Corticosteroid Therapy in Respiratory Disease
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This Fact Sheet Provides Information to Patients with Eczema and Their Carers. About Topical Corticosteroids How to Apply Topic
This fact sheet provides information to patients with eczema and their carers. About topical corticosteroids You or your child’s doctor has prescribed a topical corticosteroid for the treatment of eczema. For treating eczema, corticosteroids are usually prepared in a cream or ointment and are applied topically (directly onto the skin). Topical corticosteroids work by reducing inflammation and helping to control an over-reactive response of the immune system at the site of eczema. They also tighten blood vessels, making less blood flow to the surface of the skin. Together, these effects help to manage the symptoms of eczema. There is a range of steroids that can be used to treat eczema, each with different strengths (potencies). On the next page, the potencies of some common steroids are shown, as well as the concentration that they are usually used in cream or ointment preparations. Using a moisturiser along with a steroid cream does not reduce the effect of the steroid. There are many misconceptions about the side effects of topical corticosteroids. However these treatments are very safe and patients are encouraged to follow the treatment regimen as advised by their doctor. How to apply topical corticosteroids How often should I apply? How much should I apply? Apply 1–2 times each day to the affected area Enough cream should be used so that the of skin according to your doctor’s instructions. entire affected area is covered. The cream can then be rubbed or massaged into the Once the steroid cream has been applied, inflamed skin. moisturisers can be used straight away if needed. -
Adrenal Disorders
Adrenal Disorders Dual-release Hydrocortisone in Addison’s Disease— A Review of the Literature Roberta Giordano, MD,1 Federica Guaraldi, MD,2 Rita Berardelli, MD,2 Ioannis Karamouzis, MD,2 Valentina D’Angelo, MD,2 Clizia Zichi, MD,2 Silvia Grottoli, MD,2 Ezio Ghigo, PhD2 and Emanuela Arvat, PhD3 1. Department of Clinical and Biological Sciences; 2. Division of Endocrinology, Diabetology and Metabolism, Department of Medical Sciences; 3. Division of Oncological Endocrinology, Department of Medical Sciences, University of Turin, Turin, Italy Abstract In patients with adrenal insufficiency, glucocorticoids (GCs) are insufficiently secreted and GC replacement is essential for health and, indeed, life. Despite GC-replacement therapy, patients with adrenal insufficiency have a greater cardiovascular risk than the general population, and suffer from impaired health-related quality of life. Although the aim of the replacement GC therapy is to reproduce as much as possible the physiologic pattern of cortisol secretion by the normal adrenal gland, the pharmacokinetics of available oral immediate-release hydrocortisone or cortisone make it impossible to fully mimic the cortisol rhythm. Therefore, there is an unmet clinical need for the development of novel pharmaceutical preparations of hydrocortisone, in order to guarantee a more physiologic serum cortisol concentration time-profile, and to improve the long-term outcome in patients under GC substitution therapy. Keywords Addison’s disease, glucocorticoids, hydrocortisone, Plenadren®, limits, advantages Disclosure: The authors have no conflicts of interest to declare. Received: June 28, 2013 Accepted: August 9, 2013 Citation: US Endocrinology 2013;9(2):177–80 DOI: 10.17925/USE.2013.09.02.177 Correspondence: Roberta Giordano, MD, Division of Endocrinology, Diabetology and Metabolism, Department of Medical Sciences, Azienda Ospedaliera Città della Salute e della Scienza di Torino, C so Dogliotti 14, 10126 Turin, Italy. -
Frequently Asked Questions for Addison Patients
