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Renal System

The document discusses renal and urinary tract anatomy and function. It describes the structures of the kidneys and how they filter blood to produce urine through glomerular filtration, tubular reabsorption and secretion. Key points are that the kidneys filter 20% of cardiac output to form urine, reabsorbing most water and electrolytes while excreting wastes. The kidneys also play an important hormonal role in regulating blood pressure and red blood cell production.

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Frances Rebecca
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0% found this document useful (0 votes)
169 views14 pages

Renal System

The document discusses renal and urinary tract anatomy and function. It describes the structures of the kidneys and how they filter blood to produce urine through glomerular filtration, tubular reabsorption and secretion. Key points are that the kidneys filter 20% of cardiac output to form urine, reabsorbing most water and electrolytes while excreting wastes. The kidneys also play an important hormonal role in regulating blood pressure and red blood cell production.

Uploaded by

Frances Rebecca
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as DOCX, PDF, TXT or read online on Scribd
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Renal and urinary tract function

 Objectives
o Review anatomy and physiology of renal system
o Discuss mechanisms to maintain homeostasis
o Discuss changes associated with aging and necessary nursing intervention s
o Discuss cultural considerations
o Discuss assessment techniques
 A and P
o Two kidneys
o Each kidney has own tube- ureter
 That drains into bladder
o Abdominal aortic that goes into renal arteries
o Urinary bladder
 Expands and contracts
 In collapsed state until you start to fill it then it will expand
o Urinary meatus
 Internal sphincters to hold till you get to bathroom
o Kidney inside
 Renal cortex- outside
 Renal medulla- inside
 Stones will usually lodge at vesicoureteral junction
o Both ureters meet bladder
o Each kidney in renal capsule
 Like every organ has Layer around it
 Receives 20-25% of total cardiac output 12x an hour is circulating
 Needs to be filtered and excreted
o Within kidney
 Millions of nephrons
o Afferent arterial
 Brings blood into system
 Oxygenated blood at good pressure going into nephron
 Have millions of those
 Straining out filtrate (not urine yet)
 Every time outflow goes through nephrons
 Remove filtrate
o Toxins, water
o Bowmen’s capsule collects this
 Loop of Henle
 Lasix exerts its effect here
 Never gets rid of fluid at loop normally
 Lasix influences that loop
 Excrete 180 L per hour
 In this section reabsorb some of that fluid
 Actually excrete 1.5 L
o Efferent
o Glomerulus
o Bowman’s capsule
 If damaged
 Output will decrease
o Lasix get rid of salt, potassium
 Watch values
o Excrete BUN
 Watch value
 When body breaks down blood, body has to reabsorb that blood
 BUN will be elevated when blood is being reabsorbed
 When excrete BUN, some can be reabsorbed
 Bruise
o Cannot reabsorb Creatinine
o Bladder anatomy
 Ureters open into bladder
 Urethra
 Opening at bottom
 Urine comes down and should not go back up
 Not just reservoir
 If problem with meatus can go through wall of pelvic above suprapubic
area
 Detrusor muscle
 When put in bladder, meet resistance that is this muscle
 Hold steady and allow to relax then continue to reinsert
 Function of upper urinary tract
o Regulatory function
 FEAR
 Formation of urine
 Electrolyte balance
 Acid base balance
 Renal clearance
o Rid of body waste
o Hormonal function
 REV
 Secrete renin
o Powerful vasoconstrictor
o Make smaller
 Erythropoietin produced to stimulate bone marrow to RBC synthesis
 Vitamin D converted to an active form for calcium reabsorption and the
parathyroid hormones
 Regulatory function: urine formation
o Filtration at glomerulus
 Dump spaghetti into strainer
 Fluid start to accumulate
 About 20% of blood passing through the globe rule (1200 mL/min) is filtered
into nephron
o Absorption into peritubular capillaries
 Then absorb in tubes around
 Substances move from filtrate back into peritubular capillaries or vasa recta
o Reabsoprtion into tubule for excretion in urine
 Reabsorb more here and excrete out what is left
 Substances move from peritubular capillaries or vasa recta into tubular filtrate
