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Lecture 11. Acute and Chronic Glomerulonephritis, Pediatric Hypertension
Lecture 11. Acute and Chronic Glomerulonephritis, Pediatric Hypertension
Lecture 11. Acute and Chronic Glomerulonephritis, Pediatric Hypertension
By:
GAP Nilawati MD, PAED
I Ketut Suarta MD, PAED
(purna tugas)
URINARY BLOCK
MEDICAL FACULTY OF UDAYANA UNIVERSITY
ACUTE AND CHRONIC GLOMERULONEPHRITIS
ETIOLOGY OF GLOMERULONEPHRITIS
Alport syndrome, congenital nephrotic syndrome (Finlandia Type)
Familial hematuria, nail patella syndrome
Acquired
Primary/ idiopathic
Minimal change disease, mesangial proliferative glomerulonephritis
Focal segmental glomerulosclerosis
Membranoproliferative glomerulonephritis
Membranous glomerulonephropathy
IgA nephropathy
Rapid progressive glomerulonephritis, diffuse proliferative glomerulonephritis
Other chronic glomerulonephritis (unclassified)
Secondary
Infection
Acute poststreptococcal glomerulonephritis, Hepatitis B, subacute bacterial endocarditis
Postpneumococcal glomerulonephritis, congenital syphilis, malaria
Lepra, schistosomiasis, filariasis, HIV AIDS
Secondary due to multisystem disease
HSP, SLE, Hemolytic uremic syndrome
Diabetes mellitus, goodpasture syndrome, amyloidosis
Vascular collagen disease, wagener granulomatosis, rheumatoid arthritis
Secondary due to drug
Penisilamin, NSAID, captopril
Street heroin, trimetadion, lithium, mercury
Secondary due to neoplastic
Leukemia, lymphoma, carcinoma
Others
Chronic rejection renal transplant, reflux nephropathy, sickle cell anemia
Acute Glomerulonephritis (AGN)
▪ The proliferation & inflammation on Glomerulus as a result of immunologic
mechanism
▪ Clinical → nephritic syndrome
▪ Proteinuria
▪ Hematuria
▪ Hypertension
▪ Edema
▪ Oligouria
▪ Fluid Overload
▪ Insufficiency kidneys, C3 ↓
Etiology
▪ Post-infection
▪ Streptococcus Hemolitikus group A (GNAPS)→Most often →
Location → pharynx infections and skin
▪ Other bacteria, viruses, parasites etc.
Epidemiology
• Age: - school age (6-7 yo)
- rarely < 3 yo
• Male : female = 2:1
Pathophysiology
▪ The immune system (complex Ag-Ab) → Streptococcal antibodies (ASTO) increased
▪ Complement C3 Active →level of C3 declined
Clinically diagnosis :
- Asymptomatic Persistent proteinuria / hematuria
- Nephrotic syndrome
- Nephritic syndrome
6-10 years Renal parenchymal disease, Renal artery stenosis, Primary hypertension, Endocrine
causes.
Adolescence Primary hypertension, White coat hypertension, Renal parenchymal disease,
Substance abuse (cocaine, amphetamines, methamphetamines, phencyclidine,
methylphenidate, caffeine), Teen pregnancy, Endocrine causes.
MECHANISM OF
HYPERTENSION
THE SIZE OF THE THE CUFF TENSIMETER
▪ Neonates : the width of the cuff (2.5- 4 cm) the length of the cuff (5-9 cm)
▪ Baby : W (4-6 cm) L (11.5 - 18 cm)
▪ Children : W (7.5- 9 cm) L (17-19 cm)
▪ Adults : W (11.5 - 13 cm) L (22-26 cm)
▪ Bigger arm : W(14-15 cm) L (over 30.5- 33 cm)
▪ Thigh : W (18-19 cm)L (36-38 cm)
Description :
W: the width of the pouch
L : The length of the pouch
Definitions of BP Categories and Stages
(The American Academy of Pediatrics (AAP) and its Council on Quality Improvement and Patient Safety, 2017)
Beta blocker Propanolol 0.2-0.5 mg/kg/dose (q6-12 hrs) 2 mg/kg/dose (80 mg/dose)
Class of drugs Type Dose Maximal Dose
Calcium Nifedipine 0.25 mg/kg/dose (q 6-8 hours) 0.5 mg/kg/dose (20 mg daily)
channel
blocker
Amlodipine 0.05 mg/kg daily (q24 hours) 0.2 mg/kg daily