Circulatory Shock, types and stages, compensatory mechanisms
How to master Steroid (glucocorticoids) prescription, different scenarios, case based approach Ahmed Yehia Ismaeel, MD Beni-Suef
1. How to master
Steroid prescription,
different scenarios,
case-based approach
Ahmed Yehia, MD, Internal Medicine
(Immunology, Allergy & Rheumatology)
Beni-Suef
4. • A 30-year-old lady presented to me
with unilateral hip pain & limping.
• On probing, she admitted taking
steroids for > 1 year to gain weight.
• What is the likely hip pathology?
• How to assess?
12. Glucocorticoids (GC) adverse effects
High doses of
glucocorticoids for a
few days
• can be administered
with little risk.
Chronic therapy
• Glucocorticoids
cannot be given
chronically without
the risk of adverse
effects.
13. هل دكتور يا طيب
مشاكل؟ يعمل ممكن
Glucocorticoids cannot be
given chronically without the
risk of adverse effects.
16. Case
A 42-year-old female
with systemic lupus
erythematosus (SLE)
was prescribed
prednisolone 10 mg.
How to monitor
steroids for bone
adverse effects (AE)?
22. Let’s start our journey.
Case for discussion
• A 75 years old female patient presents with
acute severe headache, scalp tenderness, jaw
& tongue claudication & diplopia. The patient
also has bilateral shoulder & hip pain &
stiffness.
• What is the best next step?
24. ESR: 1st H.: 80 mm
CRP: +ve, 96 mg/dl
Temporal artery ultrasound?
Eye examination?
What is the expected cause of bilateral
shoulder & hip pain & stiffness?
29. High dose oral steroids.
What is the dose?
Which preparation?
30. What is low-dose, medium-dose & high-dose
daily prednisone therapy?
Very high dose >100 mg/day.
High dose ≥40 mg/day to 100 mg/day (2 mg/kg/day in children).
Medium dose 7.5 mg/day to <40 mg/day.
Low dose ≤7.5 mg/day.
31. When to give the
steroid dose?
Because natural
cortisol secretion has
a circadian rhythm
with the peak in the
morning, taking the
CS before ~ 10:00
am will result in less
suppression of the
hypothalamic–
pituitary–adrenal
(HPA) axis. When
taking CS long term
this probably is less
important.
36. • So, patients with severe liver disease may have
difficulty converting prednisone to prednisolone;
in such patients, it is possible that one might not
get the same effect from prednisone as from
prednisolone.
• Certain drug interactions can affect the
metabolism & bioavailability of prednisone. As an
example, barbiturates, phenytoin, or rifampin
attenuate the biologic effects of GCs by enhancing
their metabolism
37. While the patient is on 40 mg prednisone, she
developed vomiting & diarrhea with fever &
she can’t take her steroid. How can you
manage this situation?
• Treat the gastroenteritis as appropriate.
• Shift to IV steroids.
• Which preparation? What is the dose?
39. Should we decrease the
dose due to infection?
Doses need to be
increased at times of
serious intercurrent
illness (defined as
presence of a fever),
accident & stress.
Double doses should
be taken during
these periods.
43. • Potent synthetic glucocorticoids(eg, prednisone,
methylprednisolone, & dexamethasone) have little
mineralocorticoid, androgenic, or estrogenic activity.
• As a result, the major systemic side effects are those of suppression
of hypothalamic-pituitary-adrenal (HPA) function and Cushing's
syndrome. The time required to develop these complications
depends upon the dose and duration oftherapy and varies among
patients, probably because of differences in their rates of
glucocorticoid metabolism.
44. The mode of action of GCs
Genomic
• interactions between
the glucocorticoid
receptor & genomic
DNA
Nongenomic
• in high dosages.
45. Now after 1 month, the patient started
to feel better. How will you proceed?
• Follow up ESR 60 mm
• Follow up CRP 5 mg/dl
–Which one to follow: ESR or CRP?
46. After normalization of symptoms, ESR & CRP (usually takes
1 month) on prednisone at 30 mg twice a day,
The following tapering schedule can be tried:
• Taper the dose by 5 mg /1 to 2 weeks to 30 mg/day.
• -- the dose by 2.5 mg /1 to 2 weeks to 15 mg once a day.
• Further taper the dose by 2.5 mg /4 weeks to 10 mg daily.
• Decrease the dose by 1 mg /4 weeks until the patient is
off prednisone.
Clinical symptoms and CRP should be monitored for every
taper in dose. Spontaneous recurrences occur in up
to 50% of cases. Up to 40% of patients (especially women)
need corticosteroid therapy for years.