FREQUENTLY ASKED QUESTIONS FOR ADDISON PATIENTS TABLE OF CONTENT (Place your cursor over the subject line, hold down the Control Button and Click your mouse. To get back to the Table of Content, hold down the Control Button and press the Home key) ADDISONIAN CRISIS / EMERGENCY ADDISONS AND OTHER DISORDERS ADDISONS AND OTHER MEDICATIONS ADRENALINE BLOOD PRESSURE COMMON COLD/FLU/OTHER ILLNESS CORTISOL DAY CURVE CORTISOL MEDICATION CRAMPS DIABETES DIAGNOSING ADDISONS EXERCISE / SPORTS FATIGUE FLORINEF / SALT / SODIUM HERBAL / VITAMIN SUPPLEMENTS HYPERPIGMENTATION IMMUNIZATION MENOPAUSE, PREGNANCY, HORMONE REPLACEMENT, BIRTH CONTROL, HYSTERECTOMY MISCELLANEOUS OSTEOPOROSIS SECONDARY ADDISON’S SHIFT WORK SLEEP 1 STRESS DOSING SURGICAL, MEDICAL, DENTAL PROCEDURES THYROID TRAVEL WEIGHT GAIN 2 ADDISONIAN CRISIS / EMERGENCY How do you know when to call an ambulance? If you are careful, you should not have to call an ambulance. If someone with adrenal insufficiency has gastrointestinal problems and is unable to keep down their cortisol or other glucocorticoid for more than 24 hrs, they should be taken to an emergency department so they can be given intravenous solucortef and saline. It is not appropriate to wait until they are so ill that they cannot be taken to the hospital by a family member. If the individual is unable to retain anything by mouth and is very ill, or if they have had a sudden stress such as a fall or an infection, then it would be necessary for them to go by ambulance as soon as possible. It is important that you should have an emergency kit at home and that someone in the household knows how to use it. -
Trials of Cortisone Analogues in the Treatment of Rheumatoid Arthritis
Ann Rheum Dis: first published as 10.1136/ard.18.2.120 on 1 June 1959. Downloaded from Ann. rheum. Dis. (1959), 18, 120. TRIALS OF CORTISONE ANALOGUES IN THE TREATMENT OF RHEUMATOID ARTHRITIS BY H. W. FLADEE, G. R. NEWNS, W. D. SMITH, AND H. F. WEST Sheffield Centre for the Investigation and Treatment of Rheumatic Diseases In 1954 the first report appeared of a controlled rates and strengths of grip of the 21 patients from trial of aspirin versus cortisone in the treatment of this Centre who took part in the trial. Had a 1 to 5 early cases ofrheumatoid arthritis (Medical Research prednisone to cortisone dose been employed, the Council-Nuffield Foundation Joint Committee, therapeutic superiority of prednisone, of which 1954). The trial showed that, after treatment for we are now aware, would have been apparent. More a year, the group receiving cortisone (mean dose recently, fourteen patients from this trial who had 75 mg. daily) had fared no better than that receiving been kept on cortisone for a second year were only aspirin. Some of the patients had had radio- transferred to prednisolone. On this occasion the graphs taken of their hands and feet at the start dose ratio employed was 1 to 6 prednisolone to of the trial and at the end of the first year. Bone cortisone. By the end of 6 months their mean erosion was found to have advanced in both groups. erythrocyte sedimentation rate (Wintrobe) had The score for advance was slightly greater in the fallen from 24-6 to 15 mm./hr, and their mean aspirin group, but the difference was not statis- strength of grip had risen from 271 to 299 mm. -
Cortisone Injections
Pain & Rehab Medicine 920‐288‐8377/888‐965‐4380 Cortisone Injections Why are these procedures done? Cortisone is a treatment for inflammation. Most literature on painful conditions of the spine and joints suggest that inflammation can be a key contributor to the pain in addition to ligament, tendon and cartilage damage. It is very important to note that these injections/procedures are almost NEVER a cure for the problem. These procedures are used as a tool to advance your therapy and exercise program. When you find your therapy or exercise program too painful – cortisone injections can be of great value in lessening the inflammation/pain to allow for more effective therapeutic intervention. Possible side effects: Cortisone or Steroid Flare Reaction ‐ Sometimes people experience a delayed (within 24‐48 hours), temporary (lasting 24‐48 hours) increase in their pain. Icing can be helpful. You should not be concerned if you experience this side effect. It will not change the effectiveness of the shot. Elevated Blood Pressure ‐ Most commonly occurs in patients who are already hypertensive. This happens because of temporary fluid retention and may be accompanied by an increased swelling of the feet. This effect is temporary. Elevated Blood Sugar ‐ Most commonly seen in diabetic patients. Patients with diabetes should carefully monitor their blood sugar as cortisone can cause a temporary rise in glucose levels. If you take insulin you should be especially careful. Check your blood sugar often and adjust the insulin doses if necessary. Facial Flushing ‐ A flushing sensation and redness of the face. This reaction is more common in women and is seen in up to 15 percent of patients. -
