Comprehensive Hemophilia Management - Impact Education, LLC [PDF]

After completing this activity, the participant should be better able to: • Discuss the impact of hemophilia with and

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Idea Transcript


Educational Objectives After completing this activity, the participant should be better able to:

• Discuss the impact of hemophilia with and without inhibitors on clinical, economic, and humanistic outcomes • Assess current and emerging hemophilia therapies for children and adults, with and without inhibitors • Implement the Medical and Scientific Advisory Council (MASAC) Quality of Care Guidelines for the treatment of hemophilia • Employ collaborative care strategies and resources, including HTCs, to improve care coordination for health plan patients with hemophilia • Recommend hemophilia management policies and protocols to optimize patient outcomes in a managed care and/or specialty pharmacy setting • Provide accurate and appropriate counsel as part of the treatment team

Faculty Peg Geary, MA, MBA, MPH, LCSW, CCM Clinical Hemophilia Social Worker UMass Memorial Hospital, New England Hemophilia Center

Patrick Lynch A Patient with Hemophilia Executive Producer, Believe Digi

Sue Geraghty, RN, MBA Formerly: HTC Nurse Coordinator University of Colorado Hemophilia and Thrombosis Center University of Colorado Health Sciences Center

Vanita K. Pindolia, PharmD, BCPS Vice President, Ambulatory Clinical Pharmacy Services — PCM Henry Ford Health System/Health Alliance Plan

Marc Gilgannon, PT Lead Therapist University of Virginia Children’s Hospital

Michael D. Tarantino, MD Professor, Department of Pediatrics and Department of Medicine University of Illinois College of Medicine at Peoria Medical Director Bleeding and Clotting Disorders Institute

Faculty Disclosures The faculty reported the following financial relationships or relationships they or their spouse/life partner have with commercial interests related to the content of this continuing education activity: Name of Faculty or Presenter

Reported Financial Relationship

Peg Geary, MA, MBA, MPH, LCSW, CCM

No financial interest/relationships relating to the topic of this activity

Sue Geraghty, RN, MBA

Consulting Fees: Biogen Idec, Kedrion Biopharma, Inc., Novo Nordisk, Inc. Fees for Non-CME/CE Services: Biogen Idec, Novo Nordisk, Inc.

Marc Gilgannon, PT

No financial interest/relationships relating to the topic of this activity

Patrick Lynch

No financial interest/relationships relating to the topic of this activity

Vanita K. Pindolia, PharmD, BCPS

No financial interest/relationships relating to the topic of this activity

Michael D. Tarantino, MD

Consulting Fees: Amgen, Baxter Healthcare Corporation, Bio Products Laboratory, Ltd., Pfizer Inc. Fees for Non-CME/CE Services: Baxter Healthcare Corporation, Bio Products Laboratory, Ltd., Grifols, Novo Nordisk, Inc., Pfizer, Inc. Advisor: Amgen, Baxter Healthcare Corporation, Bayer HealthCare, Bio Products Laboratory Ltd., Cangene Corporation, Grifols, Kedrion Biopharma, Inc., Novo Nordisk, Inc., Pfizer, Inc. Grant: American Thrombosis & Hemostasis Network, Centers for Disease Control and Prevention, Health Resources and Services Administration Research: Baxter Healthcare Corporation, Cangene Corporation, Grifols, Novo Nordisk, Inc. Royalty: UpToDate Inc.

Clinical Updates in Hemophilia Treatment

Michael D. Tarantino, MD Professor, Department of Pediatrics and Department of Medicine University of Illinois College of Medicine at Peoria Medical Director Bleeding and Clotting Disorders Institute

Hemophilia: An Inherited Disorder • X-linked recessive bleeding disorder leading to spontaneous bleeding and bleeding following trauma or surgery – Typically expressed in males; female carriers may have symptoms – Characterized by a deficiency of Factor VIII (hemophilia A) or Factor IX (hemophilia B)

• Current prevalence in the United States: ~20,000 males • Occurs in ~1 of every 5,000 live male births • 30% of cases are new mutations • Affects individuals from all racial and ethnic groups

• Hemophilia A is ~4X as common as hemophilia B

CDC. Hemophilia facts. http://www.cdc.gov/ncbddd/hemophilia/facts.html.

Detection/Diagnosis Prior Family History

No Previous Family History

• • • •



Identify carriers Pre-conception counseling Cord blood testing of males Low-level carriers should be identified early to prevent bleeding with surgery or injury

CDC. http://www.cdc.gov/ncbddd/hemophilia/diagnosis.html.

• •

Bleeding with birth or post-natal, circumcision, immunizations Excessive bleeding following trauma/injury Joint bleeds and hematomas

Clinical Manifestations • • •

Bleeding into joints (hemarthrosis), muscles, soft tissues, and other locations Interference with normal activities and ability to participate fully in school or work Long-term sequelae if bleeding not prevented – – – – – –



Flexion contractures Arthritis/arthropathy Chronic pain Muscle atrophy Loss of mobility Neurologic impairment

Inhibitor development represents severe sequelae occurring in ~30% of severe FVIII patients

NHF. http://www.hemophilia.org/NHFWeb/MainPgs/MainNHF.aspx?menuid=179&contentid=45&rptname=bleeding.

Clinical Classification Classification (% of affected patients)

Severe (50%- 70%)

Moderate (10%)

Mild (30%- 40%)

FVIII or FIX activity

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