The Care Strategy for Families of Terminally Ill Cancer Patients Who Become Unable to Take Nourishment Orally: Recommendations from a Nationwide Survey of Bereaved Family Members' Experiences

Abstract Context Anorexia is one of the most common symptoms in terminally ill cancer patients and causes considerable distress for both patients and their families. Objectives The primary aims of the present study were to clarify the level of the family-perceived emotional distress and necessity fo...

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Veröffentlicht in:Journal of pain and symptom management 2010-11, Vol.40 (5), p.671-683
Hauptverfasser: Yamagishi, Akemi, RN, PhD, Morita, Tatsuya, MD, Miyashita, Mitsunori, RN, PhD, Sato, Kazuki, RN, MHlthSci, Tsuneto, Satoru, MD, PhD, Shima, Yasuo, MD
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container_end_page 683
container_issue 5
container_start_page 671
container_title Journal of pain and symptom management
container_volume 40
creator Yamagishi, Akemi, RN, PhD
Morita, Tatsuya, MD
Miyashita, Mitsunori, RN, PhD
Sato, Kazuki, RN, MHlthSci
Tsuneto, Satoru, MD, PhD
Shima, Yasuo, MD
description Abstract Context Anorexia is one of the most common symptoms in terminally ill cancer patients and causes considerable distress for both patients and their families. Objectives The primary aims of the present study were to clarify the level of the family-perceived emotional distress and necessity for improvement in professional practice when a relative becomes unable to take nourishment orally and explore the determinants of these outcomes. The ultimate aim was to develop an effective care strategy for family members of terminally ill cancer patients who become unable to take nourishment orally. Methods A cross-sectional anonymous nationwide survey was conducted involving 662 bereaved family members of cancer patients who had been admitted to 95 palliative care units throughout Japan. Results A total of 452 bereaved family members returned the questionnaires (effective response rate, 68%). Overall, 80% of family members experienced the situation where a terminally ill relative became unable to take nourishment orally. The reported level of family-perceived emotional distress was very distressing (38%) and distressing (33%). Responses to the family-perceived necessity for improvement in professional practice they received were much improvement needed (4%), considerable improvement needed (10%), and some improvement needed (46%). The independent determinants of a high level of family perceived emotional distress were a sense of helplessness and guilt, and belief that dehydration causes profound distress for dying patients. Independent determinants of a high level of family-perceived necessity for improvement in professional practice were a sense of helplessness and guilt, experience that health care providers did not pay enough attention to family members' concerns, and insufficient relief of the patient's symptoms. Conclusion A considerable number of family members experienced high levels of emotional distress when a terminally ill cancer patient became unable to take nourishment orally, and many perceived a necessity for improvement in professional practice they received. A recommended care strategy includes the following four major domains: 1) relieving the family members' sense of helplessness and guilt, 2) providing up-to-date information about hydration and nutrition at the end of life, 3) understanding family members' concerns and providing emotional support, and 4) relieving the patient's symptoms. Further research is needed to evaluate the effects o
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Objectives The primary aims of the present study were to clarify the level of the family-perceived emotional distress and necessity for improvement in professional practice when a relative becomes unable to take nourishment orally and explore the determinants of these outcomes. The ultimate aim was to develop an effective care strategy for family members of terminally ill cancer patients who become unable to take nourishment orally. Methods A cross-sectional anonymous nationwide survey was conducted involving 662 bereaved family members of cancer patients who had been admitted to 95 palliative care units throughout Japan. Results A total of 452 bereaved family members returned the questionnaires (effective response rate, 68%). Overall, 80% of family members experienced the situation where a terminally ill relative became unable to take nourishment orally. The reported level of family-perceived emotional distress was very distressing (38%) and distressing (33%). Responses to the family-perceived necessity for improvement in professional practice they received were much improvement needed (4%), considerable improvement needed (10%), and some improvement needed (46%). The independent determinants of a high level of family perceived emotional distress were a sense of helplessness and guilt, and belief that dehydration causes