Åsa Grauman
Åsa Grauman
Postdoc
Åsa Grauman uses preference studies where both qualitative and quantitative methods are included, to understand how people balance their interests and values. She studies cancer patients' (acute myological leukemia and colorectal cancer) preferences and perspectives on individualized treatment using algorithms sequences techniques. The research is part of the multidisciplinary projects MEET-AML and ONCOLOGICS. Within the IMI-research project Screen4care, she studies parents' preferences regarding newborn screening for rare diseases. She also validates an instrument (Genetic Outcome Scale) to be able to evaluate how screening affects parents' degree of empowerment in Germany and Italy.
Åsa Grauman has a master's degree in public health science and has a doctorate in medical science from Uppsala University. Her PhD project was about how people perceive their risk of suffering from heart disease, how people are affected by cardiovascular risk information and their preferences of how risk information should be conveyed.
E-mail: asa.grauman@crb.uu.se
Phone: +46 18 471 62 44
Recently in media
- Svenskarna lurar sig själva om risk för hjärtinfarkt
Vetenskapsradion, 2022-02-21 - Därför kan långvarig stress leda till hjärtinfarkt
Vetenskapsradion, 2022-02-18 - Uppsala University: Unequal Knowledge About Cardiovascular Diseases
India Education Daily, 2022-02-09 - Unequal knowledge about cardiovascular diseases
Informationsdienst Wissenschaft, 2022-02-08 - While understanding causes of cardiovascular diseases, not everyone recognizes their own risks
Medical Xpress, 2022-02-08 - Många underskattar hjärtsjukdomar
Södermanlands Nyheter, 2021-09-25 - Många underskattar sin risk för hjärt-kärlsjukdom
Örebronyheter, 2021-09-24 - Undersökning: Många underskattar risken för hjärt- och kärlsjukdom
EPOCH TIMES, 2021-09-23 - Många underskattar sin risk för hjärt-kärlsjukdom
Hjärt-Lungfonden, 2021-09-23 - Vanligt underskatta risk för hjärtinfarkt
Medicinsk Access, 2021-04-26 - Vanligt underskatta risk för hjärtinfarkt
forskning.se, 2021-04-12 - Gentest ledde inte till ändrat beteende
Vetenskapsradion 2017-03-02
Risk information
We are investigating risk information from serval perspectives.
Managing genetic risk information
Research generates huge amounts of genetic information. How should we handle it? That is what we are trying to find out in a large international research project.
Preferences
Cardiovascular risk information
Åsa Grauman will investigate how research participants perceive their personal risk for cardiovascular disease, and their perceptions on cardiovascular risk information.
Recent publications
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Attitudes and values among the Swedish general public to using human embryonic stem cells for medical treatment
Part of BMC Medical Ethics, 2022.
DOI for Attitudes and values among the Swedish general public to using human embryonic stem cells for medical treatment Download full text (pdf) of Attitudes and values among the Swedish general public to using human embryonic stem cells for medical treatment
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Health literacy and digital health information-seeking behavior - a cross-sectional study among highly educated Swedes
Part of BMC Public Health, 2022.
DOI for Health literacy and digital health information-seeking behavior - a cross-sectional study among highly educated Swedes Download full text (pdf) of Health literacy and digital health information-seeking behavior - a cross-sectional study among highly educated Swedes
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Perceptions on using surplus embryos for the treatment of Parkinson’s disease among the Swedish population: a qualitative study
Part of BMC Medical Ethics, 2022.
DOI for Perceptions on using surplus embryos for the treatment of Parkinson’s disease among the Swedish population: a qualitative study Download full text (pdf) of Perceptions on using surplus embryos for the treatment of Parkinson’s disease among the Swedish population: a qualitative study
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Public perceptions of myocardial infarction: Do illness perceptions predict preferences for health check results
Part of Preventive Medicine Reports, p. 101683-101683, 2022.
DOI for Public perceptions of myocardial infarction: Do illness perceptions predict preferences for health check results Download full text (pdf) of Public perceptions of myocardial infarction: Do illness perceptions predict preferences for health check results
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What CVD risk factors predict self-perceived risk of having a myocardial infarction?: A cross-sectional study
Part of International Journal of Cardiology Cardiovascular Risk and Prevention, 2022.
DOI for What CVD risk factors predict self-perceived risk of having a myocardial infarction?: A cross-sectional study Download full text (pdf) of What CVD risk factors predict self-perceived risk of having a myocardial infarction?: A cross-sectional study
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Grauman, Åsa
The publics’ perspective on cardiovascular risk information: Implications for practice
2021.
DOI for Grauman, Åsa Download full text (pdf) of Grauman, Åsa
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Communicating test results from a general health checkup: the public’s preferences from a discrete choice experiment survey
Part of Patient Related Outcome Measures, p. 649-660, 2021.
DOI for Communicating test results from a general health checkup: the public’s preferences from a discrete choice experiment survey Download full text (pdf) of Communicating test results from a general health checkup: the public’s preferences from a discrete choice experiment survey
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Good general health and lack of family history influence the underestimation of cardiovascular risk: A cross sectional study
Part of European Journal of Cardiovascular Nursing, p. 676-683, 2021.
DOI for Good general health and lack of family history influence the underestimation of cardiovascular risk: A cross sectional study Download full text (pdf) of Good general health and lack of family history influence the underestimation of cardiovascular risk: A cross sectional study
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Short-term mental distress in research participants after receiving cardiovascular risk information
Part of PLOS ONE, 2019.
DOI for Short-term mental distress in research participants after receiving cardiovascular risk information Download full text (pdf) of Short-term mental distress in research participants after receiving cardiovascular risk information
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Exploring research participants' perceptions of cardiovascular risk information-Room for improvement and empowerment
Part of Patient Education and Counseling, p. 1528-1534, 2019.
DOI for Exploring research participants' perceptions of cardiovascular risk information-Room for improvement and empowerment Download full text (pdf) of Exploring research participants' perceptions of cardiovascular risk information-Room for improvement and empowerment
Informing about cardiovascular risk
Any health care interventions should be made after careful consideration of the benefits and risks for the individual. But experts and the general public sometimes have different views on what the benefit actually is. Understanding how the public perceives risk is important for designing the information correctly: to build on the individual's pre-understanding, to bridge knowledge gaps, and to correct inaccuracies. From a societal perspective, it is also important to ensure that health care efforts are equal. By examining which groups benefit from the efforts, they can be directed towards particularly vulnerable groups and individuals.
This policy brief contains Åsa Grauman's recommendations for how best to inform the public about the risk of cardiovascular disease.
