Skip to main content
. 2020 Apr 28;7(3):243–249. doi: 10.1007/s40801-020-00193-9

Table 2.

INTERCheck® scores (total and divided in risk classes A, B, C, D, C + D, ACB) in outpatients (n = 98) and inpatients (n = 46) without (n = 25) and with (n = 21) severe ADEs

Total score Class ACB
A B C D C + D
Outpatients 4.5 ± 3.8 0.1 ± 0.3 3.2 ± 3.8 0.8 ± 1.2 0.3 ± 0.6 1.1 ± 1.6 0.9 ± 1.3
Inpatients 5.2 ± 4.8 0.1 ± 0.3 3.0 ± 2.9 1.1 ± 1.5 0.9 ± 1.6 2.0 ± 2.5 2.2 ± 2.1
Inpatients without severe ADEs 2.9 ± 2.6 0.0 ± 0.0 2.2 ± 2.0 0.4 ± 0.6 0.4 ± 0.9 0.8 ± 1.4 1.6 ± 1.7
Inpatients with severe ADEs 7.9 ± 5.3 0.3 ± 0.5 4.1 ± 3.4 2.0 ± 1.9 1.6 ± 2.0 3.6 ± 2.8 2.9 ± 2.4

Outpatients vs. total inpatients class D p = 0.01, class C + D p = 0.025, ACB p = 0.00001; inpatients with vs. without severe ADEs, INTERCheck® total score p = 0.001, class A p = 0.01, class B p = 0.025, class C p = 0.001, class D p = 0.01, class C + D p = 0.00001, ACB p = 0.05; inpatients with severe ADEs vs. outpatients INTERCheck® total score p = 0.001, class A p = 0.025, class C p = 0.0001, class D p < 0.000001, class C + D p < 0.000001, ACB p < 0.000001. The INTERCheck® software describes the interactions between drugs according to their clinical relevance in class A (minor, no known clinical relevance), class B (moderate, interaction associated with an uncertain or variable event), class C (major, interaction associated with a serious event, but which can be managed, e.g., by reducing the dose), and class D (contraindicated or very serious interaction associated with a serious event for which it is appropriate to avoid coadministration or to establish careful monitoring). Data are presented as mean ± standard deviation

ACB anticholinergic cognitive burden scale, ADE adverse drug event