Chronic Kidney Dz Flashcards

1
Q

Chronic Kidney Disease (CKD)- End Stage Renal Disease (ESRD)

Patients remain asymptomatic until their disease has significantly progressed, true or false?

A

True

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2
Q

Common causes of late-stage chronic kidney disease

A

most are due to DM and HTN

Some are unknown or due to other causes

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3
Q

CKD

Definition

A

-GFR less than 60 mL/min for greater than or equal to 3 months with or without kidney damage

OR

-Kidney damage for greater than or equal to 3 months with or without decreased GFR

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4
Q

CKD

disease progression

A
  • CKD is rarely reversible and leads to a progressive decline in renal function
  • reduction in renal mass leads to hypertrophy if the remaining nephrons
  • this places a burden on the remaining nephrons and leads to progressive glomerular sclerosis and interstitial fibrosis
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5
Q

CKD

Risk factors

A
  • DM
  • HTN
  • older age
  • FHx
  • drug toxicity
  • urinary obstruction
  • african american
  • american indian
  • asian
  • pacific islander
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6
Q

How many nephrons does each kidney contain?

What are the consequences of destruction of the nephrons?

At what GFR % decrease do blood urea and Cr start to show a measurable increase?

Plasma Cr value will approximately double with a ____% reduction in GFR

A

How many nephrons does each kidney contain?
-1 million

What are the consequences of destruction of the nephrons?
-hyperfiltration and compensatory hypertrophy

At what GFR % decrease do blood urea and Cr start to show a measurable increase?
-Only after GFR has decreased by 50%

Plasma Cr value will approximately double with a _50__% reduction in GFR

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7
Q

What five steps are taken during the initial assessment of CKD?

A
  1. Confirm primary renal dx
  2. Establish chronicity
  3. Identify reversible factors
  4. Detect co-morbid factors
  5. Establish a baseline database
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8
Q

What are the five stages of CKD?

At which stages do symptoms appear?

A

Stage 1: Kidney damage with normal or increased GFR (greater than 90 mL/min)

Stage 2: Mild reduction in GFR (60-89 mL/min)

Stage 3: Moderate reduction in GFR (30-59 mL/min)

Stage 4: Severe reduction of GFR (15-29 mL/min)

Stage 5: Kidney failure (GFR less than 15 mL/min or dialysis)

*sx typically appear in stages 4 and 5, 1-3 are frequently asymptomatic

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9
Q

How do you measure renal function?

A

Serum Creatinine

  • it will increase as renal function worsens
  • alone, SCr is not an accurate measurement of GFR
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10
Q

The national kidney foundation advises that what two testes be used together to improve prognostic accuracy?

A

GFR and Albuminuria

**Microalbuminuria is a key parameter for measuring nephron injury and repair (its an early sign of kidney disease)

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11
Q

What is Azotemia?

What are the types?

What can Azotemia lead to?

A

What is Azotemia?
-condition characterized by high levels of nitrogen-containing compounds in the blood

What are the types?

  • Prerenal azotemia
  • Primary renal azotemia
  • Postrenal azotemia

What can Azotemia lead to?
-If not treated, can lead to Uremia

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12
Q

What is Uremia?

When do sx occur?

A

What is Uremia?
-condition resulting from advanced stages of kidney failure in which urea and other nitrogen containing wastes are found in the blood

When do sx occur?
-sx may not occur until 90% of the nephrons are destroyed

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13
Q

Uremia

sx

signs

labs

A

sx: fatigue, weakness, easy bruising, breath “fishy odor”, metallic taste in mouth, epistaxis, dyspnea, pulm edema, pericarditis, anorexia/n/v, ED, amenorrhea, restless legs, numbness, cramps, irritability
signs: Sallow (unhealthy) appearing, pallor, ecchymosis, excoriations, edema, yellow, urinous breath, pale conjunctiva, rales, pleural effusion, HTN, cardiomegaly, friction rub, stupor, asterixis ( tremor of the hand when the wrist is extended), peripheral neuropathy
labs:
- BUN/Cr: elevated
- CBC: anemia
- CMP: hyperphosphatemia, hyperkalemia, hypocalcemia
- Serum albumin levels: low (spilling into urine)
- lipid profile: risk of CVD
- Urinalysis: broad waxy cast cells
- also look for evidence of renal bone disease by serum phosphate, Vit D, alkaline phosphatase, intact PTH levels

