Articulo 4
Articulo 4
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Abstract
We sought to determine the comparative benefits and harms of rehabilitation interventions for
patients who have undergone elective, unilateral THA surgery for the treatment of primary
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osteoarthritis. We searched PubMed, Embase, The Cochrane Register of Clinical Trials, CINAHL,
PsycINFO, Scopus, and ClinicalTrials.gov from January 1, 2005 through May 3, 2021. We
included randomized controlled trials and adequately-adjusted nonrandomized comparative
studies of rehabilitation programs reporting performance-based, patient-reported, or healthcare
utilization outcomes. Three researchers extracted study data and assessed risk of bias, verified
by an independent researcher. Experts in rehabilitation content and complex interventions
independently coded rehabilitation interventions. The team assessed strength of evidence (SoE).
Large heterogeneity across evaluated rehabilitation programs limited conclusions. Evidence from
15 studies suggests diverse rehabilitation programs may not differ in terms of risk of harm or
outcomes of pain, strength, activities of daily living, or quality of life (all low SoE). Evidence is
insufficient for other outcomes. In conclusion, no differences in outcomes were found between
different rehabilitation programs following THA. Further evidence is needed to inform decisions
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on what attributes of rehabilitation programs are most effective for various outcomes.
CORRESPONDING AUTHOR: Kristin J. Konnyu, BSc MSc BEd PhD, 121 S. Main Street, Box G-121-8, Providence, RI 02903,
USA, Center for Evidence Synthesis in Health, Department of Health Services, Policy, and Practice, Brown University School of
Public Health, Providence, Rhode Island, USA, kristin_konnyu@brown.edu.
CONFLICTS OF INTEREST
The authors have no conflicts of interest to disclose.
FINANCIAL DISCLOSURES
The authors have no relevant financial relationships to disclose.
PROTOCOL REGISTRATION
This systematic review was prospectively registered through PROSPERO (Registration Number: CRD42020199102)
Konnyu et al. Page 2
Keywords
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rehabilitation; total hip arthroplasty; total hip replacement; osteoarthritis; systematic review;
complex intervention
Background
Standard care for adults who have undergone total hip arthroplasty (THA) for end-
stage osteoarthritis is to offer rehabilitation after surgery, with the goal of optimizing
postoperative function, reducing pain, and returning to normal activities of daily living
(ADL). Rehabilitation programs are complex interventions that incorporate multiple specific
components (i.e., resistance exercises, gait training, etc.) that may be initiated at different
times after surgery, performed at different frequencies and intensities, delivered by different
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personnel in different settings, and may be personalized to individual, social and financial
circumstances and responses to surgery and rehabilitation. Thus, while rehabilitation
following THA in general has been shown to be effective1 it is unclear which specific
rehabilitation intervention(s), or components within interventions are most effective and
should be replicated in practice to achieve the best clinical outcomes and reduce avoidable
complications or joint failures.2
We conducted a systematic review (SR)3 under the Agency for Healthcare Research
and Quality (AHRQ) Evidence-based Practice Center (EPC) Program to understand the
effectiveness and comparative effectiveness of prehabilitation and rehabilitation for total
knee arthroplasty and THA (see questions for the full review in Appendix A). In this
paper, we address the comparative effects and harms of rehabilitation for patients who have
undergone THA on patient-reported outcomes, performance-based outcomes, and healthcare
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Methods
The Brown Evidence-Based Practice Center (EPC) used established SR methodologies as
outlined in AHRQ Methods Guide.6 The SR was registered in PROSPERO (registration
number CRD42020199102) and is reported in accordance with the Preferred Items for
Reporting in Systematic Reviews and Meta-Analyses7 (Appendix B). We developed the
protocol with input from a broad panel of stakeholders (https://effectivehealthcare.ahrq.gov/
products/major-joint-replacement/protocol). Detailed descriptions of the SR and methods
can be found in the full AHRQ report3 and Appendix C.
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employed since the 2000s.8 No language restrictions were employed. See Appendix C for
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search strategies.
Study Selection
We included studies of adults who had undergone elective non-revision, unilateral THA
for primary osteoarthritis and who received a rehabilitation program within 6 months
after surgery. The 6-month timepoint was selected with stakeholder input to restrict to
evidence of programs that were more recent to the THA surgery. We excluded studies
of patients with non-elective (e.g., emergency), bilateral, or revision THA, and THA for
conditions other than primary osteoarthritis. We defined rehabilitation as active, structured
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Rehabilitation could be compared with other rehabilitation (of different content), similar
rehabilitation with an additional adjunctive modality, or rehabilitation of similar content that
varied in terms of intensity or delivery personnel or delivery setting. We did not evaluate
pharmaceutical or over-the counter interventions as co-interventions with the rehabilitation
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interventions.
reviewers (one with expertise in rehabilitation content, the other with expertise in complex
intervention taxonomies) separately extracted intervention details. Based on stakeholder
input, we restricted outcome to 6 months or later.
