Glucocorticoid: Difference between revisions
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'''Glucocorticoids''' are defined as "a group of | '''Glucocorticoids''' are defined as "a group of [[corticosteroid]]s that affect carbohydrate metabolism (gluconeogenesis, liver glycogen deposition, elevation of blood sugar), inhibit adrenocorticotropic hormone secretion, and possess pronounced anti-inflammatory activity. These [[steroid]]s also play a role in fat and protein metabolism, maintenance of arterial blood pressure, alteration of the connective tissue response to injury, reduction in the number of circulating lymphocytes, and functioning of the central nervous system."<ref name="title">{{cite web |url=http://www.nlm.nih.gov/cgi/mesh/2007/MB_cgi?term=Glucocorticoids |title=Glucocorticoids|author=National Library of Medicine |accessdate=2007-11-25 |format= |work=}}</ref> | ||
Glucocorticoids are commonly used for treating rheumatological diseases and are categorised as [[disease-modifying antirheumatic drugs]] (DMARDs). | Glucocorticoids are commonly used for treating rheumatological diseases and are categorised as [[disease-modifying antirheumatic drugs]] (DMARDs). | ||
==Dosage== | |||
Equivalent dosage calculators: | |||
* http://www.globalrph.com/corticocalc.htm | |||
* http://www-users.med.cornell.edu/~spon/picu/referenc/steroids.htm | |||
==Adverse effects== | ==Adverse effects== | ||
The [http://www.eular.org/ European League Against Rheumatism] (EULAR) has made recommenations on the avoidance of adverse effects from glucocorticoids.<ref name="pmid17660219">{{cite journal |author=Hoes JN, Jacobs JW, Boers M, ''et al'' |title=EULAR evidence-based recommendations on the management of systemic glucocorticoid therapy in rheumatic diseases |journal=Ann. Rheum. Dis. |volume=66 |issue=12 |pages=1560–7 |year=2007 |pmid=17660219 |doi=10.1136/ard.2007.072157}}</ref> EULAR states that risk factors for adverse effects include "[[hypertension]], [[diabetes]], peptic ulcer, recent fractures, presence of cataract or [[glaucoma]], presence of (chronic) infections, dyslipidemia and co-medication with [[Non-steroidal anti-inflammatory agents|non-steroidal anti-inflammatory drugs]]".<ref name="pmid17660219"/> EULAR recommends monitoring of "body weight, blood pressure, peripheral oedema, cardiac insufficiency, serum lipids, blood and/or urine glucose and ocular pressure".<ref name="pmid17660219"/> | [[Drug toxicity]] from glucocorticoids is common.<ref name="pmid19066177">{{cite journal| author=Hoes JN, Jacobs JW, Verstappen SM, Bijlsma JW, Van der Heijden GJ| title=Adverse events of low- to medium-dose oral glucocorticoids in inflammatory diseases: a meta-analysis. | journal=Ann Rheum Dis | year= 2009 | volume= 68 | issue= 12 | pages= 1833-8 | pmid=19066177 | ||
| url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=clinical.uthscsa.edu/cite&email=badgett@uthscdsa.edu&retmode=ref&cmd=prlinks&id=19066177 | doi=10.1136/ard.2008.100008 }} </ref> The [http://www.eular.org/ European League Against Rheumatism] (EULAR) has made recommenations on the avoidance of adverse effects from glucocorticoids.<ref name="pmid17660219">{{cite journal |author=Hoes JN, Jacobs JW, Boers M, ''et al'' |title=EULAR evidence-based recommendations on the management of systemic glucocorticoid therapy in rheumatic diseases |journal=Ann. Rheum. Dis. |volume=66 |issue=12 |pages=1560–7 |year=2007 |pmid=17660219 |doi=10.1136/ard.2007.072157}}</ref> EULAR states that risk factors for adverse effects include "[[hypertension]], [[diabetes]], peptic ulcer, recent fractures, presence of cataract or [[glaucoma]], presence of (chronic) infections, dyslipidemia and co-medication with [[Non-steroidal anti-inflammatory agents|non-steroidal anti-inflammatory drugs]]".<ref name="pmid17660219"/> EULAR recommends monitoring of "body weight, blood pressure, peripheral oedema, cardiac insufficiency, serum lipids, blood and/or urine glucose and ocular pressure".<ref name="pmid17660219"/> | |||
===Adrenal insufficiency=== | ===Adrenal insufficiency=== | ||
| Line 27: | Line 33: | ||
A more recent [[randomized controlled trial]] suggests that teriparatide improved bone mass more than alendronate does.<ref name="pmid18003959">{{cite journal |author=Saag KG, Shane E, Boonen S, ''et al'' |title=Teriparatide or alendronate in glucocorticoid-induced osteoporosis |journal=N. Engl. J. Med. |volume=357 |issue=20 |pages=2028–39 |year=2007 |pmid=18003959 |doi=10.1056/NEJMoa071408}}</ref> | A more recent [[randomized controlled trial]] suggests that teriparatide improved bone mass more than alendronate does.<ref name="pmid18003959">{{cite journal |author=Saag KG, Shane E, Boonen S, ''et al'' |title=Teriparatide or alendronate in glucocorticoid-induced osteoporosis |journal=N. Engl. J. Med. |volume=357 |issue=20 |pages=2028–39 |year=2007 |pmid=18003959 |doi=10.1056/NEJMoa071408}}</ref> | ||
===Neuro-psychiatric=== | |||
Neuro-psychiatric [[drug toxicity]] may occur.<ref name="pmid22362393">{{cite journal| author=Fardet L, Petersen I, Nazareth I| title=Suicidal behavior and severe neuropsychiatric disorders following glucocorticoid therapy in primary care. | journal=Am J Psychiatry | year= 2012 | volume= 169 | issue= 5 | pages= 491-7 | pmid=22362393 | doi=10.1176/appi.ajp.2011.11071009 | pmc= | url= }} </ref> | |||
==References== | ==References== | ||
<references/> | <references/>[[Category:Suggestion Bot Tag]] | ||
Latest revision as of 11:01, 22 August 2024
Glucocorticoids are defined as "a group of corticosteroids that affect carbohydrate metabolism (gluconeogenesis, liver glycogen deposition, elevation of blood sugar), inhibit adrenocorticotropic hormone secretion, and possess pronounced anti-inflammatory activity. These steroids also play a role in fat and protein metabolism, maintenance of arterial blood pressure, alteration of the connective tissue response to injury, reduction in the number of circulating lymphocytes, and functioning of the central nervous system."[1]
Glucocorticoids are commonly used for treating rheumatological diseases and are categorised as disease-modifying antirheumatic drugs (DMARDs).