48. • While on 40 mg prednisolone, the patient
developed epigastric pain & nausea, so he
stopped the treatment till he meets you the
next week. 3 days later, he developed severe
vomiting, asthenia, you found BP to be 80/40.
RPG: 48mg/dl.
• How to proceed?
50. • After 3 months off steroids which she had
taken for 2 years, the patient developed a
picture of typical appendicitis, the
surgeon consults you for any
precautions for surgery?
51. Any patient who:
1. is Cushingoid in appearance,
2. has received > 20 mg of daily prednisone for > a month in
the preceding year,
3. or has been on > 3 to 5 mg for
> a year
should be considered to have a
potentially suppressed HPA axis.
52. Full recovery of the HPA axis may take
• 6 to 9 months after stopping GC therapy. The
responsiveness of the adrenal gland to stress
can be tested with a short ACTH (Cortrosyn)
stimulation test.
53. • Any patient who was on long term
steroids if faced with stress should
receive stress dose steroids during the
12 months after steroid withdrawal or
do ACTH stimulation test.
54. Case
A 25 years old
female patient
presenting with
severe hypotension.
What is the best
steroid in acute
hypotension in the
ED?
58. Case
A 30 years old female patient with lupus nephritis class II,
proteinuria 700 mg, arthritis was admitted & the resident
consulted you to give pulse Solumedrol 1 gm IV for 3 days.
What is your opinion?
59. EULAR recommendations for the management of
systemic lupus erythematosus: 2023
1. Hydroxychloroquine is recommended for all patients
(1b/A), unless contraindicated, at a target dose of 5
mg/kg real body weight/day (2b/B) but individualised
based on risk for flare (2b/B) and retinal toxicity.
2. Glucocorticoids, if needed, are dosed based on the
type & severity of organ involvement (2b/C).
60. • She is well-controlled on HCQ 400 mg daily &
prednisolone 15 mg daily.
• How to manage her GC dose?
• Withdraw.
61. أوقف ممكن هل
يا الكورتيزون
دكتور؟
?????
She is still in remission while withdrawing
prednisolone to 2.5 mg daily.
62. EULAR recommendations for the management of
systemic lupus erythematosus: 2023
2. Glucocorticoids, if needed, are
dosed based on the type &
severity of organ involvement
(2b/C) & should be reduced to
maintenance dose of ≤5 mg/day
(prednisone equivalent) (2a/B) &,
when possible, withdrawn.
64. EULAR recommendations for the management of
systemic lupus erythematosus: 2023
In patients with moderate-to-severe disease, pulses of intravenous
methylprednisolone (125–1000 mg/day, for 1–3 days) (3b/C) can be
considered.
3. In patients not responding to hydroxychloroquine (alone or in
combination with glucocorticoids) or patients unable to reduce
glucocorticoids below doses acceptable for chronic use, addition of
immunomodulating/immunosuppressive agents (eg, methotrexate (1b/B),
azathioprine (2b/C) or mycophenolate (2a/B)) and/or biological agents (eg,
belimumab (1a/A) or anifrolumab (1a/A)) should be considered.
65. While in remission,
she developed
generalized
puffiness & HTN.
Urine: glomerular
hematuria &protein
++++
Urine protein
creatinine ratio
4000 mg/gm.
S. creatinine rises
rapidly over days: 1
1.5 2 2.3
mg/dl.
What to do? Renal biopsy.
66. EULAR recommendations for the management
of
systemic lupus erythematosus: 2023
In patients with moderate-to-
severe disease, pulses of
intravenous methylprednisolone
(125–1000 mg/day, for 1–3 days)
(3b/C) can be considered.
67. EULAR recommendations for the management
of
systemic lupus erythematosus: 2023
8. Patients with active proliferative lupus nephritis
should receive low-dose (EuroLupus) IV
cyclophosphamide (1a/A) or mycophenolate (1a/A) &
GCs (pulses of IV methylprednisolone followed by
lower oral doses); combination therapy with
belimumab (either with cyclophosphamide or
mycophenolate (1b/A)) or calcineurin inhibitors
(especially voclosporin or tacrolimus, combined with
mycophenolate, 1b/A) should be considered.
68. Case
• A 22-year-old female with SLE presents with
flare of skin disease while on
hydroxychloroquine 400 mg daily. No other
organ is affected now.
• How to manage?
69. EULAR recommendations for the management
of
systemic lupus erythematosus: 2023
5. Treatment of active skin disease should include
topical agents (glucocorticoids, calcineurin inhibitors)
(2b/B), antimalarials (hydroxychloroquine, chloroquine)
(1a/A), &/or systemic
glucocorticoids (4/C) as needed.
70. Her skin didn’t improve on topical
treatment & HCQ 400 mg daily,
so, we added 10 mg prednisolone
daily & she improved but she
relapses with any trial of
prednisolone withdrawal.
