A randomised controlled comparison of injection, thermal, and mechanical endoscopic methods of haemostasis on mesenteric vessels
C C Hepworth
a GI Science Research Unit, St Bartholomew's
and The Royal London School of Medicine and Dentistry, London, UK, b Department of Medical Physics, University College, London, UK
Correspondence to: Dr P Swain,
The Royal London Hospital, Whitechapel, London E1 1BB, UK. Accepted for publication 13 November 1997 Background and aims Keywords:
endoscopic haemostasis;
mesenteric
vessels
A randomised controlled
comparison of haemostatic efficacy of mechanical, injection, and
thermal methods of haemostasis was undertaken using canine mesenteric
vessels to test the hypothesis that mechanical methods of haemostasis are more effective in controlling haemorrhage than injection or thermal
methods. The diameter of arteries in human bleeding ulcers measures up
to 3.45 mm; mesenteric vessels up to 5 mm were therefore studied.
Methods
Mesenteric vessels were randomised to
treatment with injection sclerotherapy (adrenaline and ethanolamine),
bipolar diathermy, or mechanical methods (band, clips, sewing machine, endoloops). The vessels were severed and haemostasis recorded.
Results
Injection sclerotherapy and clips failed
to stop bleeding from vessels of 1 mm (n=20) and 2 mm (n=20). Bipolar
diathermy was effective on 8/10 vessels of 2 mm but failed on 3 mm
vessels (n=5). Unstretched elastic bands succeeded on 13/15 vessels of 2 mm but on only 3/10 vessels of 3 mm. The sewing machine achieved haemostasis on 8/10 vessels of 4 mm but failed on 5 mm vessels (n=5);
endoloops were effective on all 5 mm vessels (n=5).
Conclusions
Only mechanical methods were
effective on vessels greater than 2 mm in diameter. Some mechanical
methods (banding and clips) were less effective than expected and need
modification. Thermal and (effective) mechanical methods were
significantly (p<0.01) more effective than injection sclerotherapy.
The most effective mechanical methods were significantly more effective (p<0.01) than thermal or injection on vessels greater than 2 mm.
(GUT 1998;42:462-469)
© 1998 by Gut
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