Kidney: UTI, Pyelonephritis, Glomerulonephritides Flashcards

1
Q

Classification of UTIs

A

Simple
- female
- 1st presentation
- not pregnant
- no pyelonephritis

Complicated
- male
- recurrent - 3+ in a year
- pregnant
- elderly
- catheters

Lower - bladder and distal
Upper - kidneys (pyelonephritis)

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2
Q

UTI risk factors

A

Past UTI
Sexually active
Pregnant
Low estrogen
DM, obesity, IC

Stones
Catheters
Surgery, renal transplant

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3
Q

Causative organisms for UTIs

A

MOST COMMON - Ecoli followed by staph saprophyticus

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4
Q

UTI
-presentation, history approach
-diagnosis

A

FUND
-assess triggers, sexual Hx
-DM, stones, neurology, IC
Red flags - sepsis, pyelonephritis (flank pain, fever, N+V)

Clinical diagnosis with urine dipstick (nitrites, leukocytes)
Culture if complicated, recurrent

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5
Q

UTI management

A

Non pregnant - 3 days nitro/trimeth

MCS needed if
-65+
-any form of hematuria

Pregnant - 7 days
1st trimester - nitro
3rd trimester - trimeth
2nd line - amox, cefalexin
TREAT EVEN IF ASYMPTOMATIC

Men - 7 days nitro/trimeth + MCS
-refer to urology if multiple UTIs

Catheterised - 7 days nitro/trimeth
-NO TREATMENT IF ASYMPTOMATIC

Supportive
- fluids, perineal hygiene, post coital voiding
- remove catheter if present
- if postmenopausal => HRTs to reduce future risk

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5
Q

Characteristics of nephrotic syndromes
- triad
- examples

A

Glomerular damage => proteinuria, hypoalbuminemia, peripheral edema

Foot effacement - Minimal change disease, FSGS
AB deposition - Membranous
Complex deposition - Membranoproliferative

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6
Q

Minimal change disease
- epidemiology and most common cause
- presentation, investigations
- management

A

Children - IDIOPATHIC
-NSAIDs, rifampicin
-Hodgkin, thymoma
-glandular fever

Nephrotic + hyperlipidemia - response to low albumin

Confirm nephrotic picture - urinalysis, U&E, lipids
Renal biopsy if not responding to steroids
- normal LM
- EM podocyte foot effacement

1st line - CS
2nd line - cyclophosphamide

2/3d will relapse, but will stop before adulthood

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7
Q

Focal segmental glomerular sclerosis
- epidemiology and most common cause
-presentation
- investigation
- management

A

Young adults (20-30s) - IDIOPATHIC
-HIV

Nephrotic + HTN + hyperlipidemia

Renal biopsy
-glomerular scarring on LM, EM

1st line - CS
2nd line - cyclophosphamide

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8
Q

Membranous glomerulonephritis
- epidemiology and most common cause
-presentation
- investigation
- management and prognosis

A

Adults - IDIOPATHIC - anti PLA2 IgG AB
-high association with prostate, lung, lymphoma, leukemia

Nephrotic + HTN + hyperlipidemia

EM - BM thickening ‘spike and dome’

Management
-BP and proteinuria control - ACEi/ARB
Definitive - self limiting but if severe => CS + cyclophosphamide combination
Can lead to ESRF

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9
Q

Nephritic syndrome
- triad
- urinary findings

Examples of nephritic syndromes

A

Glomerular inflammation => inflammation
- Haematuria
- Oliguria and edema
- HTN

Anti GBM
SLE
IgA nephropathy/post streptococcal
ANCA

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10
Q

What is IgA nephropathy or post streptococcal GN?
- key differences
- investigations
- management
- prognosis

A

IgA/Bergers - most common GN
- young male, nephritic
- 1-2 days after URTI, visible hematuria
- renal biopsy - mesangial hypercellularity, high IgA, C3

