Table 4. Study characteristics.
Name, publication year and country first author surname | Study design | Duration from symptoms onset to treatment | Age (years) inclusion; median age years (mean) | No. (DHC/Control) | Primary outcome | Jadad |
---|---|---|---|---|---|---|
DECIMAL 2007 [12], France, Vahedi | RCTs | Within 30 h | 18–55 years 43.5 |
20/18 | mRS as the ordinal outcome at 6 months, 12 months, blinding of outcome assessment | 5 |
DESTINY I 2007 [13], Germany, Jüttler | RCTs | 12–36 h | 18–60 years; 44.5 |
17/15 | mRS as the ordinal outcome at 6 months, 12 months, blinding of outcome assessment | 5 |
HAMLET 2009 [14], Netherlands, Hofmeijer | RCTs | Within 96 h | 18–60 years 50.0 |
32/32 | mRS as the ordinal outcome at 12 months, blinding of outcome assessment | 5 |
HeADDFIRST 2014 [15] U.S.A. and Canada, Frank | RCTs | Within 100 h | 18∼75 years 52.3 |
14/10 | Death (mRS = 6) at 21 days, 6 months, blinding of outcome assessment | 4 |
Decompressive Hemicraniectomy 2012 [16], Latvia, Slezins | RCTs | Within 48 h | ≥18 years 57.2 |
11/13 | mRS as the ordinal outcome at 12 months, not blinding of outcome assessment | 3 |
HeMMI 2015 [17], Philippina, Chua | RCTs | Within 72 h | 18–65 years 50.3 |
13/11 | mRS as the ordinal outcome at 6 months, blinding of outcome assessment | 4 |
Decompressive Hemicraniectomy 2012 [21], China, Zhao | RCTs | Within 48 h | 18–82 years 63.5 |
24/23 | mRS as the ordinal outcome at 6 months,12 months, blinding of outcome assessment | 5 |
DESTINY II 2014 [22], Germany, Jüttler | RCTs | Within 48 h | ≥60 years; 70 |
47/62 | mRS as the ordinal outcome at 6 months, 12 months, blinding of outcome assessment | 5 |
Decompressive Hemicraniectomy 2018 [23], China, Li | RCTs | Within 48 h | >60 years 65.3 |
32/31 | mRS as the ordinal outcome at 12 months, not blinding of outcome assessment | 3 |