Randomized clinical trial of symptom control after stapled anopexy or diathermy excision for haemorrhoid prolapse
- PMID: 20035531
- DOI: 10.1002/bjs.6804
Randomized clinical trial of symptom control after stapled anopexy or diathermy excision for haemorrhoid prolapse
Abstract
Background: : This multicentre randomized clinical trial studied how symptoms improved after either stapled anopexy or diathermy excision of haemorrhoids.
Methods: : The study involved 18 hospitals in Sweden, Denmark and the UK. Some 207 patients were randomized to either anopexy or Milligan-Morgan haemorrhoidectomy, of whom 90 in each group were operated on. Patients reported symptoms before surgery and after 1 year. Daily postoperative pain scores were recorded in a patient diary. Surgeons evaluated the anal anatomy before surgery and after 1 year.
Results: : Correction of prolapse in the anopexy and haemorrhoidectomy groups was similar at 1 year (88 and 90 per cent respectively; P = 0.80). Freedom from symptoms was obtained in 44 and 69 per cent respectively (P = 0.002). Stapled anopexy was associated with less postoperative pain, which resolved more quickly (P = 0.004). Significant improvements were noted in anal continence and well-being 1 year after both operations (P < 0.001). Excessive pain was the most common complication after diathermy excision and disturbed bowel function after stapled anopexy.
Conclusion: : Haemorrhoidal prolapse was corrected equally by either operation. Diathermy haemorrhoidectomy gave better symptom relief but was more painful. Neither operation provided complete cure but well-being was greatly improved.
Registration number: ISRCTN68315343 (http://www.controlled-trials.com).
Copyright (c) 2009 British Journal of Surgery Society Ltd. Published by John Wiley & Sons, Ltd.
Comment in
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Randomized clinical trial of symptom control after stapled anopexy or diathermy excision for haemorrhoid prolapse (Br J Surg 2010; 97: 167-176).Br J Surg. 2010 Jun;97(6):961; author reply 961-2. doi: 10.1002/bjs.7144. Br J Surg. 2010. PMID: 20474014 No abstract available.
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