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1
PRESENTED BY
Dr. E. RAMNATH
DEPARTMENT OF PERIODONTOLOGY
History
 By the middle of 19th century it was demonstrated
that adrenal glands were essential for life
 Later, it was appreciated that the cortex was more
important than the medulla
 A number of steroidal active principles were
isolated and their structures were elucidated by
kendall and his coworkers in the 1930s.
2
 However, the gate to their
great therapeutic potential was
opened by Hench (1949) who
obtained striking improvement
in rheumatoid arthritis by using
cortisone.
 The nobel prize was awarded
the very next year to kendall
and Hench.
 Currently, corticosteroids are
drugs with one of the broadest
spectrum of clinical utility.
3
Functional anatomy and histology of
adrenal glands

4
5
6
7
Zones of adrenal cortex Hormones
Zona glomerulosa Aldosterone
Desoxycorticosterone
Zona fasciculata
Cortisone
Cortisol
Zona reticularis
Dehydroepiandrosterone
Androstenidione
Traces of estrogens
Essentials Of Medical Physiology 3rd Edition,
K Sembulingam
8
MECHANISM OF ACTION
plasma memb
Corticosteroids
CYTOPLASMIC
RECEPTOR
PROTEIN
GLUCOCORTICOID
RESPONSE
ELEMENT
Nucleus
Transcription of
m - RNA
New protein
synthesis
TOTAL
TIME
30 – 60 mins
On resistance to stress 9
Physical or mental stress
Increases ACTH
Increase in glucocorticoid secretion
High resistance to body against stress
GOODMAN & GILMAN'S THE PHARMACOLOGICAL BASIS OF
THERAPEUTICS - 11th Ed. (2006)
Steroids in Dentistry
 Used primarily to decrease postoperative edema and
manage oral inflammatory diseases
10
Classification of steroids based on their
relative activity
11
Mineralocorticoids
• Desoxycorticosterone acetate(DOCA)
• Fludrocortisone
• Aldosterone
Classification of steroids based on their
relative activity
12
Short acting
(t1/2 < 12 hr)
• Hydrocortisone
• Cortisone
Intermediate
acting:
(t1/2 12 – 36)
• Prednisole
• Methyl prednisole
• Triamcinolone
Long acting:
(t1/2 > 36 hrs)
• Paramethasone
• Dexamethasone
• Betamethasone
13
Cortisone
Oral: 5, 10, 25 mg tablets
Parentral:22,25 mg of
solution
14
Hydrocortisone
Oral:5mg,10mg,20mgtab
Topical:
1%eye drops
0.025%nasal drops
0.25-2.5%skin cream
Parenteral:25, 50 mg for IV,IM,SC Injections
15
Prednisolone
Oral:5,10, 20 mg tablets,
15mg/5 ml syrup, 5mg
suspension as pediatric drops
Parenteral:25,50 mg
IM,IV,Intralesional
Triamcinolone
Oral:1,4,8mg syrup
Topical:0.1% eye drops, ointment
Parentral: 3,10,40 mg for I.M,
intraarticular, intralesional
injections
16
17
Dexamethasone
Oral:0.25,0.5,0.75,1,2,4,6mg tablets
Topical:0.1% eye drops, ear drops,
skin ointment
Parenteral: 4,8,10,20 mg for IV, IM,
intralesional and intraarticular.
18
Betamethasone
Oral: oral drops – 0.5 mg/ ml, tablets –
0.5 to 1 mg.
Topical – 0.1% eye drops, ointment,0.05%
nasal drops, 0.12% skin creams
Parenteral:4 mg/ml for IM, IV,
intralesional, intraarticular
ADMINISTRATION OF
STEROIDS
 TOPICAL
 SYSTEMIC
 INTRA - LESIONAL
19
Protocols for use -(TC)
 POTENCY
 RELIEF
20
JDR April 2005 vol. 84 no. 4 294-301
21
short course of
TCs
Accelerate
remission without
adverse effects
Recurrent aphthous
stomatitis (RAS), some
cases of erythema
multiforme (EM), and
Drug-induced
ulceration.
