Renal Flashcards

(359 cards)

1
Q

Blood urea nitrogen

A

Tells amount of urea nitrogen in blood that is made by liver when protein is broken down
Nitrogen then excreted into urine

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2
Q

What does a BUN/Creatinine ratio greater than 20/1 indicate

A

Decreased blood flow to kidneyes

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3
Q

Creatinine

A

Produced from muscle breakdown
Produced at constant rate and filtered through kidneys
Not the best test of kidney function because muscle mass needs to be considered (amputees, muscle wasting, malnutrition)

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4
Q

What does doubling of creatinine represent

A

50% decrease in GFR

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5
Q

Glomerular filtration rate (GFR)

A

Blood filter by glomeruli per minute
BEST way to measure kidney function and monitor progression

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6
Q

Best lab to measure kidney function and and monitor progression

A

GFR

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7
Q

What all is considered in GFR calculation

A

Serum creatinine, age, sex, race

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8
Q

What GFR indicated chronic kidney disease

A

GFR<60 for over 3 months

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9
Q

What GFR shows pt should be referred to nephrologist

A

GFR<30 chronically

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10
Q

Do healthy kidneys excrete albumin into urine

A

No

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11
Q

Microalbuminuria lab value

A

Albumin 30-300mg/L of urine

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12
Q

Albuminuria

A

> 300mg/L of urine

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13
Q

Abnormal albumin/creatinine ratio

A

30 or higer shows albumin is leaving at an accelerated rate (can be used because creatinine excreted at steady state)

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14
Q

Whats tested on urine dipstick

A

Specific gravity
pH
Protein (albumin)Glucose
Ketones
Blood
Leukocyte esterase
Nitrates
Bilirubin
Urobilinogen

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15
Q

Specific gravity definition

A

Ration of weight of urine to equal quantitiy of weight in water

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16
Q

Normal specific gravity

A

1.003-1.030
Varies depending on hydration and kidneys ability to maximally dilate

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17
Q

Normal pH of urine

A

4.5-8

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18
Q

Albumin scoring on dipstick

A

Trace - 5-30
1+ - 30-100
2+ - 100-300
3+ - 300-1000
4+ - >1000

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19
Q

What can cause false positive of albumin on dipstick

A

Alkaline (pH>7) urine

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20
Q

What plasma glucose concenctration do you start seeing glycosuria

A

180

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21
Q

What complications cause you to have ketones in urine

A

Diabetic ketoacidosis
Salicylate toxicity
Isopropyl alcohol poisoning
Starvation

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22
Q

What can cause false positive ketones

A

Sulfhdryl group drugs (captopril or levodopa)

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23
Q

What parts of blood are sensed on urine dipstick and how

A

Free hemoglobin and intact erythrocytes via peroxidase activity

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24
Q

What can cause false positive for blood on urine dipstick

A

Ascorbic acid
Myoglobin
Bacteria expressing peroxidase activity
Rifampin
Chloroquine
Other iodine forms

