Category: Ethics
Articles about end-of-life ethical issues including ethical dilemmas
Articles about end-of-life ethical issues including ethical dilemmas
You may think that CPR is a miracle that can save anyone’s life, but that is not always the case. CPR is not practical for terminally ill patients, and it can cause more harm than good. In fact, studies show that only about 5% of terminally ill patients who receive CPR survive to leave the hospital. Many of them suffer from brain damage, broken ribs, or infections because of CPR.
This article aims to help you understand the truth about CPR for terminally ill patients. We will debunk ten common myths you may have heard or believed about CPR and provide you with accurate and reliable information. We will also help you make informed and respectful decisions about CPR for your loved one based on their wishes and values.
A groundbreaking skin test has emerged as a potential game-changer in the early detection of Parkinson's disease and related disorders. This article explores the science behind the test, its accuracy, and the ethical implications of early diagnosis. Discover how this innovative approach could revolutionize Parkinson's treatment and patient care.
Choosing between full code and DNR for terminally ill patients can be challenging. This article explains the differences, benefits, and drawbacks of helping caregivers and families make informed decisions.
Hospice care is often misunderstood. A common myth suggests that once a patient with a terminal illness enters hospice, they lose control over their care. This article aims to dispel this misconception and highlight the central role of patient and family autonomy in hospice settings. It's important to note that this discussion primarily applies to patients receiving care at home or in non-facility settings, as facility-based patients may have less control over their care decisions.
Explore the complex decision of using antibiotics in end-of-life care. This article weighs the potential benefits against risks, considering comfort, quality of life, and ethical concerns. Learn how to make informed choices with your healthcare team for compassionate, patient-centered care in life's final stages.
Shielding children from death deprives them of understanding this natural part of life, leading to emotional and psychological consequences. This article explores why exposing children to the dying process is essential for their development and highlights the role of hospice care in supporting families during this time.
Discover how oral ketamine is emerging as a game-changer in palliative care, offering rapid relief for severe depression, anxiety, and emotional distress. This comprehensive guide explores its potential benefits, administration methods, and important considerations for patients and healthcare providers.
Discover how to use the CUS tool and Caring Feedback Model to advocate for your loved one's health. This guide empowers caregivers to communicate effectively with healthcare providers, ensuring their concerns are heard and addressed.
This guide covers the essentials of palliative sedation for hospice patients, including ethical dilemmas, timing, recommended medications, and monitoring effectiveness, ensuring comfort during the end-of-life journey.
Learn how to communicate effectively with healthcare professionals when caring for a loved one with a terminal illness. Improve communication, advocacy, and coping skills to ensure your loved one receives the best care possible.
This article delves into the intricate relationship between dementia and seizures, offering insights on identification, safety protocols, and advocacy for caregivers.
This article delves into the growing importance of End-of-Life Doulas in hospice care. It provides insights into their role, their support to patients and families, and their impact on the quality of end-of-life care.
Hospice care in facilities can face challenges due to facility policies, staffing issues, and lack of coordination with hospice providers. This article sheds light on the struggles patients, families, and hospice nurses face in ensuring timely, appropriate care.
Uncover the importance of regular care plan meetings at healthcare facilities. This guide details participants, goals, benefits, and risks of non-participation.
Dive into the contrasting philosophies of purist and non-purist hospice nurses and doctors. Understand how their views on medication and patient care differ, shaping the terminal phase of a patient’s journey. This article highlights the delicate balance between medical intervention and quality of life in hospice care.
Explore the profound journey of the actively dying. This article unravels the reasons behind their lingering, examining medical interventions and the emotional need for closure. Gain insight into this delicate phase of life."
An article that guides families through understanding and exercising their rights to choose the best hospice care for their loved ones, ensuring their final chapter is written with compassion and respect.
Welcome to our discussion on a topic close to many hearts: the care of our loved ones with dementia. When a family member is diagnosed with dementia, it feels like a part of them slowly fades away. But as they lose parts of themselves, your role in their life becomes even more crucial. This article isn’t just words on a page; it’s a beacon of hope and understanding, shining a light on why your voice, as a family member, is vital in the care of your loved one.
Welcome to our guide on hospice care for undocumented immigrants. This article is crafted with the utmost empathy to support family members and caregivers as they navigate the complexities of end-of-life care. Our goal is to provide a clear understanding of hospice services and the unique challenges faced by undocumented immigrants during these tender moments.
When someone you love is extremely sick and needs hospice care, you may feel scared, sad, or angry. You may not know what to do or how to help them. You are not alone. Many people go through this challenging time.
As a hospice nurse, I have met many families who have loved ones in hospice. Some of them are continually active and involved in their care. They ask questions, make decisions, and speak up for their needs. Others are more passive and trusting. They let the doctors, nurses, and staff do whatever they think is best. They don’t say much or ask for anything.
Who do you think gets better care for their loved ones? The active ones or the passive ones?
Caring for a loved one who has a terminal illness can be extremely rewarding but also particularly challenging. You may feel exhausted, overwhelmed, or isolated by the demands of caregiving. You may also feel guilty or anxious about taking a break from your loved one. But you deserve time to rest, recharge, and care for yourself. That is why hospice respite care can be a great option for you and your loved one.
Hospice respite care is a service that allows you to temporarily place your loved one in a facility, such as a hospital, nursing home, or hospice house, where they can receive professional care and support. You can use this time to do whatever you need or want, such as sleeping, working, running errands, visiting friends, or enjoying a hobby. Respite care can last up to five days at a time.
Explore how to support a loved one's decision to stop eating voluntarily and drinking (VSED) in hospice care. Learn about the ethical, emotional, and practical aspects of VSED, including its impact on patients and families, and how to provide compassionate care during this challenging end-of-life journey.
Caregivers of dementia patients in the final stage face a challenging dilemma: whether to wake their loved ones or let them sleep. This article explores the pros and cons of each approach, offering guidance on making this difficult decision while prioritizing comfort and dignity in end-of-life care.
Pharmaceutical advertisements often highlight the benefits of a particular drug, including its ability to reduce the risk of various health conditions. However, the actual risk reduction these drugs provide may differ from what is portrayed in the advertisements. It is the opinion of the author that if cardiologists and other providers told their patients the absolute risk reduction of statins is 0.8% for all-cause mortality, 1.3% for myocardial infarction and 0.4% for stroke and the side effects of going on a statin include dementia, worsening dementia, confusion, muscle problems, such as aches, pains, weakness, muscle breakdown, falls, nausea, constipation, diarrhea, and increase the risk of type 2 diabetes, would you or anyone else ever agree to take a statin?