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14
Q

Uremia

imaging

complications

A

Imaging:

  • renal ultrasound (small echogenic kidney bilaterally
  • CT
  • MRI/MRA
  • Retrograde pyelogram
  • renal bx (indicated when real impairment is present and the dx is unclear after extensive work-up

Complications

  • Hyperkalemia (especially when GFR drops below 10 mL/min, kidneys have a decreased ability to secrete potassium)
  • metabolic acidosis (damaged kidneys are unable to excrete the 1 mEq/kg/day of acid generated by metabolism of dietary proteins, this limits the production of ammonia and limits buffering of H+ in the urine…excess H+ are buffered by large calcium carbonate and calcium phosphate stores in the bone…this contributes to renal osteodystrophy of CKD)
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15
Q

(more) Complications of CKD

CV

Hematologic

Neurologic

A

CV

-HTN, pericarditis, CHF, pulmonary edema, Heart disease (LVH and Ischemic heart disease)

Hematologic

  • Anemia (normochromic, normocytic), due to decreased EPO production
  • Coagulopathy (d/t platelet dysfunction, abnormal adhesiveness and aggregation)

Neurologic

  • uremic encephalopathy
  • peripheral neuropathy (stocking glove distribution)
  • Sub-arachnoid hemorrhage
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16
Q

(more) Complications of CKD

Disorders of mineral metabolism

Skin

A

Disorders of mineral metabolism

  • hypocalcemia
  • hyperphosphatemia

Skin

  • dry, yellow, brown color
  • fingernails become thin and brittle
  • Uremic Frost
17
Q

What are disorders of calcium, phosphorus, and bone referred to in CKD?

Pathophys

A

Renal Osteodystrophy

  • hyperphosphatemia leads to hypocalcemia
  • PTH is stimulated and leads to Osteitis Fibrosa Cystica (a skeletal disorder caused by hyperparathyroidism, stimulates the activity of osteoclasts, cells that break down bone) and high level of bone turnover
18
Q

Renal Osteodystrophy

causes

Complications

A

Causes:

  • ability to excrete phosphate is lost
  • decreased production of Vit D leads to decreased intestinal absorption of calcium (to balance out phosphate)
  • hypoglycemia triggers PTH production and release
  • secondary hyperparathyroidism leads to Ca mobilization from bone and increase renal phosphate excretion to maintain electrolyte homeostasis

Complications

  • Osteomalacia
  • bony pain and proximal muscle weakness
19
Q

CKD management

A
  • Appropriately screen and dx early CKD
  • consult nephrologist

Delay or halt progression by:

  • treat underlying condition
  • BP control (ACE/ARB)
  • treat hyperlipidemia
  • control blood sugar
  • avoid nephrotoxins (contrast dye)
  • treat hypocalcemia (calcium supplements)
  • loop diuretics for volume overload
  • oral alkali supplements for metabolic acidosis
20
Q

Why is a special diet important for patients that are on dialysis?

What is the special diet?

A

Because dialysis alone will not effectively remove all waste production. Also, these products can build up between dialysis tx.

