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Narrative review discusses multimodal strategies for rebound pain after extremity fracture surgery

Narrative review discusses multimodal strategies for rebound pain after extremity fracture surgery
Photo by Nigel Hoare / Unsplash
Key Takeaway
Consider multimodal analgesic concepts for rebound pain in extremity fracture surgery.

This narrative review focuses on multimodal preventive strategies for rebound pain in patients undergoing extremity fracture surgery. The scope of the discussion centers on the concept of integrating pharmacological agents and techniques with divergent mechanisms of action. The authors propose a multimodal analgesic approach to address this clinical challenge.

The authors hypothesize that rebound pain arises from the dynamic interplay of three interrelated risk elements. This hypothesis forms the core argument of the review without relying on pooled effect sizes or specific trial data. The text explicitly notes that causal claims regarding the Triple-Hit Model should not be overstated.

Limitations regarding sample size, setting, and follow-up duration are not reported in this source. Safety data, including adverse events and tolerability, were not reported. The review serves as a conceptual framework rather than a quantitative analysis of specific interventions or outcomes.

The practice relevance is framed around the multimodal analgesic concept. Clinicians should interpret these findings as a hypothesis rather than established fact given the lack of primary trial data.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedMay 2026
View Original Abstract ↓
Extremity fracture surgery is the standard surgical intervention for traumatic musculoskeletal injuries. The maturation of ultrasound-guided visualization techniques has facilitated the widespread application of peripheral nerve block (PNB) in perioperative anesthesia and analgesia. However, rebound pain (RP)—defined as the phenomenon wherein previously suppressed nociceptive signals exhibit abrupt intensification exceeding baseline levels following the termination of regional analgesic effects—has emerged as a significant clinical challenge. RP interferes with early postoperative functional mobilization, compromises patient satisfaction, and increases healthcare resource utilization. The pathogenesis of RP involves a multifactorial pathophysiological process: hyperexcitability of nerve fibers following block resolution; compensatory neurophysiological responses subsequent to local anesthetic pharmacodynamic decline; iatrogenic neural effects attributable to needle instrumentation or surgical manipulation; localized inflammatory cascade activation triggered by tissue trauma; and interindividual variability in genetic susceptibility and psychological resilience. The cornerstone of RP prevention lies in the multimodal analgesic concept, integrating pharmacological agents and techniques with divergent mechanisms of action. This review proposes a conceptual “Triple-Hit Model of RP,” hypothesizing that RP arises from the dynamic interplay of three interrelated risk elements: the first element is the magnitude of initial peripheral nociceptive input, predominantly determined by surgical trauma severity; the second element is individual central nervous system modulation capacity and pain tolerance thresholds, influenced by chronological age, anxiety states, and related factors; the third element is the withdrawal pattern of regional analgesic protection, encompassing block duration and offset velocity. The synergistic convergence of these three hits substantially amplifies the risk of severe RP manifestation.
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