midterm #2 Flashcards

1
Q

relevant subj and obj data that should be collected to determine clinical manifestations of pts w/ CKD

A
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2
Q

age-related changed in the urinary system

A

the number of functioning nephrons decreases with age

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3
Q

describe CKD

A

involves the progressive, irreversible loss of kidney function

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4
Q

5 stages of CKD based on GFR

A

Normal GFR = 125 mL/minute
Stage 1: GFR > 90
Stage 2: GFR = 60-89
Stage 3: GFR = 30-59
Stage 4: GFR = 15-29
Stage 5 ESRD occurs when GFR < 15 mL/minute

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5
Q

select risk factors that contribute to the development of CKD

A

DM, HTN, obesity, renal vascular disease

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6
Q

summarize the significance of CV disease in pts w/ CKD

A

hypertension

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7
Q

multi-system clinical manifestations in pts w/ uremia

A

Syndrome that incorporates all signs and symptoms seen in various systems throughout the body due to the build-up of waste products and excess fluid associated with kidney failure.

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8
Q

CKD
– collaborative care

A

Detect and tx any reversable causes
Goals of CKD care:
- delay progression of renal disease
- preserve existing renal function
- treat clinical manifestations
- prevent complication
- educate pt and family regarding kidney disease and options for care
- prepare pts for renal replacement therapy or transplantation

Care must be tailored to pts stage

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9
Q

hemodialysis vs peritoneal dialysis

A

hemodialysis:
- blood leaves the body

peritoneal dialysis:
- cleaning fluid enters the body and filters the waste
- via osmosis and diffusion

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10
Q

describe composition of the major body fluid compartments

A

intracellular: 2/3
extracellular: 1/3
- plasma, interstitial fluid
transcellular:
- CSF, joints
- pleural/cardiac lubricants

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11
Q

fluid & electrolytes
– diffusion, osmosis,

A

diffusion:
[high] to [low] through a semipermeable membrane

osmosis:
movement of water between two compartments by a membrane permeable to H2O but not to solute
- moves from low [solute] to high [solute]
- requires no energy

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12
Q

hydrostatic pressure, oncotic pressure, and osmotic pressure

A

if oncotic pressure drops and you don’t have the pull pressure (12mmHg)
- the fluid is going to stay in the tissues = edema
- in a case of low albumin we can give it supplementally or synthetic intravascular bulking agents that ↑ the oncotic pull pressure
- ↑ interstitial hydrostatic push pressure (30mmHg)
- a counter pressure (compression) to overcome hydrostatic pressure

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13
Q

2nd and 3rd spacing + examples

A

2nd spacing:
- fluid moved into the interstitial space
- not useful to the body
- w/ therapy push or pull it where it can be useful

3rd spacing:
- in a cavity where we cant draw it back or push it back
- needs to be removed
- ascites
- fluid no longer available to the body

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14
Q

list and summarize the ways in which the body regulates water balance

A
  1. hypothalamic regulation - thirst, stimulates pituitary
  2. pituitary regulation
    - ADH , less urine output
  3. Adrenal Cortical Regulation
    - RAAS system; renin aldosterone (Sodium retention (therefore H2O) acts on kidneys
  4. Renal regulation
    - release Na, vasodilation
  5. Cardiac regulation
    - ANF
  6. GI regulation
    - LI, H2O absorption (c-diff, viral infections, cholera, Crohn’s,)
  7. Insensible H2O loss
    - What happens with body (900mL lost)
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15
Q

regulation of H2O balance
– hypothalamus

A

1 ) senses thirst
2 ) stimulates posterior pituitary to release ADH
3 ) ADH makes the kidneys permeable to reabsorb H2O
4 ) aldosterone released from adrenal gland makes kidneys reabsorb H20 + Na and excrete K+

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16
Q

regulation of H2O balance
– kidney

A

renin-angiotensin system

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17
Q

regulation of H2O balance
– cardiac

A

ANF/ANP released when volume and pressure ↑
- ANF causes vasodilation and ↑ urinary excretion of Na and H2O
- blood volume ↓