TCs must be used
for longer, less
predictable periods
Severe RAS, Erosive oral
lichen planus (OLP),
specific forms of EM,
and mucous membrane
pemphigoid (MMP)
Scully et al., 1999; Chan et al., 2002
Criteria for use topical and systemic
22
very severe cases
of ulceration
Short course of systemic
corticosteroids followed
by maintenance regimen
of TCs and or can also be
started simultaneously
with the systemic therapy
Pemphigus
vulgaris ,10-30%
of Pemphigoid
patients, Erosive
lichen planus
Inevitably be treated with
systemic corticosteroids
and/or other
immunosuppressant
therapies
Laskaris and Angelopoulos, 1981;
Nisengard and Neiders, 1981; Fine et al., 1984;
Domloge-Hultsch et al., 1994; Dayan et al., 1999
The key factors 23
JDR April 2005 vol. 84 no. 4 294-301
The specific diagnosis
The severity of the oral disease
The presence or absence of extra-oral lesions
The medical history of the patient
Factors that influence the
effectiveness of TCs:
24
JDR April 2005 vol. 84 no. 4 294-301
The intrinsic potency of the drug
Factors that influence the
effectiveness of TCs:
25
JDR April 2005 vol. 84 no. 4 294-301
The contact time between the
drug and lesion and the vehicle
used to apply it;
Factors that influence the
effectiveness of TCs:
26
JDR April 2005 vol. 84 no. 4 294-301
Concentration
Success of a topical medicine
27
Two main factors
Number of applications per day
High-potency
(2-3 times)
Low potency
(5-10 times)
The vehicle
used
Various vehicles
JDR April 2005 vol. 84 no. 4 294-301
Various vehicles. 28
JDR April 2005 vol. 84 no. 4 294-301
Orabase (Stoy, 1966),
Cyanoacrylate (Jasmin et al., 1993),
Bioadhesive patches made of cellulose derivatives (Mahdi et al., 1996),
Gels (Regezi and Sciubba, 1999), and
Denture adhesive paste (Lo Muzio et al., 2001).
Steroids as anti- inflammatory 29
Prevention of postoperative pain,
edema, trismus after 3rd molar surgery
Prevention of postoperative edema
after orthognathic surgery
TREATING alveolar osteitis
30
Phospholipids
Arachidonic acids
lipoxygenase Cylo - oxygenase
Leukotriene
Prostaglandins,
Thromboxane
Prostacyclins
Phospholipase A2
Lipocortin
Corticosteroids
Steroids as intra-canal
medicaments
 Ledermix
 triamcinolone acetonide + demeclocycline.
31
Journal of Interdisciplinary Dentistry / May-Aug 2014 / Vol-4
/ Issue-2
Corticosteroids in auto immune disorders and other aids
32
• Eg: Erosive LP
• RAS
Ulcerative, Vesiculoerosive
diseases
• Eg: CGCG
• HemangiomaBenign lesions
• Eg: Mucocele
Salivary gland disorders
• Eg: Osteoarthritis
• Rheumatiid arthritisTMJ Disorders
• Eg. Post herpatic neuralgia
Neuralgia Treatment
• OSMF
Miscellanous
Systemic steroids for ulcerative
vesiculobullous diseases
33
major aphthae or severe multiple
minor aphthae
 Prednisone therapy should be started at 1.0 mg/kg/day
in patients with severe RAU and should be tapered after
1 to 2 weeks.
34
35
Minor EM 20 – 40 mg/day for 4 – 6
days / PREDNISOLONE
Severe or rapidly
progressing
lesions
60 mg/day slowly
tapered by 10 mg/day
over 6 weeks
Erythema multiforme
Pemphigus Vulgaris
 Mainstay 1-2mg/kg/d.