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25
Leukocyte esterase
Enzyme in leukocytes seen on dipstick
26
Nitrites
Seen on dipstick Converted from nitrates in UTIs caused by gram negative organisms
27
What does bilirubin in urine indicate
liver disease Obstructive jaundice
28
WHat can cause false positive of bilirubin on urine dipstick
Chlorpromazine Ascorbic acid
29
Urobilinogen
Made in gut from metabolism of bilirubin --> reabsorbed --> Excreted in urine
30
What causes positive urobilinogen on dipstick
hemolytic anemia or hepatic necrosis but not from obstructive casuses
31
What would lead you to do urine microscopy
Abnormalities on dipstick Acute kidney injury Suspicion for glomerulonephritis Newly diagnosed CKD
32
What can be seen on urine microscopy
WBC RBC Bacteria Epithelial cells (shows urine wasn't properly gotten)
33
What do dysmorphic RBC on urine microscopy indicate
Glomerular disease Called cast
34
Pyuria
Excess leukocytes in urine 4 or more leukocytes/HPF
35
Most common cause of pyuria
UTI
36
Cause of hyaline cast
Hypovolemia
37
What does hypovolemia cause in kidneys
Low urine output an dhyaline casts
38
What does tubular injury casue
Pigmented epithetical tubular debris and muddy brown casts
39
What does glomerular injury cause
Erythrocyte casts with lomerulonephritis
40
What does tubulointerstitial injury of the kidney cause
Leukocyte cast with pyelonephritis
41
What will be urine sodium if there are prerenal problems
<20
42
Normal urine sodium
Around 20
43
What will be urine sodium if ther eare problems with the kidney itself
>40
44
Urine osmolality definition and normal
500-850 Number of dissolved particles or concentration of all particles per unit of water in urine
45
What does a high urine osmolality indicate
>850 Problems before kidney
46
What does low urine osmolality indicate
300-500 Problems within the kidney
47
What level of protein in urine is considered proteinuria
>300
48
What lab values define acute kidney injury
Creatinine: 0.3 or more increase in last 48 hrs
49
Oliguric
urine production 400-500mL/day
50
Anuria
Urine production <100/day
51
CKD findings on imaging
Kidneys could be smaller
52
Acute Kidney disease complications non-renal complications
Uremia causing nausea vomiting, malaise, ams, encephalopathy Pericardia effusions causing cardiac tamponade
53
AKI lab findings
Elevated BUN an creatinin Metabolic acidosis with increased aniion gap Hyperkalemia Hyperphosphatemia Hypermagnesemia Hypocalcemia Anemia
54
AKI ECG findings
Long QT segment (from hypocalcemia)\ Peaked T waves (from hyperkalmia) PR prolongation QRS widening
55
Three types of AKI
Prerenal intrinsic - in kidney itself Postrenal
56
How can decreased profusion cause AKI
Decrease in intravascular volume Changes in vascular resistance Low CO
57
Prerenal AKI lab findings
BUN/Creatinine ratio >20:1 due to decreased urea Urinary sediment shows benign or hyaline casts Urine osmolarity high (>500) Fractional excretion of Na (FENa) low (<1%)
58
Prerenal AKI treatment
Treat heart failure or infection (abx) IV hydration or blood transfusion to get euvolemia Watch electrolytes Avoid nephrotoxic drugs
59
Most common type of intrinsic AKI
Acute tubular necrosis
60
Major causes of acute tubular necrosis
Ischemia Nephrotoxin exposure
61
Sites of injury of intrinsic renal disorders
Tubules Interstitium Vasculature Glomeruli
62
Acute tubular necrosis causes
Exposure to nephrotoxins (mostly exogenous): Antimicrobial agents (aminoglycosides, amphotericin B, Vancomycin, Acyclovir, Cephalosporins) CT contrast Calcinerin inhibitor Rhabdomyolysis
63
How to prevent acute tubular necrosis caused by CT contrast
500-1000mL of normal salline over six hours before and after contrast is given Avoid nephrotoxic agent s the day before and after contrast is given (metformin, ACEi, ARB)
64
Acute tubular necrosis lab findings
Hyperkalemia Hyperphosphatemia BUN and creatininen ration <20:1 Urine osmolality is low (<350) Microscopy shows a Pigmented epithetical tubular debris and muddy brown casts
65
Acute tubular necrosis treatment
Speeding up recovery and avoiding complications Avoid volume overload and hyperkalemia Furosemide infusion, thiazide diuretics
66
What is rhabdomyolysis
Muscle fibers break down and leak contets into blood stream
67
What is found in labs for rhabdomyoliysis
Myoglobinuria (causes false positive of blood on dipstick) Elevated creatine kinase levels (>20,000) Elevated AST, ALT< and lactate dehydrogenase
68
Rhabdomyolysis causes
Distance runnng Crush injuries Seizures Substance abuse Cocaine Meds (statins)
69
Rhabdomyolysis treatment
Aggressive volume repletion with normal saline Remove offending agents
70
Intrinsic AKI (acute interstitial nephritis) causes
Drugs Infection Immunologic disorders Idiopathic conditions
71
Most common drugs to causes acute interstitial nephritis
Penicillins Cephalosporins Sulfonamides NSAIDs
72
Acute interstitial nephritis presentation
Fever Rash Arthralgias Nausea VOmiting malaise HTN Flank/lumbar pain Mild edema Can be asymptomatic Triad of fever, rash, arthralgias
73
Acute interstitial nephritis lab findings
Peripheral blood eosinophila Urine eosinophils Serum BUN/Cr ratio <20:1 WBC. RBC, Casts on UA
74
Acute interstitial nephritis treatment
Supportive and remove offending agent If persist, hygih dose methylprednisone or prednisone orally for 1-2 weeks then steroid taper for more severe cases of drug-induced interstitial nephritis
75
Postrenal causes of AKI
Urethral obstruction Bladder dysfunction Obstruction of both ureters or renal pelvises Anticholinergic drugs Neurogenc bladder due to injury, diabetes, or drugs
76
Lab findings in postrenal AKI
Initially high urine osmolality, low urine Na, high BUN/creatinine ration, low FENa, Decreased pH and bicarb Urine Na increaseds several day slater urine sediment generally bland
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Postrenal AKI treatment
Bladder catheterization and ultrasonography to check for hydroureter, hydronephrosis, large baldder volume with no sensation to void. Monitor I&O
78
Hydronephrosis
Postrenal AKI Distension of renal calyces and pelvis of one or both kidneys by urine Obstruction can occur at any level of urinarty tract
79
What causes bilateral hydronephrosis
Obstruction of urinary flow at or bleow level of bladder or urethra
80
How to diagnosis hydronephrosis
Bladder catheterization, if diuresis occurs, obstruction is below bladder neck.
81
Hydronephrosis presentatoin
Pain Caused by distention of collecting system or renal capsule that can radiate to lower abdomen, testicles, or labia Diff voiding with oliguria or anuria in complete obstruction Polyuria/nocturia can occur with partial obstruction
82
Hydronephrosis lab findings
