听力与言语-语言病理学

行为科学

医学伦理学

你正在浏览JOURNAL OF PALLIATIVE CARE期刊下所有文献
  • COP2ING With a New Normal: Navigating the Return to Society for Older Adults With Dementia and Their Caregivers.

    abstract::COVID-19 has stressed the healthcare system in ways our society has not seen before. Less visibly, elderly patients and their caregivers have been stressed as well, both by the virus and by the public health measures required to slow its spread. After months of isolating, patients with dementia and their caregivers ar...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859720984567

    authors: Hamilton CK,Paniagua MA,Jones CA

    更新日期:2021-01-12 00:00:00

  • What Is Good Advance Care Planning According to Hospitalized Palliative Patients and Their Families? An Explorative Study.

    abstract:BACKGROUND:Advance care planning is not well implemented in Belgian hospital practice. In order to obtain successful implementation, implementation theory states that the adopters should be involved in the implementation process. This information can serve as a basis for creating better implementation strategies. AIM:...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859720938583

    authors: Vanderhaeghen B,Bossuyt I,Menten J,Rober P

    更新日期:2020-10-01 00:00:00

  • Would You Be Surprised if This Patient Died in the Next 12 Months? Using the Surprise Question to Increase Palliative Care Consults From the Emergency Department.

    abstract:BACKGROUND:There is a growing movement to increase palliative care consults from the emergency department (ED) to reduce healthcare costs and improve quality of life. The surprise question is a screening tool that emergency medicine physicians may be able to use towards achieving this goal. OBJECTIVE:The objectives of...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859719866698

    authors: Zeng H,Eugene P,Supino M

    更新日期:2020-10-01 00:00:00

  • Working at the Intersection of Palliative End-of-Life and Mental Health Care: Provider Perspectives.

    abstract:OBJECTIVE:Palliative, end-of-life care (PEOLC) providers are poorly resourced in addressing the needs of patients with mental health challenges, and the dying experiences of this cohort-particularly those with a comorbid, chronic and persistent mental illness (CPMI)-are poorly documented. We sought to explore the exper...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859720951360

    authors: Park T,Hegadoren K,Workun B

    更新日期:2020-08-18 00:00:00

  • Chemotherapy at the End of Life.

    abstract:BACKGROUND AND OBJECTIVES:The use of chemotherapy at the end of life in advanced cancer patients has increased and end of life care has become increasingly aggressive. The aim of this study is to evaluate patients receiving chemotherapy in the last 3 months of life and the aggressiveness of end-of-life support of these...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859720946505

    authors: Urvay S,Civelek B,Özaslan E,Sürel AA

    更新日期:2020-08-06 00:00:00

  • The Impact of Socioeconomic Status on Place of Death Among Patients Receiving Home Palliative Care in Toronto, Canada: A Retrospective Cohort Study.

    abstract:BACKGROUND:Socioeconomic disparities in home death have been noted in the literature. Home-based palliative care increases access to home death and has been suggested as a means to decrease these disparities. AIM:Our study examines the association between socioeconomic status and other demographic factors on place of ...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859719855020

    authors: Wales J,Kalia S,Moineddin R,Husain A

    更新日期:2020-07-01 00:00:00

  • Death and End of Life: Perceptions Throughout The Career About Death, Palliative Care, and Educational Process.

    abstract:PURPOSE:To evaluate the perception of attending physicians, medical residents, and undergraduate medical students about death and dying, the end of life (EoL), and palliative care (PC) during training and clinical practice, highlighting knowledge gaps, and the changes needed in medical school curricula. METHOD:Cross-s...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859720923435

    authors: Corradi MLG,Duim E,Rodrigues CIS

    更新日期:2020-05-10 00:00:00

  • Masculinity and Military Culture in VA Hospice and Palliative Care: A Narrative Review With Clinical Recommendations.

    abstract::This article examines the intersection between masculinity, military culture, and hospice and palliative care (HPC). The authors conducted a narrative literature review, supplemented with clinical annotations, to identify the impact of masculinity and military culture on the following topics salient to end-of-life car...

