Journal of Rehabilitation Medicine 51-8 | Page 63

Outcomes after in-reach multidisciplinary rehabilitation in the acute ward rehabilitation for such patients is often now provided by an in-reach rehabilitation team. This model of care has emerged over the last decade and has been adopted by a number of Australian hospitals since 2010 (13). In- reach rehabilitation teams are mobile (treating patients on different wards), multidisciplinary (involving at least 3 disciplines), coordinated, and are staffed to provide an intensity of therapy that is comparable to the rehabilita- tion setting (at least 2 therapy sessions per day). At the time this pilot study was conceived, there were no randomized controlled trials to guide the provision of early rehabilitation for critical care survivors on an acute ward after discharge from ICU (14). This study therefore aimed to explore the feasibility, efficiency and effectiveness of a coordinated inpatient early rehabilitation programme, delivered by an in-reach rehabilitation team as early as possible to critical care survivors on the acute ward. Objectives • To assess the feasibility of an in-reach multidisci- plinary rehabilitation programme in critical care survivors, commencing soon after discharge from the ICU and delivered on the acute ward. • To determine whether in-reach rehabilitation re- duces hospital length of stay (LOS) and improves functional and psychological outcomes in critical care survivors, compared with usual ward therapy. METHODS The trial was granted ethical approval by the Human Re- search Ethics Committee of St Vincent’s Hospital Sydney (HREC/12/SVH/324), and was retrospectively registered with the Australian New Zealand Clinical Trials Registry (Trial Id: ACTRN12618000539235). The trial is reported according to the Consolidated Standards of Reporting Trials (CONSORT) guidelines. Design A single-site, prospective pilot randomized controlled trial was conducted with blinded outcome assessment at 6 and 12 months. Participants Participants were recruited from the ICU of one metropolitan hospital in Sydney, Australia. The hospital is a tertiary referral and heart and lung transplant centre. The ICU is a 15-bed unit that cares for approximately 1,100 patients per year. Critical care survivors were included in the trial if they met the follo- wing inclusion criteria: aged 18–75 years; ICU stay ≥ 5 days; predicted LOS on the acute ward ≥ 5 days; and premorbid fun- ctional independence, defined a priori as a Barthel Index score ≥ 70, obtained from a proxy describing patient function during the 2 weeks prior to admission. Patients were excluded if they were not expected to survive their admission (e.g. withdrawal of life support and considered for palliation); were unable to 599 be followed-up (e.g. overseas visitor, homeless, severe hearing impairment); were unable to speak English; had a pre-existing diagnosis of dementia (of any aetiology); severe psychiatric disorders with recent hospitalization (within 6 months) or an active substance use disorder. Recruitment and allocation Participants were recruited within 72 hours of transfer from ICU to an acute ward. After baseline assessment, participants were randomly allocated to 1 of 2 groups, either the early rehabilita- tion intervention group, or usual care. A web-based, computer- generated randomization procedure (accessed from: http://www. graphpad.com/quickcalcs/randomize1.cfm 12/11/2012) was used for random sequence generation. Group allocation was placed in sealed envelopes, prepared by an administrative staff member with no role in clinical care or the study procedures, and numbered sequentially. Intervention The intervention group received involvement of an in-reach mobile rehabilitation team. This multidisciplinary team con- sisted of a rehabilitation physician (0.2 full-time equivalent), nurse (0.2 full-time equivalent), full-time physiotherapist and full-time occupational therapist. The mobile rehabilitation team had a caseload of 6–8 patients at any one time. This team was available 5 days per week and commenced rehabilitation im- mediately after baseline assessment, as soon as possible after ICU discharge to the acute ward. Participants in the intervention group were all visited by the rehabilitation physician for an initial assessment. Subsequent vi- sits by the physician were based on clinical need, typically once or twice per week. A structured multidisciplinary rehabilitation programme was devised for each patient. This aimed to address individual patient needs, involved the patient in decision-making and goal-setting, and was reviewed regularly during the patient journey via twice weekly multidisciplinary team meetings. The in-reach therapists worked with ward therapists so that the therapy frequency delivered was over and above what the patient would normally receive from acute ward therapists. The expected frequency was a 2-fold increase in therapy sessions for the intervention group compared with usual care. The duration of the study intervention was also determined by clinical need, i.e. patients could be discharged from the service once all rehabilitation goals during the acute stay were achieved. For those patients who required inpatient rehabilita- tion, the in-reach team remained involved until acute hospital discharge and transfer to rehabilitation. Control The control group received usual care, as directed by the acute physicians or surgeons on the acute ward. This involved acute ward allied health and nursing interventions, which were not coordinated by a rehabilitation physician or nurse. Each therapy discipline prioritized their interventions based on resources, clinical need and patient flow pressures, without reference to other team members. However, the in-reach rehabilitation team is well established at the hospital, and referrals based on clinical grounds by the acute medical/surgical teams can be considered part of usual care. The treating team always had the option of referring patients for additional therapy via the in-reach reha- bilitation team at any time-point during the acute ward stay, if they perceived a clinical need. J Rehabil Med 51, 2019