作者:中华医学网发布时间:2026-01-12 08:37浏览:
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| Outcome | Key Findings | Evidence Quality |
|---|---|---|
| Pain Control | NSAIDs reduce pain vs. placebo/standard care; heterogenous data precluded meta-analysis | Low |
| Opioid Sparing | Consistent reduction in opioid dose/duration vs. opioids alone | Moderate |
| Functional Recovery | Improved early mobility with better pain control | Low |
| Risk | Association with NSAIDs | Evidence Quality | Clinical Action |
|---|---|---|---|
| Fracture Non-union | Small absolute risk increase (0.8%); no causal link confirmed | Low | Avoid prolonged use (>2 weeks) in high-risk fractures (e.g., tibial shaft, scaphoid) |
| Renal Injury | No AKI association in short-term use (≤5 days); higher risk with hypovolemia/CKD | Low | Hydrate; avoid in eGFR <30mL/min/1.73m² |
| Gastrointestinal Toxicity | Increased risk with older age, history of ulcers, or concurrent steroids | Moderate | Use PPI prophylaxis in high-risk patients; prefer COX-2 inhibitors |
| Cardiovascular Risk | Increased MI/stroke in long-term use; minimal acute risk | Low | Avoid in uncontrolled hypertension/heart failure |
| Population | Eligibility | Contraindications |
|---|---|---|
| Indicated | Adults (≥18) with traumatic fractures; acute pain requiring multimodal analgesia | Severe CKD (eGFR <30); active peptic ulcer; severe heart failure; hypersensitivity to NSAIDs |
| Caution | Elderly (≥65); CKD (eGFR 30–60); diabetes; hypertension; history of GI ulcers | — |
| Avoid | Pregnancy (third trimester); breastfeeding; coagulopathy; concurrent anticoagulants | — |
| Population/Fracture | Modification | Evidence Basis |
|---|---|---|
| Elderly (≥75) | Lower NSAID dose (e.g., ibuprofen 400mg q8h); avoid ketorolac | Increased GI/renal risk |
| High-Risk Fractures (tibial shaft, scaphoid, spine) | Limit NSAIDs to ≤5 days; switch to acetaminophen/opioids | Small non-union risk signal |
| Polytrauma with Hypovolemia | Avoid NSAIDs until hemodynamically stable | AKI risk in hypoperfusion |
| Postoperative Fracture Fixation | NSAIDs safe for 5–7 days; no implant failure link | Low-quality evidence |