Research Article

Idiopathic Intracranial Hypertension: Prognostic Factors and Multidisciplinary Management

Table 2

Population characteristics and comparison of good versus poor 6-month visual outcome.

CriteriaTotal population 
Good outcome 
Bad outcome 

Sex
 Female, (%)73/79 (92.4)33/36 (91.7)28/31 (90.3)
 Male, (%)6/79 (7.6)3/36 (8.3)3/31 (9.7)

Age years, mean ± SD33 ± 1231.5 ± 12.735 ± 11.4

Time to diagnosis, months, median (range)2 (1–48)4.7 (1–48)2.8 (1–8)

BMI at diagnosis, kg⋅m−2, mean ± SD35 ± 9.734.6 ± 9.432.9 ± 7.7
 BMI < 30, (%)21/68 (30.9)11/32 (34.4)9/28 (32.1)
 BMI 30–35, (%)13/68 (19.1)5/32 (15.6)8/28 (28.6)
 BMI 35–40, (%)11/68 (16.2)5/32 (15.6)4/28 (14.3)
 BMI > 40, (%)23/68 (33.9)11/32 (34.4)7/28 (25)

CSF opening pressure mmCSF, median (range)285 (150–540)260 (170–420)305 (150–540)

Clinical signs
 Headache, (%)65/79 (82.3)27/36 (75)27/31 (87)
 Papilledema, (%)75/78 (96)35/36 (97)31/31 (100)
 Visual acuity, median, /108.258.58.3
 Transient visual obscuration, (%)14/79 (17.7)5/36 (13.8)5/31 (16.1)
 Visual field defect, (%)62/71 (87.3)28/32 (87.5)26/28 (93)
 Eye-tracking impairment, (%)12/79 (15.2)9/36 (25)3/31 (9.7)
 Tinnitus, (%)10/79 (12.7)4/36 (11)6/31 (19.3)
 Dizziness, (%)9/79 (11.4)3/36 (8.3)6/31 (19.3)

Radiological signs
 Empty sella, (%)45/79 (57)22/36 (61)19/31 (61.3)
 Optic nerve sheath enlargement, (%)51/79 (64.6)21/36 (58.3)22/31 (71)

Transverse sinus
 Normal, (%)5/58 (8.6)3/26 (11.5)0/28
 Hypoplasia, (%)5/58 (8.6)3/26 (11.5)2/28 (7.1)
 Unilateral stenosis, (%)5/58 (8.6)4/26 (15.5)1/28 (3.6)
 Bilateral stenosis, (%)43/58 (74)16/26 (61.5)25/28 (89.3)

Treatments
 Acetazolamide daily dose, mg, median623640651
 Weight change<0.00
 Gain > 5%, (%)10/48 (20.8)0/2610/22 (45.5)
 Loss > 5%, (%)15/48 (31.2)11/26 (42.3)4/22 (18.2)
 No change, (%)23/48 (48)15/26 (57.7)8/22 (36.3)

BMI: body mass index; CSF: cerebrospinal fluid; SD: standard deviation; a: Fisher’s exact test, b: Student’s -test; : number of patients, presented as number of events/number of documented cases (and percentage). 12 patients were lost to follow-up or missed data.