Management
- Haematuria only - self limiting
- Persistent proteinuria - BP control
- Falling GFR - CS

Post strep glomerulonephritis => diffuse proliferative GN
- 1-2wks after URTI, proteinuria => edema
-confirm recent URTI with O-streptolysin test
- renal biopsy - low complement

Management - symptom relief

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11
Q

How would you manage nephrotic syndromes

A

Reduce edema => diuretics
Reduce HTN => ACEi
Reduce DVT risk => anticoagulation
Reduce cholesterol => statin
Renal biopsy to establish cause

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12
Q

How would you manage nephritic syndromes

A

Supportive
-Na, water restriction

Pharmacological
-proteinuria/HTN => ACEi, ARB, diuretics

Lupus nephritis => immunosuppressive therapy
AntiGBM AB => plasmapheresis

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13
Q

What are the rapidly progressing glomerulonephritides (crescenteric glomerulonephritides)
- what are 3 examples of this
- how might this present
- management

A

Rapid destruction of glomeruli => ESRD

Anti GBM disease
ANCA vasculitis (GPA, MPA)
Lupus with pulmonary haemorrhage

NEPHRITIC - hematuria, proteinuria, HTN
+features specific to underlying cause

Biopsy - crescent formation around glomerulus

Management - CS, cyclophosphamide, plasmapheresis

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14
Q

What is ANCA positive vasculitis
- main symptoms
- 2 main types and their associated AB

A

Renal - nephritic symptoms
Resp - SOB, haemoptysis
Systemic - fatigue, weight loss, fever
Vasculitic rash
ENT - sinusitis

GPA - cANCA (serine proteinase)
MPA - pANCA (myeloperoxidase)

If suspected => MDT approach
Definitive management - immunosuppression

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15
Q

What is Anti GBM/Goodpasture disease
- ABs are associated with Anti GBM
- investigations
- clinical presentation
- management

A

AB glomerular and alveolar BM => AKI, nephritis, pulmonary hemorrhage

Renal biopsy - IgG deposits on BM
antiGBM AB

Management
-Plasmapheresis + CS + cyclophosphamide

16
Q

What blood tests might you do in suspected glomerular disease

A

Blood cultures, virology
U&E, LFT, bone profile
CRP

RF (AB against Fc of IgG), ANCA, AntiGBM, ANA, dsDNA
C3, C4

Myeloma screen

17
Q

ANCA associated vasculitis
- types
- common findings
- investigations
- diagnosis and management

A

Granulomatosis with polyangiitis
Eosinophilic granulomatosis with polyangitis
Microscopic polyangiitis

Renal impairment
-immune complex glomerulonephritis => high creatinine, haematuria, proteinuria
Resp involvement
-SOB, haemoptysis, sinusitis
Systemic upset
Vasculitic rash

Urinalysis - hematuria, proteinuria
U&E - renal impairment
FBC - normocytic anemia, thrombocytosis
High CRP
CXR - nodular, fibrotic, infiltrative lesions

Diagnosis aided by lung and kidney biopsies
-refer to specialist teams

18
Q

Acute pyelonephritis
-causative organism
-pathophysiology
-investigations

A

Ecoli - most commonly from lower UT, but can come from bloodstream

Fever, rigors
Loin pain
N/V
LUTI signs

MSU before ABx

Hospital admission
Broad spec ABx - cephalosporin/quinolone 7-10days

19
Q

Granulomatosis with polyangiitis
-key features
-investigations
-management

A

URT - nosebleeds, sinusitis, nasal crusting, saddle nose
LRT - SOB, hemoptysis
Renal - crescenteric changes
Vasculitis

cANCA
Renal biopsy - epithelial crescents in Bowmans

CS
Cyclophosphamide
Plasma exchange

20
Q

Eosinophilic granulomatosis with polyangiitis
-key features
-investigations
-management

A

URT - sinusitis
LRT - Asthma, eosinophilic features

pANCA

Steroids
Cyclophosphamide
Plasmapheresis