How to manage?
71. EULAR recommendations for the management
of
systemic lupus erythematosus: 2023
3. In patients not responding to HCQ (alone or in
combination with GCs) or patients unable to reduce GCs
below doses acceptable for chronic use,
addition of immunomodulating/immunosuppressive
agents (eg, methotrexate (1b/B), azathioprine (2b/C) or
mycophenolate (2a/B)) &/or biological agents (eg,
belimumab (1a/A) or anifrolumab (1a/A)) should be
considered.
72. EULAR recommendations for the management
of
systemic lupus erythematosus: 2023
5. Treatment of active skin disease should include
topical agents (glucocorticoids, calcineurin inhibitors)
(2b/B), antimalarials (hydroxychloroquine, chloroquine)
(1a/A), and/or systemic glucocorticoids (4/C) as needed,
with methotrexate (1b/B), mycophenolate (4/C),
anifrolumab (1a/A), or belimumab (1a/B) considered
as second-line therapy.
73. A
steroid
sparing
drug While steroids are effective in rapidly
suppressing inflammation, their long-
term use can lead to various side effects
A medication used to treat chronic
inflammatory conditions while aiming to
reduce the reliance
on glucocorticoid
use or
minimize the
dosage needed.
74. DMARDs Usual Time to Effect
• as early as 4 to 6 weeks
MTX
• relatively rapid within 4-8 weeks
Leflunamide
• It may take 6 weeks to 3 months to see the
effects.
Sulfasalazine
• 2 to 4 months is usual. Most agree that if no
response after 5-6 months, consider HCQ failure.
Hydroxychloroquine
• rapid onset of action sometimes with
improvements seen within 2 to 4 weeks
TNF inhibitors
Why not to use the steroid sparing alone from the start?
75. Case
A 30 years old male patient with
lupus nephritis class II,
proteinuria 700 mg, arthritis
presented for severe flare of RT
knee arthritis & the resident
consulted you to give pulse
Solumedrol 1 gm IV for 3 days.
What is your
opinion?
What do you
recommend
considering that
he is diabetic?
76. Synovial fluid analysis
for 3 C
• TLC 250
• Culture: negative.
– Pain and effusion
persisted.
– What will you do?
79. Does local steroid injection
affect diabetes mellitus control?
• A steroid produces a hyperglycemic
effect that lasts for at least 5 days
after a local injection. Check the
patient’s blood glucose/ 4 to 6 hours
& adjust the doses as needed for 5 to
7 days postinjection.
80. Case
A 20-year-old RA patient on MTX 25 mg
weekly presented with moderate
disease activity with tender joint count 6
& swollen joint count 5.
She has no poor prognostic factors.
How to manage?
81.
82. • 6. Short-term glucocorticoids should be considered when initiating
or changing csDMARDs, in different dose regimens & routes of
administration, but should be tapered & discontinued as rapidly as
clinically feasible. (1a A 9.3±1.2 92)
84. Initiation of a csDMARD without short-term (<3 months) GCs is
conditionally recommended over initiation of a csDMARD with short-
term GCs for DMARD-naïve patients with moderate-to- high disease
activity.
Initiation of a csDMARD without longer term (≥3
months) GCs is strongly recommended over initiation of
a csDMARD with longer-term GCs for DMARD-naïve
patients with moderate-to-high disease activity
85. Case
A 20-year-old RA patient on
MTX 25 mg weekly presented
with low disease activity with
only right wrist tender hot red
swelling. CRP: 48 mg/l.
She has no poor
prognostic factors.
How to manage?
86. • Intralesional & intra-
articular injections of a
glucocorticoid can be very
effective & the risk of
causing a local bacterial
infection is very low.
87. • An ICU patient with
lymphoma on
chemotherapy on NPO (nil
per os) complains of severe
left big toe pain for 6 hours.
During examination, he was
found to have podagra and
serum urate 11 mg/dl. How
to manage him?
IV glucocorticoid
IM glucocorticoids
Intra-articular glucocorticoids
Arthrocentesis only with fluid analysis
88. •An ICU patient on NPO (nil
per os) complains of
severe left knee pain for 6
hours. During
examination, he was found
to have acute
monoarthritis & serum
urate 8 mg/dl. How to
manage his arthritis?
IV glucocorticoid
IM glucocorticoids
Intra-articular glucocorticoids
Arthrocentesis only with fluid analysis
89. Acute monoarthritis is septic until
proven otherwise.
Cells (WBCs)
Culture & sensitivity
Crystals by polarized
microscopy
•The 1st step is Arthrocentesis with fluid
analysis for 3C
90. We suggest arthrocentesis &
intraarticular injection of GCs in patients
who (Grade 2C).
are unable to take oral
medications &/or
have only one or two actively
inflamed joints
infection has been excluded.
