Mg. Patti et al., Laparoscopic Heller myotomy and Dor fundoplication for achalasia - Analysis of successes and failures, ARCH SURG, 136(8), 2001, pp. 870-875
Background: In the treatment of achalasia, surgery has been traditionally r
eserved for patients with residual dysphagia after pneumatic dilatation. Th
e results of laparoscopic Heller myotomy have proven to be so good, however
, that most experts now consider surgery the primary treatment.
Hypothesis: The outcome of laparoscopic myotomy and fundoplication for acha
lasia is dictated by technical factors.
Setting: University hospital tertiary care center.
Design: Retrospective study.
Patients and Methods: One hundred two patients with esophageal achalasia un
derwent laparoscopic Heller myotomy and Dor fundoplication. Fifty-seven pat
ients had been previously treated by pneumatic dilatation or botulinum toxi
n. The design of the operation involved a 7-cm myotomy, which extended 1.5
cm onto the gastric wall, and a Dor fundoplication. Esophagrams, esophageal
manometric findings, and video records of the procedure were analyzed to d
etermine the technical factors that contributed to the clinical success or
failure of the operation.
Main Outcome Measure: Swallowing status.
Results: In 91 (89%) of the 102 patients, good or excellent results were ob
tained after the first operation. A second operation was performed in 5 pat
ients to either lengthen the myotomy ( 3 patients) or talc down the fundopl
ication (2 patients). Dysphagia resolved in 4 of these patients. The remain
ing 6 patients were treated lay pneumatic dilatation, but dysphagia improve
d in only 1. At the conclusion of treatment, excellent or good results had
been obtained in 96 (94%) of the 102 patients.
Conclusions: These data chow that a Heller myotomy was unsuccessful inpatie
nts with an esophageal stricture; a short myotomy and a constricting Dor fu
ndoplication were the avoidable causes of residual dysphagia; a second oper
ation, but not pneumatic dilatation, was able to correct most failures; and
that the identified technical flaws were eliminated from the last half of
the patients in the series.