profound distress for dying patients. Independent determinants of a high level of family-perceived necessity for improvement in professional practice were a sense of helplessness and guilt, experience that health care providers did not pay enough attention to family members' concerns, and insufficient relief of the patient's symptoms. Conclusion A considerable number of family members experienced high levels of emotional distress when a terminally ill cancer patient became unable to take nourishment orally, and many perceived a necessity for improvement in professional practice they received. A recommended care strategy includes the following four major domains: 1) relieving the family members' sense of helplessness and guilt, 2) providing up-to-date information about hydration and nutrition at the end of life, 3) understanding family members' concerns and providing emotional support, and 4) relieving the patient's symptoms. Further research is needed to evaluate the effects of this care strategy on family members' outcomes, including clinical studies to obtain more accurate understanding of the symptomatic effects of hydration and nutrition in terminally ill cancer patients.</description><identifier>ISSN: 0885-3924</identifier><identifier>EISSN: 1873-6513</identifier><identifier>DOI: 10.1016/j.jpainsymman.2010.02.025</identifier><identifier>PMID: 20800425</identifier><identifier>CODEN: JSPME2</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Anesthesia &amp; Perioperative Care ; Anorexia ; artificial hydration ; Biological and medical sciences ; Cancer ; Caregivers - psychology ; Cross-Sectional Studies ; Emotional distress ; Emotions ; end of life ; family ; Family - psychology ; Humans ; Japan ; Medical sciences ; Necessity ; Neoplasms - complications ; Neoplasms - psychology ; Pain Medicine ; Perception ; Pharmacology. Drug treatments ; Professional practices ; Relatives ; Stress, Psychological - etiology ; Stress, Psychological - psychology ; Surveys and Questionnaires ; Terminal Care - psychology ; Terminally Ill ; Terminally ill people</subject><ispartof>Journal of pain and symptom management, 2010-11, Vol.40 (5), p.671-683</ispartof><rights>U.S. Cancer Pain Relief Committee</rights><rights>2010 U.S. Cancer Pain Relief Committee</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c642t-a18040080824d7abcc3d6ef2596462791576c9dd7794ee5b1b713985754bef9f3</citedby><cites>FETCH-LOGICAL-c642t-a18040080824d7abcc3d6ef2596462791576c9dd7794ee5b1b713985754bef9f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jpainsymman.2010.02.025$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,30999,45994</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=23531165$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20800425$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamagishi, Akemi, RN, PhD</creatorcontrib><creatorcontrib>Morita, Tatsuya, MD</creatorcontrib><creatorcontrib>Miyashita, Mitsunori, RN, PhD</creatorcontrib><creatorcontrib>Sato, Kazuki, RN, MHlthSci</creatorcontrib><creatorcontrib>Tsuneto, Satoru, MD, PhD</creatorcontrib><creatorcontrib>Shima, Yasuo, MD</creatorcontrib><title>The Care Strategy for Families of Terminally Ill Cancer Patients Who Become Unable to Take Nourishment Orally: Recommendations from a Nationwide Survey of Bereaved Family Members' Experiences</title><title>Journal of pain and symptom management</title><addtitle>J Pain Symptom Manage</addtitle><description>Abstract Context Anorexia is one of the most common symptoms in terminally ill cancer patients and causes considerable distress for both patients and their families. Objectives The primary aims of the present study were to clarify the level of the family-perceived emotional distress and necessity for improvement in professional practice when a relative becomes unable to take nourishment orally and explore the determinants of these outcomes. The ultimate aim was to develop an effective care strategy for family members of terminally ill cancer patients who become unable to take nourishment orally. Methods A cross-sectional anonymous nationwide survey was conducted involving 662 bereaved family members of cancer patients who had been admitted to 95 palliative care units throughout Japan. Results A total of 452 bereaved family members returned the questionnaires (effective response rate, 68%). Overall, 80% of family members experienced the situation where a terminally ill relative became unable to take nourishment orally. The reported level of family-perceived emotional distress was very distressing (38%) and distressing (33%). Responses to the family-perceived necessity for improvement in professional practice they received were much improvement needed (4%), considerable improvement needed (10%), and some improvement needed (46%). The independent determinants of a high level of family perceived emotional distress were a sense of helplessness and guilt, and belief that dehydration causes profound distress for dying patients. Independent determinants of a high level of