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18
Q

the impact of normal aging on fluid and electrolyte balance

A

structural change to kidney
loss of SUBQ
> loss of moisture
↓ thirst mechanism

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19
Q

isotonic solution

A

to ↑ intervascular fluid
NS 0.9% > not if hyponatremic
Lactated Ringers
D5W > not w/ pts who are DM or those with ↑ICP

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20
Q

hypotonic solution

A

NS 0.45%
Dextrose 5% in H2O
tx of cellular dehydration
- don’t give for ↑ICP, trauma, burns or hypovolemia

21
Q

hypertonic solution

A

5% in 0.45/0.9% Dextrose
- cerebral edema
- hyponatremia
- don’t give if HF/ CKD

22
Q

collab care
– Hyperkalemia
C big K drop

A

C- Calcium gluconate- stabilize myocardium
B- β2-adrenergic agonists such as salbutamol to shift potassium into the cells
I- IV insulin (shift K+ into cells), and
G- IV Glucose to manage hypoglycemia
K- Kayexalate
D- diuretics or Dialysis

23
Q

the process of acid-base regulation

A

buffer system:
- reacts imediately
resp system:
- responds in min
- max effectiveness reached within hrs
renal system:
- 2-3 days to reach max response
- maintain balance for a long period of time

24
Q

biochemistry and physiology involved with acid-base balance in the body

A

buffer system:
- K+ exchanged w/ H+
- alkalosis > hypokalemia
- acidosis > hyperkalemia
lungs
- rapid resps > ↓ CO2 > ↓ acidity
slow resps > ↑CO2 > ↑ acidity
kidneys
- excretion and/or retention of acids and bicarb
- ↓ H+ and ↑HCO3 > ↓ acidity

25
Q

ABG normal values

A

pH = 7.35 - 7.45
paCO2 = 35-45
HCO3 = 22-26
paO2 = 80 - 100mmHg

26
Q

metabolic acidosis

A

Accumulation of acid:
- DKA, septic shock (lactic acid accumulation), starvation
loss of bicarbonate:
- diarrhea, renal failure

27
Q

metabolic alkalosis

A

Loss of acid:
- NG suctioning
- prolonged vomiting
- loss of K+ due to diuretic therapy
Gain in bicarbonate:
- ingestion of baking soda

28
Q

respiratory acidosis

A

Anything that causes hypoventilation:
- COPD
- barbituate or sedative overdose
- severe pneumonia
- Atelectasis
- Respiratory muscle weakness
- mechanical hypoventilation

29
Q

respiratory alkalosis

A

Anything causing hyperventilation:
- sepsis, anxiety attack
- 2o to hypoxia, fear, fever
- stimulated respiratory center
- CNS disorders, brain injury, salicylate poisoning
- mechanical overventilation

30
Q

biological processes involved in cancer

A

defects in cellular proliferation
- normal cellular function vs. cancer cell
- stem cell theory
- loss of contact inhibition
defects in cellular differentiation:
- proto-oncogenes
> can be altered by mutations
> An oncogene is like a gas pedal that is stuck down causing out of control growth
- tumor-suppressor genes
> rendered inactive by mutations
* BRCA1 and BRCA2 –> mutation makes a high risk for breast and ovary cancer

31
Q

differentiate the 3 phases of cancer development

A

1 ) initiation
- genetic or carcinogen mutations
2 ) promotion
- latency period
- cells only become tumors only when they establish the ability to self-replicate and grow
3 ) progression
- growth, invasiveness and metastasis

32
Q

describe the role of the immune system in relation to cancer

A

immunological surveillance
- response to tumor-associated antigens
- lymphocytes continually check cell surface antigens and detect/destroy abnormal cells
- involves cytotoxic T cells, natural killer cells, macrophages, and B lymphocytes

33
Q

describe the use of the classification systems for cancer
– TNM table

A

tumor (T)
- T0 = no tumor
- Tis = evidence of tumor in situ
- T1, T2, T2 etc.. = progressive ↑in tumor size and involvement
- tx = unable to assess
nodes (N)
- N0 = no lymph node metastasis
- N1, N2, N3= ↑involvement of regional nodes
- Nx = cannot be assessed
Metastasis (M)
- M0 = no evidence
- M1, M2, M3 = metastatic involvement
- Mx = cannot be assessed