 Initial dose of treatment – 0.5 mg/kg/day to 3 mg/kg/d
 Dose that achieves clinical control is maintained for 2-
3 weeks and then gradually tapered.
36
Burkit’s Oral Medicine, 11th edition
Pulse therapy
 Also called short term therapy
 High dose therapy involves a 48-72 hrs course of
intensive steroid administration
 Single i.v injection of a supra-physiological dose of
steroid
 Dose of 0.5-2g of prednisolone or equivalent
37
39Cicatricial pemphigoid
Predisolone – 30
to 60 mg/day
2-3 weeks to
stop new bullae
formation
Tapered by 20%
every 2-3 weeks
until the dose of
10 mg is reached
Dose maintained on
alternate days and
reduced by 5 mg
every 2 weeks, then
stopped
40Bullous pemphigoid
Clobetasol propionate
20 -40 mg/day is more
effective for the treatment.
JIAOMR, April-June 2011;23(2):128-131
41Lichen planus
Prednisolone
1mg/kg/d for <7
days
Tapered to
10-20mg per day
for 2 weeks
Burkit’s Oral Medicine, 11th edition
JIAOMR, April-June 2011;23(2):128-131
42Lupus erythematosus
Predisolone – 20
- 30 mg/day for
2- 6 weeks
Tapered
gradually
Steroids in the treatment of benign
lesions
43
CENTRAL GIANT CELL GRANULOMA
HEMANGIOMA
44CGCG
Intralesional injection of triamcinolone
can be given in a dose of 1 to 2 mg/kg/d
(maximum of 60 mg).
The treatment interval at 4 to 6 weeks.
Hemangioma 46
Prednisone at a dose of 20-30
mg/d can be given for 2 weeks
to 4 months
( Fost and Esterly)
Intralesional triamcinolone
acetonide (4 mg/mL)
(Hawkins et al)
47
Steroids in salivary gland disorders
MUCOCELE
48Mucocele
 0.05% clobetasol
propionate 3 times a
day for 4 weeks in a
mucosal adhesive base.
 Intralesional injections
51
Steroids in neuralgia
POST HERPETIC
NEURALGIA
52Post herpetic neuralgia
To reduce incidence of post herpetic neuralgia:
 Prednisolone 20 to 30 mg/day for 7 – 10 days
tapered to 10 mg/day for 1 week
(Treatment of oral diseases, George Lascaris)
54
Steroids for TMJ disorders
OSTEOARTHRITIS
RHEUMATOID ARTHRITIS
55
Rheumatoid
arthritis
Intraarticular injection –
10 to 40 mg/ml
osteoarthritis
Intraarticular injection –
20 mg/ml(2 injections 14
days apart)
Arthritis
56
Miscellaneous
OSMF
57OSMF
Predisolone – 20
- 30 mg/day for
2 – 4 weeks
Gradually taper
Discontinue in 1-
2 months
58
Injections of triamcinolone 10mg/ml diluted
in 1 ml of 2% lidocaine with hyaluronidase 1500
IU, biweekly for 4 weeks.
(Borle et al)
dexamethasone (4mg/ml) and
two parts of hyaluronidase,
diluted in 1.0 ml of 2%
xylocaine.
59Adverse effects
Due to extention of pharmacological action occuring
with prolonged therapy
Mineralocorticoids:
 Sodium and water retention
 Edema
 Hypokalemic alkalosis
 Progressive rise in B.P
 Fluid and electrolyte disturbance
60Glucocorticoid:
Metabolic effects:
 Hyperglycemia
 Ketoacidosis
 Hyperosmolar coma
 Hypophosphatemia
61
Cushing’s Habitus:
Prolonged therapy causes
 Central obesity with moon face
 Buffalo hump
 Pink florid striae are liable to appear on the
abdomen, hips and pectoral region and skin may
become friable
62
CVS and renal system:
 Hypertension
 Salt and water retention
 Hypokalemic alkalosis
CNS:
 Influence mood, sleep pattern
 Insomnia
 Acute psychotic reactions
 Benign intracranial hypertension
 Epilepsy
63
Suppression of inflammation and immune response:
 Latent infection may flare
 Oppurtunistic infection with low grade pathogens
Retardation of linear growth:
 Occurs in children who receive more than 50 mg
of cortisone per day.
