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ANATOMY, PHYSIOLOGY, DIAGNOSTIC TESTS and THERAPY of RENAL and URINARY DISORDERS:
Objectives 1-15
1. Compare and contrast kidney function with functions of the ureters, bladder, and urethra.
What does kidney do?
Maintain body fluid volume and composition
Filter waste products
Acid base balance
Erythropoietin for RBC
Convert Vit D to active form
Note: nephron functional unit of kidney which forms urine from blood
Juxtamedullary nephrons are longer and dip deeply into medulla: concentrate urine during times of low fluid intake to allow
continued excretion of wastes with less fluid loss
Bladder: stores urine
2. Describe the physiologic processes involved in urine formation, including filtration, reabsorption,
and secretion. (glomerular filtration, tubular reabsorption, tubular secretion/ filtration, diffusion, active
Transport and osmosis)
SIMPLE NURSING
Patho Of the Kidneys Part 1
Filtration
Afferent arteriole brings blood to glomerulus ( series of specialized capillary loops with cap walls that have pores bw/endothelial and
epithelial cells for filtering) where capillaries filter water, electrolytes, and small particles (creatinine, urea nitrogen, glucose) from blood to
make urine Bowmans capsule (glomerular filtrate) PCT (tubular filtrate) Descending loop of Henle Ascending Loop of Henle
Cortex DCT Collecting ducts papillae renal pelvis
Normal GFR: 125/mL/min 1-3 L excreted each day as urine; rest absorbed back into circulatory system
GFR controlled by BP and blood flow
Kidneys self-regulate so GFR constant - selectively constricting and dilating afferent/efferent arterioles; if systolic BP<65 to 70
then self-regulation processes not effective
NOTE: large particles: blood cells, albumin and other proteins are too large to filter thru glomerular capillary walls therefore not normally
present in final urine!
Juxtaglomerular complex (afferent arteriole, efferent arteriole, DCT) - produce and store renin
Renin secreted when sensing cells in DCT (macula densa) sense changes in blood volume, pressure, or blood Na level is low renin
converts angiotensinogen Lungs ACE/ angiotensin 1 Liver angiotensin 2 Adrenal secretion of hormone aldosterone
3. Discuss the renal regulatory mechanisms related to fluid, electrolytes, acid-base balance, and blood
pressure.
Too Little volume
Juxtaglomerular complex- made of afferent (incoming) arteriole, efferent (exiting) arteriole and DCT (distal convoluted tubule).
These
structures store renin. When DCT baroreceptors called macula densa sense low volume, low blood volume or low sodium, then
renin is
released.
Renin converts to a ngiotensinogen in LUNGS the Angiotensinogen Converting Enzyme (ACE) converts it to
Angiotensin 1
Sends it to the liver it is converted to Angiotensin 2
This is a vasopressor (moves blood toward center of body and main circulation)
Angiotensin 2 acts on afferent arteriole and efferent arteriole coming in/out of glomerulus to maintain filtration
pressure.
Also sends it to adrenal gland on kidney
Adrenal releases aldosterone (increases reabsorption of H2O and Na+ in DCT)
It also promotes the excretion of K+ (sodium potassium pump - 2 Na+ out, 1 K+ out)
When volume is low, erythropoietin is secreted and action on red marrow of long bones to produce more RBC
Carotid artery has stretch receptors, when they sense low volume, the send info to pituitary. Pituitary releases ADH. That acts
on distal
tubule to reabsorb more Na+ and H2O.
Too much volume
NP stretch receptor in atria of heart secretes NP, which shuts down ADH and Aldosterone and returns balance
Decreased glomerular Monitor hydration status. The ability of the kidneys to regulate water balance
filtration rate decreases with age.
(GFR)
Ensure adequate fluid intake. The kidneys are less able to conserve water when
necessary.
Administer potentially nephrotoxic agents or Dehydration reduces kidney blood flow and
drugs carefully. increases the nephrotoxic potential of many
agents. Acute or chronic kidney failure may
result.
Nocturia Ensure adequate nighttime lighting and a Falls and injuries are common among older patients
hazard-free environment. seeking bathroom facilities.
Ensure the availability of a bedside toilet, Using these items instead of getting up to the
bedpan, or urinal. bathroom can help prevent falls.
Discourage excessive fluid intake for 2-4hr Excessive fluid intake at night may increase
before the patient goes to bed. nocturia.
Decreased bladder Encourage the patient to use the toilet, bedpan, Emptying the bladder on a regular basis may avoid
capacity or urinal at least every 2hr. overflow urinary incontinence.
Respond as soon as possible to the patient's A quick response may alleviate episodes of urinary
indication of the need to void. stress incontinence.
Weakened urinary Provide thorough perineal care after each The shortened urethra increases the potential for
sphincters and voiding. bladder infections.
shortened urethra
in women
Good perineal hygiene may prevent skin irritations
and urinary tract infection (UTI).
