| Literature DB >> 32355884 |
Olaya I Brewer Gutierrez1, Robert A Moran2, Pietro Familiari3, Mohamad H Dbouk1, Guido Costamagna3, Yervant Ichkhanian1, Stefan Seewald4, Amol Bapaye5, Joo Young Cho6, Maximilien Barret7, Nikolas Eleftheriadis8, Mathieu Pioche9, Bu' Hussain Hayee10, Marcel Tantau11, Michael Ujiki12, Rosario Landi3, Martina Invernizzi4, In Kyung Yoo6, Sabine Roman9, Amyn Haji10, H Mason Hedberg12, Nasim Parsa1, Francois Mion9, Lea Fayad1, Vivek Kumbhari1, Anant Agarwalla1, Saowanee Ngamruengphong1, Omid Sanaei1, Thierry Ponchon9, Mouen A Khashab1.
Abstract
Background and study aims Per-oral endoscopic myotomy (POEM) is associated with a short-term clinical response of 82 % to 100 % in treatment of patients with achalasia. Data are limited on the long-term durability of the clinical response in these patients. The aim of this study was to determine the long-term outcomes of patients undergoing POEM for management of achalasia. Methods This was a retrospective multicenter cohort study of consecutive patients who underwent POEM for management of achalasia. Patients had a minimum of 4 years follow-up. Clinical response was defined by an Eckardt score ≤ 3. Results A total of 146 patients were included from 11 academic medical centers. Mean (± SD) age was 49.8 (± 16) years and 79 (54 %) were female. The most common type of achalasia was type II, seen in 70 (47.9 %) patients, followed by type I seen in 41 (28.1 %) patients. Prior treatments included: pneumatic dilation in 29 (19.9 %), botulinum toxin injection in 13 (8.9 %) and Heller myotomy in seven patients (4.8 %). Eight adverse events occurred (6 mucosotomies, 2 pneumothorax) in eight patients (5.5 %). Median follow-up duration was 55 months (IQR 49.9-60.6). Clinical response was observed in 139 (95.2 %) patients at follow-up of ≥ 48 months. Symptomatic reflux after POEM was seen in 45 (32.1 %) patients, while 35.3 % of patients were using daily PPI at 48 months post POEM. Reflux esophagitis was noted in 16.8 % of patients who underwent endoscopy. Conclusion POEM is a durable and safe procedure with an acceptably low adverse event rate and an excellent long-term clinical response.Entities:
Year: 2020 PMID: 32355884 PMCID: PMC7165007 DOI: 10.1055/a-1120-8125
Source DB: PubMed Journal: Endosc Int Open ISSN: 2196-9736
Baseline demographic and pre-POEM characteristics.
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| Age; (mean ± SD) | 49.8 ± 16 | |
| BMI; (mean ± SD) | 108 | 23 ± 4.7 |
| Female; (n) (%) | 79 (54) | |
| Ethnicity; (n) (%) | ||
White | 110 (75.3) | |
Black | 8 (5.5) | |
Asian | 26 (17.8) | |
Others | 2 (1.4) | |
| Disease Classification; (n) (%) | ||
Type I | 41 (28.1) | |
Type II | 70 (47.9) | |
Type III | 9 (6.2) | |
Unspecified Achalasia | 26 (17.8) | |
| Prior therapy (yes); (n) (%) | 41 (28.1) | |
| Pneumatic dilation; (n) (%) | 29 (19.9) | |
| Botox; (n) (%) | 13 (8.9) | |
| Heller myotomy; (n) (%) | 7 (4.8) | |
| Sigmoidal esophageal shape; (n) (%) | 142 | 10 (7) |
| HRM IRP (mmHg); (mean ± SD) | 93 | 26.9 ± 13.1 |
| HRM resting pressure (mmHg); (mean ± SD) | 125 | 38.4 ± 20.8 |
| Pre-POEM Eckardt score; (median) (IQR) | 7 (6.75–9) | |
HREM, high-resolution esophageal manometry; IRP, integrated relaxation pressure; LES, lower esophageal sphincter; IQR, interquartile range; PPI, proton pump inhibitor
Fig. 1Clinical success (Eckardt score ≤ 3) at different time intervals after POEM in patients who had follow-up at 48 months.
Procedure characteristics and outcomes.
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| Full thickness LES myotomy; (n) (%) | 145 | 76 (52.4) |
| Gastric myotomy (cm); (mean ± SD) | 3.2 ± 1 | |
| Esophageal myotomy (cm); (mean ± SD) | 8.5 ± 2.5 | |
| Orientation of myotomy (anterior); (n) (%) | 144 | 112 (77.8) |
| Patients with adverse events; (n) (%) | 8 (5.5) | |
| Follow up-post poem | ||
| 48 months Eckardt; (Median) (IQR)) | 1 (0–2) | |
| 36 months Eckardt; (Median) (IQR) | 123 | 1 (0–2) |
| 24 months Eckardt; (Median) (IQR)) | 135 | 1 (0–2) |
| 12 months Eckardt; (Median) (IQR) | 123 | 1 (0–2) |
| 6 months Eckardt; (Median) (IQR) | 141 | 1 (0–1) |
| HRM Resting pressure (mmHg); (mean ± SD) | 93 | 16.9 ± 9 |
| HRM IRP (mmHg); (mean ± SD) | 89 | 10.28 ± 7.1 |
| Symptomatic reflux; (n) (%) | 140 | 45 (32.1) |
| Esophagitis; (n) (%) | 131 | 22 (16.8) |
| Abnormal acid exposure; (n) (%) | 80 | 38 (47.5) |
| DeMeester > 14.72; (n) (%) | 80 | 44 (55) |
| PPI use; (n) (%) | 136 | |
| Yes-daily | 48 (35.3) | |
| Yes-occasionally | 15 (11) | |
| No | 73 (53.7) | |
| Follow up time (months); (Median)(IQR) | 55 (49.9–60.6) | |
HREM, high-resolution esophageal manometry; IRP, integrated relaxation pressure; LES, lower esophageal sphincter; IQR, interquartile range; PPI, proton pump inhibitor