Renal 3 Flashcards

(76 cards)

1
Q

3 causes/triggers of dz for disorders of glomerular function

A

immunologic, nonimmunologic, or hereditary

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2
Q

3 names for glomerular diseases

A

proliferative, membranous, or sclerotic

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3
Q

what is the third leading cause of end stage kidney failure worldwide?

A

glomerulonephritis

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4
Q

what is glomerulonephritis?

A

inflammatory process involving the glomerular structures

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5
Q

two types of conditions OF glomerulonephritis

A

primary- glomerular abnormality is the only disease present

secondary- glomerular abnormality results from another dz (such as DM or SLE)

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6
Q

what type of syndrome is diffuse proliferative glomerulonephritis?

A

nephrITIC; mesangial/endothelial cell proliferation and large, irregularly spaced sub-epithelial deposits (“lumpy bumpy”)

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7
Q

what type of syndrome is membranous glomerulopathy? what is seen on microscopy?

A

nephrOTIC; thickening of GBM and small, evenly spaced sub epithelial deposits (“fine granularity”)

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8
Q

five glomerular syndromes

A

1) . acute nephritic syndrome
2) . rapidly progressive glomerulonephritis
3) . nephrotic syndrome
4) . asymptomatic disorders of urinary sediment (hematuria, proteinuria)
5) . chronic glomerulonephritis

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9
Q

what is acute nephritic syndrome?

A

acute proliferative inflammation that occludes the glomerular capillary lumen and damages capillary wall

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10
Q

what does acute nephritic syndrome present as? (4)

A

sudden onset hematuria, positive for RBC casts or dysmorphic RBCs, tea colored urine, salt and water retention causing edema or HTN

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11
Q

what disease is most common after group A beta hemolytic strep infection?

A

post infectious glomerulonephritis

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12
Q

interventions to prevent or slow progression of CKD (3)

A

1) . target BP less than 140/90 (130/90 if DM or proteinuria)
2) . A1C target of 7% with T2DM
3) . CKD stage 4 & 5: reduced protein intake might reduce risk of death

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13
Q

tx of CKD comorbidities (2- anemia and CVD)

A

1) . consider ESA to tx anemia with target Hb levels > 12

2) . prevent/tx CVD with statin and asp therapy

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14
Q

which two drugs should you reduce dose by 50% when GFR < 30 in CKD?

A

fluoroquilolones and trimethoprim

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15
Q

ACE/ARB for CKD: start at lower dose with GFR < ____, and assess _____ and _____ 1 week after starting

A

45; GFR and K+

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16
Q

NSAIDS for CKD: avoid GFR < _____ and avoid prolonged therapy when GFR < ______

A

30; 60

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17
Q

metformin for CKD: review use when GFR is less than ____ and avoid when GFR is less than ____

A

45; 30

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18
Q

med adjustments for CKD: may dec insulin when GFR < _____; adjust gabapentin when GFR < ____

A

30; 60

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19
Q

when using warfarin in a CKD pt, there is an increased risk of what when GFR < 30?

A

bleeding

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20
Q

post infectious glomerulonephritis: most common in ___________, characterized by _____ infection; tx with _____ to help infection; excellent ______ and ______ causes KD; kids resolve within ___-____ weeks, adults take a bit _____

A

children; strep; ABX; prognosis rarely; 6-8 weeks; longer

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21
Q

rapidly progressive glomerulonephritis: presents with progression of _____ _____ over ____ to _____, in most cases in the context of _______ ___________

A

renal failure; days to weeks; NEPHRITIC PRESENTATION

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22
Q

rapidly progressive glomerulonephritis is also called: _____________ _____________. why?

A

crescentic glomerulonephritis, bc pathologic findings of glomerular crescent formation

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23
Q

rapidly progressive glomerulonephritis does not have a _______. if left _____, it rapidly progresses to ______ ______ ______ and ____ within a few months

A

cause; untreated; acute renal failure; death

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24
Q

Good pasture syndrome is associated with what disease? what is GPS?

