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Katy Hospices

Compassionate Hearts Caring Hands

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Free In-Home Consultation 832-410-3193

  • Home
  • About Us
    • Coverage areas
    • Emergency Preparedness
    • Leadership team
    • Testimonials
    • Privacy Policy
  • Services
    • Grief Services
      • Coping Strategies That Work
      • What to Expect
    • Health Care Professionals
    • Veterans Program
    • Which Program is Right for You?
    • In-home Health Care
  • Hospice Care
    • Enter Hospice Care
    • Levels of Care
    • Hospice Settings
    • Paying For Hospice
    • Planning And Decisions
  • Giving
  • Volunteer
  • Employment
  • Blog
  • Contact Us

Understanding Hospice

We’re pleased to provide Understanding Hospice, an educational series we plan to post over the next few months that will outline different aspects of hospice care such as:

  • What is Hospice?
  • Key Questions and Concerns About Hospice
  • Truths About Hospice
  • Importance of Self Care for Caregivers
  • and more!

Be sure to Like our FaceBook page where we’ll let you know we’ve posted a new Understanding Hospice article on our blog. 

The History of Hospice

The term hospice is derived for the word “hospitality.” Dating back to medieval times, it was know as a place where ill travelers could stay during their journey. It was until 1948 was the term “hospice” used in medicine. Dame Cicely Saunders created the first modern hospice in London, St. Christopher’s Hospice.

Here is a timeline of the history of hospice.

1965: Florence Wald, then Dean of the Yale School of Nursing, invites Saunders to become a visiting faculty member of the school for the spring term.

1967: Dame Cicely Saunders creates St. Christopher’s Hospice in the United Kingdom.

1968: Wald takes a sabbatical from Yale to work at St. Christopher’s and learn all she can about hospice.

1969: A book based on more than 500 interviews with dying patients is published, entitled, On Death and Dying.  Written by Dr. Elisabeth Kubler-Ross, it identifies the five stages through which many terminally ill patients progress.  The book becomes an internationally known best seller.  Within it, Kubler-Ross makes a plea for home care as opposed to treatment in an institutional setting and argues that patients should have a choice and the ability to participate in the decisions that affect their destiny.

1972:  Kubler-Ross testifies at the first national hearings on  death with dignity, conducted by the U.S. Senate Special Committee on Aging.

1974:  Florence Wald, along with two pediatricians and a chaplain, founded Connecticut Hospice in Branford, Connecticut. The first hospice legislation is introduced by Senators Frank Church and Frank E. Moss to provide federal funds for hospice programs.

1979: The Health Care Financing Administration (HCFA) initiates demonstration programs at 26 hospices across the country to assess the cost effectiveness of hospice care and to help determine what a hospice is and what it should provide

1982: Congress includes a provision to create a Medicare hospice benefit in the Tax Equity and Fiscal Responsibility Act of 1982

1993: Hospice is included as a nationally guaranteed benefit under President Clinton’s health care reform proposal. Hospice is now an accepted part of the health care continuum.

2005: The American Heart Association and the American College of Cardiology release new guidelines about treating heart failure that includes recommendations that hospice care education be provided early in the course of an illness.

2014: Forty years after the creation of Connecticut Hospice, NHPCO and its affiliates celebrate 40 years of hospice care in the US.

Hospice and Cultural Consideration

Houston is known for being the top city for cultural diversity, passing New York City and Los Angeles. Understanding how different cultures approach death is very important. Through hospice, we provide grief services for everyone involved, but cultural practices are often overlooked. There are many transitions that happen at the end of life and through these transitions there things you should consider.

  • a patient’s perceptions of health and suffering;
  • a patient’s perceptions of death and dying;
  • accepted health care practices and remedies;
  • accepted religious and spiritual beliefs, practices, and rituals;
  • communication patterns and common forms of expression;
  • the role of family, relationships

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Once these things have been observed, the hospice provider can give the patient the proper care. The patient may believe that pain and death are a part of the journey of life. They may also believe that their family must be involved in all areas of their care. Some have religious limitations or rituals important to their end of life process.

Some may want nondisclosure about the serious illness of their loved ones. The reasoning behind this is discussing death is impolite in some cultures, or they don’t want unnecessary anxiety felt by their loved one. However, in 1990 the Federal Patient Determination Act and Patient Self Determination Act were passed, emphasizing the need for the patient’s consent.  

The way to handle these situations is to be respectful of different cultural practices. By having respect and appreciation it will be easier to form a relationship with the patient and their family. Expanding your knowledge of different practices is important as well. The goal of hospice is to bring comfort to the patient and understanding their beliefs is a big part of that.  

