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. 2013 Mar 22;142(1):200–207. doi: 10.1017/S0950268813000617

Table 3.

Results of log-linear modelling and estimated prevalence of injecting drug use (IDU) in HCV-diagnosed persons, for both full and stratified datasets; the latter were stratified by sex, birth cohort and period of HCV diagnosis. 95% confidence intervals were derived using the profile likelihood

n IDU risk, from data sources, n (%) IDU risk, total n (95% CI) Estimated prevalence Saturated model?
Full dataset 25 521 18 782 (73·6) 21 266 (20 582–22 140) 83·3% Y
Stratified analysis
 Sex
  Female 8177 5694 (69·6) 6230 (6130–6341) 76·2% Na
  Male 17 344 13 088 (75·5) 14 669 (14 235–15 229) 84·6% Nb
 Birth cohort
  <1960 5168 1958 (37·9) 2554 (2366–2801) 49·4% Nc
  1960–69 8894 6841 (76·9) 8089 (7575–8865) 91·0% Y
  1970–79 8812 7781 (88·3) 8226 (8146–8316) 93·4% Nd
  1980+ 2647 2202 (83·2) 2405 (2347–2474) 90·8% Ne
 Health board
  GGC 10 679 8174 (76·5) 8856 (8698–9045) 82·9% Nf
  Other 14 842 10 608 (71·5) 12 573 (11 914–13 491) 84·7% Y
 Period of HCV diagnosis
  <1995 2290 1211 (52·9) 1411 (1304–1600) 61·6% Ng
  1995–99 7163 5454 (76·1) 6554 (6039–7389) 91·5% Y
  2000–04 8168 6479 (79·3) 6912 (6830–7004) 84·6% Nh
  2005–09 7900 5638 (71·4) 6192 (6075–6326) 78·4% Ni

Y, Yes; N, no; CI, confidence interval; GGC, Greater Glasgow & Clyde.

‘Saturated model?’, Y refers to a log-linear model in which all main effects and all possible two- and three-way interactions were retained after applying the backward stepwise selection.

a

All two-way interactions only (residual d.f. = 4, deviance = 2·53).

b

All two-way interactions and a:b:d, a:c:d, and b:c:d only (residual d.f. = 1, deviance = 1·70).

c

All two-way interactions and a:c:d only (residual d.f. = 3, deviance = 1·66).

d

All two-way interactions only (residual d.f. = 4, deviance = 1·90).

e

All two-way interactions except a:c and b:c (residual d.f. = 6, deviance = 3·47).

f

All two-way interactions and a:b:c and a:c:d only (residual d.f. = 2).

g

All two-way interactions and a:b:c and a:c:d only (residual d.f. = 2, deviance = 2·33).

h

All two-way interactions except b:c (residual d.f. = 5, deviance = 5·50).

i

All two-way interactions and a:b:c and b:c:d only (residual d.f. = 2, deviance = 0·42).

[a, HCV Diagnosis; b, HIV Test; c, Scottish Morbidity Records hospital discharge/deaths data (SMR01/Deaths); d, Scottish drug misuse database (SDMD).]