UA shows hematuria, pyuria, proteinuria, or bacteriuria with normal sediment Check BUN/creatinine Urodynamic testing if suspect bladder causes
83
Hydronephrosis imaging
Ultrasound preferred IV urogram (aka IV pyelogram) CT
84
Hydronephrosis treatment
Abx for 3-4 weeks if infection Catheters, stents, or surgery to fix blockage
85
When to start dialysis in AKI
Serum creatinine > 5mg/dl Unresponsive acidosis Electrolyte disorders Fluid overload Uremic complications
86
First step in treatment for proteinuria
Max out ACEi (-pril) or ARB (-sartan)
87
What to do if you put them on ACEi/ARB and still have proteinuria
SGLT2 (-flozin)
88
What to do if you give them ACEi/ARB and SGLT2 and still have proteinuria
MRA (spironolactone)
89
What puts someone at highest risk for CKD
Previous acute kidney injury
90
CKD
Abormal kidney function >3 months Usually asymptomatic until near end stage
91
CKD risk factors
Diabetes mellitus HTN Chronic NSAID use Glomerulonephritis Polycystic kidney disease Systemic upus erythamatous
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CKD presentation
Fatigue Malaise Anorexia Nausea Vomiting Metallic taste Hiccups DOE Irritability Muscle cramps Restless legs Weakenss Pruritis Easy bruising Altered mentation muscle waisting Pallor Edema Ecchymosis Bruit Weight loss
93
Symptoms of CKD stages I-IV
Asymptomatic
94
CKD labs
BMP to get GFR Urinalysis: proteinuria,, albuminuria, UACR Urine microscopy: waxy casts CBC: anemia
95
Who to give Statin in CKD
>49 yo ASCVD DM Hx of TIA/CVA 10 year risk>10%
96
Who to give RAS inhibitor (ACEi/ARB) in CKD and how to go about that
BP >120/80 Proteinuria Use highest dose tolerated Recheck BMP 2-4 weeks after initiation
97
Who to give SGLT2 inhibitor in CKD
Diabetes HF Refractory proteinuria on max RAS agent
98
When to give MRA (spironolactone) in CKD
Proteinuria despite RAS agent and SGLT2
99
Who to screen for CKD
Diabetes HTN CAD Age>50 Obesity Fam hx CKD Polycystic kidney disease Systemic lupus erythematous
100
When to refer CKD to nephrology
GFR<30 UAVR>300 Urine output declines Protein/creatinine ratio >500 HTN refractory to 4 meds Associated complications
101
CKD stages I-IV management
Yearly BMP, UACR, lupuds BP<120/80 Statin in pts >50yo <1.5g Na daily
102
CKD stages III and IV management
Yearly BMP UACR Lipids PTH Ca Vitamin D CBC Phosphorus
103
CKD complications
Anemia from decreased erythropoietin production Hyperkalemia Acidemia Secondary hyperthyroid Elevated phosphorus Hypocalcemia Low vitamin D Renal osteodystrophy Vascular calcifications
104
Anemia in CKD treatment
Check iron levels first Consider erythropoietin if possible (lowest possible dose) Maintain hgb>11 Ferrous sulfate for low iron
105
Hyperkalemia in CKD treatment
Avoid ACEi/ARB and spironolactone Potassium binding agents (sodium polysytrene sulfonate, sodium zirconium cyclosilicate, patiromer)
106
Acidemia in CKD treatment
Consistent serum bicarbonate <20 Oral bicarbonate solution/tablets
107
Secondary hyperparathyroid in CKD treametn
Calcitriol, paricalcitol, deoxercalciferol Goal PTH 150-300
108
Elevated phosphorus in CKD treatment
Dietary mods Renal osteodystrophy
109
Electrolyte changes in CKD
Hyperkalemia Hyperphosphatemia Hypocalcemia Hypomagnesium
110
Meds to avoid when GFR<30
Metformin Sulfonylurea ACEi/ARB HCTZ DOAC Fenofibrates Lovenox
111
End stage renal disease presentation
Fatigue Malaise Anorexia Nausea Uremic frost Kussmaul respirations Pruritis Easy bruising Chachexia HTN
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End stage renal disease uremic syndrome complications
Pericarditis Delirium Pericardial effusion Uremic encephalopathy
113
Types of hemodialysis access
Synthetic AV graft Central venous catheter AV fistula
114
What GFR to refer to hemodialysis
15-29
115
Arteriovenous fistula dialysis
Preferred Takes 2-6 months to form Less risk of clots or infections Lasts for years Connect artery to vein
116
Arterovenous graft dialysis
If pt has small or weak feins that won't make fistula usually needs 2-4 weeks to develop Bruit and thrill on physical exam Causes increased risk of clotting and infection No venipuncture, taking BP, or heavvy lifting Don't last as long as fistula
117
Central venous catheter dialysis
Used for more temporary dialysis (ACUTE) High infection rate Veins can develop stenosis or clot Usually changes every 4 weeks Swimming/bathing not recommended
118
Peritoneal dialysis
Does not require vascular access LEss stressful Decreased side effects Can be done at home Causes increased risk of peritonitis bc of intraabdominal catheter
119
Polycystic kidney disease treatment
RAAS Tulbactam if progresses DO NOT Use statins, sglt2, GLP-1, or MRA
120
Polycystic kidney disease pathophys
>5 cysts on kidney overwhelms and replaces mass of kidney reducing kidney function leading to kidney failure
121
What gene is associated with polycystic kidney disease
APKD Can be born with or acquired with long term CKD/ESRD
122
Polycystic kidney disease presentation
Flank/back pain from kidney stones Cyst rupture/hemorrhage or infection HTN Recurrent UTI Weight loss HA Nocturia Nodular and tender kidney Cysts on pancreas and liver
123
Polycystic kidney disease extrarenal manifestations
Cerebral "berry" aneurisms Hepatic cysts Pancreatic cysts Mitral valve prolapse Diverticulosis
124
]polycystic kidney disease imaging
Renal ultrasound showing fluid filled cyst CT showing enlarged kidneys and cysts Angiography with bending of small vessels around cysts
125
Polycystic kidney disease labs
CBC showing anemia
126
Supportive treatment for polycystic kidney
BP <110/75 Pain management Normal BMI Drink more water Treat infections with abx Dialysis Transplant Tolvaptan Screening for cerebral aneurisms
127
Renal cell carcinoma presentation
Usually asymptomatic until advance Metastasis in lymph, lungs, liver, bone brian Flank pain Palpable renal mass Hematuria Abd pain and mass Weight loss HTN
128
Renal cell carcinoma risk factors
Smoking Obesity HTN
129
Renal cell carcinoma increased risk population
Family Hx ESRD on HD >3 years before kidney radiation
130
Renal cell carcinoma labs
Anemia Hypercalcemia Hematuria
131
Renal cell carcinoma imaging
CT biopsy usually done at time of nephrectomy
132
Renal cell carcinoma treatment
Nephrectomy Surveilance for 5 years post-cure
133
Renovascular hypertension
High bp that develops into renal artery disease either stenosis or fibromuscular dysplasia
134
Renal artery stenosis risk factors
Older pt with ASCVD Smoking ASCVD risk factors
135
Gold standard to confirm renal artery stenosis
Renal angiography
136
Renal artery stenosis treatment
ACEi/ARB Statin PCTA or bypass if 70% lesion
137
What is a sign of fibromuscular displacia on imaging
String of pearls sign (squiggly renal artery)on renal angiography
