-
1
-
-
77950874918
-
Do the trajectories of dysnea differ in prevalence and intensity by diagnosis at the end of life? A consecutive cohort study
-
1 Currow, D.C., Smith, J., Davidson, P.M., et al. Do the trajectories of dysnea differ in prevalence and intensity by diagnosis at the end of life? A consecutive cohort study. J Pain Symptom Manage 39 (2010), 680–690.
-
(2010)
J Pain Symptom Manage
, vol.39
, pp. 680-690
-
-
Currow, D.C.1
Smith, J.2
Davidson, P.M.3
-
2
-
-
31344445894
-
A comparison of symptom prevalence in far advanced cancer, AIDS, heart disease, chronic obstructive pulmonary disease and renal disease
-
2 Solano, J.P., Gomes, B., Higginson, I.J., A comparison of symptom prevalence in far advanced cancer, AIDS, heart disease, chronic obstructive pulmonary disease and renal disease. J Pain Symptom Manage 31 (2006), 58–69.
-
(2006)
J Pain Symptom Manage
, vol.31
, pp. 58-69
-
-
Solano, J.P.1
Gomes, B.2
Higginson, I.J.3
-
3
-
-
34547903207
-
Symptoms in patients receiving palliative care: a study on patient-physician encounters in general practice
-
3 Borgsteede, S.D., Deliens, L., Beentjes, B., et al. Symptoms in patients receiving palliative care: a study on patient-physician encounters in general practice. Palliat Med 21 (2007), 417–423.
-
(2007)
Palliat Med
, vol.21
, pp. 417-423
-
-
Borgsteede, S.D.1
Deliens, L.2
Beentjes, B.3
-
4
-
-
0031731047
-
Symptoms and attitudes of 100 consecutive patients admitted to an acute hospice/palliative care unit
-
4 Ng, K., von Gunten, C.F., Symptoms and attitudes of 100 consecutive patients admitted to an acute hospice/palliative care unit. J Pain Symptom Manage 16 (1998), 307–316.
-
(1998)
J Pain Symptom Manage
, vol.16
, pp. 307-316
-
-
Ng, K.1
von Gunten, C.F.2
-
5
-
-
33646006132
-
Breathlessness in cancer and chronic obstructive pulmonary disease: using a qualitative approach to describe the experience of patients and carers
-
5 Booth, S., Silvester, S., Todd, C., Breathlessness in cancer and chronic obstructive pulmonary disease: using a qualitative approach to describe the experience of patients and carers. Palliat Support Care 1 (2003), 337–344.
-
(2003)
Palliat Support Care
, vol.1
, pp. 337-344
-
-
Booth, S.1
Silvester, S.2
Todd, C.3
-
6
-
-
84881649403
-
Development of a Carer Support Needs Assessment Tool (CSNAT) for end of life care practice at home: a qualitative study
-
6 Ewing, G., Grande, G., Development of a Carer Support Needs Assessment Tool (CSNAT) for end of life care practice at home: a qualitative study. Palliat Med 27 (2013), 244–256.
-
(2013)
Palliat Med
, vol.27
, pp. 244-256
-
-
Ewing, G.1
Grande, G.2
-
7
-
-
77956907223
-
White paper on improving support for family carers in palliative care: recommendations from the European Association for Palliative Care Task Force on Family Carers. Part 1
-
7 Payne, S., Hudson, P., Grande, G., et al. White paper on improving support for family carers in palliative care: recommendations from the European Association for Palliative Care Task Force on Family Carers. Part 1. Eur J Palliat Care 17 (2010), 238–245.
-
(2010)
Eur J Palliat Care
, vol.17
, pp. 238-245
-
-
Payne, S.1
Hudson, P.2
Grande, G.3
-
8
-
-
52549108727
-
Respiratory disease: caring for the carers of chronic lung disease sufferers in the community
-
8 Parnell, H., Respiratory disease: caring for the carers of chronic lung disease sufferers in the community. J Commun Nurs 15 (2001), 1–3.
-
(2001)
J Commun Nurs
, vol.15
, pp. 1-3
-
-
Parnell, H.1
-
9
-
-
7944238611
-
Living with severe chronic obstructive pulmonary disease (COPD): perceptions of patients and their carers. An interpretative phenomenological analysis
-
9 Seamark, D.A., Blake, S.D., Seamark, C.J., Halpin, D.M.G., Living with severe chronic obstructive pulmonary disease (COPD): perceptions of patients and their carers. An interpretative phenomenological analysis. Palliat Med 18 (2004), 619–625.
-
(2004)
Palliat Med
, vol.18
, pp. 619-625
-
-
Seamark, D.A.1
Blake, S.D.2
Seamark, C.J.3
Halpin, D.M.G.4
-
10
-
-
3342932327
-
The dyspnea-anxiety-dyspnea cycle—COPD patients' stories of breathlessness: “It's scary/when you can't breathe.”
