Preview

Family Support

Powerful Essays
Open Document
Open Document
9764 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Family Support
Crit Care Nurs Q Vol. 35, No. 3, pp. 299–313 Copyright c 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Experiences and Needs of Families Regarding Prognostic Communication in an Intensive Care Unit
Supporting Families at the End of Life
Karen M. Gutierrez, PhD, RN
This article reports the results of a study designed to explore the experiences and needs of family members for prognostic communication at end of life in an intensive care unit (ICU). Subjects in this qualitative study included 20 family members of patients at high risk for death in 1 adult medical/surgical ICU. All subjects were interviewed once utilizing a semistructured interview format, with approximately half interviewed multiple times during the ICU stay. Families described 5 themes of information-related “work”: (1) hearing and recalling, (2) accessing, (3) interpreting, (4) retaining, and (5) utilizing information for decision making. Barriers, including accessing physicians and cognitive issues from high levels of stress, made this work difficult. Families described a need for prognostic information, especially if the prognosis was poor. Because hearing this news was difficult, they needed it communicated with respect, sensitivity, and compassion. Suggestions for clinical practice to support families in their information-related work are presented. Overall, the importance of providers approaching communication from a holistic perspective, extending beyond simply passing on information, is emphasized. Viewing communication as a therapeutic modality, and communicating with compassion, sensitivity, and a genuine sense of caring, can help provide both the information and the emotional support and comfort families desperately need. Key words: communication, critical care, end of life, family support, intensive care unit

Author Affiliation: Department of Nursing and Health Sciences, Metropolitan State University, St Paul, Minnesota. This work was done at the University of Minnesota.



References: 1. Verhaeghe S, Defloor F, Van Zuuren F, Duijnstee M, Grypdonck M. The needs and experiences of family members of adult patients in an intensive care unit: a review of the literature. J Clin Nurs. 2005;14:501509. 2. Pochard F, Azoulay E, Chevret S, Kentish-Barnes N. Symptoms of anxiety and depression in family members of intensive care unit patients: ethical hypothesis regarding decision-making capacity. Crit Care Med. 2001;29(10):1893-1897.

You May Also Find These Documents Helpful

  • Satisfactory Essays

    Chamberlain College of Nursing — NUR-351— Week 2 Discussion Board Post 1 — Jan 2015…

    • 348 Words
    • 2 Pages
    Satisfactory Essays
  • Satisfactory Essays

    U.S. Department of Health and Human Services Agency for Healthcare Research and Quality www.ahrq.gov AHRQ Pub. No. 08-IP002-A AARP Pub. No. D19005 May 2008 ISBN No. 978-1-58763-338-6…

    • 1008 Words
    • 5 Pages
    Satisfactory Essays
  • Powerful Essays

    1.1 Caring for patients at the end of life is a challenging task that requires not only the consideration of the patient as a whole but also an understanding of the family, social, legal, economic, and institutional circumstances that surround patient care.…

    • 1923 Words
    • 8 Pages
    Powerful Essays
  • Satisfactory Essays

    The team should be knowledgeable to give proactive care, understand the patient's preferences and forgive conflicts. The process of truth telling in advanced cancer or any other terminal illness can be a difficult task. Whenever a patient is too moribund and not in a suitable mental stage, the family carers are required to give informed consent. The doctor and nurse in the palliative care team have to build the communication with a responsible family carer so that confidentiality and dignity for patient's last stage are maintained.[1,2] Communication is meant to deal with ethical questions regarding two fundamental aspects of Palliative Care: To explain the concept of a good death and to resolve the conflicting needs of patient vis-à-vis family.[8]…

    • 183 Words
    • 1 Page
    Satisfactory Essays
  • Better Essays

    Anticipatory Grieving Case

    • 2870 Words
    • 12 Pages

    The family members play an important role and helping care for the patient helps them with the grieving process while providing a supportive environment to express their grief while coping with their feelings (Davidson, 2010). The second intervention would to have been to take a moment to request a chaplain or ask some one to request one for the family to talk to them about what is happening and how they are coping with this situation and if there is a need for spiritual counseling for them or the patient. This gives the family members a chance to express the desire to have any rituals performed for the patient. Also, to help them cope more effectively with the psychological and emotional stain of their family member’s illness and the dying process (Davidson, 2010). Last, the third intervention would be getting the family a list of some activities that the family members can do that will help facilitate with the anticipatory grieving and dealing with the feelings of grief. Being active gives the family members a purpose and helps them to make sense of what is happening. This helps with reshaping their lives and find new meaning in life without their family member (Davidson,…

