Intervention Protocol

Erythrocytapheresis versus phlebotomy for hereditary haemochromatosis

  1. Heba Abolaban1,
  2. Munes Fares1,
  3. Qusay Haydour1,
  4. Nazir Ibrahim2,
  5. Dona Rayess1,
  6. Maria Diab1,*,
  7. Ahmad M Al Moujahed1

Editorial Group: Cochrane Hepato-Biliary Group

Published Online: 10 NOV 2010

Assessed as up-to-date: 30 SEP 2010

DOI: 10.1002/14651858.CD008855


How to Cite

Abolaban H, Fares M, Haydour Q, Ibrahim N, Rayess D, Diab M, Al Moujahed AM. Erythrocytapheresis versus phlebotomy for hereditary haemochromatosis (Protocol). Cochrane Database of Systematic Reviews 2010, Issue 11. Art. No.: CD008855. DOI: 10.1002/14651858.CD008855.

Author Information

  1. 1

    Damascus University, Faculty of Medicine, Damascus, Syrian Arab Republic

  2. 2

    Alkalamon University, Damascus, Syrian Arab Republic

*Maria Diab, Faculty of Medicine, Damascus University, P.O. Box: 6461 Damascus, Syria, Damascus, 00963, Syrian Arab Republic. diab.maria@gmail.com.

Publication History

  1. Publication Status: Edited (no change to conclusions)
  2. Published Online: 10 NOV 2010

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Abstract

  1. Top of page
  2. Abstract

This is the protocol for a review and there is no abstract. The objectives are as follows:

To assess the benefits and harms of TEA versus phlebotomy in the treatment of hereditary haemochromatosis.