Prednisone induced vaso occlusion
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Transcript of Prednisone induced vaso occlusion
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PHARMACOVIGILANCE CASE
PRESENTATION
Dr. Pranesh PawaskarFirst Year ResidentDept. of PharmacologyL.T.M.M.C. Sion, Mumbai 400022Date : 06/01/2017
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Prednisolone induced vaso - occlusive crisis
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case• Male
• 12 Years
• K/C/O Sickle Cell Anaemia + Thalassaemia
Major.
• Chief Complaints – 4 Episodes Of Convulsion
- Severe Pain In Lower Limbs
&
- Altered Consciousness
-
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Course of reactionPatient is a k/c/o sickle cell anaemia +
thalassemia major since childhood (family history +ve)
.
.Requires periodic blood transfusion
.
.Patient got admitted with
• Excruciating pain in lower limbs (L>R) (since 2/12/16),
• 4 episodes of Convulsions (4/12/16),• Altered Consciousness
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Course of reactionOn 4/12/16
Admitted to Sion hospital Under Dr.MVM in Ward 37
.
.Patient has chronic bone pain but was
exaggerated since one monthOn 6/11/16
For which he was started with T. Prednisolone @ 2 mg/kg/dayPt was continuously taking
T. Prednisolone 60 mg in two divided doses daily
( tapered to 30mg/kg on 4/12/16, 15mg/kg on 12/12/16 and 10mg/kg on 19/12/16 )
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Course of reaction
Treatment at Sion Hospital –
• i.v. fluids. (N.S. with 5% Dextrose).
• Cap. Hydroxyurea 400 mg.
• Inj. Paracetamol 500 mg SOS.
• Inj. Pantoprazole 40mg O.D.
• Inj. Ondansetron 8 mg B.D.
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Investigations• MRI lower limbs –
• s/o Ischaemic changes Left > right.
• MRI Brain –
• S/o Normal vasculature.
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Seriousness of reaction
• Reaction was SERIOUS as it Required
Hospitalisation of patient.
• Patient Recovered And Discharged on 20/12/16
• Diagnosis- Steroid Induced Vaso-occlusive
Crisis.
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Causality assessment
• According to Naranjo Scale score is 4
POSSIBLE
BECAUSE -1) Reasonable time-event relationship.2) De-challenge response positive.
POSSIBLE
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VASO – OCCLUSIVE CRISIS
• The Vaso-occlusive Crisis is caused by
sickle-shaped red blood cells that obstruct
capillaries and restrict blood flow to an
organ.
• Resulting in Ischaemia, Pain, Necrosis, and
often Organ Damage.
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SICKLE CELL DISEASE• Inherited blood disorder.
• Inheritation of 2
abnormal copies of Hb
gene one from each
parent.
• Caused by a mutation in
the beta-globin gene that
changes the sixth amino
acid from glutamic acid
to valine.
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SICKLE CELL DISEASE• It results in an abnormal
haemoglobin found in red
blood cells.
• This leads to a rigid,
sickle-like shape under
certain circumstances.
• Problems in sickle cell
disease typically begin
around 5 to 6 months of
age.
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SICKLE CELL DISEASE• A number of health problems may develop,
such as attacks of pain ("Sickle-cell
Crisis"), Anaemia, Bacterial Infections,
And Stroke.
• Long term pain may develop as people get
older.
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CAUSES OF VASO-OCCLUSIVE CRISIS
• Infections• Severe dehydration• Exposure to very high or very low temperatures, or rapid change in temperature.• High altitudes, where oxygen levels are low• Drugs
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PREDNISOLONE
• Prednisolone is a Steroid Medication used to
treat certain types of Allergies, Inflammatory
Conditions, Autoimmune Disorders
• Some of these conditions include
Adrenocortical Insufficiency, High Blood
Calcium, Rheumatoid Arthritis, Dermatitis, Eye
Inflammation, Asthma, And Multiple Sclerosis
• It is use by oral,intravenous injection, as a
skin cream, and as eye drops.