Relative Contraindications: 64
 Peptic ulcer
 Diabetes mellitus
 Hypertension
 Pregnancy
 Herpes simplex
keratitis
 Tuberculosis
 Osteoporosis
 Psycosis
 Epilepsy
 Renal failure
65Adrenal crisis
Causes
Sudden withdrawal of
glucocorticoid treatment
Rule of 2
Adrenocortical suppression should be suspected if a patient
has received Glucocoticoid therapy through two of the
following methods
 In a dose of 20 mg or more of cortisone or its equivalent
 Via oral or parenteral route or a continuous period of 2
weeks or longer
 Within 6 months -2 years of therapy
66
Medical emergencies in dental office, Stanley F.Malamed
Complications in Anesthesia - John L. Atlee; Page-132
Drug interactions 67
Glucocorticoid dosage decreased:
 Antibiotics (Erythromycin)
 Cyclosporine
 Isoniazid
 Ketakonazole
 Estrogen
Reduce metabolic
clearance
THANK YOU
68

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Steroids in dentistry

  • 1. 1 PRESENTED BY Dr. E. RAMNATH DEPARTMENT OF PERIODONTOLOGY
  • 2. History  By the middle of 19th century it was demonstrated that adrenal glands were essential for life  Later, it was appreciated that the cortex was more important than the medulla  A number of steroidal active principles were isolated and their structures were elucidated by kendall and his coworkers in the 1930s. 2
  • 3.  However, the gate to their great therapeutic potential was opened by Hench (1949) who obtained striking improvement in rheumatoid arthritis by using cortisone.  The nobel prize was awarded the very next year to kendall and Hench.  Currently, corticosteroids are drugs with one of the broadest spectrum of clinical utility. 3
  • 4. Functional anatomy and histology of adrenal glands  4
  • 5. 5
  • 6. 6
  • 7. 7 Zones of adrenal cortex Hormones Zona glomerulosa Aldosterone Desoxycorticosterone Zona fasciculata Cortisone Cortisol Zona reticularis Dehydroepiandrosterone Androstenidione Traces of estrogens Essentials Of Medical Physiology 3rd Edition, K Sembulingam
  • 8. 8 MECHANISM OF ACTION plasma memb Corticosteroids CYTOPLASMIC RECEPTOR PROTEIN GLUCOCORTICOID RESPONSE ELEMENT Nucleus Transcription of m - RNA New protein synthesis TOTAL TIME 30 – 60 mins
  • 9. On resistance to stress 9 Physical or mental stress Increases ACTH Increase in glucocorticoid secretion High resistance to body against stress GOODMAN & GILMAN'S THE PHARMACOLOGICAL BASIS OF THERAPEUTICS - 11th Ed. (2006)
  • 10. Steroids in Dentistry  Used primarily to decrease postoperative edema and manage oral inflammatory diseases 10
  • 11. Classification of steroids based on their relative activity 11 Mineralocorticoids • Desoxycorticosterone acetate(DOCA) • Fludrocortisone • Aldosterone
  • 12. Classification of steroids based on their relative activity 12 Short acting (t1/2 < 12 hr) • Hydrocortisone • Cortisone Intermediate acting: (t1/2 12 – 36) • Prednisole • Methyl prednisole • Triamcinolone Long acting: (t1/2 > 36 hrs) • Paramethasone • Dexamethasone • Betamethasone
  • 13. 13 Cortisone Oral: 5, 10, 25 mg tablets Parentral:22,25 mg of solution
  • 15. 15 Prednisolone Oral:5,10, 20 mg tablets, 15mg/5 ml syrup, 5mg suspension as pediatric drops Parenteral:25,50 mg IM,IV,Intralesional
  • 16. Triamcinolone Oral:1,4,8mg syrup Topical:0.1% eye drops, ointment Parentral: 3,10,40 mg for I.M, intraarticular, intralesional injections 16
  • 17. 17 Dexamethasone Oral:0.25,0.5,0.75,1,2,4,6mg tablets Topical:0.1% eye drops, ear drops, skin ointment Parenteral: 4,8,10,20 mg for IV, IM, intralesional and intraarticular.