family-perceived necessity for improvement in professional practice were a sense of helplessness and guilt, experience that health care providers did not pay enough attention to family members' concerns, and insufficient relief of the patient's symptoms. Conclusion A considerable number of family members experienced high levels of emotional distress when a terminally ill cancer patient became unable to take nourishment orally, and many perceived a necessity for improvement in professional practice they received. A recommended care strategy includes the following four major domains: 1) relieving the family members' sense of helplessness and guilt, 2) providing up-to-date information about hydration and nutrition at the end of life, 3) understanding family members' concerns and providing emotional support, and 4) relieving the patient's symptoms. Further research is needed to evaluate the effects of this care strategy on family members' outcomes, including clinical studies to obtain more accurate understanding of the symptomatic effects of hydration and nutrition in terminally ill cancer patients.</description><subject>Anesthesia &amp; Perioperative Care</subject><subject>Anorexia</subject><subject>artificial hydration</subject><subject>Biological and medical sciences</subject><subject>Cancer</subject><subject>Caregivers - psychology</subject><subject>Cross-Sectional Studies</subject><subject>Emotional distress</subject><subject>Emotions</subject><subject>end of life</subject><subject>family</subject><subject>Family - psychology</subject><subject>Humans</subject><subject>Japan</subject><subject>Medical sciences</subject><subject>Necessity</subject><subject>Neoplasms - complications</subject><subject>Neoplasms - psychology</subject><subject>Pain Medicine</subject><subject>Perception</subject><subject>Pharmacology. Drug treatments</subject><subject>Professional practices</subject><subject>Relatives</subject><subject>Stress, Psychological - etiology</subject><subject>Stress, Psychological - psychology</subject><subject>Surveys and Questionnaires</subject><subject>Terminal Care - psychology</subject><subject>Terminally Ill</subject><subject>Terminally ill people</subject><issn>0885-3924</issn><issn>1873-6513</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>7QJ</sourceid><recordid>eNqNkttu0zAYgCMEYmXwCshcoF21-BA7NhdIrNpg0g6IdeLScpw_1F0SFzst5Ol4NZy1MMTNkCxZ_vX9B9tflr0ieEYwEW9Ws9XauC4ObWu6GcUpjmla_FE2IbJgU8EJe5xNsJR8yhTND7JnMa4wxpwJ9jQ7oFhinFM-yX4uloDmJgC67oPp4euAah_QqWld4yAiX6MFhNZ1pmkGdNY0Ce4sBPTJ9A66PqIvS4-OwfoW0E1nygZQ79HC3AK69Jvg4rJNGLoKY4G36PNIpkiV0n0XUR18iwy6vDt-d1WaYxO2MIyNjyGA2UK1m2ZAF9CWEOIROvmxhpC6W4jPsye1aSK82O-H2c3pyWL-cXp-9eFs_v58akVO-6khEuc43VrSvCpMaS2rBNSUK5ELWijCC2FVVRWFygF4ScqCMCV5wfMSalWzw-xoV3cd_LcNxF63LlpoGtOB30QtmeKSMSwfJilVTGDGHiQLWWCOBS4SqXakDT7GALVeB9eaMGiC9aiEXum_lNCjEhrTtHjKfbnvsilbqP5k_nYgAa_3gInWNHVIH-ziPcc4I0SM3HzHQXrnrYOgo737hMoFsL2uvPuvcd79U8U2rnOp8S0MEFfJmeRa1ETHlKCvR4dHhUmyN1dKsV_JavEe</recordid><startdate>20101101</startdate><enddate>20101101</enddate><creator>Yamagishi, Akemi, RN, PhD</creator><creator>Morita, Tatsuya, MD</creator><creator>Miyashita, Mitsunori, RN, PhD</creator><creator>Sato, Kazuki, RN, MHlthSci</creator><creator>Tsuneto, Satoru, MD, PhD</creator><creator>Shima, Yasuo, MD</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>ASE</scope><scope>FPQ</scope><scope>K6X</scope><scope>7QJ</scope></search><sort><creationdate>20101101</creationdate><title>The Care Strategy for Families of Terminally Ill Cancer Patients Who Become Unable to Take Nourishment Orally: Recommendations from a Nationwide Survey of Bereaved Family Members' Experiences</title><author>Yamagishi, Akemi, RN, PhD ; Morita, Tatsuya, MD ; Miyashita, Mitsunori, RN, PhD ; Sato, Kazuki, RN, MHlthSci ; Tsuneto, Satoru, MD, PhD ; Shima, Yasuo, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c642t-a18040080824d7abcc3d6ef2596462791576c9dd7794ee5b1b713985754bef9f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Anesthesia &amp; Perioperative Care</topic><topic>Anorexia</topic><topic>artificial hydration</topic><topic>Biological and medical sciences</topic><topic>Cancer</topic><topic>Caregivers - psychology</topic><topic>Cross-Sectional Studies</topic><topic>Emotional distress</topic><topic>Emotions</topic><topic>end of life</topic><topic>family</topic><topic>Family - psychology</topic><topic>Humans</topic><topic>Japan</topic><topic>Medical sciences</topic><topic>Necessity</topic><topic>Neoplasms - complications</topic><topic>Neoplasms - psychology</topic><topic>Pain Medicine</topic><topic>Perception</topic><topic>Pharmacology. Drug treatments</topic><topic>Professional practices</topic><topic>Relatives</topic><topic>Stress, Psychological - etiology</topic><topic>Stress, Psychological - psychology</topic><topic>Surveys and Questionnaires</topic><topic>Terminal Care - psychology</topic><topic>Terminally Ill</topic><topic>Terminally ill