B33 CAN Clinical & Professional Flashcards

1
Q

How do we dose chemotherapy?

A
Fixed Dose
BSA
Weight based dosing
AUC
Dose Banding
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2
Q

BSA

A

Body surface area, based on Weight and Height

Correlation between BSA and renal function

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3
Q

BSA disadvantages

A

effect of renal impairment
BSA is estimated
Rounding of the BSA calculation and Dose calcualation

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4
Q

Causes of variation in dose

A

Pharmacogenetics, Vial contents , Weight Height BSA, Syringe accuracy,
Residual volumes during administartion

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5
Q

AUC

A

Area under curve, Need GFR

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6
Q

Calculating GFR

A

Use ideal body weight -100 in men -105 in woman

Adjusted body weight

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7
Q

Fixed doses

A

Ease of dose preparation
Reduced cost
Lower risk of dosing errors

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8
Q

Dose banding - Benefits

A

Fewer dose calculation errors
Quicker Dispensing
Reduced patient waiting times

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9
Q

Dose banding - disadvantages

A

Admistered dose may vary from BSA calculated dose

Banded doses may be more expensive

Repeptive strain disorder from repeat syringe usage

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10
Q

Therapeutic monitoring - Benefits

A

Cytotoxic drugs fufil requirements for TDM

Help track patient adherence to treatment

Allows individual dose optimisation

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11
Q

TDM - Disadvantages

A

Tumour heterogeneity
Drugs have overlapping therapuetic & toxic effects

Practical & economical consideratiosn

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12
Q

High dose MTX is the only cytotoxic drug on TDM, what can be used to ‘rescue’…?

A

Folinic acid ‘rescure’ commenced 24 hours after MTX to block unwanted side effects

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13
Q

Cycle interval

A

Chemotherapy scheduling gbased of effects of cytotoxic drug on normal tissue

2-3 week cylce as normal cells recover in 3 weeks

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14
Q

Dose adjustments - Renal function

A

Calculate for nephrotoxicity

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15
Q

Staging

A

Staging the disease (after Diagnosis) allows for baseline for monitoring and prognostic information
Stage 0-4
4( metastised)

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16
Q

tnm STAGING

A

Primary tumour = T
REgional lymphnodes = N
m = metastasis

17
Q

Grade

A

Grade is the macroscopic assesment of the degree of cellular differentiation
(cancer cells being poorly differentiated grade 3)

18
Q

Dose adjustments Cardiotoxicity

A

Two classes of Cardiotoxings

1) Irreversible
2) Reversible

Irreversible caused by anthracyclines (dox)

Reversible caused by Mabs (trastuzumab)

19
Q

Complications of Cancer

A

SVCO (Superior vena cava obstruction)
- Narrowing of the SVC

Caused by carcinoma

20
Q

SVCO : S & S

A
Oedema in the neck
SOB
Dilation of superior neck skin veins
Headache
Cough coarse voice
21
Q

SVCO: treatment

A

Corticosteroids + Defentive treatment: RT or Chemo

22
Q

Spinal Cord Compression (SCC) : Occurs in…? , Sympotms…?

A

Occurs when bone metasates
Motor weakness
Sensory Loss
Pain at level of compression

23
Q

SCC Treatment

A

Corticosteroids and RT

24
Q

SCC prognosis

A

Ability to walk / move at time of diagnosis and treatment begininning

25
Pharmacist role in SCC
Prompt diagnoisis and delivery of Corticosteroids and Refferal Speak about DVT/PE prophylaxis Laxatives Analgesis
26
Chemotherapy induced N&V
- impact on QoL
27
Types of CINV
Acute Breakthrough Refractory Anticapatory N&V PROPHYLAXIS better than treatment
28
CINV consequences
Delayed therapy (omitted doses) Dehydration Electrolyte imbalance Patient stopping therapy
29
CINV treatment & MOA
Neurokinin 1 Receptor antagonists NK1RA - & Inhibts the action of Substrate P in both CNS & PNS
30
Neutropenic sepsis
Infection due to having no neutrophils
31
Neutropenic sepsis: T and pharmacist role
T: Gentamicin PR: Full Blood count, peniclin allergy
32
Classification
Non-vesicant (5FU) Irritant -> Pain and phelbitis (cisplatin) Vesicant - Severe tissue damage and necrosis (anthrycyline antibioitcs e.g doxorubicn)
33
Different sources of funding for cancer drugs
1) Funded by NHS via NICE approval 2) Cancer drug fund (NICE not approved yet) 3) Clinical trail (pharmecutical company funded) (If works legally obliged to continue, gives drug comp. data, cheap) 4) Compassionate use scheme (pharmaceutical company funded) (doctor asks for drug) 5) Privately funded (insurance of induvidual)
34
Incremental Cost equation
C1 - C0 =
35
Incremental benefit equation
Qaly1-Qaly0
36
Incremental Cost Effectiveness Ratio (ICER):
(c1-co) / (Qaly 1 - Qaly 0)
37
Technology acceptable if ICER < ..... per QALY Gained
Accepted if
38
EOL acceptable if ICER
EOL acceptable if