# The Role of Functional Lumen Imaging Probe (FLIP) in Addition to High‐Resolution Manometry and Timed Barium Esophagram in Treated Achalasia Patients With Persistent or Recurrent Symptoms

**Authors:** Elise M. Wessels, Niek Warringa, Gwen M. C. Masclee, Jeroen M. Schuitenmaker, Albert J. Bredenoord

PMC · DOI: 10.1111/nmo.70281 · 2026-03-10

## TL;DR

This study found that FLIP does not add value over HRM and TBE in selecting achalasia patients for retreatment.

## Contribution

The study evaluates the added value of FLIP in combination with HRM and TBE for retreatment decisions in achalasia patients.

## Key findings

- FLIP did not significantly improve prediction of treatment success compared to HRM and TBE.
- Most patients with abnormal HRM and TBE results had successful retreatment.
- FLIP showed moderate to strong correlation with HRM but no added benefit.

## Abstract

A subgroup of treated achalasia patients has recurrent symptoms which prompt consideration of additional treatment. The aim of this study was to examine the additional yield of functional lumen imaging probe (FLIP) to high‐resolution manometry (HRM) and timed barium esophagram (TBE) in selection of patients for retreatment.

This prospective observational cohort study was performed between November 2019 and October 2025 and included treated achalasia patients with recurrent or persistent symptoms who underwent FLIP in addition to HRM and TBE prior to retreatment. The primary outcome was the association between the distensibility index measured by FLIP and response to retreatment (treatment success: Eckardt score ≤ 3).

In total 84 patients were included (median age 50 years, 36.9% female). At a median follow‐up of 11 weeks after retreatment, 82.1% had treatment success (N = 69/84) and 17.9% had treatment failure (N = 15/84). The distensibility index at 40 mL on FLIP did not significantly differ between patients with and without treatment success (1.4 mm2/mmHg vs. 1.0 mm2/mmHg, p = 0.463). Almost all patients with abnormal HRM and TBE results had treatment success (N = 22/23, 95.7%). In cases with inconclusive HRM and TBE results, treatment success was 83.3% when FLIP results were normal (N = 10/12) and 74.3% when FLIP results were abnormal (N = 26/35).

FLIP did not provide added value over HRM and TBE for identifying treated achalasia patients who may benefit from further treatment. The difficulty in selecting achalasia patients for retreatment highlights the complexity of this patient population and underscores the need for further research.

Subsequent treatments tend to have lower efficacy in achalasia patients with persistent or recurrent symptoms following initial treatment, reflecting the challenges in managing this complex subgroup.Functional lumen imaging probe did not offer additional predictive value over high‐resolution manometry and timed barium esophagram in identifying which treated achalasia patients were likely to benefit from further treatment.Functional lumen imaging probe outcomes demonstrated a moderate to strong correlation to high‐resolution manometry, indicating the potential use as a substitute diagnostic tool.

Subsequent treatments tend to have lower efficacy in achalasia patients with persistent or recurrent symptoms following initial treatment, reflecting the challenges in managing this complex subgroup.

Functional lumen imaging probe did not offer additional predictive value over high‐resolution manometry and timed barium esophagram in identifying which treated achalasia patients were likely to benefit from further treatment.

Functional lumen imaging probe outcomes demonstrated a moderate to strong correlation to high‐resolution manometry, indicating the potential use as a substitute diagnostic tool.

Functional lumen imaging probe did not offer additional yield over high‐resolution manometry and timed barium esophagram in identifying which treated achalasia patients with persistent or recurrent symptoms were likely to benefit from further treatment.

## Linked entities

- **Diseases:** achalasia (MONDO:0008698)

## Full-text entities

- **Genes:** CFLAR (CASP8 and FADD like apoptosis regulator) [NCBI Gene 8837] {aka CASH, CASP8AP1, CLARP, Casper, FLAME, FLAME-1}, NPNT (nephronectin) [NCBI Gene 255743] {aka EGFL6L, POEM}
- **Diseases:** chest pain (MESH:D002637), esophageal motility disorder (MESH:D015154), esophagogastric junction outflow obstruction (MESH:D014694), Peptic strictures (MESH:D003251), epiphrenic diverticula (MESH:D004240), regurgitation (MESH:D008944), esophageal dilation (MESH:D004941), Gastroesophageal reflux (MESH:D005764), retrosternal pain (MESH:D010146), esophageal adenocarcinoma (MESH:D000230), anxiety (MESH:D001007), Achalasia (MESH:D004931), dysphagia (MESH:D003680), TBE (MESH:C537080), PD (MESH:D002311), esophageal hypersensitivity (MESH:D004935), weight loss (MESH:D015431)
- **Chemicals:** water (MESH:D014867), fentanyl (MESH:D005283), propofol (MESH:D015742), saline (MESH:D012965), midazolam (MESH:D008874), Barium (MESH:D001464), Esophagram (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12973156/full.md

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Source: https://tomesphere.com/paper/PMC12973156