Reeves - Interprofessional Collaboration
Reeves - Interprofessional Collaboration
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Scott Reeves1 , Ferruccio Pelone1 , Reema Harrison2 , Joanne Goldman3 , Merrick Zwarenstein4
1 Faculty of Health, Social Care and Education, Kingston University and St George’s, University of London, London, UK. 2 University of
Sydney, Sydney, Australia. 3 Centre for Quality Improvement and Patient Safety, University of Toronto, Toronto, Canada. 4 Department
of Family Medicine, University of Western Ontario, London, Canada
Contact address: Scott Reeves, Faculty of Health, Social Care and Education, Kingston University and St George’s, University of London,
St George’s Hospital, Grosvenor Wing, Cranmer Terrace, London, Greater London, SW17 0BE, UK. [email protected].
Citation: Reeves S, Pelone F, Harrison R, Goldman J, Zwarenstein M. Interprofessional collaboration to improve profes-
sional practice and healthcare outcomes. Cochrane Database of Systematic Reviews 2017, Issue 6. Art. No.: CD000072. DOI:
10.1002/14651858.CD000072.pub3.
Copyright © 2017 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
ABSTRACT
Background
Poor interprofessional collaboration (IPC) can adversely affect the delivery of health services and patient care. Interventions that address
IPC problems have the potential to improve professional practice and healthcare outcomes.
Objectives
To assess the impact of practice-based interventions designed to improve interprofessional collaboration (IPC) amongst health and
social care professionals, compared to usual care or to an alternative intervention, on at least one of the following primary outcomes:
patient health outcomes, clinical process or efficiency outcomes or secondary outcomes (collaborative behaviour).
Search methods
We searched CENTRAL (2015, issue 11), MEDLINE, CINAHL, ClinicalTrials.gov and WHO International Clinical Trials Registry
Platform to November 2015. We handsearched relevant interprofessional journals to November 2015, and reviewed the reference lists
of the included studies.
Selection criteria
We included randomised trials of practice-based IPC interventions involving health and social care professionals compared to usual
care or to an alternative intervention.
Two review authors independently assessed the eligibility of each potentially relevant study. We extracted data from the included studies
and assessed the risk of bias of each study. We were unable to perform a meta-analysis of study outcomes, given the small number of
included studies and their heterogeneity in clinical settings, interventions and outcomes. Consequently, we summarised the study data
and presented the results in a narrative format to report study methods, outcomes, impact and certainty of the evidence.
Interprofessional collaboration to improve professional practice and healthcare outcomes (Review) 1
Copyright © 2017 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
Main results
We included nine studies in total (6540 participants); six cluster-randomised trials and three individual randomised trials (1 study
randomised clinicians, 1 randomised patients, and 1 randomised clinicians and patients). All studies were conducted in high-income
countries (Australia, Belgium, Sweden, UK and USA) across primary, secondary, tertiary and community care settings and had a
follow-up of up to 12 months. Eight studies compared an IPC intervention with usual care and evaluated the effects of different
practice-based IPC interventions: externally facilitated interprofessional activities (e.g. team action planning; 4 studies), interprofessional
rounds (2 studies), interprofessional meetings (1 study), and interprofessional checklists (1 study). One study compared one type of
interprofessional meeting with another type of interprofessional meeting. We assessed four studies to be at high risk of attrition bias
and an equal number of studies to be at high risk of detection bias.
For studies comparing an IPC intervention with usual care, functional status in stroke patients may be slightly improved by externally
facilitated interprofessional activities (1 study, 464 participants, low-certainty evidence). We are uncertain whether patient-assessed
quality of care (1 study, 1185 participants), continuity of care (1 study, 464 participants) or collaborative working (4 studies, 1936
participants) are improved by externally facilitated interprofessional activities, as we graded the evidence as very low-certainty for
these outcomes. Healthcare professionals’ adherence to recommended practices may be slightly improved with externally facilitated
interprofessional activities or interprofessional meetings (3 studies, 2576 participants, low certainty evidence). The use of healthcare
resources may be slightly improved by externally facilitated interprofessional activities, interprofessional checklists and rounds (4 studies,
1679 participants, low-certainty evidence). None of the included studies reported on patient mortality, morbidity or complication
rates.