    journal_title:Journal of palliative care

    pub_type: 杂志文章,评审

    doi:10.1177/0825859719851483

    authors: Plys E,Smith R,Jacobs ML

    更新日期:2020-04-01 00:00:00

  • Nebulized Vasopressin for the Control of Hematemesis and Hemoptysis in a Child With Recurrent, Refractory Stage III Burkitt Lymphoma.

    abstract:BACKGROUND:Bleeding occurs with some regularity at the end of life. Patients often endure fatigue, weakness, pain, dyspnea and anxiety. These symptoms are magnified in visually apparent bleeds. Management can be particularly challenging as we attempt to balance therapies with goals of care. Children are at risk for suc...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859719883844

    authors: Dulin JD,Coyne PJ

    更新日期:2020-04-01 00:00:00

  • How Clinician-Family Interactions Potentially Impact Clinicians' Conceptualization and Discussions Regarding Prognostic Uncertainties.

    abstract:OBJECTIVES:Little is known about how clinicians perceive prognostic uncertainty. Our study objective was to identify factors that influence how prognostic uncertainty is viewed by physicians, as it relates to their communications with families. DESIGN:Thirty semi-structured interviews with qualitative content analysis...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859719845005

    authors: Peoples HA,Boone B,Blumenthal-Barby JS,Bruce CR

    更新日期:2020-01-01 00:00:00

  • Longer Duration of Palliative Care in Patients With COPD Is Associated With Death Outside the Hospital.

    abstract:BACKGROUND:Patients with advanced chronic obstructive pulmonary disease (COPD) have a significant symptom burden despite maximal medical therapy, yet few are referred for concomitant palliative care. OBJECTIVE:To evaluate the utilization and impact of palliative care on the location of death and to identify clinical v...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859719851486

    authors: Kraskovsky V,Schneider J,Mador MJ,Provost KA

    更新日期:2019-07-02 00:00:00

  • Quality of Life of Family Caregivers of Patients With Cancer in Korçe, Albania.

    abstract:PURPOSE::The primary objective of this study was to quantify cancer family caregiver (FCG) quality of life (QOL) in a Southern Albanian population and to determine whether differences exist between 4 domains of QOL (physical, psychological, social, and spiritual). This study also sought to compare QOL in our cohort to ...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859718812432

    authors: Judkins J,Laska I,Paice J,Kumthekar P

    更新日期:2019-04-01 00:00:00

  • A Canadian Academic Hospital's Initial MAID Experience: A Health-Care Systems Review.

    abstract:BACKGROUND::Following the Supreme Court of Canada's Carter Decision, medical assistance in dying (MAID) became possible with individual court orders in February 2016. Subsequently, on June 17, 2016, legislation was passed that eliminated the need for court orders, essentially making physicians the arbiters of these req...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859718812446

    authors: Ball IM,Hodge B,Jansen S,Nickle S,Sibbald RW

    更新日期:2019-04-01 00:00:00

  • When Doctors Unlearn English.

    abstract::Doctor-patient communication is a quintessential part of medical care. Yet, several factors challenge its effectiveness. The author, a third year Pediatrics resident, explores the ways medical education creates distance between doctors' and patients' ability to achieve mutual understanding in the clinical setting and ...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859718795438

    authors: Fenton R

    更新日期:2019-01-01 00:00:00

  • Physician-Assisted Suicide and Euthanasia: Emerging Issues From a Global Perspective.

    abstract::Medical professional societies have traditionally opposed physician-assisted suicide and euthanasia (PAS-E), but this opposition may be shifting. We present 5 reasons why physicians shouldn't be involved in PAS-E. 1. Slippery slopes: There is evidence that safeguards in the Netherlands and Belgium are ineffective and ...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859718777325

    authors: Sprung CL,Somerville MA,Radbruch L,Collet NS,Duttge G,Piva JP,Antonelli M,Sulmasy DP,Lemmens W,Ely EW

    更新日期:2018-10-01 00:00:00

  • Inpatient Palliative Care Consultations From a Canadian Clinical Teaching Unit: Who is Referred and When?

    abstract::Inpatient palliative care consultation has been demonstrated to improve quality of life as well as decrease hospital readmissions, intensive care unit transfers, and hospital costs for people with a life limiting illness. The clinical teaching units (CTUs) at London Health Sciences Centre (LHSC) routinely admit patien...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859718781363

    authors: Maddison AR,Malik S,Smaggus A

    更新日期:2018-10-01 00:00:00

  • Advance Care Planning in Chinese Seniors: Cultural Perspectives.