  • 18. 18 Betamethasone Oral: oral drops – 0.5 mg/ ml, tablets – 0.5 to 1 mg. Topical – 0.1% eye drops, ointment,0.05% nasal drops, 0.12% skin creams Parenteral:4 mg/ml for IM, IV, intralesional, intraarticular
  • 19. ADMINISTRATION OF STEROIDS  TOPICAL  SYSTEMIC  INTRA - LESIONAL 19
  • 20. Protocols for use -(TC)  POTENCY  RELIEF 20 JDR April 2005 vol. 84 no. 4 294-301
  • 21. 21 short course of TCs Accelerate remission without adverse effects Recurrent aphthous stomatitis (RAS), some cases of erythema multiforme (EM), and Drug-induced ulceration. TCs must be used for longer, less predictable periods Severe RAS, Erosive oral lichen planus (OLP), specific forms of EM, and mucous membrane pemphigoid (MMP) Scully et al., 1999; Chan et al., 2002 Criteria for use topical and systemic
  • 22. 22 very severe cases of ulceration Short course of systemic corticosteroids followed by maintenance regimen of TCs and or can also be started simultaneously with the systemic therapy Pemphigus vulgaris ,10-30% of Pemphigoid patients, Erosive lichen planus Inevitably be treated with systemic corticosteroids and/or other immunosuppressant therapies Laskaris and Angelopoulos, 1981; Nisengard and Neiders, 1981; Fine et al., 1984; Domloge-Hultsch et al., 1994; Dayan et al., 1999
  • 23. The key factors 23 JDR April 2005 vol. 84 no. 4 294-301 The specific diagnosis The severity of the oral disease The presence or absence of extra-oral lesions The medical history of the patient
  • 24. Factors that influence the effectiveness of TCs: 24 JDR April 2005 vol. 84 no. 4 294-301 The intrinsic potency of the drug
  • 25. Factors that influence the effectiveness of TCs: 25 JDR April 2005 vol. 84 no. 4 294-301 The contact time between the drug and lesion and the vehicle used to apply it;
  • 26. Factors that influence the effectiveness of TCs: 26 JDR April 2005 vol. 84 no. 4 294-301 Concentration
  • 27. Success of a topical medicine 27 Two main factors Number of applications per day High-potency (2-3 times) Low potency (5-10 times) The vehicle used Various vehicles JDR April 2005 vol. 84 no. 4 294-301
  • 28. Various vehicles. 28 JDR April 2005 vol. 84 no. 4 294-301 Orabase (Stoy, 1966), Cyanoacrylate (Jasmin et al., 1993), Bioadhesive patches made of cellulose derivatives (Mahdi et al., 1996), Gels (Regezi and Sciubba, 1999), and Denture adhesive paste (Lo Muzio et al., 2001).
