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Published on: March 3, 2023
Per Oral Endoscopic Myotomy (POEM) for pediatric achalasia: Institutional experience and outcomes
Mikael Petrosyan1, Shikib Mostammand2, Adil A Shah1
1The Department of General and Thoracic Surgery, Children's National Hospital, 111 Michigan Avenue NW, Washington DC 20010, United States.
Insights
Per oral endoscopic myotomy (POEM) is a safe and effective treatment for pediatric achalasia, whether used as a primary therapy or after previous procedures. This minimally invasive approach offers comparable results to traditional surgery, improving patient outcomes.
Area of Science:
- Pediatric surgery
- Gastroenterology
- Minimally invasive procedures
Background:
- Achalasia management in children typically involves surgical interventions like laparoscopic Heller myotomy (LHM) and per oral endoscopic myotomy (POEM).
- While LHM is established, there's growing global experience with endoscopic POEM for pediatric achalasia, even in centers with lower patient volumes.
Purpose of the Study:
- To evaluate the institutional experience with POEM as a primary or revisional therapy for achalasia in pediatric patients.
- To assess the safety and efficacy of POEM in this population.
Main Methods:
- A retrospective review of pediatric achalasia patients undergoing POEM between July 2015 and September 2021.
- Data collected included demographics, operative details, pre- and post-operative Eckardt scores, complications, and follow-up outcomes.
Main Results:
- 37 POEM procedures were performed (33 primary, 4 revisional).
- The mean age was 11.6 years, with a mean baseline Eckardt score of 6.73.
- Post-POEM, 100% achieved symptomatic relief (Eckardt score ≤ 3), with a 16.2% reintervention rate (5 PBD, 1 LHM).
- Intraoperative complications occurred in 43.2% but did not require reoperation; post-operative complications included recurrent dysphagia (13.5%) and GERD (8.1%).
Conclusions:
- POEM is a safe and effective treatment for pediatric achalasia, suitable as both first-line therapy and for patients with prior treatment failures.
- POEM demonstrated comparable outcomes to LHM in this cohort.
- Long-term monitoring for growth and symptom recurrence is planned.
Background:
The surgical treatment of achalasia by both laparoscopic and endoscopic approaches has been recognized as the definitive management in children. Despite reported low volumes in many centers, there has been an increasing worldwide experience with endoscopic approaches to pediatric achalasia. The aim of this study is to report our institutional experience with per oral endoscopic myotomy (POEM) as first-line or revisional therapy for achalasia.
Methods:
An IRB approved retrospective review of all patients who underwent operative procedures for achalasia, specifically with the POEM technique, from July 2015 to September 2021. Data including demographics, intra-operative details, pre and post operative Eckardt scores, complications, outcomes, and follow-up were obtained.
Results:
During the study period, a total of 43 children underwent 46 operations for achalasia including POEM and laparoscopic Heller myotomy (LHM). Operations included 37 POEMS (33 primary POEMS; 3 POEMS after failed LHM; and 1 POEM after failed POEM). Additionally, 9 LHM operations including, 4 primary LHM; 3 attempted POEMS converted to LHM; 1 attempted POEM after failed LHM converted to redo LHM; and 1 LHM after failed POEM. In the POEM group (n = 37), based on the high resolution esophageal manometry findings Chicago Classification types at diagnosis were as follows: 9 patients were type I (24.3%); 25 patients were type II (67.6%); 2 patients were type III (5.9%) and 1 patient was unknown type (2.7%). Sixteen children (43.2%) had prior endoscopic treatment of achalasia prior to POEM [Pneumatic Balloon Dilatation (PBD), and/or Botox injection (BTI)],), while prior operative intervention occurred in 4 patients (10.8%), 3 LHM and 1 POEM. Age at operation was 2-18 years (mean ± SD age: 11.6 ± 4.5 years). Weight at operation 11.8-100.7 kg (mean ± SD kg; 39 ± 19.9 kg). Range of baseline Eckardt score was 4-10 (mean ± SD: 6.73 ± 1.5). Operative time was 64-359 min (mean ± SD minutes: 138.1 ± 62.2 min). Intraoperative complications occurred in 16 patients (43.2%) but did not require reoperation during index admission including: 4 mucosotomy (11.8%); 9 pneumothoraces (24.3%); 2 pneumomediastinum (5.4%); 10 pneumoperitoneum (27%); 0 sub-mucosal tunnel bleeding (0%); 0 open conversion/death (0%). Post operative complications included: 5 recurrent dysphagia (13.5%); 0 esophageal leak (0%); 3 GERD (8.1%); 1 failed POEM (2.7%). Median length of stay was 2 days (mean ± SD days: 2.4 ± 0.9 day). Follow-up ranged from 1 to 74 months (median 15 months), mean follow-up 22.6 months ± 20 months. Post POEM Eckardt score was 0.6 ± 0.9. Five patients required a single PBD post POEM (13.5%) and 1 patient required a repeat myotomy (LHM) after POEM (2.7%) for a 16.2% reintervention rate. Subsequent normalization of Eckardt scores (≤ 3) and symptomatic relief was achieved in all patients (100%).
Conclusions:
POEM as first-line therapy for pediatric achalasia, or as a secondary procedure after failed prior myotomy or POEM, in our experience is safe and effective. We have shown equivalent results to our own prior experience with LHM. Long-term follow-up will be performed to monitor for recurrent symptoms, adequate physical growth, and general development.
Level Of Evidence:
II.
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