Determination of Steroid Hormones and Their Metabolite in Several
G Model CHROMA-359178; No. of Pages 10 ARTICLE IN PRESS Journal of Chromatography A, xxx (2018) xxx–xxx Contents lists available at ScienceDirect Journal of Chromatography A journal homepage: www.elsevier.com/locate/chroma Determination of steroid hormones and their metabolite in several types of meat samples by ultra high performance liquid chromatography—Orbitrap high resolution mass spectrometry ∗ Marina López-García, Roberto Romero-González, Antonia Garrido Frenich Research Group “Analytical Chemistry of Contaminants”, Department of Chemistry and Physics, Research Centre for Agricultural and Food Biotechnology (BITAL), University of Almeria, Agrifood Campus of International Excellence, ceiA3, E-04120, Almería, Spain a r t i c l e i n f o a b s t r a c t Article history: A new analytical method based on ultra-high performance liquid chromatography (UHPLC) coupled Received 8 November 2017 to Orbitrap high resolution mass spectrometry (Orbitrap-HRMS) has been developed for the deter- Received in revised form 23 January 2018 mination of steroid hormones (hydrocortisone, cortisone, progesterone, prednisone, prednisolone, Accepted 28 January 2018 testosterone, melengesterol acetate, hydrocortisone-21-acetate, cortisone-21-acetate, testosterone Available online xxx ␣ propionate, 17 -methyltestosterone, 6␣-methylprednisolone and medroxyprogesterone) and their metabolite (17␣-hydroxyprogesterone) in three meat samples (chicken, pork and beef). Two differ- Keywords: ent extraction approaches were tested (QuEChERS “quick, easy, cheap, effective, rugged and safe” and Meat Hormones “dilute and shoot”), observing that the QuEChERS method provided the best results in terms of recov- Steroids ery. A clean-up step was applied comparing several sorbents, obtaining the best results when florisil Metabolite and aluminum oxide were used. -
Steroid Use in Prednisone Allergy Abby Shuck, Pharmd Candidate
Steroid Use in Prednisone Allergy Abby Shuck, PharmD candidate 2015 University of Findlay If a patient has an allergy to prednisone and methylprednisolone, what (if any) other corticosteroid can the patient use to avoid an allergic reaction? Corticosteroids very rarely cause allergic reactions in patients that receive them. Since corticosteroids are typically used to treat severe allergic reactions and anaphylaxis, it seems unlikely that these drugs could actually induce an allergic reaction of their own. However, between 0.5-5% of people have reported any sort of reaction to a corticosteroid that they have received.1 Corticosteroids can cause anything from minor skin irritations to full blown anaphylactic shock. Worsening of allergic symptoms during corticosteroid treatment may not always mean that the patient has failed treatment, although it may appear to be so.2,3 There are essentially four classes of corticosteroids: Class A, hydrocortisone-type, Class B, triamcinolone acetonide type, Class C, betamethasone type, and Class D, hydrocortisone-17-butyrate and clobetasone-17-butyrate type. Major* corticosteroids in Class A include cortisone, hydrocortisone, methylprednisolone, prednisolone, and prednisone. Major* corticosteroids in Class B include budesonide, fluocinolone, and triamcinolone. Major* corticosteroids in Class C include beclomethasone and dexamethasone. Finally, major* corticosteroids in Class D include betamethasone, fluticasone, and mometasone.4,5 Class D was later subdivided into Class D1 and D2 depending on the presence or 5,6 absence of a C16 methyl substitution and/or halogenation on C9 of the steroid B-ring. It is often hard to determine what exactly a patient is allergic to if they experience a reaction to a corticosteroid. -
Drug Name Plate Number Well Location % Inhibition, Screen Axitinib 1 1 20 Gefitinib (ZD1839) 1 2 70 Sorafenib Tosylate 1 3 21 Cr
