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. 2015 Oct 16;15:206. doi: 10.1186/s12883-015-0450-x

Table 2.

Details of included study arms for the estimation of effectiveness

Intervention Study Cumulative dose Route Duration Day of assessment Fraction with reduced relapse Relapse severity (baseline EDSS) Diagnostic criteria
High-dose methylprednisolone Durelli 1986a [31] 7035 mgb IV 15 days 15 10/11 5.8 (mean) Poser 1983 [51]
Milligan 1987 [32] 2500 mg IV 5 days 28 10/13 4.0 (median) McDonald 1977 [52]
La Mantia 1994 [27] 5750 mg IV 14 days 14 8/10 4.6 (mean) McDonald 1977 [52]
Barnes 1997 [33] 3000 mg IV 3 days 28 13/38 6.0 (median) Not stated
Sellebjerg 1998 [34] 3676 mg PO 15 days 21 14/26 4.5 (median) Poser 1983 [51]
Visser 2004 [35] 2500 mgc IV 5 days 28 6/9 3.5 (median) Not stated
Ramo-Tello 2013 [36] 3000 mg IV 3 days 28 15/23 4.0 (median) McDonald 2005 [53]
Ramo-Tello 2013 [36] 3750 mg PO 3 days 28 15/22 3.0 (median) McDonald 2005 [53]
Low-dose methylprednisolone Milanese 1989 [26] 390 mg IV 14 days 30d 3/10 4.9 (mean) McDonald 1977 [52]
La Mantia 1994 [27] 390 mg IV 14 days 14 6/10 4.7 (mean) McDonald 1977 [52]
Barnes 1997 [33] 588 mg PO 21 days 28 20/42 5.0 (median) Not stated
Placebo Miller 1961 [37] - IM 21 days 21 4/18e Not stated Not stated
Rose 1970 [38] - IM 14 days 28 39.25/94f 5.2 (mean) Rose 1968 [54]
Durelli 1986a [31] - IV 15 days 15 4/10 5.9 (mean) Poser 1983 [51]
Milligan 1987 [32] - IV 5 days 28 2/9 4.0 (median) McDonald 1977 [52]
Sellebjerg 1998 [34] - PO 15 days 21 6/25 4.0 (median) Poser 1983 [51]

IV intravenous, PO per oral, IM intramuscular

a Only the 15 days controlled period of this trial is considered here

b Based on a weight of 70 kg

c Patients also received 2 % human albumin

d This study lacked reported assessments in the 14–28 day interval

e No EDSS measurement performed; the result refers to the fraction with an ‘undoubted response to treatment’

f Conversion based on the assumption that a DSS of e.g. 4 is equally likely to correspond to EDSS 4.0 as EDSS 4.5