Skip to main content
BMJ Open logoLink to BMJ Open
. 2018 May 5;8(5):e019998. doi: 10.1136/bmjopen-2017-019998

Early rehabilitation to prevent postintensive care syndrome in patients with critical illness: a systematic review and meta-analysis

Ryota Fuke 1,#, Toru Hifumi 2,#, Yutaka Kondo 3, Junji Hatakeyama 4, Tetsuhiro Takei, Kazuma Yamakawa 5, Shigeaki Inoue 6, Osamu Nishida 7
PMCID: PMC5942437  PMID: 29730622

Abstract

Introduction

We examined the effectiveness of early rehabilitation for the prevention of postintensive care syndrome (PICS), characterised by an impaired physical, cognitive or mental health status, among survivors of critical illness.

Methods

We performed a systematic literature search of several databases (Medline, Embase and Cochrane Central Register of Controlled Trials) and a manual search to identify randomised controlled trials (RCTs) comparing the effectiveness of early rehabilitation versus no early rehabilitation or standard care for the prevention of PICS. The primary outcomes were short-term physical-related, cognitive-related and mental health-related outcomes assessed during hospitalisation. The secondary outcomes were the standardised, long-term health-related quality of life scores (EuroQol 5 Dimension (EQ5D) and the Medical Outcomes Study 36-Item Short Form Health Survey Physical Function Scale (SF-36 PF)). We used the Grading of Recommendations Assessment, Development and Evaluation approach to rate the quality of evidence (QoE).

Results

Six RCTs selected from 5105 screened abstracts were included. Early rehabilitation significantly improved short-term physical-related outcomes, as indicated by an increased Medical Research Council scale score (standardised mean difference (SMD): 0.38, 95% CI 0.10 to 0.66, p=0.009) (QoE: low) and a decreased incidence of intensive care unit-acquired weakness (OR 0.42, 95% CI 0.22 to 0.82, p=0.01, QoE: low), compared with standard care or no early rehabilitation. However, the two groups did not differ in terms of cognitive-related delirium-free days (SMD: −0.02, 95% CI −0.23 to 0.20, QoE: low) and the mental health-related Hospital Anxiety and Depression Scale score (OR: 0.79, 95% CI 0.29 to 2.12, QoE: low). Early rehabilitation did not improve the long-term outcomes of PICS as characterised by EQ5D and SF-36 PF.

Conclusions

Early rehabilitation improved only short-term physical-related outcomes in patients with critical illness. Additional large RCTs are needed.

Keywords: early rehabilitation, intensive care unit, post-intensive care syndrome, sepsis


Strengths and limitations of this study.

  • This meta-analysis is the first meta-analysis of comprehensive postintensive care syndrome (PICS) based on randomised controlled trials (RCTs), in which the study intervention populations were limited to early rehabilitation.

  • This meta-analysis was mainly limited by (1) the small number of patients in the included RCTs, (2) a lack of detailed analysis of the adverse effects and PICS domains after hospital discharge and (3) no confirmation of the exact first day of rehabilitation initiation in one of the six included RCTs.

  • We used the Grading of Recommendations Assessment, Development and Evaluation approach in the review process.

Introduction

Dramatic developments and improvements in the technique, instruments and education systems used in intensive care units (ICUs) have reduced the mortality of patients with critical illness over the past four decades.1 However, this evolution of life-saving interventions has led to increasing numbers of surviving critically ill patients with an impaired ability to return to physical and mental aspects of normal life.2 These persistent physical, cognitive and mental impairments experienced by ICU survivors present serious obstacles to discharge from the hospital to a home setting and, once home, to a return to normal daily life.2 3

Postintensive care syndrome (PICS) was established as a new syndrome encompassing new or worsening impairments in physical, cognitive or mental health status that arise after critical illness and persist beyond acute care hospitalisation, with the aim initiating improvements for ICU survivors and their families across the continuum of care.4 Since the establishment of PICS in 2010, observational studies have evaluated the independent factors associated with this syndrome5; however, few intervention studies have targeted the prevention of PICS.

Physiotherapy with early rehabilitation is considered an integral component of the multidisciplinary management of patients in ICUs. In other populations, exercise has been shown to improve strength and function, decrease inflammation6–8 and affect oxidative stress,9–12 leading to suggestions that early physiotherapy may prevent or reverse some physical impairments in ICU patients. However, no systematic review has investigated the effectiveness of early rehabilitation for the prevention of PICS in ICU patients. The present systematic review aimed to assess the effectiveness of early rehabilitative interventions for the prevention of PICS in ICU patients.

