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2.
Addiction ; 114(9): 1696-1705, 2019 09.
Article in English | MEDLINE | ID: mdl-30851219

ABSTRACT

BACKGROUND AND AIMS: During the past three decades an expansive literature has emerged that is dedicated to analysing the processes of policy transfer. One neglected pathway involves subnational agents emulating crime control innovations that have emerged in subnational jurisdictions of other nations. This paper presents the case of the London Mayor's Office for Policing and Crime's (MOPAC) Alcohol Abstinence Monitoring Requirement (AAMR) Pilot to examine the multi-level factors that facilitate and/or constrain international-subnational crime and justice policy transfer. METHODS: A qualitative case study design reconstructed the (in)formal events that led to components of the South Dakota 24/7 Sobriety Project (USA) being either abandoned or integrated into MOPAC's AAMR Pilot. Evidence is drawn from elite interviews and documentary materials. RESULTS: A series of inter/transnational-, macro-domestic-, meso- and micro-level factors enabled and/or obstructed processes of complete international-subnational policy transfer. Exclusion of domestic violence perpetrators from the London Pilot was fuelled by interest-group hostility and mobilization. Use of alcohol tags rather than breathalysers to monitor compliance was a result of political-economic constraints, concern surrounding intrusion, technological innovation and policy-orientated learning. The decision to omit an 'offender pays' funding mechanism was a consequence of legal incompatibility and civil service reluctance, while 'flash incarceration' for breach was not implemented due to European policy harmonization. CONCLUSIONS: The London Alcohol Abstinence Monitoring Requirement Pilot was a policy 'synthesis' that combined ideas, goals, vocabulary, principles, technology and practices from the South Dakota model with the existing English and Welsh criminal justice framework. Structural factors and the actions of particular agents limited the extent to which policy transfer occurred.


Subject(s)
Alcohol Abstinence/legislation & jurisprudence , Alcohol Drinking/legislation & jurisprudence , Crime/prevention & control , Driving Under the Influence/prevention & control , Law Enforcement/methods , Policy Making , Public Policy , Blood Alcohol Content , Breath Tests , Criminal Law , Domestic Violence , Humans , London , Organizational Case Studies , Pilot Projects , Qualitative Research , South Dakota
3.
J Clin Neuromuscul Dis ; 9(4): 397-401, 2008 Jun.
Article in English | MEDLINE | ID: mdl-18525423

ABSTRACT

BACKGROUND: Hypogonadism has been described in patients with myotonic muscular dystrophy type 1 but has not been evaluated in other myopathies. METHODS: We measured total and free serum testosterone levels in 59 men with myotonic muscular dystrophy type 1 (N = 12), facioscapulohumeral muscular dystrophy (N = 11), dystrophinopathy (N = 12), metabolic myopathy (N = 7), and inclusion body myositis (N = 17) and compared these with the normal reference interval. RESULTS: Thirty-two of the 59 (54%) participants had low total testosterone, 23 (39%) had low total and free values, and 5 (8%) had low free with normal total levels. There were no significant differences in the prevalence of hypogonadism between those with myotonic muscular dystrophy type 1 and the other groups even after considering age as a confounder. CONCLUSIONS: Hypogonadism is common in men with myopathies, and with the importance of testosterone in the maintenance of muscle mass, treatment of hypogonadism should be considered.


Subject(s)
Hypogonadism/complications , Muscular Diseases/blood , Muscular Dystrophies/blood , Testosterone/blood , Adult , Age Distribution , Aged , Cohort Studies , Humans , Hypogonadism/blood , Male , Middle Aged , Muscular Diseases/classification , Muscular Diseases/complications , Muscular Dystrophies/complications , Muscular Dystrophy, Facioscapulohumeral/blood , Muscular Dystrophy, Facioscapulohumeral/complications , Myositis, Inclusion Body/blood , Myositis, Inclusion Body/complications , Myotonic Dystrophy/blood , Myotonic Dystrophy/complications
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