Compared to multidisciplinary audio conferencing, multidisciplinary video conferencing may reduce the average length of treatment
and may reduce the number of multidisciplinary conferences needed per patient and the patient length of stay. There was little or no
difference between these interventions in the number of communications between health professionals (1 study, 100 participants; low-
certainty evidence).
Authors’ conclusions
Given that the certainty of evidence from the included studies was judged to be low to very low, there is not sufficient evidence to
draw clear conclusions on the effects of IPC interventions. Neverthess, due to the difficulties health professionals encounter when
collaborating in clinical practice, it is encouraging that research on the number of interventions to improve IPC has increased since
this review was last updated. While this field is developing, further rigorous, mixed-method studies are required. Future studies should
focus on longer acclimatisation periods before evaluating newly implemented IPC interventions, and use longer follow-up to generate
a more informed understanding of the effects of IPC on clinical practice.
Effects of practice- based interprofessional collaboration (IPC) interventions on professional practice and healthcare
outcomes compared to usual care
Patient or population: health and social care prof essionals involved in the delivery of health services and patient care
Settings: prim ary, secondary, tertiary and com m unity care settings, prim arily in the USA and the UK
Intervention: practice-based interprof essional collaboration (IPC) interventions with an explicit objective of im proving
collaboration between two or m ore health or social care prof essionals
Comparison: usual care
a We assessed the certainty of the evidence as low because of high risk of bias (no blinding of outcom e assessm ent).
b We assessed the certainty of the evidence as very low because of the risk of bias (high risk of attrition and detection bias;
details about allocation sequence generation and concealm ent were not reported).
c We assessed the certainty of the evidence as low due to potential indirectness (both studies were conducted in one country
and the outcom es m ay not be transf erable to other settings), and risk of bias (high risk of attrition, unclear selection and
reporting risk).
d We assessed the certainty of the evidence as very low because of risk of bias (high risk of attrition and detection bias, and
Types of interventions
Search methods for identification of studies
We included any practice-based intervention with an explicit ob-
jective of improving collaboration between two or more health or
social care professionals. We used the following criterion to in-
clude interventions. Electronic searches
• Evaluations of a practice-based IPC intervention, where the
We searched the following sources.
study explicitly noted an objective to improve collaboration
1. Cochrane Central Register of Controlled Trials
amongst two or more types of health or social care professionals. (CENTRAL; 2015, issue 11) in the Cochrane Library (searched
Other terms besides IPC could have been used, and were on 24 November 2015; full strategy available in Appendix 1).
accepted as equivalent to IPC, such as communication, co- 2. MEDLINE Ovid: 2007 to 2015 (searched on 10
ordination, and teamwork. November 2015; full strategy available in Appendix 2).
The comparator was usual care or an alternative intervention, We 3. CINAHL EBSCO: 2007 to 2015 (searched on 10
placed no restrictions on interventions or settings (e.g. hospitals, November 2015; full strategy available in Appendix 3).
primary care, community-based care). 4. ClinicalTrials.gov and WHO International Clinical Trials
Registry Platform (ICTRP): 2007 to 2015 (searched on 24
November 2015; full strategy available in Appendix 4).
Types of outcome measures We placed no language restrictions on the search strategy. We did
not search Embase, as a review of the studies included previously
showed that none were indexed in this database. We included
Primary outcomes all the trials identified by the previous version of the review (
Zwarenstein 2009).
Selection of studies
At least two review authors (SR, FP) independently reviewed each Unit of analysis issues
of the titles and abstracts retrieved in the searches, to identify those We critically examined the methods of analysis of all study types.
that met the review’s inclusion criteria. We identified cluster-randomised trials, and where appropriate,
We obtained the full-text of all potentially relevant articles. At commented on unit of analysis errors in the results and discussion.
least two review authors (SR, FP) independently assessed each full-
text article to determine if it met all of the criteria. We resolved
disagreements by consultation with another review author (MZ). Dealing with missing data
As a further quality check, this additional review author reviewed It was not possible to undertake a meta-analysis of the included
all included articles. studies due to heterogeneity and therefore the issue of missing data
in statistical analysis did not arise.
Patient-assessed quality of care Collaborative working, team communication and team co-
ordination
It is uncertain if externally facilitated interprofessional activities
It is uncertain whether externally facilitated interprofessional ac-
increase patient-assessed quality of care at 12-month follow-up
tivities improve collaborative working, team communication, and
(very low-certainty evidence, 1 study, N = 1185) (Black 2013).
co-ordination (very low-certainty evidence, 3 studies, N = 1907).