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patient education, and adjunctive modalities. We extracted information on the goals of the
exercise(s) and the specific exercises used to achieve these goals; information on whether the
rehabilitation was progressed (i.e., advanced over time) and, if so, whether it was appropriate
(i.e., according to patient-specific parameters assessed by the therapist and not uniform for
all participants); and who delivered the intervention (personnel), how (mode of delivery),
and where (setting). We did not assess dose, intensity, and duration aside from minimal
criteria needed to meet our rehabilitation definition or in cases where rehabilitation content
was the same but varied only in terms of dose, intensity or duration. More details about how
we operationalized the taxonomy and our extractions of the rehabilitation interventions can
be found in Appendix C. We categorized studies by whether rehabilitation occurred during
the acute postoperative period (<2 weeks) or post-acute (≥2 weeks).
To assess study methodological quality, we used the Cochrane risk of bias tool for RCTs12
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and for NRCSs, elements from the ROBINS-I Tool13 related to confounding and selection
bias. For RCTs, we also used items from the National Heart, Lung, and Blood Institute
(NHLBI) tool on the adequacy of descriptions of study eligibility criteria, interventions,
and outcomes.14 Each study was extracted and assessed for methodological quality by one
methodologist and reviewed and confirmed by at least one other experienced methodologist.
Disagreements were resolved by discussion among the team.
For all analyses, we graded the strength of evidence (SoE) as per the AHRQ Methods
Guide.15, 16 For each SoE assessment, we considered the number of studies, their designs,
limitations/risk of bias, the directness of the comparisons to the research question,
consistency of study results, precision of estimates of effect, likelihood of reporting bias,
and other limitations. Based on these assessments, we assigned an SoE rating as being either
high, moderate, or low, or there was insufficient evidence to allow a conclusion.
protocol and full evidence report. The LHS partner and AHRQ did not participate in the
literature search, determination of study eligibility criteria, data analysis, study evaluation,
or interpretation of findings. After completion of the AHRQ report,3 we discussed draft
versions of the manuscript with the LHS partner to ensure it met the decision-making needs
of LHSs and properly conveyed our conclusions. The LHS partner did not draft any portion
of the manuscript or attempt to alter conclusions.
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Results
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The literature searches yielded 22,361 citations (for all topics addressed in the full report).
We found 1,016 citations to retrieve for full-text screening (Appendix D) of which 15 studies
(14 RCTs and 1 NRCS) in 20 articles addressed rehabilitation after THA.17–36
two in the U.S. Studies were mostly at moderate risk of bias due to lack of blinding. Four
RCTs were at high risk of bias due to additional threats to the randomization process.
The one included NRCS was adjusted for important confounders as this was part of our
eligibility criteria and was deemed moderate risk of bias (Appendices G and H).
We did not find a single rehabilitation intervention that was evaluated in more than one
study; all included RCTs evaluated a different rehabilitation program comprised of different
components delivered in varying settings, by diverse personnel, and at various points during
the rehabilitation period (Figure 1, Appendix F). For this reason, we did not perform
meta-analyses of outcomes as we decided with our stakeholders that an “average effect” of
a single concept of “rehabilitation” was not accurate given the notably diverse interventions
identified. Meta-regression (an alternative evidence synthesis approach to explore the impact
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of specific features of interventions on study outcomes) was not feasible due to the
heterogeneity of outcomes.
We, thus, summarized studies based on post-surgical timing (acute and post-acute).
Four RCTs delivered rehabilitation during the acute phase (<2 weeks) and 11 studies
(10 RCTs and 1 NRCS) during the post-acute phase (≥2 weeks). Of the four acute
rehabilitation studies, two evaluated more intensive rehabilitation programs versus less
intensive rehabilitation programs and two evaluated similar programs with varying timing
and settings of delivery (e.g., early vs. late aquatic therapy, early supervised vs. home
unsupervised). Of the 11 post-acute rehabilitation studies, six evaluated novel rehabilitation
programs versus standard care (variously defined) or alternative rehabilitation programs, and
five studies evaluated similar programs different settings or personnel.
