proteinuria Exercise Fever Orthostatic Dehydration Drugs Chemotherap y Heavy metals Antibiotics Medical conditions Hemolysis Rhabdomyolysis Multiple myeloma Amyloidosis Kidney diseases Glomerulonephritis T ubular diseases Reflux nephropathy Diabetes Mellitus Avner, et al, Pediatric Nephrology 2007 DOI 10.1007/978-3-662-43596-0
  • 23. UnderlyingAbnormality in NEPHROTIC SYNDROME Increased permeability of the glomerular capillary wall • massive proteinuria • hypoalbuminemia
  • 24. UnderlyingAbnormality in NEPHROTIC SYNDROME Podocyte - epithelial cell - foot processes - slit diaphragms - nephrin - podocin - CD2AP - α-actinin 4 Podocyte Functions • structural support of the capillary loop • major component of the glomerular filltration barrier to proteins • involved in synthesis and repair of the glomerular basement membrane
  • 25. UnderlyingAbnormality in NEPHROTIC SYNDROME Podocyte injury or genetic mutations of genes produc- ing podocyte proteins may cause nephrotic-range proteinuria • foot process effacement of the podocyte • decrease in number of functional podocytes • altered slit diaphragm integrity increased protein “leakiness” across the glomerular capillary wall into the urinary space
  • 26. Immune System ? contributes to the overall pathogenesis of the nephrotic syndrome *MCNS occur after viral infections *MCNS in children with HL and T cell lymphoma *use of immunosupressive agents in cases of SRNS
  • 28.
  • 29. Avner, et al, Pediatric Nephrology 2007 DOI 10.1007/978-3-662-43596-0 Nephrotic Syndrome History insidious onset of edema progressing to frank anasarca Decreased urine output OtherSymptoms-diarrhea,abdominal pain,poorappetite and irritability
  • 30. Avner, et al, Pediatric Nephrology 2007 DOI 10.1007/978-3-662-43596-0 Nephrotic Syndrome Clinical Consequences • Edema • Hyperlipidemia • Increased susceptibility to infections • Hypercoagulability
  • 31. Volume Expanded (Overfill) ( FeNa >0.2 , Urine K index >0.6 ) Volume Contracted (Underfill) (FeNa<0.2, Urine K index <0.6)
  • 32. Avner, et al, Pediatric Nephrology 2007 DOI 10.1007/978-3-662-43596-0 Nephrotic Syndrome:Work Up Low Serumalbumin HighSerumCholesterol CBC- Hemoconcentrated KUBUTZ - normalorenlargedkidneys Urinalysis - 3+ urineproteindipstick - MicroscopicHematuria Randomspoturine protein - >2000 mg/g (200mg/mmol) 24 hourtotal protein excretion ->40mg/m2/hr Renal Biopsy
  • 33.
  • 34. Avner et al, Pediatric Nephrology 2007 Management cause Anti-proteinuric agents ImmunosuppreS u sp sp o ir ot i v neTreatment Antibiotics prednisone or prednisolD on iue retics Dependass o i n n g u l n e d d e a r l i y l y i n d g o s eof 60 m A g l b / m u m 2 i / n d i n a f y u s o i o r n 2 mg/kg/da (A yCE inhibitors, ARBs) maximum of 60 mg daily for 4-6 wk Withdrawal of offending agf e o n llt o s wed by alternate-day prednisone (starting at 40 mg/m2 qod or 1.5 mg/kg qod) for a period ranging from 8 wk to 5 mo,with tapering of the dose
  • 35. Avner et al, Pediatric Nephrology 2007 Management Depends on underlying cause Antibiotics A lbum in infusion Anti-proteinuric agents ResponseSupportiveT reatment the attainment of remission withD i iu nr e t ti c hs einitial 4 wk of corticosteroid therapy Remissio ( n ACE inhibitors, ARBs) Witu hd ri rn aw ea p lr o o fto e fi fn en: dc in r g eatinine ratio of <0.2 or <1+ p r o a t e g i e n n t o s n urine dipstick for 3 consecutive days
  • 36. Management Referral to Nephrology Frequent Relapsers Steroid Dependent Steroid Resistant Avner et al, Pediatric Nephrology 2007
  • 37. Avner et al, Pediatric Nephrology 2007 Management cause agents Antibiotics Diuretics Albumin infusion Anti-proteinuric agents (ACE inhibitors, ARBs) Alternative Therapies to Corticosteroids in the Treatment of Nephrotic Syndro S m up e portiveTreatment • C D y e c p l e o n p d h o s s o p n h a u m n d i d e e r l y i n g • Calcineurin Inhibitors •W M it y h cd or p a h w en a o llo at feoffending • Rituximab
  • 38.
