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- Apr 11, 2008
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I have a clinical issue I would like to hear other's honest opinion. I have been dealing with our endocrinologist that wants us to raise our free T4 level upper limit of normal as he feels he is getting too many "abnormal" values referred to him by primary care and he doesn't seem (in my opinion) to want these one stop referrals.
Our current instrument has a free t4 of 0.6 to 1.12. (BC Unicel DxC 600 I). The "other" inpatient labs in town have changed their reference ranges (one even did a 1 month study with abnormal and normal free T4 to get their ranges) their range went from ours of 1.12 to 1.6 based upon this (I don't think normal reference ranges should include abnormal values in the validation studies but who listens to me). He brought me example labs reports to show me their reference ranges.
I've reviewed many articles and cannot find anything solid addressing endocrinologists wishing to change reference ranges. One unifying thought in the literature is that reference ranges may be all over the place for different instruments and clinical judgment needs to come into play (I'll leave my own thoughts of this clinician's judgment out). Our lab has done routine validation studies on this instrument to make sure it jives with the manufacturer's ranges. It is up to par on all proficiency testing that we do. The CLSI has recommendations for validating reference ranges but I feel these are too time and cost consuming to do again given we have already done validation of the instrument and PT. I cannot fathom changing these reference ranges at the whim of a single clinician, but I'm trying to give this clinician as scientific explanation of the why's and wherefores as I can.
Would like to hear your thoughts and wondering if any of you have ever bumped into a related issue.
Our current instrument has a free t4 of 0.6 to 1.12. (BC Unicel DxC 600 I). The "other" inpatient labs in town have changed their reference ranges (one even did a 1 month study with abnormal and normal free T4 to get their ranges) their range went from ours of 1.12 to 1.6 based upon this (I don't think normal reference ranges should include abnormal values in the validation studies but who listens to me). He brought me example labs reports to show me their reference ranges.
I've reviewed many articles and cannot find anything solid addressing endocrinologists wishing to change reference ranges. One unifying thought in the literature is that reference ranges may be all over the place for different instruments and clinical judgment needs to come into play (I'll leave my own thoughts of this clinician's judgment out). Our lab has done routine validation studies on this instrument to make sure it jives with the manufacturer's ranges. It is up to par on all proficiency testing that we do. The CLSI has recommendations for validating reference ranges but I feel these are too time and cost consuming to do again given we have already done validation of the instrument and PT. I cannot fathom changing these reference ranges at the whim of a single clinician, but I'm trying to give this clinician as scientific explanation of the why's and wherefores as I can.
Would like to hear your thoughts and wondering if any of you have ever bumped into a related issue.