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Treatment of Cushing's Syndrome: An Endocrine Society Clinical Practice Guideline
The Journal of Clinical Endocrinology & Metabolism · 2015 · Vol. 100(8) · pp. 2807–2831
Lynnette K. Nieman✉(Eunice Kennedy Shriver National Institute of Child Health and Human Development)Beverly M. K. Biller(Harvard University)James W. Findling(Medical College of Wisconsin)M. Hassan Murad(WinnMed)John Newell‐Price(University of Sheffield)Martin O. Savage(William Harvey Research Institute)Antoine Tabarin(Université de Bordeaux)
Abstract
Treatment of Cushing's syndrome is essential to reduce mortality and associated comorbidities. Effective treatment includes the normalization of cortisol levels or action. It also includes the normalization of comorbidities via directly treating the cause of Cushing's syndrome and by adjunctive treatments (eg, antihypertensives). Surgical resection of the causal lesion(s) is generally the first-line approach. The choice of second-line treatments, including medication, bilateral adrenalectomy, and radiation therapy (for corticotrope tumors), must be individualized to each patient.
Pituitary Gland Disorders and TreatmentsAdrenal and Paraganglionic TumorsGrowth Hormone and Insulin-like Growth FactorsMedicineGuidelineTask forceGrading (engineering)Systematic reviewEndocrine systemCushing syndromeClinical PracticeMEDLINEIntensive care medicine
MeSH terms
Adrenal Gland NeoplasmsAdrenalectomyCushing SyndromeEndocrinologyHumansPatient Care PlanningPituitary NeoplasmsRecurrenceRemission InductionEvidence-Based MedicineConsensus
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