Abstract
Background: Cardiotoxicity, which involves direct effects of the cancer treatment on heart function and structure, may be accelerated in the presence of traditional cardiovascular risk factors.
Purpose: This study developed and piloted a cardiotoxicity risk assessment questionnaire to quantify, for the first time the potential extent of cardiovascular and/or cardiotoxicity risk factors in breast cancer patients before treatment.
Methods: The study was conducted in 2 phases. Phase 1 included content and face validity testing an expert panel consensus and Phase 2 pilot testing of the questionnaire in a sample of breast cancer patients (n = 36) undergoing chemotherapy, at two Australian public hospital oncology clinics. Questionnaires were self administered, in the presence of a research assistant, during patient waiting time for third or fourth cycle of chemotherapy.
Results: Mean age of the female participants was 54.8 years. Family history CVD risk factors included hypercholesterolaemia and myocardial infarction. Participants reported their own CVD risk factors including diabetes 2.8%, hypertension 19.8%, hypercholesterolaemia 11% and sleep apnoea 5%. Lifestyle CVD risk factors included; 0% participants eating the recommended 5 vegetables per day and 78% not eating the recommend 2 fruits per day; 13% reported being current smokers and 75% regular consumers of alcohol, 75% reported being moderately active, 24% had little to no social support and 30% recorded high to very high K10 depression scores and sleeping less than the national average (6.7 hours v. 7.3 hours per night). 61% were overweight or obese. Unwillingness to undertake lifestyle changes was high; alcohol consumption 88%; dietary habits 44%; good emotional/mental health strategies 72%; improve physical activity 61%; quit smoking 68% learn more about heart health 78% and lose weight 50%.
Conclusion: This study is an important first step towards evidence-based and personalised assessment, prevention and management of treatment-associated cardiac burden after breast cancer.
Purpose: This study developed and piloted a cardiotoxicity risk assessment questionnaire to quantify, for the first time the potential extent of cardiovascular and/or cardiotoxicity risk factors in breast cancer patients before treatment.
Methods: The study was conducted in 2 phases. Phase 1 included content and face validity testing an expert panel consensus and Phase 2 pilot testing of the questionnaire in a sample of breast cancer patients (n = 36) undergoing chemotherapy, at two Australian public hospital oncology clinics. Questionnaires were self administered, in the presence of a research assistant, during patient waiting time for third or fourth cycle of chemotherapy.
Results: Mean age of the female participants was 54.8 years. Family history CVD risk factors included hypercholesterolaemia and myocardial infarction. Participants reported their own CVD risk factors including diabetes 2.8%, hypertension 19.8%, hypercholesterolaemia 11% and sleep apnoea 5%. Lifestyle CVD risk factors included; 0% participants eating the recommended 5 vegetables per day and 78% not eating the recommend 2 fruits per day; 13% reported being current smokers and 75% regular consumers of alcohol, 75% reported being moderately active, 24% had little to no social support and 30% recorded high to very high K10 depression scores and sleeping less than the national average (6.7 hours v. 7.3 hours per night). 61% were overweight or obese. Unwillingness to undertake lifestyle changes was high; alcohol consumption 88%; dietary habits 44%; good emotional/mental health strategies 72%; improve physical activity 61%; quit smoking 68% learn more about heart health 78% and lose weight 50%.
Conclusion: This study is an important first step towards evidence-based and personalised assessment, prevention and management of treatment-associated cardiac burden after breast cancer.
Original language | English |
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Article number | 197 |
Pages (from-to) | 129-130 |
Number of pages | 2 |
Journal | Heart, Lung and Circulation |
Volume | 26 |
Issue number | Suppl_2 |
DOIs | |
Publication status | Published - 2017 |