91. We prefer Triamcinolone acetonide
large joint [eg,
knee]
40mg
medium joint
[eg, wrist, ankle,
elbow]
30 mg
small joint
10 mg
or equivalent doses of methylprednisolone acetate.
92. Case
A 20-year-old SLE patient got
pregnant while on
hydroxychloroquine 300 mg/day,
prednisolone 20 mg /day &
azathioprine 100 mg/day.
She is in remission.
What else to screen for
other than disease
activity?
93. • If SLE or SLE-like disease, SS, SSc, or
RA: Test once (early) for anti-Ro/SSA &
anti-La/SSB. (Strong)
99. Case
A 20-year-old SLE patient got
pregnant while on
hydroxychloroquine 300 mg/day,
prednisolone 20 mg /day &
azathioprine 100 mg/day.
She is in remission.
Anti-Ro, anti-La are
negative.
How to manage?
102. Low to moderate doses of prednisolone during
pregnancy appear to be safe.
103. Steroid target in pregnancy
• cross the placenta.
Fluorinated
glucocorticoids, such as
dexamethasone &
betamethasone
• largely metabolized before
they reach the fetus.
Low-to-moderate–dose
nonfluorinated
glucocorticoids, such as
prednisone & prednisolone
104. The concept of health care value
clinical
benefit costs & harms
For a given
intervention
105. • The goal of glucocorticoid therapy, as
with any therapy, is to obtain
maximum benefit with minimum
adverse side effects.
110. Case
• A 40 years old female patient
with ITP resistant to steroids and
is planned for splenectomy.
• Vaccines??
111. • Vaccination against S. pneumoniae, H.
influenzae type b & N. meningitidis,
– ideally at least 2 weeks prior to surgery
• Repeat vaccination against S. pneumoniae/5 y,
annual influenza vaccine
• Education about the risk of postsplenectomy
sepsis.
112. Our GCA patient improved &
discharged with the tapering schedule.
• In one of the follow up visits, the patient
complains of polyurea, polydipsia and
nocturia.
• You request plasma glucose screening.
• FPG: 200 mg/dl
• 2H ppPG: 260 mg/dl.
• What have happened?
• How to proceed?
113. Steroid & DM
• Steroid treatment in people
without pre-existing diabetes may
result in a rise in glucose,
‘steroid-induced diabetes’.
114. It may or may not resolve when
GCs are withdrawn.
Steroid-induced
DM, will it resolve?
115. Steroid & DM
• Steroid treatment in people with pre-existing
diabetes will undoubtedly result in worsening
glucose control, and this may be termed
‘steroid-induced hyperglycaemia’, and will
• warrant temporary additional, and more
active, glycaemic management.
117. A study of 112 patients with
rheumatoid arthritis (RA)
5 to 10
mg/day
• odds ratio
4.5
10 to15
mg/day
• 32.3
There is a clear dose-dependence of AEs
Odds ratio
Data from Saag, KG, Koehnke, R, Caldwell, JR, et al. Am J Med 1994; 96:115.
118. How to decrease this effect?
Alternate
daily dose.
Use only
when highly
indicated.
Use the
lowest dose
for the
shortest
period.
Monitoring..
Monitoring..
Monitoring..
119. Alternate daily dose
Doubling the dosage &
administering the drug every
other day in the morning
more closely mimics the
endogenous corticosteroid
circadian rhythm.
This form of administration
enables the patient to
experience the therapeutic
effects while side effects are
minimized.
126. The 7 golden rules
1. Prescribe corticosteroids at the lowest possible dose and
discontinue as soon as the disease activity permits.
2. Encourage physical activities and avoid immobilization (helps
prevent myopathy).
3. Implement fall prevention program.
4. Prescribe dietary and supplemental calcium to achieve intake
of 1000-1500 mg/day.
5. Supply vitamin D at a minimum of 1000 international units per
day.
6. Consider bisphosphonate therapy implementation (if >7.5
mg/day for >3 months) particularly if postmenopausal.
(See Chapter 52).
7. Document patient education concerning the adverse effects of
therapy particularly risk of osteonecrosis.
129. Case
• A young male with & recent deep vein
thrombosis with scrotal ulcers but no
oral ulcers.
130. Case
•This 30-year-old lady presents with
recurrent oral ulcers, superficial
thrombophlebitis.
•She was on repeated frequent
doses of oral steroids for her
painful oral ulcers.
•What is your diagnosis?
•What are the labs needed for this
diagnosis confirmation?