A

rapidly progressive glomerulonephritis; its when antibodies attack the glomeruli basement membranes

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25
GPS's staining hallmark is what? what might these pts present with?
diffuse (smooth) linear staining of glomerular BM's for IgG; present with coughing up blood
26
characteristics of nephrotic syndrome (4)
1) . nephrotic range proteinuria: >3.5g/day in adults 2) . hypoalbuminemia (<3) 3) . hyperlipidemia 4) . lipiduria: free fat, urine foam, fatty casts, oval bodies
27
Nephrotic syndrome is NOT a specific ______________ disease, but a constellation of clinical findings that results from what two things?
glomerular; loss of plasma proteins and inc in glomerular permeability
28
pts with nephrotic syndrome are at an increased risk of what? it develops as a ______ or ________ disorder
thrombotic complications; primary or secondary
29
nephrITIC: 5 things nephrotic: 3 things
ITIC: inflammatory, hematuria, edema, HTN, lower degree of proteinuria (<3.5g in 24 hrs) OTIC: noninflammatory, protein >3.5g, increased lipids in blood and urine
30
two asymptomatic disorders of urinary sediment
Alport syndrome and IgA nephropathy
31
pts with asymptomatic disorders of urinary sediment present with what two asymptomatic things?
hematuria and/or proteinuria
32
what is IgA nephropathy? what does this lead to? what syndrome is it a form of?
presence of glomerular IgA immune complex deposits in mesangial cells of glomerulus; leads to damage in the basement membrane, which allows blood and proteins to pass through; form of nephritic syndrome
33
tx for IgA nephropathy
no great tx's
34
what is Alport syndrome?
hereditary defect of GBM which results in hematuria and might progress to chronic renal failure
35
Alport syndrome: _____ are more commonly affected and typically progress to _______ ________ as adults
men; renal failure
36
how to dx Alport syndrome
made by UA of a child who comes from a family of Alport syndrome (maybe microscopic hematuria/proteinuria)
37
most Alport syndrome pts have _________ _______ and _____ diseases
sensorineural deafness and eye dz
38
tx for Alport syndrome
ACEI for pts with proteinuria. maybe ARB and statin | those with CRF, transplant
39
chronic glomerulonephritis is characterized by ______ kidneys with __________ glomeruli. develops _________ and has _______ __________; slowly progresses to ________ _________
small; sclerosed; insidiously; PERSISTENT PROTEINURIA; kidney disease
40
what are three types of glomerular lesions associated with systemic dz?
systemic lupus erythematous glomerulonephritis, diabetic glomerulosclerosis, and hypertensive glomerular dz
41
systemic lupus erythematous glomerulonephritis is ____________ ______________; _______ disease is the most common complication. these pts will need _____ ______ and routine UAs if anything is abnormal. Tx is _____ and _____
tubulointerstitial inflammation; renal disease; RENAL BIOPSIES; steroids and ACEIs
42
diabetic glomerulosclerosis: look for ______________. tx: control ________, start _____ and ______
MICROALBUMINURIA (30-300 mg in 24 hrs); glucose, ACEI and ARBs
43
Hypertensive Glomerular Dz: mild to moderate HTN causes ______ changes in renal arterioles and small arteries....this leads to what? tx are what meds?
sclerotic; leads to poor perfusion of kidneys' lower BP, ACEI/ARBs
44
IgA Nephropathy is what type of syndrome?
nephritic
45
acute tubular necrosis: death of _______ _________ cells in the renal tubules. presents with ______ ________ ______ and is one of the most common causes of ________ AKI (85%)
tubular epithelial; acute renal failure; intrinsic
46
two common causes of ATN
hypotension with ischemia and use of nephrotoxic drugs
47
ATN: presence of "________ _______ _______". BUN/Cr will be less than ____ and urine Na will be less than _____
MUDDY BROWN CASTS; 20, 40
48
management of ATN relies on aggressive tx of factors that ___________ ATN; overall prognosis is ______ if the cause is corrected. recovery within ___-____ days