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Tendency to retain Observe the patient for urinary retention (e.g., Urinary stasis may result in a UTI, which may lead
urine bladder distention) or urinary tract infection to bloodstream infections, urosepsis, or septic
(e.g., dysuria, foul odor, confusion). shock.
Provide privacy, assistance, and voiding Nursing interventions can help initiate voiding.
stimulants such as warm water over the
perineum as needed.
Evaluate drugs for possible contribution to Anticholinergic drugs promote urinary retention.
retention.
Inspect for
Color, appearance and odor
Hydration/dehydration, excess bilirubin
Odor - signs of UTI, Diabetes, bladder infection
8. Relate the variations in voiding patterns with their descriptive terms and their significance to urinary
conditions, including Best Practices and patient teaching.
Continence - ability to voluntarily control bladder emptying
Urine filling and storage -Detrusor muscle relaxed (sympathetic nervous system fibers prevent contraction), internal sphincter
muscle tone, external sphincter contraction
Bladder fills stretch sensations transmitted to spinal sacral nerves
Control centers for voiding - cerebral cortex, brainstem, lower spinal cord
Urethral closure for continence must have mucosal surfaces in contact and be adhesive - contact depends on presence and
proper function of nerves and muscles; adhesion depends on adequate secretion of mucus-like substances
Maintenance continence- interaction of nerves controlling muscles of bladder, bladder neck, urethra, pelvic
floor as well as factors that close urethra
Micturition (voiding)-reflex of autonomic control triggers contraction of detrusor muscle (closing ureter at UV) to prevent backflow and
simultaneously relaxes external sphincter and muscles of pelvic floor
Voluntary voiding - learned response controlled by cerebral cortex and brainstem
Contraction of external sphincter inhibits micturition reflex and prevents voiding
9. Relate the description of pain to the specific urinary structure and the pathophysiology.
UTI (Lower tract:urethritis, cystitis, prostatitis) (Upper tract: pyelonephritis), Cystitis, kidney, and ureter
stones.
1353 Col. 1 para. 6: Pain
Flank pain and pain in the lower abdomen or pelvic region, or in the perineal area. Onset, intensity, duration, location, association w/any activity or
event.
Kidney & ureteral pain/irritation= severe and spasmodic=termed renal colic-
Renal colic pain radiates to perianal area, groin, scrotum, or labia; can be intermittent or continuous, w/pallor, diaphoresis, and
hypotension.
Occurring with distention or spasm of the ureter: obstruction or stone passing.
This happens because of the location of the nerve tracts near or in the kidneys and ureters.
Chp 66 p1385- severe pain/renal colic flank pain suggests a stone is in the kidney or upper ureter.
Flank pain extending toward abdomen or to the scrotum and testes or the vulva suggests the stones are in the ureters or bladder.
PAIN IS MOST INTENSE WHEN IN MOVING OR WHEN THE URETER IS OBSTRUCTED. Renal colic is said to begin suddenly and is
often described as unbearable. Nausea, vomiting, pallor, and diaphoresis often accompany the pain. STAGHORN CALCULUS rarely
causes pain because it is not moving.
Urethral spasm- excruciating and may cause shock from stimulation of nearby nerves. Stones fet stuck in the bends, causing ureteral obstruction,
ureter dilates; enlargement of the ureter is hydroureter.
GI manifestations happen in this same way due to the kidney and GI organs close proximity, the nerve pathways are similar. Renointestinal reflexes
often complicate the description of kidney problems.
Body manifestations r/t Uremia : Anorexia, nausea and vomiting muscle cramps, pruritus, fatigue, and lethargy.
build-up of nitrogenous waste products in blood r/t kidney impairment.
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Cystitis:
Pain and burning on urination
Suprapuberic pain
Men-midline low back (flank) pain
INFECTIOUS CYSTITIS (can lead to
sepsis or
Foley catheterization=Female entry is
by short urethra and Males -the
varmints climb-up the outside of the
catheter itself and go all the way up to
the bladder.
Catheter breaks in a closed system:
allow bacteria to sneak in and move up
the lumen-and surprise!
W/in 48hrs of cath insert.-bacterial
colonization (remember colonization is
bacteria presence w/o or before
infection) begins along urethra (F.) and
catheter (M.), ascending to the bladder,
affecting about 50% of pts. w/in 1wk of
insertion.
DISORDER COMPLICATIONS
Gyn. cancers, cancers, pelvic
inflammatory disorder, endometriosis,
Crohns disease, diverticulitis, lupus, or
Tb.
INTERSTITIAL CYSTITIS
U/K Cause.
Infections through blood and lymph.
Lack of Mucin (produced by cells lining
the bladder to maintain integrity and
make it difficult for bacteria to attach to;
concentrated urine irritation interferes
w/production).
10. Discuss the nursing management, including Best Practices and patient teaching the following
diagnostic procedures & lab work:
Serum Creatinine of 1.5mg/dl or > is risk for AKI (acute kidney injury) from contrast dye and medications.
