Estimating the probability that a donor will have or not have an adverse event is useful for staff knowledge to give blood donors reassurance upon request. STUDY DESIGN AND METHODS: One-thousand donors from the general donor pool were interviewed for seven potential adverse events 3 weeks after a 525-mL whole-blood phlebotomy. The four most common adverse events were bruise (22.7%), sore arm (10.0%), fatigue (7.8%), and donor reaction (7.0%). A stepwise logistic regression analysis was performed based on five donor characteristics that were studied: age, weight, sex, race, and first-time donor status. The contribution of each significant or marginally significant factor to each adverse event was quantified. RESULTS: For donor reaction, weig...
Aim: The aim of this study was to analyze the frequency of on-site and off-site adverse donor reacti...
Item does not contain fulltextBACKGROUND: Observational data suggest that some donors might benefit ...
INTRODUCTION: According to German legislation, reports of suspected serious adverse reactions (AR) a...
Estimating the probability of a blood donation adverse event based on 1000 interviewed whole-blood d...
Some blood donation–related adverse events (AEs) can negatively impact the blood donor return rate (...
The blood donation process is usually very safe, and blood donors are comfortable during the blood d...
Adverse events have been reported post blood donation. Donors might refrain from donating again due ...
Background: Donor reaction has the most negative impact on the blood donor return rate. Amelioration...
<div><p>Background</p><p>Adverse events have been reported post blood donation. Donors might refrain...
Objectives: Fragmented blood transfusion services along with an unmotivated blood donation culture o...
Background: Blood and apheresis donations are widely considered safe, with a low incidence of advers...
There are no reports in the transfusion medicine literature that describe adverse donor reactions af...
Background: Blood donation is associated with a number of adverse events. Most of these are both unc...
Background: Despite the advent of many synthetic and semi-synthetic products, the importance of biol...
Background: Blood donation is associated with a number of adverse events. Most of these are both unc...
Aim: The aim of this study was to analyze the frequency of on-site and off-site adverse donor reacti...
Item does not contain fulltextBACKGROUND: Observational data suggest that some donors might benefit ...
INTRODUCTION: According to German legislation, reports of suspected serious adverse reactions (AR) a...
Estimating the probability of a blood donation adverse event based on 1000 interviewed whole-blood d...
Some blood donation–related adverse events (AEs) can negatively impact the blood donor return rate (...
The blood donation process is usually very safe, and blood donors are comfortable during the blood d...
Adverse events have been reported post blood donation. Donors might refrain from donating again due ...
Background: Donor reaction has the most negative impact on the blood donor return rate. Amelioration...
<div><p>Background</p><p>Adverse events have been reported post blood donation. Donors might refrain...
Objectives: Fragmented blood transfusion services along with an unmotivated blood donation culture o...
Background: Blood and apheresis donations are widely considered safe, with a low incidence of advers...
There are no reports in the transfusion medicine literature that describe adverse donor reactions af...
Background: Blood donation is associated with a number of adverse events. Most of these are both unc...
Background: Despite the advent of many synthetic and semi-synthetic products, the importance of biol...
Background: Blood donation is associated with a number of adverse events. Most of these are both unc...
Aim: The aim of this study was to analyze the frequency of on-site and off-site adverse donor reacti...
Item does not contain fulltextBACKGROUND: Observational data suggest that some donors might benefit ...
INTRODUCTION: According to German legislation, reports of suspected serious adverse reactions (AR) a...