    abstract::In traditional Chinese culture, death was sensitive and mentioning it was sacrilegious and to be avoided. Many Chinese families object to telling the patient a "bad" diagnosis or prognosis, which may hinder the chance in advance care planning (ACP) discussion. While death remains an inevitable consequence of being bor...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859718763644

    authors: Cheng HWB

    更新日期:2018-10-01 00:00:00

  • Palliative Care Leadership.

    abstract::Palliative care is one of the newer health specialties and continues to mature. While there has been remarkable progression of clinical skills and education, there has been a lack of focus on palliative care interdisciplinary leadership or development of leadership skills. This article highlights the importance of int...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859718791427

    authors: Dahlin C,Coyne P,Goldberg J,Vaughan L

    更新日期:2018-08-16 00:00:00

  • Encounters With Health-Care Providers and Advance Directive Completion by Older Adults.

    abstract:BACKGROUND:The Patient Self-Determination Act (PSDA) requires hospitals, home health agencies, nursing homes, and hospice providers to offer new patients information about advance directives. There is little evidence regarding whether encounters with these health-care providers prompt advance directive completion by pa...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859718769099

    authors: Koss C

    更新日期:2018-07-01 00:00:00

  • Life-Sustaining Procedures, Palliative Care Consultation, and Do-Not Resuscitate Status in Dying Patients With COPD in US Hospitals: 2010-2014.

    abstract:AIM:Little is known regarding the extent to which dying patients with chronic obstructive pulmonary disease (COPD) receive life-sustaining procedures and palliative care in US hospitals. We examined temporal trends and the impact of palliative care on the use of life-sustaining procedures in this population. MATERIALS...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859718777375

    authors: Shen JJ,Ko E,Kim P,Kim SJ,Lee YJ,Lee JH,Yoo JW

    更新日期:2018-07-01 00:00:00

  • Advanced Cancer Patients' Perceptions of Dignity: The Impact of Psychologically Distressing Symptoms and Preparatory Grief.

    abstract:PURPOSE:The present study assesses the relationship between patient dignity in advanced cancer and the following variables: psychological distress, preparatory grief, and sociodemographic and clinical characteristics. METHODS:The sample consisted of 120 patients with advanced cancer. The self-administered questionnair...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859718759882

    authors: Kostopoulou S,Parpa E,Tsilika E,Katsaragakis S,Papazoglou I,Zygogianni A,Galanos A,Mystakidou K

    更新日期:2018-04-01 00:00:00

  • E-Pain Reporter: A Digital Pain and Analgesic Diary for Home Hospice Care.

    abstract::Informal hospice caregivers play a key role in managing patients' pain at home, but lack of adherence to doctor-prescribed analgesic regimens and medication errors are significant barriers to truly effective pain management. A digital pain diary may improve caregiver management of pain at home; however, most digital p...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/0825859717722466

    authors: Mayahara M,Wilbur J,O'Mahony S,Breitenstein S

    更新日期:2017-04-01 00:00:00

  • Healthcare Needs of Patients with Amyotrophic Lateral Sclerosis (ALS) in Singapore: A patient-centred qualitative study from multiple perspectives.

    abstract:BACKGROUND:One challenge for those who manage amyotrophic lateral sclerosis (ALS) is to understand patients' needs. AIM:The aim of this study was to examine the needs of Singapore ALS patients from their perspective as well as that of their caregivers and healthcare professionals in order to develop a template for bet...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/082585971503100304

    authors: Ang K,Umapathi T,Tong J,Ng J,Tseng LJ,Woo IM

    更新日期:2015-01-01 00:00:00

  • Barriers to, and Facilitators of Physical Activity in Patients Receiving Chemotherapy for Lung Cancer: An exploratory study.

