week 4 Flashcards

1
Q

common problems in PT and cancer

but not just cancer

A
  • cancer related fatigue - most common symptom
  • pain
  • spinal cord compression
  • pathologic fracture/bone mets/lytic lesions
  • lymphedema
  • altered blood counts and immunity
  • venus thromboembolism (VTE: DVT + PE)
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2
Q

cancer related fatigue (CRF)

A
  • distressing, persistent, subjective sense of physical, emotional, and/or cognitive tiredness or exhaustion related to cancer or cancer treatment that is not proportional to recent activity and interferes with usual functioning
  • associated with multiple domains: cancer, cancer treatment (chemo/radiation), surgery
  • does not improve with rest
  • limits QOL
  • affects ability to concentrate, calculate, or remember – similar to chemo brain
  • “can’t get through the day”
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3
Q

subjective and objective components of CRF

A
  • physical performance: weakness or tiredness
  • mood: depression, anxiety
  • motivation: lack of initiative
  • cognition: slowing of thought processes, distraction, or memory deficits
  • social functions: reduced ability to sustain social relationships
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4
Q

needs for improved CRF management

A
  • CRF is a multifactorial,bio-behavioral phenomenon
  • impacts: ADLs/functional capacity, mental/emotional well-being, social/behavioral, occupation, caregivers
  • multidimensional
  • CRF is under-reported, under-diagnosed, under-treated
  • fatigue should be assessed at every patient interaction
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5
Q

CRF education example

A
  • you have a battery/money, and you want to have enough to last all day
  • going up stairs on a good day takes 5%, but on a bad day, it takes 20%
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6
Q

screening

for CRF

A
  • screening tools are generally unidimensional, easy to administer, easy to interpret
  • often dichotomous - yes/no
  • may provide simplistic evaluation for severity, but should trigger a more in depth screen
  • importance: triggers need for more “in depth” assessment and referral for care for typically unmet needs and additional medical consultation
  • fatigue thermometer: pick 0-10 that describes fatigue you have had in the past week including today
  • one item fatigue scale: rate fatigue on scale 0-10, 0: no fatigue, 1-3: mild fatigue, 4-6: moderate fatigue, 7-10: severe fatigue
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7
Q

assessment of CRF

A
  • assessment tools identify extent of a problem, including impact on function and health-related QOL
  • generally multidimensional in nature
  • comprehensive in scope
  • importance: provides greater direction for treatment plan
  • multiple well-validated measures: fatigue severity scale, fatigue impact scale, brief fatigue inventory and functional assessment of chronic illness threapy - fatigue (FACIT-F)
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8
Q

eastern cooperative oncology group (ECOG)

performance scale - v important

A
  • ECOG scale: details
  • 0: normal activity
  • 1: symptoms demonstrated but patient remains ambulatory, able to perform self care
  • 2: ambulatory > 50% of the time, requires occasional assistance
  • 3: ambulatory < 50% of the time, requires nursing care
  • 4: bedridden
  • 5: death
  • cancer trials use this for cutoffs
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9
Q

karnofsky performance status scale

performance scale

A
  • able to carry on normal activity and work, no special care needed
  • 100: normal, no complaints - no evidence of disease
  • 90: able to carry on normal activity, minor signs or symptoms of disease
  • 80: normal activity with effort, some signs or symptoms of disease
  • unable to work, able to live at home and care for most personal needs, varying amount of assistance needed
  • 70: cares for self, unable to carry on normal activity or to do active work
  • 60: requires occasional assistance, but is able to care for most of his personal needs
  • 50: requires considerable assistance and frequent medical care
  • unable to care for self, institutional or hospital care, disease may be progressing rapidly
  • 40: disabled, requires special care and assistance
  • 30: severely disabled, hospital admissions is indicated although death not imminent
  • 20: very sick, hospital admission necessary, active supportive treatment necessary
  • 10: moribund, fatal processes progressing rapidly
  • 0: dead
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10
Q

physical therapy interventions

A
  • exercise: aerobic and strength training
  • complimentary and alternative therapies: acupuncture and yoga
  • lymphedema mangament
  • start easy: low and progress slow, but progress
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11
Q

caution performing exercise with any of the following

A
  • bone metastases (cancer spread to the bone)
  • thrombocytopenia (low platelets)
  • anemia (low RBCs)
  • neutropenia: avoid environments where the risk of exposure to infectious diseases (public swimming pools, crowded gyms)
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12
Q

cancer related pain

A
  • 20-50% of patients with cancer report pain as a symptom
  • prevalence increases with progression of cancer and may reach 90% in terminal patients
  • prevalence of 26-54% in cancer survivors
  • pain is often undertreated
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13
Q

characteristics of cancer pain

A

causes of cancer patients can be classified as:
1. directly related to cancer - direct invasion or compression of structures by cancer
2. related to cancer therapy - due to surgery, chemo, radiation
3. related to effects of cancers - bed sores, debility
4. age-related, comorbidities - chronic back pain, OA (not all pain is the C word)