  • 29. Steroids as anti- inflammatory 29 Prevention of postoperative pain, edema, trismus after 3rd molar surgery Prevention of postoperative edema after orthognathic surgery TREATING alveolar osteitis
  • 30. 30 Phospholipids Arachidonic acids lipoxygenase Cylo - oxygenase Leukotriene Prostaglandins, Thromboxane Prostacyclins Phospholipase A2 Lipocortin Corticosteroids
  • 31. Steroids as intra-canal medicaments  Ledermix  triamcinolone acetonide + demeclocycline. 31 Journal of Interdisciplinary Dentistry / May-Aug 2014 / Vol-4 / Issue-2
  • 32. Corticosteroids in auto immune disorders and other aids 32 • Eg: Erosive LP • RAS Ulcerative, Vesiculoerosive diseases • Eg: CGCG • HemangiomaBenign lesions • Eg: Mucocele Salivary gland disorders • Eg: Osteoarthritis • Rheumatiid arthritisTMJ Disorders • Eg. Post herpatic neuralgia Neuralgia Treatment • OSMF Miscellanous
  • 33. Systemic steroids for ulcerative vesiculobullous diseases 33
  • 34. major aphthae or severe multiple minor aphthae  Prednisone therapy should be started at 1.0 mg/kg/day in patients with severe RAU and should be tapered after 1 to 2 weeks. 34
  • 35. 35 Minor EM 20 – 40 mg/day for 4 – 6 days / PREDNISOLONE Severe or rapidly progressing lesions 60 mg/day slowly tapered by 10 mg/day over 6 weeks Erythema multiforme
  • 36. Pemphigus Vulgaris  Mainstay 1-2mg/kg/d.  Initial dose of treatment – 0.5 mg/kg/day to 3 mg/kg/d  Dose that achieves clinical control is maintained for 2- 3 weeks and then gradually tapered. 36 Burkit’s Oral Medicine, 11th edition
  • 37. Pulse therapy  Also called short term therapy  High dose therapy involves a 48-72 hrs course of intensive steroid administration  Single i.v injection of a supra-physiological dose of steroid  Dose of 0.5-2g of prednisolone or equivalent 37
  • 38. 39Cicatricial pemphigoid Predisolone – 30 to 60 mg/day 2-3 weeks to stop new bullae formation Tapered by 20% every 2-3 weeks until the dose of 10 mg is reached Dose maintained on alternate days and reduced by 5 mg every 2 weeks, then stopped
  • 39. 40Bullous pemphigoid Clobetasol propionate 20 -40 mg/day is more effective for the treatment. JIAOMR, April-June 2011;23(2):128-131
  • 40. 41Lichen planus Prednisolone 1mg/kg/d for <7 days Tapered to 10-20mg per day for 2 weeks Burkit’s Oral Medicine, 11th edition JIAOMR, April-June 2011;23(2):128-131
  • 41. 42Lupus erythematosus Predisolone – 20 - 30 mg/day for 2- 6 weeks Tapered gradually
  • 42. Steroids in the treatment of benign lesions 43 CENTRAL GIANT CELL GRANULOMA HEMANGIOMA
  • 43. 44CGCG Intralesional injection of triamcinolone can be given in a dose of 1 to 2 mg/kg/d (maximum of 60 mg). The treatment interval at 4 to 6 weeks.
  • 44. Hemangioma 46 Prednisone at a dose of 20-30 mg/d can be given for 2 weeks to 4 months ( Fost and Esterly) Intralesional triamcinolone acetonide (4 mg/mL) (Hawkins et al)
  • 45. 47 Steroids in salivary gland disorders MUCOCELE
  • 46. 48Mucocele  0.05% clobetasol propionate 3 times a day for 4 weeks in a mucosal adhesive base.  Intralesional injections
  • 47. 51 Steroids in neuralgia POST HERPETIC NEURALGIA
  • 48. 52Post herpetic neuralgia To reduce incidence of post herpetic neuralgia:  Prednisolone 20 to 30 mg/day for 7 – 10 days tapered to 10 mg/day for 1 week (Treatment of oral diseases, George Lascaris)
  • 49. 54 Steroids for TMJ disorders OSTEOARTHRITIS RHEUMATOID ARTHRITIS
  • 50. 55 Rheumatoid arthritis Intraarticular injection – 10 to 40 mg/ml osteoarthritis Intraarticular injection – 20 mg/ml(2 injections 14 days apart) Arthritis
  • 52. 57OSMF Predisolone – 20 - 30 mg/day for 2 – 4 weeks Gradually taper Discontinue in 1- 2 months
  • 53. 58 Injections of triamcinolone 10mg/ml diluted in 1 ml of 2% lidocaine with hyaluronidase 1500 IU, biweekly for 4 weeks. (Borle et al) dexamethasone (4mg/ml) and two parts of hyaluronidase, diluted in 1.0 ml of 2% xylocaine.