Monitor baselines and look for actual and risk for changes esp. If patients exposed to nephrotoxic agents
Call provider promptly if any increase above 1.5mg/dl and urine output of less than 0.5ml/hr for 6 hrs or more.
Because this is a big indicator of AKI!!! If fast response Pt. may recover.
Urinalysis
The UA is done after the urethral meatus is cleaned and it is collected in midstream during the first void of the morning (ideally)
Should be examined immediately because a delay can result in changes in the test results
Bladder catheterization or suprapubic aspiration can be done
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Urine Culture and Sensitivity (via foley catheter and other)
Clean catch or catheter-derived specimen analyzed for # and type of organisms present
Manifestations of infection and unexplained bacteria in urine specimen bacteria placed in medium w/different antibiotics
effective in killing or stopping growth sensitive or resistant
Creatinine Clearance
[(volume urine x urine creatinine at end of 24 hr)] / serum creatinine (midway thru 12 hr)
Calculated measure of GFR and kidney function based on 24 hr urine collection
Calculated from serum creatinine, age, wt, urine creatinine, gender and race
Age, gender, ht, wt, diet and activity level influence excreted creatinine
Decreases require reducing drug doses; signifies need to explore cause of kidney deterioration
Normal clearance 107-239 mL/min men and 87-107 mL/min women with 24 hr urine sample
Values decrease 6.5 mL/min per decade of life if older than 40 (age r/t decline in GFR)
Bladder Scanners
Noninvasive method of estimating bladder volume
Screen post-void residual volumes and determine need for intermittent catheterization
No discomfort; no patient prep beyond explanation of wt to expect
Explain why procedure done and sensations might experience during procedure
Use male icon on all men and women with hysterectomy
Ultrasound: Check for abnormalities in size, position, shape
To look for kidney stones
Tumors
Kidney,Ureter, Bladder X-rays (KUB)
X-ray of Kidney, ureter, bladder. Can see abdominal structure.
Used for renal calculi, abnormalities in structure
ARE THEY PREGNANT?
Teching: remove all metal, lay flat, non invasive
Intravenous Urography (IVP)
Slide: NPO before 8-12 hrs, bowel prep, nephrotoxic agent. Renal function adequate? Allergy to contrast medium? Patient IV required;
may feel warm sensation and/or salty taste as dye is injected Metformin BOOK Discontinue 24 hrs prior to procedure page 1361 NUrSING
SAFETY PRIORITY Ensure pt does not take metformin after procedure with dye contrast until adequate kidney function determined!
If you are taking metformin when you have your imaging test procedure
.What might happen:The effects of metformin may increase and cause a serious condition called lactic acidosis, especially if you have kidney
problems. Symptoms of lactic acidosis are: feeling very weak, tired, or uncomfortable, unusual muscle pain, trouble breathing, unusual or
unexpected stomach discomfort, feeling cold, dizziness or lightheadedness, suddenly developing a slow or irregular heartbeat.
X-ray exam of your urinary tract. Views kidneys, bladder and ureters
An X-ray dye (iodine contrast solution) injected into a vein in your arm. The dye flows into your kidneys, ureters and bladder,
outlining each of these structures. X-ray pictures are taken at specific times during the exam, so your doctor can clearly see your
urinary tract and assess how well it's working
May be used to help diagnose conditions that affect the urinary tract, such as:
Kidney stones
Bladder stones
Enlarged prostate
Kidney cysts
Urinary tract tumors
Structural kidney disorders
Information regarding urinary tract obstruction
The injection of X-ray dye can cause side effects such as:
Before your intravenous pyelogram, a member of your health care team will:
Lie on your back on an exam table. The X-ray machine usually is either attached to or part of the table. An X-ray image
intensifier the part of the machine that obtains the images is positioned over your abdomen. After you're positioned
comfortably on the table, the exam progresses this way:
X-rays are taken of your urinary tract before any dye is injected.
X-ray dye is injected through your IV line.
X-ray images are taken at timed intervals as the dye flows through your kidneys to the ureters and into your bladder.
Toward the end of the exam, you may be asked to urinate again.
You then return to the exam table, so that the health care team can get X-ray images of your empty bladder.
Post: monitor urine output to ensure clearance of contrast med
CT:Uses contrast dye - In some cases the dye can cause kidney failure
Can help to diagnose or detect; tumors or other lesions, obstructive conditions, such as kidney stones, congenital anomalies,
polycystic kidney disease, buildup of fluid around the kidneys, and the location of abscesses
More likely to have kidney damage after the contrast dye if the patient has kidney disease.
