NEPHROTIC SYNDROME
PREPARED BY:
PRAJNA SUBEDI
B.SC.NSG 4TH YR
6TH BATCH
INTRODUCTION:
Nephrotic syndrome is a group of symptoms which is
seen in any condition that seriously damages the
glomerular capillary membrane , causing increased
glomerular permeability with loss of protein in urine.
DEFINITION:
Nephrotic syndrome is a group of symptoms
characterized by proteinuria ( > 3.5 grams per
day), low blood protein levels , high cholesterol
levels , and edema.
INCIDENCE:
 All ages can be affected.
 Most common during 2 to 6 years.
 Affects male more than female.
CAUSES:
 Autoimmune diseases such as systemic lupus
erythematosus.
 Diabetes Mellitus
 Hypertension
 Drug toxicity : excessive use of NSAIDS
 Malaria , hepatitis infection etc.
Types:
• 90% of cases
Primary /
Idiopathic
Nephrotic
syndrome
• 10% of cases
Secondary
Nephrotic
Syndrome
• Serious and rare
Congenital
Nephrotic
syndrome
Primary / Idiopathic Nephrotic
syndrome:
 Most common in children.
 Exact cause is unknown but are mainly associated
with autoimmune cause.
 It is also known as minimal change disease : This
disorder results in abnormal kidney function , but
when the kidney tissue is examined under a
microscope , it appears normal , or nearly normal.
Secondary Nephrotic Syndrome:
 Causes may be various disorders that can damage
the glomerulus of the kidneys.
 Diseases such as Diabetes Mellitus , Hypertension ,
Systemic Lupus Erythematosus and other
infections might be the cause.
Congenital Nephrotic Syndrome:
It is serious and rare condition caused by
autosomal recessive disorder.
No therapies are effective usually.
Infants die under 1 or 2 years of age.
PATHOPHISIOLOGY:
The glomerular basement membrane is
negatively charged layer .
Due to antibody attack or other causes , this
property is lost which allows proteins
especially albumin to pass through
glomerular membrane.
CLINICAL FEATURES:
 Excessive weight gain , edema – peri-orbital
initially , then in extremities , increases in the
morning.
 Ascites , scrotal/labial swelling may be present.
 Urine changes ;
 decreased volume
 Frothy and pallor
 Edema of intestinal mucosa may lesd to loss of
appetite , poor intestinal absorption.
Contd..
 Fatigue , lethargic, irritability.
 Blood pressure may be normal or slightly
decreased due to decreased intravascular volum
 Susceptibility to infection increases
 Dyspnea may be seen due to pleural effusion ,
ascites and other type of fluid.
DIAGNOSIS:
• Family history
• Birth history
• Antenatal history
HISTORY TAKING:
• Edema can be seen
PHYSICAL EXAMINATION:
• Urinalysis
• Serum tests
• Hematology
• Kidney biopsy
• KUB X-ray
• USG
INVESTIGATIONS:
INVESTIGATION AND FINDINGS:
 Urinalysis:
 Shows marked proteinuria , cast ,few RBCs ,
increased urine specific gravity
 24 hrs urinary protein excretion : >50 mg/kg/day
 Serum:
 Markedly decreased serum protein (albumin)
 High cholesterol (450-1500 mg/dl)
 Hyponatremia
CONTD:
 Hematology:
 Normal or increased hemoglobin level
 High platelet count
 Kidney biopsy
 Done if there is recurrent relapses , non responsive
to treatment
COMPLICATIONS:
Blood clots / venous thrombosis
Poor nutrition
High blood pressure
Acute kidney failure
Chronic kidney failure
Infections
TREATMENT:
Goals of management:
 Reduce urinary protein excretion.
 Reduce fluid retention.
 Prevent infections and complications.
Pharmacological treatment:
 Diuretics : Frusemide , spironolactone
 Corticosteroids : Prednisolone
 Albumin Infusion :
 Immune suppressant therapy : For child who
continue to have proteinuria (+2 or more) after 8
weeks of steroid therapy are treated with immune
suppresant therapy such as cyclophosphamide.
Nursing managements:
 Monitor edema urine characteristics , albumin , I/O
, abdominal girth , daily weight , etc.
 Administer medications such as diuretics ,
antibiotics and corticosteroid as ordered.
 Improve nutritional status.
• Low sodium diet
• High calorie and high protein diet
• Small and frequent feeding
Contd..
 Encourage activities and exercise.
 Maintain skin integrity
• Provide skin care.
• Change position every 2 hrs.
• Check for skin break down.
 Prevent and manage side effects of steroid therapy.
 Discharge plan and home care teaching.
SUMMARY
ASSIGNMENT:
Develop a nursing care plan of child with
NEPHROTIC SYNDROME.
Nephrotic syndrome.pptx
Nephrotic syndrome.pptx

Nephrotic syndrome.pptx

  • 1.