Methods

Protocols and registration

This review protocol was registered in PROSPERO, an International Prospective Register of Systematic Reviews at the National Institute for Health Research and Centre for Reviews and Dissemination at the University of York (http://www.crd.york.ac.uk/PROSPERO/) (Registration No. CRD42016039759).13 This protocol adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Protocols (PRISMA-P) statements,14 15 and the systematic review was reported according to PRISMA guidelines.14 16 17 The protocol for this systematic review was previously published.18

Search strategy

We searched the Medline (via PubMed from 1996 to 7 June 2016), Embase (until 7 June 2016) and Cochrane Central Register of Controlled Trials (CENTRAL) databases (until 7 June 2016) for full-text clinical trials conducted in humans to retrieve relevant articles for the literature review. We also performed a manual search to retrieve all potentially relevant articles from 8 June to 31 August 2016. The key search terms used to identify potential studies are listed in online supplementary file 1. Finally, we updated our search in Medline (via PubMed from 8 June 2016 to 15 January 2018) using the same key search terms.

Supplementary data

bmjopen-2017-019998supp001.pdf (204.6KB, pdf)

Study selection and inclusion criteria

Three authors (YK, RF, SI) performed the first-line comprehensive literature search and removal of duplicates. Subsequently, two randomly selected authors independently screened the study titles and abstracts for potential relevance. The kappa value for selection bias was 0.396. When disagreements arose between reviewers, the full text of the paper was retrieved, and the disagreements were reconsidered and discussed until a consensus was reached. The full texts of articles included in the final selection were reviewed by two randomly chosen authors. We included trials with the following characteristics:

Study types: Randomised controlled trials (RCTs) were included; non-randomised and observational studies were excluded.

Population: Adult patients (aged >18 years) admitted to the ICU were included. We excluded patients with traumatic brain injury and stroke who did not fulfil the PICS criteria, specifically those with acquired physical and psychiatric/cognitive dysfunction after ICU admission.

Intervention: The intervention was early rehabilitation, defined as (1) starting at an earlier time point than usual care or (2) administration within 7 days of ICU admission. ’Rehabilitation' included all physiotherapy, occupational therapy and palliative care-related support. We excluded RCTs in which rehabilitation was initiated before ICU admission and those comparing early rehabilitation with another intervention.

Control: The control group received standard care or no early rehabilitation.

Outcome: The primary outcomes (ie, short-term outcomes assessed during hospitalisation) were as follows: (1) physical-related outcomes (incidence of ICU-acquired weakness (AW), Medical Research Council (MRC)19 scale score), (2) cognitive-related outcomes (delirium-free days) and (3) mental status-related outcomes (Hospital Anxiety and Depression Scale (HADS)).20 The secondary outcomes (long-term outcomes assessed postdischarge) included the standardised Health-Related Quality of Life with EuroQol 5 Dimensions (EQ5D) test21 22 and the Medical Outcomes Study 36-Item Short Form Health Survey Physical Function scale (SF-36 PF)23 as measures of long-term physical function.

Assessment of the risk of bias

To assess the quality of the included studies, we adopted the Cochrane risk of bias tool.24 Two randomly selected authors performed the risk of bias assessment; disagreements were resolved by discussion, with the inclusion of a third reviewer if necessary. We considered the risk of bias for each element to be ‘high’ when bias was present and likely to affect outcomes, and ‘low’ when bias was not present or present but unlikely to affect outcomes.25

Rating the quality of evidence using the Grading of Recommendations Assessment, Development and Evaluation approach

Two authors (RF and TH) independently used the Grading of Recommendations Assessment, Development, and Evaluation (GRADE) tool to rate the quality of evidence (QoE). We used the GRADE approach to rate the QoE of early rehabilitation for outcomes. Although the QoE represents a continuum, we assessed the quality of the body of evidence for each outcome categorised as high, moderate, low or very low using the GRADE pro Guideline Development Tool.

Data extraction and management

The author(s), title, journal name, year of publication, website URL and abstract of each included article were identified. Conference abstracts were excluded. Data from each study were extracted independently by two review authors. When faced with insufficient or incomplete data, we contacted the authors of the studies directly. Information related to the study population, sample size, interventions, comparators, potential biases in the conduct of the trial, outcomes (including adverse events), follow-up and statistical analysis methods were extracted from the original reports into specially designed paper forms and then entered into a spreadsheet.

Summarisation of data and treatment effects

As data from several trials were available, we performed a meta-analysis according to the Cochrane Handbook for Systematic Reviews of Interventions and PRISMA guidelines using Review Manager software (RevMan V.5.3, Copenhagen, Denmark: The Nordic Cochrane Centre, the Cochrane Collaboration 2014). We summarised the results of this meta-analysis using the generic inverse variance method to facilitate the pooling of estimates of treatment effects. We used ORs with 95% CIs for dichotomous outcomes, and mean differences or standardised mean differences (SMDs) with 95% CIs for continuous outcomes when appropriate. If a quantitative synthesis was not appropriate for a particular outcome, we devised a qualitative summary of that outcome.

