Efficacy and safety of intranasal agents for the acute treatment of migraine: a systematic review and network meta-analysis
Abstract Background Intranasal agents may be ideal for the treatment of migraine patients. Many new acute intranasal-specific therapies have been developed, but few of them have been directly compared. The aim of this network meta-analysis (NMA) was to compare the efficacy and safety of various intr...
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BMC
2023-09-01
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Series: | The Journal of Headache and Pain |
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Online Access: | https://doi.org/10.1186/s10194-023-01662-6 |
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author | Guanglu Li Shaojie Duan Tiantian Zhu Zhiying Ren Hui Xia Ziyao Wang Lei Liu Zunjing Liu |
author_facet | Guanglu Li Shaojie Duan Tiantian Zhu Zhiying Ren Hui Xia Ziyao Wang Lei Liu Zunjing Liu |
author_sort | Guanglu Li |
collection | DOAJ |
description | Abstract Background Intranasal agents may be ideal for the treatment of migraine patients. Many new acute intranasal-specific therapies have been developed, but few of them have been directly compared. The aim of this network meta-analysis (NMA) was to compare the efficacy and safety of various intranasal agents for the treatment of acute migraine in adult patients. Methods The Cochrane Register of Controlled Trials, Embase, and PubMed were searched from inception to 15 August 2023. Randomized controlled trials (RCTs) using intranasal agents (no restrictions on dose, formulation, dosing regimen or timing of the first dose) to treat adult patients with acute migraine were included. The primary efficacy endpoint was pain freedom at 2 h, and the primary safety endpoint was adverse events (AEs). The analysis process followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Results Nineteen studies (21 RCTs, 9738 participants) were included. Compared to the placebo, 5 mg of zolmitriptan using a conventional liquid nasal spray device was the most effective for pain freedom at 2 h [odds ratio (OR): 4.67, 95% confidence interval (CI): 3.43 to 6.43] and 24 h (OR: 5.49, 95% CI: 3.58 to 8.42) among all the interventions. Butorphanol nasal spray 1 mg was the most effective (OR: 8.62, 95% CI: 1.11 to 66.92) for pain freedom at 1 h, but with low-quality evidence. DFN-02 presented the highest freedom from nausea (OR: 4.95, 95% CI: 1.29 to 19.01) and phonophobia (OR: 5.36, 95% CI: 1.67 to 17.22) at 2 h, albeit with lower odds of achieving complete pain freedom. ROX-828 showed the highest improvement in freedom from photophobia at 2 h (OR: 4.03, 95% CI: 1.66 to 9.81). Dihydroergotamine nasal spray was significantly associated with the highest risk of AEs (OR: 9.65, 95% CI: 4.39 to 21.22) and was not recommended for routine use. Zavegepant nasal spray demonstrated the lowest risk of AEs (OR: 2.04, 95% CI: 1.37 to 3.03). The results of sensitivity analyses for the primary endpoints (pain freedom at 2 h and AEs) were generally consistent with those of the base case model. Conclusions Compared with other new intranasal-specific therapies in treating migraine attacks, zolmitriptan nasal spray 5 mg was the most effective agent for pain freedom at 2 h. Zavegepant nasal spray 10 mg had the fewest adverse side effects. |
first_indexed | 2024-03-10T17:19:40Z |
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issn | 1129-2377 |
language | English |
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publishDate | 2023-09-01 |
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series | The Journal of Headache and Pain |