138
Fibromuscular diysplasia risk factors
<50 Women Refractory to HTN treatment
139
Fibromuscular dysplacia treatment
PTCA/stent/bypass
140
Nephrotic syndrome features
Proteinuria from damage to glomerulus Hypoalbuminemia since albumin is being dumped into urine causing low oncotic pressure Edema from low oncotic pressure Hyperlipidemia from hepatic lipoproteins being made in response to decrease in oncotic pressure
141
Four criteria for nephrotic syndrome
Proteinuria >3.5 Low albumin Edema Hyperlipidemia
142
Nephrotic syndrome symptoms
Foamy/frothy urine Edema of lower extremities, eyelids, face, abd Weight gain Fatigue
143
Diagnostic tests used for nephrotic syndrome
BMP Lipids 24 hr urine Albumin creatinine ratio Kidney ultrasound Kidney biopsy
144
Nephrotic syndrome causes
Focal segmental glomerulosclerosis Minimal change disease Membraneous nephropathy Diabetic nephropathy Amyloidosis
145
Focal segmental glomerulosclerosis pathophys
Filtration issue from podocyte damage.
146
Focal segmental glomerulosclerosis causes
Immunologic Genetic (APOL1 gene) Overwork injuries (obesity, solitary kidney, HTN)
147
Focal segmentsal glomerulosclerosis diagnostic tests
Kidney biopsy required shwoing hyalinosis and segmental sclerosis Immunofluorescence with entrapment of IgM and C3 Light mcroscopy showing sclerosis of glomeruli Electron microscopy showing podocyte effacement
148
Primary Focal segmental glomeruloscelrosis treatment
ACEi/ARB and Na restriction CCS Calcineurin inibitor (cyclosporine and tacrolimus)
149
Secondary Focal segmental glomeruloscelrosis treatment
Treat underlying cause
150
What patients is focal segmental glomerulosclerosis commonly found in
Sickle cell HIV Black Hispanic
151
Most common nephrotic syndrome in children
Minimal change disease
152
Minimal change disease causes
MOSTLY IDIOPATHIC Infections NSAIDs Allergies mallignancy
153
Minimal change disease diagnostic testing
Most not good Biopsy only if refractory Glomeruli normal on light microscopy Effacement (thinning) of podocytes on microscopy
154
Minimal change disease pathophys
Idiopathic podocyte dysfunction T cell disorder impairs glomelrular filtration Sudden onset in children
155
Minimal change disease treatment in children
Empiric treatment preferred instead of getting biopsy Predinsone ACE/ARB if prednisone doesn't solve
156
Minimal change disease treatment in adults
Prednisone ACE/ARB Diuretics Na restricted diet Refractory may need to add immunosuppressive agents
157
Membranous nephropathy pathophys
deposits of antigen antibody complexes between glomerular basement membrane and podocytes
158
Membranous nephropathy causes
Idiopathic but associated with phospholipase A2 receptor (PLA2R) on podocytes
159
Membranous nephropathy diagnostic testing
Kidney biopsy gold standard. If anti-PLA2R positive biopsy not needed Light microscopy shows glomerular basement membrane thickening Electron microscopy shows spike and dome appearance
160
Membranous nephropathy treatment
A. Manage symptoms with diuretics, statins, ACEi/ARB, anticoag, Na restriction B. Immunosuppresive therapy: Corticosteroids alternating with cyclophosphamide, or give rituximab, or give tacrolimus or cyclosporine C. Dialysis or transplant D. treat underlying cause in secondary
161
Membranous nephropathy complications
Hypercoag (embolism, dvt) Increased risk fo bleeding Hyperlipidemia Progression to CKD Immunotherapy side affects
162
Leading cause of CKD and ESKD
Diabetic nephropathy
163
Diabetic nephropathy
Leading cause of CKD and ESKD worldwide Affects 30% of diabetics Usually present before T2DM diagnosis Highly associated with presence of retinopathy
164
Who should be screened for diabetic nephropathy
Anyone >5yo with T2DM
165
What is looked at in diabetic nephropathy screening
EGFR Urinary albumin:creatinine rati Random (spot) collection
166
Who should be monitored twice annually for diabetic nephropathy
Pt with diabetes and urinary albumin >300 or EGFR 30-60
167
Diabetic nephropathy diagnosis
Albuminuria and/or reduced eGFR in presence of high A1C and absence of other causes Retinopathy and diabetes often seen with it
168
Diabetic nephropathy treatment
Glucose control (A1C<6.5) BP control (<130/80) with ACEi/ARB Use SGLT2 or GLP1 maybe
169
Amyloidosis pathogenesis
TIssue deposition of abnormally folded proteins calle amyloid fibrils from bone marrow making amyloid light chains (primary) Or fibrils from circulating inflammatory protein in infammatory disease (secondary)
170
Renal amyloidosis diagnosis
Biopsy GOLD congo red stain with apple green birefringence under polarized light
171
Renal amyloidosis treatment
Corticosteroids reduce inflammation Melphalan and stem cell transplant is standard of care Also use cyclophosphamide, bortezomib, and dexmethazone plus daratumumab Hemodialysis or transplant if not responsive
172
Nephritic syndrome characteristics
INFLAMMATORY RBC casts Proteinuria <3.5 Hematuria HTN Edema
173
Nephritic syndrome symptoms
Edema of face, eyes, legs, abd Proteinuria Cola colored frothy urine RBC casts (acanthocytosis) HTN Decreased urine output
174
Acanthocytes
Found in nephritic syndrome RBCs damaged when filtered through glomerulus Sign of glomerulonephritis
175
Nephritic syndrome pathophys
Antigen either bacterial or autoantibody causes inflammatory response leading to tissue damage Complement overactivation can also cause it
176
Glomerulonephritis (nephritic syndrome) causes
IgA/Berger's most common in adults Goodpasture syndrome Granulomatosis Membranoproliferative glomerulonephritis Lupus Infection (strep in kids)
177
Nephretic syndrome imaging
Renal ultrasound CXR showing pulmonary edema
178
Nephritic syndrome lab findings
Elevated creatinine UA shows hematuria and proteinuria with dysmorphic red cells, red cell casts, and white cells Spot urine albumin/creatinine ratio or 24 hr urine collection to quantify proteinuria
179
What does finding red cell casts on UA suggest
Glomerulonephritis
180
Poststreptococcal glomerulonephritis presentation
MC in children 1-3 weeks after throat infection or 3-6 weeks after impetigo Group A strep HTN Decreased GFR
181
What causes poststreptococcal glomerulonephritis
Group A strep
182
Poststreptococcal glomerulonephritis diagnostic testing
Streptozyme test shwoing 5 antibodies including antistreptolysin-O UA has RBC casts (acanthocytes) and maybe proteinuria Reduced C3
183
Poststreptococcal glomerulonephritis treatment
Loop diuretics (fluorosemide) and Na and water restriction to treat HTN and edema Abx if strep infection still present
184
Most common cause of primary nephritic syndrome (glomerulonephritis)
IgA (Berger's syndrome)
185
IGA nephropathy (Berger's disease) presentation
MC cause of acute glomer Men 1-2 days after URI or GI infection HTN Fecre Dark urine Edema Hematuria