Assessment of heterogeneity

For each outcome, we assessed heterogeneity between trials using I2 statistics to quantify inconsistencies. We considered that significant heterogeneity was present when the reason for heterogeneity could not be explained and the I2 was ≥50%. The presence of strong clinical heterogeneity was considered when deciding to perform a quantitative data synthesis or a sensitivity analysis with a special focus.26

Data synthesis

Estimates were pooled using a random effects model. We performed our analysis based on all published or available data.

Results

Literature search

The PRISMA flow chart of study selection is shown in figure 1. The combined search strategy identified 5105 citations, of which 46 were judged to be potentially eligible based on the abstract. After excluding 40 of these citations following a full-text review (online supplementary file 2), six RCTs that had enrolled 709 patients were deemed eligible and were included in the review.27–32 The updated literature search in Medline also identified a total of 320 citations, but no studies were judged to be potentially eligible based on the inclusion criteria.

Figure 1.

Figure 1

Flow chart of the process of study identification and inclusion. ICU, intensive care unit.

Supplementary data

bmjopen-2017-019998supp002.pdf (325KB, pdf)

Characteristics of included studies

The study characteristics are summarised in table 1. Early rehabilitation was initiated within 3 days (median or mean) of ICU admission in five studies.27 29–32 The first day of rehabilitation was not confirmed in three studies, although early rehabilitation was described in the text, and we contacted the authors to acquire additional information.28 The rehabilitation strategies administered to each intervention group varied among protocols.

Table 1.

Characteristics of included studies

Source Population No of patients Age (years) APACHE II score Intervention Timing of first rehabilitation/
standard care
Follow-up Outcome Ref
Total Early rehab Control Early rehab Control Early rehab Control Early rehab Control Short-term
(during the hospitalisation)
Long-term (post
discharge)
Brummel 2014 Respiratory failure and/or septic, cardiogenic or haemorrhagic shock. 44 22 22 62 (48–67) 60 (51–69) 21.5 (20.0–28.8) 27.0 (17.5–31.0) Passive ROM exercises to independent ambulation, guided by the patient’s RASS (daily). Physical therapy (1–2 per week). Intervention: 1 (1–1), control: 3 (2–6) 3 months VFD, DFD EQ5D 27
Hodgson 2016 Critically ill adults mechanically ventilated >24 hours. 50 29 21 64±12 53±15 19.8±9.8 15.9±6.9 Functional rehabilitation treatment conducted at the highest level of activity. Not protocolised and all usual unit practice was continued. Intervention: 3 (2–4), control: 3 (2–4) 6 months MRC, ICU-AW, mechanical ventilation days EQ5D 31
Jones 2015 Patients ≥45 years, had a combined ICU and pre-ICU stay ≥5 days. 42 22 20 64±13 60±12 17±10 14±4 In addition to the self-help programme, a 6-week programme of supervised physiotherapy sessions. Patient-controlled self-help rehabilitation programme. NA 3 months VFD,
HAS/HADS
28
Kayambu 2015 Sepsis patients >18 years who remained mechanically ventilated >48 hour. 50 26 24 62.5 (30–83) 65.5 (37–85) 28±7.6 27±6.8 EMS, passive ROM, active ROM, sitting out of bed, transfers, ambulation for 30 min, one to two times daily. Standard ICU care, which included physical therapy. Within 48 hours of sepsis 6 months MRC, VFD,
HAS/HADS
SF-36 PF 29
Morris 2016 Patients with acute respiratory failure requiring MV. 300 150 150 55±17 58±14 NA NA Passive ROM, physical therapy and progressive resistance exercises for 7 days per week. Physical therapy weekday when ordered by the clinical team. Intervention: 1 (0–2)
Control: 7 (4–10)
6 months VFD, DFD SF-36 PF 32
Schweickert 2009 Patients who had been on MV for <72 hour. 104 49 55 57.7 (36.3–69.1) 54.4 (46.5–66.4) 20 (15.8–24) 19 (13.3–23) Early exercise and physical and occupational therapy on the day of enrolment. Therapy as ordered by the primary care team. Intervention: 1.5 (1.0–2.1)
Control: 7.4 (6.0–10.9)
NA MRC, ICU-AW, VFD, DFD 30

APACHE II score, Acute Physiology and Chronic Health Evaluation II score; AW, acquired weakness; DFD, delirium-free days; early rehab, early rehabilitation; EMS, electrical muscle stimulation; EQ5D, EuroQol 5 Dimensions; HAS/HADS, Hospital Anxiety and Depression Scale; ICU, intensive care unit; MRC, Medical Research Council; MV, mechanical ventilaltion; NA, not applicable; RASS, Richmond agitation-sedation scale; ROM, range of motion; SF-36 PF, 36-Item Short Form Health Survey Physical Function scale; VFD, ventilator-free days.