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PHARMACOLOGY
• Absorption duration – 18 -36
hr
• Protein bound 65-91 %
• Vd = 0.22 – 0.7 L/kg
• Extensively metabolised in
liver
• Half – Life = 3 hr
• Excretion = Urine
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USES
ADULT
• Rheumatoid Arthritis
• Multiple Sclerosis
• Acute Exacerbation of
COPD
• Bells Palsy
PAEDIATRIC
• Inflammation
• Acute Asthmatic
Exacerbation
• Nephrotic Syndrome
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ADVERSE EFFECTS
• Acne
• Adrenal Suppression
• Diabetes Mellitus
• Menstrual Irregularity
• Myopathy
• Neuritis
• Peptic ulcer
• Osteoporosis
• Psychosis
• Weight Gain
• Seizures
• Vertigo
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INTERACTIONS
• Mifepristone
• Live Vaccines
• Ketoconazole, Cimetidine
• Erythromycin, Carbamazepine, Rifampin
• Aceclofenac, Aspirin, Ibuprofen
• Heparin, Liraglutide
• Serolimus, Tacrolimus
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MECHANISM BEHIND VASO-OCCLUSIVE CRISIS
• The potential mechanism(s) involved in systemic
steroid-induced vaso-occlusion is unclear.
• Bone marrow infarction and likely associated
Fat Embolism may have contributed to the
adverse events.
• There is a well-documented association of
corticosteroid therapy and Bone Marrow
Necrosis.
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Mechanism Behind Vaso-occlusive Crisis
• Additionally, we speculate that Steroid-induced
Leucocytosis could be another potential factor.
• High WBC counts in steady state have been linked
to worse clinical course, and Polymorphonuclear
Leukocytes appear to play an active role in vaso
-occlusive crises.
• Granulocytes or Stimulating Agents have been
associated with the apparent triggering of
sickle-related crises and multiorgan failure in
isolated case reports.
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MECHANISM BEHIND VASO-OCCLUSIVE CRISIS
1. A patient with Hemoglobin-S/C Disease who
developed fatal sickle cell crisis after
receiving Granulocyte Colony Stimulating Factor
was also on daily Dexamethasone.
2. Severe complications were observed in ten of
the 16 patients (62%). Eight patients
experienced severe vaso-occlusive events (VOE)
within the 2 months following the initiation of
steroid treatment. Frequency of painful crises
(2X),severe pain episode, Acute Chest Syndrome,
stroke,& Renal infarction.
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Management of vaso-occlusive crisis
• For Milder Crisis, manage on Nonsteroidal
Anti-inflammatory Drugs (Diclofenac or
Naproxen.)
• For more Severe Crises, most patients require
inpatient management for Intravenous Opioids;
Patient-controlled Analgesia Devices are
commonly used in this setting.
• Vaso-occlusive crisis involving organs such as
the Penis or Lungs are considered an emergency
and treated with Red-blood Cell Transfusions.
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MANAGEMENT OF VASO-OCCLUSIVE CRISIS
• Painful Crises are treated with Hydration,
Analgesics, & Blood Transfusion; Pain
management requires Opioid Administration at
regular intervals.
• Vigorous hydration.
• Bone pain may respond as well to Ketorolac
(30–60 mg initial dose, then 15–30 mg every
6–8 h).
• Morphine (0.1–0.15 mg/kg every 3–4 h) should
be used to control severe pain
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MANAGEMENT OF VASO-OCCLUSIVE CRISIS
• Many crises can be managed at home with oral
hydration and oral analgesia.
• Most crises resolve in 1–7 days.
• Use of blood transfusion should be reserved
for extreme cases, transfusions do not
shorten the duration of the crisis.
• The most significant advance in the therapy
of sickle cell anaemia has been the
introduction of Hydroxyurea as a mainstay of
therapy for patients with severe symptoms.
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MANAGEMENT OF VASO-OCCLUSIVE CRISIS
• Hydroxyurea (10–30 mg/kg per day) increases
fetal haemoglobin.
• Exert beneficial affects on RBC Hydration,
Vascular Wall Adherence, and Suppression of the
granulocyte and Reticulocyte count.
• Maintain a white cell count between 5000 and
8000/L.
• White Cells And Reticulocytes may play a major
role in the pathogenesis of sickle cell crises,
their suppression may be an important benefit of
hydroxyurea therapy.
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CONCLUSION
• The present case emphasizes the poor tolerance
of steroids in SCD patients
• Review of literature suggest that systemic
corticosteroids play an important role in the
development of severe adverse events in some
patients with SCD.
• With better understanding of risk factors,
prevalence and pathophysiology of these
events, systemic corticosteroids should be
used with caution in this population.
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CONCLUSION
• Prompt Red-cell Transfusion or Exchange
Transfusion along with aggressive clinical
management can improve the clinical outcome
in severe cases.
• Red blood cell transfusions given with
corticosteroid therapy in SCD patients may
attenuate the risk of such complications.
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