HLTH 2501: disorders of the urinary system Flashcards

1
Q

2 lower urinary tract infections

A

cystitis and urethritis

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2
Q

an upper tract urinary infection

A

pyelonephritis

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3
Q

where do most UTIs come from?

A

most are ascending, arising from organisms in the perineal area and travelling along the continuous mucosa

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4
Q

common causative organism of UTIs

A

E coli

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5
Q

how does E coli enter the urinary tract?

A

it adheres to the mucosa of the bladder by fimbriae or pili, therefore is not washed out when emptying

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6
Q

why are women more susceptible to UTIs?

A

shorter urethra, closer proximity to the anus, and frequent irritation to the tissues

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7
Q

why may men develop UTIs?

A

prostatic hypertrophy and retention of urine

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8
Q

why are the elderly at risk for UTIs?

A

tendency towards incomplete emptying, reduced fluid intake, impaired blood supply to the bladder, and immobility

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9
Q

what may contribute to UTIs?

A

pregnancy, scar tissue, and renal calculi (kidney stones)

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10
Q

what does cystitis and urethritis cause the urinary tract to appear as?

A

inflamed, red, swollen, and ulcerated

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11
Q

cystitis causes

A

bacterial infection, reaction to drugs, radiation therapy, or irritants like feminine hygiene products or catheter

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12
Q

urethritis causes

A

STI, injury from an instrument like a catheter, or exposure to an irritating chemical like a spermicide

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13
Q

2 categories of urethritis

A

gonococcal and nongonococcal

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14
Q

gonococcal urethritis causative organism

A

neisseria gonorrhoeae (transmitted sexually)

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15
Q

nongonococcal urethritis causative organism

A

infectious agents other than N. gonorrhoeae, often being chlamydia trachomatis

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16
Q

signs of lower tract UTIs

A

pain in lower abdomen, dysuria (painful urination), urgency, and nocturia, systemic signs like fever, malaise, and nausea, reactive arthritis, conjunctivitis, and cloudy urine

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17
Q

dysuria

A

painful urination

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18
Q

complications of UTIs

A

prostatitis, pelvic inflammatory disease, cervicitis, or infertility

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19
Q

treatment for UTIs

A

antibiotics, pain management, sometimes NSAIDs, increased fluid intake, and cranberry juice as a prophylactic measure

20
Q

pyelonephritis

A

infects one or both kidneys through infection extending from the ureter, causing purulent exudate to pool and caused inflammation of the medulla

21
Q

how do the kidneys appear during pyelonephritis?

A

abscesses and necrosis can be seen in the medulla and may extend through the cortex to the surface of the capsule

22
Q

complications of pyelonephritis

A

the exudate can compress the renal artery and vein and can obstruct urine flow to the ureter, causing acute renal failure; recurrent infections can also lead to fibrous scar tissue forming over a calyx, leading to loss of tubule function and hydronephrosis

23
Q

signs of pyelonephritis

A

normal lower tract symptoms such as dysuria, but also a dull aching pain in the lower back and more marked systemic signs

24
Q

urinalysis for lower tract UTIS

A

will indicate bacteriuria, pyuria, and microscopic hematuria

25
urinalysis for upper tract UTI
will indicate bacteriuria, pyuria, and microscopic hematuria, but also urinary casts consisting of leukocyte or renal epithelial cells
26
types of antibiotics for UTIs
trimethoprim-sulfamethoxazole, nitrofurantoin, and amoxicillin
27
function of cranberry juice for UTIs?
it reduces the capability of E coli to adhere to the bladder mucosa
28
glomerulonephritis main type
acute poststreptococcal glomerulonephritis
29
acute poststreptococcal glomerulonephritis
follows streptococcal infection with certain strains of group A beta-hemolytic streptococcus which usually originate as upper respiratory infections
30
who is most commonly affected by APSGN?
young boys (3-7)
31
how does APSGN develop?
the antistreptococcal antibodies create an antigen-antibody complex (type III reaction) that lodges in the glomerular capillaries and activates the complement system to cause an inflammatory response in the glomeruli of both kidneys
32
serum levels in APSGN
immunoglobulin G and C3 are present in glomerular tissue and serum C3 is reduced
33
complications of APSGN
decreased GFR can cause acute renal failure, renin secretion can be triggered, increased BP and causing edema, and scarring of the kidneys may occur
34
signs of APSGN
dark and cloudy urine, facial and periorbital edema, elevated BP, back pain, inflammation signs, and decreased urine output
35
diagnostic tests for APSGN
blood tests showing elevated urea and creatine, anti-Dnase B, streptococcal antibodies, ASO, ASK, decreased complement levels, and decreased HCO3 due to metabolic acidosis; urinalysis will also be used to confirm the presence of proteinuria, gross hematuria, and erythrocyte casts
36
treatment for APSGN
reduced sodium, fluid, and protein intake, glucocorticoids for inflammation, and antihypertensives for BP; however, recovery is usually self occuring and is sufficient
37
nephrotic syndrome other name
nephrosis
38
nephrotic syndrome
is often secondary to other diseases (ex. lupus or exposure to drugs)
39
how does nephrotic syndrome develop
increased permeability os the glomerular capillaries allows large amounts of plasma proteins like albumin to escape into the filtrate, causing decreased osmotic pressure and low BP as a result; this activates aldosterone secretion, leading to edema
40
lipoid nephrosis
is a type of nephrotic syndrome common in young children
41
blood levels in nephrotic syndrome
hypoalbuminemia and high cholesterol
42
urinalysis of nephrotic syndrome
indicates proteinuria, lipiduria, and casts that are fatty, epithelial, and hyaline; urine is often frothy
43
signs of nephrotic syndrome
massive edema (anasarca), weight gain, pallor, causing impaired appetite, respiration, and activity levels; skin breakdown may also occur
44
treatment for nephrotic syndrome
glucocorticoids like prednisone, ACE inhibitors, antihypertensive therapy, and increased protein intake and reduced sodium
45
treatment for recurrent nephrotic syndrome
cytotoxic therapies such as cyclophosphamide
46