Guidelines on red cell transfusion in sickle cell disease. Part I: principles and laboratory aspects

被引：94

作者：

Davis, Bernard A. ^{[1
]}

Allard, Shubha ^{[2
]}

Qureshi, Amrana ^{[3
]}

Porter, John B. ^{[4
]}

Pancham, Shivan ^{[5
]}

Win, Nay ^{[2
]}

Cho, Gavin ^{[2
]}

Ryan, Kate ^{[6
]}

机构：

[1] Whittington Hlth, London, England

[2] Barts Hlth NHS Trust, London, England

[3] Oxford Univ Hosp NHS Fdn Trust, Oxford, England

[4] Univ Coll London Hosp NHS Fdn Trust, London, England

[5] Sandwell & West Birmingham Hosp NHS Trust, Birmingham, W Midlands, England

[6] Cent Manchester Univ Hosp NHS Fdn Trust, Manchester, Lancs, England

来源：

BRITISH JOURNAL OF HAEMATOLOGY | 2017年 / 176卷 / 02期

关键词：

sickle cell disease; red cell transfusion; principles; ACUTE CHEST SYNDROME; LONG-TERM ERYTHROCYTAPHERESIS; VENOUS ACCESS DEVICES; IRON OVERLOAD; BLOOD-TRANSFUSION; HYPERHEMOLYSIS SYNDROME; EXCHANGE-TRANSFUSION; RECURRENT STROKE; ANEMIA; CHILDREN;

D O I：

10.1111/bjh.14346

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：179 / 191

页数：13

共 104 条

[1] Erythrocytapheresis can reduce iron overload and prevent the need for chelation therapy in chronically transfused pediatric patients [J].

Adams, DM ;

Schultz, WH ;

Ware, RE ;

Kinney, TR .

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 1996, 18 (01) :46-50

[2]

Adams RJ, 2005, NEW ENGL J MED, V353, P2769

[3] Prevention of a first stroke by transfusions in children with sickle, cell anemia and abnormal results on transcranial Doppler ultrasonography [J].

Adams, RJ ;

McKie, VC ;

Hsu, L ;

Files, B ;

Vichinsky, E ;

Pegelow, C ;

Abboud, M ;

Gallagher, D ;

Kutlar, A ;

Nichols, FT ;

Bonds, DR ;

Brambilla, D ;

Woods, G ;

Olivieri, N ;

Driscoll, C ;

Miller, S ;

Wang, W ;

Hurlett, A ;

Scher, C ;

Berman, B ;

Carl, E ;

Jones, AM ;

Roach, ES ;

Wright, E ;

Zimmerman, RA ;

Waclawiw, M ;

Pearson, H ;

Powars, D ;

Younkin, D ;

El-Gammal, T ;

Seibert, J ;

Moye, L ;

Espeland, M ;

Murray, R ;

McKinley, R ;

McKinley, S ;

Hagner, S ;

Weiner, S ;

Estow, S ;

Yelle, M ;

Brock, K ;

Carter, E ;

Chiarucci, K ;

Debarr, M ;

Feron, P ;

Harris, S ;

Hoey, L ;

Jacques, K ;

Kuisel, L ;

Lewis, N .

NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (01) :5-11

[4] Rheologic behavior of sickle and normal red blood cell mixtures in sickle plasma: implications for transfusion therapy [J].

Alexy, Tamas ;

Pais, Eszter ;

Armstrong, Jonathan K. ;

Meiselman, Herbert J. ;

Johnson, Cage S. ;

Fisher, Timothy C. .

TRANSFUSION, 2006, 46 (06) :912-918

[5]

Alkindi Salam, 2012, J Infect Public Health, V5, P57, DOI 10.1016/j.jiph.2011.10.004

[6] EFFECT OF NORMAL CELLS ON VISCOSITY OF SICKLE-CELL BLOOD - IN VITRO STUDIES AND REPORT OF 6 YEARS EXPERIENCE WITH A PROPHYLACTIC PROGRAM OF PARTIAL EXCHANGE TRANSFUSION [J].

ANDERSON, R ;

CASSELL, M ;

CHAPLIN, H ;

MULLINAX, GL .

ARCHIVES OF INTERNAL MEDICINE, 1963, 111 (03) :286-+

[7]

[Anonymous], 2008, STANDARDS CLIN CARE

[8]

[Anonymous], 2013, 2012 ANN SHOT REPORT

[9] Clinical significance of RBC alloantibodies and autoantibodies in sickle cell patients who received transfusions [J].

Aygun, B ;

Padmanabhan, S ;

Paley, C ;

Chandrasekaran, V .

TRANSFUSION, 2002, 42 (01) :37-43

[10] Rituximab as an effective treatment of hyperhemolysis syndrome in sickle cell anemia [J].

Bachmeyer, Claude ;

Maury, Jacqueline ;

Parrot, Antoine ;

Bachir, Dora ;

Stankovic, Katia ;

Girot, Robert ;

Lionnet, Francois .

AMERICAN JOURNAL OF HEMATOLOGY, 2010, 85 (01) :91-92

← 1 2 3 4 5 6 7 8 9 10 →