  • 54. 59Adverse effects Due to extention of pharmacological action occuring with prolonged therapy Mineralocorticoids:  Sodium and water retention  Edema  Hypokalemic alkalosis  Progressive rise in B.P  Fluid and electrolyte disturbance
  • 55. 60Glucocorticoid: Metabolic effects:  Hyperglycemia  Ketoacidosis  Hyperosmolar coma  Hypophosphatemia
  • 56. 61 Cushing’s Habitus: Prolonged therapy causes  Central obesity with moon face  Buffalo hump  Pink florid striae are liable to appear on the abdomen, hips and pectoral region and skin may become friable
  • 57. 62 CVS and renal system:  Hypertension  Salt and water retention  Hypokalemic alkalosis CNS:  Influence mood, sleep pattern  Insomnia  Acute psychotic reactions  Benign intracranial hypertension  Epilepsy
  • 58. 63 Suppression of inflammation and immune response:  Latent infection may flare  Oppurtunistic infection with low grade pathogens Retardation of linear growth:  Occurs in children who receive more than 50 mg of cortisone per day.
  • 59. Relative Contraindications: 64  Peptic ulcer  Diabetes mellitus  Hypertension  Pregnancy  Herpes simplex keratitis  Tuberculosis  Osteoporosis  Psycosis  Epilepsy  Renal failure
  • 60. 65Adrenal crisis Causes Sudden withdrawal of glucocorticoid treatment
  • 61. Rule of 2 Adrenocortical suppression should be suspected if a patient has received Glucocoticoid therapy through two of the following methods  In a dose of 20 mg or more of cortisone or its equivalent  Via oral or parenteral route or a continuous period of 2 weeks or longer  Within 6 months -2 years of therapy 66 Medical emergencies in dental office, Stanley F.Malamed Complications in Anesthesia - John L. Atlee; Page-132
  • 62. Drug interactions 67 Glucocorticoid dosage decreased:  Antibiotics (Erythromycin)  Cyclosporine  Isoniazid  Ketakonazole  Estrogen Reduce metabolic clearance

Editor's Notes

  1. Mol Cell Endocrinol. 1993 Jul;94(1):111-9.
  2. the key factors that determine the selection of a topical or systemic treatment
  3. It also depends upon the concentration
  4. Logically, the success of a topical medicine depends mainly on the contact time of the drug with the lesion.
  5. TCs have been applied in various vehicles. 2.1 Lotion 2.2 Shake lotion 2.3 Cream 2.4 Ointment 2.5 Gel 2.6 Foam 2.7 Transdermal patch 2.8 Powder 2.9 Solid 2.10 Sponge 2.11 Tape 2.12 Vapor 2.13 Paste 2.14 Tincture
  6. The applications in the field of oral surgery would include, Prevention of postoperative pain, edema, trismus after 3rd molar surgery Prevention of postoperative edema after orthognathic surgery Prevention of alveolar osteitis
  7. Doses of each pulse are not standardized but are usually 500 to 1000 mg methylprednisolone or 100 to 200 mg dexamethasone.
  8. Doses of each pulse are not standardized but are usually 500 to 1000 mg methylprednisolone or 100 to 200 mg dexamethasone.
  9. 1 mg /kg/day for 7 days Followed by reduction of 10mg each subsequent day Burkits 11th edition
  10. Normal HPA suppression recovery may take time to 30 days to 12 month But according to the guideline given by John L. Atlee it is considered normal to return in 6 months