Migren atak tedavisinde triptan, NSAİİ ve kombinasyon tedavisinin karşılaştırması

Amaç: Migren atağında baş ağrısı aynı atak içinde rekürrens gösterebilmektedir. Çalışmamızın amacı migren atağını sonlandırmak için yaygın kullanılan nonsteroid antienflamatuvar ilaçlar (NSAİİ) ve triptan gruplarından seçilen birer ajanın ve bunların kombine kullanımının migren atağını sonlandırma üzerindeki etkilerini göstermek ve karşılaştırmaktır.Gereç ve Yöntem: Altmış yedi migren hastasına ait 201 atak değerlendirildi. Hastalar sıra ile üç ayrı tedavi grubuna bire birer alındılar. Birinci grup hastanın baş ağrısı atağı başladığında rizatriptan 10 mg, ikinci grubun tenoksikam 20 mg, üçüncü grubun rizatriptan 10 mg ve ek olarak tenoksikam 20 mg alması sağlandı. Hastalar ağrıyı hissettikleri ve ilaçlarını aldıkları anda, 30 dakika, 60 dakika, bir saat, iki saat, dört saat, sekiz saat sonra ve ertesi gündeki baş ağrısı şiddetlerini Vizüel Analog Skalası'nda (VAS) işaretlediler. Her hasta için toplam üç ayrı atak değerlendirildi. Ataklar, her tedavi alternatifi için ayrı ayrı değerlendirilerek karşılaştırıldı.Bulgular: Tedavi gruplarının VAS değerleri atak başlangıcında farksız iken, Rizatriptan grubunda ve kombinasyon grubunda 30. dakikadan itibaren VAS puanları tenoksikama göre daha düşük bulundu. Rizatriptan grubunda ve kombinasyon grubunda 60. dakikada VAS ortalama değeri 4'ün altına düştü. Tenoksikam grubunda ise 60. dakika VAS değeri dördün üzerinde kaldı ve bu gruptaki VAS ortalaması hem rizatriptan hem de kombinasyon grubundan anlamlı olarak daha yüksek bulundu. Yirmi dördüncü saat değerlendirmesinde ise kombinasyon ve tenoksikam gruplarının VAS puanları birbirine eşi, rizatriptan grubunun VAS ortalaması diğer iki gruptan yüksek bulundu.Sonuç: Tek ilaç ile yeterli kontrol sağlanamayan ataklarda hızlı etkili triptan ve uzun etkili NSAİİ uygun bir tedavi seçeneği olarak görünmektedir.

Comparison of triptans, NSAID and combination in migraine attack treatment

Objectives: Headache during migraine attack may recur during a single attack. The present study evaluated efficacy of both individual and combined use of agents from nonsteroidal anti-inflammatory drug (NSAID) and triptan groups widely used in treatment of migraine attacks.Methods: A total of 201 attacks in 67 migraine patients were evaluated. Patients were divided into 3 study groups: those receiving rizatriptan 10mg, tenoxicam 20 mg, and rizatriptan + tenoxicam (combination). Patients evaluated severity of headache based on visual analogue scale (VAS) at moment of drug delivery, after 30 minutes, and after 1, 2, 4, 8 and 24 hours. Attacks were evaluated separately for each treatment alternative, and results were also compared.Results: VAS values were the same at onset of attack, but were lower in rizatriptan and combination groups than in tenoxicam group at 30 minutes and onward. VAS score was above 4 at 60 minutes in tenoxicam group and mean VAS value in this group was found to be significantly higher than values in rizatriptan and combined groups. At 24 hours, VAS scores were similar in combination and tenoxicam groups, while rizatriptan group had higher mean VAS score than the other 2 groups.Conclusion: When single drug use fails to provide adequate control, combined use of a rapid-acting triptan and a long-acting NSAID appears to be a suitable treatment option.