    NEPHROTIC SYNDROME PREPARED BY: PRAJNASUBEDI B.SC.NSG 4TH YR 6TH BATCH
  • 2.
    INTRODUCTION: Nephrotic syndrome isa group of symptoms which is seen in any condition that seriously damages the glomerular capillary membrane , causing increased glomerular permeability with loss of protein in urine.
  • 3.
    DEFINITION: Nephrotic syndrome isa group of symptoms characterized by proteinuria ( > 3.5 grams per day), low blood protein levels , high cholesterol levels , and edema.
  • 4.
    INCIDENCE:  All agescan be affected.  Most common during 2 to 6 years.  Affects male more than female.
  • 5.
    CAUSES:  Autoimmune diseasessuch as systemic lupus erythematosus.  Diabetes Mellitus  Hypertension  Drug toxicity : excessive use of NSAIDS  Malaria , hepatitis infection etc.
  • 6.
    Types: • 90% ofcases Primary / Idiopathic Nephrotic syndrome • 10% of cases Secondary Nephrotic Syndrome • Serious and rare Congenital Nephrotic syndrome
  • 7.
    Primary / IdiopathicNephrotic syndrome:  Most common in children.  Exact cause is unknown but are mainly associated with autoimmune cause.  It is also known as minimal change disease : This disorder results in abnormal kidney function , but when the kidney tissue is examined under a microscope , it appears normal , or nearly normal.
  • 8.
    Secondary Nephrotic Syndrome: Causes may be various disorders that can damage the glomerulus of the kidneys.  Diseases such as Diabetes Mellitus , Hypertension , Systemic Lupus Erythematosus and other infections might be the cause.
  • 9.
    Congenital Nephrotic Syndrome: Itis serious and rare condition caused by autosomal recessive disorder. No therapies are effective usually. Infants die under 1 or 2 years of age.
  • 10.
    PATHOPHISIOLOGY: The glomerular basementmembrane is negatively charged layer . Due to antibody attack or other causes , this property is lost which allows proteins especially albumin to pass through glomerular membrane.
  • 11.
    CLINICAL FEATURES:  Excessiveweight gain , edema – peri-orbital initially , then in extremities , increases in the morning.  Ascites , scrotal/labial swelling may be present.  Urine changes ;  decreased volume  Frothy and pallor  Edema of intestinal mucosa may lesd to loss of appetite , poor intestinal absorption.
  • 13.
    Contd..  Fatigue ,lethargic, irritability.  Blood pressure may be normal or slightly decreased due to decreased intravascular volum  Susceptibility to infection increases  Dyspnea may be seen due to pleural effusion , ascites and other type of fluid.
  • 14.
    DIAGNOSIS: • Family history •Birth history • Antenatal history HISTORY TAKING: • Edema can be seen PHYSICAL EXAMINATION: • Urinalysis • Serum tests • Hematology • Kidney biopsy • KUB X-ray • USG INVESTIGATIONS:
  • 15.
    INVESTIGATION AND FINDINGS: Urinalysis:  Shows marked proteinuria , cast ,few RBCs , increased urine specific gravity  24 hrs urinary protein excretion : >50 mg/kg/day  Serum:  Markedly decreased serum protein (albumin)  High cholesterol (450-1500 mg/dl)  Hyponatremia
  • 16.
    CONTD:  Hematology:  Normalor increased hemoglobin level  High platelet count  Kidney biopsy  Done if there is recurrent relapses , non responsive to treatment
  • 17.
    COMPLICATIONS: Blood clots /venous thrombosis Poor nutrition High blood pressure Acute kidney failure Chronic kidney failure Infections
  • 18.
    TREATMENT: Goals of management: Reduce urinary protein excretion.  Reduce fluid retention.  Prevent infections and complications.
  • 19.
    Pharmacological treatment:  Diuretics: Frusemide , spironolactone  Corticosteroids : Prednisolone  Albumin Infusion :  Immune suppressant therapy : For child who continue to have proteinuria (+2 or more) after 8 weeks of steroid therapy are treated with immune suppresant therapy such as cyclophosphamide.
  • 20.
    Nursing managements:  Monitoredema urine characteristics , albumin , I/O , abdominal girth , daily weight , etc.  Administer medications such as diuretics , antibiotics and corticosteroid as ordered.  Improve nutritional status. • Low sodium diet • High calorie and high protein diet • Small and frequent feeding
  • 21.
    Contd..  Encourage activitiesand exercise.  Maintain skin integrity • Provide skin care. • Change position every 2 hrs. • Check for skin break down.  Prevent and manage side effects of steroid therapy.  Discharge plan and home care teaching.
  • 22.
  • 23.
    ASSIGNMENT: Develop a nursingcare plan of child with NEPHROTIC SYNDROME.