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dc.contributor.authorSahin, Serdar
dc.contributor.authorKarimova, Gular
dc.contributor.authorOzcan, Seyda Gul
dc.contributor.authorDurcan, Emre
dc.contributor.authorOzkaya, Hande Mefkure
dc.contributor.authorKadioglu, Pinar
dc.date.accessioned2022-07-04T14:56:51Z
dc.date.available2022-07-04T14:56:51Z
dc.date.issued2022
dc.identifier.citationSahin S., Karimova G., Ozcan S. G. , Durcan E., Ozkaya H. M. , Kadioglu P., "Pasireotide treatment in Cushing?s disease: A single tertiary center?s experience", TURKISH JOURNAL OF MEDICAL SCIENCES, cilt.52, sa.2, ss.467-476, 2022
dc.identifier.issn1300-0144
dc.identifier.othervv_1032021
dc.identifier.otherav_961c2d98-1896-4496-a2dc-3660c5aca229
dc.identifier.urihttp://hdl.handle.net/20.500.12627/183827
dc.identifier.urihttps://doi.org/10.3906/sag-2105-261
dc.description.abstractBackground/aim: Cushing's disease (CD), which cannot be controlled by surgery, requires medical treatment. In this situation, treatments with long-term effectiveness and safety profiles are needed. We aimed to evaluate the effects and adverse effects of pasireotide treatment in CD. Materials and methods: Patients who were followed up for CD and treated with pasireotide between 2014-2020 at Cerrahpa,sa Medical Faculty, were evaluated retrospectively. The efficacy and adverse effects of pasireotide were evaluated in this study. Results: Thirty-two patients were evaluated. The mean duration of treatment was 26.5 [range, 12.0-37.0] months. The 24-h urinary free cortisol (UFC) decreased 46% during the treatment and normalized in 37.5% of patients. A significant decrement was found between pretreatment and last follow-up UFC (p = 0.001). Plasma ACTH decreased by 21%. A significant decrement was found between pre-treatment and the 3rd month, 6th month, and last follow-up ACTH levels (p = 0.014, p = 0.017, and p = 0.017, respectively). Serum cortisol levels decreased by 18% and a significant decrement was found between pretreatment and the 3rd month, and between pretreatment and the last follow-up (p = 0.034 and p = 0.013, respectively). While fasting blood glucose at the 3rd month was significantly higher than pretreatment fasting blood glucose, no significant difference was found between pretreatment fasting blood glucose and 6th month and last follow-up fasting blood glucose. Although there was a significant difference between pretreatment HbA1c levels and the HbA1c levels at the 3rd month (5.9% vs. 6.6% p = 0.007), 6th month (5.9% vs. 6.7% p = 0.003), and the last follow-up (5.9% vs. 7.1% p = 0.001), in the last follow-up, the majority (77%) of patients had adequate glycemic control (HbA1c <= 7.0 %). Conclusion: Pasireotide treatment is an alternative treatment in CD, remission is obtained in the first months of treatment, and continues for an extended period. Although hyperglycemia is the most common adverse effect, it can be successfully controlled.
dc.language.isoeng
dc.subjectGeneral Medicine
dc.subjectTIP, GENEL & İÇECEK
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectFamily Practice
dc.subjectFundamentals and Skills
dc.subjectGeneral Health Professions
dc.subjectPathophysiology
dc.subjectInternal Medicine
dc.subjectAssessment and Diagnosis
dc.subjectMedicine (miscellaneous)
dc.subjectHealth Sciences
dc.titlePasireotide treatment in Cushing?s disease: A single tertiary center?s experience
dc.typeMakale
dc.relation.journalTURKISH JOURNAL OF MEDICAL SCIENCES
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume52
dc.identifier.issue2
dc.identifier.startpage467
dc.identifier.endpage476
dc.contributor.firstauthorID3432105


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