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14
Q

breakthrough pain

A

acute exacerbation of pain of short duration on teh background of stable pain pattern

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15
Q

bone lesions

A

2 types:
1. osteolytic lesions: cancer has cuased bone breakdown or thinning, destroy bone material (bone is weakened, thin)
2. osteoblastic lesions: cancer has caused overproduction of bone cells (rigid, inflexible)

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16
Q

mirels scoring system for pathologic fracture risk

A
  • rate each area on site, pain, lesion, size (1-3) - diameter
  • clinical recommendations are based on total score
  • < 7 radiation therapy and observation
  • 8 use clinical judgement
  • > 8 prophylactic surgical fixation

increased lesion = increased fracture risk

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17
Q

pain characteristics and fracture

impending fracture

A
  • pain with:
  • WB
  • groin
  • hip scour
  • hip external rotation and abduction
  • deep inspirtaion
  • bance around chest wall
  • supine
  • with valsalva
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18
Q

spinal cord compression

A
  • primary or secondary disease spreads to the vertebra and impinges on the spinal column
  • etiologies
  • vertebral collapse (85%)
  • direct invasion
  • prolonged compression can disrupt of vascular supply (infarction)
  • general S&S
  • back pain is most frequent symptom (95%) - pain increases or is unrelieved with supine
  • motor > sensory changes - DTRs change, ask about changes in bowel and bladder
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19
Q

post prostatectomy incontinence

A
  • the incidence of urinary incontinence after radical prostatectomy varies
  • incontinence immediately after catheter removal may approach an incidence of 90%
  • after one year, incontinence (very common) varies from 5% (0-1 pads daily) to 30-40%
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20
Q

most common blood testes

A
  • complete blood count (CBC) with differential
  • basic metabolic profile (BMP, somtimes called a chem 7)
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21
Q

complete blood count (CBC)

A
  • **red blood cells (RBC) **
  • male 4.7-5.5 mil cells/mm^3
  • female 4.1-4.9 mil cells/mm^3
  • white blood cells (WBC)
  • 4,500-11,000 cells/mm^3
  • hemoglobin (Hb)
  • male 14.4-16.6 gm/dL
  • female 12.2-14.7 gm/dL
  • hematocrit (Hct)
  • male 43-49%
  • female 38-44%
  • platelets (Plt)
  • 150,000-350,000 platelets per microliter (mcL)
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22
Q

plasma

A
  • liquid part of blood (55%)
  • pale yellow made up of 91% water, 9% other
  • colloid: liquid containing suspended substances that don’t settle out
  • albumin: important in regulation of water movement between tissues and blood (osmosis)
  • globulins (anti-bodies): immune system and transport molecules
  • clotting factors/fibrinogen: responsible for formation of blood clots (hemostasis), from liver
23
Q

formed elements in blood

A
  • red blood cells: RBC, erythrocytes
  • white blood cells: WBC, leukocytes
  • granulocytes: neutrophils, eosinophils, basophils
  • agranulocytes: lymphocytes, monocytes
  • thrombocytes: platelets
24
Q

erythrocytes

A
  • structure: biconcave, anucleate
  • components:
  • hemoglobin
  • lipids, ATP, carbonic anhydrase
  • function:
  • transport oxygen from lungs to tissues and carbon dioxide from tissues to lungs
  • acid:base balance
25
Q

hemoglobin

A
  • norms: women (12.2-14.7 g/dl), men (14.4-16.6 g/dl)
  • mild anemia: > 10-11.9 g/dl
  • therapy as indicated, no distinct precautions
  • moderate anemia: 8-9.9 g/dl
  • anticipate decreased cardiopulmonary reserve/limited endurance
  • monitor VS closely
  • patient symptoms: exercise intolerance/DOE/tachycardia/pallor
  • severe anemia: < 7-8 g/dl
  • therapy may be contraindicated - check institution P&P
  • blood transfusion probable Hb < 7 g/dl - more common “criital value”
  • < 5 g/dl: increased risk of cardiac event
26
Q

