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"Connection": the integration of a person-centered narrative intervention into the electronic health record - an implementation study

COATS, Heather ; MEEK, Paula M. ; SCHILLING, Lisa M. ; AKARD, Terrah Foster ; DOORENBOS, Ardith Z.
JOURNAL OF PALLIATIVE MEDICINE, 06/2020, vol.23, n°6, p. 785-791

Communication of advance care planning decisions - a retrospective cohort study of documents in general practice

PANOZZO, Laura ; HARVEY, Pam ; ADAMS, Meagan-Jane ; O'CONNOR, Dennis ; WARD, Bernadette
BMC palliative care, 14/07/2020, vol.19, n°1, p. 1-7

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Quality assessments of end-of-life care by medical record review for patients dying in intensive care units in Taiwan

LO, Mei-Ling ; HUANG, Chung-Chi ; HU, Tsung-Hui ; CHOU, Wen-Chi ; CHUANG, Li-Pang ; CHIANG, Ming Chu ; WEN, Fur-Hsing ; TANG, Siew Tzuh
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 07/07/2020, Pagination inconnue

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The usefulness of patient-reported outcomes and the influence on palliative oncology patients and health services - a qualitative study of the prospective outcomes and support initiative

HOWARD, A. Fuchsia ; MEDHURST, Kerensa ; MANHAS, Domnick S. ; YANG, Linda Y. ; BROWN, Steven ; BROWN, Erika ; OLSON, Robert A.
Cancer nursing, 17/06/2020, Pagination inconnue

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Directives anticipées - à déposer sur le DMP

MERMET, Olivier
REVUE DU PRATICIEN MEDECINE GENERALE, 02/2020, vol.34, n°1036, p. 155-156

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Quality of collaboration and information handovers in palliative care - a survey study on the perspectives of nurses in the Southwest region of the Netherlands

ENGEL, Marijanne ; VAN DER ARK, Andrée ; TAMERUS, Rosanne ; VAN DER HEIDE, Agnes
European journal of public health, 28/03/2020, p. 1-8

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Frequency of discussing and documenting advance care planning in primary care - secondary analysis of a multicenter cross-sectional observational study

HAMANO, Jun ; OISHI, Ai ; MORITA, Tatsuya ; KIZAWA, Yoshiyuki
BMC palliative care, 17/03/2020, vol.19, n°1, p. 1-8

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Thème : Soins. Cote : eD02.04.01

PROJET SOIN ANTICIPE ; COMMUNICATION ; RELATION MEDECIN PATIENT ; DOSSIER PATIENT

Background: To improve the quality of advance care planning (ACP) in primary care, it is important to understand the frequency of and topics involved in the ACP discussion between patients and their family physicians (FPs).
Methods: A secondary analysis of a previous multicenter cross-sectional observational study was performed. The primary outcome of this analysis was the frequency of and topics involved in the ACP discussion between outpatients and FPs. In March 2017, 22 family physicians at 17 clinics scheduled a day to assess outpatients and enrolled patients older than 65 years who were recognized by FPs as having regular visits. We defined three ACP discussion topics: 1) future decline in activities of daily living (ADL), 2) future inability to eat, and 3) surrogate decision makers. FPs assessed whether they had ever discussed any ACP topics with each patient and their family members, and if they had documented the results of these discussions in medical records before patients were enrolled in the present study. We defined patients as being at risk of deteriorating and dying if they had at least 2 positive general indicators or at least 1 positive disease-specific indicator in the Japanese version of the Supportive and Palliative Care Indicators Tool.
Results: In total, 382 patients with a mean age of 77.4 ± 7.9 years were enrolled, and 63.1% were female. Seventy-nine patients (20.7%) had discussed at least one ACP topic with their FPs. However, only 23 patients (6.0%) had discussed an ACP topic with family members and their FPs, with the results being documented in their medical records. The topic of future ADL decline was discussed and documented more often than the other two topics. Patients at risk of deteriorating and dying discussed ACP topics significantly more often than those not at risk of deteriorating and dying (39.4% vs. 16.8%, p < 0.001).
Conclusion: FPs may discuss ACP with some of their patients, but may not often document the results of this discussion in medical records. FPs need to be encouraged to discuss ACP with patients and family members and describe the decisions reached in medical records.

