Neurovascular Architecture of Deep Endometriosis and Postoperative Pain Outcomes after Butterfly Peritoneal Excision: A Prospective Pilot Study

Other OA: closed CC0
View on OpenAlex View on PubMed View at publisher
⚙ AI-generated summary by gemini-2.5-flash-lite, 2026-06-11 ⓘ

This pilot study examined the neurovascular architecture of deep endometriosis and its correlation with postoperative pain outcomes following butterfly peritoneal excision.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

Abstract

STUDY OBJECTIVE: To evaluate the neurovascular architecture of deep endometriosis using a standardized butterfly excision approach and to explore its association with postoperative pain outcomes. DESIGN: Prospective exploratory pilot study. SETTING: Tertiary referral center specializing in endometriosis surgery. PATIENTS: Fifteen women with advanced posterior deep endometriosis undergoing laparoscopic excision. INTERVENTIONS: Standardized butterfly peritoneal excision with systematic radial sampling from the central lesion to the peripheral peritoneum. MEASUREMENTS AND MAIN RESULTS: Each specimen was divided into 15 segments (7 per side plus central lesion), yielding 240 total samples, including normal peritoneum. Nerve-fiber density showed a significant center-to-periphery decline (β = -0.3169, p <.001), corresponding on average to an estimated 27% reduction per segment, while capillary density demonstrated a parallel but less pronounced decrease (β = -0.100, p <.001), supporting a coordinated neurovascular gradient. No right-left difference was observed. In contrast, tissue pain mediators exhibited heterogeneous spatial distribution rather than a uniform center-dominant pattern. Among evaluated markers, only bradykinin was associated with nerve-fiber density (p <.001). In exploratory multivariable analyses, central nerve growth factor concentration showed an association with 6-month dysmenorrhea improvement (β = 0.012, p = .043), whereas morphometric nerve-fiber density did not. For chronic pelvic pain, baseline pain severity was the only variable associated with postoperative improvement (β = 0.777, p = .030). Clinically, postoperative reductions were observed across multiple pain domains, accompanied by improvements in physical and mental quality-of-life measures. CONCLUSION: Deep endometriosis demonstrated spatial neurovascular gradients with dissociation between structural innervation and inflammatory mediator distribution. Central neurotrophic activity showed an exploratory association with postoperative dysmenorrhea improvement, whereas morphometric nerve-fiber density did not. These findings support the feasibility and potential biological relevance of spatial neurovascular mapping in deep endometriosis and should be considered hypothesis-generating pending validation in larger studies. CLINICAL TRIAL NUMBER: NCT06286371, https://clinicaltrials.gov/study/NCT06286371. DATE OF REGISTRATION: 22.02.2024.

My notes (saved in your browser only)

Citation neighborhood (2-hop)

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. Outer rings show 2-hop neighbours — papers reached through the immediate citers/citees. [ collapse to 1-hop ]

References (31)

Cited by (1)

SciLite annotations

chemicals 1
bradykinin

Source provenance

europepmc
last seen: 2026-10-16T06:09:50.462052+00:00
openalex
last seen: 2026-08-31T06:00:52.054077+00:00
pubmed
last seen: 2026-10-16T06:03:29.143702+00:00
scilite
last seen: 2026-07-12T09:48:33.364277+00:00
unpaywall
last seen: 2026-10-16T06:24:35.758740+00:00
License: CC0 · commercial use OK