7 Hospice Myths and Misconceptions

Hospice care isn’t always the easiest thing to talk about and many people don’t have a clear idea what hospice actually is. Even after 25 years, most Americans aren’t aware of the advantages hospice brings. This mostly comes from our country’s resistance to talk about death. However, hospice is undoubtedly this best choice for end of life care. Not only for the patient, but the family as well. It’s so important to talk about and dismiss the myths that surround the hospice community.

The definition of hospice is a type of care and philosophy of care that focuses on the palliation of a chronically ill, terminally ill or seriously ill patient’s pain and symptoms, and attending to their emotional and spiritual needs. Here are seven of the most common myths of hospice

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Hospice is a place– Actually, hospice care takes place wherever the patient needs. 70% of hospice patients are cared for in their homes.

Hospice is only for Cancer patients or AIDS patients– Statistically, more than half of hospice recipients are diagnosed with other terminal conditions. Serving families coping with the end-stages of chronic diseases, like emphysema, Alzheimer’s, cardiovascular, and neuromuscular diseases.

Choosing hospice means you have given up– The beautiful thing about hospice is that it helps families share in the end of life process, through personal and spiritual connection. Many families find immense comfort when looking back, knowing they did everything possible to make their loved ones final hours peaceful and comfortable.

Hospice is just for the patient– Hospice is a family-centered program, focusing on the grieving families just as much as the patient. Many hospice providers reach out the community as well.

Hospice is only for the elderly– Hospice care is for all ages. However, most patients are seniors.

Medicare won’t cover services–  Beneficiaries can use their Medicare hospice benefits anytime they choose.

Hospice isn’t for people who need a high level of care–   Most hospices are Medicare-certified, requiring that they employ experienced medical and nursing personnel with skills in symptom control.

Coping within the family

Contact:

Maria Patino

832.410.3193

www.katyhospices.com

May 23,2016

 

How a family handles cancer depends a lot on how the family has dealt with problems in the past. Those who are used to communicating openly and sharing feelings are usually able to talk about how cancer is affecting them. Families who solve their problems as individuals instead of a team might have more trouble coping with cancer.

Cancer treatment includes care for the patient and the family, not just the cancer. A mental health professional may already be a part of the cancer care team. If not, talk with the doctor or nurse to learn about other resources that can help you and your family cope with cancer.

People with cancer often say that lack of communication in their families is a problem. Changes in responsibilities can cause resentment and anxiety. Some family members may not feel comfortable openly discussing their feelings. Other family members may avoid the person with cancer because they feel as if they have nothing to offer, don’t know how to act, or feel they can’t do anything to help make the situation better. These factors can all make families more distant at a time when they need to pull together. Many families need help with this. Through family counseling, members can learn to deal with changes within the family and discuss their feelings more comfortably.

 

The role of a Hospice Nurse

Contact: Maria Patino

832.410.3193

katyhospices.com

Hospice and palliative care nurses work in collaboration with other health providers (such as physicians, social workers, or chaplains) within the context of an interdisciplinary team.  Composed of highly qualified, specially trained professionals and volunteers, the team blends their strengths together to anticipate and meet the needs of the patient and family facing terminal illness and bereavement.

Hospice and palliative nurses distinguish themselves from their colleagues in other nursing specialty practices by their unwavering focus on end-of-life care. Hospice and palliative care includes 24-hour nursing availability, management of pain and other symptoms, and family support. By providing expert management of pain and other symptoms combined with compassionate listening and counseling skills, hospice and palliative nurse promote the highest quality of life for the patient and family.

Regardless of the setting, hospice and palliative nurses strive to achieve an understanding of specific end-of-life issues from the perspective of each patient and his or her family.  To accomplish this, nurses collaborate in a cultural assessment of the patient and family and provide culturally sensitive care.

Hospice and palliative nursing is not only practiced at the bedside. Nurses, consistent with their individual educational preparation, experience and roles, promote the highest standards of end-of-lie care through community and professional education, participation in demonstration grants, and in end-of-life research. As society’s needs change and awareness of the issues surrounding the end of life increases, nurses are called to advocate for the terminally ill and their families through public policy forums, including the legislative process. 

Misconceptions about Hospice and Palliative Care

Contact:
Maria Patino
832.410.3193
katyhospices.com

Misconception
Hospice makes death come sooner.
Reality

Hospice neither hastens nor postpones dying. The aim is to improve the quality of remaining life so patients can enjoy time with family and friends and experience a natural, pain-free death. In some cases, hospice care can extend life.

Misconception
Hospice is giving up hope; it’s better to fight for life.

Reality
Most terminally ill patients experience less anxiety by refocusing hope on what might be realistically achieved in the time remaining. If continuing uncomfortable and painful curative treatment for an illness is fruitless, hospice patients benefit more from having their symptoms treated instead.
A hospice patient who shows signs of recovery can’t return to regular medical treatment.