precipitated; good; 7-21 days
49
acute pyelonephritis (APN): _______ infection of the ______ urinary tract. most common by ______, ____, _________ and __________
bacterial; upper; causes by E coli, Klebsiella, Enterobacter, pseudomonas
50
APN: kidneys can become infected via what two ways?
ascending infection from lower urinary tract or through blood stream
51
APN: _____ onset of infection with _____, _____, constant ache in the ______, _____ pain, positive _____ tenderness
acute; chills, fever, flank; abdominal; CVA
52
diagnosis of APN: positive ____, ____ elevated, CT indicates what
pos UA, WBC elevated, pyelo +/- abscess
53
what two pt populations ALWAYS get admitted for APN?
pregnant women and kids
54
chronic pyelonephritis: scarring and deformation of renal ______ and _______, along with ____ of the overlying cortex
calyces and pelvis; atrophy
55
chronic pyelonephritis involves a ______ or ________ bacterial infection superimposed on _____, ___ _____, or both
recurrent or persistent; UTI, urine reflex
56
chronic pyelonephritis: involves one or both sides? what is tx?
can be bilateral; tx: determine the source and tx, ABX
57
what four drugs can cause ACUTE PRERENAL FAILURE?
1) . diuretics 2) . IV dye 3) . immunosuppressive drugs (tacro/cyclosporine) 4) . NSAIDS
58
acute drug-related hypersensitivity reactions produce _________ ________. associated with what drugs? (4) ____% of the time, pt has a rash
tubulointerstitial nephritis; sulfa, methicillin, beta lactams. Lasix/thiazides; 25%
59
chronic analgesia nephritis is associated with _____ ____
analgesic abuse (pain killers)
60
ARF is caused by _______ _____ use, especially _______ or _____
illicit drug use; cocaine or NSAIDs
61
what are the three cystic diseases of the kidney?
1) . polycystic kidney dz (ADPKD or ARPKD) 2) . nephronophthisis- Medullary cystic disease complex 3) . simple and acquired renal cysts
62
PKD is an ________ disorder with many cyst sacs or segments in the _______ structures of the kidney
inherited; tubular
63
ADPKD: _____ common, appears when pt is an _____, ___-___% of pts have an associated aneurysm; ____ is preferred method for diagnosis
most; adult; 10-30%; US
64
tx for ADPKD
supportive: control HTN and UTI prevention, pain control (dialysis/transplant for those to progress to renal failure)
65
ARPKD: cystic _____ of the ______ and _________ collecting tubules. this disease is ____
dilation; cortical and medullary; rare
66
ARPKD: infant presents with bilateral ______ _____, severe _____ failure, ______ fibrosis, impaired _____ development. ____ ______ may be present
flank masses; renal; liver; lung; potter facies
67
ARPKD: ___% of infants die during the perinatal period
75%
68
tx of ARPKD
supportive, aggressive ventilator support, renal transplant
69
nephronophthisis- Medullary cystic disease complex: group of ________ ______ and ________ disorders with _______ onset
autosomal dominant and recessive; childhood
70
what happens to the kidneys in nephronophthisis- Medullary cystic disease complex? what is present on the kidneys?
small and shrunken, presence of numerous cysts at corticomedullary junction
71
progression of dz in what happens to the kidneys in nephronophthisis
progress to azotemia (high levels of nitrogen compounds in the blood) and renal failure within 5-10 yrs
72
simple cysts: single or _______, unilateral or ______, confined to the _____. if symptomatic, they can cause _____ pain, hematuria, infection. common in people
multiple, bilateral; cortex; flank; 50 yrs
73
acquired cysts: forms in people with ____ who have undergone prolonged _____ tx
CKD; dialysis
74
acquired cysts are typically _____, but may have cysts that ______, causing ____. what might develop in the walls of the cysts?
asymptomatic; bleed, causing hematuria; tumors might develop in the walls
75
what type of syndrome is FSGS? _____ urine due to ____ levels of protein; ____ and chronic _____ impairment
nephrOTIC; foamy; high; HTN and chronic renal impairment
76
microscopy for FSGS shows what?
focal and segmental glomerular sclerosis