Patients with hereditary hemochromatosis reach safe range of transferrin saturation sooner with erythrocytaphereses than with phlebotomies

Author:

Rombout‐Sestrienkova Eva12,Brandts Lloyd3,Koek Ger H.14,Deursen Cees Th. B. M15

Affiliation:

1. Department of Internal Medicine, Division of Gastroenterology and Hepatology Maastricht University Medical Centre+ Maastricht The Netherlands

2. Department of Transfusion Medicine Sanquin Blood Supply Maastricht The Netherlands

3. Clinical Epidemiology and Medical Technology Assessment (KEMTA) Maastricht University Medical Centre+ Maastricht The Netherlands

4. School of Nutrition and Translational Research in Metabolism (NUTRIM) University Maastricht Maastricht The Netherlands

5. Department of Internal Medicine Gastroenterology and Clinical Geriatrics Zuyderland Medical Center Heerlen The Netherlands

Publisher

Wiley

Subject

Hematology,General Medicine

Reference24 articles.

1. Diagnosis and management of hereditary hemochromatosis;Van Bokhoven MA;BMJ,2011

2. Revisiting hemochromatosis: genetic vs. phenotypic manifestations

3. EASL clinical practice guidelines for HFE hemochromatosis

4. Diagnosis and management of hemochromatosis: 2011 Practice Guideline by the American Association for the Study of Liver Diseases

5. Guideline Hemochromatosis of the NIV (Dutch Society of Internists).https://richtlijnendatabase.nl/richtlijn/hereditaire_hemochromatose_hh/startpagina.html

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