PMID- 30699098 OWN - NLM STAT- MEDLINE DCOM- 20190626 LR - 20210114 IS - 1872-6623 (Electronic) IS - 0304-3959 (Linking) VI - 160 IP - 4 DP - 2019 Apr TI - Flunarizine as prophylaxis for episodic migraine: a systematic review with meta-analysis. PG - 762-772 LID - 10.1097/j.pain.0000000000001456 [doi] AB - Based on few clinical trials, flunarizine is considered a first-line prophylactic treatment for migraine in several guidelines. In this meta-analysis, we examined the pooled evidence for its effectiveness, tolerability, and safety. Prospective randomized controlled trials of flunarizine as a prophylaxis against migraine were identified from a systematic literature search, and risk of bias was assessed for all included studies. Reduction in mean attack frequency was estimated by calculating the mean difference (MD), and a series of secondary outcomes-including adverse events (AEs)-were also analyzed. The database search yielded 879 unique records. Twenty-five studies were included in data synthesis. We scored 31/175 risk of bias items as "high," with attrition as the most frequent bias. A pooled analysis estimated that flunarizine reduces the headache frequency by 0.4 attacks per 4 weeks compared with placebo (5 trials, 249 participants: MD -0.44; 95% confidence interval -0.61 to -0.26). Analysis also revealed that the effectiveness of flunarizine prophylaxis is comparable with that of propranolol (7 trials, 1151 participants, MD -0.08; 95% confidence interval -0.34 to 0.18). Flunarizine also seems to be effective in children. The most frequent AEs were sedation and weight increase. Meta-analyses were robust and homogenous, although several of the included trials potentially suffered from high risk of bias. Unfortunately, reporting of AEs was inconsistent and limited. In conclusion, pooled analysis of data from partially outdated trials shows that 10-mg flunarizine per day is effective and well tolerated in treating episodic migraine-supporting current guideline recommendations. FAU - Stubberud, Anker AU - Stubberud A AD - Department of Neuromedicine and Movement Sciences, NTNU Norwegian University of Science and Technology, Trondheim, Norway. FAU - Flaaen, Nikolai Melseth AU - Flaaen NM AD - Department of Neuromedicine and Movement Sciences, NTNU Norwegian University of Science and Technology, Trondheim, Norway. FAU - McCrory, Douglas C AU - McCrory DC AD - Duke Evidence Synthesis Group, Duke Clinical Research Institute, Durham, NC, United States. AD - Department of Medicine, Duke University School of Medicine, Durham, NC, United States. AD - Center for Health Services Research in Primary Care, Durham Veterans Affairs Medical Center, Durham, NC, United States. FAU - Pedersen, Sindre Andre AU - Pedersen SA AD - Library Section for Medicine and Health Sciences, NTNU University Library, NTNU Norwegian University of Science and Technology, Trondheim, Norway. FAU - Linde, Mattias AU - Linde M AD - Department of Neuromedicine and Movement Sciences, NTNU Norwegian University of Science and Technology, Trondheim, Norway. AD - Norwegian Advisory Unit on Headaches, St. Olavs Hospital, Trondheim, Norway. LA - eng PT - Journal Article PT - Meta-Analysis PT - Systematic Review PL - United States TA - Pain JT - Pain JID - 7508686 RN - 0 (Histamine H1 Antagonists) RN - R7PLA2DM0J (Flunarizine) SB - IM MH - Databases, Bibliographic MH - Flunarizine/*therapeutic use MH - Histamine H1 Antagonists/*therapeutic use MH - Humans MH - Migraine Disorders/*prevention & control MH - Randomized Controlled Trials as Topic EDAT- 2019/01/31 06:00 MHDA- 2019/06/27 06:00 CRDT- 2019/01/31 06:00 PHST- 2019/01/31 06:00 [pubmed] PHST- 2019/06/27 06:00 [medline] PHST- 2019/01/31 06:00 [entrez] AID - 00006396-201904000-00002 [pii] AID - 10.1097/j.pain.0000000000001456 [doi] PST - ppublish SO - Pain. 2019 Apr;160(4):762-772. doi: 10.1097/j.pain.0000000000001456.