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1.
Handb Clin Neurol ; 190: 61-71, 2022.
Article in English | MEDLINE | ID: mdl-36055720

ABSTRACT

Drawing its beginnings from end-of-life care, palliative care has developed into a specialized interdisciplinary effort aiming to alleviate distress in all its form, and spanning the whole serious illness trajectory. With this evolution came the inevitable expansion to different sites and modes of care delivery. This section discusses the various models of bringing palliative care to patients with neurologic illness. It begins by distinguishing primary from specialist palliative care, then examines various models of inpatient and outpatient care. Hospital-based models include consultation service and dedicated inpatient units, while outpatient care mainly consists of palliative care specialists embedded in disease-specific clinics. Home-based palliative care and services provided through telemedicine are discussed. Hospice, a model of care often associated with end-of-life palliative care is detailed, together with suggestions on when to consider transitioning to hospice care. It is worth noting that there is not a single best model of palliative care delivery for persons living with neurologic illness. The models discussed in this chapter are complementary not competing and should be adopted by clinicians to fit the needs of patients and caregivers, the resources available in the healthcare system, and based on where patients are in the spectrum of their illness.


Subject(s)
Hospice Care , Terminal Care , Humans , Palliative Care
2.
Curr Neurol Neurosci Rep ; 19(9): 69, 2019 08 16.
Article in English | MEDLINE | ID: mdl-31420757

ABSTRACT

PURPOSE OF REVIEW: Tardive dyskinesia (TD) is caused by exposure to medications with dopamine antagonism, mainly antipsychotics. It often distresses individuals, physically and emotionally and affects their quality of life. We evaluated peer-reviewed recently published articles with a goal of providing a critically appraised update on the latest advancements in this field. RECENT FINDINGS: In 2017, FDA approved VMAT2 inhibitors, deutetrabenazine and valbenazine. They have demonstrated efficacy in several class 1 studies. Also there have been update in the evidence-based guidelines for treatment for tardive dyskinesia. Various medication classes are being used for treatment of TD with VMAT2 inhibitors to be first FDA-approved medications. Their use should be tailored to the individual patient. Long-term studies will further guide us in how to optimize treatment, especially in the real-world setting. As clinicians, we need to take into consideration all aspects of symptomatology, etiology, potential side effects of the medications, to find the best possible "match" for our patients.


Subject(s)
Tardive Dyskinesia/drug therapy , Tetrabenazine/analogs & derivatives , Valine/analogs & derivatives , Vesicular Monoamine Transport Proteins/antagonists & inhibitors , Antipsychotic Agents/adverse effects , Dopamine Antagonists/adverse effects , Drug-Related Side Effects and Adverse Reactions , Humans , Quality of Life , Tetrabenazine/therapeutic use , Valine/therapeutic use
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