Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
---|---|---|---|---|---|
O'Brien et al 1993 USA | 58 patients aged 12-65 years with exudative pharyngitis and severe dysphagia/odynophagia. Patients with cancer, AIDS, Diabetes Mellitus, recent steroid use, pregnancy or suspicion of peritonsillar abscess excluded. 10mg IM Dexamethasone vs. saline placebo. All patients received oral antibiotics. | Prospective, randomized, double blinded placebo controlled trial | Improvement in pain score (0 to 3.0) at 24 hours. | 1.8±0.8 in IM Dexamethasone group vs. 1.2±0.9 in placebo group (P<0.05) | Follow up was 88% at 24 hours, falling to 45% at 7 days. No Power Calculation given. |
Time to onset of pain relief | 6.3±5.3 hours in IM Dexamethasone group vs. 12.4±8.5 in placebo group (P<0.02) | ||||
Time to complete lack of pain | 15.0±11.4 hours in IM Dexamethasone group vs. 35.4±17.9 hours in placebo group (P<0.02) | ||||
Marvez-Valls et al 1998 USA | 92 patients aged 14-65 years with sore throat and/or odynophagia, dysphagia, fever or cervical lymphadenopathy with visible evidence of exudative pharyngeal infection and pain. Patients with AIDS, immunocompromise, peritonsillar abscess, thrush, steroid use in last 3 months, diabetes mellitus, ulcerative pharyngitis, pharyngitis without exudates, prior allergy to steroids and inability to consent were excluded. Unknown dose of IM Betamethasone vs. saline placebo. All patients received antibiotics. | Randomized, double blind, placebo controlled trial | Mean decrease in 10cm visual analogue pain score at 24 hours | 5.5±2.7 in IM Betamethasone group vs. 3.9± 2.7 in placebo group. P=0.004 | Patient and prescribing physician blinded, but nurse administering drug unblinded. 50% of patients reminded of previous pain score at telephone follow up. |
Mean decrease in 10cm visual analogue pain score at 48 hours | 6.8±2.7 in IM Betamethasone group vs. 6.2±2.7 in placebo group. P=0.28 | ||||
Time to first experiencing pain relief | 6.3±8.1 hours in IM Betamethasone group vs. 11.3± 8.1 hours in placebo group. P=0.013 | ||||
Time to complete pain relief | 42.0±43.3 hours in IM Betamethasone group vs. 55.8±43.9 hours in placebo group. P=0.013 | ||||
Number of days school / work missed | 0.4±1.4 days in IM Betamethasone group vs. 0.7±1.4 days in placebo group. P=0.19 | ||||
Wei et al 2002 USA | 120 patients aged 15 and above with clinical diagnosis of acute pharyngitis/tonsillitis and physical examination showing erythema with or without exudate in oropharynx. Immunosupressed patients, diabetes mellitus, HIV positive, history of head or neck malignancy, recent (last 3 months) steroid use, adenotonsillectomy in last 3 months, return visit to the ED but not previously enrolled, suspected peritonsillar abscess, unavailability for follow up and those requiring admission excluded. 10mg IM Dexamethasone vs. 10mg PO Dexamethasone vs. saline placebo. All patients were given antibiotics. | Randomized, double blind, placebo controlled trial | Decrease in 10cm pain visual analogue score at 12 hours | 4.2±2.3 in IM Dexamethasone group vs. 3.8±2.3 in PO Dexamethasone group vs. 2.1±2.0 in placebo group. P<0.001 | Not an Intention to Treat Analysis. No Power Calculation given. |
Percentage with complete resolution of pain within 12 hours | 7±18.9 in IM Dexamethasone group vs. 8±20.0 in PO Dexamethasone group vs. 1±2.9 in placebo group. P=0.052 | ||||
Percentage returning to normal activity at 12 hours | 25±67.6 in IM Dexamethasone group vs. 26±66.7 in PO Dexamethasone group vs. 12±35.3 in placebo group. P=0.001 | ||||
Percentage able to take liquids and solids at 12 hours | 36±97.3 in IM Dexamethasone group vs. 40±100.0 in PO Dexamethasone group vs. 31±91.2 in placebo group. P=0.071 | ||||
Decrease in 10cm pain visual analogue score at 24 hours | 5.0±2.4 in IM Dexamethasone group vs. 4.6±1.9 in PO Dexamethasone group vs. 3.6±2.6 in placebo group. P<0.097 | ||||
Percentage with complete resolution of pain within 24 hours | 13±33.3 in IM Dexamethasone group vs. 12±29.3 in PO Dexamethasone group vs. 4±11.1 in placebo group. P<0.057 | ||||
Percentage returning to normal activity at 24 hours | 33±84.6 in IM Dexamethasone group vs. 29±70.7 in PO Dexamethasone group vs. 20±55.6 in placebo group. P<0.018 | ||||
Percentage able to take liquids and solids at 24 hours | 38±97.4 in IM Dexamethasone group vs. 40±97.6 in PO Dexamethasone group vs. 33±91.7 in placebo group. P>0.05 |