Other
things we do that place your health at risk.
1) All vaccines
and temperature-sensitive medications that require refrigeration should be
stored in refrigerators with continuous temperature monitoring that alarms and
records when temperatures fall out-of-range - and for how long.
- A digital or manual log of
out-of-range temperatures needs to be reviewed on a regular basis by the
Pharmacy Department and maintained.
- This log should also include
actions taken for each out-of-range temperature.
- Some vaccines require frozen
storage, but the aforementioned requirements should also apply.
- Deviation from the required
storage conditions for any medication or vaccine can reduce or eliminate their
effectiveness.
- Not all hospitals follow these
important principles of maintaining AND monitoring storage conditions for
medications and vaccines – especially outside of the central Pharmacy where
medications and vaccines are stored at the point-of-care.
2)
Hospitals should maintain policies and procedures that outline actions
to be taken for deviations from the required storage conditions in both the
central Pharmacy Department and point-of-care areas. These actions should include all
possibilities up to and including the disposal of medications and/or vaccines.
- Many hospitals do not have
these policies and procedures.
3) Food
and food products should never be stored in a medication refrigerator. Foods, and even the outside of food
containers, provide an ideal environment for the growth of bacteria.
- Some hospitals and/or
point-of-care areas store drinks, pudding, yogurt, applesauce, etc. (that are
used to administer medications to certain patient populations) in medications
refrigerators for the sake of convenience.
4)
Refrigerators used for the storage of microbiology specimens (and
other specimens) in the central Laboratory and in point-of-care areas must be separate and have the
same requirements for maintaining and monitoring storage conditions, as well as
policies and procedures outlining actions to be taken for out-of-range
temperatures – up to and including the disposal of specimens.
5) Refrigerators
used for the storage of blood or blood products (for transfusion) in the hospital’s Blood
Bank and in point-of-care areas must
be separate and have the same requirements for maintaining and
monitoring storage conditions, as well as policies and procedures outlining
actions to be taken for out-of-range temperatures – up to and including the
disposal of blood or blood products.
6)
Hospitals need to have a process for monitoring and auditing compliance
with required storage conditions for medications, vaccines, microbiology
specimens, and blood/blood products.
- Public Health Departments, government/regulatory agencies, and
Accreditation Canada all need to audit these practices during their
inspections.
- Logs need to be reviewed
spanning back to the previous visit (i.e previous Public Health inspection or
Accreditation Canada survey).
And on a slightly different
note….
7) All intravenous (IV) lines
attached to a central venous line (CVL) must run via an infusion pump
to prevent the risk of (life threatening) “air embolus”.
- IVs connected to CVLs should never
be run via gravity.
- Sometimes an infusion pump is
not in the room when a CVL is inserted in an emergent situation.
- Simply bumping an IV bag around
can let air into the tubing – that you may not notice during a crisis
situation.
- Infusion pumps need to be
considered part of the equipment necessary for central line insertion.
- Infusion pumps have air-detectors
and will alarm and stop infusing if air is detected.
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