IV Gamma Globulin Presentation

Download Report

Transcript IV Gamma Globulin Presentation

What's Happening in IV Gamma Globulin: Clinical Use and Costs Stacy M. Borans, MD

Chief Medical Officer

Advanced Medical Strategies [email protected]

Learning Objectives For Gamma Globulin

     Understand the diseases for which IVIG therapy is appropriate Identify when IVIG therapy is inappropriate Understand the mechanism of action of IVIG therapy Identify IVIG therapy dosage and duration for indicated diseases Estimate the costs associated with IVIG therapy

What is Gamma Globulin?

 A major class of immunoglobulins found in the blood, including many of the most common antibodies circulating in the blood.

 Also called immunoglobulin G (IgG).

 And immunoglobulins are????

What is Gamma Globulin?

    Monomeric immunoglobulin which isbuilt of two heavy chains (γ) and two light chains Each molecule has two antigen binding sites Most abundant immunoglobulin only immunoglobulin that can pass through the placenta

What is Gamma Globulin?

How does Gamma Globulin Work?

 Binds to pathogens:  Viruses   Bacteria Fungi  Protects the body from them in 3 ways:   Complement Activation Opsonization for Phagocytosis  Toxin Neutralization

How does Gamma Globulin Work?

 Complement Activation:     System of serum proteins interact in a cascade Classical Pathway: activated by antibody antigen complexes Trigger for the classical pathway is either IgG or IgM antibody bound to antigen Major part of human immune response

How does Gamma Globulin Work?

 Phagocytosis:  Large particles are enveloped by larger particles’ cell membranes    Specialized cells perform phagocytosis to reduce inflammation Involved in immune tolerance-prevents inflammation against normal body components IGG coats the surface of foreign bodies making them more attractive to phagocytic cells

When should Gamma Globulin be given?

 Primary Immunodeficiency Disorders:       congenital agammaglobulinemia hypogammaglobulinemia common variable immunodeficiency severe combined immunodeficiency (SCID) X-linked immunodeficiency with hyperimmunoglobulin M Wiskott-Aldrich syndrome

When should Gamma Globulin be given?

     Idiopathic thrombocytopenic purpura Secondary immunodeficiency in chronic lymphocytic leukemia (CLL) Pediatric HIV infection Kawasaki syndrome Prevention of graft versus host disease (GVHD) and infection in adult transplant recipient

Primary Immunodeficiency Disorders

   Many different types of this Genetic disorders: defective or mutative genes Children with these disorders develop frequent, severe or unusual infections  Pneumonia   Thrush Infections of the skin and mucous membranes in the eyes, mouth, and genital area

Primary Immunodeficiency Disorders

   Diagnosis usually made with blood tests Circulating IgG levels typically low in pertinent disorders Treatment is usually multi-focused:  Antibiotics to target specific infections: May be used for preventative treatment   Gamma Globulin to increase antibody response Cytokine Therapy: boost the immune system

Primary Immunodeficiency Disorders

   Treatments do not cure the underlying disorder Gamma Globulin administration:  200-400 mg/kg administered monthly   Can be given more frequently Minimum IgG level not established Only curative treatment for these patients is bone marrow transplantation

When should Gamma Globulin be given?

   CLL: B-cell type, prevention of recurrent bacterial infections Pediatric HIV/ARC: prevention of serious bacterial infections Allogenic Transplant Patients:   20 years of age or older and administered in the first 100 days after BMT and  manifested by interstitial pneumonia or infections

Gamma Globulin Dosage

   B-cell Chronic Lymphocytic Leukemia:  400 mg/kg every 3 to 4 weeks is recommended Allogenic Transplant:  500 mg/kg body weight on days -7 and -2 pretransplant  weekly through day 90 post-transplant Pediatric HIV:  400 mg/kg (8 mL/kg) body weight every 28 days

Idiopathic Thrombocytopenic Purpura

    Low platelet count (thrombocytopenia) of no known cause (idiopathic). Occurs most often in women over 40 years of age Symptoms include bruising, nosebleeds, and bleeding gums Acute and Chronic Forms:   lasting for 6 months or less or Lasting for over 1 year

Idiopathic Thrombocytopenic Purpura

  Mild ITP does not require treatment Treat when:   platelets are under 10,000 or Platelets under 50,000 and hemorrhage   Steroids are first line Gamma Globulin reserved for life threatening cases

Idiopathic Thrombocytopenic Purpura

    Gamma Globulin effect only temporary Given in order to prevent splenectomy or To help make the splenectomy procedure more safe Usual Gamma Globulin Dosage:   Adults: 1-2 g/kg IV administered over 1-5 d Peds: 1 g/kg once

Kawasaki Disease

    Febrile Illness of childhood Fever lasts for longer than 5 days and usually is quite high Involves the skin, mouth, and lymph nodes Untreated, the disorder can lead to cardiac complications-aneurysms

Kawasaki Disease

    Has 3 phases:    Acute febrile phase (days 1-11) Subacute phase (days 11-21) Convalescent phase (days 21-60): Some do add a 4 th phase: chronic Cardiac aneurysms are the only clinically significant manifestation of 4 th phase Treatment should begin within first 10 days