Drug Name Plate Number Well Location % Inhibition, Screen Axitinib 1 1 20 Gefitinib (ZD1839) 1 2 70 Sorafenib Tosylate 1 3 21 Crizotinib (PF-02341066) 1 4 55 Docetaxel 1 5 98 Anastrozole 1 6 25 Cladribine 1 7 23 Methotrexate 1 8 -187 Letrozole 1 9 65 Entecavir Hydrate 1 10 48 Roxadustat (FG-4592) 1 11 19 Imatinib Mesylate (STI571) 1 12 0 Sunitinib Malate 1 13 34 Vismodegib (GDC-0449) 1 14 64 Paclitaxel 1 15 89 Aprepitant 1 16 94 Decitabine 1 17 -79 Bendamustine HCl 1 18 19 Temozolomide 1 19 -111 Nepafenac 1 20 24 Nintedanib (BIBF 1120) 1 21 -43 Lapatinib (GW-572016) Ditosylate 1 22 88 Temsirolimus (CCI-779, NSC 683864) 1 23 96 Belinostat (PXD101) 1 24 46 Capecitabine 1 25 19 Bicalutamide 1 26 83 Dutasteride 1 27 68 Epirubicin HCl 1 28 -59 Tamoxifen 1 29 30 Rufinamide 1 30 96 Afatinib (BIBW2992) 1 31 -54 Lenalidomide (CC-5013) 1 32 19 Vorinostat (SAHA, MK0683) 1 33 38 Rucaparib (AG-014699,PF-01367338) phosphate1 34 14 Lenvatinib (E7080) 1 35 80 Fulvestrant 1 36 76 Melatonin 1 37 15 Etoposide 1 38 -69 Vincristine sulfate 1 39 61 Posaconazole 1 40 97 Bortezomib (PS-341) 1 41 71 Panobinostat (LBH589) 1 42 41 Entinostat (MS-275) 1 43 26 Cabozantinib (XL184, BMS-907351) 1 44 79 Valproic acid sodium salt (Sodium valproate) 1 45 7 Raltitrexed 1 46 39 Bisoprolol fumarate 1 47 -23 Raloxifene HCl 1 48 97 Agomelatine 1 49 35 Prasugrel 1 50 -24 Bosutinib (SKI-606) 1 51 85 Nilotinib (AMN-107) 1 52 99 Enzastaurin (LY317615) 1 53 -12 Everolimus (RAD001) 1 54 94 Regorafenib (BAY 73-4506) 1 55 24 Thalidomide 1 56 40 Tivozanib (AV-951) 1 57 86 Fludarabine -
Corticosteroids in Terminal Cancer-A Prospective Analysis of Current Practice
Postgraduate Medical Journal (November 1983) 59, 702-706 Postgrad Med J: first published as 10.1136/pgmj.59.697.702 on 1 November 1983. Downloaded from Corticosteroids in terminal cancer-a prospective analysis of current practice G. W. HANKS* T. TRUEMAN B.Sc., M.B., B.S., M.R.C.P.(U.K.) S.R.N. R. G. TWYCROSS M.A., D.M., F.R.C.P. Sir Michael Sobell House, The Churchill Hospital, Headington, Oxford OX3 7LJ Summary Introduction Over half of a group of 373 inpatients with advanced Corticosteroids have a major role to play in the malignant disease were treated with corticosteroids control of symptoms in patients with advanced for a variety of reasons. They received either pred- malignant disease. They may be employed in a non- nisolone or dexamethasone, or replacement therapy specific way to improve mood and appetite; or they with cortisone acetate. Forty percent of those receiv- may be indicated as specific adjunctive therapy in the ing corticosteroids benefited from them. A higher relief of symptoms related to a large tumour mass or response rate was seen when corticosteroids were to nerve compression. The management of a numberProtected by copyright. prescribed for nerve compression pain, for raised of other symptoms and syndromes may also be intracranial pressure, and when used in conjunction facilitated by treatment with corticosteroids (Table with chemotherapy. No significant difference in 1). efficacy was noted between the 2 drugs. The results, The use of corticosteroids in patients with ad- however, suggest that with a larger sample, dexame- vanced cancer is empirical, as it is in other non- thasone would have been shown to be significantly endocrine indications. -
Endogenous Steroid Hormones in Hair: Investigations on Different Hair Types, Pigmentation Effects and Correlation to Nails
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 2020 Endogenous steroid hormones in hair: investigations on different hair types, pigmentation effects and correlation to nails Voegel, Clarissa D ; Hofmann, Mathias ; Kraemer, Thomas ; Baumgartner, Markus R ; Binz, Tina M Abstract: Steroid hormone analysis is widely used in health- and stress-related research to get insights into various diseases and the adaption to stress. Hair analysis has been used as a tool for the long-term monitoring of these steroid hormones. In this study, a liquid chromatography-tandem mass spectrome- try method was developed and validated for the simultaneous identification and quantification of seven steroid hormones (cortisone, cortisol, 11-deoxycortisol, androstenedione, 11-deoxycorticosterone, testos- terone, progesterone) in hair. Cortisol, cortisone, androstenedione, testosterone and progesterone