Black 2013 reported differences between the intervention and con-
trol groups in the mean change from baseline to follow-up in staff
Patient mortality, morbidity or complication rates role scores assessed using the Chronic Care Team Profile (CCTP).
These differences were in the non-GP clinical staff function (P
None of the included studies reported patient mortality, morbidity
= 0.023), the administrative staff function (P < 0.001), and the
or complication rates.
total score (P = 0.03). These changes included, for example, the
creation of a diabetes care co-ordinator to perform tasks such as
managing the recall and reminder system for patients with dia-
Clinical process or efficiency outcomes
betes, and organising staff meetings to improve communication
and practice systems.
Cheater 2005 report that Collaborative Practice Scale (CPS) scores
on co-operation went from 83.5 at baseline to 88.5 after the inter-
Adherence to recommended practices
vention in the intervention group, compared to 84.5 at baseline
The use of interprofessional activities with an external facilitator to 84.5 after the intervention in the control group. These differ-
may slightly improve adherence to recommended practices and ences are presented with no measures of variability and the change
prescription of drugs (low-certainty evidence, 2 studies, N = 722). appears small in relation to the value at baseline.
Cheater 2005 reported an increase in collaborative audit activity, Deneckere 2013 found little effect of the intervention on relational
with six of the 11 intervention teams completing the full audit co-ordination, which assessed the process of communication and
cycle. Only three control teams undertook any audit (first data relationship between team members in order to complete the task.
collection).
Deneckere 2013 reported improvements in the following out-
comes: conflict management (slope of difference between inter- Interprofessional rounds
vention and control group (β) 0.30, 95% confidence interval (CI)
0.08 to 0.53); team climate for innovation (β 0.29, 95% CI 0.09
Patient health outcomes
to 0.49); and level of organised care (β 5.56, 95% CI 1.35 to
9.76). Deneckere 2013 also reported that the intervention group None of the included studies reported patient health outcomes.
scored lower in emotional exhaustion (β 0.57, 95% CI 0.14 to
1.00) and higher in level of competence (β 0.39, 95% CI 0.15 to Clinical process or efficiency outcomes
0.64).
Effects of practice- based interprofessional collaboration (IPC) interventions on professional practice and healthcare
outcomes compared with alternative IPC intervention
Patient or population: health and social care prof essionals involved in the delivery of health services and patient care
Settings: two hospitals in Australia
Intervention: m ultidisciplinary video conf erencing
Comparison: m ultidisciplinary audio conf erencing
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Black 2013
Methods Cluster-randomised trial to test the effectiveness of an intervention involving non GP-
staff in GP practices, on the quality of care for patients with diabetes or cardiovascular
disease
Interventions To assist non-GP staff (e.g. nurses, administrative staff (practice managers, receptionists)
) to work as a team with GPs, the intervention included a number of activities including:
the use of structured appointment systems, recall and reminders, planned care, the use
of roles, responsibilities, and job descriptions, as well as communication and meetings
Notes
Risk of bias
Baseline outcome measurements similar - Low risk At baseline, the quality of care PACIC out-
All outcomes comes in the intervention group (3.01, SD
0.30) and control group (2.87, SD 0.34)
were similar
Baseline characteristics similar Low risk Intervention and control teams look rea-
sonably similar.
Quote: “Control practices were more likely
to be in an urban location compared with
the intervention practices, have a lower full-
time equivalent level of practice nurses and
were also more likely to have a higher score
Blinding of outcome assessment (detection High risk It did not appear that there was any blind-
bias) - All outcomes ing.
Incomplete outcome data (attrition bias) - High risk Acknowledged sites dropped out, but ITT
All outcomes is not mentioned in the text
Practice level:
Quote: “Of these, 69% (60/87) finally par-
ticipated in the study, and three of these
(3/60) withdrew at follow up…Reasons for
withdrawal of three practices included con-
cern about the extent of data collection and
other reasons not pertaining to the study.”
Patient level:
There were 3349 patients invited to partic-
ipate in the study, with 2642 (79%) provid-
ing informed consent. Of these, 2552 (96.