Dosage
Equivalent dosage calculators:
- http://www.globalrph.com/corticocalc.htm
- http://www-users.med.cornell.edu/~spon/picu/referenc/steroids.htm
Adverse effects
Drug toxicity from glucocorticoids is common.[2] The European League Against Rheumatism (EULAR) has made recommenations on the avoidance of adverse effects from glucocorticoids.[3] EULAR states that risk factors for adverse effects include "hypertension, diabetes, peptic ulcer, recent fractures, presence of cataract or glaucoma, presence of (chronic) infections, dyslipidemia and co-medication with non-steroidal anti-inflammatory drugs".[3] EULAR recommends monitoring of "body weight, blood pressure, peripheral oedema, cardiac insufficiency, serum lipids, blood and/or urine glucose and ocular pressure".[3]
Adrenal insufficiency
EULAR recommends:[3]
- "All patients on glucocorticoid therapy for longer than 1 month, who will undergo surgery, need perioperative management with adequate glucocorticoid replacement to overcome potential adrenal insufficiency"
- "For moderate physical stress-inducing procedures, a single dose of 100 mg of hydrocortisone intravenously has been proposed, and for major surgery, 100 mg of hydrocortisone intravenously before anaesthesia and every 8 h 4 times thereafter. The dose can be gradually tapered by half per day afterwards."
Gastrointestinal toxicity
EULAR recommends:[3]
- "Patients treated with glucocorticoids and concomitant non-steroidal anti-inflammatory drugs (NSAIDs) should be given appropriate gastro-protective medication, such as proton pump inhibitors (PPIs) or misoprostol, or alternatively could switch to a cyclo-oxygenase-2 selective inhibitor (coxib)."
- "For moderate physical stress-inducing procedures, a single dose of 100 mg of hydrocortisone intravenously has been proposed, and for major surgery, 100 mg of hydrocortisone intravenously before anaesthesia and every 8 h 4 times thereafter. The dose can be gradually tapered by half per day afterwards. However, several other schemes of GC-replacement exist."
Growth retardation in children
The European League Against Rheumatism (EULAR) recommends:[3]
- "Children receiving glucocorticoids should be checked regularly for linear growth and considered for growth-hormone replacement in case of growth impairment."
Osteoporosis
The European League Against Rheumatism (EULAR) recommends:[3]
- "patient is started on prednisone >=7.5 mg daily and continues on prednisone for more than 3 months, calcium and vitamin D supplementation should be prescribed".
- "Antiresorptive therapy with bisphosphonates to reduce the risk of glucocorticoid-induced osteoporosis should be based on risk factors, including bone-mineral density (BMD) measurement."
A more recent randomized controlled trial suggests that teriparatide improved bone mass more than alendronate does.[4]
Neuro-psychiatric
Neuro-psychiatric drug toxicity may occur.[5]
References
- ↑ National Library of Medicine. Glucocorticoids. Retrieved on 2007-11-25.
- ↑ Hoes JN, Jacobs JW, Verstappen SM, Bijlsma JW, Van der Heijden GJ (2009). "Adverse events of low- to medium-dose oral glucocorticoids in inflammatory diseases: a meta-analysis.". Ann Rheum Dis 68 (12): 1833-8. DOI:10.1136/ard.2008.100008. PMID 19066177. Research Blogging.
- ↑ 3.0 3.1 3.2 3.3 3.4 3.5 3.6 Hoes JN, Jacobs JW, Boers M, et al (2007). "EULAR evidence-based recommendations on the management of systemic glucocorticoid therapy in rheumatic diseases". Ann. Rheum. Dis. 66 (12): 1560–7. DOI:10.1136/ard.2007.072157. PMID 17660219. Research Blogging.
- ↑ Saag KG, Shane E, Boonen S, et al (2007). "Teriparatide or alendronate in glucocorticoid-induced osteoporosis". N. Engl. J. Med. 357 (20): 2028–39. DOI:10.1056/NEJMoa071408. PMID 18003959. Research Blogging.
- ↑ Fardet L, Petersen I, Nazareth I (2012). "Suicidal behavior and severe neuropsychiatric disorders following glucocorticoid therapy in primary care.". Am J Psychiatry 169 (5): 491-7. DOI:10.1176/appi.ajp.2011.11071009. PMID 22362393. Research Blogging.