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The content of the specific rehabilitation programs varied across interventions. Most
interventions included exercises to address the goal components of strength (14/15 studies;
21/31 arms) and flexibility (11/15 studies; 15/31arms). Fewer studies included components
to address task-specific training (8/15 studies; 13/31 arms), patient education (7/15
studies; 11/31 arms), and balance-motor-learning-agility (5/15 studies; 7/31 arms). Few
studies included exercises targeted at aerobic endurance (3/15 studies; 3/31 arms). Three
studies included an adjunctive modality, including massage and mindfulness/stress reducing
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activities (in 4 arms). Seven of the 15 studies reported some form of progression, of which
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we assessed five to be appropriate progression (i.e., patients were not progressed based on
patient-specific parameters).
Specific codes for intervention (and control arm, where present) goals and exercises, use of
progression (and assessment of appropriateness), and details on personnel, mode of delivery,
and setting are detailed in Figures 2 and 3 and Appendix F.
activities of daily living, quality of life (QoL) or risk of harms (all low SoE) (Table
1). Evidence is insufficient on the impact of rehabilitation on hip range of motion and
satisfaction with care. Interventions and outcomes were too heterogeneous to explore
whether outcomes varied by the presence of specific factors (i.e., intervention content,
personnel, setting, progression). Complete data on all outcomes by outcome domain (e.g.,
pain, strength, QoL) can be found in Appendix I.
and Hip Disability and Osteoarthritis Outcome Score [HOOS]), seven18, 20, 22, 23, 25, 27, 30–32
observed no differences between groups at follow-up ranging from six months to five years
post-THA. The two studies that reported differences found reduced stiffness with ergometer
cycling and “standard physical therapy” compared with “standard physical therapy” alone
with (MD −5.2; P=0.047)24 and with task-oriented exercises compared with open chain
kinetic exercises (MD −9.0, P=0.037).28
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Eleven studies reported pain data using six different measurement instruments (the pain
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components of HOOS and WOMAC, the bodily pain component of the 36-Item Short
Form Survey [SF-36], the visual analogue scale [VAS] of the EuroQol-5 dimensions, VAS,
and the Latinen scale measuring pain intensity).18, 20–32 As with symptoms, most studies
(n=8) found no difference in pain between comparison groups. Three studies18, 20, 28
reported statistically significant reduced pain in their respective intervention groups (sport
therapy; hydrotherapy; task-oriented exercises) compared with controls (no sports therapy;
no hydrotherapy; open-chain kinetic exercises; respectively). Effective programs in these
three studies varied in terms of their component goals but all included strength and
flexibility.
Five studies or fewer reported data on strength (n=5)18, 21, 22, 26, 27, 30, 31, emotional
functioning (n=4) 17, 19, 28, 30, 31, range of motion (n=3)21, 22, 26, 35, 36, and energy and vigor
(n=1)28 and generally observed comparable effects between intervention groups at follow-up
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Twelve studies17–25, 27, 28, 30–34 reported data on patient-reported physical function and
ADLs using various scales (function component of WOMAC, ADL and sports and
recreation scales of the HOOS, physical component scale of the SF-36) measured at follow-
ups between 6 months and 5 years after THA surgery. Eight studies found no difference
between groups in terms of patient-reported function and ADL17–19, 25, 27, 30–34; four
studies20–24, 28 reported significant differences between groups. Interventions associated
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with significant improvements in at least one measure of function and ADL included
a hydrotherapy-based program,20 a walking skills program, 21–23 ergometer cycling
program,24 an early supervised and task-oriented exercise program.28
Five studies reported data on mobility19, 21, 22, 27, 30, 31, 35, 36 and two studies reported data
on transfers 22, 23, 27 using various outcome measures (e.g., 6-meter walk test, 40-meter
fast paced walk test, stair climb tests, step test, figure eight test, speed in a 5-meter
walkway, timed up-and-do test, and step length, 20-second time chair stand test). Three
studies reported no differences between groups. Heiberg 2012 found patients randomized
to the walking skill training program performed significantly better than “standard care”
patients on the 6-meter walk test (mean difference [MD] 52 meters, P<0.001) at 12 months21
although the effect was no longer significant at 5 years.23 Nelson et al. reported patients
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studies reported data on satisfaction with care;24, 25; no differences were observed in these
outcomes between groups. Eleven studies17–19, 21–25, 28, 29, 32–36 reported data on patients’
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self-reported global assessment of their health using ten different measurement instruments.