6%) returned the PACIC questionnaire at
baseline, with 2135 (73.7%) completing all
20 items. To be included in the factor anal-
ysis, at least 17 questions needed to be com-
pleted, and 2438 participants met this cri-
terion. The multilevel regression included
data for which all relevant variables were
available, resulting in a final sample size of
1853 patients
Selective reporting (reporting bias) Unclear risk All relevant outcomes in the method sec-
tion (p B) were reported in the results sec-
tion (p D-E). A study protocol was not
available and there was insufficient infor-
mation to permit judgement of high or low
risk of bias
Outcomes Clinical process or efficiency outcomes: length of operation, discharge status, readmission
rates and technical proficiency. Collaborative behavioural outcomes: team behaviours (e.
g. team communication and co-ordination)
Notes
Risk of bias
Random sequence generation (selection Unclear risk Randomisation was mentioned: “a total of
bias) 65 cases were randomized (by attending
surgeon) to…”, but method not specified
Baseline characteristics similar Low risk Quote: “Length of operation, discharge sta-
tus, and readmission rates as indication of
case outcome showed nonstatistical differ-
ences between groups.”
Blinding of outcome assessment (detection High risk It did not appear that there was any blind-
bias) - All outcomes ing.
Incomplete outcome data (attrition bias) - High risk Acknowledged sites dropped out but ITT
All outcomes was not mentioned in the text
Patient level:
Quote: “A total of 65 cases were random-
ized...”
Quote: “Eighteen subjects/cases dropped
out between randomization and analysis:
two in the checklist group declined to use
the checklist or requested that their cases
be withdrawn after videotaping, three cases
Selective reporting (reporting bias) Unclear risk All relevant outcomes in the method sec-
tion (p 1132-3) were reported in the results
section (p 1133-6). A study protocol was
not available and there was insufficient in-
formation to permit judgement of high or
low risk of bias
Cheater 2005
Methods A RT where 22 multidisciplinary teams from five acute care hospitals were randomised to
an intervention group that participated in a facilitated programme on multidisciplinary
audit or a control group
Participants Country: UK
Nurses, physicians and other professionals (e.g. pharmacist, social worker, physiother-
apist), service support staff (e.g. ward clerk, care assistant), and managers. A range of
specialties (e.g. surgery, medicine, and nephrology) were included. There were 11 teams
with a total of 77 participants in the intervention group and 11 teams with a total of 64
participants in the control group
Interventions Five facilitated meetings over 6 months with activities designed to support multidisci-
plinary teams to undertake an audit
Notes
Risk of bias
Random sequence generation (selection Low risk Quote: “Teams within the same hospi-
bias) tal were stratified on mean self-reported
KSA scores, perceived level of team collab-
oration and medical or surgical specialty
before randomisation. The project secre-
tary under the supervision of [a researcher]
randomised 22 teams to intervention or
control groups, using a computer random
number generator
Allocation concealment (selection bias) Low risk Quote: “With the exception of two ac-
cident and emergency teams in different
hospitals, teams from the same organisa-
tion were randomised in pairs. Other re-
searchers were blind to allocation.”
Baseline outcome measurements similar - Low risk At baseline, both groups were equivalent
All outcomes for baseline variables in relation to KSA
scores, and on the scores for the Collabo-
rative Practice Scale
Baseline characteristics similar Low risk Quote: “At baseline, both groups were
equivalent for all outcome variables except
two. In comparison to the intervention
group, the control arm reported higher lev-
els of audit knowledge (median score 32.5
vs 25.0, z = -3.001, P = 0.003) and skills
(median score 32.5 vs. 24.6, z = - 2.990, P =
0.003). Baseline differences were adjusted
for in the analysis. Baseline differences were
not found for WWTs.”
Blinding of outcome assessment (detection Low risk Quote: “Two members of the research team
bias) - All outcomes (RB and HH) independently assessed the
quality of the reports (blind to group alloca-
tion) and the percentage inter-rater agree-
ment did not fall below 82%.”