Cystography and Cystourethrography (diagnosis or treatment)
NPO night before; light meal can be eaten, bowel prep w/laxative or enemas
Series of x-rays or continuous radiographic visualization w/fluoroscopy
Dye fills bladder; bladder is emptied
Images: structure and function of bladder and urethra
Tumors, rupture or perforation of bladder and urethra, abnormal backflow , distortion from trauma or other pelvic masses
Explain urinary catheter temporary to instill contrast dye into bladder (enhances visibility of lower urinary tract; not absorbed into
blood) (NOT nephrotoxic)
X-rays taken front, back, and side positions.
Voiding cystourethrogram (VCUG) x -ray while pt voids to determine if backflow into ureter; urethral or bladder injury or
pyelonephritis (kidney infection) to examine for urethral trauma and identify causes of urinary tract obstruction
Monitor for infection from catheter
Encourage fluid intake-dilute urine/reduce burning from catheter irritation
Monitor for changes in urine output
(Retrograde)Cystography and urethrography identify structural problems, i.e. fistulas, diverticula, and tumors
Doctors inject dye, contrast material, into your blood vessels which will show up on the x-ray.
This procedure allows doctors to see your veins. Possible problems include:
blood clots
blockages
abnormal structural issues
spasms in the vessels
tumors
high blood pressure in the vessels
widened blood vessels
If you have kidney disease or kidney failure, your doctor may perform this procedure to help monitor your condition. They may also use this
test to assess the extent of these conditions.
NPO 8 hrs
10
Meds: Aspirin, for example, can affect your bloods ability to clot. Your doctor may tell you to temporarily stop taking some or all of your
medications before the procedure.
Allergies to:
any medications
latex
iodine substances
any anesthetics
contrast dye
Make sure you let your doctor know if youre pregnant or breastfeeding.
Your doctor will then insert a narrow tube, called a catheter, into your artery. Theyll inject the dye through this tube.
Before injecting the dye, your doctor has to get the catheter into the right position. They do this by carefully guiding it through your blood
vessels until it reaches your aorta.
When the catheter is in position, the dye is injected. Your doctor will take multiple X-rays as the dye travels through your blood vessels. The
dye makes the vessels appear on the X-ray so that your doctor to see if there are blockages.
In some cases, your doctor may choose to treat a problem during the procedure. For example, if they find a clot or tumor, they may inject
medication on the spot to help treat it.
infections
blood clots
nerve injury
damage to an artery
You shouldn't drive for 24 hours, so you should arrange for someone to pick you up after the procedure. Avoid exercise or heavy lifting for
about a week. Your doctor may give you additional instructions
Renal Biopsy
Most performed percutaneously using ultrasound or CT guidance
Prone position
Preliminary images/area prepped and sterile draped; local anesthetic
Needle depth and placement confirmed by ultrasound or CT
Pt holds breath while needle advanced into renal cortex; spring loaded coring biopsy needle
Informed consent required
NPO 4-6 hrs prior
Coagulation studies i.e. platelet count, aPTT, PT, and bleeding time performed prior to surgery
Hypertension aggressively managed before and after
Uremia increases risk of bleeding; dialysis maybe before procedure
Possible blood transfusion to correct anemia
Follow up care: major risk bleeding from biopsy site; monitor 24 hrs dressing site, vital signs, urine output, hemoglobin level, hematocrit
Internal bleed suspected with flank pain, decreasing BP, decreasing urine output or s/s of hypovolemia or shock
Strict bed rest, supine position w/back roll for 2-6 hrs after biopsy; HOB elevated, oral intake of food and fluids ok
After bedrest, limited bathroom privileges
Monitor for hematuria-most common complication; resolves on own 46-72 hrs
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Monitor for aching at site radiating to flank and around front of abdomen-possible bleeding or hematoma
If bleeding IV fluid, packed RBC or both to prevent shock
No bleeding resume general activities after 24 hrs; no heaving lifting, exercising or performing strenous activities for 1-2 weeks; possible
driving restrictions
BPH PSA (prostate specific antigen) Normal PSA <4ng/mL Following info from Hesi case study:
The presence of prostate-specific antigen (PSA), which is secreted only by prostate tissue, suggests prostate disease. Levels are
extremely high with advanced prostate cancer. Low levels reflect prostate hyperplasia or early prostate cancer. PSA levels are generally
higher in older men than in younger men, even when cancer is not present. The American Cancer Society recommends PSA blood test
yearly for all men over age 50. Men in high-risk groups (African Americans and those with a first degree relative diagnosed with prostate
cancer at an early age) should be tested earlier.
Anatomically, the prostate surrounds the urethra and bladder neck. Positioned in the pelvic cavity, it rests upon the rectum. The American
Cancer Society recommends annual digital rectal exam for all men over age 50. Palpation of hard, irregular nodes on the prostate
suggests cancer. Men in high-risk groups (African Americans, those with a family history) should be tested earlier. The prostate cancer
screening blood test can be falsely elevated if the blood is drawn immediately after a digital rectal exam is done.
Serum sodium is usually monitored in clients who have a TURP, to detect TURP syndrome. Serum osmolality may also be monitored.