132. ISG criteria for BD
Required Criteria (Recurrent oral ulcerations observed by
physician or patient, ≥ 3 times in 1 year: (minor or major
aphthous ulcers or herpetiform ulcers))
Minor
Criteria
Recurrent genital ulceration
(aphthous or scarring) observed by
physician or patient
Eye lesions
observed by
physician
Anterior uveitis Posterior uveitis
Cells in vitreous
on slit lamp
exam
Retinal vasculitis
observed by
ophthalmologist
Skin lesions
present
Erythema
nodosum (patient
or physician)
Pseudo folliculitis
(observed by
physician)
Papulopustular
lesions
(observed by
physician)
Acneiform nodules
(observed by
physician)
Positive pathergy
(Behcetine) test
read by physician
within 24-28 hours
1 required criteria
2 minor criteria
Patient meets
diagnostic criteria for
BD with:
133. ICBD
Ocular lesions 2
Genital aphthosis 2
Oral aphthosis 2
Skin lesions 1
Neurological symptoms 1
Vascular manifestations 1
+ve Pathergy test
*
1
*
*Pathergy test is optional, & the primary scoring system does not include pathergy testing. However, where
pathergy testing is conducted one extra point may be assigned for a positive result.
OGO (2) - BPCC (1)
134. ISG criteria for BD
Required Criteria (Recurrent oral ulcerations observed by
physician or patient, ≥ 3 times in 1 year: (minor or major
aphthous ulcers or herpetiform ulcers))
Minor
Criteria
Recurrent genital ulceration
(aphthous or scarring) observed by
physician or patient
Eye lesions
observed by
physician
Anterior uveitis Posterior uveitis
Cells in vitreous
on slit lamp
exam
Retinal vasculitis
observed by
ophthalmologist
Skin lesions
present
Erythema
nodosum (patient
or physician)
Pseudo folliculitis
(observed by
physician)
Papulopustular
lesions
(observed by
physician)
Acneiform nodules
(observed by physician
in post-adolescent
patients not on
steroids)
Positive pathergy
(Behcetine) test
read by physician
within 24-28 hours
1 required criteria
2 minor criteria
Patient meets
diagnostic criteria for
BD with:
136. Case
•A 10-year-old asthmatic &
allergic rhinitis patient
presented with these oral
white lesions.
•What are important items to
consider in history taking?
137. ICS, systemic GCs or antibiotics
Diabetes Cancer
Human
immunodeficiency
virus (HIV)
Dry mouth Pregnancy
Also, don’t forget.
138. Preventing Oral Thrush
From an Inhaler
Practicing good oral
hygiene is essential
to preventing
thrush.
Rinse your mouth
out with water or
brush your teeth
after every inhaler
use
Brush and floss
regularly
Avoid high sugar
foods or foods that
contain yeast
Stop smoking
139.
140. Case •A 14-year-old female with a
history of comorbid allergic
asthma, eczema &allergic
rhinitis.
141. • The patient is attending the clinic because she has been
experiencing frequent asthma exacerbations. In total, 3
exacerbations in the past year, of which 2 were in the last
6 months. She currently uses rescue medications about 3
to 4 times/week & wakes up due to her asthma at least
once a week.
• Her ICS dose was increased to a medium dose about 10
months ago.
• What is the best next step?
144. • The patient is attending the clinic because she has been
experiencing frequent asthma exacerbations. In total, 3
exacerbations in the past year, of which 2 were in the last
6 months. She currently uses rescue medications about 3
to 4 times/week & wakes up due to her asthma at least
once a week.
• Her ICS dose was increased to a medium dose about 10
months ago & then a high dose approximately 5
months ago.
• What is the best next step?
148. Case
• A 13-year-old boy presented with bilateral knee arthritis.
• His physician prescribed him Betafos (Durafos) ampoule.
• The ampoule relieved the symptoms markedly.
149.
150. Case
A 4-year-old girl presents with 2 months history of
bilateral knee & right wrist arthritis.
What’s the best next step?
Put a D.D. to guide diagnosis plan.
151. Is this rheumatic fever? ASOT 600 800
Mostly no, duration, echocardiography: normal
Is this JIA?
JIA is a diagnosis of exclusion.
So, we requested ESR, CRP, ANA (IF) with titre, rheumatoid factor,
TSH, calcium, s. 25 OH vitamin D. All were non-significant.
156. GC AEs
Displeasing to
patients (eg,
Cushingoid
appearance)
Varying
degrees of
morbidity
Life-
threatening
(eg, serious
infections).
