Oral nifedipine reduces resting anal pressure and heals chronic anal fissure

Background: Topical preparations have been used in the treatment of anal fissure. However, they are not universally successful and there is confusion over the site and dose of application. This study assessed the effectiveness of oral nifedipine in reducing resting anal pressure and on fissure heali...

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Bibliographic Details
Published in:British journal of surgery Vol. 86; no. 10; pp. 1269 - 1273
Main Authors: Cook, T. A., Humphreys, M. M. Smilgin, Mortensen, N. J. McC
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Science Ltd 01-10-1999
Wiley
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Summary:Background: Topical preparations have been used in the treatment of anal fissure. However, they are not universally successful and there is confusion over the site and dose of application. This study assessed the effectiveness of oral nifedipine in reducing resting anal pressure and on fissure healing. Methods: Anal manometry was performed on eight healthy volunteers and 15 patients with chronic anal fissure before and after oral administration of nifedipine 20 mg. Nifedipine was taken twice daily. Fissure healing was assessed over an 8‐week period and pain scores were monitored. Results: Oral nifedipine produced an initial reduction in maximum resting anal pressure (MRP) of 35 per cent (P < 0·001) and of 28 per cent after 5 days (P < 0·001) in healthy volunteers. A reduction in MRP of 36 per cent (P < 0·001) was observed in patients with fissure. Pain scores were significantly reduced during the treatment period. Healing was complete in nine patients after 8 weeks and a further three were asymptomatic. Ten patients experience flushing and four had mild headaches. There were no episodes of postural hypotension or incontinence. Conclusion: Oral nifedipine reduces resting anal pressure. It is well tolerated and offers an alternative treatment for chronic anal fissure. © 1999 British Journal of Surgery Society Ltd
Bibliography:ark:/67375/WNG-82C2F1ZP-7
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ArticleID:BJS70
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0007-1323
1365-2168
DOI:10.1046/j.1365-2168.1999.01292.x