    • 2870 Words
    • 12 Pages
    Better Essays
  • Powerful Essays

    As stated by Fields, “Do not resuscitate does not mean no care; it means a different kind of care that can be best achieved through end-of-life protocols and education” (2007, p. 294). According to Lachman (2010), do- not-resuscitate orders, or DNRs, are not being initiated early enough in their hospital stay for identified terminal patients. The purpose of this paper is to investigate and focus on a few reasons why this is happening, as well as to provide a few solutions. The terminal patients are the patients with chronic diseases such as end-stage renal disease, congestive heart failure, and diabetes, who have had an exacerbation in their symptoms which has now rendered them terminal. Prognostic tools and evidence-based predictor tools are being implemented more frequently to define these critical, “terminal” patients (Papadimos, 2011). These tools are especially important, because they apply mainly to non-cancer patients, whose terminal prognoses often overlooked. DNRs are not being initiated earlier in the hospital due to barriers such as the semantics of a DNR, doctors not setting the time to have the conversation with the family early enough in the hospital stay, and the miscommunication between healthcare providers, patients, and family members.…

    • 3724 Words
    • 15 Pages
    Powerful Essays
  • Good Essays

    Family caregivers and family members provide valuable information about the patient and issue. Furthermore, goals will be more easily obtained with family input because family members may have better understanding of what tasks are practical. When family members are communicating the health care team, the information should be relevant to the patient’s situation. Additionally, this information should be clear, concise, complete, and correct. When family caregivers are communicating with the patient they can employ therapeutic communication techniques. Moreover, employing these techniques will help in resolving issues that of concern to the patient. Effective communication will benefit a positive patient outcome; conversely, if there is a lack of or ineffective communication within the health care team, a patient’s health outcome may be adversely affected. Therefore, all members of the health care team should strive to improve their communication techniques; this includes interpersonal and patient…

    • 1119 Words
    • 5 Pages
    Good Essays
  • Good Essays

    In hospitals, especially emergency rooms and intensive care units, nurses encounter many critically ill patients. “One-fifth of the patients cared for by critical care nurses die in the intensive care unit” (Browning, 144), when these patients are nearing the end of their lives there are many decisions that need to be made by the patient if they are able and their family. Healthcare workers are put under tremendous amounts of stress in these situations, especially when they disagree with what the current code status of their patient.…

    • 1026 Words
    • 5 Pages
    Good Essays
  • Better Essays

    Advanced Directives

    • 2140 Words
    • 9 Pages

    Advance Directives are a type of blueprint for individuals to map out their plan of care in case they become mentally unable to make decisions. Two highly published cases involving women who lacked decisional capacity started the ball rolling for what became known as the Patient Self- determination Act of 1990 (Odom, 2012). This act required medical professionals to advice patients of their rights once be admitted as a patient. There are moral, ethical and spiritual factors that come into play when a patient is making end of life plans and keeping the family informed will help with the caring through of those decisions even if the patient can no longer make their own choices. As Nurses it our job to educate and inform the patient of these rights and what choices they have in making these types of decisions. We must obtain written consent and document as much information as possible so that a patient feels we are making choices in their best interest.…

    • 2140 Words
    • 9 Pages
    Better Essays
  • Good Essays

    Assistant Professor, University of Maryland School of Nursing, Department of Material and Clinical Health, Baltimore, Maryland, U.S.A. (Received 20 March 1995;revised 13 January 1996;accepted 11 March 1996)…

    • 6406 Words
    • 26 Pages
    Good Essays
  • Better Essays

    Early access to palliative care can make a devastating experience easier for everyone involved. The majority of children with advanced, life-limiting illnesses only receive the support and care they need during their last days. Weeks and even months go by during which they experience unnecessary physical pain, emotional distress, and receive unwanted or unneeded treatment. This is why effective communication between health care providers, the child, and the family members is a vital part of this process.…

    • 1305 Words
    • 6 Pages
    Better Essays
  • Powerful Essays

    A review of journal articles that address the needs of critical care family members reveals ongoing research on this subject. Evidence of needed change in the routine of critical care is revealed in multiple research projects. From the perspective of nursing practice, a more open communication with the family would be a step in resolving emotional stress experienced with the hospitalization of a significant other.…

    • 1850 Words
    • 8 Pages
    Powerful Essays
  • Good Essays

    Communicating information about possible life threatening issues can be difficult, but if it is not done well, the communicator…

    • 882 Words
    • 3 Pages
    Good Essays
  • Best Essays

    Rogers, N. (2012, June 27). Handout: NURS2002 [Inter-Professional Paper Outline]. Vancouver: Vancouver Community College, Licensed Practical Nursing Program.…

    • 1707 Words
    • 7 Pages
    Best Essays
  • Powerful Essays

    Compassion Fatigue

    • 1480 Words
    • 6 Pages

    Compassion fatigue is most frequently reported amongst nurses, doctors and other frontline care providers in direct interaction with patients. This condition significantly effects these professionals’ interaction with patients, with families of patients and even with other health workers. In extreme cases, problems in interaction with own family has been reported according to Reese (2009). Reese (2009) further states there is an increasingly awareness of the profound emotional disturbances that occur in health care providers when they witness the pain and suffering of the patients in the face of an incurable disease such as cancer. Care providers are often partners in the journey of the patients they are attending. At present, an understanding of the effects of the treatment of terminally ill on the caregiver is limited.…

    • 1480 Words
    • 6 Pages
    Powerful Essays