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Clopidogrel can be an effective complementary prophylactic for drug-refractory migraine with patent foramen ovale
The present study aims to determine the potential prophylactic effect of clopidogrel for migraine with patent foramen ovale (PFO) in patients who are poor responders to two or more common preventive medications. Migraineurs underwent contrast-enhanced transcranial doppler examination to confirm the...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525787/ https://www.ncbi.nlm.nih.gov/pubmed/32848048 http://dx.doi.org/10.1136/jim-2020-001342 |
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author | Guo, Yichen Shi, Yujie Zhu, Dan Liu, Rui Qi, Yi Luo, Guogang |
author_facet | Guo, Yichen Shi, Yujie Zhu, Dan Liu, Rui Qi, Yi Luo, Guogang |
author_sort | Guo, Yichen |
collection | PubMed |
description | The present study aims to determine the potential prophylactic effect of clopidogrel for migraine with patent foramen ovale (PFO) in patients who are poor responders to two or more common preventive medications. Migraineurs underwent contrast-enhanced transcranial doppler examination to confirm the presence of PFO and determine the right-to-left shunt degree. Clopidogrel 75 mg/day was added to the existing prophylactic regimen for 3 months and 6 months. The presence of PFO was found in 56.8% (151/266) of all patients with migraine and 70.2% (59/84) of migraine with aura (MHA), and among MHA a large shunt was observed in 36 patients. Twenty-six patients with drug-refractory migraine took clopidogrel 75 mg/day for 3 months. Compared with those at baseline, headache frequencies and attack durations were significantly lower (6.17±3.93/month (M) vs 3.28±2.67/M, p=0.003; 13.62±13.98/hour (H) vs 7.36±7.33/H, p=0.0049, respectively); visual analog scale scores and migraine disability assessment scores were also obviously decreased (6.32±1.97 vs 4.71±1.20, p<0.001; 22.14±7.13 vs 16.00±5.92, p=0.001, respectively). These improvements were maintained for 6 months in 12 patients. We concluded that PFO was closely correlated with migraine, especially in MHA. Clopidogrel could act as an effective complementary prophylactic for migraine with PFO in patients with poor response to routine prophylactics. |
format | Online Article Text |
id | pubmed-7525787 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-75257872020-10-19 Clopidogrel can be an effective complementary prophylactic for drug-refractory migraine with patent foramen ovale Guo, Yichen Shi, Yujie Zhu, Dan Liu, Rui Qi, Yi Luo, Guogang J Investig Med Original Research The present study aims to determine the potential prophylactic effect of clopidogrel for migraine with patent foramen ovale (PFO) in patients who are poor responders to two or more common preventive medications. Migraineurs underwent contrast-enhanced transcranial doppler examination to confirm the presence of PFO and determine the right-to-left shunt degree. Clopidogrel 75 mg/day was added to the existing prophylactic regimen for 3 months and 6 months. The presence of PFO was found in 56.8% (151/266) of all patients with migraine and 70.2% (59/84) of migraine with aura (MHA), and among MHA a large shunt was observed in 36 patients. Twenty-six patients with drug-refractory migraine took clopidogrel 75 mg/day for 3 months. Compared with those at baseline, headache frequencies and attack durations were significantly lower (6.17±3.93/month (M) vs 3.28±2.67/M, p=0.003; 13.62±13.98/hour (H) vs 7.36±7.33/H, p=0.0049, respectively); visual analog scale scores and migraine disability assessment scores were also obviously decreased (6.32±1.97 vs 4.71±1.20, p<0.001; 22.14±7.13 vs 16.00±5.92, p=0.001, respectively). These improvements were maintained for 6 months in 12 patients. We concluded that PFO was closely correlated with migraine, especially in MHA. Clopidogrel could act as an effective complementary prophylactic for migraine with PFO in patients with poor response to routine prophylactics. BMJ Publishing Group 2020-10 2020-08-26 /pmc/articles/PMC7525787/ /pubmed/32848048 http://dx.doi.org/10.1136/jim-2020-001342 Text en © American Federation for Medical Research 2020. Re-use permitted under CC BY-NC. No commercial re-use. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, an indication of whether changes were made, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Original Research Guo, Yichen Shi, Yujie Zhu, Dan Liu, Rui Qi, Yi Luo, Guogang Clopidogrel can be an effective complementary prophylactic for drug-refractory migraine with patent foramen ovale |
title | Clopidogrel can be an effective complementary prophylactic for drug-refractory migraine with patent foramen ovale |
title_full | Clopidogrel can be an effective complementary prophylactic for drug-refractory migraine with patent foramen ovale |
title_fullStr | Clopidogrel can be an effective complementary prophylactic for drug-refractory migraine with patent foramen ovale |
title_full_unstemmed | Clopidogrel can be an effective complementary prophylactic for drug-refractory migraine with patent foramen ovale |
title_short | Clopidogrel can be an effective complementary prophylactic for drug-refractory migraine with patent foramen ovale |
title_sort | clopidogrel can be an effective complementary prophylactic for drug-refractory migraine with patent foramen ovale |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7525787/ https://www.ncbi.nlm.nih.gov/pubmed/32848048 http://dx.doi.org/10.1136/jim-2020-001342 |
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