2.8 Managing resources Flashcards

1
Q

What are some of the key points to consider when introducing a new test?
(clinician rings up to ask for this new assay to be performed)

A
  1. Clarify w clinician regarding
    - clinical utility
    - if dissatisfied w current lab procedure regarding sendaway
    - opportunity for education
    - review literature
    - take it seriously
  2. New assay considerations
    - preanalytical: sample collection, transport, storage, triage
    - analytical: platform, numbers, TAT/demand, staffing level/expertise,
    - post analytical: interpretation, LIS, data entry
  3. Discuss with colleagues, EQA program, rv literature

If possible
4. Order kit- verification
5. Compare with current - cross validation
(kappa if binary, linear regression if correlation important, bland altman if agreement important)
6. SOP/ update/communicate/education/staff training
7. Documentation for NATA
8. QAP

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2
Q

What are the factors which determine the cost of a test?

How does your lab do this?

A
  • Predominantly done by lab manager
  • consult financial advisor of laboratory services

Direct vs Indirect costs
Fixed (doesn’t vary with # tests performed) vs variable cost

Direct
Fixed
- equipment/ maintenance
- lab staff employed
- QAP program

Variable:

  • lab staff time/after hours
  • kits, reagents, consumables

Indirect

  • utility (heating/lighting)
  • building
  • specimen collection storage/freezers
  • cleaning
  • administration
  • IT
  • QC housekeeping
  • safety monitoring
  • record keeping
  • training, teaching, secretarial/clerical work
  • salaries senor staff,

OTHER strategy is to take total indirect cost and divide by total number of request to calculate “handling charge per request””
total cost= cost per request (+per test)

Review

  • number of tests reqested/demand
  • medicare rebate 25% hospital
  • charging patients privately
  • other support for testing

Can divide indirect costs by total number of requests to calculate

Who signs off on the test at ACT Pathology?

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3
Q

Who decides about Medicare rebate of a test? What are the regulations that govern this decision making?

A

MSAC- medical services advisory committee:

  • expert panel decides on scientific quality of evidence /utility of test for a condition
  • comprehensive evaluation
  • recommends test to minister of health and ageing

PSTC- pathology services table committee

  • panel determine dollar value
  • make recomm to minister to sign off
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4
Q

How do you manage your lab in the COVID pandemic?

A

Caveat

  1. MDT input; institution wide but also heads of diff pathology disciplines
  2. Health chief officer; instructions top -> down ensuring dissemination of information effectively
  3. Planning for testing
    - urgent vs non urgent, rationalising tests
    - methods (ANCA IFA vs mpo/pr3)
    - samples having same test, serology on already diagnosed patients
    - alternative platforms
    - TAT; especially sendaways may not work
    - communication to clinicians
  4. Stock take
    - suppliers/manufacturers
    - back up stock
    - prioritise test kits
  5. Staffing
    - rostering different shifts; staggered shifts
    - expertise level
    - cross training of staff
    - cancel unnecessary leave
    - pathologists remote reporting
  6. Staff safety
    - PPE
    - social distancing measures; meetings
    - contact web; unwell, calling in sick
    - psychological wellbeing
  7. Contingency planning
    - if <50%, 75% staff
    - EQAP engagement
    - education programmes
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5
Q

What are some of the strategies you would employ to try and reduce lab costs?

A
  • reduce overheads ( unecessary lighting, space, electricity)
  • tests offered vs sendaway tests- analysis
  • competitive tender for courier services
  • discontinue redundant tests
  • reduce call back
  • increase batching of tests/reduce waste from kits/reagents/controls
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6
Q

What is a WELCAN unit?

A

1 min of scientific/technical/pathology assistant/clerical time

ave time involved in performance of ix including pre-a, a, post a work

divide salary of relevant staff by total number of welcan units worked

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7
Q

Considerations when purchasing a new piece of equipment

A
  1. Need
    - why is it needed
    - current platform
    - demand/requests
  2. Equipment in question
    - pre-analytical: processing, sample storage, handling, test volume
    - analytical:
    - - methodlogy; any kits or company kits
    - - performance capacity, precision, performance eqa, colleagues
    - - practically: physical space, workflow, workload, TAT, random access, multi functions, LIS, automated vs manual- compatibility , waste disposal
    - post analytical:
    - - interfacing, LIS, data entry need, friendly programing /operations
  3. Other
    - access to service, maintenance requirements, waste produce/disposal
  4. EQA
  5. Cost/financial
    - Direct fixed: outright purchase/lease/maintenance
    - Direct variable: test kits/reagents/consumables/Qc/labour/batch testing
    - indirect: specimen collection /processing/ transport/staff/space/other facilites
    - medicare rebate
  6. Staff
    - training, expertise
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8
Q

A patient was not made aware of a non MBS genetic profile test cost and doesnt want to pay, how would you resolve this?

A
  1. Investigate
    - who requested, what, why, test performed already
    - non MBS rebate test consent (ACT Pathology)
    • usually requester needs to discuss
    • awareness? policy/procedural? education?
      – send letter/update test guide/ consent
  2. Either waiver OR discuss with patient
  3. Document/ complaint/QIR, discuss at management meeting, monitor
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9
Q

You have to set up a new lab in the a new city what are some of the points of focus?

A
  • caveat: familiarise self with funding (Medicare/MBS), type of laboratory/supervision, staffing levels/disciplines
  • also range of tests, purpose, client base, population, other labs in the area, space, funding
  1. Quality manual for quality systems in parallel to test implementation
  2. Organisational
    - hierarchy
    - facilities
    - safety
    - personnel
    - equipment
    - LIS
    - inventory
  3. Services
    - test range/ scope of accreditation
    - QC
    - documents/records
    - information management
  4. Post service
    - incident management
    - accreditation
    - QAP
    - billing
    - liaison/communication with requestors and customers
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10
Q

What type of equipment related records are part of NATA requirements?

A

Retention of records- equipment records lifespan + 3years

  • instructions (manufacturer, model, serial number, contact information)
  • acceptance testing
    (date receiving, entering, condition when received)
  • calibration
  • maintenance/repair log
    (mx preventative q6-12months)
  • adverse incident/troubleshooting
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11
Q

How often do you have to maintain equipment?

A
  • preventative maintenance q6-12months
  • pipette q3-6monthly (but may depend on its indication for use) if fails sent to NATA accredited calibration facility
  • scale monthly?
  • temperature daily; thermometer check, acceptable range (refrid, freezer, incubator, water bath)
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12
Q

What are some of the benefits and disadvantages of automation?

A

Benefits

  • faster TAT
  • high throughput
  • less labour cost
  • improved precision/accuracy
  • ease of use/less training
  • eliminate human error
  • interface with LIS

Disadvantages

  • set up cost/equipment/LIS/program
  • dependent on servicing/maintenance third party
  • Staff less competent/skill level decrease
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13
Q

How to improve TAT

A
  • ordering
  • collection
  • transport
  • preparation
  • analysis
  • reporting
  • release of result

At each step see where the delay could be/improved

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14
Q

What does preventative equipment maintenance include?

A

systematic and routine cleaning, adjustment and replacement of equipment parts at scheduled intervals

daily, weekly, monthly or yearly tasks

Equipment plan

  • assign responsibility
  • logs
  • policy/procedure
  • train staff
  • inventory log of all equipment
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