Origine : PubMed

Who are hospice patients and what care is provided in hospices? - a pilot study

KOORN, Remco M. ; VAN KLINKEN, Merel ; DE GRAAF, Everlien ; BRESSERS, Rick E. G. W. ; JOBSE, Adri P. ; VAN DER BAAN, Frederieke ; TEUNISSEN, Saskia C. C. M.
The American journal of hospice and palliative care, 06/2020, vol.37, n°6, p. 448-454

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Passing on death - an audit of the terminology utilized in discharge summaries for deceased patients

HABECK-FARDY, Anna
DEATH STUDIES, 08/08/2019, p. 1-7

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Documentation of palliative and end-of-life care process measures among young adults who died of cancer - a natural language processing approach

POORT, Hanneke ; ZUPANC, Sophia N. ; LEITER, Richard E. ; WRIGHT, Alexi A. ; LINDVALL, Charlotta
Journal of adolescent and young adult oncology, 14/08/2019, p. 1-5

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Advance care planning in the palliative phase of people with intellectual disabilities - analysis of medical files and interviews

VOSS, H. ; VOGEL, A. ; WAGEMANS, A. M. A. ; FRANCKE, A. L. ; METSEMAKERS, J. F. M. ; COURTENS, A. M. ; DE VEER, A. J. E.
Journal of intellectual disability research, 24/06/2019, Pagination inconnue

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The impact of advance care planning on end-of-life care - do the type and timing make a difference for patients with advanced cancer referred to hospice?

PRATER, Laura C. ; WICKIZER, Thomas ; BOWER, Julie K. ; BOSE-BRILL, Seuli
The American journal of hospice and palliative care, 12/2019, vol.36, n°12, p. 1089-1095

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Palliative care specialists in hospice and hospital/community teams predominantly use low doses of sedative medication at the end of life for patient comfort rather than sedation - findings from focus groups and patient records for I-CAN-CARE

VIVAT, Bella ; BEMAND-QURESHI, Lucy ; HARRINGTON, Jane ; DAVIS, Sarah ; STONE, Patrick
PALLIATIVE MEDICINE, 06/2019, vol.33, n°6, p. 578-588

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Patient healthcare passports in community specialist palliative care - a mixed methods study

WHITE, Clare ; SPROULE, Jenny ; BROGAN, Paula ; WATSON, Max
BMJ supportive and palliative care, 18/08/2018, Pagination inconnue

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Describing transitional palliative nursing care using a standardized terminology

HOLLAND, Diane E. ; VANDERBOOM, Catherine E. ; DOSE, Ann Marie ; DELGADO, Adriana M. ; AUSTIN, Christine M. ; INGRAM, Cory J. ; WILD, Ellen M. ; MONSEN, Karen A.
JOURNAL OF HOSPICE AND PALLIATIVE NURSING, 06/2017, vol.19, n°3, p. 275-281

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Use of standardized assessment tools to improve the effectiveness of palliative care rounds - a quality improvement initiative

SPANER, Donna ; CARAISCOS, Valerie B. ; MUYSTR, Christina ; FURMAN, Margaret Lyn ; ZALTZ-DUBIN, Jodi ; WHARTON, Marilyn ; WHITEHEAD, Katherine
JOURNAL OF PALLIATIVE CARE, 10/2017, vol.32, n°3-4, p. 134-140

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Access to medical records for assisted death - clarifying the guidance

TEED, Paul
The British journal of general practice, 11/2017, vol.67, n°664, p. 515

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Understanding factors contributing to inappropriate critical care - a mixed-methods analysis of medical record documentation

NEVILLE, Thanh H. ; TARN, Derjung M. ; YAMAMOTO, Myrtle ; GARBER, Bryan J. ; WENGER, Neil S.
JOURNAL OF PALLIATIVE MEDICINE, 11/2017, vol.20, n°11, p. 1260-1266

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Comparison of methods to identify advance care planning in patients with severe chronic obstructive pulmonary disease exacerbation

STEPHENS, Amanda Renee ; WIENER, Renda Soylemez ; IEONG, Michael H.
JOURNAL OF PALLIATIVE MEDICINE, 03/2018, vol.21, n°3, p. 284-289

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Disenfranchised grief and physician burnout

LATHROP, Deborah
Annals of family medicine, 07/2017, vol.15, n°4, p. 375-378

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