Acute and glomerulonephritis. Nephrotic syndrome

Содержание

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The concept of glomerulonephritis. Classification. Etiology. Diagnostics Analyzes Сontent

The concept of glomerulonephritis.
Classification.
Etiology.
Diagnostics
Analyzes

Сontent

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Acute glomerulonephritis is an acute diffuse immune-mediated inflammation that has developed

Acute glomerulonephritis is an acute diffuse immune-mediated inflammation that has developed

after sensitization with an antigen (more often bacterial or viral) and manifested by acute nephritic syndrome.

WHAT IS IT?

Chronic glomerulonephritis is a chronic immune-mediated inflammation of the glomeruli of the kidneys with a stable change in urine tests (proteinuria and / or hematuria)

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Acute glomerulonephritis

Acute glomerulonephritis

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Chronic glomerulonephritis

Chronic glomerulonephritis

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Acute (10%): - with acute arthritis syndrome - with isolated urinary

Acute (10%): - with acute arthritis syndrome
- with isolated urinary

syndrome
- with nephrotic syndrome
Chronic (70% b, jktt): - a latent variant
- hematuric
- hypertensive
- nephrotic
- mixed
Subacute (1%): (rapidly progressive GN)

Classification of glomerulonephritis (Tareyev EM)

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Glomerulonephritis develops from infections, poisonings, allergies, because of the complications of

Glomerulonephritis develops from infections, poisonings, allergies, because of the complications of

other diseases.
getting into the human body of infections (streptococcus, staphylococcus), viruses (hepatitis, herpes, rubella), bacteria, parasites that cause inflammation in the glomerulus of the kidneys;
poisoning with poisons, chemicals, alcohol, or some medication;
allergic complications;
re-vaccination;
the transfer of certain diseases (lupus, periarteritis, vasculitis) as a complication.

Сauses?

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The acute form progresses rather quickly, after a couple of weeks

The acute form progresses rather quickly, after a couple of weeks

the following symptoms are observed:
edema;
pain in the lower back;
headache, general weakness in the body;
nausea, sometimes vomiting;
high body temperature;
lowering of urine leakage;
urine leaves with an admixture of blood;
increased blood pressure in the kidneys.

Difference in symptoms

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nephrotic (small admixtures of blood in the urine, problems with urination,

nephrotic (small admixtures of blood in the urine, problems with urination,

in the analysis of blood detect protein); hypertensive (increased pressure); mixed (there are signs of nephrotic and hypertensive syndromes); hematuric (most often in men on the background of drinking alcohol).

What other differences in symptoms?

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It happens quite difficult because of the absence of obvious symptoms

It happens quite difficult because of the absence of obvious symptoms

(latent leakage), in contrast to acute. The patient can feel quite normal, not have puffiness, his urine without blood. Chronic often the form is discovered by chance. Increased protein in the blood, an increase in the number of red blood cells can mean the presence of the disease. If it is not treated for a long time, kidney failure develops.

Detect HG

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ANALYSIS

ANALYSIS

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During the exacerbation of the nephrotic form of CG, an early

During the exacerbation of the nephrotic form of CG, an early

manifestation is a decrease in the level of the total protein due to albumin, an increase in alpha-2 and gamma globulins, as well as levels of sialic acids, seromucoid, fibrinogen. With hypertensive form, there is a decrease in glomerular filtration rate. Electrophoretic determination of protein fractions of urine allows differentiating selective and nonselective proteinuria in chronic glomerulonephritis.

Analyzes for CG

In the analysis of urine, a decrease in the relative density of urine, nocturia and polyuria. Proteinuria is noted, especially pronounced in the nephrotic form of the disease. A characteristic symptom of this disease is macro- and microhematuria. In the analysis of urine sediment, hyaline and granular cylinders, less often waxy, especially pronounced cylindruria with nephrotic and mixed form of the disease, reveal yellowish filaments of fibrin.

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OAK leukocytosis, eosinophilia, elevated ESR, often thrombocytopenia BH blood - the

OAK leukocytosis, eosinophilia, elevated ESR, often thrombocytopenia BH blood - the total

protein content is reduced. The level of creatinine and urea increases. the level of fibrinogen and other proteins of the acute phase increases. They show hypercoagulability - a shortening of prothrombin time, an increase in the prothrombin index. Immunological analyzes - increased levels of immunoglobulins A and immunoglobulins M (subspecies of blood globulins), circulating immune complexes, decreased C3 and complement fractions, high antibody titers to streptococcal antigens.

Analyzes for AG

In the analysis of urine in the initial period of OG is noted (oliguria) and an increase in the relative density. A few days later, proteinuria and microhematuria, but in a number of cases in the first days there is also a macrohematuria - urine acquires a red color or the color of "meat slops".
Half of the patients with exhaust gas in the analysis of the urine sediment find hyaline and granular cylinders, leukocytes, sometimes cells of the renal epithelium.

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Nephrotic range proteinuria, (>40mg/m2/hour), (> 50mg/kg/day), urine to protein creat ratio

Nephrotic range proteinuria, (>40mg/m2/hour), (> 50mg/kg/day), urine to protein creat ratio

(>2mg/mg), +3-4 on dipstick
Hypoalbumenia (<2.5g/dl)
Hyperlipidemia
edema
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Primary or idiopathic(MCD,FSGS,Membranous, Mesangial proliferation) 2. Secondary to infections,systemic diseases (HSP,SLE) ETIOLOGY

Primary or idiopathic(MCD,FSGS,Membranous,
Mesangial proliferation)
2. Secondary to infections,systemic diseases (HSP,SLE)

ETIOLOGY

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Podocytes and the slit diaphragm

Podocytes and the slit diaphragm

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Electrolytes: low Na,low albumin and calcium ANA,C3,C4,hepatitis B,C Hemoglobin high,platlet high

Electrolytes: low Na,low albumin and calcium
ANA,C3,C4,hepatitis B,C
Hemoglobin high,platlet high
Urine Na less

than 10
Urine analysis: proteinuria,microscopic hematuria
Urine protein/creatinine more than 2 mg/mg
Elevated cholesterol and triglycerides

Laboratory investigation

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First episode :Steriods 2mg/kg/day,60 mg/m2/day single daily dose for 4 weeks,followed

First episode :Steriods 2mg/kg/day,60 mg/m2/day single daily dose for 4 weeks,followed

by alternate dose for 3-6 months.
Response in 10 to 14 days
Recent Cockrane metaanalysis found that treatment for 3m compared to 2m reduces risk of relapse by 30% at 12-24m
No significant diff in risk of side effects or cumulative steriod dose
With each 1 m over 2m,RR of relapse falls by 11%

TREATMENT

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Treatment of relapses:2mg/kg/day till remission for 3 days,then alternate days for

Treatment of relapses:2mg/kg/day till remission for 3 days,then alternate days for

2-3m.
Treatment of FR or SD SSNS:
1.Long alternate steriods for 12-18 m
2.Cyclophosphamide
3.cyclosporine
4.Levimazole
5.Mycophenolate acetate
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1-Infections:losses of IgG in urine,abn T cell function,low factor B (C3

1-Infections:losses of IgG in urine,abn T cell function,low factor B (C3

proactivator),steriod use,impaired opsonization
Encapsulated bact streptococcus pneumonia,staph,Ecoli
Primary bacterial peritonitis
Immunization against pneumococcus,varicella

COMPLICATIONS