Patient level:
Results were provided about the quality of
the audits in relation to their compliance
with the 55 quality criteria, but no further
information was provided in relation to any
patient level outcomes
Selective reporting (reporting bias) Unclear risk All relevant outcomes in the method sec-
tion (p 781-2) were reported in the results
section (p 785-7). A study protocol was not
available and there was insufficient infor-
mation to permit judgement of high or low
risk of bias
Curley 1998
Methods Randomised trial - Firm trial: patients and staff from inpatient medical wards at an acute
care hospital were randomised to one of six medical wards. Three wards were allocated
to the intervention group that implemented daily interdisciplinary work rounds, and
three wards were allocated to the control group that continued traditional work rounds
Notes Unit of analysis error - allocated intervention to wards but analysed patients without
correction for clustering. However, this correction may not substantially change the
conclusion because randomisation of staff and patients limits variation between clusters
Risk of bias
Random sequence generation (selection Low risk Quote: “The firm system randomization
bias) procedures and their validation have been
reviewed extensively in the literature. Each
inpatient firm has two physician teams or
ward services. For this trial the six ward ser-
Allocation concealment (selection bias) Low risk Quote: “The firm system randomization
procedures and their validation have been
reviewed extensively in the literature. Each
inpatient firm has two physician teams or
ward services. For this trial the six ward ser-
vices were divided so that three ward ser-
vices continued traditional work rounds as
usual and the three ward services imple-
mented the CQI designed interdisciplinary
work rounds.”
Baseline characteristics similar Low risk Quote: “After controlling for baseline dif-
ferences in case-mix using a multivariate
propensity score, the length of stay and to-
tal charges for the hospital stay for the pa-
tients included in the trial were evaluated.
”
Blinding of outcome assessment (detection Low risk Quote: “Patient data were retrieved from
bias) - All outcomes the hospital’s administrative and billing sys-
tem. Thus, patient specific cost and effi-
ciency outcomes were limited to resource
utilization in the form of hospital length of
stay and total charges.”
“...the Respiratory Therapy (RT) Depart-
ment conducted a study of aerosol use
appropriateness, as determined by criteria
previously devised and tested by the RT
Department.”
Selective reporting (reporting bias) Unclear risk All relevant outcomes in the method sec-
tion (AS6) were reported in the results sec-
tion (AS7-9). There was no published pro-
tocol so we cannot be sure all planned anal-
yses were conducted
Deneckere 2013
Methods A post-test-only cluster-RT of 30 teams caring for patients with COPD and PFF. 17
intervention teams and 13 control teams examined how the use of CPs improved team-
work in an acute hospital setting
Interventions The intervention involved the development and implementation of CPs including 3
components: 1) feedback on team’s performance before CP implementation; 2) receipt
of evidence-based key-indicators for implementing CPs in practice to review; 3) training
in CP development. Control teams: usual care
Outcomes Conflict management, team climate for innovation, level of organised care, emotional
exhaustion, level of competence, relational co-ordination
Notes
Risk of bias
Random sequence generation (selection Low risk Quote: “Stratified randomisation was used
bias) to assign the teams to an intervention
group (using care pathways) and a control
group (usual care). Interprofessional teams
were randomised. COPD/PFF was used as
blocking factor.”
Allocation concealment (selection bias) Low risk Quote: “Before the start of the randomi-
sation process, random numbers were as-
signed to each cluster by a researcher not
involved in the study, using the online
available tool ’Research Randomizer’ www.
randomizer.org). Next, the researcher ran-
domly allocated the coded clusters to the
intervention or control group using the
same online tool.”
Baseline characteristics similar Low risk Intervention and control teams were rea-
sonably similar.
Quote: “No significant differences in or-
ganizational or team member characteris-
tics were found, except for the number of
years of experience, which was significantly
higher in the control group” (Table 2)
Blinding of outcome assessment (detection High risk It did not appear that there was any blind-
bias) - All outcomes ing.
Incomplete outcome data (attrition bias) - Low risk Practice level ITT was not mentioned. Au-
All outcomes thors acknowledged that sites dropped out
Quote: “A potential weakness of the study
is the dropout of 7 teams and its possible
impact on the results.”
Selective reporting (reporting bias) Low risk All relevant outcomes in the method sec-
tion (p 100-1) were reported in the re-
sults section (p 102-4). There was also a
published protocol and all planned analy-
ses were conducted
Schmidt 1998
Interventions Pharmacist led team meetings once a month over a period of 12 months
Outcomes Proportion of patients receiving drugs, number of psychotropic drugs, use of non-rec-
ommended hypnotics, use of non-recommended anxiolytics, use of non-recommended
antidepressant drugs
Notes
Risk of bias
Allocation concealment (selection bias) Low risk Quote: “Thirty-six nursing homes, repre-
senting 5% of all nursing homes in Swe-
den, participated in the study. The sam-
pling process consisted of three steps. At the
time of the study, the National Corpora-
tion of Swedish Pharmacies was organized
into 36 regions, 18 of which were randomly
selected for this study. Each regional phar-
macy director then selected two facilities in
his or her region using several criteria....Re-
searchers randomly assigned one home in
each pair to receive the intervention.”