157. Accelerated
reductions in
bone mineral
density
Acute vertebral
collapse
Early cataracts
Cataract
requiring
surgical
extraction
Some AEs may be largely asymptomatic until later
manifestations develop that require medical attention
There is ill-defined mixed sclerotic & lytic lesion of the left femoral head. Additional cortical collapse of the superior aspect of the femoral head is noted with a linear area of lucency below it (crescent sign), measuring around 20mm. No evidence of secondary degenerative changes.
Early recognition of this complication is of imperative importance as the prognosis is affected by the stage of the disease. MRI is more sensitive than plain radiograph for diagnosing in early-stage.
This is a plain radiography from a patient with established osteonecrosis of the right femoral head.
Collapse of the femoral neck, extensive degenerative changes, joint-space narrowing & subchondral sclerosis.
Active disease: New, persistent, or worsening clinical signs and/or symptoms attributed to GCA/TAK and not related to prior damage
A low or maintenance dosage is approximately 0.1 to 0.25 mg per kg per day of prednisone, a moderate dosage is approximately 0.5 mg per kg per day of prednisone, a high dosage is 1 to 3 mg per kg per day of prednisone, and a massive dosage is approximately 15 to 30 mg per kg per day of prednisone
The systemic bioavailability of prednisone is nearly equivalent to that of prednisolone (0.77 to 0.80).
Prednisone itself is biologically inactive, but it is rapidly converted to the active form prednisolone.
These dose relationships only apply to oral or IV administration.
Glucocorticoid potencies may differ greatly following IM or intra-articular administration.
Fludrocortisone is not used for glucocorticoid effects (only for its mineralocorticoid properties)
Remember to consider not just potency but also duration of effect. Dexamethasone typically requires much less frequent dosing due to its very long half-life and duration of action.
Assuming normal cardiovascular function, the following are required:
• 1 L of 0.9% saline should be given over 30–60 min with 100 mg of i.v. bolus
hydrocortisone
• Subsequent requirements are several litres of saline within 24 h (assessing with central
venous pressure line if necessary) plus hydrocortisone, 100 mg i.m., 6-hourly, until the
patient is clinically stable
• Glucose should be infused if there is hypoglycaemia
• Oral replacement medication is then started, unless the patient is unable to take oral
medication: initially, hydrocortisone 20 mg, 8-hourly, reducing to 20–30 mg in divided
doses over a few days
*Potency is expressed in milligram comparisons to cortisol reference
value of 1.
3. Glucocorticoid-induced osteoporosis results from suppressed bone formation, impaired osteocyte
function, and enhanced bone resorption, accounting for the rapid bone loss and disproportionately
low bone strength seen in glucocorticoid-treated patients.
Whether dexamethasone given for fetal first-or second-degree heart block changes outcome is a matter of controversy.
Treatment should be limited to several weeks, depending on response, because of the risk of irreversible fetal and maternal toxicity. Whether dexamethasone improves long-term survival for a fetus with CHB is controversial, but recent analyses do not support its use.
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Survival curves demonstrating the time to development of the firstserious adverse event (ie, the probability of remaining free of anadverse event) in patients with rheumatoid arthritis treated with noor different doses of prednisone.
The preselected adverse effectsincluded in the analysis were fracture, serious infections, gastrointestinal bleed or ulcer, andcataracts. The glucocorticoid-adverse effect association persisted after statistical adjustment forsignificant disease severity factors, such as the presence of rheumatoid nodules and bonyerosions. There are also some data that have suggested that very low doses of glucocorticoids(eg, prednisone <5 mg/day) are associated with fewer adverse effects
The rationale for an alternate-day steroid dosing regimen (often referred to as alternate-day therapy or QOD therapy) stems from several potential benefits it offers compared to daily dosing:
Reduced side effects:
Pituitary-adrenal axis suppression: Daily steroid use can suppress the body's natural production of cortisol, leading to long-term complications like weight gain, mood swings, osteoporosis, and increased susceptibility to infections. QOD dosing allows the hypothalamic-pituitary-adrenal (HPA) axis to partially recover during the off-day, mitigating these side effects.
Overall side effect burden: By reducing the total steroid dose over time, QOD therapy may decrease the incidence and severity of other common side effects like skin thinning, cataracts, and muscle weakness.
Improved therapeutic efficacy:
Pulse therapy effect: Studies suggest that providing the steroid in larger doses every other day might be as effective or even more effective than smaller daily doses for certain conditions. This "pulse therapy" effect may be due to improved receptor sensitivity and reduced receptor downregulation.
Potential disease-modifying effects: In some chronic inflammatory conditions like lupus or inflammatory bowel disease, QOD therapy might have disease-modifying effects beyond just symptom control. However, more research is needed in this area.
Other potential benefits:
Improved patient adherence: Some patients find QOD dosing easier to stick to than daily regimens, leading to better overall treatment outcomes.
