NAPLEx > compounding I: basics > Flashcards

compounding I: basics Flashcards

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1
Q

U.S Pharmacopeia

A

sets the standard for compounding preperations.

795 for non-sterile
797 for sterile

+800 if it is hazard..

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2
Q

non-sterile compounding

A
  • prepare a dose or formulation taht is not commercially available: such as
    —> Changing a solid tab to liquid
    —> compounding an ointment 10% when only 5% and 15% available
  • avoid an excipient (ex. dye, gluten)
  • add a flavor to med

non-sterile prep admin include: by mouth, via tube, rectally, vaginally, topically, nasally or in the ear

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3
Q

USP 795 divides non-sterile compounding into three categories based on complexity

A
  • simple: following instructions (kits, w/ step by step)
  • moderate: specialized calculations or procedures, or making a preparation that no established stability data. (ex. mixing two topical creams when stability data for mixture is not available)
  • complex: requires specialized training, equipment, facilities or procedures (ex. transdermal dosage forms)
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4
Q

specifically designated for non-sterile compounding

A
  • separate location
  • performed in ambient air (room air)
  • separated from the dispensing part of pharm
  • all components, equipment should be stored off the floor

two types of water:
- portable (drinkable)
- purified (distilled) for water-containing formulations and for rinsingequipment..

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5
Q

sterile compounding used to prep:

A
  • IV
  • IM and subq
  • radio pharm
  • eye drops
  • irrigation
  • pulmonary inhalation (not include nasal inhalation)
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6
Q

