Submitted:
24 January 2026
Posted:
27 January 2026
You are already at the latest version
Abstract
Keywords:
Introduction

Methods
Eligibility Criteria
Searching and Screening
Data Collection Process
Planned Data Synthesis
Current Review Stage
Conceptual Role in Preoperative Planning
Intraoperative Guidance and Execution
Postoperative Monitoring and Outcomes
Limitations, Safety Concerns, and Barriers to Adoption
| Nano Application | Evidence Level | Clinical Status |
|---|---|---|
| Fluorescence probes | Preclinical / early human pilots | Experimental |
| Drug-eluting particles | Preclinical | Not approved in US/EU |
| Targeted contrast agents | Animal models / phase I trials | Investigational |
| Nano-sensors for monitoring | Preclinical concepts | Not in clinical use |
Evidence for Hybrid Systems
| Aspect | Single-Technology (e.g., AI Alone, Robotics Alone, Nano Alone) | Hybrid Systems (e.g., AI-Robotics-Nano Integration) |
| Strengths | Simpler implementation; lower cost; focused on specific pain points (e.g., AI for prediction, robotics for dexterity). | Potential synergies for adaptive workflows; addresses multiple challenges simultaneously (e.g., real-time margin adjustment). |
| Weaknesses | Limited scope; may not handle complexity like deformation or heterogeneity. | Increased complexity; higher risk of compounded errors; regulatory hurdles. |
| Evidence Maturity | Higher for AI/robotics (trials); lower for nano (preclinical). | Mostly preclinical/pilot; lacks RCTs. |
| Clinical Value | High for routine cases; reduces cognitive load in isolated tasks. | May add value in complex resections; could degrade performance in routine ones due to latency/setup. |
| Adoption Barriers | Cost/learning curve for robotics; bias for AI. | Vendor lock-in; interoperability issues; equity gaps. |
| When to Prefer | Standard procedures where one tech suffices. | High-risk cases needing multi-layered support, pending validation. |
When Hybrid Systems May NOT Add Value
Future Roadmap
Conclusions
References
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