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Cisplatin’e Bağlı Böbrek Toksisitesi ve Sentetik Oral Prostaglandin E1 Analoğunun Etkinliğinin Değerlendirilmesi

Cisplatin-Induced Renal Toxicity and Evaluation of the Efficacy of Synthetic Oral Prostaglandin E1 Analogue

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Abstract (2. Language): 
Despite the demonstration of the protective effects of misoprostol, an oral prostaglandin E1 analogue, on the nephrotoxicity of non-steroidal antiinflammatory drugs (NSAID) and cyclosporine, its role in cisplatin nephrotoxicity has not been investigated. In our study, we planned to investigate cisplatin-induced acute renal failure and the efficacy of misoprostol on acute cisplatin nephrotoxicity. For this purpose, 28 lung cancer patients who had been planned to receive the cisplatin+etoposide chemotherapy regimen were included in the study. Patients then were divided into two groups. In addition to chemotherapy, Misoprostol group received misoprostol at the dose of 100 µg qid during the study. Control group received only chemotherapy. Renal functions were evaluated in both groups before the onset of chemotherapy and 2nd and 6th days of chemotherapy. In conclusion, it was demonstrated that misoprostol could not produce any protective effect on the functional disturbances due to cisplatin administration.
Abstract (Original Language): 
Bir oral prostaglandin E1 analoğu olan misoprostolün steroid olmayan antienflamatuar ilaçlar (NSAID) ve siklosporin nefrotoksisitesinde protektif etkisi olduğu gösterilmesine karşın, cisplatin nefrotoksisitesindeki rolü incelenmemiştir. Çalışmamızda cisplatine bağlı gelişen akut böbrek yetmezliğinin ve misoprostolün akut cisplatin nefrotoksisitesindeki etkinliğinin incelenmesi amaçlanmıştır. Bu amaçla cisplatin+etoposid kemoterapi rejimi alması planlanan 28 akciğer kanserli hasta çalışmaya dahil edildi. Hastalar iki gruba ayrıldı. Misoprostol grubu kemoterapinin yanısıra çalışma süresince günde 4 kez 100 µg dozda misoprostol aldı. Kontrol grubu sadece kemoterapi aldı. Her iki grupta renal fonksiyonlar kemoterapi başlamasından önce ve kemoterapinin 2. ve 6. günlerinde değerlendirildi. Sonuç olarak, cisplatin kullanımına bağlı gelişen fonksiyonel bozukluklarda misoprostolün koruyucu etkinlik gösteremediği saptandı.
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