Professional Documents
Culture Documents
Annex3 m7
Annex3 m7
1 Haematological disorders
Question
What selection criteria should be applied to prospective blood donors with a
current or past history of anaemia?
22
#11Search (#10) AND iron-deficiency anemia Limits: Humans, English, published in the
last 10 years07:55:38 1420
#10Search (#6) AND#9 Limits: Humans, English, published in the last 10 years07:52:43
1558
#9Search (#7) AND#8 Limits: Humans, English, published in the last 10 years07:48:14
4736
#8Search iron-deficiency OR megaloblastic OR macrocytic OR pernicious OR
hypochromic Limits: Humans, English, published in the last 10 years07:47:48 5443
#7Search anaemia OR anemia Limits: Humans, English, published in the last 10
years07:46:28 36056
#6Search pre-donation haemoglobin OR haemoglobin screening OR haematocrit OR
ferritin Limits: Humans, English, published in the last 10 years07:44:25 19317
#5Search (#3) NOT#4 Limits: Humans, English, published in the last 10 years07:43:02
1635
#4Search cord blood OR stem cell OR transplantation OR organ donation OR organ
transplantation OR organ transplant OR liver OR kidney OR renal transplant OR (twin-twin
transfusion) OR allogeneic transplant Limits: Humans, English, published in the last 10
years07:42:07 374406
#3Search (#2) AND#1 Limits: Humans, English, published in the last 10 years07:37:25
4857
#2Search blood Limits: Humans, English, published in the last 10 years07:37:00 648600
#1Search (donor suitability) OR (donor deferral) OR (donor risk) OR (donor
safety) Limits: Humans, English, published in the last 10 years07:36:24 9964
Decision-making process
The Guideline Development Group agreed on the following recommendations
based on their medical knowledge and experience from best practice.
Recommendations
Accept
Individuals who:
— Have a past history of iron deficiency anaemia, with a known cause
that is not a contraindication to donation, and who have completed
treatment and are fully recovered
— Have a past history of B12 or folate deficiency, are fully recovered and
are taking maintenance treatment with B12 or folic acid
Defer
Individuals who:
— Do not meet the minimum haemoglobin level for blood donation
— Are under investigation or on treatment for anaemia
— Defer permanently
— Individuals who have chronic anaemia of unknown cause or associated
with systemic disease: e.g. renal failure, rheumatoid disease
23
5.1.2 Haemoglobinopathies
Question
What selection criteria should be applied to prospective blood donors with
inherited red cell disorders such as sickle cell disease, sickle trait, thalassaemia
and thalassaemia trait?
24
#3Search (#2) AND#1 Limits: Humans, English, published in the last 10 years07:37:25
4857
#2Search blood Limits: Humans, English, published in the last 10 years07:37:00 648600
#1Search (donor suitability) OR (donor deferral) OR (donor risk) OR (donor
safety) Limits: Humans, English, published in the last 10 years07:36:24 9964
Key references
1 Stroncek DF et al. Sickle Hb polymerization in RBC components from donors with sickle
trait prevents effective WBC reduction by filtration. Transfusion, 2002, 42(11):1466–
1472.
2 Ould Amar AK. Red blood cells from donors with sickle cell trait: a safety issue for
transfusion? Transfusion Medicine, 2006, 16(4):248–253.
Decision-making process
The Guideline Development Group agreed on the following recommendations
based on data from the above studies, their medical knowledge and experience
from best practice.
Recommendations
Accept
Individuals with:
— Thalassaemia traits, provided they are well and meet the minimum
haemoglobin level for blood donation
— Sickle cell trait: accept for whole blood donation provided they meet
the minimum haemoglobin level for blood donation; blood donated by
sickle cell trait individuals is, however, not suitable for leucodepletion,
intrauterine transfusion, neonatal exchange transfusion or for patients
with sickle cell disease
Defer permanently
Individuals with:
— Thalassaemia major or sickle cell disease
— Sickle cell trait for blood donation by apheresis procedure or for whole
blood donation if the blood is to be leucofiltered
Question
What selection criteria should be applied to prospective blood donors with
inherited red cell enzymopathies and membrane defects such as G-6-PD deficiency,
hereditary spherocytosis?