Cost-effectiveness: In some cases, QOD therapy can be more cost-effective than daily dosing due to reduced drug use.
However, it's important to remember that QOD therapy is not appropriate for everyone and has its own limitations:
Not suitable for all conditions: QOD may not be as effective for some conditions requiring continuous suppression, such as organ transplantation rejection or severe asthma.
Flare risk: During the steroid-free day, some patients may experience symptom flares, requiring dose adjustments or additional medications.
Monitoring needs: Close monitoring of disease activity and potential side effects is crucial during QOD therapy.
The potency of GC therapy roughly correlates with the duration of hypothalamic–pituitary axis suppression.
Cushingoid facies
Cushingoid facies is the result of exogenous or iatrogenic Cushing syndrome in patients treated
with CS for a long period of time. Patients develop a rounded appearance (moon facies) due to fat
deposits on the sides of the face (Fig. 16.1a, b). Weight gain with fat redistribution such as moon
facies is one of the most common signs of CS use. Nevertheless, moon facies does not always
mean that it is the result of steroid intake. This is a reversible effect and dose-dependent. Usually,
when steroid dose decreases, there is improvement of the signs too. To avoid steroid adverse
effects, the lowest effective dose should be prescribed. In Fig. 16.1b you can also notice the extensive
face telangiectasias (black arrows) as well as hypertrichosis around the mouth which are sideeffects
of prolonged treatment with CS. In Fig. 16.1c, the same patient as in Fig. 16.1a after
minimizing the CS.
Steroid-related skin atrophy
Steroid atrophy or CS-induced dermal atrophy could be the result of topical or systemic CS. In
Rheumatology, systemic treatments are commonly used. Patients on long-term systemic CS usually
present with notable skin atrophy on the upper and lower limbs. Topical CS are absorbed at
different rates depending on the thickness of the stratum corneum and are also dependent of the
form, potency and the content of other agents (e.g. keratolytic agents such as salicylic acid).
In Fig. 16.2, skin atrophy is significant with the characteristic “cigarette paper” appearance and
increased visibility of the vessels. Non-palpable purpuric lesions (black thick arrows) and telangiectasias
are common. Ecchymoses are found in up to one-third of rheumatologic patients treated
with CS, instead of 2% without CS in their treatment. Newer ecchymoses have a more vivid red
colour (black arrows), unlike the old ones, which get a brown colour due to haemosiderin deposition
in the nearby tissue (yellow arrows). Finally, superficial ulcers (black circle) may appear
which are difficult to treat and are prone to bacterial infections.
The sensitivity of the ISG 1990 criteria is 92% with a specificity 97% making it an effective tool to rule in cases. It has been suggested that given the low prevalence of Behcet's disease, a more sensitive criteria ought to be adopted. The International Criteria for Behcet's Disease (ICBD) was created in 2006 and has a more sensitive but less specific tool to mitigate this issue. They both continue to be used in clinical practice and research studies, among others.
A positive pathergy test (PPT) is an optional score in
the ICBD criteria, and therefore, might not be performed
by all clinicians. As such, and considering the fact that
we routinely perform a pathergy test for our patients, we
sought to determine how many patients benefited from
the addition of a PPT. Only two patients had a score of
3 prior to the pathergy test, both of whom had oral and
skin lesions only. In these cases, a PPT added the 1 score
needed to establish a BD diagnosis. In the other 38
patients (95%), a diagnosis of BD was made regardless of
the result of the pathergy test.
ICBD are the latest diagnosis/classification criteria, created by the participation of 27 countries from different parts of the world. The large number of Behcet's disease patients and control patients, from inside and outside of the Silk Road, assures the variability needed to create an international criteria that can work in any country with different ethnicities. The validation of the criteria in the Far East, Middle-East, and Europe demonstrates its validity.
The sensitivity of the ISG 1990 criteria is 92% with a specificity 97% making it an effective tool to rule in cases. It has been suggested that given the low prevalence of Behcet's disease, a more sensitive criteria ought to be adopted. The International Criteria for Behcet's Disease (ICBD) was created in 2006 and has a more sensitive but less specific tool to mitigate this issue. They both continue to be used in clinical practice and research studies, among others.
A positive pathergy test (PPT) is an optional score in
the ICBD criteria, and therefore, might not be performed
by all clinicians. As such, and considering the fact that
we routinely perform a pathergy test for our patients, we
sought to determine how many patients benefited from
the addition of a PPT. Only two patients had a score of
3 prior to the pathergy test, both of whom had oral and
skin lesions only. In these cases, a PPT added the 1 score
needed to establish a BD diagnosis. In the other 38
patients (95%), a diagnosis of BD was made regardless of
the result of the pathergy test.