were detected and quantified in authentic hair samples of different individuals. Significantly higher concen- trations for body hair were found for cortisone and testosterone compared to scalp hair. Furthermore, missing correlations for the majority of steroids between scalp and body hair indicate that body hair is not really suitable as alternative when scalp hair is not available. The influence of hair pigmentation was analyzed by comparing pigmented to non-pigmented hair of grey-haired individuals. The results showed no differences for cortisol, cortisone, androstenedione, testosterone and progesterone concentrations (p> 0.05) implying that hair pigmentation has not a strong effect on steroid hormone concentrations. Cor- relations between hair and nail steroid levels were also studied. Higher concentrations of cortisol and cortisone in hair were found compared to nails (p< 0.0001). -
Quantification of Hair Corticosterone, DHEA and Testosterone As
animals Article Quantification of Hair Corticosterone, DHEA and Testosterone as a Potential Tool for Welfare Assessment in Male Laboratory Mice Alberto Elmi 1 , Viola Galligioni 2, Nadia Govoni 1 , Martina Bertocchi 1 , Camilla Aniballi 1 , Maria Laura Bacci 1 , José M. Sánchez-Morgado 2 and Domenico Ventrella 1,* 1 Department of Veterinary Medical Sciences, University of Bologna, 40064 Ozzano dell’Emilia, BO, Italy; [email protected] (A.E.); [email protected] (N.G.); [email protected] (M.B.); [email protected] (C.A.); [email protected] (M.L.B.) 2 Comparative Medicine Unit, Trinity College Dublin, D02 Dublin, Ireland; [email protected] (V.G.); [email protected] (J.M.S.-M.) * Correspondence: [email protected]; Tel.: +39-051-2097-926 Received: 11 November 2020; Accepted: 14 December 2020; Published: 16 December 2020 Simple Summary: Mice is the most used species in the biomedical research laboratory setting. Scientists are constantly striving to find new tools to assess their welfare, in order to ameliorate husbandry conditions, leading to a better life and scientific data. Steroid hormones can provide information regarding different behavioral tracts of laboratory animals but their quantification often require stressful sampling procedures. Hair represents a good, less invasive, alternative in such scenario and is also indicative of longer timespan due to hormones’ accumulation. The aim of the work was to quantify steroid hormones in the hair of male laboratory mice and to look for differences imputable to age and housing conditions (pairs VS groups). Age influenced all analysed hormones by increasing testosterone and dehydroepiandrosterone (DHEA) levels and decreasing corticosterone. -
LCMS Saliva Steroid & Steroid Synthesis Inhibitor Profile
PROVIDER DATA SHEET LCMS Saliva Steroid & Steroid Synthesis Inhibitor Profile ZRT Laboratory now offers a comprehensive LC-MS/MS saliva assay that measures the levels of 18 endogenous steroid hormones (see Steroid Hormone Cascade Tests Included diagram on the next page) including estrogens, progestogens, androgens, Estrogens glucocorticoids, and mineralocorticoids. In addition to endogenous hormones Estradiol (E2), Estriol (E3), Estrone (E1), the new assay quantifies the level of melatonin and the synthetic estrogen ethinyl Ethinyl Estradiol (EE) estradiol, present in most birth control formulations, as well as several synthetic Progestogen Precursors and Metabolites aromatase inhibitors (anastrozole and letrozole) and the 5α-reductase inhibitor Pregnenolone Sulfate (PregS), Progesterone (Pg), finasteride. Allopregnenolone (AlloP), 17-OH Progesterone (17OHPg) The LC-MS/MS assay expands beyond the 5-steroid panel of parent hormones Androgen Precursors and Metabolites (estradiol, progesterone, testosterone, DHEAS, and cortisol) currently tested Androstenedione (Adione), Testosterone (T), by immunoassay (IA) at ZRT Laboratory. Testing the levels of both upstream Dihydrotestosterone (DHT), DHEA (D), precursors and downstream metabolites of these parent active steroids, listed DHEA-S (DS), 7-Keto DHEA (7keto) above and shown in the diagram on the next page, will help determine which steroid Glucocorticoid Precursors and Metabolites synthesis enzymes are low, overactive, blocked by natural or pharmaceutical 11-Deoxycortisol (11DC) Cortisol