JCPSLP Vol 22 No 2 2020
Table 2. Mean scores from audits using the three devices
Total number audited
Mean score LST (in cm)
Mean score Flow Test (in mls)
Mean score Bostwick (in cm)
17.09 (SD = 1.3, Range = 14–19.5) Prescribed acceptable norm range: 12–18, mean 15 10 (SD = 1.17, Range 7–11.5) Prescribed acceptable norm range: 10–12, mean 11 4.9 (SD = 1.07, Range = 3–6.25) Prescribed acceptable norm range: 5–7, mean 6
7.7 (SD = 1.12, Range = 5–9.4) Prescribed acceptable norm range: Between 4–8mls remaining in the syringe 9.8 (SD = 0.19, Range 9.2–10) Prescribed acceptable norm range: More than 8mls remaining in the syringe, but some liquid still flows through the syringe 10 (SD = 0, Range = 10–10) Prescribed acceptable norm range: No liquid flows at all through the syringe
Mildly thick
37
4.2 (SD = 0.39, Range 3.49–5.22)
Prescribed acceptable norm range: 3.9–5.0, mean 4.2
Moderately thick 22
2.9 (SD = 0.31, Range 2.04-3.35)
Prescribed acceptable norm range: 2.9–3.89, mean 3.2
Extremely thick
18
1.8 (SD = 0.36, Range = 0.99– 2.31)
Prescribed acceptable norm range: 1.5–2.89, mean 2.2
Table 3- Non-compliant audit results
Audit method
Bostick LST Flow
Bostick LST Flow
Bostick LST Flow
MILDLY thick
MODERATELY thick
EXTREMELY thick
4
6
8
18
12
0
11
5
0
Non- compliant by consistency
Too thin
Total
4
2
0 Total
0
0
0 Total
0
0
0
Old
3
0
– Old
-
-
– Old
–
-
–
New
1
2
– New
-
-
– New
–
-
–
Room
2
1
– Room
-
-
– Room
–
-
–
Cold
2
1
– Cold
-
-
– Cold
–
-
–
Too thick
Total
0
4
8 Total
18
12
0 Total
11
5
0
Old
–
2
1 Old
18
8
– Old
11
5
–
New
–
2
7 New
0
4
– New
0
0
–
Room –
0
2 Room
7
7
– Room
4
2
–
Cold
–
4
6 Cold
11
5
– Cold
7
3
–
different flavour categories at both fridge and room temperature. Line Spread Test Of the 62 samples audited using the LST, a total of 3% (n = 2) were excluded due to missing audit information; therefore a total of 60 samples were subject to analysis. A total of 62% (n = 37) were within acceptable norms for the line spread test. Of those that failed (n = 23), 91% (n = 21) were considered too thick and 9% (n = 2) were considered too thin. Of the samples that failed because they were too thin (9%, n = 2), both samples were mildly thick fluids, from two different flavour categories at both fridge and room
Flow Test. Of those that failed (13%, n = 8), all were considered too thick. Of the total that failed, 100% were mildly thick fluids and were from both room and fridge temperature. Non-compliant samples are outlined in Table 3 with compliance of thickened fluids across the three low technology methods illustrated in Figure 1. Agreement between the three auditing methods When the same sample could be compared across each of the three audit methods (n = 41) with the supplier phasing out old stock and introducing new stock on 37% of occasions (n = 15), there was complete agreement between the three auditing methods that the thickened fluid samples were compliant with viscosity norms. On 5% of occasions (n = 2) there was agreement between two auditing methods as to compliance. There was no agreement between all three auditing methods (the
temperature. Flow Test
Of the 62 samples audited using the Flow Test, a total of 3% (n = 2) were excluded due to missing audit information; therefore a total of 60 samples were subject to analysis. Of these 87% (n = 52) were within acceptable norms for the
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JCPSLP Volume 22, Number 2 2020
Journal of Clinical Practice in Speech-Language Pathology
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