Exploring patient participation in reducing health-care-related safety risks
Exploring patient participation in reducing health-care-related safety risks
Exploring patient participation in reducing health-care-related safety risks
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<strong>Explor<strong>in</strong>g</strong> <strong>patient</strong> <strong>participation</strong> <strong>in</strong> reduc<strong>in</strong>g <strong>health</strong>-<strong>care</strong>-<strong>related</strong> <strong>safety</strong> <strong>risks</strong><br />
158<br />
Box A3 .2 . Categories of reactions<br />
Categories of reactions<br />
FNHTR<br />
Increase of body temperature of >=2°C (with or without rigors) dur<strong>in</strong>g or <strong>in</strong> the first two hours after a blood<br />
transfusion, if no other cause for the fever can be found and haemolysis has been excluded. Exclusion of<br />
bacteriological or blood group serological causes and TRALI.<br />
Acute haemolytic transfusion reaction<br />
Signs start<strong>in</strong>g with<strong>in</strong> m<strong>in</strong>utes or up to 24 hours after commenc<strong>in</strong>g transfusion, due to (usually complementmediated<br />
<strong>in</strong>travascular) destruction of red blood cells. Most often caused by transfusion of AB0-<strong>in</strong>compatible<br />
blood components, sometimes by irregular erythrocyte antibodies or occasionally by transfusion of a haemolytic<br />
red blood cell concentrate or <strong>in</strong>fusion of hypotonic fluids.<br />
Delayed haemolytic transfusion reaction<br />
Immune-mediated destruction of red blood cells occurr<strong>in</strong>g >24 hours after, and as a result of, transfusion of a<br />
blood component.<br />
TRALI<br />
Cl<strong>in</strong>ical picture of adult respiratory distress syndrome: dyspnoea, hypoxia and a f<strong>in</strong>ely mottled appearance on<br />
chest X-ray with onset up to six hours after adm<strong>in</strong>istration of a (plasma-conta<strong>in</strong><strong>in</strong>g) blood component, if other<br />
causes, such as anaphylaxis, <strong>in</strong>fection and circulatory overload, have been excluded.<br />
Circulatory overload<br />
Onset with<strong>in</strong> a few hours of transfusion of dyspnoea, orthopnoea, cyanosis, oedema of dependent parts, raised<br />
central venous pressure, with congestive picture on chest X-ray.<br />
Anaphylactic reaction<br />
Serious allergic reaction with onset with<strong>in</strong> seconds to m<strong>in</strong>utes of commenc<strong>in</strong>g transfusion, with signs such as<br />
airway obstruction, circulatory collapse or gastro<strong>in</strong>test<strong>in</strong>al signs as well as m<strong>in</strong>or allergic manifestations.<br />
Other allergic reactions<br />
With<strong>in</strong> m<strong>in</strong>utes to hours of start<strong>in</strong>g transfusion, occurrence of allergic signs such as itch<strong>in</strong>g, erythema and<br />
urticaria, without serious allergic manifestations.<br />
Post-transfusion purpura<br />
Severe temporary thrombocytopenia aris<strong>in</strong>g roughly 9 (1–24) days after a transfusion of red blood cells and/or<br />
platelets, usually <strong>in</strong> a <strong>patient</strong> who has previously had a blood transfusion or been pregnant.<br />
Bacterial contam<strong>in</strong>ation<br />
Bacterial septicaemia that can be traced to a transfused blood component. May be difficult to dist<strong>in</strong>guish from<br />
a haemolytic transfusion reaction. Confirm diagnosis by bacteriological culture on the <strong>patient</strong> and the blood<br />
component and/or another blood component result<strong>in</strong>g from the same donation.<br />
Viral <strong>in</strong>fection<br />
Any viral <strong>in</strong>fection that can be traced to a transfused blood component (hepatitis A, HBV, HCV, non-ABC,<br />
HIV, human T-cell lymphotropic virus, Epste<strong>in</strong>-Barr virus, cytomegalovirus etc.)<br />
Post-transfusion hepatitis<br />
Significant rise <strong>in</strong> transam<strong>in</strong>ases between 14 and 180 days after transfusion or a serologically confirmed new<br />
<strong>in</strong>fection with HBV or HCV <strong>in</strong> a <strong>patient</strong> who has been transfused. Transfusion-associated cytomegalovirus<br />
<strong>in</strong>fection A (probably) – primary cytomegalovirus <strong>in</strong>fection <strong>in</strong> a recipient of a blood component should be<br />
reported.<br />
Transfusion-associated graft-versus-host disease reaction<br />
Reaction 1–6 weeks (usually 8–10 days) after a T-cell blood component is adm<strong>in</strong>istered, with (<strong>in</strong>itially central)<br />
erythema, watery diarrhoea, elevated liver enzymes and pancytopenia – generally <strong>in</strong>volv<strong>in</strong>g a high risk of<br />
mortality and caused by an immunological reaction of the donor’s T lymphocytes to the tissues of the recipient<br />
(who had suppressed immunity).