# Efficacy of NSAIDs and corticosteroids as premedication for post-endodontic pain management: A systematic review and meta-analysis

**Authors:** Radia Mrini, Marcela Salamanca-Ramos, Priscilla Ledezma, Alejandro R. Pérez, José Aranguren, Javier Montecinos, Elías Utreras, Nicolas Pinto-Pardo

PMC · DOI: 10.4317/jced.63455 · Journal of Clinical and Experimental Dentistry · 2025-12-30

## TL;DR

This study finds that NSAIDs and corticosteroids both reduce post-dental pain, with NSAIDs acting quickly and corticosteroids providing longer-lasting relief.

## Contribution

The study provides a systematic review and meta-analysis comparing preemptive NSAID and corticosteroid use for post-endodontic pain management.

## Key findings

- NSAIDs and corticosteroids both significantly reduce postoperative pain compared to placebo.
- NSAIDs offer rapid early pain relief, while corticosteroids provide sustained analgesia over 12-48 hours.
- Both drug classes reduce rescue analgesic use, with corticosteroids showing slightly better long-term efficacy.

## Abstract

Post-endodontic pain remains a common clinical challenge. This systematic review and meta-analysis evaluated the preemptive efficacy of NSAIDs and corticosteroids as premedication for managing postoperative pain in patients with symptomatic irreversible pulpitis undergoing non-surgical root canal treatment. Objectives: To compare the preemptive efficacy of NSAIDs and corticosteroids as single-dose premedication in reducing postoperative pain and rescue medication use after endodontic treatment.

Following PRISMA 2020 guidelines, a systematic search was conducted in PubMed, Cochrane Library, and Embase up to April 2024. Eligibility criteria included randomized controlled trials comparing single-dose NSAIDs or corticosteroids with placebo. Primary outcomes were postoperative pain intensity measured by validated scales (VAS, NRS, HP-VAS) and need for rescue analgesics. Risk of bias was assessed with RoB2, and certainty of evidence with GRADE. Meta-analysis used random-effects models, with standardized mean differences (SMD) and 95% confidence intervals (CI). Protocol registered in PROSPERO (CRD42024499723).

Seven RCTs (n=820) published between 2009 and 2023 were included. Both corticosteroids (SMD = -1.28; 95 % confidence interval (CI): -1.96 to -0.61) and NSAIDs (SMD = -0.61; 95% CI: -1.11 to -0.10) significantly reduced postoperative pain versus placebo. NSAIDs provided rapid analgesia at 6 h, while corticosteroids achieved sustained analgesia from 12-48 h. Rescue analgesic use decreased substantially in both active groups compared with placebo (NSAIDs 4.6%, corticosteroids 5.5%, placebo 34.4%). High heterogeneity (I² = 90%) was partly explained by drug class, dose, and administration route. Sensitivity analysis excluding imputed data confirmed robustness of results.

Both NSAIDs and corticosteroids are effective preemptive agents for managing post-endodontic pain in symptomatic irreversible pulpitis. NSAIDs should be preferred for rapid early relief, while corticosteroids provide extended analgesia. Findings highlight their opioid-sparing potential and support their inclusion in evidence-based endodontic pain management protocols. Further multicenter RCTs are warranted to refine patient-tailored regimens.

## Linked entities

- **Chemicals:** doxorubicin (PubChem CID 31703)

## Full-text entities

- **Genes:** COX8A (cytochrome c oxidase subunit 8A) [NCBI Gene 1351] {aka COX, COX8, COX8-2, COX8L, MC4DN15, VIII}, PLA2G1B (phospholipase A2 group IB) [NCBI Gene 5319] {aka PLA2, PLA2A, PPLA2}, MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, NR3C1 (nuclear receptor subfamily 3 group C member 1) [NCBI Gene 2908] {aka GCCR, GCR, GCRST, GR, GRL}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** gastrointestinal bleeding (MESH:D006471), neurogenic inflammation (MESH:D020078), SIP (MESH:D011671), renal impairment (MESH:D007674), chronic pain (MESH:D059350), bacterial infections (MESH:D001424), gastrointestinal issues (MESH:D005767), systemic diseases (MESH:D034721), analgesia (MESH:D000699), Orofacial pain (MESH:D005157), opioid (MESH:D009293), Anxiety (MESH:D001007), Postoperative pain (MESH:D010149), Dental pain (MESH:D010146), apical periodontitis (MESH:D010485), inflammation (MESH:D007249)
- **Chemicals:** tramadol (MESH:D014147), morphine (MESH:D009020), dexamethasone (MESH:D003907), naproxen (MESH:D009288), Prednisolone (MESH:D011239), tenoxicam (MESH:C032801), piroxicam (MESH:D010894), ketorolac (MESH:D020910), methylprednisolone (MESH:D008775), diclofenac (MESH:D004008), prostaglandin (MESH:D011453), betamethasone (MESH:D001623), acetaminophen (MESH:D000082), ibuprofen (MESH:D007052)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12916047/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12916047/full.md

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Source: https://tomesphere.com/paper/PMC12916047