Kawasaki Disease

    Gamma Globulin and Aspirin are mainstays of therapy Patients also placed on anticoagulation Gamma Globulin appears to be effective in improving the inflammation in the disease Dosage/Duration  400 mg/kg/d IV in a single daily infusion for 4 d or  single dose of 2 g/kg IV infused over 12 h

“Off-Label” Gamma Globulin Use

 Several disorders have generally accepted use:  Guillain-Barré Syndrome      Lambert-Eaton Myasthenic Syndrome Multifocal Motor Neuropathy Multiple Sclerosis-Relapsing/Remitting Chronic Inflammatory Demyelinating Polyneuropathies Dermatomyositis/Polymyositis

Guillain-Barré Syndrome

(Acute Inflammatory Demyelinating Polyneuropathy)

    immune-mediated process generally characterized by motor, sensory, and autonomic dysfunction Symptoms:   progressive symmetric ascending muscle weakness Paralysis  Hyporeflexia (diminished reflexes) Severe cases progress to respiratory failure Patients may have prior infection

Guillain-Barré Syndrome

(Acute Inflammatory Demyelinating Polyneuropathy)     Other causes are linked to GBS Muscle weakness ascends from distal to proximal Pain is most pronounced in shoulder, back, buttocks and thighs Autonomic dysfunction is usually present:    Tachycardia/bradycardia Blood pressure fluctuations Urinary retention/constipation

Guillain-Barré Syndrome

(Acute Inflammatory Demyelinating Polyneuropathy)     Diagnosis is usually made on clinical signs/symptoms Lumbar Puncture and nerve conduction studies can be very helpful Treatment is generally supportive and most patients make a complete recover within 6-12 months Maximal recovery is seen 18 months after onset

Guillain-Barré Syndrome

(Acute Inflammatory Demyelinating Polyneuropathy)     Treatment:    Steroids alone are ineffective Plasma Exchange Gamma Globulin: 400 mg/kg/d IV for 5 d Both Plasma Exchange and Gamma Globulin are equally effective Goal is to shorten recovery time by 50% Mechanism of Action is unclear

Multifocal Motor Neuropathy

    Acquired immune-mediated polyneuropathy Progressive weakness, fasciculations and cramping No sensory involvement May resemble amyotrophic lateral sclerosis   No muscle atrophy Slower progression

Multifocal Motor Neuropathy

    Weakness is asymmetric and distal Progresses over long time period  Duration of disease prior to diagnosis ranges from several months to more than 15 years. Patients can remain productive and employed even with symptoms Events leading to motor nerve dysfunction not completely understood

Multifocal Motor Neuropathy

    50% of cases have elevated titers of anti GM1 antibodies Electrodiagnostic testing documents conduction blocks Upper Motor Neuron symptoms absent Creatinine Kinase is usually elevated although less than 3 times normal

Multifocal Motor Neuropathy

  Treatment:   Gamma Globulin and Cyclophosphamide are most effective Plasmapheresis and steroids alone are ineffective Gamma Globulin Dosage:   Initial dose: 2 g/kg IV over 2-5 days Maintenance Dose: 1-2 g/kg IV q4-8wk

Toxic Shock Syndrome

    Symptoms include fever, rash, hypotension and multi-organ involvement Typically associated with tampon use in women Organisms responsible are Staph Aureus and Strep Pyogenes Patients are usually critically ill, often requiring respiratory and ventilatory support

Toxic Shock Syndrome

  Staphylococcus TSS:    Fever, hypotension, and rash Involvement of 3 or more organ systems Absence of other diseases Streptococcus TSS:    Isolation of group A strep from a site Hypotension Involvement of 2 or more organ systems

Toxic Shock Syndrome

     An absence of immunity is considered to be a major risk factor Gamma Globulin has been reported to be effective in toxin neutralization in TSS Requires further studies to evaluate its use Dosage:  400 mg/kg IV as single dose infused over several hours Patients require aggressive support and antibiotic therapy

Other Diseases

      Chronic Fatigue Syndrome Amyotrophic lateral sclerosis Autoimmune neutropenia Stevens Johnson Syndrome Recurrent Spontaneous Miscarriage Epilepsy         Hemolytic Uremic Syndrome Rheumatoid Arthritis Alzheimer’s Disease Parkinson’s Disease Huntington’s Chorea Asthma Myocarditis Polymyositis

Gamma Globulin Preparations

More Common:

     Gammagard Gamimune Gammar-P Sandoglobulin Gamunex 

Less Common:

     Flebogamma Iveegam Octagam Polygam Venoglobulin-S

Gamma Globulin Costs

 Average Wholesale Price for 5 gram vial:   $600 UCR (200% AWP): $1,200  Average Wholesale Price for 10 gram vial:   $1,100 UCR (200% AWP): $2,200

Gamma Globulin Costs

 Average Reasonable Charges (75 kg patient):    400mg/kg = 30,000 mg = 30 grams AWP for three 10 gram vials = $3,300 UCR Charges: $6,600/dose    Dose of 2g/kg = 150 grams AWP for fifteen 10 gram vials = $16,500 UCR Charges: $33,000/dose

Questions/Comments

Thank you for attending!