25
Population Intervention Outcome
Prospective blood Acceptance or Minimize adverse effects related to
donors deferral for blood blood donation
donation
Avoid unnecessary deferral of
suitable blood donors
Minimize risk of adverse reactions in
recipients of blood transfusion
26
#7Search (#6) AND#5 Limits: Humans, English, published in the last 10 years06:32:17 817
#6Search anaemia OR anemia Limits: Humans, English, published in the last 10
years06:31:55 36064
#5Search glucose phosphate dehydrogenase deficiency OR (G-6-PD) OR favism OR pyruvate
kinase deficiency OR hereditary spherocytosis06:30:40 8023
#1Search donor suitability OR donor deferral OR recipient risk or recipient
safety Limits: Humans, English, published in the last 10 years06:25:44 3849
Background paper
1 Beutler E. G6PD deficiency. Blood, 1994, 84:3613–3636.
Decision-making process
The Guideline Development Group agreed on the following recommendations
based on data from the background paper above, their medical knowledge and
experience from best practice.
Recommendations
Policies for the assessment of prospective donors should be developed by
BTS in regions where there is a high incidence of enzymopathies and inherited
membrane defects.
Accept
Individuals with G6PD deficiency or other inherited red cell membrane defects,
without a history of haemolysis; however, their blood is not suitable for
intrauterine transfusion, neonatal exchange transfusion or for patients with
G6PD deficiency
Defer permanently
Individuals with G6PD deficiency or inherited red cell membrane defects, with
a history of haemolysis
5.1.4 Thrombocytopenia
Question
What selection criteria should be applied to prospective blood donors with current
or past thrombocytopenia?
27
Key search and MeSH words
bruising OR haematoma
Key reference
1 Guidelines for the blood transfusion services in the United Kingdom: donor selection
guidelines, 7th edition. London, UK Blood Transfusion & Tissue Transplantation Services,
2005
28
Decision-making process
The Guideline Development Group agreed on the following recommendations
based on the above reference and on their medical knowledge and experience
from best practice.
Recommendations
Accept
Individuals with a past history of acute autoimmune thrombocytopenia more
than 5 years previously, provided they are well and no longer require treatment,
other than prophylactic antibiotics following splenectomy
Defer permanently
Individuals with thrombocytopenia of unknown cause or associated with long-
term haematological or systemic disease
Question
What selection criteria should be applied to prospective blood donors with
inherited or acquired coagulation disorders, including familial carriers?
29
#16Search (blood donation) AND#417:36:53 447
#15Search (#3) AND haemophilia17:36:00 42
#14Search (#13) NOT#1117:23:52 37
#13Search (#3) AND haemostatic disorder17:22:19 81
#12Search (#10) NOT#1117:20:49 26
#11Search cord blood OR autologous transplant OR hepatic OR liver OR stem cell OR
cancer OR myeloma OR Creutzfeldt-Jakob disease OR vCJD Limits: Humans, English,
published in the last 10 years17:18:06 861926
#10Search (#3) AND haemorrhagic disorders Limits: Humans, English, published in the
last 10 years17:14:58 98
#9Search (#6) NOT#8 Limits: Humans, English, published in the last 10 years17:06:49 60
#8Search liver OR kidney transplant OR kidney graft OR vCJD Limits: Humans, English,
published in the last 10 years16:56:29 148228
#6Search (#3) AND blood coagulation disorders Limits: Humans, English, published in
the last 10 years16:53:12 81
#7Search (#3) AND blood coagulation disorders[Title/Abstract] Limits: Humans, English,
published in the last 10 years16:52:38 0
#5Search (#3) AND#4 Limits: Humans, English, published in the last 10 years16:50:17 158
#4Search blood coagulation disorders OR haemorrhagic disorders OR haemostatic disorders
OR haemophilia Limits: Humans, English, published in the last 10 years16:49:51 34396
#3Search (#1) AND#2 Limits: Humans, English, published in the last 10 years16:48:28
6583
#2Search donor safety OR donor suitability OR donor risk OR donor well-being Limits: Humans,
English, published in the last 10 years16:48:02 14482
#1Search blood Limits: Humans, English, published in the last 10 years16:46:44 649489
Decision-making process
In the absence of relevant published evidence, the Guideline Development Group
agreed on the following recommendations based on their medical knowledge and
experience from best practice.
Recommendations
Accept
Individuals with carrier states for inherited coagulation disorders including
haemophilia A or B, provided they have normal or near normal coagulation
factor levels, do not have a history of abnormal bleeding and have not received
treatment with blood products
Defer permanently
Individuals with coagulation factor deficiencies, whether inherited or acquired
30