o Processes are dependent on osmolarity and osmolarity
o If blood glucose level reaches 220 or higher
 Will spill into urine
 Not normally be sugar in urine
 If sugar in urine, blood sugar was high, but took time to get there so not high
anymore
 Urine formation by glomerular filtration
o About 20% of blood passing through the glomeruli is filtered into nephron
 1200 mL/min
o 180 L/day
o Normal GFR= 120-130 mL/min
 Controlled by BP and blood flow
 As long as maintained at certain amount then will have enough pressure
to work as it should
 BP decrease= less pressure so filtration decrease
 Self regulating mechanism is not effective with BP below 65- 70 mm Hg
systolic = perfusion problem or MAP of less than 65 mm HG
o Map
 Mean arterial pressure
 ((DBP x2) + SBP then /3)* on test
 If too low, not perfuse as should so hurt kidney
 Systolic= top number
 Diastolic= bottom number
 Water, electrolytes, and small particles filtered
 Enters proximal convoluted tubules (PCT) and is known as “tubular
filtrate”
 Urine formation by tubular reabsorption
o Keep normal urine output at 1-3 L /day
o Most water and electrolytes are reabsorbed from filtrate and returned into blood
o 50% of urea in filtrate is reabsorbed – except creatinine
o Reabsorb some of glucose filtered
 Renal threshold for reabsorption= 220 mg/dL
 > 220 mg/dL stays in filtrate
 Present in urine
o Bicarbonate, calcium, and phosphate are reabsorbed
 Maintain acid base balance
o Tubules return all filtered water back into body
 Vasopressin (ADH- anti diuretic hormone) and aldosterone
 More permeable to water with Vasopressin (ADH) and aldosterone
 Increased arteriole constriction
o Alters bp and amount of fluid that exits the glomerular
capillaries
 Aldosterone promotes the reabsorption of Na in the DCT
o Water reabsorption occurs as result of movement of Na
 Where sodium goes- water goes
 Urine formation by tubular secretion
o Transfer materials from peritubular capillaries to renal tubular lumen
o Secretion of Hydrogen (H+) and NH4+ (ammonia) from blood into tubular fluid that
helps to keep blood pH at its normal level
 Hormonal function
o Renin- powerful vasoconstrictor
 Assist in BP control
 Triggers chain of events
 RAAS pathway
 Renin angiotensin aldosterone system
o In response to low Bp or serum sodium, kicks in to help
compensate for that
 Serum sodium
 Low sodium= low fluid volume
 Not a lot of fluid= BP decreases
 Regulate bp and bring it up
 Liver Releases hormone called antiotensinogen
 Response to that kidney shoots out renin
 Together they react and end up with angiotensin 1
 When angiotensin 1 gets to lungs, they release ACE
 Level where ACE inhibitors work
 When they take ACE inhibitors, stop enzyme
from being released
 ACE causes raise in blood pressure
 Ace and angiotensin 1 together make angiotensin 2
 Angiotensin 2 works on level of kidney and adrenal
glands
 Go to adrenal glands and create aldosterone
 Aldosterone effect in body
o When created, helps BP regulation
 When have aldosterone,
increase reabsorption of
sodium, so increase fluid on
board that also increases BP
o Aldosterone decreases K so watch
levels and provide preventative
measures
 Angiotensin 2 at kidney
o Cause vasoconstriction in arterioles
 Going to increase BP
 More narrow arteries and
vessels= higher Bp goes
o Diagram information
 Stimuli for renin secretion
 Decreased renal perfusion pressure and/or
decreased salt delivery to kidney tubules
o Examples
 Hemorrhage
 Heart failure
 Cirrhosis
 Loop diuretics
 Decreased salt intake
 Angiotensin to liver
 Renin release
 Angiotensin 1
 Renal autoregulation
o Efferent arterioles constrict
o GFR maintained
 Increased blood pressure
o Vasoconstriction
o Increased myocardial contractility
o Prostaglandin release
 Increased circulating volume
o Aldosterone release
o Sodium and water reabsorption
o K excrete
o ADH release
o Prostaglandins
 Regulate glomerular filtration, kidney vascular resistance and renin production
 Increase sodium and water excretion
o Erythropoietin
 Triggers RBC production in bone marrow
o Vit D
 Processing occurs from sunlight and in liver
 Converted to active form in kidney
 Needed to absorb calcium
 Renal clearance
o Renal clearance test
 How well Kidney clear solutes form plasma
o 24 hr urine collection
 Throw away first
 End of time void and put in container
 On ice or in cool place
 Dark place
o Creatine: waste product of skeletal myo breakdown
 Filtered via glomerulus
 Passes through tubules with minimal change
