Trial reportInternational orthopaedics2026
Optimizing tourniquet pressures in knee arthroscopy: an international survey on current practice and a double-blind randomized trial.
Trial report in International orthopaedics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.
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Corrections and comments
- Erratum issued
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
BACKGROUND & PURPOSE: Pneumatic tourniquets improve surgical visualization during knee arthroscopy, but fixed high pressures may increase postoperative pain. This study investigated whether a minimal effective individualized occlusion pressure (MEIOP), calculated as limb occlusion pressure plus a safety margin, maintains surgical field quality while reducing pain compared to a standardized occlusion pressure (SOP).
methodsA preliminary survey of 79 orthopaedic surgeons identified 350 mmHg as the routine SOP. In a subsequent double-blind randomized clinical trial, patients undergoing elective knee arthroscopy were assigned to SOP (350 mmHg) or MEIOP, defined as Doppler-derived limb occlusion pressure plus a safety margin (mean ≈ 230 mmHg). Outcomes included surgical field quality, postoperative using a visual analog scale (VAS) up to 15 days, overall 15-day pain perception, and analgesic consumption.
resultsBoth groups achieved 100% excellent surgical field ratings. Pain trajectories differed significantly between groups over time (group × time interaction, p = 0.022). The MEIOP group experienced significantly lower pain at discharge (~ 6 h; p = 0.013, d = 1.14) and lower overall 15-day pain perception (p = 0.043, d = 0.89). Analgesic consumption showed a consistent descriptive trend favoring MEIOP throughout follow-up.
conclusionThis proof-of-concept study suggests that individualizing tourniquet pressure using predefined MEIOP protocol preserves satisfactory surgical visualization and is associate with lower postoperative pain compared with a standard high-pressure protocol. This trial was prospectively registered at the Brazilian Clinical Trials Registry (ReBEC; RBR-4xd6cxm).
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