Diagnosis and treatment of Takayasu arteritis in Turkey: A single center results
Amaç: Bu çalışmada hastanemizdeki Takayasu arteritlihastaların klinik, laboratuvar ve radyolojik özellikleriile beraber cerrahi ve endovasküler girişim sonuçlarıincelendi.Çalışmaplanı: Nisan 2002 - Ocak 2014 tarihleri arasındaTakayasu arteriti tanısı ile takip edilen 38 hastanın hastanekayıtları geriye dönük olarak incelendi. Kayıtlar Takayasuarteritinin klinik öyküsünü, eşlik eden hastalıkları, tanısırasındaki laboratuvar bulgularını, anjiyografik bulgularıve tedavi şeklini içeriyordu.Bul gu lar: Kadın/erkek oranı 3.75:1 idi. Anjiyografiksınıflamaya göre; 11 hasta tip 1, üç hasta tip 2a,üç hasta tip 2b, dört hasta tip 3, altı hasta tip 4ve 11 hasta tip 5 idi. Otuz sekiz hastanın 18ineendovasküler veya cerrahi girişim uygulandı (8cerrahi, 10 endovasküler girişim). Erken mortaliteolmadı.Sonuç: Hastalarımızın demografik ve anjiyografiközellikleri Japonya ve Akdeniz toplumları ile benzerdi.Endovasküler işlemlerin uzun dönem sonuçları verestenoz yönetimi gelecekte karşılaşılabilecekzorluklardan olabilir. Baypas cerrahisi uzun dönemaçıklık elde etmek için altın standart olmaya devametmektedir. Endovasküler tedavi, cerrahi tedaviyeuygun olmayan hastaların semptomlarında kısa sürelirahatlama sağlayabilir.
Türkiye de Takayasu arteritinin tanı ve tedavisi: Tek merkez sonuçları
Background: This study aims to evaluate clinical,laboratory, and radiological features as well as the surgicaland endovascular procedure outcomes of patients withTakayasu arteritis in our hospital. Methods: Hospital records of 38 patients who were followedwith the diagnosis of Takayasu arteritis between April2002 and January 2014 were retrospectively evaluated.Records included the clinical history of Takayasu arteritis,comorbid diseases, laboratory and angiographic findings atthe time of diagnosis, and mode of treatment. Results: The female/male ratio was 3.75:1. According toangiographic classification; 11 patients were type 1, threepatients were type 2a, three patients were type 2b, fourpatients were type 3, six patients were type 4, and 11 patientswere type 5. Eighteen of 38 patients were administeredendovascular or surgical intervention (8 surgeries and 10endovascular procedures). There was no early mortality. Conclusion: Demographic and angiographic featuresof our patients were similar to those of Japan andMediterranean populations. The long-term follow-up ofendovascular procedure success, and the managementof restenosis may be among challenges to be faced inthe future. Bypass surgery remains the gold standard forachieving long-term patency. Endovascular treatment mayprovide short-term symptom relief in patients who are notsuitable for surgical treatment.
___
- 1. Bicakcigil M, Aksu K, Kamali S, Ozbalkan Z, Ates A, Karadag O, et al. Takayasus arteritis in Turkey - clinical and angiographic features of 248 patients. Clin Exp Rheumatol 2009;27:S59-64.
- 2. Mason JC. Takayasu arteritis--advances in diagnosis and management. Nat Rev Rheumatol 2010;6:406-15.
- 3. Perera AH, Youngstein T, Gibbs RG, Jackson JE, Wolfe JH, Mason JC. Optimizing the outcome of vascular intervention for Takayasu arteritis. Br J Surg 2014;101:43-50.
- 4. Mukhtyar C, Guillevin L, Cid MC, Dasgupta B, de Groot K, Gross W, et al. EULAR recommendations for the management of large vessel vasculitis. Ann Rheum Dis 2009;68:318-23.
- 5. Arend WP, Michel BA, Bloch DA, Hunder GG, Calabrese LH, Edworthy SM, et al. The American College of Rheumatology 1990 criteria for the classification of Takayasu arteritis. Arthritis Rheum 1990;33:1129-34.
- 6. Hata A, Noda M, Moriwaki R, Numano F. Angiographic findings of Takayasu arteritis: new classification. Int J Cardiol 1996;54 Suppl:S155-63.
- 7. Isobe M. Takayasu arteritis revisited: current diagnosis and treatment. Int J Cardiol 2013;168:3-10.
- 8. Wen D, Du X, Ma CS. Takayasu arteritis: diagnosis, treatment and prognosis. Int Rev Immunol 2012;31:462-73.
- 9. Vanoli M, Bacchiani G, Origg L, Scorza R. Takayasu's arteritis: a changing disease. J Nephrol 2001;14:497-505.
- 10. Lee TH, Chen IM, Chen WY, Weng CF, Hsu CP, Shih CC. Early endovascular experience for treatments of Takayasu's arteritis. J Chin Med Assoc 2013;76:83-7.
- 11. Türkoğlu C, Memiş A, Payzin S, Akin M, Kültüsay H, Akilli A, et al. Takayasu arteritis in Turkey. Int J Cardiol 1996;54 Suppl:S135-6.
- 12. Ureten K, Oztürk MA, Onat AM, Oztürk MH, Ozbalkan Z, Güvener M, et al. Takayasu's arteritis: results of a university hospital of 45 patients inTurkey. Int J Cardiol 2004;96:259-64.
- 13. Lee GY, Jang SY, Ko SM, Kim EK, Lee SH, Han H, et al. Cardiovascular manifestations of Takayasu arteritis and their relationship to the disease activity: analysis of 204 Korean patients at a single center. Int J Cardiol 2012;159:14-20.
- 14. Sharma BK, Sagar S, Singh AP, Suri S. Takayasu arteritis in India. Heart Vessels Suppl 1992;7:37-43.
- 15. Yajima M, Numano F, Park YB, Sagar S. Comparative studies of patients with Takayasu arteritis in Japan, Korea and India- -comparison of clinical manifestations, angiography and HLA-Bantigen. Jpn Circ J 1994;58:9-14.
- 16. Tada Y, Sato O, Ohshima A, Miyata T, Shindo S. Surgical treatment of Takayasu arteritis. Heart Vessels Suppl 1992;7:159-67.
- 17. Suwanwela N, Piyachon C. Takayasu arteritis in Thailand: clinical and imaging features. Int J Cardiol 1996;54 Suppl:S117-34.
- 18. Bilge NS, Kaşifoğlu T, Cansu DU, Korkmaz C. Retrospective evaluation of 22 patients with Takayasu's arteritis. Rheumatol Int 2012;32:1155-9.
- 19. Perera AH, Mason JC, Wolfe JH. Takayasu arteritis: criteria for surgical intervention should not be ignored. Int J Vasc Med 2013;2013:618910.