The effect of restructuring of healthcare on the quality, quantity, and nat
ure of aphasia management is largely unknown. The current study is the firs
t to examine access, diagnostic, treatment, and discharge patterns of patie
nts with aphasia in Australia, Canada, the UK, the US private sector (US-Pr
ivate), and the US Veterans Health Administration in the Department of Vete
rans Affairs (US-VA).
The authors developed a 37-item survey to be completed by clinicians workin
g with aphasic patients. The survey focused on eight areas: access to care,
evaluation procedures, group treatment, number and duration of treatment s
essions, limitations of the number of sessions, termination of treatment, f
ollow-up practices, and resumption of treatment. 394 surveys were distribut
ed and 175 were returned completed (44% return rate). Respondents represent
ed a range of ages, work experiences, and work settings. There was consider
able consistency among respondents from our five healthcare systems. Result
s suggest that patients may be routinely denied treatment in direct contrad
iction to the research literature. Just as we carefully monitor the progres
s of patients receiving our treatment, we are obliged to monitor the effect
s of managed care on our patients, fellow clinicians, and our profession.