MedPath

POEM Anterior Versus Posterior Approach

Not Applicable
Completed
Conditions
Achalasia
Interventions
Procedure: Peroral Endoscopic Myotomy
Registration Number
NCT02454335
Lead Sponsor
Johns Hopkins University
Brief Summary

Per-oral endoscopic myotomy (POEM) is an incisionless procedure used to treat esophageal achalasia, performed by GI endoscopist without cutting any surface of the human body. The main constituent of the procedure is the myotomy part, through which the endoscopist cuts the muscle fibers in the submucosa. Since this procedure is completely new to the area of treatment of achalasia, it is unknown whether a posterior or an anterior myotomy is better in relieving the symptoms. Thenceforth, this study aims at randomizing patients with achalasia presenting for POEM to getting either the posterior or the anterior myotomy. Patients will be followed up for symptoms and complications; data will be extracted and the appropriate analysis will be employed to determine if there is any difference of outcome between the two techniques of myotomy.

Detailed Description

Peroral Endoscopic Myotomy (POEM) is an effective, minimally-invasive treatment for achalasia that has been adopted over the past few years. As more programs attempt to adopt the novel technique, there is an increased need for trials to help guide the growth of the procedure. Review of the current literature reveals that most endoscopists prefer an anterior approach, with an incision in the anterior/ anterolateral wall of the esophagus. This approach has been used with tremendous success in decreasing the symptoms of dysphagia and lowering esophageal sphincter (LES) pressure since the first description of the procedure in humans in 2010. However, it can be technically challenging in patients with anterior scarring from prior surgery or radiation, in whom a posterior approach has typically been used. Alternatively, the posterior approach, with incision in the posterolateral wall of the esophagus, has been adopted with great success by several endoscopists as the primary approach to myotomy. Reports involving the posterior approach have also shown significant symptom relief as defined by symptoms score (Eckardt score) \< 3, decreased LES pressure, and low complication rates.

However, despite high rates of technical and clinical success, the posterior approach has not been as widely adopted as the anterior approach. Without comparison of the two approaches in terms of efficacy and safety, the optimal technique to myotomy for POEM is yet to be defined. The investigators main hypothesis is that the posterior myotomy is as efficacious as the anterior myotomy in terms of improvement of achalasia symptoms as indicated by reduction in the Eckardt score and LES pressure. Adaptation of both techniques may increase options in approach for routine POEM and increase the number of patients that are able to undergo the procedure, thereby promoting its applicability.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
150
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Anterior ApproachPeroral Endoscopic MyotomyFor the anterior approach, an incision will be made in the 1 to 2 o'clock position of the esophageal wall.
Posterior ApproachPeroral Endoscopic MyotomyFor the posterior approach, a mucosal incision will be made at the 5 to 6 o'clock position
Primary Outcome Measures
NameTimeMethod
Change in Eckardt Scoreup to 24 months

The standardized clinical scoring system for achalasia will be assessed at 2 weeks, 3 months, 6 months, and 1 year post procedure. The score is based on the results of a self- administered questionnaire using 4 items related to digestive symptoms including weight loss, dysphagia, retrosternal pain, and regurgitation. Each item is rated from 0 to 3 (0= none, 1= occasional, 2=daily, 3=with every meal).

Secondary Outcome Measures
NameTimeMethod
Total procedure time and times of different stepsup to 24 months
Dysphagia by the Dysphagia Scoreup to 24 months

Dysphagia scoring system scores dysphagia as follows:

0 = able to eat normal diet / no dysphagia; 1 = able to swallow some solid foods; 2 = able to swallow only semi solid foods; 3 = able to swallow liquids only; 4 = unable to swallow anything / total dysphagia.

Rate of GERD by pH-impedanceup to 24 months

This is assessed by the DeMeester score. The score is comprised of the following: Percent total time pH \< 4, Percent Upright time pH \< 4, Percent Supine time pH \< 4, Number of reflux episodes, Number of reflux episodes ≥ 5 min, Longest reflux episode (minutes). The abnormal reflux is defined as DeMeester score \>14.72

Quality of Life by QoL S36 questionnaireup to 2 years

The SF-36 general health questionnaire consists of 36 questions evaluating the patient's perception of their quality of life (QoL) in the following eight subscales: physical functioning (PF), role limitations due to physical problems (RP), role limitations due to emotional problems (RE), energy/fatigue (EF), emotional well-being (EW), social functioning (SF), bodily pain (BP) and general health (GH). Subscale scores range from 0 to 100, with 100 being the best and 0 being the worst quality of life.

Postoperative pain by VAS analogue scale2 years

The visual analogue scales scores the severity of the pain from zero (minimum) to 10 (maximum).

Operative and post-operative complicationsup to 2 years
Technical successup to 24 months

Defined as completion of the procedure using the assigned approach

Analgesic use by Analgesic Quantification Algorithmup to 24 months

Analgesic Quantification Algorithm scoring scores analgesic use from zero (minimum) to 7 (maximum) as follows:

0= No analgesic; 1= Non-opioid analgesics; 2= Weak opioids (For example, codeine and tramadol); 3= Strong opioids ≤75 mg OME per day; 4= Strong opioids \>75-150 mg OME per day; 5= Strong opioids \>150-300 mg OME per day; 6= Strong opioids \>300-600 mg OME per day ; 7=Strong opioids \>600 mg OME per day

Hospital stay in daysup to 24 months
LES pressure by Manometryup to 2 years
Ease of procedure measured by the Lickerdt scaleup to 24 months

The ease of the procedure scored by the endoscopist on a Likert scale rated from 1 (easy) to 5 (impossible).

Trial Locations

Locations (1)

Johns Hopkins Hospital

🇺🇸

Baltimore, Maryland, United States

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