Risk of bias in the included trials

The evaluation of the risk of bias in each included RCT is shown in the risk of bias summary for PICS-related outcomes without in figure 2. Regarding blinding, six trials involved open-label RCTs. The blinding of outcome assessments was described for all RCTs. In all RCTs, attrition bias was observed because of a per-protocol analysis, the inclusion of many patients who dropped out of the study and death. The performance bias of mortality as an outcome measure was low, however, because blinding did not affect mortality.

Figure 2.

Figure 2

Risk of bias summary.

Outcomes

The quality assessment and a summary of each outcome measure are shown in table 2.

Table 2.

Quality assessment and summary of findings for the main comparison

Quality assessment No of patients Effect Quality Importance
No of studies Study design Risk of bias Inconsistency Indirectness Imprecision Other considerations Early rehabilitation Control Relative
(95% CI)
Absolute
(95% CI)
Incidence of ICU-AW
2 Randomised trials Serious* Not serious Not serious Serious† None 22/78 (28.2%) 37/76 (48.7%) OR 0.42
(0.22 to 0.82)
202 fewer per 1000
(from 49 fewer to 314 fewer)
⨁⨁◯◯
Low
Critical
MRC
3 Randomised trials Serious* Not serious Not serious Serious† None 97 99 SMD 0.38 higher
(0.1 higher to 0.66 higher)
⨁⨁◯◯
Low
Critical
Delirium-free days
3 Randomised trials Serious* Not serious Not serious Serious† None 164 162 SMD 0.02 lower
(0.23 lower to 0.2 higher)
⨁⨁◯◯
Low
Critical
Incidence of HADS/HAS
2 Randomised trials Serious* Serious Not serious Serious† None 10/48 (20.8%) 11/44 (25.0%) OR 0.79
(0.29 to 2.12)
42 fewer per 1000
(from 162 fewer to 164 more)
⨁◯◯◯
Very low
Critical
Health related QOL score (EQ5D)
2 Randomised trials Serious* Serious‡ Not serious Serious† None 35 28 SMD 0.11 SD higher
(0.86 lower to 1.09 higher)
⨁◯◯◯
Very low
Critical
SF-36 PF
2 Randomised trials Serious* Not serious Not serious Serious† None 93 98 SMD 2.41 higher
(0.75 lower to 5.58 higher)
⨁⨁◯◯
Low
Critical

*Most of the studies are classified as unclear or high risk of bias (performance bias and attrition bias).

†CIs for absolute effects are wide and include no effect and important harm and/or small sample size (the number of events is <300).

‡Substantial heterogeneity present.

AW, acquired weakness; EQ5D, EuroQol 5 Dimensions; HADS/HAS, Hospital Anxiety and Depression Scale; ICU, intensive care unit; MRC, Medical Research Council; QOL, quality of life; SF-36 PF, 36-Item Short Form Health Survey Physical Function scale; SMD, standardised mean difference.

GRADE working group grades of evidence: High quality—further research is very unlikely to change our confidence in the estimate of effect. Moderate quality—further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate. Low quality—further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate. Very low quality—we are very uncertain about the estimate.

Primary outcomes (short-term outcomes)

Physical-related outcomes

Incidence of ICU-AW: Two RCTs reported the incidence of ICU-AW (figure 3). There was a significant reduction in the incidence of ICU-AW in the early rehabilitation group according to the random effects model (two trials, n=154; OR 0.42, 95% CI 0.22 to 0.82, p=0.01; I2=0%).

Figure 3.

Figure 3

The effect of early rehabilitation on short-term outcomes in postintensive care syndrome (PICS) in intensive care unit (ICU) patients. (1) Physical-related outcomes (A) Incidence of ICU-acquired weakness (AW). (B) Medical Research Council (MRC) sum score. (2) Cognitive-related outcomes, characterised by delirium-free days. (3) Mental status-related outcomes, characterised by the Hospital Anxiety and Depression Scale (HAS/HADS) score.

The risk of bias was determined to be serious because all RCTs included a moderate risk of bias. Imprecision was also determined to be serious because of the small number of included patients as per the optimal information size (OIS) criteria. Therefore, the QoE was downgraded from high to low because of these serious risks.

MRC: Three RCTs reported MRC scores (figure 3). We observed a significant improvement in the early rehabilitation group (MRC (three trials, n=196; SMD 0.38, 95% CI 0.10 to 0.66, p=0.009; I2=0%)).

Cognitive-related outcomes

Delirium-free days: Two RCTs reported the incidence of delirium-free days (figure 3). There was no significant increase in this parameter in the early rehabilitation group according to a random effects model (two trials, n=326; SMD −0.02, 95% CI −0.23 to 0.20, p=0.62; I2=0%). The risk of bias was determined to be serious because all RCTs included a moderate risk of bias, and imprecision was also determined to be serious because of the small number of included patients as per OIS criteria. These serious risks led to the downgrading of the QoE from high to low.

