Incidence, predictors and severity of adverse events among whole blood donors
Autor: | Abdulaziz Alajlan, Faisal Wani, Khaled Al-Surimi, Mahmoud Salam, Bushra Al-Shammari, Hamdan Almutairi |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: |
Male
Physiology Health Care Providers lcsh:Medicine Nurses Blood Donors Blood Pressure 030204 cardiovascular system & hematology Biochemistry Vascular Medicine 0302 clinical medicine Risk Factors Epidemiology Medicine and Health Sciences 030212 general & internal medicine lcsh:Science Whole blood Multidisciplinary Incidence (epidemiology) Incidence Age Factors Body Fluids Professions Blood Research Design Hypertension Chills Female medicine.symptom Anatomy Research Article Adult medicine.medical_specialty Nausea Clinical Research Design Saudi Arabia Research and Analysis Methods 03 medical and health sciences Internal medicine medicine Humans Hemoglobin Blood Donation Adverse effect Retrospective Studies business.industry lcsh:R Body Weight Biology and Life Sciences Proteins Retrospective cohort study Surgery Health Care Blood pressure People and Places lcsh:Q Population Groupings Adverse Events business |
Zdroj: | PLoS ONE PLoS ONE, Vol 12, Iss 7, p e0179831 (2017) |
ISSN: | 1932-6203 |
Popis: | Background Adverse events have been reported post blood donation. Donors might refrain from donating again due to such events which lowers the blood supply in collection centers. Aim This study measured the incidence, predictors and severity of adverse events among donors of a single whole blood unit at one of the largest donation centers in Saudi Arabia. Methods A retrospective cohort was conducted in 2015 to investigate the adverse events immediately post donation. Donor characteristics such as age, blood pressure, hemoglobin level, weight and history of donation were described and tested as potential risk predictors. Eligible blood donors were 18,936/24,634 (76.8%). Results Incidence of adverse events found 1.1% (208 donors), of which 0.65% had mild symptoms (chills; nausea; pallor; dizziness; nervousness; headache), while 0.45% had severe symptoms (hypotension; convulsions; syncope; respiratory distress; emesis). Multiple logistic regression showed that, the incidence of adverse events was significantly higher among young age donors |
Databáze: | OpenAIRE |
Externí odkaz: |