 Excreted in urine
 Creatinine clearance good indicator of GFR (kidney function)
 Test question
o Factors that affect renal clearance
 Speed across filter
 Affected by pressure
 Substance reabsorption along tubules
 Quantity of substances secreted back into tubules
 some med nephrotoxic
 Normal urinary output
o UO (urinary output)/kg decreases as child ages bc kidney becomes more efficient at
concentrating urine
 Infant
 2ml/kg/hr
 Children
 0.5-1 ml/kg/hr
 Adolescents
 40-80 ml/hr
 Adults
 1-3 L/day
 Ureters, urinary bladder, urethra
o Ureters
 Connects the renal pelvis to urinary bladder
o Urinary bladder
 Muscular sac
 Men
 Front of rectum
 Women
 In front of vagina
o Urethra
 Narrow tube to eliminate urine from bladder
 Men 6-8 in
 Women 1-1 ½ in
 Kidney changes associated with aging *
o Reduced ability to filter and excrete
 Smaller with age
 Reduced blood flow
 Nephrons at risk for damage during BP changes
 Number of glomeruli and GFR decreases
 GFR around 65ml/hr
o ½ the rate of young adult
 Risk for fluid overload
 Decline more rapid in DM, HTN, HF
 Greater risk or damage from drugs and contrast dye
o Why hold metformin when going for dye bc both hard on kidney
and could cause renal failure
o Tubule length decreases
 Decrease ability to concentrate urine
 Urgency
 Nocturnal polyuria
o Regulation of sodium, acids, and bicarbonate less effective
o Risk for dehydration and hypernatremia
 Impairment in thirst mechanism in addition to age related changes
o Decreased bladder capacity
o Reduced ability to retain urine r/t decreased bladder capacity change secondary to
detrusor muscle
o Urinary sphincters become weak
o Women
 Urinary incontinence
 Wreaked myo in pelvic wall = shorten urethra
o Men
 Urinary retention
 Enlarged prostate gland
 Difficulty starting stream
 Nursing interventions with older adult
o Monitor hydration status and snacks provide adequate fluid intake
 Regulation of water balance decreases with age changes secondary to
decreased GFR
o Administer all drugs carefully especially nephrotoxic
 Blood flow reduced
 Decrease blood clearance secondary to decrease GFR
 Some drugs increase urine output
 Anticholinergic drugs promote urinary retention
o Safety with nocturia
 Ensure lighted and clear pathways
 Bedside toilet/urinal
 No fluid intake 2-4 hr before bedtime
 Home teaching
o Urination needs
 Encourage urination at least every 2 hr
 Scheduled urination may avoid overflow incontinence
 Respond to pt urination need ASAP
 May alleviate stress incontinence
o Perineal care in women
 Shortened urethra increase risk for bladder infections
 Cultural considerations
o African Americans greater risk for kidney failure
 Greater age related decreases in GFR than white people
 Excretion of sodium is less effective in hypertensive pt
 20% less blood flow secondary to changes in small vessels and intrarenal
responses to renin
o Education about yearly urinalysis to check for microalbuminuria and evaluating serum
creatinine
 Microalbuminuria
 Small protein in urine
 Dip stick tests
o Indication of clearance and function of kidney
 Pt history assessment
o Pt history
 Age, gender, race, ethnicity
 Nonmodifiable risk factors
 Sudden onset HTN after 50 could indicate HTN
 Men older than 50 with urine pattern changes could indicate prostate disease
 Women have shorter urethras increase risks for cystitis
 Previous kidney and urologic problems
 Chronic problems
 DM
 HTN
 Vessel damage with these diseases
 Chemical exposure
 Illegal drugs
 Recent travels
 Socioeconomic status
 Lack of insurance
 Access to health care
 Lack of transportation
 Education
 Completing antibiotic therapy
 Which meds do not need to be taken together
 Watch self medication due to socioeconomic factors
o Only take BP pill every other day
 Language barriers
o Nutrition history
 Diet including recent changes in diet
 Increase in protein with poor fluid intake could = calculi
 Fluid amount and type
 2L/day recommended to prevent dehydration and cystitis
 Changes in appetite
 Possible buildup of nitrogenous waste product as result of kidney
impairment
o Medication history
 Identify ALL medications as many can cause impaired kidney function
 Gentamicin can cause ACUTE KIDNEY INJURY (AKI)- NEPHROTOXIC
 OTC
o APAP and NSAIDS
 HTN, DM, cardiac, etc
o Family history and genetic risk
o Current health problems
 URI, GI, arthralgia, myalgia can be related to kidney function problems
 Renal colic
