A new scale for assessing severity in PDA (Panic Disorder with/without
Agoraphobia) has recently been developed: the Panic and Agoraphobia S
cale [P&A (Bandelow, 1995)]. The objective of this study was to test w
hether the scale is sensitive to changes during a treatment trial. Thi
rty-seven patients (mean age, 32.7; S.D., 6.3) with PDA were treated w
ith imipramine (75-150 mg/day) for 8 weeks in an open prospective tria
l. Patients with concurrent agoraphobia were instructed in practising
self-exposure to agoraphobic situations. The total scores on the P&A,
the Hamilton Anxiety Scale (HAMA) and the Clinical Global Impression S
cale (CGI) were used as the main efficacy criteria. Treatment results
were excellent, as could be shown by a decrease in the average severit
y scores of the P&A observer-sated version from 28.9 (S.D., 8.1) to 13
.3 (S.D., 11.8; rank statistic T-N = 6.7; P < 0.0001). The largest eff
ect size r(w) of all clinician-rated scales was seen with the observer
-rated version of the P&A, although closely followed by the CGI and th
e HAMA. Among the self-rated scales, the P&A (self-rated version) also
showed the largest effect size. All five subscores of the P&A showed
significant improvements. The highest treatment effect sizes could be
seen in the 'panic attacks' subscore, followed by the 'anticipatory an
xiety' subscore. The new Panic and Agoraphobia Scale (P&A) is a useful
tool for measuring treatment efficacy in panic disorder trials. (C) 1
998 Elsevier Science Ireland Ltd.