186
IGA nephropathy (Berger's disease) lab findings
Hematuria RBC casts Proeinuria Specific gravity >1.02 Elevated BUN and creatinine Normal complement
187
IGA nephropathy (Berger's disease) diagnostic testing
Renal biopsy shows IGA deposits
188
IGA nephropathy (Berger's disease) treatment
ACEi Loop diuretics CCS if rapid progression
189
Anti-glomerular basement membrane disease pathophys
Autoimmune against glomerular and alveolar basement membranes
190
Anti-glomerular basement membrane disease presentation
Younger Develop pulmonary hemorrhage (hemoptysis) and glomerulonephritis Critically ill Older Isolated glomerulonephritis Less severe course Malaise, fever, chills, arthralgia, weight loss
191
Anti-glomerular basement membrane disease Diagnostic testing
UA shows low-grade proteinuria, Gross or microscopic hematuria, and RBC and granular casts Increased BUN and creatinine ANTI-GBM antibodies in serum confirms CXR or CT shows bilateral, diffuse Ground glass or consolidative opacities
192
Membranoproliferative glomerulonephritis causes
Hep B or C
193
Membranoproliferative glomerulonephritis presentation
Nephritic syndrome
194
Membranoproliferative glomerulonephritis daignostic testing
Biopsy showing enlarged hypercellular glomeruli with thickened glomerular membrane
195
Membranoproliferative glomerulonephritis treatment
Supportive and immunosuppressant
196
Granulomatosis with polyanagitis pathophys
Vasculitis causing necrotizing granulomas
197
Granulomatosis with polyangitis presentation
Cough Dyspnea Flu-like joint pain
198
Granulomatosis with polyangitis diagnostic tests
ANCA in blood Kidney biopsy with pauci-immune crescentic glomerulonephritis with necrotizing vasculitis
199
Pauci-immune
Lacking immune complexes on biopsy
200
Rapidly progressive glomerulonephritis diagnostiv tests
Kidney biopsy shows cellular cescent formation in glomeruli
201
Rapidly progressive glomerulonephritis treatment
Immmunosuppresion (CCS or cyclophosphamide) Plasmapheresis if immunosuppression contraindicated)
202
Nephrolithiasis
Stones located in kidney
203
Urolithiasis
Stones formed in kidney exit renal pelvis into urinary collection system
204
Most common type of kidney stones
Calcium oxalate
205
Calcium oxalate stone causes
Hyperoxaluria (urinary oxylate >40mg/day) Ingestion of foods with oxalate (spinach, cocoa, nuts, pepper, tea, beets, rhubarb) Intestinal disease can effect oxalate metaobolism
206
Calcium phosphate stones causes
Urine pH > 7.2 Too much Ca and P Too little citrate Hyperparathyroidism Renal tubular acidosis
207
Uric acid stones cause
Elevated urinary uric acid from breakdown of purines in meat Low urine pH and low urine volumes
208
Uric acid stones risk factors
Gout Diarrhea Diabetes Metabolic syndrome
209
Cystine stones cause
Genetic metabolic disorder on SLC3A1 or SLC7A Kidneys not reabsorbing cystine
210
Strutvite (staghorn) kidney stones causes
Infection stones (aka magnesium ammonium phosphate stones) More commonly seen in women with UTI
211
What diet modifications can prevent kidney stones
Less animal protein DASH diet Mediterranian diet DO NOT decrease Ca intake Drink more water
212
What meds are linked to causing kidney stones
Carb anhydrase inhibitors (Acetazolamide) Systemic corticosteroids Antiretroviral Gout meds Diuretics (loop) Decongestants Abx Laxatives
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Kidney stone symptoms
Renal colic pain Sx start when stons pass from renal pelvis into ureter Pain waxes and wanes with severe spasms Unilateral Hematura NV Penile or testicular pain Dysuria, urinary urgency, suprapubic pain CVA tenderness
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Where is the stone when it causes urinary frequecy and urgency
Ureterovesicular junction
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Common places for stone to be lodged
Ureteropelvic junction Distal ureter at level of iliac vessels Uterovesical junction
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how is the pain when kidney stone is passed into bladder
Relieved
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Kidney stone diagnostic imaging
CT without contrast (most reliable) US of kidneys and bladder (first in pregnant) Plain radiographs
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Hydronephrosis
Kidney stretched and swollen from build up of urine inside (could be form stone blockage) Seen on US
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uncomplicated kidney stone treatment
Pain management Increase fluid intake Dietary mod 24 hr urinalysis Routine followup Unnula imaging with ultrasound Surgery if can't be passed
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Kidney stone <5mm treatment
Pass spontaneously Fluids and analgesics
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Kidney stone 5-10mm treatment
Might pass spontaneously Fluids Analgesia Medical expulsino therapy (alpha one antagonist or calcium channel blocker) (tamsulosin or nifedipine) (only give for 4 weeks then we need surgery if still there)
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Kidney stone >10mm
Probably won't pass to bladder Need scope and stent if distal to kidney Lithropasty if proximal or near kidney
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When to urgent consult for kidney stone
Associated with infection Urosepsis Acute kidney injury renal failure Unstable Stone not passing after 4 weeks treatment >10mm
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Procedural options in kidney stones
Ureteroscoy with laser lithotripsy Extracorporeal shock wave lithotripsy Percutaneous nephrolithotomy
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When to use percutaneous nephrostomy
Pt with infection and obstructing stone, ureteral stent, or percutaneous nephros
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What diuretic to give someone with high urine calcium
THiazides
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High urine oxalate level treatment
Calcium carbonate
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What to give for uric acid stone prevention
Potassium bicarbonate/citrate Can also bring down uric acid levels with allopurinol
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What to give for struvite stone prevention
Acetohydroxamic acid to stop bacteria from making ammonia
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Bladder calculi and cause
Stones formed in bladder from pt not being able to empty bladder completely Dehydration
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Bladder calculi presentation
Irritated bladder SEvere suprapubic pain Bleeding DYsuria Increased urine freq Cloudy, dark, bloody urine