Misconception
If a patient’s condition improves, they can be discharged from hospice and return to curative treatment, or resume their daily lives. If need be, they can later return to hospice care.

Reality
A hospice patient can’t change his or her mind and return to curative treatment even if their prognosis hasn’t changed.

Misconception
A patient can go on and off hospice care as needed—or if they change their mind and decide to return to curative treatment. They may also enter hospital for certain types of treatment if it involves improving their quality of life.
Hospice care is limited to a maximum of six months.

Reality
In the U.S., many insurance companies, as well as the Medicare Hospice Benefit, require that a terminally ill patient has a prognosis of six months or less to start hospice, but a terminally-ill patient can receive hospice care for as long as necessary.

Help With Advance Care Planning

Advance care planning is making decisions about the care you would want to receive if you become unable to speak for yourself. These are your decisions to make, regardless of what you choose for your care, and the discussions with your loved ones. If you are in an accident or have an illness that leaves you unable to talk about your wishes, who will speak for you? You can tell your family, friends and healthcare providers Accredited Hospices of America what your wishes and personal beliefs are about continuing or withdrawing medical treatments at the end of life.
Advance care planning includes:
Getting information on the types of life-sustaining treatments that are available.
Deciding what types of treatment you would or would not want should you be diagnosed with a life-limiting illness.
Sharing your personal values with your loved ones.
Completing advance directives to put into writing what types of treatment you would or would not want should you be unable to speak for yourself.

Communicating Your End-of-Life Wishes

Decisions about end-of-life care are deeply personal, and are based on your values and beliefs. Because it is impossible to foresee every type of circumstance or illness, it is essential to think in general about what is important to you. Conversations that focus on your wishes and beliefs will relieve loved ones and healthcare providers of the need to guess what you would want.

For more information, visit accreditedhospicesofamerica.com

14511 Old Katy Rd. Suite 394
Houston, Tx 77079
832.408.7999 (Office)
866.708.0821 (Fax)

What is Hospice

Contact:

Jerry Mosbacher

832.410.3192

[email protected]

Accredited Hospices of America is specialized type of care for those facing a life-limiting illness, their families and their caregivers.

Accredited Hospices of America care addresses the patient’s physical, emotional, social and spiritual needs.

Accredited Hospices of America care also helps the patient’s family caregivers.

Accredited Hospices of America care takes place in the patient’s home or in a home-like setting.

Accredited Hospices of America care concentrates on managing a patient’s pain and other symptoms so that the patient may live as comfortable as possible and make the most of the time that remains.

Accredited Hospices of America care believes the quality of life to be as important as length of life.

Choosing to elect hospice care is an important decision that can greatly benefit the quality of life for a patient with a life-limiting illness in addition to proving support to a patient’s family during a difficult time.

To help you better understand how hospice care can benefit you or a loved one, we recommend that you review our list of Frequently Asked Questions (FAQs) listed below:

Is hospice for those with cancer only?

No, Hospice patients are living with a wide range of diagnoses including heart disease, cancer, dementia, lung disease and others. However, regardless of a patient’s condition or age hospices open their doors and their hearts to all persons diagnosed with life-limiting illnesses and their families.

Hospice is NOT a place.

Hospice services can be provided to a person with limited life expectancy and his/her family, wherever they live. This means a patient living in a nursing facility or long-term care facility and his/her family can receive specialized visits/contacts from physicians, nurses, aides, chaplains, social workers, and volunteers, in addition to other care and services provided by the nursing facility. The hospice and nursing home will have a written agreement in place in order for the hospice to serve residents of the facility.

How does hospice care begin?

Typically, hospice care starts as soon as a formal request or a ‘referral’ is made. Accredited Hospices of America will visit the patient within 48 hours of referral, pending the physician’s approval, providing the visit meets the needs and schedule of the patient and family/primary caregiver. Hospice care begins within a day of two of referral. However, in urgent situations, hospice services may begin sooner. The patient of a family member may “self-refer” and request an evaluation for eligibility for receiving hospice services.

What specific assistance does hospice provide?

Accredited Hospices of America hospice patients and their families are cared for by a team of doctors, nurses, social workers, counselors, aides, spiritual, caregivers, therapist, and volunteers- working together in a team to address the patient’s and family’s identified needs. In addition, hospices help provide medications, supplies, equipment, hospital services, and additional helpers in the home, as appropriate.

How does hospice manage pain?

Accredited Hospices of America’s nurses and physicians are experts in the latest medications and devices for pain and symptom relief. In addition, physical and occupational therapists assist patients to be as mobile and self-sufficient as possible, and they are often joined by specialists schooled in music therapy, are therapy, diet counseling,and other therapies. Accredited hospices of America believes that emotional and spiritual pain are just as real and in need of attention as physical pain, so it addresses these, as well. Counselors, including spiritual caregivers, are available.