TURP syndrome occurs when irrigation fluid (usually sterile normal saline) is absorbed systemically. Irrigation fluid may be absorbed
rapidly (through the prostate venous plexus) or gradually (from retroperineal spaces). TURP syndrome can occur during TURP surgery or
up to 24 hours after surgery. With TURP syndrome, a severe hypervolemic, hyponatremic state occurs. Neurologic and hypovolemic
changes occur. Signs and symptoms vary greatly and may change. These include nausea and vomiting, confusion, hypotension,
hypertension, bradycardia, and visual disturbances. Treatment is symptomatic.
Postop/discharge:
After transurethral resection of the prostate (TURP), a high fluid intake will ensure adequate urine output, which will flush the bladder, keep
it free of clots, and reduce risk of ascending urinary tract infection. Residual bleeding and clots may occur up to six weeks after surgery.
After transurethral resection of the prostate (TURP), regular walking will promote venous return from the lower extremities. Walking is
preferred over sitting, which puts pressure on the surgical area and can cause bleeding. Strenuous exercise should initially be avoided.
Perineal exercises are often prescribed after transurethral resection of the prostate (TURP) to improve muscle tone and promote
continence. Post-void dribbling is common after TURP. This generally subsides as muscle tone improves with perineal exercises. Mr.
Sumo should be taught to contract his anal sphincter for up to 10 seconds without tensing his abdominal, buttock, or inner thigh muscles. It
is recommended that this exercise be performed often, at least 20-30 times per day. In addition, he should attempt to shut off and resume
his urine flow with each voiding.
Heavy lifting increases venous pressure and could cause bleeding. The HCP will advise Mr. Sumo when heavy lifting can be resumed.
11. Describe the methods for collection of the following types of specimens of urine: first-voided morning specimen, midstream
voided, from a catheter, 24-hour, and residual.
TABLE 65-3
Collection of Urine Specimens
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Voided Urine
Collect the first specimen voided in the morning. Urine is more concentrated in the early
morning.
Send the specimen to the laboratory as soon as possible. After urine is collected, cellular breakdown
results in more alkaline urine.
Clean-Catch Specimen
Explain the purpose of the procedure to the patient. Correct technique is needed to obtain a valid
specimen.
Instruct the patient to self-clean before voiding: Surface cleaning is necessary to remove
secretions or bacteria from the urethral
Instruct the female patient to separate the labia and use the sponges and meatus.
solution provided to wipe with three strokes over the urethra. The first two
wiping strokes are over each side of the urethra; the third wiping stroke is
centered over the urethra (from front to back).
Instruct the male patient to retract the foreskin of the penis and to similarly
clean the urethra, using three wiping strokes with the sponge and solution
provided (from the head of the penis downward).
Instruct the patient to initiate voiding after cleaning. The patient then stops and A midstream collection further removes
resumes voiding into the container. Only 1 ounce (30mL) is needed; the secretions and bacteria because urine
remainder of the urine may be discarded into the commode. flushes the distal portion of the internal
urethra.
Ensure that the patient understands the procedure. An improperly collected specimen may result
in inappropriate or incomplete treatment.
Assist the patient as needed. The patient's understanding and the nurse's
assistance ensure proper collection.
Catheterized Specimen
Follow the facility's procedures for catheterization technique. These procedures minimize bacterial entry.
13
Apply a clamp to the drainage tubing, distal to the injection port. Clamping allows urine to collect in the
tubing at the location where the specimen
is obtained.
Clean the injection port cap of the catheter drainage tubing with an Surface contamination is prevented by
appropriate antiseptic. Povidone-iodine solution or alcohol is acceptable. following the cleaning procedures.
Attach a sterile 5-mL syringe into the port, and aspirate the quantity of urine A minimum of 5mL is needed for culture
required. and sensitivity (C&S) testing.
Inject the urine sample into a sterile specimen container. A sterile container is used for C&S
specimens.
Provide written materials to assist in instruction. Instructional materials for patients, signs, etc.
remind patients and staff to ensure that
the total collection is completed.
Place signs appropriately.
Check laboratory or procedure manual on proper technique for maintaining the Proper technique prevents breakdown of
collection (e.g., on ice, in a refrigerator, or with a preservative). elements to be measured.
On initiation of the collection, ask the patient to void, discard the urine, and note Proper techniques ensure that all urine
the time. If a Foley catheter is in use, empty the tubing and drainage bag at formed within the 24-hr period is
the start time and discard the urine. collected.
Twenty-four hours after initiation, ask the patient to empty the bladder and add
that urine to the container.
Do not remove urine from the collection container for other specimens. Urine in the container is not considered a
fresh specimen and may be mixed with
preservative.
