# Cooling the burn: EMLA alone vs. paravertebral block plus EMLA for improving tolerability of 8% capsaicin patch application in thoracic postherpetic neuralgia—a retrospective cohort study

**Authors:** Hassan A. Moria

PMC · DOI: 10.3389/fnagi.2026.1762229 · Frontiers in Aging Neuroscience · 2026-02-16

## TL;DR

Combining EMLA with a paravertebral block significantly improves the tolerability and effectiveness of capsaicin patch treatment for thoracic postherpetic neuralgia compared to EMLA alone.

## Contribution

This study demonstrates that adding a paravertebral block to EMLA significantly reduces procedural pain and opioid use during capsaicin patch application for thoracic PHN.

## Key findings

- Patients receiving TPVB plus EMLA had significantly lower intraprocedural pain and no need for IV tramadol.
- TPVB improved post-procedural pain control, sleep quality, and treatment acceptability.
- The combination reduced reliance on oral analgesics and enhanced patient comfort.

## Abstract

The 8% capsaicin patch (Qutenza®) is an effective localized treatment for postherpetic neuralgia (PHN), yet intense application-related burning pain remains a major barrier to its broader use. Optimizing procedural tolerability is particularly important in elderly patients who are vulnerable to systemic analgesic side effects. Thoracic paravertebral block (TPVB) provides segmental analgesia and may attenuate procedural pain during capsaicin patch application.

To compare procedural tolerability and short-term analgesic outcomes of topical EMLA alone versus EMLA combined with TPVB before 8% capsaicin patch application in patients with thoracic PHN.

This retrospective cohort study included adults with thoracic PHN treated with 8% capsaicin patches at Prince Fahd bin Sultan Hospital, Tabuk, Saudi Arabia, between January 2022 and February 2025. Patients received either EMLA alone (n = 9) or EMLA plus ultrasound-guided TPVB (n = 8). The primary outcome was procedural tolerability, assessed using peak intraprocedural Numeric Pain Rating Scale (NPRS), area under the curve of NPRS over 60 min (AUC-NPRS), and need for intravenous (IV) tramadol. Secondary outcomes included NPRS at 8, 24, and 48 h; change in Pittsburgh Sleep Quality Index (PSQI); oral tramadol use over 48 h; and patient-reported acceptability.

Baseline characteristics were comparable between groups. Patients who received TPVB demonstrated markedly superior procedural tolerability compared with those pretreated with EMLA alone. Intraprocedural pain was substantially reduced, with a markedly lower cumulative pain burden and no requirement for IV rescue in the TPVB group, whereas all EMLA patients required opioid rescue and reported intense burning pain during application. Post-procedural pain scores remained consistently lower in the TPVB group, accompanied by significant improvements in sleep quality and reduced reliance on oral analgesics during the following 48 h. Treatment acceptability was also substantially higher with TPVB, indicating a considerably more comfortable peri-procedural experience.

TPVB combined with EMLA yielded profound improvements in procedural tolerability, early pain control, sleep quality, and patient acceptability during 8% capsaicin patch therapy for thoracic PHN, while markedly reducing opioid rescue needs. These findings support TPVB-assisted capsaicin therapy as a promising multimodal strategy deserving evaluation in prospective controlled trials.

## Linked entities

- **Chemicals:** capsaicin (PubChem CID 1548943), EMLA (PubChem CID 9911821), tramadol (PubChem CID 19472)
- **Diseases:** postherpetic neuralgia (MONDO:0041052)

## Full-text entities

- **Genes:** TRPV1 (transient receptor potential cation channel subfamily V member 1) [NCBI Gene 7442] {aka VR1}
- **Diseases:** falls (MESH:C537863), mood impairment (MESH:D019964), respiratory depression (MESH:D012131), PHN (MESH:D051474), analgesia (MESH:D000699), burn (MESH:D002056), somatic and sympathetic nerve blockade (MESH:D013001), rib fracture (MESH:D012253), Pain (MESH:D010146), Sleep disturbance (MESH:D012893), anxiety (MESH:D001007), edema (MESH:D004487), neurological complications (MESH:D002493), chronic pain (MESH:D059350), neuropathic pain (MESH:D009437), constipation (MESH:D003248), allergy (MESH:D004342), herpes zoster (MESH:D006562), limitation (MESH:D045745), erythema (MESH:D004890), cognitive impairment (MESH:D003072), pneumothorax (MESH:D011030), coagulopathy (MESH:D001778), infection (MESH:D007239), dizziness (MESH:D004244), toxicity (MESH:D064420)
- **Chemicals:** triamcinolone (MESH:D014221), EMLA (MESH:D000077442), ropivacaine (MESH:D000077212), Qutenza (MESH:D002211), bupivacaine (MESH:D002045), gabapentin (MESH:D000077206), tramadol (MESH:D014147), calcium (MESH:D002118), pregabalin (MESH:D000069583), Lidocaine (MESH:D008012), Paravertebral Block (-), sodium (MESH:D012964), Prilocaine (MESH:D011318)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

73 references — full list in the complete paper: https://tomesphere.com/paper/PMC12950785/full.md

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Source: https://tomesphere.com/paper/PMC12950785