Mental health-related outcomes

Incidence of HAS/HADS: Two RCTs reported the incidence of HAS/HADS (figure 3). These groups did not differ significantly according to a random effects model (two trials, n=92; OR 0.79, 95% CI 0.29 to 2.12, p=0.64; I2=0%). The risk of bias was determined to be serious because all RCTs included a moderate risk of bias, and imprecision was also determined to be serious because of the small number of included patients. These serious risks led to the downgrading of the QoE from high to low.

Secondary outcomes (long-term outcomes)

EQ5D: Two RCTs reported the EQ5D scores (figure 4). No significant difference was observed between the two groups according to a random effects model (two trials, n=63; SMD 0.11, 95% CI −0.86 to 1.09, p=0.82; I2=72%). The risk of bias was deemed serious because all RCTs demonstrated a moderate risk of bias, and inconsistency was deemed serious because of severe heterogeneity (p=0.06, I2=72%). Imprecision was also considered serious because of the small number of included patients. These serious risks led to the downgrading of the QoE from high to very low.

Figure 4.

Figure 4

The effect of early rehabilitation on long-term outcomes in postintensive care syndrome (PICS) in intensive care unit (ICU) patients. The effect of early rehabilitation on health-related quality of life (QOL) scores and in ICU patients. (1) Health-related quality of life (QOL) scores calculated from the EuroQol 5 Dimensions (EQ5D). (2) Medical Outcomes Study 36-Item Short Form Health Survey Physical Function scale (SF-36 PF).

SF-36 PF: Two RCTs reported SF-36 PF scale scores (figure 4). However, these scores were evaluated several months later. Moreover, the timing of SF-36 PF evaluation varied greatly among studies (ie, at hospital discharge and 2, 4 and 6 months after enrolment,32 or at 6 months after hospital discharge).29 We observed a significant improvement in the early rehabilitation group (SF-36 PF (two trials, n=191; SMD 2.41, 95% CI −0.75 to 5.58, p=0.14; I2=98%)). However, the different timings of SF-36 PF scale evaluation among the various studies led to significant heterogeneity. Imprecision was also considered serious because of the small number of included patients as per the OIS criteria. Therefore, these serious risks led to the downgrading of the QoE from high to very low.

Discussion

Summary of the main results

This meta-analysis revealed that early rehabilitation significantly improved short-term physical function in patients with critical illness, as assessed by the MRC scoring system and the incidence of ICU-AW. However, it did not significantly improve the patients' cognitive and mental status-related outcomes. These results suggest that early rehabilitation has a limited effect on the prevention of PICS in patients with critical illness, and only reflect improvements in short-term physical function.

Strengths of the review

To our knowledge, the present work is the first meta-analysis of comprehensive PICS based on RCTs in which the study intervention populations were limited to early rehabilitation. Additionally, we used the GRADE approach in the review process which allowed us to make judgements about the QoE and strength of recommendations in a systematic and transparent manner. Thus, the present meta-analysis allowed us determine whether critical care physicians should initiate early rehabilitation for patients with critical illness, and provided new evidence about the effectiveness of physiotherapy interventions aimed at early mobilisation.33

Agreements and disagreements with other studies or reviews

Four systematic reviews have addressed the effect of rehabilitation33–35 or early rehabilitation36 during an ICU stay on functional status. Through a meta-analysis, Kayambu et al found that physical therapy in the ICU may improve muscle strength, physical function, quality of life, ventilator-free days, ICU stay and hospital stay; however, the authors included one RCT involving patients who underwent laparotomy (among 10 total RCTs), and another study initiated physical therapy 30 days after bed rest.34 Therefore, the results cannot be directly applied to our clinical practice because of the heterogeneity of the study population. The present meta-analysis showed that early rehabilitation did not improve patients’ quality of life. The inconsistency of these results might be attributable to differences in the methods used to assess quality of life. Kayambu et al used the Medical Outcomes Study 36-Item Short Form survey score, whereas the present review used the EQ5D.

Castro-Avila et al conducted a systematic review and meta-analysis of the effect of early rehabilitation during an ICU stay on functional status34 and included the study reported by Denehy et al.37 However, we did not include this study in our systematic review, as it implemented early active rehabilitation in the control group. This implementation was the main reason underlying the authors’ conclusion that early rehabilitation was not associated with improvements in the walking distance and incidence of ICU-AW. Furthermore, Tipping et al reported a systematic review regarding the effects of active mobilisation and rehabilitation in the ICU on mortality and function,35 and included a study by Moss et al.38 However, that study did not initiate rehabilitation during the early phase and therefore was also not included in the current systematic review.

Clinical implementation

The initiation of early rehabilitation improved short-term outcomes, such as the physical function score and the incidence of ICU-AW in the present systematic review; however, it did not improve. The tendency to favour early rehabilitation during mechanical ventilation suggests that early rehabilitation could potentially improve short-term survival and maintain and increase muscle strength.

