Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
---|---|---|---|---|---|
Anker et al 1983 Australia | 12 healthy volunteers who received a subcutaneous injection in lower leg with mock venom (radioactively labeled insulin) | Nonrandomised controlled trial with comparison groups: a) firm pad and bandage (80-100 mmHg); b) air splint (50 to 65 mmHg); c)elastic bandage and splint (55 mmHg); d) no treatment | % of maximum radioactivity in blood after 60 minutes | After 60 minutes: 1.5 to 8% with firm pad and bandage; 32 to 36% with air splint; 36 to 45% with elastic bandage and splint; 37 to 65% without treatment | small sample size, indirectness through use of a mock venom, risk of performance bias through different treatment times, no statistical tests |
% of maximum radioactivity in blood at release of treatment | At release of treatment: 2 to 16% with firm pad and bandage (release after 64 to 116 minutes); 64 to 69% with air splint (release after 120 to 130 minutes); 41 to 67% with elastic bandage and splint (release after 60 to 99 minutes) | ||||
Anker et al. 1982 Australia | 12 healthy volunteers who received a subcutaneous injection in lower leg with mock venom (radioactive sodium iodide | Nonrandomised controlled trial with comparison groups: a) firm pad and bandage (70-120 mmHg); b) air splint (55 mmHg); c) elastic bandage and splint (55 mmHg); d) no treatment | Time to 80 % of maximum radioactivity in blood | 70 to 77 minutes with firm pad and bandage (treatment was discontinued after 58 to 67 minutes); 20 to 35 minutes with air splint; 12 to 45 minutes with elastic bandage and splint; 22 to 29 minutes without treatment | small sample size, indirectness through use of a mock venom, no statistical tests |
Howarth et al. 1994 USA | 15 healthy volunteers who received a subcutaneous injection in wrists and ankles with mock venom (99m technetium antimony sulfur colloid) (9 additional volunteers received an intradermal injection with mock venom, but did not receive first aid treatments) | Within subjects study design with comparison groups: a) bandage and splint for one lower limb; b) bandage and splint for one upper limb; c) bandage and splint for either both lower/upper limbs (no results reported) d)local pressure over injection site. Target bandage pressure was 50 to 70 mmHg, the applied bandage pressure ranged from 20 to 110 mmHg; the unbandaged limbs acted as control. | Prevention of mock venom transit from periphery to systemic circulation while in rest | In rest: No transit in lower limbs of 9 out of 13 volunteers; No transit in upper limbs of 6 out of 13 volunteers; No transit with local pressure in 1 out of 4 volunteers | small sample size, indirectness through use of a mock venom, no statistical tests |
Prevention of mock venom transit from periphery to systemic circulation while walking with bandage and splints in place | While walking: subjects without transit in rest, all showed transit in upper and lower limbs after walking. | ||||
Tun-Pe et al. 1994 Myanmar | 22 healthy volunteers who received a subcutaneous injection in lower leg with mock venom (radioactive natrium iodide) | Nonrandomised controlled trial with comparison groups: a) firm pad and bandage and splint (mean 60 ± 10 mmHg); b) no treatment | Prevention of mock venom transit | No transit in 12 out of 14 volunteers with pad and bandage and splint | small sample size, indirectness through use of a mock venom, bandage pressures and mock venom dosages varied in the intervention group, no statistical tests |
Time to 80 % of maximum radioactivity in blood | 50 to 87 minutes with firm pad and bandage and splint (treatment was discontinued after 45 to 79 minutes); 40 to 54 minutes without treatment | ||||
Canale et al. 2009 Australia | 96 volunteers ( 78 healthcare workers and 18 laypersons) | RCT with comparison groups: a)crepe bandage; b)elastic bandage | Median (IQR) bandage pressure | Without information about the requirements of the technique: 28 mmHg (IQR 17–42 mmHg) with crepe bandage; 47 mmHg (IQR 26–83 mmHg) with elastic bandage. Following training: 65 mmHg (IQR 56–71 mmHg) with elastic bandage; there was no comparison group | Indirectness through use of healthcare workers and absence of stress of a situation with a real snakebite |
Simpson et al. 2008 India | 40 volunteers (laypersons) | RCT with comparison groups: a)written instructions on application of compression bandage and splint; b)focused training on application of compression bandage and splint | Pressure bandage application within range of 55 to 70 mmHg | 0 out of 20 with written instructions; 12 out of 20 with focused training measured 1 hour after training, 7 measured 1 day after training, 5 measured 3 days after training, 3 (upper limb) measured 3 months after training, 5 (lower limb) measured 3 months after training. No significant differences for bandage materials used (crepe bandage versus turban cloth) |