The studies mostly observed no differences between groups at follow-up times between 6
months and 5 years after THA. Beck 2019 found a significant difference in favor of sports
therapy compared with control (not defined) on the EQ-5D scale at 6-month follow-up, but
this difference was not sustained at the 12-month follow-up.
groups.24, 25
Heterogeneity
Only two studies formally analyzed whether effects from rehabilitation versus its various
comparators differed among subgroups and focused on factors associated with the implant
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itself. Lyp 201626 found that the type of prosthesis used (cemented or uncemented) did not
impact the relative effects of rehabilitation on range of motion or strength. Smith 200933, 34
found outcomes from the Iowa Level of Assistance scale and SF-12 did not vary among
groups by the type of prosthesis used (cemented or uncemented) or surgical approach
(posterior or anterolateral). No study reported heterogeneity of intervention effects due to
patients’ baseline risk (e.g., patients with higher vs. lower measures of strength, flexibility,
function, at baseline).
Discussion
Based on evidence from 15 studies included in our review, it remains unclear which
rehabilitation program should be chosen for patients who have undergone THA, or what
specific attributes of programs are effective in achieving optimal patient outcomes. Each
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study evaluated unique rehabilitation interventions, which differed in content and delivery
method (e.g., timing, progression, personnel, and setting) and reported the effects of these
interventions on disparate outcomes measures. Risk of bias was moderate at best largely
due to the challenge of blinding of rehabilitation interventions. Given this, we found low
SoE of comparable effects among diverse rehabilitation programs in terms of outcomes of
pain, strength, ADLs, QoL, or risk of harms. There was insufficient evidence on outcomes
of hip range of motion or satisfaction with care, precluding conclusions on these outcomes.
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And for all outcomes there was insufficient evidence to explore the effects of any specific
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The findings of this review are consistent with two earlier systematic reviews published
in 2009 and 2013 which noted that the evidence “neither supported nor denied” 1 the
effectiveness of different rehabilitation protocols after THA and there is insufficient
evidence “to build up a detailed evidence-based exercise protocol”, respectively.2 The
persistence of systematic review findings over 12 years despite the accumulation of more
evidence should give stakeholders pause. It means that patient-care and healthcare services
for nearly half a million adults who undergo THA annually (estimated to increase to 635,000
by 2030),37 is lacking an evidence-base to guide practice and new studies are not improving
on the limitations of earlier ones.
paired with evidence synthesis (including meta-regression models) are needed to isolate the
interependent effects of various factors on key outcomes of interest to the field. To work
however, rehabilitation studies moving forward would need to address two main limitations
of the evidence to date: 1) lack of standardized intervention reporting and 2) lack of
standardized outcomes.
and providers) without first understanding what rehabilitation is being delivered? (i.e.,
if differences exist in the outcomes, how do we know if these are due to differences
in the setting, the rehabilitation program, or both?). Unfortunately, studies to date
have employed different terminologies to define their rehabilitation programs and these
descriptions have varied extensively in the level of detail provided. Some studies use
few words like “inpatient rehabilitation” while other studies provide comprehensive multi-
page supplemental protocols to detail the contents of the rehabilitation. Standardization of
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terminology is also lacking. Consistent with other complex scientific problems, the science
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of rehabilitation can only advance if the field as a collective can agree upon and use a shared
taxonomy to define intervention content and consistently report content in a complete and
transparent manner. As a starting point, we would recommend trialists consider using the
taxonomy defined by Oatis and Franklin used in this review to define intervention content,10
and the Template for Intervention Description and Replication (TIDieR) checklist to ensure
comprehensive reporting of all intervention elements.39
Standardized outcomes
Adding to the complexity of the diverse interventions, studies reported highly diverse
outcomes. These not only included different outcome domains, but also different scales
and metrics within shared outcome domains, at various points of follow-up (6 months
to 5 years). Learning across studies was difficult since we could not adequately evaluate
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review, only five studies were rated as low risk of bias for the domain of blinding outcome
assessors; five studies were rated as unclear risk of bias and three were rated as high risk
of bias. Thus, in addition to considering what core outcomes should be included in studies,
stakeholders should consider standards for how such core outcomes should be collected and
analyzed to minimize threats to bias.