However, the initiation of rehabilitation during acute phase may inflict tremendous physical stress and exhaustion on patients in the ICU, thus increasing ICU mortality.39 Although several studies included in the present meta-analysis described the safety of early physiotherapy in the ICU,27 29–32 40 only two outcomes related to the safety of early rehabilitation, the blood lactate level29 and early physiotherapy termination rate,31 were compared between two groups. Therefore, the study conclusions should be approached with caution.

Limitations of the review

The current meta-analysis had several limitations. First, the analysis of each outcome included only a small number of patients. Although Schweickert et al reported data concerning delirium, we could not extract cognitive-related outcomes because no data about delirium-free days were not addressed directly.30 Second, the studies included in the current systematic review did not measure the domains of PICS beyond hospital discharge. Third, two of the included studies were pilot/feasibility trials and not powered to identify differences in physical or cognitive outcomes.27 31 However, it was reasonable to initiate RCTs in the context of feasibility studies because no large multicentre trials of the effects of early mobilisation in the ICU had been published before the study conducted by Brummel et al, and little evidence to support the feasibility of individual patient randomisation across multiple sites using a complex intervention (ie, early mobilisation) had been reported before the study conducted by Hodgson et al. Moreover, these two RCTs demonstrated the same level of risk as other RCTs, according to risk of bias summary conducted in this meta-analysis (figure 2).

Fourth, we could not confirm the exact first day of rehabilitation initiation in the three studies, although ’early rehabilitation' was described in the text, and we contacted the authors to acquire additional information.28 40 Fifth, we could not find any data regarding direct cognitive assessment in the selected papers. Although cognitive impairment at hospital discharge may not predict long-term cognitive impairment,41 Pandharipande et al reported that a longer duration of delirium on admission was associated with worse global cognition and executive function scores in the surgical ICU at 3 and 12 months.42 Therefore, we believe that the assessment of delirium in the ICU and hospital is a very important predictor of long-term cognitive impairment postdischarge. Sixth, as this meta-analysis included studies that had implemented various ‘early rehabilitation’ protocols, further analyses should include large trials with strict and comparable rehabilitation algorithms adjusted for the initiation time, type and intensity. Despite these several limitations, our meta-analysis clarifies the effectiveness of early rehabilitation for the prevention of PICS in survivors of critical illness.

Conclusion

Early rehabilitation has a limited effect on the prevention of PICS, although it led to significant improvements in short-term physical-related outcomes, including MRC scores and the incidence of ICU-AW. However, early rehabilitation had no significant effect on cognitive function and mental health-related outcomes or mortality in patients with critical illness. Additional large-scale, rigorous RCTs are needed to confirm our results.

Supplementary Material

Reviewer comments
Author's manuscript

Footnotes

RF and TH contributed equally.

Contributors: YK, RF, TH, JH, TT and SI conceived the idea for this systematic review. YK, RF, TH, JH, TT and SI developed the methodology for the systematic review, and KY and ON supervised the methodological process. The manuscript was drafted by YK and SI. RF, TH, JH, TT and KY, and revised by ON. All authors critically reviewed and approved the final manuscript.

Funding: This research received no specific grant from any funding agency in the public, commercial or not-for-profit sectors.

Competing interests: None declared.

Patient consent: Not required.

Provenance and peer review: Not commissioned; externally peer reviewed.

Data sharing statement: Extra data can be accessed via the Dryad data repository at http://datadryad.org/ with the doi:10.5061/dryad.12q6c78

