コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 ost often associated with symptoms requiring palliative care.
2 hrough 2014, of which 76,659 (1.5%) involved palliative care.
3 mpt treatment of early invasive cancers, and palliative care.
4 insurance) were also less likely to receive palliative care.
5 for heart transplantation, or initiation of palliative care.
6 ng improving access to effective hospice and palliative care.
7 dy expressed negative attitudes toward early palliative care.
8 tice gap between curative models of care and palliative care.
9 e barriers to timely referral and receipt of palliative care.
10 emoving ICU patients identified as receiving palliative care.
11 ome, and less likely to receive high-quality palliative care.
12 the key point of entry for timely access to palliative care.
13 l barriers to optimal health care, including palliative care.
14 models to further improve access to quality palliative care.
15 been routinely incorporated into oncology or palliative care.
16 st practices recognized for dissemination of palliative care.
17 he best possible care to patients, including palliative care.
18 tom relief and other essential components of palliative care.
19 members to explore challenges in delivering palliative care; 10 filmed semi-structured interviews wi
21 (SOC) (103), investigational therapy (28) or palliative care (40); 9 died before treatment assignment
22 of family members agreed with the concept of palliative care (90.4%) with 17.3% of the family members
24 is required to evaluate the cost effects of palliative care across the entire disease trajectory.
28 ges to the quality measurement framework for palliative care and a new way to match palliative care s
30 that a widely-held but paradoxical view that palliative care and dying patients are different from th
32 ering as defined by the Lancet Commission on Palliative Care and Pain Relief, by combining WHO mortal
33 ian responses should develop and incorporate palliative care and symptom relief strategies that addre
34 is very limited evidence about the need for palliative care and symptom relief to guide the implemen
35 s when making decisions on whether to select palliative care and transition to hospice or whether to
36 h increased caregiver willingness to endorse palliative care and withdraw life-sustaining agents in a
40 tinuum of cancer control, from prevention to palliative care, and in the development of high-quality
42 uch as refractory breathlessness; short-term palliative care; and, in settings with limited access to
46 logy organizations' recommendations of early palliative care as a cancer care best practice for patie
48 er, in the Eastern Mediterranean Region, the palliative care available is variable and inconsistent.
51 nce-based delirium care for people receiving palliative care, both in specialist units, and the wider
53 strated more complex dynamics, but expanding palliative care capacity to meet clinical guidelines and
54 ts (knowledge, attitude, and experiences) of palliative care, caregiver burden, family function, pati
56 lies, whether done by oncology clinicians or palliative care clinicians, requires patient-centered co
58 care in minority hospitals had lower odds of palliative care compared with those treated in white hos
59 norities had a lower likelihood of receiving palliative care compared with whites in any hospital str
61 f patients with primarily noncancer illness, palliative care, compared with usual care, was statistic
62 ility of any of one hospital-based resource (palliative care consultants) or four ICU-based resources
63 (median, 3 vs 2 d; p = 0.001), less frequent palliative care consultation (17.6% vs 32.4%; p = 0.0006
64 rather than PAC were more likely to receive palliative care consultation (OR, 4.44; 95% CI, 2.12 to
66 s and communication, propose indications for palliative care consultation in paediatric advanced hear
72 e-sustaining therapy, triggers for automated palliative care consultation, protocol for family meetin
75 are; and, in settings with limited access to palliative care, consultation only in specific circumsta
77 spital bills for them), stillbirths averted, palliative care, contraception, and child physical and i
78 Palliative care education and guidelines for palliative care could improve the self-efficacy of care
83 rs exist to the development and expansion of palliative care delivery in this region, including the a
85 ch of the five clinical models of specialist palliative care delivery, including outpatient clinics,
87 15 staff members about their experiences of palliative care delivery; 5 focus groups with 64 staff m
89 prioritization of both active treatments and palliative care, despite limited evidence that cancer is
90 view of peer-reviewed, published articles on palliative care development between 2005-16 for each Afr
91 ver, there is still minimal to no identified palliative care development in most African countries.
92 tients potentially benefitting from directed palliative care discussions and reduce the number of ICU
93 Yet, an increase in attention to primary palliative care (e.g., basic physical and emotional symp
95 r-resourced rural practices; and using novel palliative care education delivery methods to increase c
96 es, little partnership working, insufficient palliative care education for health-care professionals
97 urpose The early integration of oncology and palliative care (EIPC) improves quality of life (QOL) an
102 tes in any hospital stratum, but the odds of palliative care for both white and minority intracerebra
106 ease during the study period in provision of palliative care for inpatients with ESKD, significant ra
107 und studies to clearly elucidate the role of palliative care for patients and families living with th
108 ncludes education, screening, treatment, and palliative care for refugees and nationals and prioritis
109 dations related to treatment, follow-up, and palliative care from the 2018 version of this guideline.