people</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamagishi, Akemi, RN, PhD</creatorcontrib><creatorcontrib>Morita, Tatsuya, MD</creatorcontrib><creatorcontrib>Miyashita, Mitsunori, RN, PhD</creatorcontrib><creatorcontrib>Sato, Kazuki, RN, MHlthSci</creatorcontrib><creatorcontrib>Tsuneto, Satoru, MD, PhD</creatorcontrib><creatorcontrib>Shima, Yasuo, MD</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>British Nursing Index</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>British Nursing Index</collection><collection>Applied Social Sciences Index &amp; Abstracts (ASSIA)</collection><jtitle>Journal of pain and symptom management</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamagishi, Akemi, RN, PhD</au><au>Morita, Tatsuya, MD</au><au>Miyashita, Mitsunori, RN, PhD</au><au>Sato, Kazuki, RN, MHlthSci</au><au>Tsuneto, Satoru, MD, PhD</au><au>Shima, Yasuo, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Care Strategy for Families of Terminally Ill Cancer Patients Who Become Unable to Take Nourishment Orally: Recommendations from a Nationwide Survey of Bereaved Family Members' Experiences</atitle><jtitle>Journal of pain and symptom management</jtitle><addtitle>J Pain Symptom Manage</addtitle><date>2010-11-01</date><risdate>2010</risdate><volume>40</volume><issue>5</issue><spage>671</spage><epage>683</epage><pages>671-683</pages><issn>0885-3924</issn><eissn>1873-6513</eissn><coden>JSPME2</coden><abstract>Abstract Context Anorexia is one of the most common symptoms in terminally ill cancer patients and causes considerable distress for both patients and their families. Objectives The primary aims of the present study were to clarify the level of the family-perceived emotional distress and necessity for improvement in professional practice when a relative becomes unable to take nourishment orally and explore the determinants of these outcomes. The ultimate aim was to develop an effective care strategy for family members of terminally ill cancer patients who become unable to take nourishment orally. Methods A cross-sectional anonymous nationwide survey was conducted involving 662 bereaved family members of cancer patients who had been admitted to 95 palliative care units throughout Japan. Results A total of 452 bereaved family members returned the questionnaires (effective response rate, 68%). Overall, 80% of family members experienced the situation where a terminally ill relative became unable to take nourishment orally. The reported level of family-perceived emotional distress was very distressing (38%) and distressing (33%). Responses to the family-perceived necessity for improvement in professional practice they received were much improvement needed (4%), considerable improvement needed (10%), and some improvement needed (46%). The independent determinants of a high level of family perceived emotional distress were a sense of helplessness and guilt, and belief that dehydration causes profound distress for dying patients. Independent determinants of a high level of family-perceived necessity for improvement in professional practice were a sense of helplessness and guilt, experience that health care providers did not pay enough attention to family members' concerns, and insufficient relief of the patient's symptoms. Conclusion A considerable number of family members experienced high levels of emotional distress when a terminally ill cancer patient became unable to take nourishment orally, and many perceived a necessity for improvement in professional practice they received. A recommended care strategy includes the following four major domains: 1) relieving the family members' sense of helplessness and guilt, 2) providing up-to-date information about hydration and nutrition at the end of life, 3) understanding family members' concerns and providing emotional support, and 4) relieving the patient's symptoms. Further research is needed to evaluate the effects of this care strategy on family members' outcomes, including clinical studies to obtain more accurate understanding of the symptomatic effects of hydration and nutrition in terminally ill cancer patients.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>20800425</pmid><doi>10.1016/j.jpainsymman.2010.02.025</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
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subjects Anesthesia & Perioperative Care
Anorexia
artificial hydration
Biological and medical sciences
Cancer
Caregivers - psychology
Cross-Sectional Studies
Emotional distress
Emotions
end of life
family
Family - psychology
Humans
Japan
Medical sciences
Necessity
Neoplasms - complications
Neoplasms - psychology
Pain Medicine
Perception
Pharmacology. Drug treatments
Professional practices
Relatives
Stress, Psychological - etiology
Stress, Psychological - psychology
Surveys and Questionnaires
Terminal Care - psychology
Terminally Ill
Terminally ill people
title The Care Strategy for Families of Terminally Ill Cancer Patients Who Become Unable to Take Nourishment Orally: Recommendations from a Nationwide Survey of Bereaved Family Members' Experiences
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