    abstract:AIM:Physical activity (PA) has a positive effect on the cardiorespiratory fitness, lung cancer symptoms, and quality of life of lung cancer patients. The aim of our study was to identify barriers to, and facilitators of PA in lung cancer patients. METHODS:We collected data from five patients diagnosed with primary, ad...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/082585971503100204

    authors: Mas S,Quantin X,Ninot G

    更新日期:2015-01-01 00:00:00

  • Evaluation of the Utility of the Edmonton Symptom Assessment System (revised) Scale on a Tertiary Palliative Care Unit.

    abstract:AIM:The aim of this study was to evaluate the utility of the Edmonton Symptom Assessment System (ESAS-r) Scale on a tertiary palliative care unit. METHOD:There were 92 admitted patients who participated in the study; the scale was administered to those able to participate on day 1 (n = 35, 38 percent), on day 4 (n = 2...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:10.1177/082585971503100107

    authors: Beddard-Huber E,Jayaraman J,White L,Yeomans W

    更新日期:2015-01-01 00:00:00

  • Initiation of chemotherapy in cancer patients with poor performance status: a population-based analysis.

    abstract:OBJECTIVE:Practice guidelines indicate that patients who have months to weeks left to live should not be offered chemotherapy. We examined factors associated with clinician-reported poor performance status as determined by the Palliative Performance Scale (PPS) and subsequent initiation of intravenous (IV) chemotherapy...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Porter J,Earle C,Atzema C,Liu Y,Howell D,Seow H,Sutradhar R,Dudgeon D,Husain A,Sussman J,Barbera L

    更新日期:2014-10-01 00:00:00

  • The survival time of terminal cancer patients: prediction based on clinical parameters and simple prognostic scores.

    abstract:AIM:By examining clinical parameters associated with survival time and analyzing patients' survival times using prognostic scores, this study aimed to provide helpful information related to the treatment of terminal cancer patients. METHODS:We retrospectively reviewed the medical records of 415 inpatients who died in ...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Kim AS,Youn CH,Ko HJ,Kim HM

    更新日期:2014-04-01 00:00:00

  • Living fully in the shadow of mortal time: psychosocial assets in advanced cancer.

    abstract:OBJECTIVE:This study aimed to characterize the strategies and psychosocial conditions that influence how resilient people live in the face of advanced cancer. METHODS:Grounded theory interviews and a survey of 10 resilient people with advanced cancer were collected and analyzed. FINDINGS:Personal assets - including p...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Wise M,Marchand L

    更新日期:2013-07-01 00:00:00

  • Attitudes of terminally ill older adults toward complementary and alternative medicine therapies.

    abstract:AIM:The aim of this study was to characterize the attitudes of older adults on an inpatient palliative care unit toward complementary and alternative medicine (CAM) therapies. METHODS:A consecutive sample of 33 inpatients (61 to 98 years old) completed a questionnaire that examined their attitudes toward CAM to determ...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Grief CJ,Grossman D,Rootenberg M,Mah L

    更新日期:2013-01-01 00:00:00

  • What is symptom burden: a qualitative exploration of patient definitions.

    abstract::Current definitions of "symptom burden" are largely derived from clinicians, and there are many variations in the way the term is used, defined, and operationalized. The aim of this study was to explore patient perceptions of symptom burden in the context of advanced and incurable disease. A group of 58 cancer patient...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Gill A,Chakraborty A,Selby D

    更新日期:2012-07-01 00:00:00

  • Paramedics' perceptions of their role in palliative care: analysis of focus group transcripts.

    abstract::Paramedics play an important role in out-of-hospital health care. They provide unscheduled care, assisting both patients with minor injuries and those experiencing life-threatening emergencies. Increasingly, paramedics are called on to manage chronic and complex health needs, including symptom relief for patients at t...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Lord B,Récoché K,O'Connor M,Yates P,Service M

    更新日期:2012-04-01 00:00:00

  • Pediatric palliative care education for medical students: development and evaluation of a pilot program.

    abstract:UNLABELLED:In Poland, medical curricula cover palliative care for adults, not for children. This paper evaluates feedback of students who participated in a pilot pediatric palliative care education program. METHOD:An anonymous questionnaire was designed for the students; they were asked to assess each aspect of the pr...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Korzeniewska-Eksterowicz A,Kedzierska B,Cynker-McCarthy M,Przysło Ł,Stolarska M,Nowicki GF,Młynarski W