References

  • 1. Bemis-Dougherty AR, Smith JM. What follows survival of critical illness? Physical therapists' management of patients with post-intensive care syndrome. Phys Ther 2013;93:179–85. 10.2522/ptj.20110429 [DOI] [PubMed] [Google Scholar]
  • 2. Iwashyna TJ, Ely EW, Smith DM, et al. Long-term cognitive impairment and functional disability among survivors of severe sepsis. JAMA 2010;304:1787–94. 10.1001/jama.2010.1553 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Desai SV, Law TJ, Needham DM. Long-term complications of critical care. Crit Care Med 2011;39:371–9. 10.1097/CCM.0b013e3181fd66e5 [DOI] [PubMed] [Google Scholar]
  • 4. Needham DM, Davidson J, Cohen H, et al. Improving long-term outcomes after discharge from intensive care unit: report from a stakeholders' conference. Crit Care Med 2012;40:502–9. 10.1097/CCM.0b013e318232da75 [DOI] [PubMed] [Google Scholar]
  • 5. Elliott D, Davidson JE, Harvey MA, et al. Exploring the scope of post-intensive care syndrome therapy and care: engagement of non-critical care providers and survivors in a second stakeholders meeting. Crit Care Med 2014;42:2518–26. 10.1097/CCM.0000000000000525 [DOI] [PubMed] [Google Scholar]
  • 6. Gielen S, Adams V, Möbius-Winkler S, et al. Anti-inflammatory effects of exercise training in the skeletal muscle of patients with chronic heart failure. J Am Coll Cardiol 2003;42:861–8. 10.1016/S0735-1097(03)00848-9 [DOI] [PubMed] [Google Scholar]
  • 7. Nuhr MJ, Pette D, Berger R, et al. Beneficial effects of chronic low-frequency stimulation of thigh muscles in patients with advanced chronic heart failure. Eur Heart J 2004;25:136–43. 10.1016/j.ehj.2003.09.027 [DOI] [PubMed] [Google Scholar]
  • 8. Vivodtzev I, Pépin JL, Vottero G, et al. Improvement in quadriceps strength and dyspnea in daily tasks after 1 month of electrical stimulation in severely deconditioned and malnourished COPD. Chest 2006;129:1540–8. 10.1378/chest.129.6.1540 [DOI] [PubMed] [Google Scholar]
  • 9. Laaksonen DE, Atalay M, Niskanen L, et al. Increased resting and exercise-induced oxidative stress in young IDDM men. Diabetes Care 1996;19:569–74. 10.2337/diacare.19.6.569 [DOI] [PubMed] [Google Scholar]
  • 10. Mercken EM, Hageman GJ, Schols AM, et al. Rehabilitation decreases exercise-induced oxidative stress in chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2005;172:994–1001. 10.1164/rccm.200411-1580OC [DOI] [PubMed] [Google Scholar]
  • 11. Nishiyama Y, Ikeda H, Haramaki N, et al. Oxidative stress is related to exercise intolerance in patients with heart failure. Am Heart J 1998;135:115–20. 10.1016/S0002-8703(98)70351-5 [DOI] [PubMed] [Google Scholar]
  • 12. Vincent HK, Morgan JW, Vincent KR. Obesity exacerbates oxidative stress levels after acute exercise. Med Sci Sports Exerc 2004;36:772–9. 10.1249/01.MSS.0000126576.53038.E9 [DOI] [PubMed] [Google Scholar]
  • 13. Moher D, Booth A, Stewart L. How to reduce unnecessary duplication: use PROSPERO. BJOG 2014;121:784–6. 10.1111/1471-0528.12657 [DOI] [PubMed] [Google Scholar]
  • 14. Moher D, Shamseer L, Clarke M, et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement. Syst Rev 2015;4:4:1 10.1186/2046-4053-4-1 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Shamseer L, Moher D, Clarke M, et al. Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015: elaboration and explanation. BMJ 2015;349:g7647 10.1136/bmj.g7647 [DOI] [PubMed] [Google Scholar]
  • 16. Liberati A, Altman DG, Tetzlaff J, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. J Clin Epidemiol 2009;62:e1–34. 10.1016/j.jclinepi.2009.06.006 [DOI] [PubMed] [Google Scholar]
  • 17. Moher D, Liberati A, Tetzlaff J, et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. PLoS Med 2009;6:e1000097 10.1371/journal.pmed.1000097 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18. Kondo Y, Fuke R, Hifumi T, et al. Early rehabilitation for the prevention of postintensive care syndrome in critically ill patients: a study protocol for a systematic review and meta-analysis. BMJ Open 2017;7:e013828 10.1136/bmjopen-2016-013828 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Paternostro-Sluga T, Grim-Stieger M, Posch M, et al. Reliability and validity of the Medical Research Council (MRC) scale and a modified scale for testing muscle strength in patients with radial palsy. J Rehabil Med 2008;40:665–71. 10.2340/16501977-0235 [DOI] [PubMed] [Google Scholar]
  • 20. Yang ZZ, Grote DM, Xiu B, et al. TGF-β upregulates CD70 expression and induces exhaustion of effector memory T cells in B-cell non-Hodgkin’s lymphoma. Leukemia 2014;28:1872–84. 10.1038/leu.2014.84 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. Mozzi A, Meregaglia M, Lazzaro C, et al. A comparison of EuroQol 5-Dimension health-related utilities using Italian, UK, and US preference weights in a patient sample. Clinicoecon Outcomes Res 2016;8:267–74. 10.2147/CEOR.S98226 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Obradovic M, Lal A, Liedgens H. Validity and responsiveness of EuroQol-5 dimension (EQ-5D) versus Short Form-6 dimension (SF-6D) questionnaire in chronic pain. Health Qual Life Outcomes 2013;11:110 10.1186/1477-7525-11-110 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23. Yang X, Fan D, Xia Q, et al. The health-related quality of life of ankylosing spondylitis patients assessed by SF-36: a systematic review and meta-analysis. Qual Life Res 2016;25:2711–23. 10.1007/s11136-016-1345-z [DOI] [PubMed] [Google Scholar]