Protein restriction (1 gram/kg/day)

salt and water restriction

potassium restriction

iron supplements

21
Q

Who to screen for CKD

A
  • FHx (especially in african americans)
  • metabolic syndrome and smoking
  • patients greater than 65 years old with associated CV risk factors and normal plasma creatinine
22
Q

How to screen for CKD

A
  • GFR (24 hour urine no longer required, eGFR (estimated) can be calculated)
  • Proteinuria (urine dipstick)
  • Screening for proteinuria, albuminuria, and microalbuminuria can reveal a decrease in kidney function when GFRs are normal
23
Q

CKD tx Overall

A
  • Restriction of daily protein
  • fluid restriction
  • daily caloric intake of 40-50 cal/kg/day
  • control HTN, DM, lipids
  • sodium restriction (2-4 g/day)
  • potassium restriction
  • calcium and phosphorus control
  • management of metabolic acidosis and anemia
  • vascular access for dialysis
  • transplantation
24
Q

Dialysis

Indications

how often?

A

Indications

  • hyperkalemia
  • severe metabolic acidosis
  • pericarditis

how often?
-3x/week, takes 3-5 hours

25
Q

Hemodialysis

types of access

A

Types of access

  • vascular shunt (surgically constructed)
  • Prosthetic graft (common to get infection, thrombosis, aneurysm formation)
  • Temporary indwelling catheters (PICC lines)
26
Q

Peritoneal dialysis

what is the “dialyzer”?

benefits?

Complications

A

what is the “dialyzer”?

-peritoneal membrane

benefits?

-permits greater pt autonomy

-minimizes the symptomatic swings observed in
hemodialysis pts

-phosphates are better cleared

Complications

  • n/v
  • abd pain
  • fever
  • diarrhea/constipation
  • infection (staph aureus)
27
Q

To be considered for an Kidney transplant, patient must:

A
  • have a condition for which transplantation is considered an effective tx
  • have severe and progressive disease
  • be willing to accept the risks of surgery and subsequent medical tx
  • be physically and emotionally capable of undergoing surgery and subsequent medical tx
28
Q

Kidney transplant requirements

A
  • pre-transplant exam
  • CXR
  • complete medical and surgical hx
  • EKG
  • ultrasound with doppler
  • blood tests
  • pulmonary function test
  • viral testing (hepatitis, CMV, EBV, HIV
  • histocompatability testing
29
Q

Who is excluded from Kidney transplant consideration?

A
  • Age greater than 70
  • high risk pts for major surgery (severe CV dz)
  • high risk pts for:cancer, acute or chronic infections
  • surgical impediments: calcified vessels, bladder diseases
30
Q

What do all transplant patients need to be started on before surgery?

A
  • Pre-transplant immunosuppression
  • gancyclovir
  • broad spectrum abx
  • monitor drugs and levels
31
Q

Who is exculded from donating a kidney?

A
  • age greater then 70
  • carriers of chronic infections (HIV, Hep B/C)
  • carriers of chronic diseases (DM, cancer, amyloidosis, vascular pts, autoimmune
  • and of course someone with just one functioning kidney
32
Q

Post-transplant complications

A
  • rejection
  • infection
  • CV (CAD, CHF, CVA, HTN)
  • Cancer (Skin, blood, solid organs)
  • Drug toxicity
  • DM/cataract/hirtruism/alopecia….etc
33
Q

Follow up schedule for kidney transplant pts

A

1st month: 3x week

1-3 months: once a week

3-6 months: once every 2 weeks

6 months-2 years: once a month

2 years and over: every 2 months

34
Q

What should the kidney transplant follow up visit include?

A
  • hematology
  • general biochemistry
  • urine
  • drug level monitoring
  • detailed clinical exam
  • diagnostic imaging (when necessary)
  • biopsy
  • special attention to: CV dz, neoplastic dz, infection, parathyroid function
35
Q

Kidney transplant rejection

clinical signs

A

Clinical signs

  • malaise
  • fever
  • oliguria
  • HTN
  • graft tenderness
  • dx hinges on serial creatinine measurements
36
Q

What vaccinations should all CKD patients have?

A

H1N1

Hep A/B

Influenza

Pneumococcal (PPV)