-
10 Bailey, P.H., The dyspnea-anxiety-dyspnea cycle—COPD patients' stories of breathlessness: “It's scary/when you can't breathe.”. Qual Health Res 14 (2004), 760–778.
-
(2004)
Qual Health Res
, vol.14
, pp. 760-778
-
-
Bailey, P.H.1
-
11
-
-
43049134755
-
Health care utilization of patients with chronic obstructive pulmonary disease and lung cancer in the last 12 months of life
-
11 Goodridge, D., Lawson, J., Duggleby, W., et al. Health care utilization of patients with chronic obstructive pulmonary disease and lung cancer in the last 12 months of life. Respir Med 102 (2008), 885–891.
-
(2008)
Respir Med
, vol.102
, pp. 885-891
-
-
Goodridge, D.1
Lawson, J.2
Duggleby, W.3
-
12
-
-
59749087492
-
Active carers: living with chronic obstructive pulmonary disease
-
12 Spence, A., Hasson, F., Waldron, M., et al. Active carers: living with chronic obstructive pulmonary disease. Int J Palliat Nurs 14 (2008), 368–372.
-
(2008)
Int J Palliat Nurs
, vol.14
, pp. 368-372
-
-
Spence, A.1
Hasson, F.2
Waldron, M.3
-
13
-
-
54249089930
-
Access to services for patients with chronic obstructive pulmonary disease: the invisibility of breathlessness
-
13 Gysels, M., Higginson, I., Access to services for patients with chronic obstructive pulmonary disease: the invisibility of breathlessness. J Pain Symptom Manage 36 (2008), 451–460.
-
(2008)
J Pain Symptom Manage
, vol.36
, pp. 451-460
-
-
Gysels, M.1
Higginson, I.2
-
14
-
-
0036715863
-
‘The Hidden Client’—women caring for husbands with COPD: their experience of quality of life
-
14 Bergs, D., ‘The Hidden Client’—women caring for husbands with COPD: their experience of quality of life. J Clin Nurs 11 (2002), 613–621.
-
(2002)
J Clin Nurs
, vol.11
, pp. 613-621
-
-
Bergs, D.1
-
15
-
-
65949122327
-
Supporting lay carers in end of life care: current gaps and future priorities
-
15 Grande, G., Stajduhar, K., Aoun, S., et al. Supporting lay carers in end of life care: current gaps and future priorities. Palliat Med 23 (2009), 339–344.
-
(2009)
Palliat Med
, vol.23
, pp. 339-344
-
-
Grande, G.1
Stajduhar, K.2
Aoun, S.3
-
16
-
-
78349275770
-
White paper on improving support for family carers in palliative care: recommendations from the European Association for Palliative Care Task Force on Family Carers. Part 2
-
16 Payne, S., Hudson, P., Grande, G., et al. White paper on improving support for family carers in palliative care: recommendations from the European Association for Palliative Care Task Force on Family Carers. Part 2. Eur J Palliat Care 17 (2010), 286–290.
-
(2010)
Eur J Palliat Care
, vol.17
, pp. 286-290
-
-
Payne, S.1
Hudson, P.2
Grande, G.3
-
17
-
-
79959749511
-
Family caregivers and palliative care: current status and agenda for the future
-
17 Hudson, P., Payne, S., Family caregivers and palliative care: current status and agenda for the future. J Palliat Med 14 (2011), 864–869.
-
(2011)
J Palliat Med
, vol.14
, pp. 864-869
-
-
Hudson, P.1
Payne, S.2
-
18
-
-
84555178558
-
How can informal caregivers in cancer and palliative care be supported? An updated systematic literature review of interventions and their effectiveness
-
18 Harding, R., List, S., Epiphanious, E., Jones, H., How can informal caregivers in cancer and palliative care be supported? An updated systematic literature review of interventions and their effectiveness. Palliat Med 26 (2011), 7–22.
-
(2011)
Palliat Med
, vol.26
, pp. 7-22
-
-
Harding, R.1
List, S.2
Epiphanious, E.3
Jones, H.4
-
19
-
-
64549139382
-
A systematic review of informal caregivers' needs in providing home based end-of-life care to people with cancer
-
19 Bee, P.E., Barnes, P., Luker, K.A., A systematic review of informal caregivers' needs in providing home based end-of-life care to people with cancer. J Clin Nurs 18 (2008), 1379–1393.