Is there any special equipment or changes I have to make in my home before hospice care begins?

Accredited Hospices of America will asses your needs, recommend any necessary equipment, and help make arrangements to obtain it. Often the need for equipment is minimal at first and increases as the patient’s needs change.

Is hospice covered by insurance?

Hospice coverage is widely available provided by Medicare nationwide, by Medicaid in Texas, and by most private health insurance policies. To be sure of coverage, families should, of course, check with their employer or health insurance provider.

If the patient is eligible for Medicare, will there be any additional expenses to be paid?

Medicare covers all services and supplies related to the life-limiting illness for the hospice patient. In some hospices, the patient may be required to pay a 5% “co-payment” on mediation and a 5% co-payment for respite care.

When should a decision about entering a hospice Program be made and who should make it?

At any time during a life-limiting illness, it is appropriate to discuss all of a patient’s care options, including hospice. By law the decision belongs to the patient. Because hospice care includes family members and other caregivers, they are also considered an important part of the decision-making process. Sometimes, people have concerns about changing the focus of care from disease-modifying to focus on comfort care and quality of life. Accredited Hospices of America’s staff members are highly sensitive to these concerns and are always available to discuss them with the patient, family and physician.

What is Palliative Care?

If you are not familiar with the term ”palliative” care, it is a medial specialty focused on managing the physical and emotional impact of serious illness. Sometimes people think palliative and hospice care are synonymous. They are not. Some organizations provided both hospice and palliative care. Hospice is a specific branch of palliative care for those with a terminal diagnosis. It is important to know you DO NOT have to forgo curative treatment or have a terminal diagnosis to receive palliative care.

ACCREDITED HOSPICES AWARDED GOLD SEAL

June 12, 2015 Contact:

Debbie Mosbacher 832.408.7999 [email protected]

ACCREDITED HOSPICES OF AMERICA AWARDED GOLD SEAL OF APPROVAL FROM THE JOINT COMMISSIONM

HOUSTON, TX, JUNE 12, 2015, Accredited Hospices of America today announced that it has earned The Joint Commission’s Gold Seal of Approval® for Hospice Accreditation by demonstrating continuous compliance with its performance standards. The Gold Seal of Approval® is a symbol of quality that reflects an organization’s commitment to providing safe and effective care.
Accredited Hospices of America underwent a rigorous on-site survey in June, 2015. During the survey, compliance with hospice care standards reflecting key organization areas was evaluated, including the provision of care, treatment and services, emergency management, human resources, individual rights and responsibilities, and leadership.

Established in 1988, The Joint Commission’s Hospice Accreditation program supports the efforts of its accredited organizations to help deliver safe, high quality care and services. Accreditation by The Joint Commission and the gold seal serve as an indication that the organization has demonstrated compliance to these recognized standards of safe and quality care.”

Accredited Hospices of America is pleased to receive accreditation from The Joint Commission, the premier health care quality improvement and accrediting body in the nation,” added Jerry Mosbacher, Administrator, Accredited Hospices of America. “Staff from across our organization continue to work together to straighten the continuum up Care and to deliver and maintain optimal hospice services for those in our community.”

The Joint Commission Hospice standards are developed in consultation with health care experts, home care providers and researchers, as well as industry experts, purchasers and consumers. The standards are informed by scientific literature and expert consensus to help organizations measure, Accesss and improve performance.

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The Joint Commission

Founded in 1951, the Joint Commission seeks to continuously improve health care for the public, in collaboration with other stakeholders,by evaluating health care organizations and inspiring them to excel in providing safe and effective care of the highest quality and value. The Joint Commission accredits and certifies nearly 21000 health care organizations and programs in the United States. An independent, non-profit organization, The Joint Commission is the nation’s oldest and largest standards – setting and accrediting body in health care. Learn more about the Joint Commission at www.Jointcommission.org.

Accredited Hospice of America in Houston, Texas is a leading provider of hospice care in our goal is to provide the best and most comprehensive hospice care services available. Hospice care is not a standardized service; therefore, Hospice cannot, and you’re not, for Riley same level of care. We are different from other Hospice and the Houston area because of our dedication to excellence and the inclusion of families in our care plans.

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Common questions:

  • What Is Hospice?
  • Truths About Hospice
  • Paying For Hospice

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Katy Hospices
14520 Old Katy Road, Suite 97
Houston, TX 77079832-410-3193

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Accredited Hospices of America™ has received
accreditation by the Joint Commission, which
is recognized nationally as the Gold Seal of
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