hematocrit

Hct

A
  • ratio or volume of red blood cells to total volume of blood
  • male: 43-49%
  • female: 38-44%
  • Hct < 25% often cited as a critical value and correlates to Hb < 7-8 g/dL
27
Q

anemia and PT

A
  • S&S of anema (low H/H)
  • symptoms: weakness, fatigue, dyspnea
  • signs: tachycardia, pallor
  • confounding factors: rapid or slow change in values
  • medical history: chronic illness, heart disease, cancer or cancer treatment, surgery
28
Q

transfusion reactions

A
  • febrile non-hemolytic reaction: most common
  • fever, chills, SOB –> benign, reactions are small
  • acute hemolytic reaction: rapid destruction of donor erythrocytes by preformed recipient antibodies
  • triad of fever, flank pain, red/brown urine (hemoglobinuria)
  • decreases H&H
  • anaphylactic reaction:
  • shock, hypotension, angioedema, respiratory distress –> life threatening
  • transfusion-associated acute lunk injury (TRALI):
  • pulmonary edema –> life threatening
29
Q

thrombocytes

platelets

A
  • small fragments of megakaryocytes
  • platelets contain granules that are secreted in response to “activation”
  • important in preventing blood loss: platelet plugs, promoting formation and contraction of clots
30
Q

thrombocytes

platelets

A
  • small fragments of megakaryocytes
  • platelets contain granules that are secreted in response to “activation”
  • important in preventing blood loss: platelet plugs, promoting formation and contraction of clots
31
Q

platelets and therapy considerations

A
  • normal: 150,000-350,000/mm^3
  • subnormal - thrombocytopenia: < 150,000/mm^3
  • 50,000-149,999: low intensity progressive resistive exercise (PRE) and aerobic exercise (none to minimal elevations/resistance)
  • 30,000-50,000: typically not associated with spontaneous bleeding, AROM exercise, walking ad lib
  • <10,000-20,000: risk of spontaneous bleeding, petechiae, ecchymosis, therapy may be contraindicated/minimla AROM
  • elevated - thrombocytosis: > 350,000/mm^3
  • no distinct recommendation, paradoxical increased risk of bleeding
32
Q

venus thromboemoblism (VTE)

pulmonary emoblism

A
  • PE hospitalization rates increased substantially from 1999 to 2010, with a higher rate for black patients
  • PE mortality increases with age
  • overall mortality rates decreased but remains high
  • PE hospitalization rates have increased
  • increase in hospitalization and continued high mortality confirm significant burden of PE (especially for black and older adult patients)
33
Q

who is at risk for VTE

A
  • **virchow’s triad **
  • hypercoagulable state
  • malignancy
  • pregnancy and peri-partum pareiod
  • oestrogen therapy
  • truama or surgery of LE, hip, abdomen, or pelvis
  • inflammatory bowel disease
  • nephrotic syndrome
  • sepsis
  • thrombophilia
  • vascular wall injury
  • trauma or surgery
  • venepuncture
  • chemical irritation
  • heart valve disease or replacement
  • atherosclerosis
  • indwelling catheters
  • circulatory stasis
  • atrial fibrillation
  • left ventricular dysfunction
  • immobility or paralysis
  • venous insufficiency or varicose veins
  • venous obstruction from tumor, obestiy, or pregnancy
34
Q

venous thromboembolism

VTE

A
  • DVT and/or PE
  • disease that includes both deep vein thrombosis and pulmonary embolism
  • 3rd most common cardiovascular illness: acute coronary syndrome (ACS) and CVS, 2/3 associated with hospitalization
35
Q

wells prediction rule for DVT and PE

A
36
Q

pulmonary embolism

A
  • hallmark clinical features
  • tachypnea: 16 breaths per minute or greater
  • tachycardia (> 100 bpm)
  • sudden onset dyspnea
  • chest pain (acute onset)
  • other features
  • hypotension - dizziness, lightheadedness
  • desaturation - decreasing pulse oximetry
  • couch
37
Q

is there a correlation between exercise and DVT

A

no, patient should already be on anticoagulants anyway

38
Q

if on coumadin, check

A

INR

39
Q

if on heparin, check

A

PTT

40
Q

major complications of DVT and PE

A
  • DVT: venous stasis syndrome (post-thrombotic syndrome), venous ulcer
  • PE: chronic thromboembolic disease/pulmonary hypertension, post PE syndrome
41
Q

post thrombotic syndrome (PTS)

