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SUMMARY A study of a modified Canadian unit system of measuring laboratory workload was
undertaken in five joint Public Health Laboratory Service and hospital microbiology laboratories.
Ten percent of the specimens received over six months were sampled, the number of units
expended on each was recorded, and the results were analysed on a central computer. The
process of gathering information in the absence of laboratory computers was time consuming
and, despite careful planning, differences were found in the recording practices of the
laboratories. The analysis of results did not lead to major changes in data gathering techniques
because the same information about laboratory workload could be obtained by collecting num-
bers of clearly defined specimens. Analysis of workload units could be useful for particular
purposes, such as comparing differences between laboratories using different techniques for the
same investigation or assessing the possible benefits of automation. It must be appreciated,
however, that workload units are measures of quantity not of laboratory performance.
For some years there has been dissatisfaction with laboratories. Within the laboratory this information
the methods of assessing laboratory work. They is necessary for the best allocation to be made of
have been criticised as being both inaccurate and manpower and space. It should be sufficiently pre-
uninformative. Attempts to improve the methods cise to enable assessment of trends in workload lead-
have led in Britain to redefinitions of requests and ing to the review of methods so as to provide, for
specimens and in North America to the use of work- example, information on the cost effectiveness of
load units. These different approaches may be a automation.
reflection of the different methods of financing Health authorities need information to allocate
laboratory work. resources between laboratories more rationally. If
The complexity of microbiological investigations costing of laboratory services to particular users,
compared with the more stereotyped and mechan- such as individual clinical disciplines, can be made
ised techniques used in haematology and chemical sufficiently accurate, realistic forecasts of the
pathology make for more difficulty in workload resource requirements of the laboratory can be
measurement. In general, the information required made to accommodate changes in clinical workload.
of a microbiology laboratory is the total workload, Accurate statistics of workload would be of particu-
the distribution of specimen types, and the work lar value to the Public Health Laboratory Service
entailed in the examination of each type. It may also (PHLS), in which there are a number of closely
be desirable to record the source of specimens and comparable laboratories, because they would pro-
to provide a means of costing the examination. None vide opportunities for the evaluation of different
of these measurements is of any value unless the methods and techniques as well as providing the
method of calculating the workload is reliable, administrative information already discussed.
reproducible, and provides for uniformity between Before the present study, discussion in Britain'
different types of specimen and between different about the Canadian unit system2 of measuring work-
load led to an experimental assessment of unit work-
load measurement in pathology by the South West-
Accepted for publication 9 October 1984 ern Regional Health Authority (SWRHA). A
208
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DATE IN OUT
P. H.; L. EXETER WS/241/50/01 SPUTA AND SPECIMENS FOR T.B.
CLER'CAL 037 SENSITMVITY ( CULTURE) 30' 224
VISUAL EXAMINATION 262 STOKES PLATE 225 LAB. NUMBER
HOMOGENISATION 093 BLOOD AGAR SUB 02 043
LIQUEFACTION/DIGESTION 131 CO2 044
METHYLENE BLUE STAIN 155 AnO2 044
DIRECT BLOOD AGAR 02 043 GRAM (CULTURE) 153 G.P. HOSP. HOSP. ENV. OTHER
CO2 044 X+'VDISCS 280
AnO2 044 BETA-LACTAMASE 021 TELEPHONED REPORT 241 |
CHOCOLATE AGAR CO2 '044 OPTOCHIN 182 SEND FOR PHAGE TYPING 183
CLED 043 BILE SOLUBILITY 023 " " FUNGUS 183
McC 043 SLIDE COAGULASE 039 " " HISTOLOGY 183
NALIDIXIC BLOOD AGAR 044 TUBE COAGULASE 040 " CYTOLOGY 183
MANNITOL SALT AGAR 043 UREA 251 REF. LAB. (EXTERNAL) 210
SAB C 270 043 AESCULIN 001
.,370 043 OXIDASE 184
SUCROSE BROTH 045 GERM TUBE 082
MYCOPLASMA MEDIUM 044 NaOH TREATMENT 242
BROTH CULTURE 045 LJ PLAIN 370 C 046
P
ED
PYRUVATE 370 C
GRAM (SPECIMEN)
ZN (SPECIMEN)
153
161 PLAIN 300 C
046
046
I
EOSINOPHIL STAII4 154 PYRUVATE 300 C 046
CENTRIFUGE 034 KIRCHNER 046
WET PREP (DIRECT) 159 ZN (CULTURE) 160
READ DIP SLOPE 054 LI 250C 046
WET PREP (SPUN DEPOSIT)
SENSITIVITY (DIRECT) 370
159
223
_ 370 C (DARK)
370 C (LIGHT)
046
046
I ~~~~~~
Jl
T I
., 300 223 450C 046
(CULTURE) 370 224 __ OXYGEN PREFERENCE 045
No of specimens
sampled
- _lr
.. I
Workload units
recorded f:::::: ,
-2 aio M r variation
Lower
respiratory Mycology
16 i, Blood .D-
1'U _
culture Virology. Culture/
11, Non- electronmicroscopy
gexg >s ciia
Tuberculosis clinical;
0l 0 0- Laliboratories
0- 0-
[DA
OB
Eu
oc
ED
-8
-9. C1E
Wide variation -13- -14.
Fig. 3 Variation between laboratories in mean workload units per specimen. Laboratory A did not undertake mycology
and laboratory E did no virology (culture or electron microscopy).
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Notes