___

  • Tepper SJ, Stillman MJ. What is the best drug-delivery ap- proach for the acute treatment of migraine? Expert Rev Neurother 2012;12(3):253-5.
  • Burstein R, Jakubowski M, Rauch SD. The science of mi- graine. J Vestib Res 2011;21(6):305-14.
  • Krymchantowski AV. Acute treatment of migraine. Break- ing the paradigm of monotherapy. BMC Neurol 2004;4:4.
  • Ferrari MD, James MH, Bates D, Pilgrim A, Ashford E, Ander- son BA, et al. Oral sumatriptan: effect of a second dose, and incidence and treatment of headache recurrences. Cepha- lalgia 1994;14(5):330-8.
  • Teall J, Tuchman M, Cutler N, Gross M, Willoughby E, Smith B, et al. Rizatriptan (MAXALT) for the acute treatment of migraine and migraine recurrence. A placebo-controlled, outpatient study. Rizatriptan 022 Study Group. Headache 1998;38(4):281-7.
  • Dahlöf CG, Lipton RB, McCarroll KA, Kramer MS, Lines CR, Ferrari MD. Within-patient consistency of response of rizat- riptan for treating migraine. Neurology 2000;55(10):1511- 6.
  • Block GA, Goldstein J, Polis A, Reines SA, Smith ME. Efficacy and safety of rizatriptan versus standard care during long- term treatment for migraine. Rizatriptan Multicenter Study Groups. Headache 1998;38(10):764-71.
  • Krymchantowski AV. The use of combination therapies in the acute management of migraine. Neuropsychiatr Dis Treat 2006;2(3):293-7.
  • Tasaki Y, Yamamoto J, Omura T, Noda T, Kamiyama N, Yoshi- da K, et al. Oxicam structure in non-steroidal anti-inflam- matory drugs is essential to exhibit Akt-mediated neuro- protection against 1-methyl-4-phenyl pyridinium-induced cytotoxicity. Eur J Pharmacol 2012;676(1-3):57-63.
  • Headache classification committee of the IHS. Classifica- tion and diagnostic criteria for headache disorders, cranial neuralgias and facial pain. Cephalalgia 2004;24;1:9-95.
  • Cameron C, Kelly S, Hsieh SC, Murphy M, Chen L, Kotb A, et al. Triptans in the Acute Treatment of Migraine: A Sys- tematic Review and Network Meta-Analysis. Headache 2015;55 Suppl 4:221,35.
  • Allais G, Rolando S, De Lorenzo C, Benedetto C. The effi- cacy and tolerability of frovatriptan and dexketoprofen for the treatment of acute migraine attacks. Expert Rev Neu- rother 2014;14(8):867-77.
  • Krymchantowski AV, Bigal ME. Rizatriptan versus rizatrip- tan plus rofecoxib versus rizatriptan plus tolfenamic acid in the acute treatment of migraine. BMC Neurol 2004;4:10.
  • Fumal A, Schoenen J. Current migraine management - pa- tient acceptability and future approaches. Neuropsychiatr Dis Treat 2008;4(6):1043-57.
  • Moskowitz MA. Genes, proteases, cortical spreading de- pression and migraine: impact on pathophysiology and treatment. Funct Neurol 2007;22(3):133-6.
  • Block GA, Goldstein J, Polis A, Reines SA, Smith ME. Efficacy and safety of rizatriptan versus standard care during long- term treatment for migraine. Rizatriptan Multicenter Study Groups. Headache 1998;38(10):764-71.
  • Bell CF, Foley KA, Barlas S, Solomon G, Hu XH. Time to pain freedom and onset of pain relief with rizatriptan 10 mg and prescription usual-care oral medications in the acute treatment of migraine headaches: a multicenter, prospec- tive, open-label, two-attack, crossover study. Clin Ther 2006;28(6):872-80.
  • Amoozegar F, Pringsheim T. Rizatriptan for the acute treat- ment of migraine: Consistency, preference, satisfaction, and quality of life. Patient Prefer Adherence 2009;3:251,8.
  • Becker WJ. Acute Migraine Treatment in Adults. Headache 2015;55(6):778-93.
  • Longmore J, Hargreaves RJ, Boulanger CM, Brown MJ, Desta B, Ferro A, et al. Comparison of the vasoconstrictor properties of the 5-HT1D-receptor agonists rizatriptan (MK-462) and sumatriptan in human isolated coronary ar- tery: outcome of two independent studies using different experimental protocols. Funct Neurol 1997;12(1):3-9.
  • Cumberbatch MJ, Hill RG, Hargreaves RJ. Rizatriptan has central antinociceptive effects against durally evoked re- sponses. Eur J Pharmacol 1997;328(1):37-40.
  • Williamson DJ, Shepheard SL, Hill RG, Hargreaves RJ. The novel anti-migraine agent rizatriptan inhibits neurogenic dural vasodilation and extravasation. Eur J Pharmacol 1997;328(1):61-4.
  • Sciberras DG, Polvino WJ, Gertz BJ, Cheng H, Stepanavage M, Wittreich J, et al. Initial human experience with MK-462 (rizatriptan): a novel 5-HT1D agonist. Br J Clin Pharmacol 1997;43(1):49-54.
  • Okazawa H, Tsuchida T, Pagani M, Mori T, Kobayashi M, Tanaka F, et al. Effects of 5-HT1B/1D receptor agonist rizat- riptan on cerebral blood flow and blood volume in normal circulation. J Cereb Blood Flow Metab 2006;26(1):92-8.
  • Vyas KP, Halpin RA, Geer LA, Ellis JD, Liu L, Cheng H, et al. Disposition and pharmacokinetics of the antimi- graine drug, rizatriptan, in humans. Drug Metab Dispos 2000;28(1):89-95.
  • Ferrari MD, Goadsby PJ, Roon KI, Lipton RB. Triptans (sero- tonin, 5-HT1B/1D agonists) in migraine: detailed results and methods of a meta-analysis of 53 trials. Cephalalgia 2002;22(8):633-58.
  • Cutler NR, Jhee SS, Majumdar AK, McLaughlin D, Brucker MJ, Carides AD, et al. Pharmacokinetics of rizatriptan tablets during and between migraine attacks. Headache 1999;39(4):264-9.
  • Kelley NE, Tepper DE. Rescue therapy for acute migraine, part 3: opioids, NSAIDs, steroids, and post-discharge medi- cations. Headache 2012;52(3):467-82.
  • Heintz RC, Guentert TW, Enrico JF, Dubach UC, Brandt R, Jeunet FS. Pharmacokinetics of tenoxicam in healthy hu- man volunteers. Eur J Rheumatol Inflamm 1984;7(2):33-44.