  • 24. Jpt H. Chapter 8: Assessing risk of bias in included studies. 2011.
  • 25. Duan EH, Oczkowski SJ, Belley-Cote E, et al. β-Blockers in sepsis: protocol for a systematic review and meta-analysis of randomised control trials. BMJ Open 2016;6:e012466 10.1136/bmjopen-2016-012466 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26. Klotz R, Klaiber U, Grummich K, et al. Percutaneous versus surgical strategy for tracheostomy: protocol for a systematic review and meta-analysis of perioperative and postoperative complications. Syst Rev 2015;4:105 10.1186/s13643-015-0092-5 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27. Brummel NE, Girard TD, Ely EW, et al. Feasibility and safety of early combined cognitive and physical therapy for critically ill medical and surgical patients: the Activity and Cognitive Therapy in ICU (ACT-ICU) trial. Intensive Care Med 2014;40:370–9. 10.1007/s00134-013-3136-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28. Jones C, Eddleston J, McCairn A, et al. Improving rehabilitation after critical illness through outpatient physiotherapy classes and essential amino acid supplement: a randomized controlled trial. J Crit Care 2015;30:901–7. 10.1016/j.jcrc.2015.05.002 [DOI] [PubMed] [Google Scholar]
  • 29. Kayambu G, Boots R, Paratz J. Early physical rehabilitation in intensive care patients with sepsis syndromes: a pilot randomised controlled trial. Intensive Care Med 2015;41:865–74. 10.1007/s00134-015-3763-8 [DOI] [PubMed] [Google Scholar]
  • 30. Schweickert WD, Pohlman MC, Pohlman AS, et al. Early physical and occupational therapy in mechanically ventilated, critically ill patients: a randomised controlled trial. Lancet 2009;373:1874–82. 10.1016/S0140-6736(09)60658-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. Hodgson CL, Bailey M, Bellomo R, et al. A binational multicenter pilot feasibility randomized controlled trial of early goal-directed mobilization in the ICU. Crit Care Med 2016;44:1145–52. 10.1097/CCM.0000000000001643 [DOI] [PubMed] [Google Scholar]
  • 32. Morris PE, Berry MJ, Files DC, et al. Standardized rehabilitation and hospital length of stay among patients with acute respiratory failure: a randomized clinical trial. JAMA 2016;315:2694–702. 10.1001/jama.2016.7201 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33. Stiller K. Physiotherapy in intensive care: an updated systematic review. Chest 2013;144:825–47. 10.1378/chest.12-2930 [DOI] [PubMed] [Google Scholar]
  • 34. Kayambu G, Boots R, Paratz J. Physical therapy for the critically ill in the ICU: a systematic review and meta-analysis. Crit Care Med 2013;41:1543–54. 10.1097/CCM.0b013e31827ca637 [DOI] [PubMed] [Google Scholar]
  • 35. Tipping CJ, Harrold M, Holland A, et al. The effects of active mobilisation and rehabilitation in ICU on mortality and function: a systematic review. Intensive Care Med 2017;43 10.1007/s00134-016-4612-0 [DOI] [PubMed] [Google Scholar]
  • 36. Castro-Avila AC, Serón P, Fan E, et al. Effect of Early Rehabilitation during Intensive Care Unit Stay on Functional Status: Systematic Review and Meta-Analysis. PLoS One 2015;10:e0130722 10.1371/journal.pone.0130722 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. Denehy L, Skinner EH, Edbrooke L, et al. Exercise rehabilitation for patients with critical illness: a randomized controlled trial with 12 months of follow-up. Crit Care 2013;17:R156 10.1186/cc12835 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38. Moss M, Nordon-Craft A, Malone D, et al. A randomized trial of an intensive physical therapy program for patients with acute respiratory failure. Am J Respir Crit Care Med 2016;193:1101–10. 10.1164/rccm.201505-1039OC [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39. Greening NJ, Williams JE, Hussain SF, et al. An early rehabilitation intervention to enhance recovery during hospital admission for an exacerbation of chronic respiratory disease: randomised controlled trial. BMJ 2014;349:g4315 10.1136/bmj.g4315 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40. Cameron JI, Chu LM, Matte A, et al. One-Year outcomes in caregivers of critically ill patients. N Engl J Med 2016;374:1831–41. 10.1056/NEJMoa1511160 [DOI] [PubMed] [Google Scholar]
  • 41. Woon FL, Dunn CB, Hopkins RO. Predicting cognitive sequelae in survivors of critical illness with cognitive screening tests. Am J Respir Crit Care Med 2012;186:333–40. 10.1164/rccm.201112-2261OC [DOI] [PubMed] [Google Scholar]
  • 42. Pandharipande PP, Girard TD, Jackson JC, et al. Long-term cognitive impairment after critical illness. N Engl J Med 2013;369:1306–16. 10.1056/NEJMoa1301372 [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Supplementary data

bmjopen-2017-019998supp001.pdf (204.6KB, pdf)

Supplementary data

bmjopen-2017-019998supp002.pdf (325KB, pdf)

Reviewer comments
Author's manuscript

Articles from BMJ Open are provided here courtesy of BMJ Publishing Group

RESOURCES