CSPs

A

compounding sterile products

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7
Q

SVP

A

small volume parenteral
<100ml

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8
Q

LVP

A

large volume parenteral
>100ml

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9
Q

PPI

A

personal protective equipment
“don”- put on
“doff”- take off

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10
Q

PEC

A

primary engineering control

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11
Q

LAFW

A

Laminar Airflow Workbench

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12
Q

C-PEC

A

containment Primary engineering control

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13
Q

BSC

A

biologic safety cabinet

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14
Q

SEC

A

secondary engineering control

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15
Q

C-SEC

A

containment secondary engineering control

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16
Q

SCA

A

segregated compounding area

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17
Q

C-SCA

A

containment segregated compounding area

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18
Q

CAI

A

compounding aseptic isolator

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19
Q

CACI

A

compounding aseptic containment isolator

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20
Q

RABS

A

restricted access barrier system

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21
Q

CSTD

A

closed system transfer device

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22
Q

CVE

A

containment ventilated enclosure

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23
Q

air quality

A

particles per volume of air, lower particle= cleaner air

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24
Q

critical areas, closet to exposed sterile drugs

A

ISO 5
particles in the count 0.5 microns or larger

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25
buffer area anteroom (garbing)
buffer ISO 7- the SEC contains PEC anteroom- at least ISO 8 if it opens into positive-pressure room, but at least ISO7 if negative pressure room
26
ISO 5 ISO 6 ISO 7 ISO 8
3,520 35,200 352,000 3,520,000
27
high efficiency article air filters
HEPA are >99.97% efficient at removing particle as small as 0.3 must be recertified every 6 month
28
vertical flow
HEPA filter at at the top of the sterile hood
29
laminar flow
HEPA filter at the back- horizontal flow
30
direct compounding and first air
- PEC provides ISO 5 air quality for sterile compounds. air coming directly out of HEPA is first air - do not obstruct first air - do not block airflow to prevent contamination, injection port of the villa and syringe needle must be kept in the first air
31
Prevent contamination of air in PEC
- wipe off outsides of all material w/ 70% isopropyl alcohol before bring into PEC - open packages along designed tear lines - compound 6" inside the sterile hood - move waste outside shortly after it is created
32
non-hazardous compounding
pressure inside PEC and SEC is positive
33
hazardous
PEC (C-PEC) and SEC (C-SEC) is negative pressure
34
types of sterile compounding area
- cleanroom suite: one or more ISO-5 PECs (sterile hoods) inside an ISO 7 buffer room that is entered through an adjacent anteroom - segregated sterile compounding area (SCA) w/ ISO 5-PEC: sterile hood often an isolated (glovebox) w/ closed front. -unclassified air
35
NIOSH general categories of hazardous meds
- carcinogenic - teratogenic - genotoxic - toxic to organs at low doses - labeled by the manufacturer w/ special handling instructions
36
Key hazardous drugs on NIOSH list abortifacient
Mifepristone, misoprostol
37
Key hazardous drugs on NIOSH list antiretrovirals antiviral
abacivr, entecavir, zidovudine cidofovir, ganciclovir, valganciclovir
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Key hazardous drugs on NIOSH list antibiotics antifungal anticoagulants
chloramphenicol fluconazole, voriconazole warfarin
39
Key hazardous drugs on NIOSH list acne arrhythmias
isotretinoin dronedarone
40
Key hazardous drugs on NIOSH list autoimmune condition
acitretin, azathioprine, leflunomide fingolimod, teriflunomide
41
Key hazardous drugs on NIOSH list benign prostatic hyperplasia (BPH) biphosphate
dutasteride, finasteride pamidronate, zoledronic acid
42
Key hazardous drugs on NIOSH list chemoprotectant (cardiac) depression diabetes
dexrazoxane paroxetine exenatide, liraglutide
43
Key hazardous drugs on NIOSH list dyslipidemia seizure/epilepsy
lomitapide clobazam, clonazepam carbamazepine, oxcarbamazepine, eslicarbazepine, divalproex, fosphenytoin, phenytoin, topiramate, vigabatrin, zonisamide
44
Key hazardous drugs on NIOSH list gout HF Hepatitis
colchicine ivabradine, spironolactone ribavarin
45
Key hazardous drugs on NIOSH list hormonal agents
androgens estrogens oxytocin, dinoprostone progesterones SERD/SERMs ulipristal
46
Key hazardous drugs on NIOSH list hyperthyroid insomnia
methimazole, propylthiouracil temazepam, triazolam
47
Key hazardous drugs on NIOSH list iron overload migraine Parkinson
deferiprone dihydroergotamine apomorphine, rasagiline
48
Key hazardous drugs on NIOSH list pulmonary arterial hypertension schizophrenia transplant
ambrisentan, bosentan, macitentan, riociguat ziprasidone cyclosporine, mycophenolate, tacrolimus, sirolimus
49
as part of assessment of risk (AoR), standard operating procedures (SOPs) must be developed:
- putting HDs in distinctive shelf bins to alert staff - wearing ASTM D6978 rated gloves when counting or packaging drugs - dedicating a counting tray and spatial for HDs and decontaminating both after use - placing prepared HD containers into a sealable plastic bag AoR doc reviewed every 12 months or whenever a new drug or dosage form is stocked or used
50
HD hoods and buffer room include word containment
C-PEC C-SEC C-SCA CACI C-PEC is located inside C-SEC or C-SCA
51
type of C-PEC for HD BSCs
biological safety cabinets have vertical laminar airflow and negative air pressure for sterile hazardous drugs
52
type of C-PEC for HD CVEs
containment ventilated enclosures are powder containment hood w/ HEPA filter air and negative air pressure used for non-sterile compounding only
53
type of C-PEC for HD CACIs
are closed-front C-PECs (gloveboxes) located in buffer room (SEC) but are often located in C-SCA external vent, negative air pressure
54
it is perferred that non-sterile and sterile compounding space separate, an exception can be made to prepare a non-sterile hazardous drug in a C-PEC inside a C-SEC if these requirements are met
- C-SEC must maintain ISO 7 - separate sterile and non-sterile C-PEC in same C-SEC y at least 1 meter apart - particle-generating activity (powders) can not be performed at the same time - occasional non-sterile HD compounding can be completed C-PEC but it must be properly decontaminated, cleaned, and disinfected before using again with sterile HDs
55
negative pressure
C-PECs, C-SECs, and C-SCAs
56
air changes
non-sterile HD (C-SEC) 12ACPH sterile C-SEC 30 ACPH C-SCA 12 ACPH ACPH- air changes per hour
57
hazardous drug storage
stored separately from non-hazardous drugs, negative pressure 12 ACPH
58
temp monitoring
SEC buffer room- once daily, kept at 20 C or 68F or cooler refrigerator and freezer monitor daily unless they contain vax which is twice daily monitoring refrigerator: 2 to 8C freezer: -25 to -10C- w/vax -50 to-15 per CDC
59
air sampling
every 6 months
60
Keep PEC running
running at all times, if there is a power outage, all compounding must stop, and PEC cleaned w/ germicidal detergent and then disinfected w/ sterile 70% isopropyl alcohol must be on for least 30min before compounding
61
deactivation and decontamination
2%bleach (sodium hypochlorite) or peroxide
62
cleaning
germicadal detergetn such as Quat, ammonium, phenolics (removes dirt and microbial contamination)
63
Disinfection
sterile 70% isopropyl alcohol (PA) inhibits or destroys microorganism; required in sterile compounding
64
black waste bin
black is for bulk HD waste: any containers (drug vials, IV bags) that contain a clearly visible amount of HD and any supplies that were used to admin HDs or to clean HD spills
65
Yellow waste bin
trace HD waste: empty syringes, IV bags, used PPE, including gowns, gloves, masks, and shoes red sharps contain is only for non-hazardous sharps
66
disposal hazard
- outer chemotherapy gloves worn during compounding is discarded in yellow waste bin inside C-PEC. or put in a sealable bag if discarding outside - chemo gown and outer shoe covering ist take off before exiting the negative-pressure area and thrown in yellow bin
67
garb for HD general Nonsterile HD
- double ASTM D6978 (chemotherapy) rated golves when compounding or cleaning up spills - single gloves can be used for HD receiving and storage - double gloves, gown, a mask and - disposable pad to protect the work surface
68
garb for HD sterile HD
- head covers, face mask, and beard covers if applicable - two pairs of shoe covers - gown impermeable to liquid - two pairs of ASTM D6978 gloves - full-facepiece respirator or a face shield w/ googles
69
garbing for sterile
-remove coat, rings, watches, etc. no make up - don head and facial coverings, facemask and then shoe covers (2nd pair are needed for HD) - perform hand hygiene w/ sopa and warm water --> clean under fingernails, fingertips to elbow, circular motion for 30 seconds --> Dry hands -don nonshedding gown and disposable gown - enter buffer area (SEC) --> apply an alcohol-based surgical hand scrub --> don sterile, powder-free gloves, two pairs of chemo for HD --> stanize gloves w/ 70% IPA
70
garbing for HD
- N95 - fae shield w/googles or respirator - gloves must be changed every 30min or when torn, punctured or contaminated - gloves powder free - for non-sterile HD, glove one pair is ok - glove two pairs must be to admin drug - gown changed every 2-3 hrs or immediately after spill - two pairs of shoe covering
71
Admin HD
- two pairs of chemo drugs - gown required when IV HD -
72
test to ensure pharmacists and techs are performing sterile compounds safely good and properly
- gloved fingerprint test - media-fill test (tryptic soy broth)
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