Testosterone Therapy in Men With Hypogonadism
Published: March 2018
$9.95
Print Copy Information:
- 18 pages
- Spiral Bound
- 80# Aqueous Coating
- 4.25" x 7.25"
- Ships in 5 – 10 business days
What's Inside
Bulk and Institutional Ordering
About the Authors
Additional Information
- Key Points
- Diagnosis of Hypogonadism in Men
- Treatment of Hypogonadism with Testosterone
- Monitoring of Testosterone Replacement Therapy
- Algorithm
- An Approach for the Diagnostic Evaluation of Adult Men Suspected of Having T Deficiency
- Tables
- Classification of Hypogonadism and Causes of Primary and Secondary Hypogonadism
- Symptoms and Signs Suggestive of T Deficiency in Men
- Conditions in Which Measurement of FT Concentration is Recommended
- Conditions in Which T Administration Is Associated With a High Risk of Adverse Outcomes
- Clinical Pharmacology of T Formulations Approved in the United States and Europe
- Testosterone Formulations Available Outside the United States, but Not Approved by the FDA
- Potential Adverse Effects of T Replacement
- Monitoring Men Receiving T Therapy
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Contact Us for more details
Founded in 1916, The Endocrine Society is the world's oldest, largest, and most active organization devoted to research on hormones and the clinical practice of endocrinology. The Society works to foster a greater understanding of endocrinology amongst the general public and practitioners of complementary medical disciplines and to promote the interests of all endocrinologists at the national scientific research and health policy levels of government. The Hormone Foundation, the Society's public education affiliate, is a leading source of hormone-related health information for the public, physicians, allied health professionals and the media.
Description
This pocket guide attempts to define principles of practice that should produce high-quality patient care. It is applicable to specialists, primary care, and providers at all levels. This pocket guide should not be considered exclusive of other methods of care reasonably directed at obtaining the same results. The ultimate judgment concerning the propriety of any course of conduct must be made by the clinician after consideration of each individual patient situation. Neither IGC, the medical associations, nor the authors endorse any product or service associated with the distributor of this clinical reference tool.
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Included Guidelines:
- Acromegaly
- Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency
- Cushing's Syndrome Treatment
- Diabetes and Pregnancy
- Diabetes Technology—Continuous Subcutaneous Insulin Infusion Therapy and Continuous Glucose Monitoring in Adults
- Diagnosis of Cushing's Syndrome
- Evaluation and Management of Adult Hypoglycemic Disorders
- Evaluation and Treatment of Hypertriglyceridemia
- Functional Hypothalamic Amenorrhea
- Gender-Dysphoria / Gender-Incongruence
- Hirsutism in Premenopausal Women
- Hyperglycemia in Hospitalized Adult Patients
- Hypothalamic–Pituitary and Growth Disorders in Survivors of Childhood Cancer
- Lipid Management in Patients with Endocrine Disorders
- Menopause
- Obesity
- Paget's Disease of Bone
- Pediatric Obesity
- Pharmacological Management of Osteoporosis in Postmenopausal Women
- Primary Adrenal Insufficiency
- Primary Aldosteronism
- Primary Prevention of ASCVD and T2DM in Patients at Metabolic Risk
- Testosterone Therapy in Men With Hypogonadism
- Treatment of Diabetes in Older Adults
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