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Bladder calculi diagnostic studies
UA shows UTI and blood CT scan DIAGNOSTIC Radiographs and US Cystoscopy to see stones in bladder
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Acute simple cystitis
Begins with colonization of vaginal introitus with pathogens from fecal flora (usually e. coli) and ascension into urethra and bladder
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Most common pathogen of acute simple cystitis
E. coli
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Acute simple cystitis presentation
Increased urine freq and urgency Hematuria Suprapubic pain Foul smelling urine AMS and nocturia in elderly NO fever
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Acute simple cystitis risk factors
Sex Spermicide Prev UTI New sexual partners in past year Diabetes Structural abnormalities
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acute simple cystitis diagnostic testing
Leukocyte esterase Nitrites WBC on microscopy Hematuria Don't always need urine culture but should be done to specify pathogen
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Who can we start treating in acute simple cystitis before UA results come back
Dysuria with or without change in urinary freq No vaginal discharge
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Treatment for cystitis with high risk aabx resistant bacteria
in patient Fluoroquinolone, bactrim, third gen cephalosporin
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Acute simple cystitis treatment
Nitrofurantoin FOsfomycin Trimethoprim-sulfamethoxazole
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Recurrent cystitis treatment
Change abx and get culture
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Most common UTI in pregnancy
E. coli
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UTI in preg treatment
Beta-lactam Nitrofurantoin Fosfomycin DO NOT give bactrim
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UTI in preg diagnostic studies
UA and culture
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Male cystitis diagnostic tests
Positive nitrates and leukocyte esterase Urine culture usually with E. coli
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Do you give abx for asymptomatic UTI
Only if preg
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Complicated UTI presentatoin
Fever Chills, rigors, fatigue, malaise Flank pain CVA tenderness NV
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Complicated UTI complications
Shock Sepsis Multi-organ failure Acute-renal failure
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Comlicated UTI diagnostic studies
UA with pyruia hematuria Leukocyte esteraase Nitrites Preg test
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COmplicated UTI imaging
Only for severely ill even after antimicrobial theray CT scan with no contrast
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Complicated UTI treatment
Outpatient: Fluoroquinolones Inpatient: 3rd or 4th gen cephalosporin, fluoroquinolones, aminglycosides 14 days
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EABV
Effective arterial blood volume
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How does your body regulate blood volume
RAAS Sympathetics ADH
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Is osmoregulation or volume regulationo more important
Volume
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Oncotic pressure
Pressure effect of proteins on movement of water
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Osmotic pressure
Pressure effect of solutes on movement of water
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Where is osmolality monitored
Hypothalamus
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Where is osmolality controlled
Hypothalamus
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Do we have more water in intracellular or extracellular space
Intracellular
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Hypovolemia clinical findings
Dry mucus membranes Decreased skin turgor Tachycardia Cool extremeties Edema Ascites Pleural efussions
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Hypovolemia treatment
Treat underlying cause Fluid resuscitation
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Hypervolemia presentation
Edema Pulmonary crackles Ascites Anasarca Weight gain Increased JVP Electrolyte probs Kidney injury
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Hypervolemia treatment
Treat underlying condition Diuresis Salt restriction
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Most common electrolyte to have problems with
Sodium
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When is hyponatremia considered severe
<125
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What to check if Na is low
osmolality If also hyposmolar it is bad. If normal or high osmolality, its not right
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How fast should you correct sodium
Within 48 hrs if acute and severe. Slowly if it has slowly come on
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What does hyponatremic with normal osmolality indicate
Lab arttifact (hyperlipidemia or hyperproteinemia)
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What does Hyponatremia with high osmolality indicate
Na effectively low due to H2O movement bc of stuff like glucose or mannitol
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What can excess water intake more than kidneys can take result in
Hyponatremia
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Hypovolemic hyponatremia causes
Fluid loss (diarrhea, vomiting, burns, diuretics)
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How to differentiate between renal and extra-renal losses of water
Urine sodium Extrarenal: <20 Renal: >20
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Hypovolemic hyponatremia treatment
Restore colume with Normal saline ADH secretion will stop once volume restored
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Euvolemic hyponatremia causes
SIADH Hypothyroidism Adrenal insufficiency Psychogenic polydipsia
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Euvolemic hyponatreamia with increased urine sodium and osmolality workup
TSH, cortisol, ACTH tests If thyroid normal suspect SIADH
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SIADH lab findings
Hyponatremia (<135) Hypoosmolality (<285) Urine Na > 20
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SIADH treatment
Fluid restriction Increase Na intake urea tablets Diuretics (loop, SGLT-2) Vasopressin
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SIADH presentation