    更新日期:2012-01-01 00:00:00

  • Emergency department use among end-of-life home care clients.

    abstract::Emergency department (ED) use is a quality-of-care indicator for community-based end-of-life (EOL) care. This study examined ED use by EOL home care clients. The sample included all EOL home care clients who received care from one community care access centre in Ontario, Canada. Information on health was gathered usin...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Brink P,Partanen L

    更新日期:2011-10-01 00:00:00

  • Bereaved family members' assessments of the quality of end-of-life care: what is important?

    abstract::Families of patients are well poised to comment on the end-of-life (EOL) care received by those patients and can provide feedback to care providers and decision makers. To better understand family-member evaluations of the quality of in-patient EOL care, this study draws on qualitative interview data (n = 24) to ident...

    journal_title:Journal of palliative care

    pub_type: 杂志文章,多中心研究

    doi:

    authors: Stajduhar KI,Funk L,Cohen SR,Williams A,Bidgood D,Allan D,Norgrove L,Heyland D

    更新日期:2011-01-01 00:00:00

  • The effectiveness and adverse effects profile of "burst" ketamine in refractory cancer pain: The VCOG PM 1-00 study.

    abstract::This multi-centre study of adjuvant "burst" ketamine in palliative care in-patients documents its effectiveness, duration of pain relief, and adverse effects (AE) profile. Patients received a three-to-five day continuous subcutaneous infusion (CSCI) of ketamine escalated from 100 to 300 to 500 mg/24 hours if required....

    journal_title:Journal of palliative care

    pub_type: 临床试验,杂志文章,多中心研究

    doi:

    authors: Jackson K,Ashby M,Howell D,Petersen J,Brumley D,Good P,Pisasale M,Wein S,Woodruff R

    更新日期:2010-10-01 00:00:00

  • Adaptation, dissemination, and evaluation of a cancer palliative care curriculum for the Indian health system.

    abstract::In 2006, the Indian Health Service (IHS) and the National Cancer Institute (NCI) collaborated to develop an interdisciplinary palliative training program for health professionals in the Indian health system. Their goal was to improve clinician knowledge and skills in palliative care, to train future trainers, and to i...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Arenella C,Finke B,Domer T,Kaur JS,Merriman MP,Ousley A

    更新日期:2010-04-01 00:00:00

  • Determinants of place of death for recipients of home-based palliative care.

    abstract:INTRODUCTION:Health system restructuring combined with the preferences of many terminally ill care recipients and their caregivers has led to an increase in home-based palliative care, yet many care recipients die within institutional settings such as hospitals. This study sought to determine the place of death and its...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Masucci L,Guerriere DN,Cheng R,Coyte PC

    更新日期:2010-01-01 00:00:00

  • Bad news for the patient and the family? The worst part of being a health care professional.

    abstract::In Spain, there is a general tendency to conceal the prognosis from a terminally ill patient. We conducted grounded-theory-based, phenomenological, qualitative research on this using a final sample of 42 in-depth interviews with doctors and nurses from different fields. We found that most health professionals believe ...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Schmidt Rio-Valle J,García Caro MP,Montoya Juarez R,Prados Peña D,Muñoz Vinuesa A,Pappous A,Cruz Quintana F

    更新日期:2009-10-01 00:00:00

  • Referrals of cancer versus non-cancer patients to a palliative care consult team: do they differ?

    abstract::This retrospective study compared 100 consecutive non-cancer (NC) patients referred to a palliative care consult team (PCT) in a Swiss university hospital to 506 cancer (C) patients referred during the same period. The frequencies of reported symptoms were similar in both groups. The main reasons for referral in the N...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Cantin B,Rothuisen LE,Buclin T,Pereira J,Mazzocato C

    更新日期:2009-07-01 00:00:00

  • Volunteers in palliative care make a difference.

    abstract::Family care giving is important for the quality of life of terminally ill patients and their family members. Although family caregivers are generally eager to provide palliative care, at some point it may become too demanding, and then volunteers can make a difference. This four-study paper presents the experiences of...

    journal_title:Journal of palliative care

    pub_type: 杂志文章

    doi:

    authors: Luijkx KG,Schols JM

    更新日期:2009-04-01 00:00:00

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