Clinical Foundations - Week 10 PP Flashcards

1
Q

Reprocessing Steps

A
  1. Transport
  2. Cleaning
    a) Rinsing
    b) Drying
    c) Corrosion Control
    d) Inspection
  3. Packaging
  4. Sterilization
  5. Storage
  6. Delivery
  7. Quality assurance
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2
Q

How do we know what we are doing is
effective?

A
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3
Q
  • What is our assurance that sterilization
    procedures are working?
A
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4
Q

How can we assure patients that we are
providing them with the best possible care?

A
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5
Q

Forms of Monitoring

A

To ensure the condition of sterility, three forms of monitoring are used:

1.Phyisical/Mechanical (cycle, temp and pressure)
2. Chemical (heat sensitive, colour changes)
3. Biologic

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6
Q

Physical Mechanical Monitoring

A
  • Displayed data on the sterilizer as each cycle progresses
    -Physical printout or electronic data / digital
    -Any cycles that fial to reach “cycle complete” will require all insruments to be repackaged
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7
Q

Chemical Monitoring - 6 types/classes

A

Process Indicators
-Placed outside instrument packages
-They respond to a signle change not combination of pressure, temperature, or time
-Indicication that item whent through sterilizer
-Does not indicate if instruments are sterile inside the package

Process Integrators
-Plced inside the instrument packages
-They respond to a combination of pressure, temperature, and time
-Process integrators are also known as multiparameter indicators
-All sterilization factors are integrated

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8
Q

Chemical Monitoring

A

Involves the use of a heat-sensitive chemical
that changes color when exposed to certain
conditions
* Does not prove sterilization has been achieved
* 6 classes

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9
Q

Chemical Monitoring - Class #1

A

Single Variable:

Responds to temperature or time

External! “Steam to Cocoa”

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10
Q

Chemical Monitoring - Class #2

A

indicates rapid and even penetration of steam and adequate aire removal

Example: Bowie Dick test used on pre-post vaccum (dynamic air removal) steam sterilizers

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11
Q

Chemical Monitoring - Class #3

A

responds to a single parameter (not used in dentistry)

-Pressure or Steam heat

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12
Q

Chemical Monitoring - Class #4 - multiparameter integrator

A

Placed internal (inside the self-sealing pouch)
-Heat and pressure or heat and steam

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13
Q

Chemical Monitoring - Class 5

A

Integrating Indicator

-Time
-Temperature
-Presence of Steam

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14
Q

Chemical Monitoring - Class 6 - Emulating Indicator

A

-Time
-Temperature
-Steam &
-Pressure

Can be used with specified sterilization cycle (eg.. 10 min, 18 min, 40 min)

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15
Q

Biological Monitoring (BI) - 3M Attest Auto-reader 490 for Steam Sterilizers

A

The 3M™ Attest™ Auto-reader 490 is
designed to incubate and automatically read
3M™ Attest™ Super Rapid Readout
Biological Indicators 1492V at 56°C for a
final negative fluorescence reading

  • Takes 1 hour for Midmark
  • Test should be negative - no spores detected (positive will have presense of spores)

Other Biological indicators (BIs) are NOT compatible with this device and cannot be used

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16
Q

PCD (Process challenging device)

A

is assembled and
placed in the least favorable to sterilization (cold point) - Closest to FRONT of door

17
Q

Control Vial

A
  • is not sterilized
    -is activated to verify the viability of the test indicator itself
    (+) Spores are detected
    The anticipated results of the sterilized BI testing shall
    be negative (spores are not detected) (-)
  • All instruments must be quarantined until sterilized BI
    results are negative. (-) This takes 60 minutes or
    less
18
Q

Biological Monitoring (BI)

A

Complete BI test with full load, including test cassette

BI challenge pack or PCD placed the 1st full load of the day.

Cycle used at SAIT: “Handpieces”

19
Q

Complete BI test with full load, including test cassette

A

Placement of the BI Challenge pack /Test Pack and Class 5 Chemical Strip

Cassette with instruments is never used on patients

Class 5 indicator strip used

BI vial is placed in the center (toughest area to reach)

Label vial with sterilizer number used and date

20
Q

Quarantine

A

-All Instruments must be quarantined until the BI reading is negative (-) no spores are detected
-At Sait the BI Vials are kept all day

21
Q

Biological Indicator (BI) Failure

A

Positive for spores result in positive (+)

22
Q

Biological Indicator Faillure

A
  • BI tests positive; follow CDSA IPC Standards
  • Items from suspect loads dating back to the last negative
    -BI test should be recalled, re-wrapped, and re-sterilized
    (remove from quarantine)
  • Repeat BI test
  1. Test results are negative and chemical and mechanical monitoring is adequate the sterilizer may be put back into service.
  2. Test results are positive, and chemical and mechanical monitoring is adequate the sterilizer
    should remain out of service until it has been inspected, repaired, and re-challenged with BI tests in (3) three consecutive empty chamber sterilization
    cycles.
23
Q

Quality Insurance - Tracking Instruments

A

✓ Ensure BI was done for the day

✓ Ensure Mechanical/ Digital print – Cycle Complete
-package integrity
-dryness
-presence of label
-date, sterilizer number, cycle number, initials

✓ The correct change in an external chemical indicator
✓ Intact seal if used and evidence of potential contamination

24
Q

Logbooks

A

“Results of All monitoring must be recorded and retained as long as necessary for medical legal purposes”

-Digital
-Analog
-Keep track and record everything!!