Dizziness, fatigue, headache, vomiting Confusion, seizure, coma, brainstem herniation
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ADH independent causes of hyponatremia
Psychogenic polydipsia Beer potomania (only drink beer) Tea and toast diet (low protein leads to less solutes) Renal impairment (GFR<15)
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Hypervolemic hyponatremia causes
Cirrhosis and HF
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Primary response to hypernatremia
Increased thirst Increased ADH
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Hypervolemic hyponatremia treatment
Diuretics (no thiazides) Fluid restriction Hypertonic salene Paracentesis
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Hypernatremia presentation
Cerebral dehydration ethargy Irritability Weakness hyperthermia Delirium Seizure Coma
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What can be caused by fixing hyponatremia too fast
Osmotic demyelnation
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Non-oliguric hypernatremia causes
Diabetes insipidus Osmotic diuresis
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Oliguric hypernatremia causes
Reduced water intake Diarrhes, sweat, hyperventilation Rhabdomyolysis
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Hypernatremia treatmen
Rate of fixing electrolytes depends on severity and acuity ACute 1.5-2/hr Chronic or asymptomatic 0.5/hr Normal saline for hypovolemic until euvolemia reached then D5W Euvolemic needs D5W Hypervolemic needs diuretics and D5W
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Hypokalemia treatment
Treat underlying Stop diuretics, beta blockers, insulin Correct Mg deficiency PO dietary or supplementation of K (20-40/day) IV K in severee
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Hypokalemia ECG changes
Inverted T wave Just flat T wave early on
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What can be caused by fixing hyernatremia too fast
Cerebral edema
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Hyperkalemia ECG abnormalities
Peaked T waves Long PR segment Wide and bizarre WRS
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Hyperkalemia causes
Kidney failure Shift from ICC to ECF
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Hypomagnesemia presentation
Tremors Cramps Confusion Disorientation Weakness HTN Tachycardia Arrhythmia Difficult to distinguish from Hypo-K and hypo-Ca
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Hyperkalemia presentation
Muscel weakness and spasms Cardiac conductoin abnormalities reducing myocardial excitability Impaired amonium excretion and may lead to metabolic acidosis
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Hypomagnesemia ECG findings
V-Tach (Torsades de Pointes) Prolonged PR Peaked T waves Prolonged QRS and QT
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Hyperkalemia treatment
Confrm laab vale to rule out pseudohyperkalemia IV calcium gluconates Insulin, beta agoniast, Na bicarbonate Loop diuretics, K binders, Hemodialysis
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Hypomagnesium treatment
Magnesium oxide PO daily IV mag if symptomatic
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Hypermagnesemia presentation
Muscle weakness Decreased reflexes Mental obtundation Confusion Hypotension Paralysis Heart block Cardiac arrest
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Hypermagnesemia treatment
Remove magnesium sources IV calcium chloride Hemodialysis maybe
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Hypermagnesemia ECG findings
INcreased PR interval Widened QRS QT proongation
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Hypocalcemia clincical findings
Tetany Laryngospasm Convulsions Paresthesia Abd pain Chovstek sign Trousseau sign
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Hypocalcemia treatment
IV calcium gluconate with D5W for symptomatic Asymptomatic: Oral calcium, vitamin D., Mg if thats low too No treatment if low albumin is the cauee
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Hypercalcemia causes
Hyperparathyroidism Malignancy
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Hypercalcemia presentation
Anxiety Lethargy Constipation ANorexia Cognitive changes Kidney stones
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Hypercalcemia management
Treat underlying no therapy for asymptomatic and still <12 Normal saline Calcitonin Bisphosphonates
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Hyperphosphatemia clinical findings
Asymptomatic Similar to hypocalcemia
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Hyperphosphatemia treatment
IV calcium gluconate for acute Hemodialysis for impaired kidney function In chronic decrease dietary intake and add phosphate binders
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Hypophosphatemia clinical findings
Related to ATP deficiency Weakness, paresthesia, encephalopathy
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Hypophosphatemia treatment
PO phosphate for moderate and asymptomatic IV phosphate for severe or unable to tolerate PO Monitor phosphate and calcium levels every 6 hrs
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Contraindications to phosphate replacement
Advanced CKD Tissue damage/necrosis Hypercalcemia
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Hyperphosphatemia clinical findings
Asymptomatic Similar to hypocalcemia
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Hyperphosphatemia treatment
Acute and symptomatic: IV calcium gluconate Impaired kidneys: Hemodialysis Chronic: Decrease dietary intake and add oral phaosphate binders
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Hypophosphatemia presentation
Related to ATP deficiency Weakness Paresthesia Encephalopathy
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Hypophosphatemia lab tests
Urine phosphate (24 hrs) distinguishes between renal and non-renal causes CBC, CMP, ABG to see other causes
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hypophosphatemia treatment
Moderate and asymptomatic: PO phosphate Severe and symptomatic: IV phosphate Monitor every 6 hrs
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High anion gap metabolc acidosis causes
Ketoacidosis (uncontrolled diabetes) Uremia (kidney failure) Lactic acidosis (tissue damage) Toxic ingestion (antifreeze, aspirin, pesticides, ethylene glycol, methanol, salicylates)
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Ketoacidosis pathophys
Not enough insulin so blood glucose not used causing Muscle, adipose, and glucagon breakdown
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Lactic acidosis values
Lactate>2
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Lactic ac
