Table 4. Estimated multivariate polynomial distributed lag (PDL) model for monthly %MRSA (R2=0.902)a.
Explaining variable | Lag (mo.) | Direct effectb |
Indirect effectc |
Sum of both effectsd |
||||
---|---|---|---|---|---|---|---|---|
Coeff | T-stat | p | Coeff | Coeffe | T-stat | p | ||
%MRSA | 1 | 0.420 | 3.96 | 0.0003 | ||||
Macrolide use | ||||||||
Each month | 1 | 0.083 | 0.083 | 4.02 | 0.0003 | |||
2 | 0.055 | 0.035 | 0.090 | 5.34 | < 0.0001 | |||
3 | 0.027 | 0.038 | 0.065 | 6.02 | < 0.0001 | |||
4 | 0.027 | 0.027 | 3.16 | 0.003 | ||||
Overall | 1–3 | 0.165 | 4.02 | 0.0003 | ||||
2–4 | 0.100 | |||||||
1–4 | 0.265 | |||||||
Third-generation cephalosporin use | ||||||||
Each month | 4 | 0.116 | 0.116 | 2.75 | 0.009 | |||
5 | 0.087 | 0.049 | 0.136 | 3.27 | 0.002 | |||
6 | 0.058 | 0.057 | 0.115 | 3.70 | 0.0007 | |||
7 | 0.029 | 0.048 | 0.077 | 3.91 | 0.0004 | |||
8 | 0.032 | 0.032 | 2.75 | 0.009 | ||||
Overall | 4–7 | 0.290 | 2.75 | 0.009 | ||||
5–8 | 0.186 | |||||||
4–8 | 0.476 | |||||||
Fluoroquinolone use | ||||||||
Each month | 4 | 0.170 | 0.170 | 3.43 | 0.002 | |||
5 | 0.085 | 0.071 | 0.156 | 3.37 | 0.002 | |||
6 | 0.066 | 0.066 | 2.31 | 0.03 | ||||
Overall | 4–5 | 0.255 | 3.43 | 0.002 | ||||
5–6 | 0.137 | |||||||
4–6 | 0.392 | |||||||
Constant | –36.7 | –4.42 | 0.0001 |
aMRSA, methicillin-resistant Staphylococcus aureus. bPast %MRSA as well as past use of these three antimicrobial drug classes had direct effects on %MRSA. These direct effects diminished the longer the lag time. cBecause every increase in %MRSA by the value 1 was followed the next month by a significant increase in %MRSA by the value 0.420, use of the three antimicrobial drug classes also had indirect effects on the %MRSA. As 0.420 is <1, these indirect effects necessarily vanished over time. As an example, decreasing indirect effects are only presented for a few months. There were substantial indirect effects of macrolide use up to month 8 (final coefficient for sum of both effects = 0.284), of third-generation cephalosporin use up to month 12 (final coefficient for sum of both effects = 0.499), and of fluoroquinolone use up to month 11 (final coefficient for sum of both effects = 0.440). dEach month, the total effect of each class of antimicrobial on the %MRSA resulted from the sum of the direct and indirect effects. eThe estimated coefficients indicate the values by which the %MRSA would increase in response to an increase in 1 DDD per 1,000 patient-days for each of the three significant antimicrobial classes, when all other variables remain constant. Since the average figure for monthly patient-days at Aberdeen Royal Infirmary is 22,800, 10 DDD per 1,000 patient-days correspond to approximately 230 DDD per month or thirty 7- to 8-day antimicrobial courses. For example, an increase in macrolide use by 10 DDD per 1,000 patient-days on a certain month, or 30 more patients treated with a macrolide as compared with the previous month, would lead to a direct increase in %MRSA by 0.83, 1 month later, by 0.55, 2 months later and by 0.27, 3 months later. The total direct effect would therefore be evident after 3 months, amounting to an increase in %MRSA by the value 1.65. Additionally, %MRSA indirectly attributable to macrolide use would increase by the value 0.35 (i.e., 0.83 x 0.42) after 2 months and by 0.38 (i.e.. [0.83 x 0.42] + [0.55 x 0.42]) after 3 months. From the 4th month onwards, there would be no direct effect of macrolide use on the %MRSA, only ever-decreasing indirect effects that would practically disappear after 8 months (decreasing effects in months 5 to 8 not shown).