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Botulinum toxin type A improves nasal symptoms in refractory allergic rhinitis with SMD -2.07 at 4 weeks

Botulinum toxin type A improves nasal symptoms in refractory allergic rhinitis with SMD -2.07 at 4…
Photo by CDC / Unsplash
Key Takeaway
Consider BTX-A for refractory allergic rhinitis, noting symptom improvement but limited safety data.

This is a meta-analysis of studies on botulinum toxin type A (BTX-A) for refractory allergic rhinitis, pooling data from 187 patients. The primary outcome was the total nasal symptom score (TNSS). The analysis found a significant improvement in TNSS at 4 weeks (SMD -2.07, 95% CI -3.58 to -0.56, P < 0.001) and at 12 weeks (SMD -2.42, 95% CI -4.22 to -0.62, P < 0.001). Compared to triamcinolone injection, BTX-A showed no significant difference in TNSS (SMD -0.51, 95% CI -1.25 to 0.24, P = 0.18). Compared to oral cetirizine, there was also no significant difference (SMD 0.50, 95% CI -0.07 to 1.06, P = 0.08). Individual nasal symptom scores at 4 weeks, including rhinorrhea (SMD -2.18), sneezing (SMD -1.88), and itchiness (MD -1.57), all showed significant improvement. Safety data were not reported, and the authors noted no serious adverse events. Limitations include the small sample size and lack of reported adverse events. The authors suggest BTX-A may be a promising adjunctive therapy, but this conclusion is based on limited evidence.

Study Details

Study typeMeta analysis
Sample sizen = 187
EvidenceLevel 1
PublishedJun 2026
View Original Abstract ↓
PURPOSE OF REVIEW: Botulinum toxin type A (BTX-A) is emerging as a promising intervention for refractory allergic rhinitis. This study evaluates its effectiveness in treating refractory allergic rhinitis. RECENT FINDINGS: The primary outcome was total nasal symptom score (TNSS), while secondary outcomes included individual nasal symptom scores, quality of life (QOL), and adverse effects. Five trials involving 187 patients (mean age: 31.8 years) were included. BTX-A significantly improved TNSS at 4 weeks [SMD -2.07, 95% confidence interval (95% CI) -3.58 to -0.56; P  < 0.001] and 12 weeks (SMD -2.42, 95% CI -4.22 to -0.62; P  < 0.001). Neither comparison of BTX-A with triamcinolone injection nor oral cetirizine showed a significant difference in TNSS (SMD - 0.51, 95% CI -1.25 to 0.24; P  = 0.18 and SMD 0.50, 95% CI -0.07 to 1.06; P  = 0.08, respectively). In the BTX-A group, significant improvements were observed in rhinorrhea (SMD -2.18, 95% CI -3.74 to -0.62; P  < 0.001), sneezing (SMD -1.88, 95% CI -2.60 to -1.15; P  < 0.001), and itchiness (MD -1.57, 95% CI -2.45 to -0.69; P  < 0.001) at 4 weeks, with these effects persisting up to 12 weeks. No serious adverse events occurred following BTX-A administration. SUMMARY: BTX-A shows promise as an adjunctive therapy for refractory allergic rhinitis.
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