Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
---|---|---|---|---|---|
Ariyasu L.et al 1990 Japan | 20 patients (18-65 years of age), divided into study group and control group. 32 mg methylprednisolone was given orally on the first day and then decreased to 4 mg gradually over the next 7 days. | PRCT and Crossover study | Subjective relief of symptoms within first 24 hours | Methylprednisolone was beneficial,p=0.02 | Small number of patients Poor randomization and blinding procedure No prior estimation of sample size No use of intention to treat analysis Short follow-up period |
One-month ENG | No difference,p=0.06 | ||||
Ohbayashi S.et al 1993 Japan | 111 patients (17-73 years of age), divided into study group and control group. 500 mg intravenous hydrocortisone was given initially and then decreased gradually by 100 mg every 2 days for 10 days. Oral prednisolone was given for 10 days at a starting dose of 30-40mg and decreased gradually | Prospective Comparative study | Subjective relief of symptoms | 1 month:no difference,3 months:no difference,6 months:no difference,12 months:no difference | Small number of patients No randomization and blinding procedure |
Disappearance of spontaneous nystagmus | 1 month:no difference,3 months:steroids were beneficial,p<0.05,6 months:no difference,12 months:no difference | ||||
Recovery of canal paralysis | Steroids were beneficial,p<0.05 | ||||
Kitahara T.et al 2003 Japan | 36 patients (18-75 years of age), divided into study group and control group. 500 mg intravenous methylprednisolone was given initially and then decreased gradually to zero in one week. | PRCT | SPEV after 2 years | No difference, p=0.07 | Small number of patients Poor randomization and blinding procedure No prior estimation of sample size |
Canal improvement ratio after 2 years | No difference | ||||
Subjective relief of symptoms | Methylprednisolone was beneficial,p<0.05 | ||||
Michael Strupp,et al 2004 Germany | 141 patients (18-80 years of age), divided into placebo group, methylprednisolone group, valacyclovir group and methylprednisolone-plus- valacyclovir group. 100 mg methylprednisolone was given daily for 3 days, then tapered off to 10 mg over the next 19 days. 1000 mg valacyclovir was given three times daily for 7 days | PRCT | Vestibular function determined by Jongkee’s formula within 3 days after the onset of symptoms and 12 months afterward | Jongkee’s formula (extent of vestibular paresis):At baseline (%): Placebo:78.9±24.0, Methylprednisolone:78.7±15.8, Valacyclovir:78.4±20.0, Methylprednisolone-plus-Valacyclovir:78.6±21.1, At 12 months (%): Placebo: 39.0±19.9, Methylprednisolone:15.4±16.2, P<0.001, Valacyclovir:42.7±32.3, P=0.63, Methylprednisolone-plus-Valacyclovir:20.4±28.4, P=0.006 | Small number of patients Unclear blinding procedure No use of intention to treat analysis 27 patient (20%) were lost during follow up |
Ali Akbar Rezaie et al. 2006 Iran | 40 patients (15-55 years of age), devided into placebo group and study group. Study group was treated by Dexamethasone 18mg plus Deminohydrinate 100mg daily, and the placebo group was treated by placebo plus Deminohydrinate 100mg daily for 3 days | PRCT | Mean time for relief of Vertigo (hours) | Study group:45.6±15.3, Control group:68.4±11.7, P<0.001 | Small number of patients Poor randomization Unclear blinding procedure No prior estimation of sample size Short follow-up period |
Mean time for relief of nausea (hours) | Study group:28.8±15.3, Control group:54±20.4, P<0.001 | ||||
Mean time for relief of nystagmus (hours) | Study group:28.8±9.8, Control group:63.6±16.1, P<0.001 | ||||
Avi Shupak et al 2008 Israel | 30 patients (22-72 years of age), divided into study group and control group. Prednisolone 1mg/kg was given daily for 5 days, followed by gradually reduced doses for the next 15 days | PRCT | Presence of symptoms and signs | 1 month: no difference,3 months:no difference,6 months:no difference,12 months:no difference | Small number of patients Unclear randomization and blinding procedure No prior estimation of sample size |
DHI score | 1 month:no difference,3 months:no difference,6 months:no difference,12 months:no difference | ||||
Caloric lateralization on ENG | 1 month:prednisolone was beneficial,p<0.03,3 months:prednisolone was beneficial,p<0.01,6 months:no difference,12 months:no difference | ||||
Pathologic finding on ENG | 1 month:no difference,3 months:prednisolone was beneficial,p<0.03,6 months:no difference,12 months:no difference | ||||
Complete resolution | 1 month:no difference,3 months:prednisolone was beneficial,p<0.03,6 months:prednisolone was beneficial,p<0.03,12 months:no difference |