 Pain radiating into perineal area, groin, scrotum, or labia
o Occurs when stones are present as they obstruct or are being
passed and the ureter is distended
o Occurs with pallor, diaphoresis, hypotension
o Pain occurs bc of nerve tracts near kidneys and ureters
 Pattern and control of urination and characteristic of urine
 Encourage diary
 Anorexia, NV, myalgia, pruritus, fatigue and lethargy
 Signs of uremia
o Buildup of nitrogenous, waste products in the blood secondary
to kidney impairment
 Commonly used terms
o Anuria
 Total urine output of less than 100 ml in 24 hr
o Azotemia
 Increased blood urea nitrogen and serum creatinine levels suggestive of kidney
impairment but without outward symptoms of kidney failure
o Bruit
 Audible swishing sound produced when volume of blood or diameter of blood
vessel changes
o Dysuria
 Discomfort or pain associated with micturition
o Frequency
 Feeling need to void often, usually voiding small amounts of urine each time
 May void every hour or even more frequently
o Hesitancy
 Difficulty in initiating the flow of urine, even when the bladder has sufficient
urine to initiate a void and the sensation of need to void is present
o Micturition
 Act of voiding
o Nocturia
 Awaken prematurely from sleep bc of need to empty bladder
o Oliguria
 Decreased urine output
 Total urine outpu between 100-400 ml in 24 hr
o Polyuria
 Increased urine output
 Total urine output usually greater than 2000 ml in 24 hr
o Uremia
 Full blown manifestations of kidney failure
 Sometimes referred to as the uremic syndrome
 Especially if cause of the renal failure is unknown
o Urgency
 Sudden onset to feeling of need to void immediately
 May result in incontinence if pt is unable to get to toileting facilities quickly
 Physical assessment
o General appearance
 Skin
 Rashes
 Ecchymosis
 Yellow discoloration
 Pallor
 Dry and scaly skin
o Uremic pruritus
 Edema
 Pedal, pretibial (shin next to bone), sacral (mostly bed bound), and
periorbital (around eyes, fluid volume overload, heart failure- heart not
pump effectively then kidney will not perfuse)
o Lung auscultation
 Determine if fluid is present
 Crackles, wet lung sounds
 Overload
o Weight
 Water weight
 Weigh every day, same time, same way
 Best assessment of fluid retention
o Vital signs
 BP
 Up
 HR
 Bounding with excessive fluid
 Tachycardia and Brady or faintly felt
o LOC, alertness, and cognitive changes
 Deficit= result of waste buildup
 Lethargy bc toxin not excreted out of system
 Kidney, ureters, and bladder physical assessment
o Inspect
 Abdomen and flank area supine and sitting
 observe for symmetry/ discoloration in CVA (costovertebral angle) region
 outline of bladder may be seen with severe distention
o Auscultate
 Over midclavicular line
 Bruit over renal artery= renal artery stenosis
o Palpate
 Ask about tenderness
 Palpate non tender areas first
 Lightly palpating would be harmful if tumor or aneurism is suspected
o Urethra physical assessment
 Inspect
 Meatus and surrounding tissue
o Discharge
 Blood, mucous, pus
o Lesions, rashes on penis, scrotum, labia, or vaginal opening
 Psychosocial assessment
o Fear
o Anger
o Embarrassment
o Anxiety
o Guilt
o Sadness
 Laboratory diagnostic assessment
o Urine test
 Urinalysis
 1st morning urine best
 Collection methods voided urine
o Clean catch urine
o Catherterized specimen
o 24 hr urine collection
 Urine color
o Can be altered by concentration of urine and drug metabolites
o Colorless to pale (straw)
 Should be this color
 Darker color more concentration
 Can be altered by drugs
o Pink to red
 Medication
 Pyridium
 Beets, blackberries, rhubarb
 Blood
o Blue/green
 Results from dyes
 Reaction of pH of urine with plastic of catheter bag
 Blue bag syndrome
o Orange to amber
 Dehydration
 Liver Problems
 AZO
 Pyridium
o Brown to black
 Macrobid
 Iron supplements
o Specific gravity
 Normal value- 1.010-1.030
 Scale
 Low, well hydrated, lighter urine 1.010
 High, dehydration, darker urine
 Concentration of particles
 Refers to density of urine compared to distilled water
 High
o Dehydration
 Diarrhea
 Vomit
 Sweating
 Low kidney blood flow
 Excess ADH (vasopressin)
 Surgery
 Anesthetic agents
 Certain drugs of SIADH
o Urine osmolality
 High fluid loss = high concentration bc the kidney’s response to save water
 Diet, drugs, and activity can change osmolarity
o Urinalysis
 RBC (hematuria)
 WBC (pyuria infection inflammation)
 Proteinuria
 High
o Stress, infection, glomerular disorders (increased permeability