14
12. State the classification, pharmacokinetics, pharmacodynamics, pharmacotherapeutics, main
common side effects and nursing implications, including patient teaching for the following GU/Renal
medications:
13. Discuss the altered drug response for the individual with kidney disease.
Page 1351 Combo of reduced kidney mass, reduced kidney flow, decreased GFR all contributes to
reduced drug clearance and greater risk for rxns and kidney damage from drugs and contrast dyes in older
adults
14. Discuss drug nephrotoxicity and the effects on kidney function. List most common drugs that are
nephrotoxic
Simple nursing:
Metformin
Vancomycin
Gentamycin
IV contrast
WATCH FOR THESE DRUG CLASSES: (top ten classes from Corinne)
Antibiotics-cipro, vancomycin
Analgesics- acetaminophen, NSAID
Cox-2 inhibitor- Celebrex
Proton Pump Inhibitor-Omeprazole
Antivirals-acyclovir
HTN-captopril
Rheumatoid arthritis-infliximab
Psychiatric- lithium
Anticonvulsants-phenytoin
Chemotherapeutics-interferons, cyclosporine
16. Describe the epidemiology, clinical findings, diagnostic studies, treatments, complications and
nursing management, including prevention and reduction of risk factors, for u rinary tract infections
(cystitis).
Uti
Cystitis
17. Describe the pathophysiology, clinical findings, and treatment (including surgical treatments such as
bladder suspension and related surgical procedures) and nursing management for patients with
dysfunctional voiding patterns (such as retention and incontinence).
18. Describe the clinical findings, treatment, and related nursing management for the patient with
ureteral and bladder stones.
19. Describe the epidemiology, clinical findings, treatment, types of urinary diversion and related
nursing management for cancer of the bladder and other urinary tumors.
Ileal reservoir- surgically created pouch can hold urine instead of bladder, inside the body
16
Can be like a colostomy bag on outside as well
Think risk for infection
20. Describe the incidence, pathophysiology, clinical findings, diagnostic studies, treatment, complications and related nursing
management for prostatic hypertrophy: benign and cancerous.
21. Discuss the pathophysiology, assessment, diagnostic findings, medications, and nursing management of the patient with a
neurogenic bladder.
23. Describe the nursing management for care of patients with problems of incontinence to include teaching about Cred voiding,
Kegel exercises, bladder training and trigger voiding.
24. Discuss incontinence issues and the nursing management in the aging population.
26. Explain how diabetic nephropathy can affect glucose metabolism and control in the client with diabetes mellitus. Page 1406
Diabetes #1 leading cause of ESKD
Always considered at risk for ESKD
Avoid nephrotoxic agents (iodinated contrast media aminoglycosides) and dehydration
Poor control of hyperglycemia problems of:
Hypertension
Atherosclerosis
Neuropathy (promotes loss of bladder tone, urinary stasis, UTI) more severe/more likely kidney damage
Diabetic nephropathy - vascular complication of diabetes
First manifestation - microalbuminuria (begin screening after 5 years of diagnosis of DM type 1, annually type 2)
Diabetic kidney disease - progressive structural/functional changes
Initially slight increase in size; GFR increased
Any proteinuria needs aggressive treatment/diagnostic workup
Worsening - frequent hypoglycemic episodes and a reduced need for insulin or antidiabetic agents due to kidney metabolize and
excrete insulin so kidney function decreased insulin available longer and less needed indicates worsening complications
Outcomes:
Achieve glycemic control <6.5%
Normalize BP 130/80 mmHg or 125/75 mmHg if proteinuria > 1.0 g/24 hr, serum crea > 1.5 mg/dL
Use drug that block renin-angiotensin-aldosterone system (aldosterone)
Treat dyslipidemia so LDL < 100mg/dL
27. Describe the etiology, pathophysiology, clinical manifestations, diagnostic studies, treatments, complications, and nursing
management of the following conditions, across the lifespan:
nephrotic syndrome pg.1404
Nephrosis (Nephrotic Syndrome) SIMPLE NURSING
Etiology: many causes
Most common is immune or inflammatory process
Can be genetic (Fabry disease)
Increases glomerular permeability allows larger molecules to pass through
Clinical Manifestations:
Protein in urine, decreased albumin levels, edema (less solutes so fluid 3rd spacing)
Severe proteinuria (>3.5g in 24 hour sample)
Low serum albumin (<3g/Dl)
Renal vein thrombosis
May harm liver function
Can cause EKD
Treatment: treat cause of problem. (steroid for inflammation ect.)
ACE inhibitors can decrease protein loss in urine
Heparin can reduce risk of renal thrombosis
If GFR is normal- intake more protein
If GFR Low-dietary protein decreased (Protein follows GFR -If high increase, if low decrease intake of protein)
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Pyelonephritis pg. 1400
Clinical manifestations:
Chronic pyelonephritis (less dramatic) Acute pyelonephritis
HTN Fever
Inability to conserve sodium chills
Cant concentrate urine tachycardia, tachypnea
Nocturia flank, back, and loin pain
Risk of hyperkalemia tender CVA costovertebral angle
Risk of acidosis N&V
Malaise or fatigue
Burning urgency
Nocturia
Diagnostics: inspect flank, palpate for tenderness, Inspect CVA for symmetry, edema, and redness
Urine dip for positive leukocyte esterase, nitrite, blood, WBC, and bacteria.
