LAB Rules | Compliance | Safety | Front Desk | Clinic Operations |
---|---|---|---|---|
Can you have food/drink in the lab
Eating, drinking, smoking, applying cosmetics or lip balm and handling contact
lenses is prohibited in work areas where there is potential for exposure to blood borne pathogens. |
What must you do when you open a new box of HIV or pregnancy tests
Perform control tests and document on QA logs
|
Where do we need to put the ER cart at the end of the night
In the locked storage room
|
Do you need to offer everyone a receipt
Yes
|
What are the situations by law, that require us to break confidentiality?
Court Order
Report to Local Health Department for follow up of tx Express harm self or others |
What would you do if the refrigerator temperature is out of range
Document the out of range temperature. Recheck temperature. Contact Meggan Leary
|
What do you need to write on a sterile pack of equipment
Center Number, Autoclave number (if more than one), date, initials
|
When do sharps containers need to be changed
When they reach the fill line (approx. 2/3 full)
|
Can we email patients test results
No.
|
Where are patients paper charts and is there a way to retrieve them?
o Bonus point if they know how many years they are stored
Iron Mountain Storage
Yes, work with CM to retrieve them |
What should you do to your computer if you are walking away from it or going to lunch
Log out- restrict access to patients and peers to use your log in
|
What would you do if spore testing failed
1. Immediately check the autoclave for proper use and function and repeat the spore
test. A single positive spore test result probably does not indicate sterilizer malfunction. Objects do not need to be re-sterilized because of a single positive spore test unless the sterilizer or the sterilization process is found defective. Sterilizer should be removed from service and sterilization operating procedures reviewed to determine whether operator error could be responsible. 2. All sterilization indicator strips must continue to turn the appropriate color. 3. If a spore test remains positive: • discontinue use of the autoclave • immediately notify supervisor • remove all sterilized packs from inventory dated after the last negative spore test result • use alternative equipment (e.g. disposable speculum) • call for service When repair is completed, rerun biological spore test prior to sterilizing equipment for use. |
What items need to be put in a biohazard bag instead of the garbage
Discarded blood, products of blood and anything caked, soaked or dripping with
blood. |
Do you need to offer everyone notice of privacy practice
Yes
|
When do you need to give out an IPV card
Minimum of annually to women having sex with men or with any change in sex partner
|
What do we do with a multi- dose vial that has been opened
Vials must be discarded if there is evidence of contamination.If a multi-dose vial has been opened or accessed (e.g., needle-punctured) the vial must be dated and discarded in accordance with manufacturer’s instructions and state/local regulations. If no specific guidelines are provided, CDC recommends discarding the vial within 28 da
|
Where can you find the most current STI treatment guidelines
CDC website
Sharepoint |
What needs to happen after we use the ER cart
Need to track what was used and reorder supplies to stay stocked.
|
How do we track EC OTC
Sale is completed as an donation in the EHR/PM system. No patient information is collected.
|
What do you do with expired/ recalled medication
I.Package — the package of medication in question must be held in a secure place at the affiliate, as later transfer to the manufacturer or the FDA may be necessary. There must be no attempt to manipulate or otherwise alter the package, as it may constitute evidence in a criminal suit or other action.
II.Remaining Stock — Remaining stock of medication with the same lot number must be identified, put aside, and not dispensed to patients until the problem has been resolved. III.Notifications — ARMS must be notified immediately by telephone for evaluation of the situation and provision of further instructions. The affiliate must not take any additional steps (such as notification of the pharmaceutical company, FDA, other patients who may have been exposed to the product, and the media) until it receives guidance from ARMS. |
Describe your process for packing up specimens (how do you know what you are sending out)
Manifest with specimen labels, kept with tracking number of shipment. Kept for 30 days.
|
How does PPWI track inventory for medications/BCM
Inforth in EHR system
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Is there a process in place to ensure that all the testing we send out is resulted in EHR
CFU follows up with test results and with the lab
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What do you need to do if you take a call from a patient who has medical questions
Create an encounter in EHR labeled as COMMUNICATION. Document how the contact was made, what was requested, what the resolution was, and who they spoke with.
|
Describe your process for dispensing & labeling medication
The label must also include the following information, which may be added by hand at the time of dispensing:
A.Date of the prescription B.Name of the patient C.Directions for use including frequency and route of administration D.Name of the prescriber E.Number of refills, if applicable |