allows proteins to pass)
 Microalbuminuria
 Albumin in urine could mean early kidney disease especially in DM pt
 Glucose
 Filtered by glomerulus and reabsorbed by proximal tubule of nephron
 When BG rises above 220 mg/dL
o Renal threshold for reabsorption is exceeded and glucose spills
over into urine
 Ketone bodies
 Present when fat is used instead of glucose for energy
 Leukoesterase
 Indication of UTI
 Sediment
o Urine test
 Urine for culture and sensitivity
 Clean catch or catheterized specimen
 Analyzed for numbers and types of organism
 Culture and sensitivity report
o Blood urine test
o Creatinine clearance
 Measure progression of kidney disease (KD) staging
 Measures volume of blood cleared of endogenous creatinine in 1 min
 Approximates GFR
 Sensitive indicator of KD used to follow progression of disease
 Age, gender, height, weight, diet, and activity level influence expected
results
 Drug dosing may need to be decreased
o Collect urine for 24 hr
o Blood drawn at end of urine collection
o Blood test
 Serum creatinine level
 Muscle and protein break down excreted by kidney
 Normal range
o 0.6-1.2 mg/dL
 Higher in men bc of increased muscle mass
o Older adults have decrease in muscle mass and a decrease rate
of creatinine clearance
 Caution noted
o Iodinated contrast dyes and some drugs with a serum creatinine
of 1.5 mg/dL or greater
 Notify MD if elevated
o BUN
 Measures effectiveness of kidney excretion of urea nitrogen (by product of
protein breakdown in liver) that has been filtered by kidneys from blood
 Not best indicator for kidney function
 Normal range
 7-18 mg/dL
 >60 yo 8-20 mg/dL
o BUN/serum creatinine ratio
 Determines if non kidney related factors are causing increase in BUN
 Blood volume low or CO low the BUN will rise more rapidly then serum
creatinine= ratio high
 Increase in BUN and serum creatinine= kidney dysfunction unrelated to
dehydration or poor perfusion
 Normal range
 6-25
 BUN divided by creatinine
o Blood osmolarity
 Good indicator of hydration status
 Measures concentration of particles in blood and urine
 Normal range blood
 285-295 MOSM/L
 ADH (vasopressin) is released when levels are high so water can be reabsorbed
 Imaging diagnostic assessment
o Kidney, ureter, and bladder x-ray (KUB)
 No preparation
 Supine position
 Measure kidney size and detect obstruction
o Computed tomography/magnetic resonance imaging of kidney
 Measure size, detect obstruction or masses, assess renal flow
 Dye may be used
 May be NPO
 Hold metformin 24 hr before and 48 hr after
 Evaluate kidney function before restarting
 Increase fluid intake to maintain UO at 1-2 mL/kg/hr for 6 hr
 No metal implants with MRI
 Dye contrast allergies
 Hellfish/iodine
o Renal scan/Nuclear
 PIV for radioisotopes (not dye)
 Preferred with allergies to dye or renal insufficiency
 Examines perfusion, function, and structure
 Encourage increase fluid intake to aid in eliminating isotope
o Renal angiography
 Determines renal blood vessel size and abnormality
 Catheter femoral artery with contrast
o Cystography and cystourethrography
 X-ray to determine structure and function of the bladder and urethra
 Catheter inserted to instill contrast dye to visualize lower urinary tract
 Not absorbed in bloodstream
o Not nephrotoxic
o Retrograde procedures
 Examines structural abnormalities or obstruction
 Contrast dye is instilled in bladder or urethra
 Not nephrotoxic
 Common urological procedures
o Cystoscopy and cystourethroscopy
 General or local anesthesia
 NPO/permit
 Examines bladder trauma or urethral damage
 Remove bladder tumors/stones or plant radium seeds in tumor
 Dilate ureters or urethra
 Place stents if necessary
 Resection of enlarged prostate
 Catheter may be in place after procedure
 Pink tinged urine
o Expected finding
 Monitor urine output, possible clots and s/s of infection
o Kidney biopsy- percutaneously
 Preoperative
 NPO 4-6 hr
 Consent
 CBC/PLT/ PT/ Serum urea
o Blood transfusion may be needed before biopsy (anemia)
o Hold anticoagulants
o HTN managed before and after as it affects clotting
o Dialysis for uremia before as it can affect clotting times
 Postoperative
 Monitor dressing, VS, UO, hematuria, HgB/Hct, flank pain (bleeding),
signs of hypovolemic shock
 Bed rest
o Supine position for 2-6 hr
 Pain med as needed
 Resume activity in 24 hr
o Avoid heavy lifting/strenuous activity for 1-2 weeks

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