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
Q

urinalysis for upper tract UTI

A

will indicate bacteriuria, pyuria, and microscopic hematuria, but also urinary casts consisting of leukocyte or renal epithelial cells

26
Q

types of antibiotics for UTIs

A

trimethoprim-sulfamethoxazole, nitrofurantoin, and amoxicillin

27
Q

function of cranberry juice for UTIs?

A

it reduces the capability of E coli to adhere to the bladder mucosa

28
Q

glomerulonephritis main type

A

acute poststreptococcal glomerulonephritis

29
Q

acute poststreptococcal glomerulonephritis

A

follows streptococcal infection with certain strains of group A beta-hemolytic streptococcus which usually originate as upper respiratory infections

30
Q

who is most commonly affected by APSGN?

A

young boys (3-7)

31
Q

how does APSGN develop?

A

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
Q

serum levels in APSGN

A

immunoglobulin G and C3 are present in glomerular tissue and serum C3 is reduced

33
Q

complications of APSGN

A

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
Q

signs of APSGN

A

dark and cloudy urine, facial and periorbital edema, elevated BP, back pain, inflammation signs, and decreased urine output

35
Q

diagnostic tests for APSGN

A

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
Q

treatment for APSGN

A

reduced sodium, fluid, and protein intake, glucocorticoids for inflammation, and antihypertensives for BP; however, recovery is usually self occuring and is sufficient

37
Q

nephrotic syndrome other name

A

nephrosis

38
Q

nephrotic syndrome

A

is often secondary to other diseases (ex. lupus or exposure to drugs)

39
Q

how does nephrotic syndrome develop

A

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
Q

lipoid nephrosis

A

is a type of nephrotic syndrome common in young children

41
Q

blood levels in nephrotic syndrome

A

hypoalbuminemia and high cholesterol

42
Q

urinalysis of nephrotic syndrome

A

indicates proteinuria, lipiduria, and casts that are fatty, epithelial, and hyaline; urine is often frothy

43
Q

signs of nephrotic syndrome

A

massive edema (anasarca), weight gain, pallor, causing impaired appetite, respiration, and activity levels; skin breakdown may also occur

44
Q

treatment for nephrotic syndrome

A

glucocorticoids like prednisone, ACE inhibitors, antihypertensive therapy, and increased protein intake and reduced sodium

45
Q

treatment for recurrent nephrotic syndrome

A

cytotoxic therapies such as cyclophosphamide

46
Q
A