Baseline outcome measurements similar - Low risk Quote: “At baseline, we found no signifi-
All outcomes cant differences in the proportion of resi-
dents with scheduled psychotropics (64%
vs 65%), number of drugs among residents
with psychotropics (2.07 vs 2.06).”
Baseline characteristics similar Low risk Quote: “There were no significant differ-
ences in the demographic, functional, or
psychiatric characteristics of residents in ex-
perimental and control homes at baseline.
”
Quote: “The overall level of prescribing was
similar in experimental and control homes
before the intervention (Table 2). At base-
line, we found no significant differences in
the proportion of residents with scheduled
psychotropics (64% vs 65%), number of
drugs among residents with psychotropics
(2.07 vs 2.06), or proportion of residents
with polymedicine (46% vs 47%). Baseline
rates of therapeutic duplication were also
comparable in the experimental and con-
trol homes.”
Blinding of outcome assessment (detection Low risk Quote: “Lists of each resident’s prescrip-
bias) - All outcomes tions were collected 1 month before and
1 month after the 12-month intervention
in both experimental homes and control
homes. Trained coders, supervised by phar-
macists, classified and coded all scheduled
and PRN (pro re nata) orders.”
Incomplete outcome data (attrition bias) - Low risk 3 intervention homes out of 18 became in-
All outcomes eligible.
Selective reporting (reporting bias) Unclear risk Insufficient information to permit judge-
ment of high or low risk of bias. There was
no published protocol so we cannot be sure
all planned analyses were conducted
Methods RT, in which patients with a stroke were treated by 31 teams from 31 Veteran Affair
rehabilitation units before and after a multifaceted intervention, aimed at improving
interprofessional collaboration
Interventions Intervention teams: received the following multifaceted intervention: 1) an off-site work-
shop emphasising team dynamics, problem-solving, and the use of performance feed-
back data; 2) action plans (specific team performance profiles with recommendations)
for process improvement; 3) telephone and video conference consultations to sustain
improvement in collaboration
Control teams only received specific team performance profile Information
Outcomes Functional improvement (as measured by the change in motor items of the FIM instru-
ment), length of stay (LOS), rates of community discharge
Notes
Risk of bias
Random sequence generation (selection Low risk Quote: “... we randomized sites to either
bias) intervention or control group using a com-
puter; each stratum was force randomized
to have 4 sites in 1 arm.”
Allocation concealment (selection bias) Unclear risk Method of concealment was not described.
Baseline outcome measurements similar - Low risk The mean FIM scores at baseline were sim-
All outcomes ilar for the intervention group (52.2 ± 3.9)
and for the control group (52.4 ± 3.8)
Baseline characteristics similar Low risk Quote: “…There were no differences be-
tween study conditions in demographic
characteristics (table 2). Control sites ad-
mitted stroke patients with lower initial
(admission) motor FIM scores during the
pre-intervention periods (P.002); thus, we
adjusted all analyses using FRGs … a clas-
sification based on initial motor FIM and
age.”
Blinding of outcome assessment (detection High risk It did not appear that there was any blind-
bias) - All outcomes ing.
Incomplete outcome data (attrition bias) - High risk Acknowledged sites dropped out but ITT
All outcomes was not mentioned in the text
Practice level
Quote: “Of 33 eligible sites, a total of 31
sites agreed to participate, initiated the IRB
approval, and were randomized. One con-
trol site was unable to complete the IRB
process and withdrew, and 1 intervention
site did not report data to the FSOD, leav-
ing 15 sites in the control group and 14 in
the intervention group
Selective reporting (reporting bias) Low risk All relevant outcomes in the methods sec-
tion (p 11) were reported in the results sec-
tion (p 14). There was a published protocol
and all planned analyses were conducted
Wild 2004
Methods Randomised trial in which patients in inpatient telemetry ward in a community hospital
were randomised to the intervention medical team, which conducted interdisciplinary
rounds or to the control team, which provided standard care
Notes
Risk of bias
Random sequence generation (selection Low risk Quote: “Randomization was performed us-
bias) ing random numerical assignments in pre-
sealed envelopes.”