Steroid acne most often occurs on the chest but may also develop on the face, neck, back and arms.
CS acne folliculitis is a relatively common skin manifestation in patients who receive treatment
with high-dose CS. With high-doses, an abrupt onset of CS acne after 1–2 weeks is observed. This
drug-induced acne may appear as a side effect of short-term or long-term therapy. Usually, it
appears commonly in early-adulthood, but it can appear at any age. Patients with a history of acne
are particularly at risk. The distribution of CS acne folliculitis resembles that of severe acne vulgaris.
The most common affected areas are the chest and back (as in the presented patient), face
and shoulders.
The lesions are relatively uniform in shape and the colour is vivid-red at the beginning which later
turns to a dull-red colour. At a later stage, dome-shaped papules appear (black arrows), sometimes
topped by a soft abscess. Usually they do not scar but a slight scarring may remain after healing.
Steroid acne may clear despite continuing the steroid medication. It usually, however, persists until the steroid medication is discontinued.
Treatment depends on the severity of the condition and its cause.
Acne is often treated with topical antiacne agents and tetracycline (eg doxycycline)
Malassezia folliculitis is treated with a topical antifungal (eg, ketoconazole shampoo) or oral antifungal medication such as itraconazole.
Severe steroid acne may be treated with oral isotretinoin. This is effective for both types of steroid acne.
Approximately 3% of people who use inhaled corticosteroids get thrush.
Oral candidiasis (oral thrush) is a not so uncommon manifestation in immunocompromised
patients. Pseudomembranous and erythematous candidiasis are the most common forms. Some
researchers consider pseudomembranous and erythematous candidiasis stages of the same entity,
because of the fact that an erythematous surface is revealed beneath the pseudomembranes if
wiped away. Sometimes there is minimal bleeding. Any part of the mouth can be affected but it
usually appears on the tongue, buccal mucosae or palate. This is a 56-year old patient on a longterm
CS use and the presence of oral candidiasis.
Asthma medication options: Adjust treatment up and down for individual’s needs
SPEAKERS: Changes in GINA 2023 for adults and adolescents :
Year added at top left, to avoid use of out-of-date versions of GINA figures
Rationale for Track 1 being the preferred regimen has been updated (see details on later slides)
As-needed ICS-SABA (if available) has been added as a reliever option in Track 2 for Steps 3–5, with most of the benefit seen in Step 3
Anti-inflammatory relievers have been identified with an asterisk (see next 2 slides for details)
NOTE: in Step 5, ‘add-on LAMA’ can be combination (triple) or separate inhalers. If a patient is prescribed triple therapy with a non-formoterol LABA, the reliever should be SABA or ICS-SABA (not ICS-formoterol).
Asthma medication options: Adjust treatment up and down for individual’s needs
SPEAKERS: Changes in GINA 2023 for adults and adolescents :
Year added at top left, to avoid use of out-of-date versions of GINA figures
Rationale for Track 1 being the preferred regimen has been updated (see details on later slides)
As-needed ICS-SABA (if available) has been added as a reliever option in Track 2 for Steps 3–5, with most of the benefit seen in Step 3
Anti-inflammatory relievers have been identified with an asterisk (see next 2 slides for details)
NOTE: in Step 5, ‘add-on LAMA’ can be combination (triple) or separate inhalers. If a patient is prescribed triple therapy with a non-formoterol LABA, the reliever should be SABA or ICS-SABA (not ICS-formoterol).
SPEAKERS: Changes for children 6–11 years in GINA 2023
Anti-IL5 (mepolizumab) included in Step 5 as an add-on option for children with severe exacerbation-prone eosinophilic asthma, following publication of the MUPPITS2 study (Jackson et al, Lancet 2022)
Anti-inflammatory relievers are flagged with asterisk
NOTE: ICS doses for children 6–11 years are found in Box 3-14. Doses for MART for children are in Box 3-15
SPEAKERS: Changes for children 5 years and younger in GINA 2023
Step 1: for children with infrequent viral wheezing and no or few interval symptoms, the recommendation has been clarified as “Insufficient evidence for daily controller”. Intermittent should course ICS at onset of viral illness may be considered if the physician is confident that it will be used appropriately
30-years old JIA patient with stunted growth due to steroids. His
height is 148 cm. Depending on the type of JIA, NSAIDs, CS, csDMARDs as well as bDMARDs are used to
reduce inflammation. CS should only be used sparingly because of their undesirable side effects at
younger age in combination with the slower-than-normal growth observed in patients with JIA. In
Fig. 16.4c patient’s hand in more detail showing short digits, whereas in Fig. 16.4d patient’s hand
with a hand of a subject of the same age. Note the short digits of the patient in comparison with a
healthy individual of the same age.