493.941—Hematology (including routine hematology and coagulation).
(a) Program content and frequency of challenge.
To be approved for proficiency testing for hematology, a program must provide a minimum of five samples per testing event. There must be at least three testing events at approximately equal intervals per year. The annual program must provide samples that cover the full range of values that would be expected in patient specimens. The samples may be provided through mailed shipments or, at HHS' option, may be provided to HHS and or its designee for on-site testing.
(b) Challenges per testing event.
The minimum number of challenges per testing event a program must provide for each analyte or test procedure is five.
Analyte or Test Procedure
Cell identification or white blood cell differential
Erythrocyte count
Hematocrit (excluding spun microhematocrit)
Hemoglobin
Leukocyte count
Platelet count
Fibrinogen
Partial thromboplastin time
Prothrombin time
(1)
An approved program for cell identification may vary over time. The types of cells that might be included in an approved program over time are—
Neutrophilic granulocytes
Eosinophilic granulocytes
Basophilic granulocytes
Lymphocytes
Monocytes
Major red and white blood cell abnormalities
Immature red and white blood cells
(2)
White blood cell differentials should be limited to the percentage distribution of cellular elements listed above.
(c) Evaluation of a laboratory's analyte or test performance.
HHS approves only those programs that assess the accuracy of a laboratory's responses in accordance with paragraphs (c) (1) through (5) of this section.
(1)
To determine the accuracy of a laboratory's responses for qualitative and quantitative hematology tests or analytes, the program must compare the laboratory's response for each analyte with the response that reflects agreement of either 80 percent of ten or more referee laboratories or 80 percent or more of all participating laboratories. The score for a sample in hematology is either the score determined under paragraph (c) (2) or (3) of this section.
(2)
For quantitative hematology tests or analytes, the program must determine the correct response for each analyte by the distance of the response from the target value. After the target value has been established for each response, the appropriateness of the response is determined using either fixed criteria based on the percentage difference from the target value or the number of standard deviations (SDs) the response differs from the target value.
The criteria for acceptable performance are:
| Analyte or test | Criteria for acceptable performance |
|---|---|
| Cell identification | 90% or greater consensus on identification. |
| White blood cell differential | Target ±3SD based on the percentage of different types of white blood cells in the samples. |
| Erythrocyte count | Target ±6%. |
| Hematocrit (Excluding spun hematocrits) | Target ±6%. |
| Hemoglobin | Target ±7%. |
| Leukocyte count | Target ±15%. |
| Platelet count | Target ±25%. |
| Fibrinogen | Target ±20%. |
| Partial thromboplastin time | Target ±15%. |
| Prothrombin time | Target ±15%. |
(3)
The criterion for acceptable performance for the qualitative hematology test is correct cell identification.
(4)
To determine the analyte testing event score, the number of acceptable analyte responses must be averaged using the following formula:
(5)
To determine the overall testing event score, the number of correct responses for all analytes must be averaged using the following formula:
[57 FR 7151, Feb. 28, 1992, as amended at 58 FR 5229, Jan. 19, 1993; 68 FR 3702, Jan. 24, 2003]