Urinalysis with culture and sensitivity. (can determine gram pos or neg bacteria)
Blood culture can look for inflammatory markers (c reactive protein, and erythrocyte sedimentation)
Treatment: pain management (NSAIDS,analgesics)
Antibiotics (broad septum 1st line)
Adequate nutrition and at least 2L fluid/day for light yellow urine
Teaching: purpose of drugs, understand diet and fluid restrictions, hand hygiene, daily weights, daily B/P. Notify provider with
sudden
increase in weight or B/P
Manifestations: mild proteinuria and hematuria, HTN, fatigue, occasional edema may be only signs
Changes in kidney result from infection, inflammation, or poor perfusion
Diagnostics: Urine output decrease <2g/24hrs.
Specific gravity is fixed at constant dilution level even with variable fluid intake
May see hematuria.
GFR is low
Serum creatinine is high >6mg/DL can be as high as 30
BUN increased often as high as 100-200 mg/DL
Sodium retention but dilution of plasma from fluid excess may result in false low or normal level.
If oliguria, potassium is not excreted and possible hyperkalemia
Hyperphosphatemia is possible
Acidosis is possible (h+ retention, and loss of bicarb)
Cysts can move to other body systems like liver (reduces liver function)
Higher risk of cerebral aneurysms, may rupture and L/T bleeding/sudden death.
Higher risk of kidney stones
Clinical manifestations: PAIN, distended abdomen, flank pain, nocturia, decreased ability to
concentrate urine.
As kidney function declines may see: edema, HTN, anorexia, N&V, pruritus, fatigue.
Paraneoplastic syndrome: (systemic effects of cancer) are anemia, erythrocytosis(extra rbcs), hypercalcemia, liver dysfunction,
with elevated
enzymes, hormonal effects, and increased sedimentation rate.
Have either anemia OR erythrocytosis not both at the same time
May have blood loss, but that does not cause anemia
Kidney cell production of erythropoietin
Either tumor cells produce large amts of erythropoietin OR
Tumor cells destroy erythropoietin producing kidney cells = anemia
Tumor cells produce parathyroid hormone-causes hypercalcemia
Increase in renin causes HTN
Increase in hCG decreases libido and secondary sex features
Large amount of sodium and fluid loss via urine followed by hypotension
And decreased output (<400ml/24 hr, or <25 ml/hr) may indicate adrenal insufficiency.
Check RBC, hemoglobin, and WBC every 6-12 hours first few days
28. Discuss the etiology, pathophysiology, clinical findings, diagnostic studies, treatments,
complications, and related nursing management of the client with renal calculi and other obstructive
disorders.
Obstructive disorders:Primary problems: urinary retention and potential infection
Hydronephrosis-kidney enlarges/urine collects in renal pelvis and kidney tissue
Hydroureter-enlargement of ureter; obstruction where iliac vessels cross or ureters enter bladder
Causes: tumors, stones, trauma, structural defects, fibrosis
Urethral stricture (low in urinary tract) -bladder distention hydroureter hydronephrosis
Urinary obstruction:
increase tubular filtrate pressure,
increase GFR,
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necrosis of kidney
Nitrogen wastes retained (urea, creatinine, uric acid) and electrolytes (Na, K, CL, P) retained/acid base imbalances
Permanent damage within 48 hrs - several weeks
Assess:
Hx of childhood urinary tract problems
Usual patterns of elimination
Recent flank or abd pain
Chills, fever, malaise (UTI)
Inspect each flank for symmetry
Gently palpate abd and bladder ( if urine leakage reflects full bladder and possible obstruction)
Urinalysis - bacteria or WBC/infection; tubular epithelial cells present if prolonged obstruction
Normal blood chemistries unless decreased GFR
Decreased GFR increase blood urea and blood urea nitrogen
Serum electrolyte levels off w/increase blood K,P, Ca metabolic acidosis (decreased bicarb)
Diagnosis: ultrasound, CT
Stone - cystoscopic or retrograde urogram procedures
stricture/hydronephrosis - nephrostomy (internal or external drainage/tubes drain to bag or bladder)
NPO 4-6 hrs
CLotting studies (INR, PT,PTT normal or corrected)
Drugs used to decrease hypertension
Moderate sedation w/procedure
Prone position
Ultrasound or fluoroscopic
Local anesthetic needle/wire/catheter ti left in renal pelvis/exterior end to bag or bladder
IMMEDIATELY decreases pressure, prevents further kidney damage leave tube in place until obstruction resolved
Follow up care:
Assess amt in bag hourly for 24 hrs; expected 30 mL/hr
Type of urine drainage bag clear communication in chart
Decrease drainage, back pain tube clogged or dislodged
Assess for leaking urine or blood; red tinged normal for 12-24 hrs gradually clear, watch for fever and change in urine character
NURSING PRIORITY: nephrostomy
Notify provider:
Decrease drainage or stops
Cloudy or foul smelling