A
  • develops 20-50% of patients within 1-2 years
  • severe PTS results in vvenous stasis ulcer: 1/4 to 1/3 of PTS
  • common symptoms: pain, heaviness, cramps, itching, tingling, aggravated by standing/walking
  • physical exam: edema, hyperpigmentation, telangiectasis, varicosities
  • risk factors: proximal DVT (above knee), recurrent DVT, prolonged symptoms (> 1 month post event), obesity, inadequate and/or delayed anticoagulation
42
Q

functions of lymphatic system

A
  • functions: tissue drainage, fat transport, immune responses
  • movement of lymph: lymphatic vessel contraction (like peristalsis), skeletal muscle contraction compression to lymph vessels
43
Q

lymphedema

A
  • accumulation of protein rich fluid: most often in the extremities (in area of treatment)
  • injury/blockages to the lymphatic vessels, nodes, etc
  • surgery, radiation, tumor
  • acute or chronic
  • treatments: surgery, complete decongestive therapy, pressure garments, pneumatic pressure pumps

diagnosis based on history: CA, symptoms

44
Q

what is lymphedema

A

abnormal circulation of protein rich fluid in the interstitium and often accompanied by reactive fibrosis and skin change

45
Q

no edema vs lymphedema

A
  • edema: excess fluid in the body tissues which is a result of abnormal leakage of fluid across capillaries from the plasma to interstitial spaces
  • classified into: generalized (whole body), local (only in 1 part of body)

no complete digestive therapy (CDT) for HF

46
Q

stages of lymphedema

A
  • stage 0: latent, sub-clinical
  • stage 1: spontaneously reversible, present during the day but goes away overnight and/or with elevation, typically soft, no skin changes –> pitting starts between stage 1 and 2
  • stage 2: spontaneously irreversible, does not fully reduce overnight or with elevation, skin becomes hard, brawny, hyperkeratosis –> need intervention but still modifiable, + Stemmers sign of digits, swelling of dorsum of hand/foot
  • stage 3: lymphostatic elephantiasis –> change in limb morphology, more advanced skin changes, still manageable

stage 2 and 3 require intervention (lymphatic massage) to clear interstitial proteins – increased risk of cellulitis. diuretics aren’t helpful

47
Q

stemmer sign

A
  • pinch and lift skinfold at base of the second toe or middle finger
  • A: if you can pinch and lift the skin, negative
  • B: if you cannot life the skin, positive
  • C: a negative test doesn’t always rule out lymphedema
48
Q

patient reports with lymphedema

A
  • tightness or heaviness in limb
  • achy
  • pins and needles
  • pain of congestion
  • not unbearable pain - would imply something more sinister
49
Q

common ways to reduce risk of developing/worsening lymphedema

A
  • skin care
  • activity and lifestyle: gradual increases in intensity/duration, monitor size/shape/texture
  • avoiding limb constriction: BP cuff
  • compression garments (if apprpriate): especially with exercise (weight training) and air travel, garments should be well fitting
  • avoiding extremes of temperature: hot tub, sauna
50
Q

UE lymphedema and XRT

A
51
Q

how is lymphedema treated

A
  • most common treatment for lymphedema is complete decongestive therapy (CDT)
  • manual lymphatic drainage (MLD)
  • bandaging
  • compression garments
  • exercise
  • self care
52
Q

complete decongestive therapy

A
  • phase 1: decongestion
  • meticulous skin drainage
  • manual lymph drainage
  • gradient compression bandaging
  • remedial exercises
  • compression garment
  • phase 2: maintenance
  • meticulous skin care
  • day: compression garment
  • night: gradient compression bandaging
  • self-manual lymph drainage
  • remdial exercises
  • follow-up assessment
53
Q

lymph nodes

A
  • 600-700 lymph nodes in body
  • major groupings: abdomen/intesintes, inguinal, axillary, supraclavicular
  • 2-30 mm in length
  • functions: filter and concentrate lymph through immune system
54
Q

when to refer/consult certified lymphedema therapist (CLT)

A
  • if patient has lymphedema diagnosis or you suspect lymphedema
  • if patient is at risk of developing lymphedema – post-axillary lymph node dissection
  • if swelling is interfering with function
  • if patient is experiencing uncontrolled pain due to swelling
  • if patient needs compression stockings or sleeve
  • if patient has non-healing wounds due to swelling
  • help coordinating outpatient referrals