Susan M. Calne
Research Subjects
Susan M. Calne has a total of 10 co-authors. Here are the top co-authors by number of shared publications:
Ajit Kumar
3 shared publicationsEdwin Mak
1 shared publicationGermaine McInnes
1 shared publicationJeanne Hall
1 shared publicationLinda Grantier
1 shared publicationMarie-Jose Fortin
1 shared publication
Latest Publications
- 31 March 2008
- Published by Elsevier in Parkinsonism & Related Disorders
- Vol. 14 (2) , 133-142
Young onset Parkinson's disease. Practical management of medical issues
- 31 March 2008
- Published by Elsevier in Parkinsonism & Related Disorders
- Vol. 14 (2) , 133-142
Young onset Parkinson's disease. Practical management of medical issues
- 1 March 2008
- Published by Elsevier in Parkinsonism & Related Disorders
- Vol. 14 (2) , 143-150
Psychosocial issues in young-onset Parkinson's disease: Current research and challenges
- 1 March 2008
- Published by Elsevier in Parkinsonism & Related Disorders
- Vol. 14 (2) , 143-150
Psychosocial issues in young-onset Parkinson's disease: Current research and challenges
- 1 December 2003
- Published by Wolters Kluwer Health in Journal of Neuroscience Nursing
- Vol. 35 (6) , 306-313
The Psychosocial Impact of Late-Stage Parkinsonʼs Disease
The late stage of Parkinson's disease (PD) can be protracted with inexorable changes in physical and mental health, loss of autonomy and self-esteem, altered relationships, and social isolation. Severely affected patients (Hoehn & Yahr stage 4-5) present a challenge to nurses who care for them; addressing their needs takes time and patience. Changes in mental status have profound implications for the welfare of the late-stage PD patient as well as of the caregiver(s). Depression and dementia in patients with PD are two factors that interfere with the ability to deliver effective care in late-stage PD as they lead to loss of initiative and cooperation. Primary caregivers often have their own medical problems, with limited stamina and support; relationships may change, leading to sadness or conflict. Nurses can be powerful advocates for the physical and mental health of both the patient with late-stage Parkinson's disease and the primary caregiver.
- 1 December 2003
- Published by Wolters Kluwer Health in Journal of Neuroscience Nursing
- Vol. 35 (6) , 306-313
The Psychosocial Impact of Late-Stage Parkinsonʼs Disease
The late stage of Parkinson's disease (PD) can be protracted with inexorable changes in physical and mental health, loss of autonomy and self-esteem, altered relationships, and social isolation. Severely affected patients (Hoehn & Yahr stage 4-5) present a challenge to nurses who care for them; addressing their needs takes time and patience. Changes in mental status have profound implications for the welfare of the late-stage PD patient as well as of the caregiver(s). Depression and dementia in patients with PD are two factors that interfere with the ability to deliver effective care in late-stage PD as they lead to loss of initiative and cooperation. Primary caregivers often have their own medical problems, with limited stamina and support; relationships may change, leading to sadness or conflict. Nurses can be powerful advocates for the physical and mental health of both the patient with late-stage Parkinson's disease and the primary caregiver.
- 1 October 2003
- Published by Wolters Kluwer Health in Journal of Neuroscience Nursing
- Vol. 35 (5) , 242-251
Nursing Care of Patients with Late-Stage Parkinsonʼs Disease
Patients in the late stages of Parkinson's disease may be significantly disabled for many years, often because of their increasing inability to tolerate therapeutic doses of antiparkinson drugs. Their status and management have been overlooked in the literature. Few current healthcare professionals have cared for patients with Parkinson's disease in the prelevodopa era and do not understand how severe and protracted the illness can be without effective treatment. This article describes a practical approach to the nursing management of severely affected patients (i.e., Hoehn and Yahr Stage 4-5) who no longer derive consistent, therapeutic benefit from their drugs. Specific problems these patients face are adverse drug reactions such as postural hypotension, psychosis, and confusion, as well as difficulties with nutrition, elimination, mobility and falling, communication, sexuality, memory, and mood. Nursing interventions can help minimize the effect of these problems on the patient.
- 1 October 2003
- Published by Wolters Kluwer Health in Journal of Neuroscience Nursing
- Vol. 35 (5) , 242-251
Nursing Care of Patients with Late-Stage Parkinsonʼs Disease
Patients in the late stages of Parkinson's disease may be significantly disabled for many years, often because of their increasing inability to tolerate therapeutic doses of antiparkinson drugs. Their status and management have been overlooked in the literature. Few current healthcare professionals have cared for patients with Parkinson's disease in the prelevodopa era and do not understand how severe and protracted the illness can be without effective treatment. This article describes a practical approach to the nursing management of severely affected patients (i.e., Hoehn and Yahr Stage 4-5) who no longer derive consistent, therapeutic benefit from their drugs. Specific problems these patients face are adverse drug reactions such as postural hypotension, psychosis, and confusion, as well as difficulties with nutrition, elimination, mobility and falling, communication, sexuality, memory, and mood. Nursing interventions can help minimize the effect of these problems on the patient.
- 1 January 2003
- Vol. 91, 115-22
Validating a quality-of-life scale in caregivers of patients with Parkinson's disease: Parkinson's Impact Scale (PIMS).
- 1 January 2003
- Vol. 91, 115-22
Validating a quality-of-life scale in caregivers of patients with Parkinson's disease: Parkinson's Impact Scale (PIMS).