Detailed Information on Publication Record
2011
Cognitive effects of long-term treatment with waking-hour subcutaneous apomorphine infusions in patients with advanced Parkinson's disease
KUBÍKOVÁ, Radka, Mojmír TYRLÍK and Irena REKTOROVÁBasic information
Original name
Cognitive effects of long-term treatment with waking-hour subcutaneous apomorphine infusions in patients with advanced Parkinson's disease
Authors
KUBÍKOVÁ, Radka (203 Czech Republic, belonging to the institution), Mojmír TYRLÍK (203 Czech Republic, belonging to the institution) and Irena REKTOROVÁ (203 Czech Republic, guarantor, belonging to the institution)
Edition
Ceska a Slovenska Neurologie a Neurochirurgie, Czech Medical Association J.E. Purkyne, 2011, 1210-7859
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30000 3. Medical and Health Sciences
Country of publisher
Czech Republic
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 0.279
RIV identification code
RIV/00216224:14740/11:00060542
Organization unit
Central European Institute of Technology
UT WoS
000294035900009
Keywords in English
Affective; Apomorphine; Cognitive; Dementia; Parkinson's disease
Tags
International impact, Reviewed
Změněno: 23/4/2013 07:30, Olga Křížová
Abstract
V originále
Aims: To determine whether long-term treatment with continuous subcutaneous apomorphine infusions (CSAI) is safe for patients with Parkinson's disease (PD) with a history of hallucinations and/or marked cognitive deficit. Methods: 12 PD patients (9 men, 3 women; age 71.8 +- 6 years) were given neuropsychological assessment prior to continuous administration of CSAI and fourteen months after it. Results: CSAI led to clinical improvement, at least minimal, in all subjects. However, the treatment led to statistically significant impairment in verbal fluency tasks, the Mattis dementia rating scale (MDRS) score and the attention and initiation subtests. No mood changes were detected. Conclusions: We observed significant impairment in "frontal-like" tasks after continuous treatment with CSAI in our PD patients with baseline cognitive impairment. Further longitudinal controlled studies are needed to assess the impact of both CSAI and PD progression. We suggest cautious selection of patients eligible for CSAI therapy with respect to their cognitive profiles and/or neuropsychiatric complications.
Links
ED1.1.00/02.0068, research and development project |
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MSM0021622404, plan (intention) |
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