34
Q

explain the role of the nurse in the prevention and detection of cancer

A

Change in bowel or bladder habits
A sore that doesn’t heal
Unusual bleeding or discharge
Thickening or lump I the breast or else where
Indigestion or difficulty swallowing
Obvious change in a wart or a mole
Nagging cough or hoarseness

Cancer cachexia

35
Q

explain the use of surgery, radiation therapy, chemo, and biological therapy in tx of cancer

A

surgery:
- diagnostic, preventative, eliminative, reconstructive, or palliative
chemo:
- exerts chemical influence on cellular division (rapid producing cells)
radiation:
- local destruction of cancer cells
- adjuvant > supplements surgery
- palliative
biotherapy:
- uses the body’s immune system to kill cancer cells

36
Q

describe the 3 goals of cancer tx
– cure, control, palliative

A

cure:
- usual life-span
control
- usual or reduced lifespan
palliative
- comfort measures
- reduced lifespan

37
Q

describe the effects of radiation and chemo on normal tissues

A

chemo attacks all fast growing cells (systemic)
- hair follicles > alopecia
- GI issues > lining
- bone marrow > pain, ↓WBC, RBC,

radiation
- worksby making small breaks in the DNA inside cells

38
Q

nursing management of pts receiving rad. therapy and chemo
– adverse rxns

A

chemo
- labs; WBC, platelets, RBC, Hmg
- G-CSF
- reverse precautions for infection
- transfusion of RBC or platelets
- GI: N/V, constipation
- Intg: skin
-

radiation
general side effects:
- skin problems and fatigue
- other side effects reflect the location of the XRT

39
Q

complications that can occur in advanced cancer
– assessments and collab intervention for each

40
Q

common indications for bone marrow transplant and nursing considerations for pts after transplant

A

stem cells to produce new blood cells
infection control
> reverse precautions

41
Q

identify S/S of inadequate oxygenation and the implications of these findings

42
Q

pathophysiology and types
– pneumonia

A
  • acute inflammation of lung parenchyma caused by an agent
  • ↑interstitial fluid & alveolar fluid
    types:
    lobar:
  • consolidation of 1 lobe of 1 lung
    lobular/bronchopneumonia
  • patchy consolidation throughout
43
Q

clinical manifestations and collab care
– pneumonia

A

manifestations:
- chest pain, SOB, cough
- OA > confused
collab care:
- antibiotics
- support measures
- vaccines
- nutrition > 3L of fluid/day
> (IV -> cautious of OA, renal failure and HF)
- fluid/electrolyte management

44
Q

pathophysiology and types
– COPD

A

chronic inflammation found in airways & lung parenchyma
> bronchioles & alveoli
Inability to expire air is main characteristic of COPD
types:
chronic bronchitis
- chronic productive cough
emphysema
- abnormal & permanent enlargement of alveoli due to rupture and damage reducing the surface area for gas exchange

45
Q

clinical manifestations
– COPD

A
  • cough, sputum production, dyspnea, ↑WOB, barrel chest…
46
Q

collab care
– COPD

A

smoking cessation
improved ventilation
- bronchodilators
remove bronchial secretions
reduce complications
- DVT prophylaxis
- pneumococcal vaccines
promote exercise in moderation
improve general health
surgical theraphy

47
Q

nursing management of the client w/ COPD

A

1 ) Prevent disease progression
2 ) Reduce the frequency and severity of exacerbations
3 ) Alleviate breathlessness and other respiratory symptoms
4 ) Improve exercise tolerance and daily activity
5 ) Treat exacerbations and complications
6 ) Improve health status and QOL
7 ) Promote client comfort and participation in care
8 ) Reduce risk of mortality

48
Q

nursing management of the client w/ pneumonia

A

Subj.: focused, questions, meds, hx of smoking/lung diseases, how long have they been sick, sx,
Obj.: breath sounds, RR, accessory muscles, SpO2, productive vs. nonproductive cough

49
Q

indicators for O2 therapy, methods of delivery, and the complications of O2 administration