Finally, studies had relatively small sample sizes, which may have resulted in underpowered
studies and, thus, misleadingly statistically nonsignificant findings. This is especially
important for comparison of two or more active interventions like two rehabilitation
programs as large samples are needed to demonstrate an advantage of a likely smaller
relative effect size. Jette et al. make similar calls for action in rehabilitation research for
TKA and noted that the challenge of sample size may necessitate the need for coordinated
multisite programs of research to facilitate larger sample sizes.42
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and delivery factors using a novel and comprehensive taxonomy. These codes are a crucial
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first step in articulating the challenge of understanding rehabilitation evidence to date and
setting a benchmark for intervention design and reporting to come. While the taxonomy was
not able to be used to its full advantage in meta-regression models to isolate the unique
effect of specific components, such analyses could be feasible in the future if sufficient
number of studies (or real world data) were available on specific outcomes. A limitation
of our synthesis is that we did not capture timing, intensity, or dosage, in any form (e.g.,
challenge of the exercise, duration of the session in minutes, duration of the program in
days/weeks, number of sessions). Finally, in terms of applicability there was wide variation
in the sex ratios (27 to 100 percent of participants being female) and mean age (54 to
71 years) across studies and most studies did not report whether patients had undergone
previous contralateral replacement surgery (although of those that that did, proportions
were less than 25%). As such, the conclusions in this SR are likely most applicable to
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middle-to-older-aged adults in high-income countries who are receiving their first total THA
for osteoarthritis.
Supplementary Material
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ACKNOWLEDGEMENTS
The authors gratefully acknowledge the contribution of David W. Niebuhr, M.D., M.P.H., M.Sc., our AHRQ
Task Order Officer; members of the Key Informant and Technical Expert Panels, reviewers of our overall review
(all listed in the AHRQ full report); Jennifer Racine-Avila, M.B.A. for early feedback and development of the
protocol; Carol A. Oatis, P.T., Ph.D., for sharing her taxonomy and providing important conceptual feedback in its
application; Shivani Mehta B.A., a research associate who played a role in conduct of the overall review
FUNDING SOURCE
This project was funded under Contract No. HHSA 75Q80120D00001 from the Agency for Healthcare Research
and Quality (AHRQ), U.S. Department of Health and Human Services (DHHS). The authors of this paper are
responsible for its content. Statements in the report should not be construed as endorsement by AHRQ or DHHS.
AHRQ retains a license to display, reproduce, and distribute the data and the report from which this manuscript was
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derived under the terms of the agency’s contract with the author.
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Figure 1. Overview of studies of acute and post-acute rehabilitation interventions versus various
controls for total hip arthroplasty
Figure presents categorization of studies that evaluated acute and post-acute rehabilitation
programs for THA. The first column lists a novel (more intensive) acute rehabilitation
program compared to a different program (first group hypothesized to be better); the second
column lists studies with comparatively similar acute rehabilitation programs in both arms
that were delivered with different timing or intensity (first group hypothesized to be better);
the third column lists a novel (more intensive) post-acute rehabilitation program compared
to a different program (first group hypothesized to be better); the fourth column lists studies
with comparatively similar rehabilitation programs delivered in different settings or by
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different personnel
Abbreviations: Adj = adjunctive, A = aerobic exercise, B= balance-motor-learning-agility
exercise, E = patient education, F = flexibility exercise, S = strengthening exercise, T =
task-specific training, THA = total hip arthroplasty.
* Intervention included progression which was deemed appropriate
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Figure 2. Goal components strength, aerobic, and flexibility and their specific exercise
components for rehabilitation interventions versus various controls for total hip arthroplasty
See Figure 3 for goal components Balance-motor-learning-agility, task specific training,
patient education, and adjunctive modalities. The color is added for visual display and does
not provide unique information.
Group I: kinesiotherapy, low-frequency magnetic field and water exercises; Group II:
undergoing kinesiotherapy and low-frequency magnetic field, without water exercises;
Group V: awaiting rehabilitation
Abbreviations: PRT = progressive resistance training, PT = physical therapy, rehab =
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Table 1.
Evidence profile: Rehabilitation versus various controls for total hip arthroplasty
Outcome Category Outcome N Studies RoB Consistency Precision Directness Intervention SoE Conclusions
(Participants) Replication
Konnyu et al.
Body structure and Pain 11 (1297) Moderate Consistent Precise Direct All unique Low Similar pain
function
ROM 3 (178) Moderate Inconsistent Precise Direct All unique Insufficient No conclusion
Strength 5 (370) Moderate Consistent Precise Direct All unique Low Similar strength
Activity and participation ADLs 12 (1247) Moderate Consistent Precise Direct All unique Low Similar ADL
Other outcomes Satisfaction with care 2 (372) Moderate Consistent Precise Direct All unique Insufficient No conclusion
QoL 4 (335) Moderate Consistent Precise Direct All unique Low Similar QoL
Harms Harms from 4 (534) Moderate Consistent Precise Direct All unique Low Similar harms
prehabilitation
Abbreviations: ADLs = activities of daily living, QoL = health-related quality of life, NA = not applicable, QoL = quality of life, RoB = risk of bias, ROM = range of motion, SoE = strength of evidence.
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