  • 39. Bed 2 6yo Male URTI 2 weeks prior to consult facial edema and dark colored urine blood pressure = 120/80mm/Hg Urinalysis = RBCTNTC/WBC8-10/ Protein +4 80% dysmorphic RBCon phase constrast microscopy
  • 40. Diagnosis? A.Acute Hemorrhagic Cystitis B.Minimal Change Nephrotic Syndrome C.Post Infectious Glomerulonephritis D.UricAcid Urolithiasis
  • 41. Clinical Approach to a child with Hematuria Confirm the presence of hematuria Differentiate glomerular from non-glomerular causes Detailed history and physical examination to determine the underlying cause Assess severity and associated complications of the hematuria
  • 42. HEMA TURIA Hematuria presence of RBCs in urine Microscopic Hematuria 5 red blood cells (RBCs)/mL of urine in a counting chamber or 2 RBCs/high-power field (hpf) of urinary sediment
  • 43. Dela Cena, 2017 NKTI PNAA 5th Symposium
  • 44. HISTORY & PE PROBABLE DISEASES Recent throat infection, skin infection Post -Infectious Glomerulonephritis Presence/Family history of hearing loss Presence of purpuric rashes over the lower extremities Hypertension History of fever, flank pain, dysuria Chronic medical problems, multisystemic disease History of trauma Alport’s Syndrome Henoch-Schonlein Purpura Acute nephritis/ nephritic syndrome UTI SLE, Wegener’s granulomatosis, Goodpasture syndrome Bleeding in urinary tract Causes of Hematuria Dela Cena, 2017 NKTI PNAA 5th Symposium
  • 45. Glomerular vs Non- glomerular Hematuria • • Evaluation of hematuria in children. Kevin E. C. MeyersPublished 2004 in The Urologic clinics of North America
  • 46. Acute Nephritic Syndrome • glomerular hematuria • hypertension • edema • moderate proteinuria
  • 47. Hematuria &Acute Nephritic Syndrome History acute onset of edema and dark colored urine *oliguria Physical Examination Hypertension due to fluid overload Localized periorbital /facial edema
  • 48. Hematuria &Acute Nephritic Syndrome Pertinent Laboratory • ** 5RBCs/HPF in the urine w/ CG casts • Dysmorphic RBCs in phase contrast microscopy • Non-Nephrotic Range Proteinuria
  • 49. Hematuria &Acute Nephritic Syndrome Complications • Hypertensive Encephalopathy • Congestive Heart Failure • Acute Kidney Injury • Rapidly Progressive Glomerulonephritis
  • 50. Hematuria &Acute Nephritic Syndrome -Differential Diagnosis- Post Streptococcal Glomerulonephritis IgA nephropathy HSP Nephritis
  • 51. Hematuria &Acute Nephritic Syndrome Post Streptococcal Glomerulonephritis immune complex mediated process for Group A Beta Hemolytic Streptococcus *gross hematuria ~2-4 weeks post respiratory or skin infection *low C3 *+ /-ASO/ Anti DNAse
  • 52. Hematuria &Acute Nephritic Syndrome Ig A Nephropathy recurrent episodes of gross hematuria 1-2 days after a viral respiratory infection or GI infection *absent latent phase *mesangial IgA deposits on renal biopsy initially considered a benign condition spontaneous remission in IgAN patients with minor glomerular abnormalities or focal mesangial proliferation 20–50 % of adults would ultimately progress to end-stage renal failure
  • 53. Hematuria &Acute Nephritic Syndrome Henoch Schonlein Purpura Nephritis within 3 months of onset of a palpable rash, joint pains and GI complaints *Hallmark - HEMATURIA ** 8 0 % will manifest in 4 weeks *** 9 5 % within 3 months
  • 54. Management Depends on underlying cause Supportive (PSGN) Fluid and salt limitation Diuretics Anti-hypertensive drugs Immunosuppression Nephrology Referral
  • 55. Hematuria &Acute Nephritic Syndrome:PSGN- Patient Follow Up Gross Hematuria - 3 weeks C3 - 2-3 months Proteinuria - 3-6 months Microscopic Hematuria - 1 year