110 s included facility type and availability of palliative care guidelines, palliative care team and pal
112 Early research studies on the economics of palliative care have reported a general pattern of cost
113 t palliative care services and 19 specialist palliative care health professionals (predominantly comm
114 ons and supplies can provide pain relief and palliative care; however, the practical availability of
116 cology services (eg, paediatric oncology and palliative care), improving access to opioids, and devel
117 ients (11%), treatment was redirected toward palliative care in 14 patients (13%), and surveillance f
118 ation can introduce patients and families to palliative care in a nonthreatening way, build patient t
119 e team for more complex cases-is unique from palliative care in adults given its focus on care of the
120 ensive review on the development of national palliative care in Africa was undertaken 12 years ago, i
122 In a secondary analysis of the PAL-HF trial (Palliative Care in Heart Failure), we analyzed differenc
125 ery in this region, including the absence of palliative care in national policies, little partnership
127 ge and achieve health equity with respect to palliative care in patient groups that have been underst
128 plant recipients, and emphasizes the role of palliative care in patients with cardiorenal syndrome.
129 assess attitudes toward early integration of palliative care in pediatric oncology patient-parent pai
131 e the illness-related suffering and need for palliative care in Rohingya refugees and caregivers in B
134 advance the field and improve integration of palliative care in the care of children with heart disea
135 ry capacity survey to identify the status of palliative care in the Eastern Mediterranean Region, inc
137 Limitations to understanding disparities in palliative care include the fact that much of the availa
138 are many delirium evidence-practice gaps in palliative care, including that the condition is under-r
139 robust evidence demonstrates that specialty palliative care integrated into oncology care improves p
140 nt autologous or allogeneic HCT to inpatient palliative care integrated with transplant care (n = 81)
143 Accumulating data demonstrate that early palliative care, integrated with oncology care, not only
144 ific, cultural, and system-based barriers to palliative care integration and optimal end-of-life care
147 mptom-related causes, attitudes toward early palliative care integration, and patient-parent concorda
149 15, to usual care (UC) (n = 75) or UC plus a palliative care intervention (UC + PAL) (n = 75) at a si
151 rs investigated whether an interdisciplinary palliative care intervention in addition to evidence-bas
153 there may be a sex disparity in response to palliative care intervention, suggesting that sex-specif
154 search is needed to define the standards for palliative care interventions and to refine the models t
155 studies show that advance care planning and palliative care interventions are associated with a redu
156 In this context, advance care planning and palliative care interventions designed to clarify patien
160 provement of depression resulting from early palliative care interventions; results for quality of li
163 procedures to guide integration of specialty palliative care into oncology have led to a proliferatio
164 idence regarding the need for integration of palliative care into routine oncology care and describes
165 clinical opinion (PCO) on the integration of palliative care into standard oncology care for all pati
167 en and parents expressed opposition to early palliative care involvement (2 [1.6%] and 8 [6.2%]) or p
168 ents and their families may not need or want palliative care involvement early in the disease traject
171 Addressing the quality gap in ICU-based palliative care is limited by uncertainty about acceptab
172 ng a deeper understanding of the barriers to palliative care is necessary from patients, families, re
176 rstanding of decision-making concepts (e.g., palliative care) is impaired; 5) treatment limitations a
182 erefore, little is known about whether early palliative care models are applicable in these low-resou
183 rs and mediators of the effect of integrated palliative care models on patient-reported outcomes and
188 Patients with glioma present with complex palliative care needs throughout their disease trajector
189 tic expectations about return home and unmet palliative care needs, suggesting the need for integrati
191 nce in palliative care unit populations; and palliative care nurses had unmet delirium knowledge need
194 sts in medicine, surgery, radiation therapy, palliative care, nursing, and pathology, along with pati
197 stralia and New Zealand for the purposes of "palliative care of a dying patient" or "potential organ
198 sible evidence-based recommendations for the palliative care of adult patients with glioma, with the
199 tions, and provide a practical framework for palliative care of caregivers in oncology settings.
201 vidence supporting the beneficial effects of palliative care on patient coping as well as the mechani
204 has ever explored the willingness to receive palliative care or terminal withdrawal and the factors i
205 5, p < 0.001), and to not receive specialist palliative care (OR 1.13, 95% CI 1.07-1.19, p < 0.001).
206 e were more likely to not receive specialist palliative care (OR 1.26, 95% CI 1.07-1.49, p = 0.005).