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Lactic acidosis causes
Sepsis shock Mesenteric ischemia Resp failure Carbon monoxide poisoning Intense exercise Seizures Alcoholism HIV infection
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Normal anionic gap acidosis causes
DIarrhea Renal tubular acidosis both losses of HCO3
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Metabolic acidosis clinical findings
Kussmaul respirations (deep and labored) headache Lethargy Stupor Coma
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Chloride responsive alkalosis causes
Vomiting NG tube suction Diuretics
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Chloride unresponsive alkalosis causes
Hyperaldosteronism Antacids
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Metabolic alkalosis lab findings
High blood pH High HCO3 Low Cl Low K
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Respiratory acidosis presentation
Somnolence Confusion Asterixis Myoclonus Pursed lip breathing Barrel chest
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Respiratory alkalosis cause
Hyperventilation leading to hypocapnea
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Second most common urologic cancer
Bladder (mostly urothelial cell aka transitional cell carcinoma)
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Bladder cancer symptoms
Hematuria Can have change in urine freq and consistancy Abd masses hepatomegaly Lymphadenopathy Lymphedema of lower extremeties
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Bladder cancer lab findings
Hematuria Pyuria and azotemia maybe Anemia cytology maybe positive
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Bladder cancer imagin
Confirmed with cytoscopy and biopsy US CT MRI
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What is looked at in Bladder cancer staging
Size Pleomorphism Mitotic rate Hyperchromatism staining Extent of bladder wall penetration and presence of metastasis
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Bladder cancer screening levels
T- primary N- regional lymph nodes M- Distant metastasis
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Bladder cancer treatment
Surgery (transurethral resction is FIRST LINE) Partial cystectomy for muscle invasive Give chemo on top of surgery to prevent recurrence INtravesical therapy Chemotherapy Radiotherapy Immunotherapy (anti-PDL-1)
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What treatment option for T2 bladder cancer
Chemo first Then radical cystectomy
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Interstitial cystitis (interstitial pain syndrome) symptoms
pain with bladder filling relieved with emptying Urine freq and urgency Dramatic exaggeration of normal sensation
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Interstitial cystitis diagnosis
Exclusion Lots of times presents with IBS/IBD or allergies
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Interstitial cystitis treatment
Hydrodistension (stretching our bladder every couple months) Amitriptyline Nifedipune Pentosan DMSO + heparin Nerve stimulation Remove bladder is last resort No cure
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Urinary incontinence transienct causes
Infection most common Delirium Infection Atrophic urethritis and vaginitis Pharmeceuticals Stool impaction Restricted mobility
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Urinary incontinence established causes
Detrusor overactivity Urethral inocmpetence (stress incontinence) Overflow incompetence
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What meds can cause urinary incompetence
Diuretics Anticholinergics Psychotropics Opioid analgesics Alpha blockers Alpha antagonists Ca channel blockers
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Detrusor overactivity/urge incontinence physical exam
Fill bladder with water and have them cough vigorously Delayed leakage shows urge incontinence
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Detrusor overactivity/urge incontinence treatment
Piss schedule Weight loss if obese Pelvic floor muscle (Kegel) exercises If that doesn't work, put on antimuscarinci/anticholinergic (tolterodine or oxybutynin) Boxtox Beta-3-agonists (mirabegron)
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Stress incontinence pathophys
Hypermobility of bladder (displacement of bladder neck and urethra) during increased abd pressure (coughing or valsalva maneuver)
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Stress incompetence treatment
Limit caffeine and fluid intake Weight loss in obese Pelvic floor muscle exercises Vaginial cones or pessaries Surgery last resort
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Overflow incontinence presentation
Dribbling Urge incontinence due to detrusor overactivity Nocturia Can't fully empty bladder
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Overflow incontinence causes
Meds Sacral lower motor neuron dysfunction
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Overflow incontinence treatment
Bladder decompression with catheter first Then Alpha blocking agent (tamsulosin and finnasteride) Double voiding Press on bladder Straight cath before bed
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Cystocele
Bladder prolapse Occurs when pt stands or strains Usually from pelvic floor injury in childbirth
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Dyspareunia
Painful intercourse
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Cystocele is located at what aspect of vaginal wall
Anterior
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Cystocele symptoms
Vaginal heaviness Sensation of sitting on ball Straining or coughing Urinary freq changes Sensation of incomplete emptying Constipation Dyspareunia
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Cystocele imaging
Sonography or MRI
342
Cystocele treatment
Pessary pelvic floor muscle exercises Estrogen for some Surgery maybe Weight loss in obese High fiber diet and laxatives to improve constipation
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Diabetic autonomic neuropathy
Poor glucose control causes bladder dysfunction
344
Diabetic autonomic neuropathy treatment
Bethanechol to improve emptying Stirct urine schedule and Crede maneuver Advanced need catheterization
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Female urethritis causes
Gonorrhea Chlamydia Mycoplasma Ureaplasma Trichomonas
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Female urethritis presentation
Urethral discharge Tenderness Congested mucosa Induration of urethra
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Female urethritis treatment
Estrogen cream