Site leaks blood or urine
Back pain
29. etiology, pathophysiology, clinical manifestations, diagnostic studies, treatments, complications, and nursing management of:
acute prerenal failure 60-70% of cases; before kidney, 20:1 BUN to Crea ratio
Reduced perfusion - most common cause of AKI in acute care as seen in hemorrhage, renal losses from diuretics, GI losses from
vomiting, diarrhea
Impaired cardiac output 2ndary to MI, heart failure, dysrhythmias, cardiogenic shock
Vasodilation from sepsis, anaphylaxis, antihypertensive meds
Key features of prerenal-hypotension, tachycardia, decreased CO, decreased urinary output, lethargy
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Damage to kidney tissue classed as intra or intrinsic renal failure/ reflects injury to glomeruli,
nephrons, or tubules
Key features of postrenal -oliguria or anuria, hypertension, tachycardia, SOB, orthopenea, n?V, generalized edema and wt gain, lethargy,
confusion
Kidney compensation with prerenal or postrenal pathology:
Constricting kidney blood vessels
Activating renin-angiotensin-aldosterone pathway
Releasing antidiuretic hormone (ADH)
Which increases blood volume and improve kidney perfusion BUT also
Reduces urine volume oliguria (<400 mL/day) and
Azotemia (retention and buildup of nitrogenous wastes in blood)
Toxins can also cause blood vessel constriction in kidney reduced kidney blood flow, oliguria, azotemia
Inflammation, infection, and damage intracellular damage of tubular system
Immune mediated complexes damage nephrons
Extensive tubular damage tubular cells slough nephrons lose ability to repair themselves
Timely interventions to remove cause of AKI may prevent ESKD page 141
Severe blood depletion can cause kidney injury even if no known kidney problems
Drink 2-3 L/day of water
Hx: ask about imaging procedures w/dye, acute illnesses (influenza, colds, gastroenteritis, sore throats), urine color dark or smoky, any hx of urinary
obstructive problems, manifestations of fluid overload (crackles, dependent and generalized edema, decreased oxygenation, increased resp rate,
and dyspnea
USUALLY NO ANEMIA unless blood loss from another condition or high BUN levels lyse RBCs
Hospital:
Nurses watch for impending kidney dysfunction in assessments/monitoring lab values
Watch for fluid and electrolyte balance
Accurately measure I/Os, check wt and peripheral edema
Note characteristics of urine, report new sediment, hematuria (smoky or red color), foul odor
Immediately report urine output< 0.5 mL/kg/hr persisting more >2 hrs
Report increase in creatinine occurring over hrs or a few days
Watch BUN, serum K, Na, osmolarity, urine specific gravity and electrolytes, serum monitoring
Be aware of nephrotoxic substances, antibiotics, NSAIDs- administer pretreatment oral or IV bolus of fluid volume; watch drug
peak and trough levels
Critical rescue: recognize volume depletion (low urine output, decreased systolic bp, decreased pulse pressure, orthostatic
hypotension, thirst, rising blood osmolarity) Intervene early w/oral fluids or request increase in IV fluid rate to prevent permanent
kidney damage
acute renal failure
Reversible clinical syndrome with sudden and pronounced loss of kidney function
Occurs over hours to days
Results in kidneys failure to excrete nitrogenous wastes
Diagnostics: Early AKI - urine tests (Na level -inability to concentrate urine, specific gravity; presence of urine sediment, myoglobin, or
hemoglobin
Ultrasonography - kidney size/patency, dilation of renal calyces and ducts, stones, hydronephrosis
CT w/out contrast dye-adequacy of blood flow, identify obstruction or tumors
MRI
X-rays of pelvis or kidneys, ureters, bladder -determine cause of AKI - hydronephrosis, stones
Nuclear medicine study( MAG3) -measure GFR and nature of kidney failure
Renal scan - sufficient blood flow
Cystoscopy or retrograde pyelography-identify obstructions of lower urinary tract
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Kidney biopsy - uncertain cause, persistent manifestations, immunologic disease suspected
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Indications:: dysuria
sodium polystyrene sulfonate (Kayexalate) Class:potassium removing resin, cation exchange resin
Action: cat ion exchange agent of sodium and potassium
pharmacodynamics:
Uses: Hyperkalemia particularly in pts with chronic kidney
disease (can take time for it to work) Can be oral or retention
enima dose
side effects: Can cause digoxin toxicity (N&V blurred vision,
anorexia),
Teaching: Don't take with sorbitol( can cause diarrhea and
increase colonic necrosis)
Class:
action:
dopamine (Intropin) pharmacodynamics:
uses:
side effects:
teaching:
Insulin, Ca and dextrose to treat hyperkalemia in emergent situation for cardiac changes bc exchange in cells
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