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1.
Physiother Res Int ; 23(4): e1724, 2018 Oct.
Article in English | MEDLINE | ID: mdl-29961973

ABSTRACT

PURPOSE: To describe how appreciative management occurs in the working environment of physiotherapists. METHODS: Cross-sectional survey. The data was collected with an electronic questionnaire. The survey instrument was Appreciative Management Scale. The participants were 474 physiotherapists working in clinical or managerial positions from public or private sector. RESULTS: Appreciative management was realized on an average level within physiotherapy. The highest scoring dimension was Equality and the weakest was Systematic Management. Appreciative management and all of its four categories were associated with the management education received by the manager, the respondent's position, and his or her current duties. The dimension of Appreciation of Know-how and its subdimensions of Guidance and Autonomy were recognized more often when the manager's basic training was in physiotherapy rather than another field. CONCLUSIONS: It is important that managers in physiotherapy recognize the characteristics of appreciative management, so they can include them as part of their good practice and as part of their own leadership style. Managers in physiotherapy need to be encouraged to participate in management education and also enable the participation of others. A background in physiotherapy can be seen to further the practice and development of physiotherapy. Offering physiotherapists challenging assignments and enabling their career development in physical therapy units is therefore of great importance.


Subject(s)
Administrative Personnel , Personnel Management , Physical Therapists , Private Sector , Public Sector , Adult , Aged , Career Mobility , Cross-Sectional Studies , Female , Humans , Leadership , Male , Middle Aged , Organizational Culture , Surveys and Questionnaires , Young Adult
2.
Synapse ; 51(2): 119-27, 2004 Feb.
Article in English | MEDLINE | ID: mdl-14618679

ABSTRACT

In order to characterize the sensitivity of an analog of levodopa and a dopamine transporter ligand to detect defects in nigrostriatal function, the uptake of [(18)F]FDOPA and [(18)F]CFT was studied ex vivo in a rat model of Parkinson's disease. The brains of these rats were unilaterally lesioned with an intranigral injection of 6-hydroxydopamine. The lesioned animals were divided into three groups subject to their behavior after pharmacological challenges. Circling behavior was recorded after amphetamine, apomorphine, and L-DOPA challenge in order to predict lesion size. The spatial distribution of radioactivity after [(18)F]FDOPA or [(18)F]CFT injection in brain sections was determined with digital autoradiography. Regions of interest were left/right striatum, left/right substantia nigra, and cerebellum. The degree of unilateral lesion for each animal was confirmed by counting of nigral tyrosine hydroxylase-positive cell bodies. With both tracers the uptake in the lesioned side was lower than in the intact side in the striatum and in the substantia nigra. In conclusion, both tracers clearly demonstrated nigrostriatal dopaminergic hypofunction and correlated with the number of nigral dopaminergic neurons. However, [(18)F]FDOPA showed a much higher unspecific uptake of radioactivity, due to extensive metabolism; therefore, this tracer was less sensitive than the transporter tracer [(18)F]CFT to detect these defects.


Subject(s)
Dihydroxyphenylalanine/analogs & derivatives , Dihydroxyphenylalanine/pharmacokinetics , Parkinson Disease/metabolism , Propionates/pharmacokinetics , Substantia Nigra/metabolism , Amphetamine/pharmacology , Animals , Apomorphine/pharmacology , Autoradiography , Behavior, Animal/drug effects , Brain/anatomy & histology , Brain/metabolism , Brain Mapping , Central Nervous System Stimulants/pharmacology , Disease Models, Animal , Dopamine Agonists/toxicity , Functional Laterality , Immunohistochemistry , Levodopa/pharmacology , Male , Oxidopamine/toxicity , Radioligand Assay , Rats , Rats, Sprague-Dawley , Stereotyped Behavior/drug effects , Sympatholytics/toxicity , Tyrosine 3-Monooxygenase/metabolism
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