207 arities, enhancing education and research in palliative care, overcoming disparities, and innovating
208 e; 10 filmed semi-structured interviews with palliative care patients or their family members; a co-d
209 We evaluated the impact of early integrated palliative care (PC) in patients with newly diagnosed lu
212 g group representing critical care medicine, palliative care, pediatric medicine, nursing, social wor
213 formational and supportive meetings led by a palliative care physician and nurse practitioner for sur
214 perts-a nephrologist and a general internist-palliative care physician-reflect on the care of a patie
217 urgical, mechanical circulatory support, and palliative care practices; advocates for the development
218 eys that assessed attitudes about specialist palliative care presence and integration into the ICU se
220 harge from a hospital that had an outpatient palliative care program (IRR, 0.90; 95% CI, 0.83 to 0.97
221 ng, as well as acceptability of 23 published palliative care prompts (triggers) for specialist consul
222 ric palliative oncology-encompassing primary palliative care provided by the multidisciplinary oncolo
223 linary oncology team as well as subspecialty palliative care provided by the palliative care team for
224 nterprofessional team led by board-certified palliative care providers within 48 hours of ICU admissi
227 at mentioned at least one dimension of WHO's palliative care public health strategy (implementation o
230 ionship was found between the CriSTAL score, palliative care referral, and in-hospital mortality in p
231 pilot study was to investigate the timing of palliative care referrals in patients receiving rapid re
234 tional Assessment of Chronic Illness Therapy-Palliative Care scale (115.7 versus 120.3; P=0.27) score
235 tional Assessment of Chronic Illness Therapy-Palliative Care scale (FACIT-Pal), assessed at 6 months.
236 tional Assessment of Chronic Illness Therapy-Palliative Care scale (range, 0 [worst] to 184 [best]; m
237 tional Assessment of Chronic Illness Therapy-Palliative Care score mean difference, 4.7 [95% CI, -6.3
238 Each of these five models of specialist palliative care serve a different patient population alo
239 y less likely than white patients to receive palliative care services (adjusted odds ratio [aOR], 0.7
240 under the care of community-based specialist palliative care services and 19 specialist palliative ca
241 ite these substantial unmet needs, specialty palliative care services are infrequently consulted for
242 isparities is necessary to improve access to palliative care services for the vulnerable ESKD populat
243 formation showed an increased development of palliative care services in a subset of African countrie
244 Little is known about disparity in use of palliative care services in such patients in the inpatie
245 k for palliative care and a new way to match palliative care services to patients with advanced cance
246 lyses from RCTs in the 2012 PCO on providing palliative care services to patients with cancer and/or
247 creening, pathology, oncology, surgical, and palliative care services, although some examples of inno
248 revention, improving cancer surveillance and palliative care services, and developing targeted treatm
249 ent, disease management, rehabilitation, and palliative care services, coordinated across the differe
250 ith advanced cancer should receive dedicated palliative care services, early in the disease course, c
253 th increasing numbers of deaths from cancer, palliative care should be available to relieve suffering
255 f life and increased family understanding of palliative care significantly associated with increased
256 Here, 2 oncologists, 1 of whom is also a palliative care specialist, debate the guideline and dis
258 patients, family and friend caregivers, and palliative care specialists to update the 2012 American
259 ion; differences arise from diverse roles of palliative care specialists within cancer care globally.
261 using the CriSTAL tool to stimulate earlier Palliative Care Team (PCT) referral served as an underly
263 l competency training for all members of the palliative care team and referring providers needs to be
264 subspecialty palliative care provided by the palliative care team for more complex cases-is unique fr
265 pports that timely involvement of specialist palliative care teams can enhance the care delivered by
266 ng the growing demand for the involvement of palliative care teams in the management of the dying pat
267 Referral of patients to interdisciplinary palliative care teams is optimal, and services may compl
270 , acceptability, and efficacy of integrating palliative care to improve the quality of life and care
271 therapy, orthopaedic surgery and specialist palliative care to minimize the impact of metastatic bon
273 ng in this population, highlight the role of palliative care to promote effective coping strategies i
274 patient preferences for communication about palliative care topics, best practices for communication
275 .22 [1.53-3.21] and 3.11 [2.05-4.71]; formal palliative care training (1.71 [1.32-2.21]); working in
276 to diagnosis and treatment (five practices), palliative care (two practices), imaging (two practices)
277 domized clinical trial conducted at an acute palliative care unit at MD Anderson Cancer Center, Texas
278 erate to high rate of delirium occurrence in palliative care unit populations; and palliative care nu
281 clinics, inpatient consultation teams, acute palliative care units, community-based palliative care,
287 f serious health-related suffering requiring palliative care until 2060 by world regions, age groups,
291 e the association between race/ethnicity and palliative care use within and between the different hos
292 08, p < 0.001), and not receiving specialist palliative care was more likely (OR 1.03, 95% CI 1.02-1.
295 from surgery, anesthesia, critical care, and palliative care were notified of the patient's frailty a
296 was based on a series of trials showing that palliative care, when added to standard oncology treatme
297 rong indicators for expert multidisciplinary palliative care, which incorporates assessment and manag
299 eeds, suggesting the need for integration of palliative care within the long-term acute care hospital
300 e cancer trajectory, combined with a limited palliative care workforce, means that new models of care