spelling | doaj.art-d63c891a9ba2443a9f5914ea7ef654722023-11-20T10:22:47ZengBMCThe Journal of Headache and Pain1129-23772023-09-0124111710.1186/s10194-023-01662-6Efficacy and safety of intranasal agents for the acute treatment of migraine: a systematic review and network meta-analysisGuanglu Li0Shaojie Duan1Tiantian Zhu2Zhiying Ren3Hui Xia4Ziyao Wang5Lei Liu6Zunjing Liu7Graduate School of Beijing, University of Chinese MedicineDepartment of Geriatrics, Taizhou Central Hospital (Taizhou University Hospital)Beijing Tiantan Hospital, Capital Medical UniversityGraduate School of Beijing, University of Chinese MedicineGraduate School of Beijing, University of Chinese MedicineGraduate School of Beijing, University of Chinese MedicineDepartment of Neurology, China-Japan Friendship HospitalDepartment of Neurology, Peking University People’s HospitalAbstract Background Intranasal agents may be ideal for the treatment of migraine patients. Many new acute intranasal-specific therapies have been developed, but few of them have been directly compared. The aim of this network meta-analysis (NMA) was to compare the efficacy and safety of various intranasal agents for the treatment of acute migraine in adult patients. Methods The Cochrane Register of Controlled Trials, Embase, and PubMed were searched from inception to 15 August 2023. Randomized controlled trials (RCTs) using intranasal agents (no restrictions on dose, formulation, dosing regimen or timing of the first dose) to treat adult patients with acute migraine were included. The primary efficacy endpoint was pain freedom at 2 h, and the primary safety endpoint was adverse events (AEs). The analysis process followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Results Nineteen studies (21 RCTs, 9738 participants) were included. Compared to the placebo, 5 mg of zolmitriptan using a conventional liquid nasal spray device was the most effective for pain freedom at 2 h [odds ratio (OR): 4.67, 95% confidence interval (CI): 3.43 to 6.43] and 24 h (OR: 5.49, 95% CI: 3.58 to 8.42) among all the interventions. Butorphanol nasal spray 1 mg was the most effective (OR: 8.62, 95% CI: 1.11 to 66.92) for pain freedom at 1 h, but with low-quality evidence. DFN-02 presented the highest freedom from nausea (OR: 4.95, 95% CI: 1.29 to 19.01) and phonophobia (OR: 5.36, 95% CI: 1.67 to 17.22) at 2 h, albeit with lower odds of achieving complete pain freedom. ROX-828 showed the highest improvement in freedom from photophobia at 2 h (OR: 4.03, 95% CI: 1.66 to 9.81). Dihydroergotamine nasal spray was significantly associated with the highest risk of AEs (OR: 9.65, 95% CI: 4.39 to 21.22) and was not recommended for routine use. Zavegepant nasal spray demonstrated the lowest risk of AEs (OR: 2.04, 95% CI: 1.37 to 3.03). The results of sensitivity analyses for the primary endpoints (pain freedom at 2 h and AEs) were generally consistent with those of the base case model. Conclusions Compared with other new intranasal-specific therapies in treating migraine attacks, zolmitriptan nasal spray 5 mg was the most effective agent for pain freedom at 2 h. Zavegepant nasal spray 10 mg had the fewest adverse side effects.https://doi.org/10.1186/s10194-023-01662-6MigraineAcute treatmentIntranasal agentsNetwork meta-analysis |
spellingShingle | Guanglu Li Shaojie Duan Tiantian Zhu Zhiying Ren Hui Xia Ziyao Wang Lei Liu Zunjing Liu Efficacy and safety of intranasal agents for the acute treatment of migraine: a systematic review and network meta-analysis The Journal of Headache and Pain Migraine Acute treatment Intranasal agents Network meta-analysis |
title | Efficacy and safety of intranasal agents for the acute treatment of migraine: a systematic review and network meta-analysis |
title_full | Efficacy and safety of intranasal agents for the acute treatment of migraine: a systematic review and network meta-analysis |
title_fullStr | Efficacy and safety of intranasal agents for the acute treatment of migraine: a systematic review and network meta-analysis |
title_full_unstemmed | Efficacy and safety of intranasal agents for the acute treatment of migraine: a systematic review and network meta-analysis |
title_short | Efficacy and safety of intranasal agents for the acute treatment of migraine: a systematic review and network meta-analysis |
title_sort | efficacy and safety of intranasal agents for the acute treatment of migraine a systematic review and network meta analysis |
topic | Migraine Acute treatment Intranasal agents Network meta-analysis |
url | https://doi.org/10.1186/s10194-023-01662-6 |
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