Updated analysis: central venous access device infection rates in an expanded cohort of paediatric patients with severe haemophilia receiving prophylactic recombinant tissue plasminogen activator

Author:

McCarthy C. E.1,O'Brien M.2,Andrews J.13,Zoland J. M.1,Macasiray E.1,Wong W.1,Lo C.1,Glader B.13,Tamaresis J.4,Jeng M.1

Affiliation:

1. Department of Pediatrics; Stanford University School of Medicine; Palo Alto CA USA

2. Cancer and Blood Disorders Institute; Cincinnati Children's Hospital Medical Center; Cincinnati OH USA

3. Department of Pathology; Stanford University School of Medicine; Palo Alto CA USA

4. Department of Health Research and Policy; Stanford University School of Medicine; Palo Alto CA USA

Publisher

Wiley

Subject

Genetics (clinical),Hematology,General Medicine

Reference21 articles.

1. Prophylaxis versus episodic treatment to prevent joint disease in boys with severe hemophilia;Manco-Johnson;N Engl J Med,2007

2. Associations between intracranial haemorrhage and prescribed prophylaxis in a large cohort of haemophilia patients in the United States;Witmer;Br J Haematol,2011

3. Twenty-five years' experience of prophylactic treatment in severe haemophilia A and B;Nilsson;J Intern Med,1992

4. National Hemophilia Foundation Medical and Scientific Advisory Council (MASAC) Recommendations Concerning Prophylaxis: Regular Administration of Clotting Factor Concentrate to Prevent Bleeding New York 2007

5. Survey of current prophylaxis practices and bleeding characteristics of children with severe haemophilia A in US haemophilia treatment centres;Ragni;Haemophilia,2011

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