Table 1—

Details of 11 patients with cystic fibrosis and allergic bronchopulmonary aspergillosis showing a pathological adrenocorticotropic hormone test

PatientItraconazole treatmentTime monthsp‐ACTH pmol·L−1#p‐cortisol nmol·L−1
no.AgeMedian doseDurationAccumulated dose0 min30 min60 min
yrsmg·day−1monthsmg
1244004480<1<154716
31205566
66437186
910396355
2213001006690<1<30143183
21152367459
3+20200776350<1<15<15<15
44189320367
58170290321
859222239
10<30140155
4+19500487680<15<15<15
14266280372
27223313310
519305366382
7191208213
518200966780<1<1571122
32114186229
6153218243
10163292324
63003826401<15<15<15
2372825
33<15<15<15
51<15<15<15
985112123
7§9100130<1<15<1525
8136003540<153655
3112181220
6259324372
9233314352
9204005578803103285348
23190277368
76271453521
1015200754200760342405
211208362438
3463286340
613239401439
11ƒ13100572550<1
11<305781
7618280
  • The daily dose, accumulated dose and duration of itraconazole treatment, results of plasma ACTH and spontaneous and stimulated plasma-cortisol measurements after 30 and 60 min are shown. All patients were treated with budesonide. Itraconazole treatment was withdrawn at time=0. P‐ACTH and p‐cortisol were measured during the following period (given as number of months after time=0)

  • p‐ACTH: plasma adrenocorticotropic levels

  • p‐cortisol: plasma cortisol levels

  • #: p‐ACTH normal range 2–10 pmol·L−1

  • : patient receiving concomitant treatment with prednisolone (10 mg·2nd day−1)

  • +: Clanthromycin (500 mg·day−1)

  • §: prednisolone (30 mg·day−1)

  • ƒ: prednisolone (7.5 mg·2nd day−1)