Chapter 3 Quslity Assessment And Aquility Control In Clinical Laboratory Flashcards
The value quality talk about the roles of the laboratory preventing
Patient safety involve
Making sure specimen received properly obtain, explain
properly how the patient collect specimen like urine, stool.
Analyze the specimen we are reporting the the quality result
If something is wrong we don’t look at the control unit, that give us that the result are accurate,precise. We could harm the the patients the cliticization on result they are received to diagnosis to receive treatment.
How we hurt the patient ordering wrong test but we don’t order the test but we received the the acquisition from the clinitation. Not doing the right testing. Delayeing or missing test that hurt patient.
Discussing Quality management think of it as management
a organization level that is there to implement acquirement an overall quality policy.
We reporting :
High quality result educated laboratory and extended specimen Collection staff,
appreciate valid testing method, properly function instruments, quality assurance and quality control process, and peer - referenced proficiency testing.
This two are important pieces Quality management
encompasses quality
assurance and quality control.
Talk about quality assurance and quality control Patient specimen
Important specimen is properly identify and collected
24 hours urine specimen to discuss with the patient the important what really mean is confusion on the first specimen in a 24hr collection is not collected in the brown container, we discuss the patient what is date it fit for them and usually is Sunday because is a 24hr specimen collection 7 and 7 pm go right through the Monday the first urine special ends is collected that is urine that been in the bladder, maybe was urine night before 6 plus hr urine that why we have the patient urine the first sample and then the second urine to collected all it of urine carefully every time is convenient but collect it how is instructed for them this is 24hr collection.
Quality assessment (QA) ensures reliability of results.
Valid results can be reported only when pre-analytical quality control (QC) has been ascertained.
ClIA 88 improvement amendment
Because the laboratory result was preforming reading where the was no regulation to fallow. Anyone can do the testing. That can cause an Errors occurring during the analytical phase testing with in clinical laboratory are now relatively rare.
Quality control material
When we running the quality control specimen they are 3 level of control
Of blood.
Low abnormal / critical control
normal control,
high abnormal/ critical control
We run an result where the white
Give us a range of between.
