Open Access
CC BY 4.0 · Journal of Digestive Endoscopy 2024; 15(01): 059-104
DOI: 10.1055/s-0044-1786294
Abstracts of presentation during ENDOCON 2024, New Delhi

Medium- and Long-Term Outcomes of Per Rectal Endoscopic Myotomy for Hirschsprung’s Disease

Arun Arora Pagadapelli
1   Shivanand Desai Centre for Digestive Disorders, Deenanath Mangeshkar Hospital and Research Center, Pune, Maharashtra, India
,
Rohan Yewale
1   Shivanand Desai Centre for Digestive Disorders, Deenanath Mangeshkar Hospital and Research Center, Pune, Maharashtra, India
,
Parag Dashatwar
1   Shivanand Desai Centre for Digestive Disorders, Deenanath Mangeshkar Hospital and Research Center, Pune, Maharashtra, India
,
Rajendra Pujari
1   Shivanand Desai Centre for Digestive Disorders, Deenanath Mangeshkar Hospital and Research Center, Pune, Maharashtra, India
,
Harshal Gadhikar
1   Shivanand Desai Centre for Digestive Disorders, Deenanath Mangeshkar Hospital and Research Center, Pune, Maharashtra, India
,
Amol Bapaye
1   Shivanand Desai Centre for Digestive Disorders, Deenanath Mangeshkar Hospital and Research Center, Pune, Maharashtra, India
› Author Affiliations
 
 

    Introduction: Hirschsprung's disease (HSCR) is characterized by absence of ganglion cells in the submucosal and myenteric plexus of colon. Surgery—standard treatment but has significant morbidity. Per rectal endoscopic myotomy (PREM) is a novel third space procedure described for treatment of HSCR.

    Aim: To evaluate technical outcomes and clinical success (measured as stool frequency, unit laxative usage, and improvement in HSCR Anorectal malformation Quality of life questionnaire [HAQL]) pre- and post-PREM.

    Methods: Single-arm, single-center prospective observational study of HSCR patients treated with PREM. HSCR diagnosis: history, contrast enema, anorectal manometry, rectal EMR biopsies. Stool frequency, laxative usage, HAQL before and after PREM were compared.

    Results: N = 16 (age 14 [± 14.4] years; 11 male) underwent PREM during a 7-year period. Majority (68.8%): symptoms from birth. Transition zone on barium enema + in all (100%), spastic colonic segment with proximal dilation on colonoscopy in 93.8%. Mean aganglionic segment length was 7.0 cm ± 3.9, RAIR was absent in 11 cases (68.75%), present in 5 cases (31.25%). HSCR subtypes: ultrashort segment (8/16, 50%), short segment (5/16, 31.25%), long segment (3/16, 18.75%). Mean procedure time: 91 minutes ± 28.9, mean length of hospital stay: 3.5 days. Median follow up: 8 months (IQR: 4.5–19.5). Median of the first stool frequency: 2 days (IQR: 2–2.5). Stool frequency: 1 in 4.1 (±1.3) days pre versus 1 in 1.4 (±0.8) days post-PREM (p < 0.0001). Mean laxative usage: 4.7 (±3.8) units of laxative (UL) pre versus 0.8 (±0.9) UL post-PREM (p < 0.0001). HAQL scores of 8.5 (±3.9) pre-PREM improved to 1.3 (±0.9) post-PREM (p < 0.0001) ([Table 1]).

    Conclusions: PREM is a safe and effective minimally invasive procedure to treat SS-HSCR. Outcomes are sustained in the long term as demonstrated by improved stool frequency rates, mean laxative use, and HAQL questionnaire.

    Table 1

    Characteristics at baseline and follow-up (post-PREM)

    N

    %

    Total subjects

    16

     

    Gender

    Male

    11

    68.75

    Female

    5

    31.25

    Age (in years)

    mean ± SD; (range min–max)

    14 ± 14.4; (1–49)

    Duration of symptoms

    Since birth

    11

    68.8

    6 months

    1

    6.3

    1 year

    2

    12.5

    2 year

    2

    12.5

    RAIR

    Absent

    11

    68.75

    Present

    5

    31.25

    Ganglion cells

    Absent

    12

    75

    Present

    4

    25

    Length of aganglionic segment in cm

    Mean ± SD; median (IQR)

    7 ± 3.9; 7 (7)

    Length of myotomy in cm

    11 ± 3.3; 10 (2)

    Time to completion in min

    90.9 ± 28.9; 85 (35)

    Time to first stool POD in days

    2.1 ± 0.7; 2 (2–2.5)

    Follow-up duration (in months)

    14.4 ± 15.9; 8(4.25–19.25)

    Follow-up characteristics

    N

    %

    Need for laxatives post-PREM

    Lactitol 13.3 g/day (20 mL/day)—half of the initial dose

    3

    18.8

    Lactitol 26.6 g/day (40 mL/day)

    1

    6.3

    Lactulose 6.67 g/day—two-third of initial dose

    3

    18.8

    PEG 17 g/day—half of the initial dose

    2

    12.5

    None

    7

    43.8

    Fecal incontinence post-PREM

    Complete improvement

    2

    12.5

    Partial improvement

    2

    12.5

    Comparison of clinical outcomes pre- and post-PREM

    Mean ± SD

    Median (IQR)

    Mean ± SD

    Median (IQR)

    Pre-PREM

    Post-PREM

    p -Value

    Stool frequency

    4.1 ± 1.3

    4 (2)

    1.4 ± 0.8

    1 (1)

    <0.0001a

    Laxative usage

    4.7 ± 3.8

    4 (4)

    0.8 ± 0.9

    0.6 (1.3)

    <0.0001a

    HAQL questionnaire

    8.5 ± 3.9

    7 (3)

    1.3 ± 0.9

    1 (1)

    0.0001a

    Note: Groups where compared using paired t-test where p <0.05 is considered statistically significant.



    No conflict of interest has been declared by the author(s).

    Publication History

    Article published online:
    22 April 2024

    © 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

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