A Roadmap to Diagnosing the Next Patient With Hereditary Angioedema

Slides:

Advertisements

Similar presentations

Immune Response and Hormonal Alterations in C1-inhibitor Deficiency Vojtech Thon University Centre for Primary Immunodeficiencies Department of Clinical.

Advertisements

C1 Esterase Inhibitor (Human) (Cinryze™) Lev Pharmaceuticals, Inc. Felice D’Agnillo, PhD Division of Hematology OBRR/CBER/FDA.

 Points from case  ? When to give Epi pen to patients with allergic Rxn’s/ angioedema  Documentation ( how to RTN to ER ?)  Admission criteria for.

Angioedema by.. Kunkanit Suntipraron. Angioedema swellings occur deeper in the dermis and in the subcutaneous or submucosal tissue. They may also affect.

Hereditary Angioedema

C1 Esterase Inhibitor Deficiency

Anaphylaxis: Racing to Diagnosis

Ocular Allergy: A Focus on Allergic Conjunctivitis

The Nurse’s Role in Inflammatory Bowel Disease

Pain Management Clinic

Erika Kajdácsi, MSc, Péter K

Diagnosis, Prognosis, and Management of aHUS

Burden of Atrial Fibrillation The Percentage of Strokes Attributable to AF Increases With Age.

Torsten Zuberbier, MD, Jonathan A. Bernstein, MD

ICD-10 and Clinical Documentation

A Practical Guide to the Prevention of Surgical Adhesions

Acute Heart Failure.

Centre for Primary Immunodeficiencies, Masaryk University Brno, CR

Progression After Cancer Immunotherapy in Advanced NSCLC

Emergency Department Management of Hereditary Angioedema Attacks: Patient Perspectives Iris M. Otani, MD, Sandra C. Christiansen, MD, Paula Busse, MD,

Introduction to Checkpoint Inhibitors

Epilepsy Treatment Across the Spectrum

Epidemiology Venous Pathophysiology Etiology.

New Standards of Care in ALK-Translocated Advanced NSCLC

Medication Nonadherence in Gout

Managing Hereditary Angioedema

Direct-To-Consumer Genetic Testing

Introduction. Risk Communication With Patients: Your Guide to Resources and Recommendations.

فرایند تسهیلگری در مددکاری جامعه ای

Addressing Iron Deficiency in Chronic HF

Managing RA: Telepartnership Between PCP and Rheumatologist

Chronic Idiopathic Urticaria

Integrating Epilepsy Performance Measures Into Clinical Practice

Recombinant Human C1-Esterase Inhibitor to Treat Acute Hereditary Angioedema Attacks in Adolescents James W. Baker, MD, Avner Reshef, MD, Dumitru Moldovan,

Screening and Diagnosing Postpartum Depression

Tailoring Hemophilia Prophylaxis Therapy

Checkpoint Inhibition

Overview. Maximizing the Safety of CAR T-Cell Therapy: Prevention, Early Recognition, and Management.

Correction The Journal of Allergy and Clinical Immunology: In Practice

Rheumatoid Arthritis 2015 Guidelines What's New? What's Different?

Pseudobulbar Affect or Psychiatric Condition?

Activation of the ficolin-lectin pathway during attacks of hereditary angioedema Dorottya Csuka, PhD, Lea Munthe-Fog, PhD, Estrid Hein, MSc, Zsuzsanna.

Use of Combination of Saxagliptin/ Dapagliflozin in Patients With Poorly Controlled Diabetes on Metformin.

Erika Kajdácsi, MSc, Péter K

Improving Outcomes in Psoriatic Arthritis

Program Goals. Accurate Diagnosis and Treatment of Patients With Thrombotic Microangiopathy.

Identifying High-Risk AF Patients

Novel Insulin/GLP-1 Combinations: Of Interest to the Primary Care Physician?

Prophylaxis Strategies in Hereditary Angioedema Weighing the Evidence

Case 1 Presentation Case 1 (cont) Assessment and Recommendations.

Hereditary angioedema: Safety of long-term stanozolol therapy

Hereditary Angioedema: New Findings Concerning Symptoms, Affected Organs, and Course Konrad Bork, MD, Gabriele Meng, MD, Petra Staubach, MD, Jochen Hardt,

Expanding the Horizons in Hereditary Angioedema

Clinical Issues in AIP:

Moving the Goal Post: Multidisciplinary Management of Advanced NSCLC

Severe Asthma and Comorbidities

A focused parameter update: Hereditary angioedema, acquired C1 inhibitor deficiency, and angiotensin-converting enzyme inhibitor–associated angioedema

Hereditary angioedema: Key role for kallikrein and bradykinin in vascular endothelial- cadherin cleavage and edema formation Laurence Bouillet, MD, PhD,

Treating Atypical Hemolytic Uremic Syndrome A Case Discussion

Renal Function and Myeloma Therapeutics

Selecting Treatment Approaches in Hemophilia

The ABCs of Diagnosing Tardive Dyskinesia

Diagnosing Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome

So Many Guidelines, So Little Time:

What Is Acute Intermittent Porphyria? Why AIP Is Often Undiagnosed or Misdiagnosed.

Clinical Pearls in the Management of Patients With Advanced Non-Small Cell Lung Cancer.

Navigating the Journey

Fresh perspectives ON BASAL Insulins in diabetes care

Presentation transcript:

A Roadmap to Diagnosing the Next Patient With Hereditary Angioedema

Hereditary Angioedema (HAE): The Basics

Acute/ED Presentations of HAE

Etiology of HAE

Mast-Cell Mediated Angioedema

Bradykinin-Mediated Angioedema

Clinical Features of HAE

Clinical Features of HAE (cont)

Abdominal Attacks in HAE

Abdominal Attacks in HAE (cont)

When to Consider HAE

Complement Testing

Complement Testing (cont)

Tips for ED Communication

ABC Stabilization

Summary

Abbreviations

References

References (cont)

References (cont)