-
(2008)
J Clin Nurs
, vol.18
, pp. 1379-1393
-
-
Bee, P.E.1
Barnes, P.2
Luker, K.A.3
-
20
-
-
58349119450
-
A review of the information and support needs of family carers of patients with chronic obstructive pulmonary disease
-
20 Caress, A., Luker, K.A., Chalmers, K.I., Salmon, M.P., A review of the information and support needs of family carers of patients with chronic obstructive pulmonary disease. J Clin Nurs 18 (2009), 479–491.
-
(2009)
J Clin Nurs
, vol.18
, pp. 479-491
-
-
Caress, A.1
Luker, K.A.2
Chalmers, K.I.3
Salmon, M.P.4
-
21
-
-
84973909629
-
What are the key elements of educational interventions for lay carers of patients with advanced disease? A systematic literature search and narrative review of structural components, processes and modes of delivery
-
e27
-
21 Farquhar, M., Penfold, C., Walter, F., Kuhn, I., Benson, J., What are the key elements of educational interventions for lay carers of patients with advanced disease? A systematic literature search and narrative review of structural components, processes and modes of delivery. J Pain Symptom Manage 52 (2016), 117–130 e27.
-
(2016)
J Pain Symptom Manage
, vol.52
, pp. 117-130
-
-
Farquhar, M.1
Penfold, C.2
Walter, F.3
Kuhn, I.4
Benson, J.5
-
22
-
-
55549083502
-
Developing and evaluating complex interventions: the new Medical Research Council guidance
-
22 Craig, P., Dieppe, P., Macintyre, S., et al. Developing and evaluating complex interventions: the new Medical Research Council guidance. BMJ, 337, 2008, a1655.
-
(2008)
BMJ
, vol.337
, pp. a1655
-
-
Craig, P.1
Dieppe, P.2
Macintyre, S.3
-
23
-
-
85010077580
-
‘Teaching adults’, Chapters 3 & 7
-
Open University Press Buckingham, England
-
23 Rogers, A., ‘Teaching adults’, Chapters 3 & 7. 1986, Open University Press, Buckingham, England.
-
(1986)
-
-
Rogers, A.1
-
24
-
-
15944406084
-
Prescribing palliative oxygen: a clinician survey of expected benefit and patterns of use
-
24 Abernethy, A.P., Currow, D.C., Frith, P., Fazekas, B.S., Prescribing palliative oxygen: a clinician survey of expected benefit and patterns of use. Palliat Med, 19, 2005, 168.
-
(2005)
Palliat Med
, vol.19
, pp. 168
-
-
Abernethy, A.P.1
Currow, D.C.2
Frith, P.3
Fazekas, B.S.4
-
25
-
-
85031828017
-
Developing an educational intervention on breathlessness in advanced disease for informal carers
-
Abstracts of the 11th Palliative Care Congress, Glasgow, March 9–11, 2016
-
25 Penfold, C., Ewing, G., Mahadeva, R., et al. Developing an educational intervention on breathlessness in advanced disease for informal carers. Palliat Med 30 (2016), S1–S130 Abstracts of the 11th Palliative Care Congress, Glasgow, March 9–11, 2016.
-
(2016)
Palliat Med
, vol.30
, pp. S1-S130
-
-
Penfold, C.1
Ewing, G.2
Mahadeva, R.3
-
26
-
-
54549109927
-
Situated/being situated: client and co-worker roles of family caregivers in hospice palliative care
-
26 Stajduhar, K.I., Nickel, D.D., Martin, W.L., Funk, L., Situated/being situated: client and co-worker roles of family caregivers in hospice palliative care. Soc Sci Med 67 (2008), 1789–1797.
-
(2008)
Soc Sci Med
, vol.67
, pp. 1789-1797
-
-
Stajduhar, K.I.1
Nickel, D.D.2
Martin, W.L.3
Funk, L.4
-
27
-
-
84939980208
-
The interaction between informal cancer caregivers and health care professionals: a survey of caregivers' experiences of problems and unmet needs
-
27 Lund, L., Ross, L., Petersen, M., Groenvold, M., The interaction between informal cancer caregivers and health care professionals: a survey of caregivers' experiences of problems and unmet needs. Support Care Cancer 23 (2015), 1719–1733.
-
(2015)
Support Care Cancer
, vol.23
, pp. 1719-1733
-
-
Lund, L.1
Ross, L.2
Petersen, M.3
Groenvold, M.4
-
28
-
-
69549105809
-
Delivering palliative care in an acute hospital setting; views of referrers and specialist providers
-
28 Ewing, G., Farquhar, M., Booth, S., Delivering palliative care in an acute hospital setting; views of referrers and specialist providers. J Pain Symptom Manage 38 (2009), 327–340.
-
(2009)
J Pain Symptom Manage
, vol.38
, pp. 327-340
-
-
Ewing, G.1
Farquhar, M.2
Booth, S.3
|