Baseline outcome measurements similar - Low risk Mean length of stay (days) was similar in
All outcomes the intervention group (3.04 ± 1.8) com-
pared with the control group (2.7 ± 1.8)
Baseline characteristics similar Low risk Quote: “There were no significant differ-
ences between groups for admission diag-
nosis; number of co-morbidities; number
of abnormal laboratory data; ability to per-
form activities of daily living; presence of
dementia or diabetes, or whether there was
a home health aide. In spite of random-
ization, the gender composition between
groups was somewhat different...and the
number of readmissions in the IR Team was
higher than in the non-IR Team (P = 0.
003).”
Blinding of outcome assessment (detection Low risk Quote: “Charts were surveyed to determine
bias) - All outcomes patient characteristics and LOS. LOS was
measured as the difference between dis-
charge and admission date.”
Selective reporting (reporting bias) Unclear risk All relevant outcomes in the method sec-
tion (p 64) were reported in the results sec-
tion (p 67). There was no published proto-
col so we cannot be sure all planned analy-
ses were conducted
Interventions Multidisciplinary audio conferences and video conferences. At each conference session,
the audio conferences were conducted before the video conferences, with the same mul-
tidisciplinary team
Outcomes Number of audio conferences held per patient, number of video conferences held, length
of treatment
Notes
Risk of bias
Random sequence generation (selection Low risk Quote: ”The random allocation was done
bias) by an independent administrative assistant,
using a table of random numbers.“
Allocation concealment (selection bias) Low risk Quote: ”The random allocation was done
by an independent administrative assistant,
using a table of random numbers.“
Baseline characteristics similar Low risk Quote: ”The two groups were similar in
terms of age, sex and diagnosis (Table 1).“
Blinding of outcome assessment (detection Low risk Quote: ”Conference times were recorded
bias) - All outcomes by an independent observer and files were
reviewed by an independent medical prac-
titioner blinded to the randomization.“
Selective reporting (reporting bias) Unclear risk All relevant outcomes in the method sec-
tion (p 353-4) were reported in the results
section (p 354). Insufficient information
was provided to permit judgement of high
or low risk of bias. There was no published
protocol so we cannot be sure all planned
analyses were conducted
APPENDICES
13 November 2015 New citation required but conclusions have not This update found four new studies. As a result, the
changed review now includes nine studies. While the num-
ber of studies has increased slightly, the main con-
clusions from the previous update remain unchanged
(Zwarenstein 2009). There have been changes to the
author team, with the inclusion of two new authors
10 November 2015 New search has been performed New searches performed to 10 November 2015. Four
new studies identified
HISTORY
Protocol first published: Issue 3, 1996
Review first published: Issue 2, 1997
13 May 2009 New citation required and conclusions have changed Conclusions changed, based on additional studies. Crite-
ria for included study designs, included participants and
specification of the intervention changed from the 1997
review. This first review included randomised trials, con-
trolled before-after studies and interrupted time series de-
signs, whereas this update included only randomised tri-
als. The types of participants included in the first review
were physicians and nurses, whereas this update included
all types of healthcare professionals. The first review in-
cluded studies in which the interventions may not have
specified their intent to change interprofessional collabo-
ration, whereas this update only included studies with an
explicit focus on collaboration. These changes were in-
tended to increase the validity of the conclusions, and to
widen their applicability to professions other than nurs-
ing and medicine
13 May 2009 New search has been performed New search and four additional studies identified and
included in the review
20 August 2008 New search has been performed Converted to new review format.
11 January 2000 New citation required and conclusions have changed Substantive amendment
DECLARATIONS OF INTEREST
Scott Reeves: none known.
Ferruccio Pelone: none known
Reema Harrison: none known
Joanne Goldman: none known
Merrick Zwarenstein: none known.
The authors have no personal or professional interests as to whether this review shows benefits of practice-based interventions on
interprofessional collaboration.
SOURCES OF SUPPORT
Internal sources
• Faculty of Health, Social Care and Education, Kingston University and St George’s, University of London, UK.
• Continuing Education and Professional Development, Faculty of Medicine, University of Toronto, Canada.
External sources
• Canadian Institutes of Health Research, Canada.