Transcutaneous Auricular Vagus Nerve Stimulation for Postpartum Contraction Pain During Elective Cesarean Delivery: A Randomized Clinical Trial.
Summary
In a single-center randomized, sham-controlled trial of 156 women undergoing elective cesarean delivery under combined spinal-epidural anesthesia, taVNS reduced moderate-to-severe uterine contraction pain on postoperative day 3 (5.1% vs 28.2%; RR 0.18) and improved incision pain, depression, anxiety, recovery quality, and sleep. Analyses followed intention-to-treat.
Key Findings
- Incidence of moderate-to-severe uterine contraction pain on postoperative day 3: 5.1% with taVNS vs 28.2% with sham (RR 0.18, 95% CI 0.07-0.50; P < .001).
- Lower incision pain on day 3 (median VAS 2.20 vs 3.00) and improved sleep on day 2 (LSEQ 52.00 vs 47.50).
- Reduced depression (EPDS) and anxiety (PRAQ-R2) and higher recovery quality (ObsQoR-11 104 vs 99) with taVNS.
Clinical Implications
taVNS could be incorporated as an adjunct to standard postoperative analgesia after cesarean delivery to reduce uterine contraction pain and improve recovery metrics, with minimal safety concerns. Implementation would require training and device availability.
Why It Matters
This RCT introduces a nonpharmacologic, scalable neuromodulation approach that improves multiple patient-centered outcomes postpartum, potentially reducing opioid exposure and enhancing ERAS pathways in obstetric anesthesia.
Limitations
- Single-center study with short follow-up limited to early postoperative period
- Generalizability across diverse settings and long-term outcomes not assessed
Future Directions
Multicenter trials with longer follow-up should assess sustainability, safety, and opioid-sparing effects, and explore dosing parameters and subgroups (e.g., multiparity, breastfeeding).
Study Information
- Study Type
- RCT
- Research Domain
- Treatment
- Evidence Level
- I - Randomized, sham-controlled clinical trial with intention-to-treat analysis.
- Study Design
- OTHER