TY - JOUR
T1 - Randomized, placebo-controlled trials of dichlorphenamide in periodic paralysis
AU - Sansone, Valeria A.
AU - Burge, James
AU - McDermott, Michael P.
AU - Smith, Patty C.
AU - Herr, Barbara
AU - Tawil, Rabi
AU - Pandya, Shree
AU - Kissel, John
AU - Ciafaloni, Emma
AU - Shieh, Perry
AU - Ralph, Jeffrey W.
AU - Amato, Antony
AU - Cannon, Steve C.
AU - Trivedi, Jaya
AU - Barohn, Richard
AU - Crum, Brian
AU - Mitsumoto, Hiroshi
AU - Pestronk, Alan
AU - Meola, Giovanni
AU - Conwit, Robin
AU - Hanna, Michael G.
AU - Griggs, Robert C.
N1 - Funding Information:
This study was supported by NIH National Institute of Neurological Disorders and Stroke award R01 NS045686 (Robert C. Griggs, principal investigator); the Muscular Dystrophy Association award 93615; NIH NCATS awards UL1 TR000042, UL1 TR000040, UL1TR001070, UL1TR000001, UL1TR000124, UL1 TR000004, UL1 TR001105, UL1 TR000135, and NIH NCRR; NCATS awards UL1 RR024160 and UL1 RR024131; NIH NCRR awards C06 RR20092, M01-02635, and 1 UL1 RR025758; NIH NINDS awards U10NS077384, R37-AR42703, and RO1-AR063182 (S. Cannon, principal investigator); and MRC Centre Grant and UCL Biomedical Research Centre Grant (M. Hanna, principal investigator, Institute of Neurology, Queen Square, London). NINDS and MDA funding was provided for participant travel support.
Publisher Copyright:
© 2016 American Academy of Neurology.
PY - 2016/4/12
Y1 - 2016/4/12
N2 - Objective: To determine the short-term and long-term effects of dichlorphenamide (DCP) on attack frequency and quality of life in hyperkalemic (HYP) and hypokalemic (HOP) periodic paralysis. Methods: Two multicenter randomized, double-blind, placebo-controlled trials lasted 9 weeks (Class I evidence), followed by a 1-year extension phase in which all participants received DCP. Forty-four HOP and 21 HYP participants participated. The primary outcome variable was the average number of attacks per week over the final 8 weeks of the double-blind phase. Results: The median attack rate was lower in HOP participants on DCP than in participants on placebo (0.3 vs 2.4, p 0.02). The 9-week mean change in the Physical Component Summary score of the Short Form-36 was also better in HOP participants receiving DCP (treatment effect 7.29 points, 95% confidence interval 2.26 to 12.32, p 0.006). The median attack rate was also lower in HYP participants on DCP (0.9 vs 4.8) than in participants on placebo, but the difference in median attack rate was not significant (p 0.10). There were no significant effects of DCP on muscle strength or muscle mass in either trial. The most common adverse events in both trials were paresthesia (47% DCP vs 14% placebo, both trials combined) and confusion (19% DCP vs 7% placebo, both trials combined). Conclusions: DCP is effective in reducing the attack frequency, is safe, and improves quality of life in HOP periodic paralysis. Classification of evidence: These studies provide Class I evidence that DCP significantly reduces attack frequency in HOP but lacked the precision to support either efficacy or lack of efficacy of DCP in HYP.
AB - Objective: To determine the short-term and long-term effects of dichlorphenamide (DCP) on attack frequency and quality of life in hyperkalemic (HYP) and hypokalemic (HOP) periodic paralysis. Methods: Two multicenter randomized, double-blind, placebo-controlled trials lasted 9 weeks (Class I evidence), followed by a 1-year extension phase in which all participants received DCP. Forty-four HOP and 21 HYP participants participated. The primary outcome variable was the average number of attacks per week over the final 8 weeks of the double-blind phase. Results: The median attack rate was lower in HOP participants on DCP than in participants on placebo (0.3 vs 2.4, p 0.02). The 9-week mean change in the Physical Component Summary score of the Short Form-36 was also better in HOP participants receiving DCP (treatment effect 7.29 points, 95% confidence interval 2.26 to 12.32, p 0.006). The median attack rate was also lower in HYP participants on DCP (0.9 vs 4.8) than in participants on placebo, but the difference in median attack rate was not significant (p 0.10). There were no significant effects of DCP on muscle strength or muscle mass in either trial. The most common adverse events in both trials were paresthesia (47% DCP vs 14% placebo, both trials combined) and confusion (19% DCP vs 7% placebo, both trials combined). Conclusions: DCP is effective in reducing the attack frequency, is safe, and improves quality of life in HOP periodic paralysis. Classification of evidence: These studies provide Class I evidence that DCP significantly reduces attack frequency in HOP but lacked the precision to support either efficacy or lack of efficacy of DCP in HYP.
UR - http://www.scopus.com/inward/record.url?scp=84964882316&partnerID=8YFLogxK
U2 - 10.1212/WNL.0000000000002416
DO - 10.1212/WNL.0000000000002416
M3 - Article
C2 - 26865514
AN - SCOPUS:84964882316
SN - 0028-3878
VL - 86
SP - 1408
EP - 1416
JO - Neurology
JF - Neurology
IS - 15
ER -